547 results
Search Results
2. Guideline for the laboratory diagnosis of iron deficiency in adults (excluding pregnancy) and children.
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Fletcher, Andrew, Forbes, Adam, Svenson, Nicola, and Wayne Thomas, D.
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IRON deficiency ,CLINICAL pathology ,IRON deficiency anemia ,LIQUID chromatography-mass spectrometry ,ACUTE phase proteins - Abstract
Recommendations Serum ferritin of <12 g/l in children aged < 5 years and <15 g/l in those aged > 5 years is indicative of iron deficiency (1B) Serum ferritin within the laboratory reference range cannot exclude iron deficiency in the context of raised inflammatory markers or a history of acute or chronic disease, so further investigation may be warranted (2B) Iron studies: serum iron, total iron binding capacity (TIBC) and transferrin saturation (TSAT... Serum iron Serum iron measures only the oxidised ferric form bound to transferrin and not the functional iron component of Hb. Recommendation Inspection of a peripheral blood film should be performed in cases of diagnostic uncertainty (2C) Serum ferritin Ferritin represents the main bulk of protein-bound tissue iron storage. Clin Chem. 1991; 37: 484 - 5. 28 Romslo I, Talstad I. Day-to-day variations in serum iron, serum iron binding capacity, serum ferritin and erythrocyte protoporphyrin concentrations in anaemic subjects. Keywords: iron; anaemia; haemoglobin; ferritin; iron deficiency EN iron anaemia haemoglobin ferritin iron deficiency 523 529 7 01/28/22 20220201 NES 220201 Methodology This Good Practice Paper was compiled according to the British Society for Haematology (BSH) process at: https://b-s-h.org.uk/media/16732/bsh-guidance-development-process-dec-5-18.pdf. [Extracted from the article]
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- 2022
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3. Comment on the paper by Ebrahimi et al published in Journal of Oral Pathology & Medicine, 2011; 40: 281-285.
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Ögmundsdóttir, Helga M. and Holbrook, W. Peter
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LETTERS to the editor , *ORAL medicine , *ORAL mucosa diseases , *ORAL cancer , *P53 protein , *LICHEN planus , *CLINICAL pathology - Published
- 2011
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4. Electronic charting of transfusion medicine consults: implementation, challenges and opportunities.
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Mohammad, Mohammad K., Wooten, Melanie S., Maier, Cheryl L., Hill, Charles E., Guarner, Jeannette, Roback, John D., Winkler, Anne M., and Sullivan, Harold C.
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BLOOD transfusion ,WEB-based user interfaces ,CLINICAL pathology ,ACCESS to information ,CLINICAL chemistry - Abstract
Background: The Joint Commission lists improving staff communication (handoffs) as part of several National Safety Goals. In this study, we developed an electronic web‐based charting system for clinical pathology handoffs, which primarily consist of transfusion medicine calls, and evaluated the advantages over a paper‐based handwritten call log. Materials and Methods: A secure online web browser application using Research Electronic Data Capture (REDCap) was designed to document on‐call pathology resident consults. A year after implementation, an online survey was administered to our pathology residents in order to evaluate and compare the usability of the electronic application (e‐consults) to the previous handwritten call log, which was a notebook where trainees hand wrote different components of the consult. Results: The REDCap web‐based application includes discrete fields for patients' information, requesting physician contact, type of consult, action items for follow‐up and faculty responses, as well as other information. These components have eventually progressed to be an online consult call catalog. With approximately 1079 consults per year, transfusion medicine‐related calls account for ~90% of the encounters, while clinical chemistry, microbiology and immunology calls constitute the remainder. The overall response rate of the survey was 96% (29 of 30 participants). Of the 16 respondents who experienced both call log systems, 100% responded that REDCap was an improvement over the handwritten call log (P < 0·0001). Conclusion: E‐consult documentation entered into a web‐based application was a user‐friendly, secure clinical information access and effective handoff system as compared to a paper‐based handwritten call log. [ABSTRACT FROM AUTHOR]
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- 2020
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5. Recommendations for cellular and molecular pathology input into clinical trials: a systematic review and meta‐aggregation.
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Lim, Shujing Jane, Gurusamy, Kurinchi, O'Connor, Daniel, Shaaban, Abeer M, Brierley, Daniel, Lewis, Ian, Harrison, David, Kendall, Timothy James, and Robinson, Max
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CLINICAL pathology ,CELLULAR pathology ,CLINICAL trials ,MOLECULAR pathology ,META-analysis ,EXPERIMENTAL design ,MEDICAL protocols ,THEMATIC analysis - Abstract
The SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013 Statement was developed to provide guidance for inclusion of key methodological components in clinical trial protocols. However, these standards do not include guidance specific to pathology input in clinical trials. This systematic review aims to synthesise existing recommendations specific to pathology practice in clinical trials for implementation in trial protocol design. Articles were identified from database searches and deemed eligible for inclusion if they contained: (1) guidance and/or a checklist, which was (2) pathology‐related, with (3) content relevant to clinical trial protocols or could influence a clinical trial protocol design from a pathology perspective and (4) were published in 1996 or later. The quality of individual papers was assessed using the AGREE‐GRS (Appraisal of Guidelines for REsearch & Evaluation – Global Rating Scale) tool, and the confidence in cumulative evidence was evaluated using the GRADE‐CERQual (Grading of Recommendations Assessment, Development and Evaluation–Confidence in Evidence from Reviews of Qualitative research) approach. Extracted recommendations were synthesised using the best fit framework method, which includes thematic analysis followed by a meta‐aggregative approach to synthesis within the framework. Of the 10 184 records screened and 199 full‐text articles reviewed, only 40 guidance resources met the eligibility criteria for inclusion. Recommendations extracted from 22 guidance documents were generalisable enough for data synthesis. Seven recommendation statements were synthesised as follows: (1) multidisciplinary collaboration in trial design with early involvement of pathologists, particularly with respect to the use of biospecimens and associated biomarker/analytical assays and in the evaluation of pathology‐related parameters; (2) funding and training for personnel undertaking trial work; (3) selection of an accredited laboratory with suitable facilities to undertake scheduled work; (4) quality assurance of pathology‐related parameters; (5) transparent reporting of pathology‐related parameters; (6) policies regarding informatics and tracking biospecimens across trial sites; and (7) informed consent for specimen collection and retention for future research. [ABSTRACT FROM AUTHOR]
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- 2021
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6. A meta‐analysis of SARS‐CoV‐2 patients identifies the combinatorial significance of D‐dimer, C‐reactive protein, lymphocyte, and neutrophil values as a predictor of disease severity.
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Singh, Kunwar, Mittal, Sasha, Gollapudi, Sumanth, Butzmann, Alexandra, Kumar, Jyoti, and Ohgami, Robert S.
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C-reactive protein ,CLINICAL pathology ,BIOMARKERS ,ONLINE information services ,DISEASE progression ,COVID-19 ,SARS-CoV-2 ,META-analysis ,MULTIPLE regression analysis ,PROGNOSIS ,NEUTROPHILS ,SEVERITY of illness index ,MEDLINE ,LYMPHOCYTE count ,FIBRIN fibrinogen degradation products - Abstract
Background: Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), known to be the causative agent of COVID‐19, has led to a worldwide pandemic. At presentation, individual clinical laboratory blood values, such as lymphocyte counts or C‐reactive protein (CRP) levels, may be abnormal and associated with disease severity. However, combinatorial interpretation of these laboratory blood values, in the context of COVID‐19, remains a challenge. Methods: To assess the significance of multiple laboratory blood values in patients with SARS‐CoV‐2 and develop a COVID‐19 predictive equation, we conducted a literature search using PubMed to seek articles that included defined laboratory data points along with clinical disease progression. We identified 9846 papers, selecting primary studies with at least 20 patients for univariate analysis to identify clinical variables predicting nonsevere and severe COVID‐19 cases. Multiple regression analysis was performed on a training set of patient studies to generate severity predictor equations, and subsequently tested on a validation cohort of 151 patients who had a median duration of observation of 14 days. Results: Two COVID‐19 predictive equations were generated: one using four variables (CRP, D‐dimer levels, lymphocyte count, and neutrophil count), and another using three variables (CRP, lymphocyte count, and neutrophil count). In adult and pediatric populations, the predictive equations exhibited high specificity, sensitivity, positive predictive values, and negative predictive values. Conclusion: Using the generated equations, the outcomes of COVID‐19 patients can be predicted using commonly obtained clinical laboratory data. These predictive equations may inform future studies evaluating the long‐term follow‐up of COVID‐19 patients. [ABSTRACT FROM AUTHOR]
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- 2021
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7. Highlights of recent clinically relevant papers.
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Wright, S.
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VETERINARY medicine ,HORSE diseases ,CLINICAL pathology ,DISEASE prevalence ,RETROSPECTIVE studies - Published
- 2018
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8. Unsupervised EHR‐based phenotyping via matrix and tensor decompositions.
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Becker, Florian, Smilde, Age K., and Acar, Evrim
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MATRIX decomposition ,ELECTRONIC health records ,NONNEGATIVE matrices ,MACHINE learning ,CLINICAL pathology ,INDIVIDUALIZED medicine - Abstract
Computational phenotyping allows for unsupervised discovery of subgroups of patients as well as corresponding co‐occurring medical conditions from electronic health records (EHR). Typically, EHR data contains demographic information, diagnoses and laboratory results. Discovering (novel) phenotypes has the potential to be of prognostic and therapeutic value. Providing medical practitioners with transparent and interpretable results is an important requirement and an essential part for advancing precision medicine. Low‐rank data approximation methods such as matrix (e.g., nonnegative matrix factorization) and tensor decompositions (e.g., CANDECOMP/PARAFAC) have demonstrated that they can provide such transparent and interpretable insights. Recent developments have adapted low‐rank data approximation methods by incorporating different constraints and regularizations that facilitate interpretability further. In addition, they offer solutions for common challenges within EHR data such as high dimensionality, data sparsity and incompleteness. Especially extracting temporal phenotypes from longitudinal EHR has received much attention in recent years. In this paper, we provide a comprehensive review of low‐rank approximation‐based approaches for computational phenotyping. The existing literature is categorized into temporal versus static phenotyping approaches based on matrix versus tensor decompositions. Furthermore, we outline different approaches for the validation of phenotypes, that is, the assessment of clinical significance. This article is categorized under:Algorithmic Development > Structure DiscoveryFundamental Concepts of Data and Knowledge > Explainable AITechnologies > Machine Learning [ABSTRACT FROM AUTHOR]
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- 2023
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9. Distribution–free hyperrectangular tolerance regions for setting multivariate reference regions in laboratory medicine.
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Liu, Wei, Bretz, Frank, and Cortina–Borja, Mario
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CLINICAL pathology , *KIDNEY physiology - Abstract
Reference regions are important in laboratory medicine to interpret the test results of patients, and usually given by tolerance regions. Tolerance regions of p (≥2)$$ p\;\left(\ge 2\right) $$ dimensions are highly desirable when the test results contains p$$ p $$ outcome measures. Nonparametric hyperrectangular tolerance regions are attractive in real problems due to their robustness with respect to the underlying distribution of the measurements and ease of intepretation, and methods to construct them have been recently provided by Young and Mathew [Stat Methods Med Res. 2020;29:3569‐3585]. However, their validity is supported by a simulation study only. In this paper, nonparametric hyperrectangular tolerance regions are constructed by using Tukey's [Ann Math Stat. 1947;18:529‐539; Ann Math Stat. 1948;19:30‐39] elegant results of equivalence blocks. The validity of these new tolerance regions is proven mathematically in [Ann Math Stat. 1947;18:529‐539; Ann Math Stat. 1948;19:30‐39] under the only assumption that the underlying distribution of the measurements is continuous. The methodology is applied to analyze the kidney function problem considered in Young and Mathew [Stat Methods Med Res. 2020;29:3569‐3585]. [ABSTRACT FROM AUTHOR]
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- 2024
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10. An analytical model for 2D consolidation of unsaturated soil with semi‐permeable boundaries considering self‐weight stress and time‐dependent loading.
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Liu, Yang, Zheng, Jun‐Jie, and Lu, Jia‐Tai
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SOIL consolidation ,SEPARATION of variables ,ANALYTICAL solutions ,CLINICAL pathology ,DRAINAGE - Abstract
This paper proposes an analytical solution for 2D (two‐dimensional) consolidation of unsaturated soil with impeded drainage boundaries by considering the combined effects of self‐weight stress of soil and time‐dependent loading. The governing equation of the 2D consolidation model was first formulated, followed by an analytical solution employing the methods of the Laplace transform technique and separation of variables. The solution is then degraded to validate the correctness against two classical lab tests and existing solutions. Subsequently, the proposed solution is further verified against finite element calculations. The results indicate that the self‐weight stress of soil acts as an additional load applied to the unsaturated soil, the larger the self‐weight stress, the greater the value of initial EPPs (excess pore pressures). Meanwhile, it can be easily found that the larger the value of self‐weight stress, the larger the consolidation settlement. Without accounting for the effect of self‐weight stress, the settlement of the soil will certainly be underestimated and the dissipation characteristics of EPPs will not be accurately captured. It can be also found that the ratio of ka/kw also significantly influenced the consolidation behavior. [ABSTRACT FROM AUTHOR]
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- 2023
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11. Taking after a parent: Phenotypic resemblance and the professional familialisation of genomics.
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Hedgecoe, Adam, Job, Kathleen, and Clarke, Angus
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CLINICAL pathology , *SEQUENCE analysis , *SOCIOLOGY , *GENETIC counselors , *UNCERTAINTY , *DOCUMENTATION , *GENOMICS , *DESCRIPTIVE statistics , *PHOTOGRAPHY , *GENETIC markers , *RESEARCH funding , *DECISION making in clinical medicine , *ETHNOLOGY , *GENETIC counseling , *PARENTS , *PHENOTYPES - Abstract
This article draws on 2 years' worth of ethnographic observation of team meetings to explore decision‐making in an NHS clinical genomics service. The focus of discussions was on ambiguous genomic results known as VUS or Variants of Uncertain Significance, which may be pathogenic but which also may turn out to be benign. In examining decision‐making around such results, we note how, in contrast to much policy and promotional material in this area, clinicians in these meetings (clinical geneticists and genetic counsellors) place great emphasis on parental phenotypes and whether the parents of a patient share the symptoms and signs of the suspected condition. This information is then combined with the result of genomic tests to decide whether the variant a patient has is responsible for their condition. This article explores the way in which clinicians attempt to flexibly enrol parents into genomic explanations through informal diagnosis of their possible phenotypes and the way in which actually meeting parents allows some clinicians to trump explanations based on documentary or photographic data. The paper sheds light on the way that earlier scholarly understandings of such decisions (around, say dysmorphology) remain relevant and explores claims that laboratory tests overrule clinical decision‐making. [ABSTRACT FROM AUTHOR]
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- 2024
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12. Systematic and scoping reviews to assess biological parameters.
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Feres, Magda, M. Duarte, Poliana, Figueiredo, Luciene C., Gonçalves, Cristiane, Shibli, Jamil, and Retamal‐Valdes, Belen
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CLINICAL pathology ,SYSTEMATIC reviews ,ORAL health ,PERIODONTITIS ,LITERATURE reviews ,DENTISTRY ,PERI-implantitis - Abstract
Introduction: An evidence synthesis approach compiling biological/laboratory data is effective in advancing health‐related knowledge. However, this approach is still underused in the oral health field. Methods: This commentary discusses the opportunities and challenges of systematic and scoping reviews of laboratory data in dentistry. Special focus is on the potential of these reviews to elucidate etiological and treatment concepts of oral diseases, such as periodontitis and peri‐implantitis. Results: The following difficulties associated with such studies are discussed: (i) selection of ideal study design, (ii) assessment of "risk of bias" and definition of "certainty of evidence", (iii) evidence assembly and summary, and (iv) the paper review process. Discussion: Despite those challenges, high‐quality reviews integrating laboratory data may generate relevant scientific information and help identify new avenues for future investigations. Experts in different oral health topics should build a process capable of helping researchers assemble and interpret these types of data. [ABSTRACT FROM AUTHOR]
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- 2022
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13. Facilitating the adoption of high‐throughput sequencing technologies as a plant pest diagnostic test in laboratories: A step‐by‐step description.
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Lebas, Benedicte, Adams, Ian, Al Rwahnih, Maher, Baeyen, Steve, Bilodeau, Guillaume J., Blouin, Arnaud G., Boonham, Neil, Candresse, Thierry, Chandelier, Anne, De Jonghe, Kris, Fox, Adrian, Gaafar, Yahya Z. A., Gentit, Pascal, Haegeman, Annelies, Ho, Wellcome, Hurtado‐Gonzales, Oscar, Jonkers, Wilfried, Kreuze, Jan, Kutjnak, Denis, and Landa, Blanca
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PLANT parasites ,CLINICAL pathology ,NUCLEOTIDE sequencing ,PHYTOSANITATION ,SHOTGUN sequencing ,IMPORT quotas ,WEEDS ,WOLBACHIA - Abstract
Copyright of EPPO Bulletin is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2022
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14. Serious consequences of Epstein‐Barr virus infection: Hemophagocytic lymphohistocytosis.
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Xu, Lingyue, Guo, Xiaofang, and Guan, Hongzai
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HIV infections ,CLINICAL pathology ,HEMOPHAGOCYTIC lymphohistiocytosis ,GRAFT versus host disease ,DIFFERENTIAL diagnosis ,GENETIC testing ,MOLECULAR biology ,CYTOGENETICS ,EPSTEIN-Barr virus diseases ,DISEASE complications - Abstract
Human is the host of the Epstein‐Barr virus (EBV) especially in childhood and adolescence. Most of them are asymptomatic infection and self‐limiting. However, for those patients who suffer from immune dysfunction, EBV infection will be life‐threatening. Epstein‐Barr virus‐associated hemophagocytic lymphohistocytosis (EBV‐HLH) is one of the severe effects. The diagnosis and differential diagnosis of EBV‐HLH and other EBV infectious diseases are mentioned in this paper. The molecular biology mechanism and complications of EBV‐HLH are equally briefly presented. It also provides a practical method for the genetic diagnosis of such diseases and the differential diagnosis with other human immunodeficiency diseases for medical scientists in routine clinical practice. [ABSTRACT FROM AUTHOR]
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- 2022
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15. Clinicopathological analysis and survival outcomes of primary salivary gland tumors in pediatric patients: A systematic review.
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Louredo, Brendo Vinícius Rodrigues, Santos‐Silva, Alan Roger, Vargas, Pablo Agustin, Ajudarte Lopes, Márcio, Martins, Manoela Domingues, Guerra, Eliete Neves da Silva, Prado Ribeiro, Ana Carolina, Brandão, Thaís Bianca, Mendonça, Regina Maria Holanda, Kowalski, Luiz Paulo, Speight, Paul M., Khurram, Syed Ali, and Pérez‐de‐Oliveira, Maria Eduarda
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CLINICAL pathology ,SALIVARY gland tumors ,CHILD patients ,SYSTEMATIC reviews ,SURVIVAL analysis (Biometry) ,SURVIVAL rate ,PROGRESSION-free survival - Abstract
Background: Salivary gland tumors are a diverse group of uncommon neoplasms that are rare in pediatric patients. The aim of this study was to evaluate the clinicopathological profile and survival outcomes of pediatric patients affected by salivary gland tumors. Materials and methods: An extensive search was carried out using the MEDLINE/PubMed, EMBASE, Scopus databases, and grey literature. The risk of bias was available in all papers included. Results: A total of 2,830 articles were initially retrieved with 54 remaining for data extraction, resulting in 2,937 cases. This comprised forty‐five case series' and nine cohort studies. These tumors were slightly more prevalent in females (57.4%). The patients' age ranged from 0.3 to 19 years old, with a mean age of 13.3 years. Parotid was the most affected site (81.9%), and 99.2% of cases clinically exhibited a swelling. Presence of pain/tenderness was reported in 13.5% of the cases, with an average duration of 12.6 months for the appearance of symptoms. Most of the reported cases were malignant tumors (75.4%), with mucoepidermoid carcinoma the most common tumor of all tumors (44.8%), followed by pleomorphic adenoma (24.1%). Surgery alone was the leading treatment choice in 74.9% cases, and the 5‐year overall survival rate of patients was 93.1%. Patients with symptoms (P =.001), local recurrence (P <.001), metastasis (P <.001), and those not undergoing surgery or surgery combined with radiotherapy (P <.001) showed lower survival rates. Conclusion: The pediatric patients present a high frequency of malignant salivary neoplasms and a high overall survival rate. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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16. Animal models of rheumatoid arthritis‐associated interstitial lung disease.
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Xiong, Li, Xiong, Liang, Ye, Hong, and Ma, Wan‐Li
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ANIMAL models in research ,PULMONARY fibrosis ,ANIMAL disease models ,INTERSTITIAL lung diseases ,RHEUMATOID arthritis ,CLINICAL pathology - Abstract
Background: Rheumatoid arthritis‐associated interstitial lung disease (RA‐ILD) is an irreversible pathologic condition of unknown cause, commonly involving the joint and the lung with variable amounts of fibrotic change. In contrast to rheumatoid arthritis or other chronic interstitial lung diseases such as interstitial pulmonary fibrosis, there is so far no extensively accepted or implemented animal model for this disease. Aims: To provide guidance for those who are investigating the pathogenesis of RA‐ILD with animal models. Materials and Methods: An analysis of papers from PubMed during 1978‐2020. Results: We outline the present status quo for animal models of RA‐ILD about their modeling methods and pathogenesis, compare their pros and cons with respect to their ability to mimic the clinical and histological features of human disease and discuss their applicability for future research. Discussion: There is no doubt that these animal models do provide valuable information relating to the pathogenesis of RA‐ILD and the development of effective therapeutic drugs. Nevertheless, these animal models can not entirely recapitulate clinical pathology and have some limitations in experimental research application. Therefore, it should be emphasized that we should improve and explore animal models in more accordance with the pathogenesis and clinical characteristics of human RA‐ILD. Conclusion: These established animal models of the disease can significantly progress our understanding of the etiology of RA‐ILD, the fundamental mechanisms of its pathogenesis and the identification of new bio‐markers, and can contribute to the development and implementation of novel treatment strategies. [ABSTRACT FROM AUTHOR]
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- 2021
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17. Performance assessment of medical diagnostic laboratories: A network DEA approach.
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Ghafari Someh, Niloufar, Pishvaee, Mir Saman, Sadjadi, Seyed Jafar, and Soltani, Roya
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CLINICAL pathology ,HOSPITAL laboratories ,MEDICAL care costs ,QUALITY assurance ,DECISION making in clinical medicine - Abstract
Rationale, aims, and objectives: The main purpose of this paper is to measure the efficiency and ranking of medical diagnostic laboratories by applying a network data envelopment analysis (NDEA). Methods: In this study, each medical diagnostic laboratory is considered as a decision‐making unit (DMU), and an NDEA model is utilized to calculate the efficiency of each medical diagnostic laboratory. Therefore, we design a series of four‐stage system composed of three main laboratory processes (the pretest process, the test process, and the posttest process). We also consider sustainability criteria in order to cover social, economic, and environmental problems of health care organizations. Results: The results show that three of the 22 considered laboratories are efficient. Therefore, the NDEA approach can lead to performance scores and ultimately real ranking. Also, the average efficiency scores show that the decrease of the reception unit's efficiency results in a decrease of the efficiency of each laboratory. Therefore, the laboratories can increase the number of patients. Along with the intermediate values of the reception unit and the sampling unit, the efficiency of the reception unit increases, which results in an increase for the overall efficiency of each laboratory. Conclusion: The proposed model can appropriately help the administrators and managers to identify inefficient units in their laboratory and ultimately improve the laboratory performance. [ABSTRACT FROM AUTHOR]
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- 2020
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18. Hemolysis interference in 10 coagulation assays on an instrument with viscosity‐based, chromogenic, and turbidimetric clot detection.
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Hedeland, Ylva, Gustafsson, Christina M., Touza, Zinah, and Ridefelt, Peter
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BLOOD coagulation factors ,BLOOD coagulation tests ,BLOOD plasma ,CLINICAL pathology ,DIAGNOSTIC errors ,FIBRIN ,HEMOGLOBINS ,HEMOLYSIS & hemolysins ,DESCRIPTIVE statistics ,PARTIAL thromboplastin time ,PROTHROMBIN time - Abstract
Introduction: Hemolysate in plasma samples from patients may cause misleading results in coagulation assays. Even though modern coagulation instruments often are equipped with modules that can detect hemolysis, icterus, and lipemia (HIL), studies that report the influence of these interferences are still limited. The present paper focuses on the influence of hemolysis on 10 coagulation assays. Methods: Artificial hemolysis was created by freezing/thawing, and the hemolysates generated were added to pools of patient plasma. Pathological and normal levels were pooled separately. These spiked samples were analyzed on a STA R Max 2 instrument. The coagulation assays evaluated utilize clot, chromogenic, or immunoturbidimetric detection. Results: Four of the evaluated assays were not influenced by hemolysis: fibrinogen, von Willebrand factor antigen, activated partial thromboplastin time, and factor VIII. Interestingly, normal and slightly elevated prothrombin time (INR < 2.0) was insensitive to hemolysis, whereas samples with a high INR (≥2.0) exhibited falsely high readings. The assays for antithrombin and fibrin D‐dimer displayed an intermediate sensitivity to hemolysis. The most sensitive assay turned out to be anti‐Xa, followed by protein C and protein S. For the anti‐Xa assay, the results are decreased by 10% already at 0.5 g/L hemoglobin. Conclusion: The present study shows that hemolysis affects several of commonly used coagulation assays. Since the sensitivity for hemolysis is dependent on the brand of the assay as well as the instrument and principle of measurement, it is necessary to evaluate the influence of each specific combination. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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19. High‐precision attitude determination and control system design and real‐time verification for CubeSats.
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Gaber, Khaled, El_Mashade, Mohamed B., and Abdel Aziz, Ghada A.
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REAL-time control ,GYROSCOPES ,CLINICAL pathology - Abstract
Summary: This paper presents the design and real‐time verification of a high‐precision and low‐cost attitude determination and control system (ADCS) for CubeSat based on a micro‐electro‐mechanical (MEMS) gyroscope. The CubeSat new missions require accurate and sophisticated ADCS with attitude drift adjustment. Moreover, designing an effective ADCS for the CubeSat poses a difficult challenge. The satellite comprises of a two‐unit CubeSat, which denotes that the ADCS is designed with small size, tight mass, and energy limitations. The ADCS has been enhanced in the former few years from fairly small resolution of 10 to around 0.6 m. This attitude drift, if not properly compensated, will cause a slow attitude information loss as the error in attitude rises between the actual and estimated. To correct the attitude adrift, the proposed system utilizes a MEMS gyroscope sensor which offers a comparative attitude to the Kalman filter for estimated attitude update. Real‐time verification and validation for the ADCS are performed through Matlab/Simulink environment and lab testing to prove the efficacy of the proposed system. Simulation of the ADCS shows accurate results with error of no more than 1°. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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20. The objective function controversy for group testing: Much ado about nothing?
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Hitt, Brianna D., Bilder, Christopher R., Tebbs, Joshua M., and McMahan, Christopher S.
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COMMUNICABLE diseases ,BEST practices ,CLINICAL pathology ,DIAGNOSTIC specimens ,GROUP size ,ALGORITHMS - Abstract
Group testing is an indispensable tool for laboratories when testing high volumes of clinical specimens for infectious diseases. An important decision that needs to be made prior to implementation is determining what group sizes to use. In best practice, an objective function is chosen and then minimized to determine an optimal set of these group sizes, known as the optimal testing configuration (OTC). There are a few options for objective functions, and they differ based on how the expected number of tests, assay characteristics, and testing constraints are taken into account. These varied options have led to a recent controversy in the literature regarding which of two different objective functions is better. In our paper, we examine these objective functions over a number of realistic situations for infectious disease testing. We show that this controversy may be much ado about nothing because the OTCs and corresponding results (eg, number of tests and accuracy) are largely the same for standard testing algorithms in a wide variety of situations. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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21. Dataset for reporting of carcinoma of the urethra (in urethrectomy specimens): recommendations from the International Collaboration on Cancer Reporting (ICCR).
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Shanks, Jonathan H, Srigley, John R, Brimo, Fadi, Comperat, Eva, Delahunt, Brett, Koch, Michael, Lopez‐Beltran, Antonio, Reuter, Victor E, Samaratunga, Hemamali, Tsuzuki, Toyonori, Kwast, Theo, Varma, Murali, and Grignon, David
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URETHRA ,CARCINOMA ,CLINICAL pathology ,CANCER ,PATHOLOGISTS ,PHYSICIANS - Abstract
The International Collaboration on Cancer Reporting (ICCR) is a not‐for‐profit organisation sponsored by the Royal Colleges of Pathologists of Australasia and the United Kingdom, the College of American Pathologists, the Canadian Association of Pathologists in association with the Canadian Partnership Against Cancer, the European Society of Pathology, the American Society of Clinical Pathology and the Faculty of Pathology, Royal College of Physicians of Ireland. Its goal is to produce standardised, internationally agreed‐upon, evidence‐based datasets for cancer pathology reporting throughout the world. This paper describes the development of a cancer dataset by the multidisciplinary ICCR expert panel for the reporting of carcinoma of the urethra in urethrectomy specimens. The dataset is composed of 'required' (mandatory) and 'recommended' (non‐mandatory) elements, which are based on a review of the most recent evidence and supported by explanatory commentary. Fourteen required elements and eight recommended elements were agreed by the international dataset authoring committee to represent the essential/required (core) and recommended (non‐core) information for the reporting of carcinoma of the urethra in urethrectomy specimens. Use of an internationally agreed, structured pathology dataset for reporting carcinoma of the urethra (in urethrectomy specimens) will provide the necessary information for optimal patient management, will facilitate consistent data collection and will provide valuable data for research and international benchmarking. The dataset will be valuable for those countries and institutions that are not in a position to develop their own datasets. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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22. Evidence‐based criteria for palaeopathological recognition: New methodology suggests that the rotator cuff condition will be amenable to reliable identification in the archeologic record.
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Rothschild, Bruce M.
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ROTATOR cuff ,VALUE engineering ,DEMOGRAPHIC surveys ,MEDICAL literature ,CLINICAL pathology - Abstract
Purpose/research question: Pitting or new bone formation on or around tendon insertions, marginal osteophytes, eburnation, cystic changes, and altered contours have been utilized by some palaeopathologists for recognition of the rotator cuff condition, with the purpose of this paper to evaluate the reliability for diagnosis (sensitivity and specificity) of these criteria as documented in the clinical literature. Materials and methods: The spectrum of medical literature is examined without time limitation, utilizing the phrase "rotator cuff" to assess criteria utilized for diagnosis of a rotator cuff conditions, the reliability of those criteria, and the relationship to symptoms and limitations/disability. Results: None of the skeletal features previously referred to by palaeopathologists have reliable indicators for recognition and may simply be age‐related phenomena. New methodology is described, offering the opportunity for confident diagnosis. Conclusions: There have been no validated evidence‐based criteria applicable for recognizing rotator cuff conditions in skeletons, in the absence of soft tissue structures. Greater tuberosity osteopenia has been noted but not yet evaluated for specificity. Rotator cuff conditions may actually be unrelated to lifestyle but may simply represent the accumulation/culmination of lifetime stresses (aging). The ratio of acromial lateral extension and height provides greater opportunity for confident diagnosis. Given the disconnection between presence or extent of pathology and clinical symptoms and limitations/disability, identification of any of the components utilized in previous consideration of rotator cuff disease diagnosis does not permit extrapolation to confidently hypothesize lifestyle or occupation. Contribution to knowledge/originality/value: Documents a methodology for confident diagnosis of rotator cuff disease and the challenge of confident attribution of skeletal conditions and clinical/lifestyle implications Limitations of this study: Evidence, rather than conjecture/consensus‐based. Suggestions for further research: Population survey utilizing ratio of acromial length extension and height. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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23. History of the Discovery of the Thymosins.
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GOLDSTEIN, ALLAN L.
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THYMOSIN ,THYMUS ,CLINICAL medicine ,IMMUNODEFICIENCY ,PEPTIDES ,MEDICAL sciences ,CLINICAL pathology ,SCIENTISTS ,STUDENTS - Abstract
From a historical perspective, the studies that led to the isolation and characterization of the thymosins began in earnest in the early 1960s in the laboratory of Abraham White at the Albert Einstein College of Medicine in New York. In a 1966 paper in the Proceedings of the National Academy of Sciences, U.S., we first named these thymic-derived factors “Thymosins.” By 1972, the thymosin team had moved to the University of Texas Medical Branch in Galveston (UTMB) where an extremely talented group of young scientists and students succeeded over the next 6 years in preparing and testing a highly active partially purified calf thymus preparation, termed thymosin fraction-5 (TF5), which was amenable for scale-up and suitable for clinical use. In 1974, we received the first IND for a thymic hormone preparation from the FDA to begin a phase-I study with TF5 in children with primary immunodeficiency diseases at the University of California Medical Center in San Francisco. The immunorestorative and potentially life-saving properties of TF5 in clinical medicine were first documented in a landmark paper in 1975 by Drs. Arthur Ammann and Diane Wara in the New England Journal of Medicine. TF5 consists of a family of at least 40 mostly small acidic polypeptides, with molecular weights ranging from 1000 to 15,000 Da. This article will identify the key scientists and the milestones involved in the initial studies with TF5 that have led to the chemical characterization of the thymosins and to translational studies from the lab bench to the clinic. [ABSTRACT FROM AUTHOR]
- Published
- 2007
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24. ORIGINAL ARTICLE Three-dimensional reconstruction of the mucosa from sequential sections of biopsy specimens of patients with ulcerative colitis: Relationship between crypt structure and vascular architecture.
- Author
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Furukawa, Hiroo, Inoue, Fumihiko, Miyake, Naoki, Moriyasu, Takayuki, Moriti, Hisako, and Saiga, Tatuyosi
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ULCERATIVE colitis ,COLITIS ,INFLAMMATORY bowel diseases ,BIOPSY ,DIAGNOSTIC specimens ,CLINICAL pathology - Abstract
In a previous paper, the stereographic reconstruction of the crypt structure of ulcerative colitis using the RATOCK System was described. The relationship between the blood vessels and the crypt structure is the focus of the current paper, using two kinds of tissue staining color in which the color differs. Stereographic images make the relationship between the crypt structure and blood vessel distribution understandable at a glance. The methods used here are identical to those described in a previous paper. In the present paper, five cases of ulcerative colitis (UC) are examined. Biopsy specimens were obtained from the diseased, normal, and transitional zones (the area between the normal and diseased zones) from each patient. Three-dimensional reconstruction was created using TRI for Windows (RATOC System Tokyo, Japan) software. In the present paper, two kinds of dyeing method between H&E and monoclonal antibody staining of the tissue was used. It was proven that the distribution of gland and blood vessel is very clear in the 3-D reconstruction shown. (i) The blood vessels in the normal zones run parallel to the crypt in a regular manner and are almost identical to one another in diameter. (ii) In the transitional and diseased zones, the blood vessels show no clear direction and produce many branches without any apparent order. The blood vessels are, moreover, irregular in diameter. (iii) In short, clear parallelism is lost in both the transitional and diseased zones. Stereographic reconstruction of endoscopically obtained biopsy specimens of UC-affected tissues makes it possible to understand at a glance the distribution of blood vessels and their relationship to crypts. The relationship of these was clarified by the combined use of two kinds of dyeing method with three-dimensional reconstruction. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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25. The original scores of traditional Chinese medicine constitutions are risk and diagnostic factors in middle‐aged and older adults with sarcopenia.
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Nie, Xin, Wang, Chi, Zhang, He, Liu, Qianhui, Hou, Lisha, Deng, Yiping, Ye, Wenbin, Yue, Jirong, and He, Yong
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RISK assessment ,CHINESE medicine ,CROSS-sectional method ,LIFESTYLES ,SELF-evaluation ,MEDICAL history taking ,PREDICTIVE tests ,RESEARCH funding ,RECEIVER operating characteristic curves ,T-test (Statistics) ,QUESTIONNAIRES ,FUNCTIONAL status ,DESCRIPTIVE statistics ,MULTIVARIATE analysis ,MANN Whitney U Test ,CHI-squared test ,HUMAN constitution ,CLINICAL pathology ,ENERGY metabolism ,STATISTICS ,SOCIODEMOGRAPHIC factors ,SARCOPENIA ,REGRESSION analysis ,OLD age ,MIDDLE age - Abstract
Objective: Sarcopenia is a geriatric syndrome that occurs with age and is characterized by a gradual decline in muscle mass, power, and functionality. It serves as a prominent contributor to frailty, disability, and mortality among older individuals. Currently, no standardized global guidelines exist for the diagnosis of sarcopenia. This study aimed to establish the correlation between sarcopenia and the constitutions of traditional Chinese medicine (TCM), considering the connection between physical functioning and sarcopenia. Methods: A total of 1441 participants in this study were diagnosed with sarcopenia. The Asian Working Group for Sarcopenia (AWGS) proposed a sarcopenia definition algorithm. To determine the constitution of each participant, classification and determination standards were used in traditional Chinese medicine. This study evaluated the demographics, lifestyles, and self‐reported medical history of individuals diagnosed with sarcopenia through a self‐administered questionnaire. The constitution of the participants was determined using TCM classification and determination standards. Subsequently, we analyzed the results of univariate analysis and multivariate regression and constructed a receiver operating characteristic (ROC) curve. Results: Participants who were diagnosed with sarcopenia had substantially lower original Neutral constitution scores (P < 0.050). In comparison to those without sarcopenia, individuals with sarcopenia exhibited notably elevated original Qi‐deficiency, Yang‐deficiency, Yin‐deficiency, Blood‐stagnation, and Qi‐stagnation scores in contrast to those in the healthy group (P < 0.050). The identified risk factors associated with sarcopenia included the following: Neutral (OR = 0.903), Qi‐deficiency (in males, OR = 1.126), Yang‐deficiency (OR = 1.062), Phlegm‐dampness (in males, OR = 0.833), and Blood‐stagnation (in females, OR = 1.089). The highest area under the curve (AUC) was observed for the original neutral constitution score, followed by the Yang‐deficiency and blood‐stagnation scores (0.644, 0.613, and 0.611, respectively). Additionally, the AUC for the combined original scores of all nine constitutions among males reached 0.778. Conclusions: In this cross‐sectional study of older people with higher original Qi‐deficiency, Yin deficiency, Yang‐deficiency, Blood‐stagnation, and Qi‐stagnation were associated with sarcopenia. Notably, various TCM constitutions are significantly linked to sarcopenia. There was a significant occurrence of various body constitution types among individuals diagnosed with sarcopenia. The mixture of the nine original constitution scores exhibited good diagnostic performance for sarcopenia in males. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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26. Numerical modeling of fracturing in permeable rocks via a micromechanical continuum model.
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Eghbalian, Mahdad, Wan, Richard, Pouragha, Mehdi, and Fung, Larry S.
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MICROCRACKS ,POROELASTICITY ,BOUNDARY value problems ,LOGNORMAL distribution ,MULTISCALE modeling ,ROCK properties ,CLINICAL pathology - Abstract
Summary: The paper presents a micromechanical approach to describe the failure of low‐permeability brittle rocks as a multiscale fracturing process based on a poroelastic microcrack‐damage model. Failure is formulated deep down at the fine pore scale as a material degradation phenomenon driven by microcrack growth that also impacts upon hydromechanical properties. A set of damage tensors describes the effect of dual‐scale porosities (nanopores and microcracks) on both the hydraulic and poroelastic rock properties. Essentially, the multiscale model reconstructs the coupling effect of hydromechanical forces at the continuum level from the ground up through the upscaling of multiphase interactions at the fundamental structural level of the material. As a result, many macroscopic characteristics emerge naturally such as friction angle, fracture properties, and most importantly, Biot's coefficient taking on a tensorial form that is generally anisotropic. The model is validated within the framework of finite elements to illustrate various baseline constitutive features such as the effect of microcrack growth on the nonlinear stress‐strain response and the induced anisotropy in the context of lab experimental tests and boundary value problems. Heterogeneities of the rock samples were incorporated by choosing material properties to be stochastic following Weibull and lognormal distributions. Numerical results appropriately replicated typical experimental observations where fracture localization and propagation are shown to be a multiscale phenomenon emerging from microcrack growth and coalescence at the microscale, with concomitant enhancement in fluid conductivity. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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27. From the Bench to the Field in Low-Cost Diagnostics: Two Case Studies.
- Author
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Kumar, Ashok A., Hennek, Jonathan W., Smith, Barbara S., Kumar, Shailendra, Beattie, Patrick, Jain, Sidhartha, Rolland, Jason P., Stossel, Thomas P., Chunda-Liyoka, Catherine, and Whitesides, George M.
- Subjects
CLINICAL pathology ,BUSINESS partnerships ,RAPID prototyping ,DEVELOPING countries - Abstract
Despite the growth of research in universities on point-of-care (POC) diagnostics for global health, most devices never leave the laboratory. The processes that move diagnostic technology from the laboratory to the field--the processes intended to evaluate operation and performance under realistic conditions--are more complicated than they might seem. Two case studies illustrate this process: the development of a paper-based device to measure liver function, and the development of a device to identify sickle cell disease based on aqueous multiphase systems (AMPS) and differences in the densities of normal and sickled cells. Details of developing these devices provide strategies for forming partnerships, prototyping devices, designing studies, and evaluating POC diagnostics. Technical and procedural lessons drawn from these experiences may be useful to those designing diagnostic tests for developing countries, and more generally, technologies for use in resource-limited environments. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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28. Dermatopathologists' concerns and challenges with clinical information in the skin biopsy requisition form: a mixed-methods study.
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Comfere, Nneka I., Peters, Margot S., Jenkins, Sarah, Lackore, Kandace, Yost, Kathleen, and Tilburt, Jon
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DERMATOLOGISTS ,DERMATOLOGY ,DERMATOPATHOLOGY ,SKIN diseases ,BIOPSY ,CLINICAL pathology - Abstract
Background Communication failures between clinicians and dermatopathologists are prevalent. Our primary objective was to characterize the concerns and challenges of dermatopathologists posed by incomplete or inaccurate clinical information in the skin biopsy requisition form. Methods An explanatory sequential, mixed-methods study design comprised of a survey sent to 1103 members of the American Society of Dermatopathology ( ASDP), followed by two focus group sessions. Results A total of 54% (598/1103) of dermatopathologists completed the questionnaire. Most dermatopathologists (80%; 436/548) viewed their roles to be providers of histopathological diagnosis and a report that is clinically meaningful. Paper or electronic requisition forms were the most common communication method (85%; 458/541) and were associated with the highest rates of dissatisfaction in 36% (193/537) of respondents. Inadequacy of specimens emerged as an important factor influencing judgment of the quality of provided clinical information. 44.7% (261/584) of dermatopathologists spent 30 minutes or more on average every day searching for relevant clinical information to assist with their histopathologic interpretation. Conclusion ASDP dermatopathologists expressed significant dissatisfaction with the quality of clinical information in the requisition form and the time spent gathering information necessary for accurate, timely and clinically meaningful diagnosis. These findings have implications for the quality, safety and efficiency of dermatologic care. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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29. Interference of an algal nutritional supplement with a urinary metabolic screening test for glycosaminoglycans in a dog suspected to have a storage disease.
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Sewell, Adrian C. and Pankraz, Alexander
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GLYCOSAMINOGLYCANS ,MUCOPOLYSACCHARIDOSIS ,TOLUIDINE blue ,CLINICAL pathology ,CHONDROITINASE ,DERMATAN sulfate - Abstract
The finding of excess urinary glycosaminoglycans ( GAG) is the first step in the laboratory diagnosis of mucopolysaccharidosis ( MPS). Urinary screening tests are based upon the binding of GAG to dimethylmethylene blue. Alternatively, paper spot tests using toluidine blue are used in human and veterinary laboratory medicine. Positive samples undergo GAG isolation for subsequent characterization. Here, we describe a 3-year-old English Cocker Spaniel with a positive urinary GAG test, but without other clinical signs of MPS. Urine samples were strongly positive with the dimethylmethylene blue test, and isolated GAG subjected to electrophoresis on cellulose acetate revealed a band co-migrating with dermatan sulfate. However, the isolated GAG were resistant to digestion with chondroitinase ABC, suggesting that the band did not represent dermatan sulfate. This was confirmed by mobility of the isolated GAG different from dermatan sulfate on agarose gel electrophoresis. MPS types VI and VII were excluded by enzyme assay. To test the hypothesis of a nutritional source, a healthy control dog was fed the same dog food as the index case. His urine showed a comparable abnormal GAG screening test and electrophoretic pattern. In addition, the analysis of an algal supplement present in the administered dog food showed a similar electrophoretic GAG pattern. The Cocker Spaniel was not available for further testing after withdrawal of the supplement. Algae contain highly sulfated fucans and galactans, and it appears that commercial dog food containing such algal, and possibly other, supplements can give rise to false-positive urinary MPS screening tests. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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30. Clinicopathological findings, treatment, and outcome in 60 cats with gastrointestinal eosinophilic sclerosing fibroplasia.
- Author
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Černá, Petra, Lopez‐Jimenez, Cristobal, Fukushima, Kenjiro, Nakashima, Ko, Nakagawa, Taisuke, Adam, Fiona, Groth, Anna, Denning, Andrew, Israeliantz, Nicolas, and Gunn‐Moore, Danièlle A.
- Subjects
CATS ,CLINICAL pathology ,SMALL intestine ,GASTROINTESTINAL system ,LYMPH nodes ,PET owners - Abstract
Background: Gastrointestinal eosinophilic sclerosing fibroplasia (GESF) in cats presents as mass(es) associated with the gastrointestinal tract, mesentery, and abdominal lymph nodes. Hypothesis/Objectives: To report the clinicopathological findings, treatment, and outcome of cats with GESF. Animals: Sixty client‐owned cats diagnosed with GESF. Methods: Retrospective review of medical records of cats with histopathologically confirmed GESF. Results: The median age was 5.4 years (interquartile range [IQR], 3.3‐8.9.); 30% were Domestic Shorthairs and 12% were Domestic Longhair cats, with the most prevalent pedigree breeds being Ragdolls (25%), Exotic Shorthair (10%) and Persian (8%) cats. The median duration of clinical signs was 90 days (IQR, 17.5‐247.0); the most common clinical signs were weight loss (60%), hyporexia/anorexia (55%), chronic vomiting (37%), lethargy (35%) and chronic diarrhea (27%). Masses were located in the small intestine (32%), stomach (27%), ileocolic junction (15%), colon (10%), lymph node (8%) and mesentery (8%) and 15% of cats had >1 mass. Eosinophilia was present in 50% and hypoalbuminemia in 28% of cats. The mass was removed surgically in 37% of cases. Most cats (98%) were treated with corticosteroids. Survival was not statistically different between cats treated with surgical resection and cats treated with medical therapy alone, 88% of the cats were still alive at the time of writing. Conclusions and Clinical Importance: GESF is an important differential diagnosis for abdominal masses in cats, and has a much better prognosis than previously reported. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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31. Closing the loop – the role of pathologists in digital and computational pathology research.
- Author
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Rau, Tilman T, Cross, William, Lastra, Ricardo R, Lo, Regina C‐L, Matoso, Andres, and Herrington, C Simon
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PATHOLOGISTS ,CLINICAL pathology ,PATHOLOGY ,ARTIFICIAL intelligence ,TISSUE analysis ,FORENSIC pathology - Abstract
An increasing number of manuscripts related to digital and computational pathology are being submitted to The Journal of Pathology: Clinical Research as part of the continuous evolution from digital imaging and algorithm‐based digital pathology to computational pathology and artificial intelligence. However, despite these technological advances, tissue analysis still relies heavily on pathologists' annotations. There are three crucial elements to the pathologist's role during annotation tasks: granularity, time constraints, and responsibility for the interpretation of computational results. Granularity involves detailed annotations, including case level, regional, and cellular features; and integration of attributions from different sources. Time constraints due to pathologist shortages have led to the development of techniques to expedite annotation tasks from cell‐level attributions up to so‐called unsupervised learning. The impact of pathologists may seem diminished, but their role is crucial in providing ground truth and connecting pathological knowledge generation with computational advancements. Measures to display results back to pathologists and reflections about correctly applied diagnostic criteria are mandatory to maintain fidelity during human–machine interactions. Collaboration and iterative processes, such as human‐in‐the‐loop machine learning are key for continuous improvement, ensuring the pathologist's involvement in evaluating computational results and closing the loop for clinical applicability. The journal is interested particularly in the clinical diagnostic application of computational pathology and invites submissions that address the issues raised in this editorial. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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32. Tau maturation in the clinicopathological spectrum of Lewy body and Alzheimer's disease.
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Arezoumandan, Sanaz, Cousins, Katheryn A.Q., Ohm, Daniel T., Lowe, MaKayla, Chen, Min, Gee, James, Phillips, Jeffrey S., McMillan, Corey T., Luk, Kelvin C., Deik, Andres, Spindler, Meredith A., Tropea, Thomas F., Weintraub, Daniel, Wolk, David A., Grossman, Murray, Lee, Virginia, Chen‐Plotkin, Alice S., Lee, Edward B., and Irwin, David J.
- Subjects
ALZHEIMER'S disease ,LEWY body dementia ,TAU proteins ,CLINICAL pathology ,PURE red cell aplasia ,MONOCLONAL antibodies ,CHRONIC traumatic encephalopathy - Abstract
Objective: Alzheimer's disease neuropathologic change and alpha‐synucleinopathy commonly co‐exist and contribute to the clinical heterogeneity of dementia. Here, we examined tau epitopes marking various stages of tangle maturation to test the hypotheses that tau maturation is more strongly associated with beta‐amyloid compared to alpha‐synuclein, and within the context of mixed pathology, mature tau is linked to Alzheimer's disease clinical phenotype and negatively associated with Lewy body dementia. Methods: We used digital histology to measure percent area‐occupied by pathology in cortical regions among individuals with pure Alzheimer's disease neuropathologic change, pure alpha‐synucleinopathy, and a co‐pathology group with both Alzheimer's and alpha‐synuclein pathologic diagnoses. Multiple tau monoclonal antibodies were used to detect early (AT8, MC1) and mature (TauC3) epitopes of tangle progression. We used linear/logistic regression to compare groups and test the association between pathologies and clinical features. Results: There were lower levels of tau pathology (β = 1.86–2.96, p < 0.001) across all tau antibodies in the co‐pathology group compared to the pure Alzheimer's pathology group. Among individuals with alpha‐synucleinopathy, higher alpha‐synuclein was associated with greater early tau (AT8 β = 1.37, p < 0.001; MC1 β = 1.2, p < 0.001) but not mature tau (TauC3 p = 0.18), whereas mature tau was associated with beta‐amyloid (β = 0.21, p = 0.01). Finally, lower tau, particularly TauC3 pathology, was associated with lower frequency of both core clinical features and categorical clinical diagnosis of dementia with Lewy bodies. Interpretation: Mature tau may be more closely related to beta‐amyloidosis than alpha‐synucleinopathy, and pathophysiological processes of tangle maturation may influence the clinical features of dementia in mixed Lewy‐Alzheimer's pathology. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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33. New aspects of hereditary ataxia in smooth-haired fox terriers.
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Rohdin, C., Lüdtke, L., Wohlsein, P., and Jäderlund, K. Hultin
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ATAXIA ,FOX terriers ,DOMESTIC animal diseases ,VETERINARY pathology ,HISTOPATHOLOGY ,DEGENERATION (Pathology) ,ETIOLOGY of diseases ,CLINICAL pathology ,DIAGNOSIS - Abstract
Hereditary ataxia was diagnosed in three smooth-haired fox terrier puppies from Sweden, 25 years after the previous known case in the breed. In addition to the characteristic spinal cord pathology, brain involvement was evident clinically, in the form of behavioural changes and bilaterally decreased menace responses, and histopathologically, with degenerative changes in the brainstem. The striking similarities to hereditary ataxia in the Jack Russell terrier suggest the same disease process in both breeds. A common ancestor, a female dog born in 1951 and considered a carrier of the disease at that time, was found in both the maternal and paternal lines of the three puppies. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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34. Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations.
- Author
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HERMANS, C., ALTISENT, C., BATOROVA, A., CHAMBOST, H., DE MOERLOOSE, P., KARAFOULIDOU, A., KLAMROTH, R., RICHARDS, M., WHITE, B., and DOLAN, G.
- Subjects
HEMOPHILIA ,BLOOD coagulation disorders ,OPERATIVE surgery ,CLINICAL trials ,CLINICAL pathology ,HEMORRHAGIC diseases - Abstract
Although most surgical and invasive procedures can be performed safely in patients with haemophilia, the optimal level and duration of replacement therapy required to prevent bleeding complications have not been established conclusively. For providing more insight into optimal therapy during invasive procedures, a literature review of surgical procedures in patients with haemophilia was conducted. Concomitantly, current practice was surveyed in 26 European Haemophilia Comprehensive Care Centres, representing 15 different countries. The review identified 110 original papers published between 1965 and 2007. Of these, only two studies were randomized controlled trials. Target levels and the duration of replacement therapy in the published studies were as follows. For major orthopaedic surgery: preoperative targets were 80–90%; postoperative targets showed a high degree of variation, with trough levels ranging from 20% to 80%, duration 10–14 days; for liver biopsy, 70–100%, 1–7 days; tonsillectomy: 90–100%, 5–11 days; indwelling venous access device insertion: 100%, 3–10 days; circumcision: 50–60%, 2–4 days; dental surgery: 30–50%, single treatment. With the exception of dental surgery, current practice in Europe, as assessed by the survey, was largely in agreement with published data. In conclusion, this study provides both a comprehensive review and a large survey of replacement therapy in patients with haemophilia undergoing invasive procedures; these data have informed the consensus practical treatment recommendations made in this paper. This study highlights the need for better-designed studies in order to better define minimal haemostatic levels of replacement therapy and optimal treatment duration. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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35. The development of the referral outcome diagram and an analysis of laboratory cancer detection rates in the English NHS cervical screening programme – is there an optimum level of detection of CIN 1 and CIN 2 lesions?
- Author
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Blanks, R. G.
- Subjects
CANCER diagnosis ,CERVICAL cancer treatment ,CLINICAL pathology ,COLPOSCOPY ,MEDICAL screening - Abstract
Objective: To use routine annual data from the English cervical screening laboratories (KC61 returns) to evaluate individual laboratory return characteristics with particular reference to factors associated with sensitivity and specificity. Methods: A graphical technique has been developed using data on referral to colposcopy and histological outcomes called a referral outcome (ROUT) diagram. The average grade of cervical intraepithelial neoplasia (CIN) detected (the mean CIN score, MCS) is plotted against the odds of a false-positive referral. Further analysis has been conducted to examine the relationship between the MCS and screen-detected invasive cancer rate. Results: There are large variations in ROUT diagram positions of individual laboratories and the diagram can be used to identify laboratories for further investigation. These variations are strongly influenced by substantial differences in the rate of low-grade referrals and the MCS (and positive predictive value) are inversely related to the referral rate for low-grade cytology ( P < 0.001). There is a strong association between high MCS values and increased screen-detected cancer rates ( P < 0.001) particularly above an MCS of 2.2. The data can be re-formulated in terms of CIN 2 and CIN 3 only where it can be shown that the invasive cancer rate rapidly increases if the numbers of CIN 2 lesions detected drops below 50% of the number of CIN 3 lesions. Given the complexity of cervical screening this may best be viewed as a hypothesis generating observation, best tested by interventional studies. Conclusions: The ROUT diagram represents a new and potentially interesting way of presenting annual return data. The national programme in England needs to balance the prevention of cancer against too many unnecessary referrals to colposcopy and the ROUT diagram, and associated data given in this paper may help toward this. Further research is required including examining the role of referral policy and threshold criteria in influencing low-grade referrals and the relationship between MCS and cancer detection rate. [ABSTRACT FROM AUTHOR]
- Published
- 2008
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36. Silodosin, a new α1A-adrenoceptor-selective antagonist for treating benign prostatic hyperplasia: results of a phase III randomized, placebo-controlled, double-blind study in Japanese men.
- Author
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Kawabe, Kazuki, Yoshida, Masaki, and Homma, Yukio
- Subjects
URINARY tract infections ,BENIGN prostatic hyperplasia ,ADRENERGIC alpha blockers ,DRUG efficacy ,CLINICAL pathology ,ULTRASONIC imaging - Abstract
This section contains papers from Japan, Austria, the UK, and joint papers from France, Denmark, Switzerland, Australia and the USA. A wide variety of lower urinary tract topics is covered, from BPH to overactive bladder and urodynamic stress incontinence. OBJECTIVE To verify the efficacy and safety of the new α
1A -adrenoceptor-selective antagonist silodosin compared with tamsulosin and placebo in patients with lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH). PATIENTS AND METHODS This randomized, double-blind, placebo-controlled study was conducted at 88 centres in Japan. Men aged ≥50 years with an International Prostate Symptom Score (IPSS) of ≥8, a quality-of-life (QoL) score of ≥3, a maximum urinary flow rate (Qmax ) of <15 mL/s, a prostate volume of ≥20 mL and a postvoid residual urine volume of <100 mL were eligible for enrolment. Patients were randomized to receive silodosin 4 mg twice daily, tamsulosin 0.2 mg once daily, or placebo, for 12 weeks. The primary endpoint was the change in IPSS from baseline. Safety was assessed by adverse events, physical examination, vital signs and laboratory tests. RESULTS In all, 457 patients were randomized (silodosin 176, tamsulosin 192 and placebo 89). The change in the total IPSS from baseline in the silodosin, tamsulosin and placebo groups was −8.3, −6.8 and −5.3, respectively. There was a significant decrease in the IPSS vs placebo in the silodosin group from 1 week. In the early-stage comparison, silodosin showed a significant decrease in IPSS vs tamsulosin at 2 weeks. The change in QoL from baseline was −1.7, −1.4 and −1.1 in the silodosin, tamsulosin and placebo groups, respectively; silodosin showed a significant improvement in the QoL score vs placebo. In the subgroup of patients with severe symptoms (IPSS ≥20) silodosin also gave a significantly better improvement than placebo (−12.4 vs −8.7). The incidence rates of adverse events and drug-related adverse events were, respectively, 88.6%, 82.3% and 71.6% and 69.7%, 47.4% and 36.4%, respectively. The most common adverse event in the silodosin group was abnormal ejaculation, which occurred more often in the silodosin than in the tamsulosin group (22.3% vs 1.6%). However, only five men (2.9%) discontinued treatment for abnormal ejaculation. CONCLUSION Silodosin was generally effective in the absence of obtrusive side-effects. This study suggests that silodosin is clinically useful for treating LUTS associated with BPH. [ABSTRACT FROM AUTHOR]- Published
- 2006
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37. Chamber test versus patch test for epicutaneous testing.
- Author
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Pirilä, Veikko
- Subjects
SKIN tests ,SKIN inflammation ,INDUSTRIAL equipment ,ECZEMA ,CLINICAL pathology - Abstract
A new modification of the chamber test for epicutaneous testing, and improved auxiliary equipment are presented. Compared with the customary patch test, the chamber test in its present form has several remarkable advantages, which are described in detail. [ABSTRACT FROM AUTHOR]
- Published
- 1975
- Full Text
- View/download PDF
38. Familial gigantiform cementoma with recurrent ANO5 p.Cys356Tyr mutations: Clinicopathological and genetic study with literature review.
- Author
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Zhou, Zheng, Zhang, Ye, Zhu, Lijing, Cui, Yajuan, Gao, Yan, and Zhou, Chuan‐Xiang
- Subjects
LITERATURE reviews ,DYSPLASIA ,GENETIC mutation ,SYMPTOMS ,FIBROMAS ,CLINICAL pathology - Abstract
Background: Familial gigantiform cementoma (FGC) is a rare tumor characterized by the early onset of multi‐quadrant fibro‐osseous lesions in the jaws, causing severe maxillofacial deformities. Its clinicopathological features overlap with those of other benign fibro‐osseous lesions. FGC eventually exhibits progressively rapid growth, but no suspected causative gene has been identified. Methods: In this study, three patients with FGC were recruited, and genomic DNA from the tumor tissue and peripheral blood was extracted for whole‐exome sequencing. Results: Results showed that all three patients harbored the heterozygous mutation c.1067G > A (p.Cys356Tyr) in the ANO5 gene. Furthermore, autosomal dominant mutations in ANO5 at this locus have been identified in patients with gnathodiaphyseal dysplasia (GDD) and are considered a potential causative agent, suggesting a genetic association between FGC and GDD. In addition, multifocal fibrous bone lesions with similar clinical presentations were detected, including five cases of florid cemento‐osseous dysplasia, five cases of polyostotic fibrous dysplasia, and eight cases of juvenile ossifying fibromas; however, none of them harbored mutations in the ANO5 gene. Conclusion: Our findings indicate that FGC may be an atypical variant of GDD, providing evidence for the feasibility of ANO5 gene testing as an auxiliary diagnostic method for complex cases with multiple quadrants. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
39. Getting clearer on overdiagnosis.
- Author
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Rogers, Wendy A. and Mintzker, Yishai
- Subjects
THYROID gland tumors ,CHRONIC kidney failure ,BIOMARKERS ,CLINICAL pathology ,DIAGNOSTIC errors ,THEORY of knowledge ,MEDICINE ,PHILOSOPHY ,DIAGNOSIS - Abstract
Overdiagnosis refers to diagnosis that does not benefit patients because the diagnosed condition is not a harmful disease in those individuals. Overdiagnosis has been identified as a problem in cancer screening, diseases such as chronic kidney disease and diabetes, and a range of mental illnesses including depression and attention deficit hyperactivity disorder. In this paper, we describe overdiagnosis, investigate reasons why it occurs, and propose two different types. Misclassification overdiagnosis arises because the diagnostic threshold for the disease in question has been set at a level where many people without harmful disease are nonetheless diagnosed. We illustrate misclassification overdiagnosis using the example of chronic kidney disease. Misclassification occurs in diseases diagnosed using biomarkers or based on patient reported phenomena. Maldetection overdiagnosis arises because, at the time the diagnosis is made and despite the presence of a 'gold standard' diagnostic test, it is not possible to discriminate between harmful and non-harmful cases of the index disease. We illustrate maldetection overdiagnosis using the example of thyroid cancer. While there is some overlap between misclassification and maldetection overdiagnosis, this conceptual analysis helps to clarify the phenomenon of overdiagnosis and is a necessary first step in developing strategies to address the problem. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
40. Volatile organic compounds as new biomarkers for colorectal cancer: a review.
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Di Lena, M., Porcelli, F., and Altomare, D. F.
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VOLATILE organic compound analysis ,COLON cancer diagnosis ,MEDICAL screening ,METABOLOMICS ,CLINICAL pathology - Abstract
Analysis of the volatile part of the metabolome (volatile organic compounds, VOC) present in the gas phase of excreted materials is a promising new screening tool for several cancers, including colorectal cancer ( CRC). The VOC signature can reflect health status, like a 'fingerprint', and can be modified in several diseases. Technical difficulties still limit the widespread use of VOC analysis in the clinical setting, but this approach has already been applied successfully in the diagnosis of CRC. The present study reviews the available data on VOC present in the headspace (the gaseous constituents of a closed space above a liquid or solid) of blood, urine, faeces and breath as a potential screening tool for CRC. A systematic electronic literature search was conducted in PubMed, Scirus and Google using the following keywords: Metabolomic, Volatile Organic Compounds ( VOC), Electronic-nose and Colorectal Cancer. Only articles published in English between 2000 and 2015 were selected and these were independently checked by two of the authors. Ten papers describing the reliability of VOC analysis in breath and faeces, blood and urine were selected; all indicated good reliability in detecting CRC. The use of different substrates and different analytical platforms has led to the identification of different patterns of VOC. The reliability of a metabolomic approach as a noninvasive biomarker for use in CRC screening is supported by this review despite several limitations due to the number of patients included in each study, the different analytical platforms and biological materials used and different VOC identified. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
41. Gouty arthropathy: Review of clinico-pathologic and imaging features.
- Author
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Parathithasan, Nishanthinie, Lee, Wai‐Kit, Pianta, Marcus, Oon, Shereen, and Perera, Warren
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GOUT diagnosis ,JOINT disease diagnosis ,CLINICAL pathology ,GOUT ,SYNOVIAL fluid ,DISEASE prevalence ,DISEASE risk factors - Abstract
Gout is a common inflammatory arthropathy in adults, with the prevalence increasing in males of older age. It occurs when monosodium urate (MSU) crystals are deposited in joints and connective tissue causing inflammation. The gold standard for the diagnosis of gout is the demonstration of negatively birefringent, needle-shaped MSU crystals through synovial fluid aspiration. However, this is an invasive technique and may not always be conclusive or feasible. Imaging techniques have been developed to aid in diagnosis of gout non-invasively. Radiography has a low utility in the early diagnosis of gout and demonstrates erosions in late stages. Ultrasound (US) has a high overall sensitivity in diagnosing gout with the 'double contour' sign having a high specificity. Magnetic resonance imaging is good at detecting tophi, bone marrow oedema and erosions, but has a limited role in diagnosis because of its high cost and limited availability. Conventional computed tomography (CT) has no role in the routine diagnosis of gout before development of erosions and tophi. A newer technology, dual-energy CT (DECT) has been shown to be able to detect MSU crystals burden with high accuracy. It has a higher specificity and lower sensitivity that US in gout diagnosis. However, because of radiation exposure and cost, it has a better utility in diagnosing clinically suspected gout complicated by other concurrent rheumatologic conditions or if radiography, US and synovial aspiration are inconclusive or not feasible. This paper will review the clinico-pathologic and imaging features of gouty arthropathy. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
42. Rural emergency departments: A systematic review to develop a resource typology relevant to developed countries.
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Kerr, Lachlan, Kealy, Benjamin, Lim, David, and Walters, Lucie
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CLINICAL pathology ,RURAL hospitals ,WORK experience (Employment) ,CINAHL database ,HOSPITAL emergency services ,HEALTH services accessibility ,DEVELOPED countries ,MEDICAL information storage & retrieval systems ,SYSTEMATIC reviews ,OPERATIVE surgery ,DIAGNOSTIC imaging ,WORKING hours ,MEDLINE ,MEDICAL specialties & specialists ,HEALTH care rationing ,EDUCATIONAL attainment - Abstract
Objective: Despite low patient numbers, rural emergency departments have a similar diversity of case presentations as urban tertiary hospitals, with the need to manage high‐acuity cases with limited resources. There are no consistent descriptions of the resources available to rural emergency departments internationally, limiting the capacity to compare clinical protocols and standards of care across similarly resourced units. This review aimed to describe the range of human, physical and specialist resources described in rural emergency departments in developed countries and propose a typology for use internationally. Design and setting: A systematic literature search was performed for journal articles between 2000 and 2019 describing the staffing, access to radiology and laboratory investigations, and hospital inpatient specialists. Results: Considerable diversity in defining rurality and in resource access was found within and between Australia, New Zealand, Canada and USA. Discussion: A typology was developed to account for (a) emergency department staff on‐floor, (b) emergency department staff on‐call, (c) physical resources and (d) access to a specialist surgical service. This provides a valuable tool for relevant stakeholders to effectively communicate rural emergency department resources within a country and internationally. Conclusion: The proposed five‐tiered typology draws together international literature regarding rural emergency department services. Although further research is required to test this tool, the formation of this common language allows a base for effective communication between governments, training providers and policy‐makers who are seeking to improve health systems and health outcomes. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
43. A modelling study of a new malignant hyperthermia diagnosis device.
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Ganesan, Adarsh V. and Ricardez‐Sandoval, Luis A.
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MALIGNANT hyperthermia ,DIAGNOSTIC equipment ,SUCCINYLCHOLINE ,CLINICAL pathology ,NEAR infrared spectroscopy ,DIAGNOSIS - Abstract
This paper presents a mathematical model for better understanding of the functionality of a newly-proposed Malignant Hyperthermia (MH) diagnosis device. MH is a rare life-threatening condition that is usually triggered by exposure to certain drugs such as a volatile anesthetic agent, neuromuscular blocking agent, or succinylcholine. It is highly recommended to have this condition diagnosed immediately after its common symptoms appear. However, it is often only when the patient has had a severe or fatal reaction to anesthetic that a diagnosis is finally made. Due to this, many deaths have been reported before a patient has been diagnosed with this condition. Further for the diagnosis, the patients are subject to an expensive clinical diagnostic procedure and it is also necessary to continuously monitor the condition. In this study, a micro-total analysis system for MH diagnosis through the assessment of the end-tidal CO
2 concentration level that can also aid point-of-care testing is presented. Various model parameters of the system are considered and their effects on the behaviour of the system are assessed. The results presented in this study are based on the proposed mathematical model for the new MH diagnosis device and can be used to evaluate the device's functionality and performance prior to its manufacture. [ABSTRACT FROM AUTHOR]- Published
- 2015
- Full Text
- View/download PDF
44. Assembly and evaluation of an inventory of guidelines that are available to support clinical hematology laboratory practice.
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Hayward, C. P. M., Moffat, K. A., George, T. I., and Proytcheva, M.
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CLINICAL pathology ,RESEARCH methodology ,MEDICAL technology ,REFERENCE sources ,PROFESSIONAL practice - Abstract
Introduction Practice guidelines provide helpful support for clinical laboratories. Our goal was to assemble an inventory of publically listed guidelines on hematology laboratory topics, to create a resource for laboratories and for assessing gaps in practice-focused guidelines. Methods PubMed and website searches were conducted to assemble an inventory of hematology laboratory-focused guidelines. Exclusions included annual, technical, or collaborative study reports, clinically focused guidelines, position papers, nomenclature, and calibration documents. Results Sixty-eight guidelines were identified on hematology laboratory practice topics from 12 organizations, some as joint guidelines. The median year of publication was 2010 and 15% were >10 years old. Coagulation topics had the largest numbers of guidelines, whereas some areas of practice had few guidelines. A minority of guidelines showed evidence of periodic updates, as some organizations did not remove or identify outdated guidelines. Conclusions This inventory of current practice guidelines will encourage awareness and uptake of guideline recommendations by the worldwide hematology laboratory community, with the International Society for Laboratory Hematology facilitating ongoing updates. There is a need to encourage best guideline development practices, to ensure that hematology laboratory community has current, high-quality, and evidence-based practice guidelines that cover the full scope of hematology laboratory practice. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
45. Consensus guidelines for the treatment of yeast infections in the haematology, oncology and intensive care setting, 2014.
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Chen, S. C., Sorrell, T. C., Chang, C. C., Paige, E. K., Bryant, P. A., and Slavin, M. A.
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CANDIDA diagnosis ,CANDIDIASIS treatment ,AMPHOTERICIN B ,ANTIFUNGAL agents ,ANTIGENS ,CANCER patient medical care ,CRITICAL care medicine ,CLINICAL pathology ,HEMATOLOGY ,IMMUNOGLOBULINS ,MEDICAL protocols ,MICROBIAL sensitivity tests ,NEONATAL intensive care ,NEONATAL intensive care units - Abstract
Pathogenic yeast forms are commonly associated with invasive fungal disease in the immunocompromised host, including patients with haematological malignancies and patients of haemopoietic stem cell transplants. Yeasts include the C andida spp., C ryptococcus spp., P neumocystis jirovecii and some lesser-known pathogens. Candida species remain the most common cause of invasive yeast infections (and the most common human pathogenic fungi). These guidelines present evidence-based recommendations for the antifungal management of established, invasive yeast infections in adult and paediatric patients in the haematology/oncology setting. Consideration is also given to the critically ill patient in intensive care units, including the neonatal intensive care unit. Evidence for 'pre-emptive' or 'diagnostic-driven antifungal therapy' is also discussed. For the purposes of this paper, invasive yeast diseases are categorised under the headings of invasive candidiasis, cryptococcosis and uncommon yeast infections. Specific recommendations for the management of P neumocystis jirovecii are presented in an accompanying article (see consensus guidelines by Cooley et al. appearing elsewhere in this supplement). [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
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46. Lab and Field Tests of a Low‐Cost 3‐Component Seismometer for Shallow Passive Seismic Applications.
- Author
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Arosio, D., Aguzzoli, A., Zanzi, L., Panzeri, L., and Scaccabarozzi, D.
- Subjects
SEISMIC waves ,CLINICAL pathology ,SEISMOMETERS ,MICROSEISMS ,PASSIVITY (Psychology) ,ANTENNAS (Electronics) ,FIELD research - Abstract
We performed laboratory tests and field surveys to evaluate the performance of a low‐cost 3‐component seismometer, consisting of three passive electromagnetic spring‐mass sensors, whose 4.5 Hz natural frequency is extended down to 0.5 Hz thanks to hyper damping. Both lab and field datasets show that the −3 dB band of the seismometer ranges approximately from 0.7 to 39 Hz, in agreement with the nominal specifications. Median magnitude frequency response curves obtained from processing field data indicate that lower corner of the −3 dB band could be extended down to 0.55 Hz and the nominal sensitivity may be overestimated. Lab results confirm the non‐linear behavior of the passive spring‐mass sensor expected for high‐level input signals (a few to tens of mm/s) and field data confirm relative timing accuracy is ±10 ms (1 sample). We found that absolute timing of data collected with USB GPS antennas can be affected by lag as large as +0.5 s. By testing two identical units, we noticed that there could be differences around 0.5 dB (i.e., about 6%) between the components of the same unit as well as between the same component of the two units. Considering shallow passive seismic applications and mainly focusing on unstable slope monitoring, our findings show that the tested seismometer is able to identify resonance frequencies of unstable rock pillars and to generate interferograms that can be processed to estimate subsurface velocity variations. Plain Language Summary: This study describes some tests that we did to evaluate a seismometer that is cheaper than similar products on the market. A seismometer is able to sense and collect seismic waves and can be used for several applications including global seismology and hydrocarbon exploration. In our work, we consider passive seismic applications, that is, we focus on seismic waves generated by non‐controlled sources (aka seismic noise). Either the seismic sources are natural or man‐made, a valuable seismometer should allow to record weak signals in a wide frequency band, especially at relatively low frequency (<5 Hz). The results of our tests show that the cheap seismometer can record frequencies down to approximately 0.5 Hz, while, to keep costs low, the highest frequency is limited to about 40 Hz. Field tests show that the seismometers can retrieve information from seismic noise as weak as a few micrometers per second, while lab test with higher inputs shows that the response of the seismometer is dependent upon the input velocity. Overall, we found that the nominal specifications of the seismometers are met, thus the tested unit is a valuable tool for shallow passive‐seismic applications with relatively‐low‐frequency, low‐amplitude signals, and a limited budget. Key Points: A low‐cost 3‐component seismometer has been tested for passive shallow applicationsThe seismometer has non‐linear response for high‐amplitude (mm/s) excitation signalsLab and field tests confirm the −3 dB band ranges from 0.7 to 39 Hz and an offset of about 0.5 s was found in the filed data whose timing was provided by a USB GPS antenna [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
47. The significance of increased influenza notifications during spring and summer of 2010-11 in Australia.
- Author
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Kelly, Heath A., Grant, Kristina A., Tay, Ee Laine, Franklin, Lucinda, and Hurt, Aeron C.
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RESPIRATORY infections ,INFLUENZA diagnosis ,BLOOD agglutination ,SEASONAL variations of diseases ,CLINICAL pathology - Abstract
Please cite this paper as: Kelly et al. (2012) The significance of increased influenza notifications during spring and summer of 2010-11 in Australia. Influenza and Other Respiratory Viruses. DOI: 10.1111/irv.12057. Background & objective During the temperate out-of-season months in Australia in late 2010 and early 2011, an unprecedented high number of influenza notifications were recorded. We aimed to assess the significance of these notifications. Methods For Australia, we used laboratory-confirmed cases notified to the WHO FluNet surveillance tool; the percentage of these that were positive; notifications by state and influenza type and subtype; and surveillance data from Google FluTrends. For the state of Victoria, we used laboratory-confirmed notified cases and influenza-like illness (ILI) proportions. We compared virus characterisation using haemagglutination-inhibition assays and phylogenetic analysis of the haemagglutinin gene for seasonal and out-of-season notifications. Results The increase in notifications was most marked in tropical and subtropical Australia, but the number of out-of-season notifications in temperate Victoria was more than five times higher than the average of the previous three seasons. However, ILI proportions in spring-summer were not different to previous years. All out-of-season viruses tested were antigenically and genetically similar to those tested during either the 2010 or 2011 influenza seasons. An increase in the number of laboratories testing for influenza has led to an increase in the number of tests performed and cases notified. Conclusion An increase in influenza infections in spring-summer of 2010-11 in tropical and temperate Australia was not associated with any differences in virus characterisation compared with viruses that circulated in the preceding and following winters. This increase probably reflected a natural variation in out-of-season virus circulation, which was amplified by increased laboratory testing. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
48. Best practices for veterinary toxicologic clinical pathology, with emphasis on the pharmaceutical and biotechnology industries.
- Author
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Tomlinson, Lindsay, Boone, Laura I., Ramaiah, Lila, Penraat, Kelley A., Beust, Barbara R., Ameri, Mehrdad, Poitout‐Belissent, Florence M., Weingand, Kurt, Workman, Heather C., Aulbach, Adam D., Meyer, Dennis J., Brown, Diane E., MacNeill, Amy L., Bolliger, Anne Provencher, and Bounous, Denise I.
- Subjects
VETERINARY toxicology ,CLINICAL pathology ,BIOTECHNOLOGY industries ,PHARMACEUTICAL industry ,PATHOLOGISTS - Abstract
The purpose of this paper by the Regulatory Affairs Committee ( RAC) of the American Society for Veterinary Clinical Pathology ( ASVCP) is to review the current regulatory guidances (eg, guidelines) and published recommendations for best practices in veterinary toxicologic clinical pathology, particularly in the pharmaceutical and biotechnology industries, and to utilize the combined experience of ASVCP RAC to provide updated recommendations. Discussion points include (1) instrumentation, validation, and sample collection, (2) routine laboratory variables, (3) cytologic laboratory variables, (4) data interpretation and reporting (including peer review, reference intervals and statistics), and (5) roles and responsibilities of clinical pathologists and laboratory personnel. Revision and improvement of current practices should be in alignment with evolving regulatory guidance documents, new technology, and expanding understanding and utility of clinical pathology. These recommendations provide a contemporary guide for the refinement of veterinary toxicologic clinical pathology best practices. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
49. Clinical approach for molecular testing on thyroid fine needle aspirates.
- Author
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Özden, Sabri, Er, Sadettin, and Tez, Mesut
- Subjects
NEEDLE biopsy ,THYROID gland function tests ,CLINICAL pathology - Abstract
This letter has been written in response to the paper by Decaussin‐Petrucci et al. published in Cytopathology, Volume 28, issue 6 ('Molecular testing of BRAF, RAS and TERT on thyroid FNAs with indeterminate cytology improves diagnostic accuracy'). Indeterminate FNAB results (Bethesda 3) can be controversial in regards to treatment. In their article, Decaussin‐Petrucci et al. demonstrated that molecular tests can be routinely performed and are strong predictors of malignancy. In our letter we comment on this hypothesis from the clinicians' perspective. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
50. The phenotypic and genetic assessment of protein C deficiency.
- Author
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COOPER, P. C., HILL, M., and MACLEAN, R. M.
- Subjects
BLOOD coagulation disorders ,GENETIC disorder diagnosis ,PROTEIN analysis ,CLINICAL pathology ,BLOOD coagulation tests ,CHROMOGENIC compounds ,GENES ,GENETIC techniques ,PHENOTYPES ,DIAGNOSIS - Abstract
This paper outlines the methods and approaches used for the laboratory detection and investigation of protein C (PC) deficiency. It does not make recommendations as to which patients should have thrombophilia testing performed; this should be done in line with local guidance. Interpretation of PC level is complicated because level varies with age, and many conditions can cause acquired deficiency. Protein C is most usually measured by chromogenic assay as a part of the thrombophilia screen. There exists, however, a very small group of individuals with significant PC deficiency, in whom the chromogenic PC assay is normal. The coagulometric assay of PC is more sensitive to these rare defects, but these assays may lack specificity. Genetic analysis allows definitive diagnosis and may be useful in confirming that deficiency is inherited and not acquired and is particularly valuable in families with severe PC deficiency. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
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