6 results on '"Elizabeth Spiwak"'
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2. Pediatric kidney transplant recipients with and without underlying structural kidney disease have a comparable risk of hospitalization associated with urinary tract infections
- Author
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Elizabeth Spiwak, Corina Nailescu, and Andrew Schwaderer
- Subjects
pyelonephritis ,immunosuppression ,congenital anomalies of the kidney and urinary tract (CAKUT) ,allograft ,E. coli ,Pediatrics ,RJ1-570 - Abstract
IntroductionUrinary tract infections (UTIs) are a common and potentially serious kidney transplant complication. Pediatric kidney transplants are potentially at increased risk for UTIs when structural kidney disease is the underlying end-stage kidney disease (ESKD) etiology. The objective of this manuscript is to determine if children with structural kidney disorders are more prone to UTIs post kidney transplant.Materials and methodsHospitalizations for pediatric kidney transplant recipients were retrospectively reviewed over a 4-year period for UTIs in the diagnostic codes. The patient’s age, sex, graft age, underlying diagnosis for cause of ESKD, symptoms at presentation, urinalysis results, and urine culture results were recorded. UTI rates, febrile UTI rates, and UTI rates in the 1st year post-transplant were compared between children with ESKD due to structural vs. non-structural kidney disease.ResultsOverall, 62 of 145 pediatric patients with kidney transplants accounted for 182 hospitalizations for kidney transplant complications over the 4-year study period. UTIs were components of 34% of the hospitalizations. Overall, UTI rates, febrile UTI rates, and UTI rates for the 1st year post kidney transplant were comparable for children with vs. without structural ESKD etiologies.ConclusionUrinary tract infections are frequent components of hospitalizations for pediatric kidney transplant recipients. Children with and without structural kidney disease as an ESKD etiology have similar UTI rates indicating that UTI susceptibility is primarily due to the transplant process and/or medication regimens. UTIs represent a potentially modifiable risk factor for pediatric kidney transplant complications.
- Published
- 2022
- Full Text
- View/download PDF
3. The kidney transplant rate is outpaced by the rate of readmission for complications
- Author
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Elizabeth Spiwak, Andrew L. Schwaderer, and Corina Nailescu
- Subjects
Graft Rejection ,medicine.medical_specialty ,medicine.medical_treatment ,Kidney transplant ,Patient Readmission ,Allograft survival ,medicine ,Humans ,Healthcare Cost and Utilization Project ,Kidney transplantation ,Immunosuppression Therapy ,Kidney ,business.industry ,Incidence (epidemiology) ,Graft Survival ,Immunosuppression ,General Medicine ,Emergency department ,medicine.disease ,Kidney Transplantation ,Transplant Recipients ,surgical procedures, operative ,medicine.anatomical_structure ,Nephrology ,Emergency medicine ,business - Abstract
Hospital readmissions experienced by kidney transplant recipients may be secondary to a range of conditions, including infections and rejection episodes. The objective was to identify trends in patients with kidney transplant complications, in regard to hospital discharges, ED visits, and charges over the years available from 1993 to 2015. Using the Healthcare Cost and Utilization Project database, trends were identified in hospitalizations, emergency department visits, and charges from 1993 to 2015 for complications following kidney transplantation. Hospital discharges have significantly increased over time and at a faster rate than the increase in number of kidney transplants performed, while emergency department visits numbers and rates remain unchanged. The type of kidney transplant complications experienced were analyzed by incidence and proportion of total charges. Rejection made up the largest proportion of hospitalizations and of total cost in patients suffering from kidney transplant complications. Improved immunosuppression regimens have resulted in longer allograft survival. We speculate that the overlap between infection and rejection is compounding and contributing to graft injury and thus, it is important to try to prevent and/or properly identify those episodes as well in order to improve graft survival.
- Published
- 2022
4. Coronavirus disease 2019 ( COVID ‐19) in two pediatric patients with kidney disease on chronic immunosuppression: A case series
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Bethanne Johnston, Michelle C. Starr, Amy C. Wilson, Shannon Anderson, Corina Nailescu, John C. Christenson, Elizabeth Spiwak, David S. Hains, Ashley Rawson, Andrew L. Schwaderer, and Sushil Gupta
- Subjects
medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,pediatrics ,medicine.medical_treatment ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,030232 urology & nephrology ,Severe disease ,Case Report ,Case Reports ,030204 cardiovascular system & hematology ,Virus ,SARS‐CoV‐2 ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,end‐stage kidney disease ,hemodialysis ,business.industry ,Immunosuppression ,Hematology ,medicine.disease ,Coronavirus ,Infectious disease (medical specialty) ,Nephrology ,Hemodialysis ,business ,Kidney disease - Abstract
Coronavirus disease 2019 (COVID‐19) is a highly infectious disease caused by the severe acute respiratory syndrome coronavirus 2 virus (SARS‐CoV‐2). While children appear to experience less severe disease than adults, those with underlying conditions such as kidney disease may be more susceptible to infection. Limited data are present for children with kidney disease, and there are limited prior reports of pediatric hemodialysis patients with COVID‐19. This report describes the mild clinical disease course of COVID‐19 in two pediatric patients with chronic kidney disease, one on hemodialysis and both on chronic immunosuppression. We review treatment in these patients, as well as our measures to reduce transmission among our hemodialysis patients and staff.
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- 2020
- Full Text
- View/download PDF
5. Use of Pleuroperitoneal Shunt in Chylothorax Related to Central Line Associated Thrombosis in Sickle Cell Disease
- Author
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Ashok Raj, Chad A. Wiesenauer, Elizabeth Spiwak, and Arun R Panigrahi
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Erythrocytapheresis ,medicine.medical_specialty ,pleuroperitoneal shunt ,central vein thrombosis ,Case Report ,Disease ,030204 cardiovascular system & hematology ,Cardiovascular ,03 medical and health sciences ,Rare Diseases ,0302 clinical medicine ,chylothorax ,Superior vena cava ,030225 pediatrics ,medicine ,cardiovascular diseases ,Stroke ,Sickle Cell Disease ,Central line ,business.industry ,Chylothorax ,Hematology ,medicine.disease ,Thrombosis ,Surgery ,Venous thrombosis ,Blood ,Pediatrics, Perinatology and Child Health ,sickle cell disease ,business - Abstract
Central vein thrombosis as a cause of chylothorax is uncommon, and in a few cases in the literature was related to thrombotic complications of central venous access devices (CVAD). Superior vena cava (SVC) occlusion-induced chylothorax has been described in adult sickle cell disease (SCD) in a setting of chronic indwelling CVAD. There are limited reports on chylothorax induced by central venous thrombosis secondary to chronic CVAD in children with SCD. We describe an 8-year-old male patient, with a history of SCD, maintained on long term erythrocytapheresis for primary prevention of stroke, and whose clinical course was complicated by chylothorax which was successfully treated with a pleuroperitoneal shunt.
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- 2018
6. Inhaled epoprostenol improves oxygenation in severe hypoxemia
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Miren A. Schinco, Elizabeth Spiwak, Joseph J. Tepas, Maryam B. Tabrizi, James Hwang, and Andrew J. Kerwin
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Adult ,Male ,ARDS ,Pulmonary Circulation ,Adolescent ,medicine.medical_treatment ,Critical Illness ,Vasodilator Agents ,Subgroup analysis ,Critical Care and Intensive Care Medicine ,Risk Assessment ,Cohort Studies ,Young Adult ,Oxygen Consumption ,Administration, Inhalation ,Medicine ,Intubation ,Humans ,Hypoxia ,Survival rate ,Aged ,Retrospective Studies ,Aged, 80 and over ,Respiratory Distress Syndrome ,Inhalation ,business.industry ,Pulmonary Gas Exchange ,Retrospective cohort study ,Oxygenation ,Hypoxia (medical) ,Middle Aged ,medicine.disease ,Epoprostenol ,Respiration, Artificial ,respiratory tract diseases ,Survival Rate ,Intensive Care Units ,Treatment Outcome ,Anesthesia ,Wounds and Injuries ,Surgery ,Female ,medicine.symptom ,business ,Follow-Up Studies - Abstract
BACKGROUND Epoprostenol (Flolan), an inhalational epoprostenol vasodilator, increases pulmonary arterial flow and decreases pulmonary pressures, thereby improving gas exchange and arterial oxygenation. We evaluated the benefits of inhaled epoprostenol as a less expensive alternative to nitric oxide in ventilated surgical intensive care patients with severe hypoxemia. METHODS After institutional review board approval was obtained, the records of mechanically ventilated surgical intensive care unit patients who received epoprostenol as a therapy for severe hypoxia (SaO₂ < 90%) in a tertiary care referral center were retrospectively reviewed. Initial PaO₂/FIO₂ (P/F) ratio and oxygen saturation were compared with values at 12 and 48 hours after the administration of epoprostenol. One-way repeated-measures analysis of variance compared improvements in oxygenation. Further subgroup analyses evaluated differences among trauma, nontrauma patient subgroups, time to initiation of epoprostenol, and age. RESULTS During a 20 month-interval beginning February 2009, 36 patients (23 trauma and 13 nontrauma; age, 15-80 years) were treated. Epoprostenol significantly improved both P/F ratio and oxygen saturation in both trauma and nontrauma patients. Therewas no difference between subgroups. Larger improvements in P/F ratiowere seen when epoprostenolwas started within 7 days. Response between age groups did not differ significantly. Subgroup analysis of mortality (trauma, 60.9% vs. nontrauma, 61.5%) failed to show any differences. CONCLUSION Treatment with inhaled epoprostenol improved gas exchange in severely hypoxemic surgical patients. Earlier intervention (within 7 days of intubation) was more efficacious at improving oxygenation.
- Published
- 2012
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