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Dive into the research topics where Dhuly Chowdhury is active.

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Featured researches published by Dhuly Chowdhury.


The Journal of Infectious Diseases | 2016

Transfusion-Transmitted Dengue and Associated Clinical Symptoms During the 2012 Epidemic in Brazil

Ester C. Sabino; Paula Loureiro; Maria Esther Lopes; Ligia Capuani; Christopher McClure; Dhuly Chowdhury; Claudia Di-Lorenzo-Oliveira; Lea Campos de Oliveira; Jeffrey M. Linnen; Tzong-Hae Lee; Thelma T. Gonçalez; Donald Brambilla; Steve Kleinman; Michael P. Busch; Brian Custer

BACKGROUND A linked donor-recipient study was conducted during epidemics in 2 cities in Brazil to investigate transfusion-transmitted (TT) dengue virus (DENV) by DENV RNA-positive donations. METHODS During February-June 2012, samples were collected from donors and recipients and retrospectively tested for DENV RNA by transcription-mediated amplification. Recipient chart review, using a case (DENV positive)-control (DENV negative and not known to be exposed) design, was conducted to assess symptoms. RESULTS Of 39 134 recruited blood donors, DENV-4 viremia was confirmed in 0.51% of donations from subjects in Rio de Janeiro and 0.80% of subjects in Recife. Overall, 42 DENV RNA-positive units were transfused into 35 recipients. Of these, 16 RNA-positive units transfused into 16 susceptible recipients were identified as informative: 5 cases were considered probable TT cases, 1 possible TT case, and 10 nontransmissions. The TT rate was 37.5% (95% confidence interval [CI], 15.2%-64.6%), significantly higher than the viremia rate of 0.93% (95% CI, .11%-3.34%) in nonexposed recipients (P < .0001). Chart review did not find significant differences between cases and controls in symptoms or mortality. CONCLUSIONS During a large epidemic of DENV-4 infection in Brazil, >0.5% of donations were RNA positive, and approximately one third of components resulted in TT. However, no significant clinical differences were evident between RNA-positive and RNA-negative recipients.


Maternal and Child Health Journal | 2011

Understanding the Association of Biomedical, Psychosocial and Behavioral Risks with Adverse Pregnancy Outcomes Among African-Americans in Washington, DC

Michele Kiely; Ayman El-Mohandes; Marie G. Gantz; Dhuly Chowdhury; Jutta S. Thornberry; M. Nabil El-Khorazaty

This study investigates the relationship between adverse pregnancy outcomes in high-risk African American women in Washington, DC and sociodemographic risk factors, behavioral risk factors, and the most common and interrelated medical conditions occurring during pregnancy: diabetes, hypertension, preeclampsia, and Body Mass Index (BMI). Data are from a randomized controlled trial conducted in 6 prenatal clinics. Women in their 1st or 2nd trimester were screened for behavioral risks (smoking, environmental tobacco smoke exposure, depression, and intimate partner violence) and demographic eligibility. 1,044 were eligible, interviewed and followed through their pregnancies. Classification and Regression Trees (CART) methodology was used to: (1) explore the relationship between medical and behavioral risks (reported at enrollment), sociodemographic factors and pregnancy outcomes; (2) identify the relative importance of various predictors of adverse pregnancy outcomes; and (3) characterize women at the highest risk of poor pregnancy outcomes. The strongest predictors of poor outcomes were prepregnancy BMI, preconceptional diabetes, employment status, intimate partner violence, and depression. In CART analysis, preeclampsia was the first splitter for low birthweight; preconceptional diabetes was the first splitter for preterm birth (PTB) and neonatal intensive care admission; BMI was the first splitter for very PTB, large for gestational age, Cesarean section and perinatal death; employment was the first splitter for miscarriage. Preconceptional factors strongly influence pregnancy outcomes. For many of these women, the high risks they brought into pregnancy were more likely to impact their pregnancy outcomes than events during pregnancy.


Patient Education and Counseling | 2014

Presenting efficacy information in direct-to-consumer prescription drug advertisements

Amie C. O’Donoghue; Helen W. Sullivan; Kathryn J. Aikin; Dhuly Chowdhury; Rebecca Moultrie; Douglas J. Rupert

OBJECTIVE We evaluated whether presenting prescription drug efficacy information in direct-to-consumer (DTC) advertising helps individuals accurately report a drugs benefits and, if so, which numerical format is most helpful. METHODS We conducted a randomized, controlled study of individuals diagnosed with high cholesterol (n=2807) who viewed fictitious prescription drug print or television ads containing either no drug efficacy information or efficacy information in one of five numerical formats. We measured drug efficacy recall, drug perceptions and attitudes, behavioral intentions, and drug risk recall. RESULTS Individuals who viewed absolute frequency and/or percentage information more accurately reported drug efficacy than participants who viewed no efficacy information. Participants who viewed relative frequency information generally reported drug efficacy less accurately than participants who viewed other numerical formats. CONCLUSION Adding efficacy information to DTC ads-both in print and on television-may potentially increase an individuals knowledge of a drugs efficacy, which may improve patient-provider communication and promote more informed decisions. PRACTICE IMPLICATIONS Providing quantitative efficacy information in a combination of formats (e.g., absolute frequency and percent) may help patients remember information and make decisions about prescription drugs.


Transfusion | 2015

A multicenter study of plasma use in the United States

Darrell J. Triulzi; Jerome L. Gottschall; Edward L. Murphy; Yanyun Wu; Paul M. Ness; Daryl J. Kor; Nareg Roubinian; Debra Fleischmann; Dhuly Chowdhury; Donald Brambilla

Detailed information regarding plasma use in the United States is needed to identify opportunities for practice improvement and design of clinical trials of plasma therapy.


The Journal of Infectious Diseases | 2016

Duration of Dengue Viremia in Blood Donors and Relationships Between Donor Viremia, Infection Incidence and Clinical Case Reports During a Large Epidemic

Michael P. Busch; Ester C. Sabino; Donald Brambilla; Maria Esther Lopes; Ligia Capuani; Dhuly Chowdhury; Christopher McClure; Jeffrey M. Linnen; Harry E. Prince; Graham Simmons; Tzong-Hae Lee; Steven Kleinman; Brian Custer

BACKGROUND Dengue viruses (DENV-1-4) pose a transfusion-transmission risk. This study estimated the dengue RNA detection period in asymptomatic blood donors and relationships between donor viremia and dengue incidence during a large epidemic. METHODS Donor samples from the 2012 dengue transmission season in Rio de Janeiro, Brazil, were tested for DENV RNA by a transcription-mediated amplification (TMA) assay, with DENV types and viral loads determined by polymerase chain reaction. Samples collected during the first and last weeks of enrollment were tested for DENV immunoglobulin (Ig) G and IgM to estimate incidence during the study period, which was analyzed relative to nucleic acid amplification technology (NAT) yield to estimate the duration of NAT-detectable viremia and compared with reported clinical dengue cases in Rio. RESULTS Samples from 16 241 donations were tested; 87 (0.54%) were confirmed as DENV-4 RNA positive. Dengue IgM-positive/IgG-positive reactivity increased from 2.8% to 8.8%, indicating a 6.2% incidence (95% confidence interval [CI], 3.2%-9.1%) during the study period. Based on these data, we estimated a 9.1-day period (95% CI, 4.4-13.9 days) of RNA detectable with TMA. With 100 475 reported cases of clinical dengue, 1 RNA-positive donation was identified per 800 DENV cases. CONCLUSIONS These parameters allow projections of dengue incidence from donor NAT yield data and vice versa, and suggest that viremic donations will be rare relative to clinical disease cases.


Transfusion | 2016

Incidence of transfusion reactions: a multicenter study utilizing systematic active surveillance and expert adjudication

Jeanne E. Hendrickson; Nareg Roubinian; Dhuly Chowdhury; Don Brambilla; Edward L. Murphy; Yanyun Wu; Paul M. Ness; Eric A. Gehrie; Edward L. Snyder; R. George Hauser; Jerome L. Gottschall; Steve Kleinman; Ram Kakaiya; Ronald G. Strauss

Prevalence estimates of the serious hazards of transfusion vary widely. We hypothesized that the current reporting infrastructure in the United States fails to capture many transfusion reactions and undertook a multicenter study using active surveillance, data review, and adjudication to test this hypothesis.


Vox Sanguinis | 2017

Incidence and clinical characteristics of transfusion-associated circulatory overload using an active surveillance algorithm

Nareg Roubinian; Jeanne E. Hendrickson; Darrell J. Triulzi; Jerome L. Gottschall; Dhuly Chowdhury; Daryl J. Kor; Mark R. Looney; Michael A. Matthay; Steve Kleinman; Donald Brambilla; Edward L. Murphy

The concordance of haemovigilance criteria developed for surveillance of transfusion‐associated circulatory overload (TACO) with its clinical diagnosis has not been assessed. In a pilot study to evaluate an electronic screening algorithm, we sought to examine TACO incidence and application of haemovigilance criteria in patients with post‐transfusion pulmonary oedema.


Vox Sanguinis | 2018

A multicentre study investigating vital sign changes occurring in complicated and uncomplicated transfusions

Eric A. Gehrie; Nareg Roubinian; Dhuly Chowdhury; Donald Brambilla; Edward L. Murphy; Jerome L. Gottschall; Yanyun Wu; Paul M. Ness; Ronald G. Strauss; Jeanne E. Hendrickson

Many hospitals require transfusions to be discontinued when vital signs stray from predetermined ranges, regardless of clinical symptoms. Variations in vital signs may be unrelated to transfusion, however, and needlessly stopping a transfusion may delay medical care while increasing donor exposures and healthcare costs. We hypothesized that a detailed study of vital sign changes associated with transfusion of blood product by component, including those associated with potential reactions (complicated) and those deemed to be uncomplicated, would establish a useful framework of reference for treating clinicians and transfusion services alike.


Critical Care Medicine | 2018

Contemporary risk factors and outcomes of transfusion-associated circulatory overload

Nareg Roubinian; Jeanne E. Hendrickson; Darrell J. Triulzi; Jerome L. Gottschall; Michael Michalkiewicz; Dhuly Chowdhury; Daryl J. Kor; Mark R. Looney; Michael A. Matthay; Steven H. Kleinman; Donald Brambilla; Edward L. Murphy

Objectives: Transfusion-associated circulatory overload is characterized by hydrostatic pulmonary edema following blood transfusion. Restrictive transfusion practice may affect the occurrence and severity of transfusion-associated circulatory overload in critically ill patients. We sought to examine contemporary risk factors and outcomes for transfusion-associated circulatory overload. Design: Case-control study. Setting: Four tertiary care hospitals. Patients: We prospectively enrolled 200 patients with transfusion-associated circulatory overload identified by active surveillance and 405 controls matched by transfusion intensity. Interventions: None. Measurements and Main Results: Among 20,845 transfused patients who received 128,263 blood components from May 2015 until July 2016, transfusion-associated circulatory overload incidence was one case per 100 transfused patients. In addition to cardiovascular comorbidities, multivariable analysis identified the following independent predictors of transfusion-associated circulatory overload: acute kidney injury, emergency surgery, pretransfusion diuretic use, and plasma transfusion—the latter especially in females. Compared with matched controls, transfusion-associated circulatory overload cases were more likely to require mechanical ventilation (71% vs 49%; p < 0.001), experienced longer intensive care and hospital lengths of stay following transfusion, and had higher mortality (21% vs 11%; p = 0.02) even after adjustment for other potentially confounding variables. Conclusions: Despite restrictive transfusion practice, transfusion-associated circulatory overload remains a frequent complication of transfusion and is an independent risk factor for in-hospital morbidity and mortality. In addition to cardiovascular and renal risk factors, plasma transfusion was associated with transfusion-associated circulatory overload after controlling for other covariates. Additional research is needed to examine the benefit of reduced erythrocyte or plasma exposure in patients at high risk for transfusion-associated circulatory overload.


Emerging Infectious Diseases | 2017

Use of Blood Donor Screening to Monitor Prevalence of HIV and Hepatitis B and C Viruses, South Africa

Marion Vermeulen; Ronel Swanevelder; Dhuly Chowdhury; Charlotte Ingram; Ravi Reddy; Evan M. Bloch; Brian Custer; Edward L. Murphy

Among 397,640 first-time blood donors screened in South Africa during 2012–2015, HIV prevalence was 1.13%, hepatitis B virus prevalence 0.66%, and hepatitis C virus prevalence 0.03%. Findings of note were a high HIV prevalence in Mpumalanga Province and the near absence of hepatitis C virus nationwide.

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Edward L. Murphy

Systems Research Institute

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Jerome L. Gottschall

Medical College of Wisconsin

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Nareg Roubinian

Systems Research Institute

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Steve Kleinman

University of British Columbia

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Brian Custer

Systems Research Institute

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