13 results on '"Galang H"'
Search Results
2. Genetic Variation and Prevalence of Amantadine-Resistant Influenza A (H3N2) Viruses in Two Consecutive Seasons in Japan and the Philippines
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Furuse, Y., primary, Suzuki, A., additional, Kamigaki, T., additional, Saito, M., additional, Fuji, N., additional, Galang, H., additional, Lupisan, S., additional, Olveda, R., additional, and Oshitani, H., additional
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- 2008
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3. Detection of Human Metapneumovirus and Human Bocavirus from Patients with Influenza-Like Illness in the Philippines
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Suzuki, A., primary, Furuse, Y., additional, Galang, H., additional, Fuji, N., additional, Kamigaki, T., additional, Miranda, E., additional, Lupisan, S., additional, Olveda, R., additional, and Oshitani, H., additional
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- 2008
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4. Enterovirus 68 among children with severe acute respiratory infection, the Philippines.
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Imamura T, Fuji N, Suzuki A, Tamaki R, Saito M, Aniceto R, Galang H, Sombrero L, Lupisan S, Oshitani H, Imamura, Tadatsugu, Fuji, Naoko, Suzuki, Akira, Tamaki, Raita, Saito, Mariko, Aniceto, Rapunzel, Galang, Hazel, Sombrero, Lydia, Lupisan, Soccoro, and Oshitani, Hitoshi
- Abstract
Enterovirus 68 (EV68) is a rare enterovirus associated with respiratory illness that, unlike other enteroviruses, has been identified only from respiratory specimens. We identified EV68 from respiratory specimens of children hospitalized with a diagnosis of severe pneumonia in Leyte, Republic of the Philippines. Twenty-one samples showed high similarity with EV68 by sequencing of 5' nontranslated region; 17 of these samples were confirmed as EV68 by sequencing of viral protein 1 capsid coding region. Most previously reported EV68 cases had been identified as sporadic cases. All 21 patients we identified had severe illness, and 2 died, possibly the first reported fatal cases associated with EV68 infection. Our study suggests that EV68 may be a possible causative agent of severe respiratory illnesses. [ABSTRACT FROM AUTHOR]
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- 2011
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5. Respiratory viruses from hospitalized children with severe pneumonia in the Philippines
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Suzuki Akira, Lupisan Socorro, Furuse Yuki, Fuji Naoko, Saito Mariko, Tamaki Raita, Galang Hazel, Sombrero Lydia, Mondoy Melisa, Aniceto Rapunzel, Olveda Remigio, and Oshitani Hitoshi
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Infectious and parasitic diseases ,RC109-216 - Abstract
Abstract Background Pneumonia remains a leading cause of child death in developing countries. The viruses in severe pneumonia remain poorly defined. Methods The study was conducted at the Eastern Visayas Regional Medical Center in Tacloban City, Philippines from May 2008 to May 2009. Patients aged 8 days to 13 years old who were admitted to the Department of Pediatrics with severe pneumonia were enrolled for the study. Upon admission, polymerase chain reaction was performed using nasopharyngeal swabs and blood cultures to detect respiratory viruses and bacteria, respectively. Result Among the 819 patients enrolled, at least one virus was detected in 501 cases (61.2%). In addition, 423 cases were positive for a single virus while bacteria were detected in the blood culture sample of 31 cases. The most commonly detected viruses were human rhinoviruses (n = 189), including types A (n = 103), B (n = 17), and C (n = 69), and respiratory syncytial virus (RSV) (n = 165). Novel viruses such as human metapneumovirus, human coronavirus NL63, human bocavirus, and human polyomaviruses WU and KI were also detected. There were 70 deaths, and one or more viruses were detected in 35 (50%) of these cases. Positivity only for influenza A virus (OR = 4.3, 95% CI = 1.3-14.6) was significantly associated with fatal outcome. From the blood culture, Burkholderia cepacia group (n = 9), Streptococcus pneumoniae (n = 4), Staphylococcus aureus (n = 4), Haemophilus influenzae (n = 1), and Salmonella C1 (n = 1) were also isolated. Conclusion Viruses were commonly detected in children with severe pneumonia in the Philippines. Hence, viral etiologies should be considered while developing better effective strategies to reduce child pneumonia-related deaths in developing countries.
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- 2012
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6. A Randomized Trial Comparing Outcomes of 3 Types of Peripheral Intravenous Catheters.
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Galang H, Hubbard-Wright C, Hahn DS, Yost G, Yoder L, Maduro RS, Morgan MK, and Zimbro KS
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- Adult, Aged, Aged, 80 and over, Catheterization, Peripheral methods, Catheterization, Peripheral standards, Catheters, Indwelling adverse effects, Catheters, Indwelling statistics & numerical data, Cost-Benefit Analysis, Equipment Design statistics & numerical data, Female, Humans, Male, Middle Aged, Outcome Assessment, Health Care statistics & numerical data, Prospective Studies, Time Factors, Catheterization, Peripheral instrumentation, Catheters, Indwelling standards, Equipment Design standards, Outcome Assessment, Health Care standards
- Abstract
Background: There was an increase in peripheral intravenous catheter (PIVC) complications and adverse patient events after product conversion during the merger between a rural hospital and a larger hospital system. A review of the existing literature identified a gap in evidence evaluating 2 closed PIVC systems compared with an open PIVC system., Purpose: The purpose of the current project was to ascertain whether open or closed PIVCs are best for patients, staff, and the health care system in terms of 3 main criteria: quality, safety, and cost., Methods: A prospective, 2-site randomized controlled trial was used to compare outcomes., Results: There were no differences in the complication rates between catheter types. There was a statistically significant increase in blood leakage and a decrease in clinician satisfaction with the open-system catheter., Conclusions: Our project supports current clinical recommendation that a closed PIVC system, regardless of type, is not only safer and cost-effective but also preferred by patients and clinicians.
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- 2020
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7. Etiology and epidemiology of community-acquired pneumonia in adults requiring hospital admission: A prospective study in rural Central Philippines.
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Lupisan S, Suzuki A, Macalalad N, Egos R, Sombrero L, Okamoto M, Dapat C, Mondoy M, Galang H, Zeta VFF, de la Pena F, Romano V, Olveda R, and Oshitani H
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- Adolescent, Adult, Aged, Bacteria classification, Bacteria isolation & purification, Community-Acquired Infections microbiology, Community-Acquired Infections virology, Female, Haemophilus influenzae isolation & purification, Humans, Male, Middle Aged, Mycobacterium tuberculosis isolation & purification, Nasopharynx microbiology, Nasopharynx virology, Orthomyxoviridae isolation & purification, Philippines epidemiology, Pneumonia microbiology, Pneumonia virology, Prospective Studies, Risk Factors, Sputum microbiology, Sputum virology, Tuberculosis, Pulmonary epidemiology, Young Adult, Community-Acquired Infections epidemiology, Hospitalization, Pneumonia epidemiology
- Abstract
Background: Community-acquired pneumonia (CAP) is a common cause of morbidity and mortality among adults worldwide. However, the distribution of the etiology of CAP varies from one country to another, with limited data from rural areas., Methods: A prospective hospital-based study on adult CAP was conducted in Leyte, Central Philippines from May 2010 to May 2012. Blood, sputum, and nasopharyngeal samples obtained from patients were used to identify pathogens using standard microbiological culture methods and PCR., Results: Of the 535 patients enrolled, 38% were younger than 50 years old. More than half of the patients had an underlying disease, including pulmonary tuberculosis (22%). The detection rate was higher for bacteria (40%) than viruses (13%). Haemophilus influenzae (12%) was the most commonly detected bacterium and influenza virus (5%) was the most commonly detected virus. The proportion of CAP patients with Mycobacterium tuberculosis infection was higher in the younger age group than in the older age group. Among CAP patients, 14% died during hospitalization, and drowsiness on admission and SpO
2 <90% were independent risk factors for mortality., Conclusions: Bacterial infections contribute substantially to the number of hospitalizations among CAP patients in rural Philippines. This study also highlights the importance of treatment of tuberculosis in reducing the burden of adult CAP in the country., (Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.)- Published
- 2019
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8. Clinical experience with dolutegravir/abacavir/lamivudine in HIV-HCV co-infected patients treated with a sofosbuvir-based regimen-safety and efficacy.
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Johnson TM, Sison R, Fallon JP, Shukla PP, Bhattarai S, Galang H, Habeeb R, and Slim J
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- CD4 Lymphocyte Count, Dideoxynucleosides administration & dosage, Drug Therapy, Combination, Female, HIV Infections immunology, HIV Infections virology, HIV-1, Hepacivirus genetics, Hepatitis C virology, Heterocyclic Compounds, 3-Ring administration & dosage, Humans, Lamivudine administration & dosage, Male, Middle Aged, Oxazines, Piperazines, Pyridones, Sofosbuvir administration & dosage, Sofosbuvir adverse effects, Treatment Outcome, Viral Load, Antiretroviral Therapy, Highly Active adverse effects, Coinfection, HIV Infections drug therapy, Hepatitis C drug therapy, Sofosbuvir therapeutic use
- Abstract
Background: There is no known reason to suspect an adverse drug interaction between dolutegravir-based antiretroviral therapy and sofosbuvir, simeprevir, or ledipasvir. There is a paucity of clinical data for this combination., Methods: Prospective, open-label study of patients with HIV well controlled on dolutegravir, abacavir, and lamivudine, who were co-infected with HCV genotype 1, and required therapy with simeprevir plus sofosbuvir or sofosbuvir/ledipasvir single-tablet regimen (STR) for 12 weeks. The two primary endpoints were percentage of patients achieving sustained virologic response (SVR) at 12 weeks post-treatment and percentage of patients with a HIV-1 viral load <50 copies/ml at end of the combination therapy., Results: Twenty-eight subjects were enrolled from August 2014 to September 2015. Thirteen patients were treated with simprevir plus sofosbuvir, and 15 subjects were treated with sofosbuvir/ledipasvir. 23 genotype 1a, and 5 genotype 1b were included. Nineteen were treatment naïve, and 2 patients had compensated cirrhosis. The mean age was 59 years (95% CI 58.21-59.78 years). The mean age was 59 years (95% CI: 58.21-59.78 years), and 25 patients were black. Out of the 28 patients who completed this study, SVR 12 was achieved in 27 of 28 patients (96%, 95% CI 89.6-100.0%), and all patients had an HIV virus load <50 copies/ml at week 12 of therapy, for an intent-to-treat rate of 100%. No patients ended therapy secondary to adverse events., Conclusion: Our study suggests a good safety and efficacy for the combination of a dolutegravir, abacavir, and lamivudine with sofosbuvir-based DAA therapy.
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- 2016
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9. Genetic characterization of human respiratory syncytial virus detected in hospitalized children in the Philippines from 2008 to 2012.
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Ohno A, Suzuki A, Lupisan S, Galang H, Sombrero L, Aniceto R, Okamoto M, Saito M, Fuji N, Otomaru H, Roy CN, Yamamoto D, Tamaki R, Olveda R, and Oshitani H
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- Adolescent, Amino Acid Sequence, Child, Child, Preschool, Cluster Analysis, Genotype, Hospitalization, Humans, Infant, Infant, Newborn, Molecular Epidemiology, Molecular Sequence Data, Morbidity, Nasopharynx, Philippines epidemiology, Phylogeny, Prospective Studies, Respiratory Syncytial Virus Infections epidemiology, Respiratory Syncytial Viruses classification, Respiratory Syncytial Viruses isolation & purification, Sequence Alignment, Viral Envelope Proteins genetics, Respiratory Syncytial Virus Infections virology, Respiratory Syncytial Viruses genetics
- Abstract
Background: Human respiratory syncytial virus (HRSV) is the leading cause of acute lower respiratory tract infection in infants and young children. However, molecular characteristic of HRSV is still unknown in the Philippines., Objective: To describe the molecular epidemiology of circulating HRSV detected in the Philippines., Study Design: From May 2008 to April 2012, nasopharyngeal swabs were collected from infants and children aged between 7 days and 14 years who were hospitalized with severe pneumonia. HRSV was detected by nested PCR targeting M2 gene, and C-terminus of the G gene was sequenced for phylogenetic analysis., Result: Out of total 2150 samples, 19.3% (n = 415) were positive for HRSV, and 65.0% of them (n = 270) were identified as HRSV-A and 35.0% (n = 145) as HRSV-B. There were two major HRSV outbreaks: between June 2008 and February 2009, and between June and March 2012. Majority of HRSV strains detected during the former outbreak were HRSV-A (97.5%, 203/208) whereas during the later outbreak, both HRSV-A (54/158, 34.2%) and HRSV-B (104/158, 65.8%) were detected. All HRSV-A strains were classified as genotype NA1 and all HRSV-B as genotype BA, which had 60-nucleotide duplication in secondary hypervariable region of the G gene. Among HRSV-B positive samples, there were 2 distinct clusters with unique amino acid changes and low homology in compared to other strains in BA, suggesting emergence of new variant of HRSV-B., Conclusion: The study provides an overview of the genetic variation in circulating HRSV viruses in the Philippines along with identification of possibly a novel variant of HRSV-B., (Copyright © 2013 Elsevier B.V. All rights reserved.)
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- 2013
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10. Detection of non-polio enteroviruses from 17 years of virological surveillance of acute flaccid paralysis in the Philippines.
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Apostol LN, Suzuki A, Bautista A, Galang H, Paladin FJ, Fuji N, Lupisan S, Olveda R, and Oshitani H
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- Adolescent, Child, Child, Preschool, Enterovirus immunology, Feces virology, Genotype, Humans, Infant, Neutralization Tests, Phenotype, Philippines epidemiology, Prevalence, Reverse Transcriptase Polymerase Chain Reaction, Enterovirus classification, Enterovirus isolation & purification, Enterovirus Infections complications, Enterovirus Infections epidemiology, Paraplegia epidemiology, Paraplegia virology
- Abstract
Acute flaccid paralysis (AFP) surveillance has been conducted as part of the World Health Organization (WHO) strategy on poliomyelitis eradication. Aside from poliovirus, which is the target pathogen, isolation, and identification of non-polio enteroviruses (NPEVs) is also done by neutralization test using pools of antisera which can only identify limited number of NPEVs. In the Philippines, despite the significant number of isolated NPEVs, no information is available with regard to its occurrence, diversity, and pattern of circulation. In this study, a total of 790 NPEVs isolated from stool samples submitted to the National Reference Laboratory from 1992 to 2008 were analyzed; neutralization test was able to type 55% (442) of the isolates. Of the remaining 356 isolates, which were untyped by using neutralization test, 348 isolates were analyzed further by RT-PCR targeting the VP1 gene. A total of 47 serotypes of NPEV strains were identified using neutralization test and molecular typing, including 28 serotypes of human enterovirus B (HEV-B), 12 serotypes of HEV-A, and 7 of HEV-C. The HEV-B group (625/790; 79%) constituted the largest proportion of isolates, followed by HEV-C (108/790; 13.7%), HEV-A (57/790; 7.2%), and no HEV-D. Coxsackievirus (CV) B, echovirus (E)6, E11, and E13 were the most frequent isolates. E6, E11, E13, E14, E25, E30, E33, CVA20, and CVA24 were considered as endemic strains, some NPEVs recurred and few serotypes existed only for 1-3 years during the study period. Despite some limitations in this study, plural NPEVs with multiple patterns of circulation in the Philippines for 17 years were identified., (Copyright © 2012 Wiley Periodicals, Inc.)
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- 2012
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11. Interruption of the circulation of an indigenous measles genotype and the introduction of other genotypes after a mass vaccination campaign in the Philippines.
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Fuji N, Suzuki A, Saito M, Centeno R, Galang H, Lupisan S, Olveda R, and Oshitani H
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- Genotype, Humans, Measles virology, Measles Vaccine immunology, Measles virus isolation & purification, Molecular Epidemiology, Molecular Sequence Data, Philippines epidemiology, Prevalence, RNA, Viral genetics, Sequence Analysis, DNA, Mass Vaccination, Measles epidemiology, Measles prevention & control, Measles Vaccine administration & dosage, Measles virus classification, Measles virus genetics
- Abstract
Molecular analysis of measles viruses in the Philippines was conducted from 2000 to 2008. No confirmed measles cases were detected in the surveillance in 2005 after the mass vaccination campaign in 2004. However, a re-emergence of measles cases occurred in 2007, which was caused by other genotypes and the previous circulating genotype had disappeared., (Copyright © 2011 Wiley-Liss, Inc.)
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- 2011
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12. Assessment of the heat stability of seven rapid HIV assays.
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Learmonth KM, Chiu CY, Galang H, Nawang MJ, and Dax EM
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- HIV Seropositivity immunology, Humans, Tropical Climate, HIV Antibodies analysis, HIV Seropositivity diagnosis, HIV-1 immunology, Hot Temperature, Reagent Kits, Diagnostic standards
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Human Immunodeficiency Virus Rapid Diagnostic Tests (HIV RDTs) are robust, quick to perform, effective diagnostic tools. The stability of seven commonly used RDTs for detecting antibody to HIV was assessed during exposure to temperatures above 30°C, the usual maximum recommended by manufacturers. The aim of the study was to determine if HIV RDTs retain their testing outcomes after exposure to higher temperatures. At two testing sites, seven RDTs were exposed to a short heat shock (60°C for 72 hours) as might occur during transport. RDTs were exposed to ambient (22 or 30°C), warm (35 or 37°C) or hot (45°C) temperatures for up to 90 days. Testing was performed at five intervals on a panel of seven positive and three negative plasma samples. Results showed no changes consistent with altered testing outcomes over time and/or temperature when test indicators were compared with the control indicators. Only one HIV RDT achieved 100% consensus with reference results at all four storage temperatures (median 97.5%, lowest 74% for RDT5 at 45°C). Testing outcomes in a limited sample panel showed six of seven HIV RDT kits were relatively robust despite exposure to higher than recommended temperatures., (Copyright © 2011 Royal Society of Tropical Medicine and Hygiene. Published by Elsevier Ltd. All rights reserved.)
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- 2011
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13. Detection of human rhinovirus C viral genome in blood among children with severe respiratory infections in the Philippines.
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Fuji N, Suzuki A, Lupisan S, Sombrero L, Galang H, Kamigaki T, Tamaki R, Saito M, Aniceto R, Olveda R, and Oshitani H
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- Age Factors, Child, Child, Preschool, Genotype, Humans, Philippines epidemiology, Reverse Transcriptase Polymerase Chain Reaction, Rhinovirus genetics, Species Specificity, Viremia diagnosis, Viremia virology, Genome, Viral, Picornaviridae Infections diagnosis, Respiratory Tract Infections virology, Rhinovirus isolation & purification
- Abstract
Human rhinovirus (HRV) C was recently identified as the third species of HRV using a molecular technique. Infections caused by previously identified HRVs (A and B) are thought to be limited to the respiratory tract; however, pathogenesis of HRVC is still largely unknown. A total of 816 nasopharyngeal swabs from hospitalized children with severe respiratory infections in the Philippines (May 2008-May 2009) were tested for HRV by reverse transcription polymerase chain reaction (RT-PCR), and 243 samples (29.8%) were positive for HRV. Among these patients, serum samples were also tested to determine whether specific HRV species were associated with viremia. Only 30 serum samples (12.3%) were positive for HRV. However, the HRV positive rates were different among HRV species, 3% (4/135) for HRVA, 0% (0/25) for HRVB, and 31% (26/83) for HRVC, and were the highest on 2 days after the onset of symptoms. These results suggest that HRVC may have a different pathogenicity and can more commonly cause viremia than HRVA and HRVB. Serum positive rates for HRV are affected by age, i.e., higher positive rates for those aged 1 year or more. HRVC that were detected from serum exhibited the same level of sequence diversity as those positive only for nasopharyngeal samples in phylogenetic analysis. However, all HRVA which were detected from serum were clustered in a monophyletic clade based on their 5' non-coding region (NCR) sequences, which is closely related with a certain HRVC genotype (A2) in 5'-NCR. This finding suggests that the 5'NCR region may be associated with viremia.
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- 2011
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