9 results on '"Nipunie S. Rajapakse"'
Search Results
2. Pediatric antimicrobial stewardship practices at discharge: A national survey
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Marie E. Wang, Hayden T. Schwenk, Jason G. Newland, Zachary Willis, Louise E. Vaz, Nipunie S Rajapakse, Kimberly Felder, Ritu Banerjee, Jeffrey S. Gerber, and Adam L. Hersh
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Microbiology (medical) ,2019-20 coronavirus outbreak ,medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Epidemiology ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Antimicrobial ,Patient Discharge ,Anti-Bacterial Agents ,Antimicrobial Stewardship ,03 medical and health sciences ,Prescriptions ,0302 clinical medicine ,Infectious Diseases ,Anti-Infective Agents ,030225 pediatrics ,Family medicine ,medicine ,Humans ,Antimicrobial stewardship ,030212 general & internal medicine ,Business ,Stewardship ,Child - Abstract
We surveyed pediatric antimicrobial stewardship program (ASP) site leaders within the Sharing Antimicrobial Reports for Pediatric Stewardship collaborative regarding discharge stewardship practices. Among 67 sites, 13 (19%) reported ASP review of discharge antimicrobial prescriptions. These findings highlight discharge stewardship as a potential opportunity for improvement during the hospital-to-home transition.
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- 2021
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3. Mediastinal Histoplasmosis With Esophageal Perforation Presenting as Recurrent Polymicrobial Empyema and Pericarditis in a Previously Healthy Child
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Sayeh Fattahi, Theresa Madigan, Nipunie S Rajapakse, and Elizabeth H Ristagno
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medicine.medical_specialty ,Esophageal Perforation ,business.industry ,Perforation (oil well) ,General Medicine ,medicine.disease ,Empyema ,Histoplasmosis ,Surgery ,Pericarditis ,Infectious Diseases ,Pediatrics, Perinatology and Child Health ,medicine ,Humans ,Child ,business - Published
- 2019
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4. Randomized Trial Evaluating Clinical Impact of RAPid IDentification and Susceptibility Testing for Gram-negative Bacteremia: RAPIDS-GN
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Nicolynn C. Cole, Peggy C. Kohner, Sukantha Chandrasekaran, Sherry M. Ihde, Annabelle de St Maurice, Jennifer Curello, Michelle Earley, Nipunie S Rajapakse, William Swearingen, Abinash Virk, Katelyn A. Reed, Lauren Komarow, Lisa E. Hines, Robin Patel, Audrey N. Schuetz, Omai B. Garner, Brenda L. Dylla, Meganne Kanatani, Rubi Arias, Sarah B Doernberg, Judith J. Lok, and Ritu Banerjee
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Microbiology (medical) ,medicine.medical_specialty ,Randomization ,medicine.drug_class ,gram negative ,Clinical Trials and Supportive Activities ,Antibiotics ,Bacteremia ,bloodstream infection ,Microbial Sensitivity Tests ,Medical and Health Sciences ,Microbiology ,law.invention ,Vaccine Related ,Randomized controlled trial ,blood cultures ,Clinical Research ,law ,Interquartile range ,Sepsis ,Internal medicine ,Gram-Negative Bacteria ,medicine ,Gram-negative bacteremia ,Humans ,Blood culture ,Online Only Articles ,medicine.diagnostic_test ,business.industry ,Prevention ,Hematology ,Biological Sciences ,Anti-Bacterial Agents ,antibiotic susceptibility testing ,Clinical trial ,Emerging Infectious Diseases ,Good Health and Well Being ,Infectious Diseases ,Gram staining ,Blood Culture ,Antimicrobial Resistance ,Gram-Negative Bacterial Infections ,Infection ,business ,rapid diagnostic - Abstract
Background Rapid blood culture diagnostics are of unclear benefit for patients with gram-negative bacilli (GNB) bloodstream infections (BSIs). We conducted a multicenter, randomized, controlled trial comparing outcomes of patients with GNB BSIs who had blood culture testing with standard-of-care (SOC) culture and antimicrobial susceptibility testing (AST) vs rapid organism identification (ID) and phenotypic AST using the Accelerate Pheno System (RAPID). Methods Patients with positive blood cultures with Gram stains showing GNB were randomized to SOC testing with antimicrobial stewardship (AS) review or RAPID with AS. The primary outcome was time to first antibiotic modification within 72 hours of randomization. Results Of 500 randomized patients, 448 were included (226 SOC, 222 RAPID). Mean (standard deviation) time to results was faster for RAPID than SOC for organism ID (2.7 [1.2] vs 11.7 [10.5] hours; P Conclusions Rapid organism ID and phenotypic AST led to faster changes in antibiotic therapy for gram-negative BSIs. Clinical Trials Registration NCT03218397.
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- 2020
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5. Unilateral Phrenic Nerve Palsy in Infants with Congenital Zika Syndrome
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Rachael M. Liesman, Elitza S. Theel, Nancy Henry, Luisa Medeiros de Mello, Mai Lan Ho, Kevin Ellsworth, Ana Catarina Matos Ishigami Alvino, Adam Wallace, Nipunie S. Rajapakse, and Jucille do Amaral Meneses
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Microbiology (medical) ,Adult ,Microcephaly ,Pediatrics ,medicine.medical_specialty ,Unilateral Phrenic Nerve Palsy in Infants with Congenital Zika Syndrome ,congenital Zika syndrome ,Adolescent ,Epidemiology ,Central nervous system ,Diaphragm ,lcsh:Medicine ,Diaphragmatic paralysis ,phrenic nerve ,Virus ,Zika virus ,lcsh:Infectious and parasitic diseases ,fetal diseases ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Pregnancy ,peripheral nervous system ,phrenic nerve palsy ,Medicine ,Humans ,viruses ,lcsh:RC109-216 ,030212 general & internal medicine ,Pregnancy Complications, Infectious ,Phrenic nerve ,Arthrogryposis ,biology ,business.industry ,Zika Virus Infection ,lcsh:R ,Infant, Newborn ,Peripheral Nervous System Diseases ,biology.organism_classification ,medicine.disease ,medicine.anatomical_structure ,Infectious Diseases ,Peripheral nervous system ,Synopsis ,Female ,medicine.symptom ,business ,030217 neurology & neurosurgery - Abstract
This case series of right unilateral diaphragmatic paralysis suggests peripheral nervous system involvement., Since the first identification of neonatal microcephaly cases associated with congenital Zika virus infection in Brazil in 2015, a distinctive constellation of clinical features of congenital Zika syndrome has been described. Fetal brain disruption sequence is hypothesized to underlie the devastating effects of the virus on the central nervous system. However, little is known about the effects of congenital Zika virus infection on the peripheral nervous system. We describe a series of 4 cases of right unilateral diaphragmatic paralysis in infants with congenital Zika syndrome suggesting peripheral nervous system involvement and Zika virus as a unique congenital infectious cause of this finding. All the patients described also had arthrogryposis (including talipes equinovarus) and died from complications related to progressive respiratory failure.
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- 2018
6. 1136. Trends in Speaker Representation at the Infectious Diseases Society of America (IDSA) IDWeek Conference, 2013-2019
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Jasmine R Marcelin, Rohan Khazanchi, Elizabeth Lyden, Kelly Cawcutt, Ravina Kullar, Nipunie S Rajapakse, David R Ha, and Elizabeth H Ristagno
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Infectious Diseases ,AcademicSubjects/MED00290 ,Oncology ,business.industry ,Poster Abstracts ,Representation (systemics) ,Medicine ,business ,Linguistics - Abstract
Background Over the last decade, there have been sustained efforts to diversify the healthcare workforce. In 2016, the IDWeek Program Committee was charged to ensure gender equity in speaker sessions. Whether this intervention also resulted in more opportunities for underrepresented speakers has not been determined. Methods This project was supported by IDSA, who provided demographic information on IDWeek speakers (excluding poster sessions) from 2013-2019. Data were summarized using descriptive statistics, and chi-square analysis evaluated changes over time. Each speaker slot was considered an independent event. Data was combined for 2013-2016 (≤2016) and 2017-2019 (>2016). IDSA membership demographics were available from 2014 for gender, race/ethnicity, from 2016 for age, and from 2018 for professional degree. Results A total of 3640 speaker slots were filled by 2504 individuals from 2013-2019. A larger proportion of speaker slots were filled by women >2016 (51%) vs ≤ 2016 (43%), with a linear increase from 38.6% in 2013 to 52.1% in 2019 (p< 0.001). Averaged across 2013-2019, IDSA membership was 67.5% White, 20.6% Asian, 7.7% Latinx, 3.9% Black, and 0.4% Other. IDWeek Speakers during that timeframe were 77.7% White, 13.9% Asian, 4.7% Latinx, 2.7% Black, and 1.0% Other; a larger proportion of slots were filled by Asian speakers >2016 (16.3%) vs ≤ 2016 (12.8%) (p=0.005). The proportion of pharmacist speakers increased over time; 5.1% of speakers in 2019 reflected IDSA pharmacist membership (5.4%). The proportion of individuals invited to speak more than once differed by age (19% in < 40yo, 28% 40-49yo, 32% 50-59yo, and 22% >60yo; p< 0.001), and professional degree (28% physicians, 18% pharmacists, 9% other doctorates, and 7% non-doctorate speakers; p< 0.001). Figure 1: Trends in Gender Distribution of IDWeek Speakers and IDSA Members, 2013-2019 Figure 2: Trends in Race/Ethnicity Distribution of IDWeek Speakers and IDSA Members, 2013-2019 Conclusion Intentional consideration of gender equity by the Program Committee significantly improved equitable gender representation of invited speakers at IDWeek. This effort has not resulted in increased diversity of invited speakers from groups underrepresented in IDSA membership. To ensure that invited speakers represent the membership of IDSA/IDWeek partner organizations and more importantly, the communities we serve, we call for continued application of the principles of Inclusion, Diversity, Access, and Equity at IDWeek. Disclosures All Authors: No reported disclosures
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- 2020
7. 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
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Ritu Banerjee, Lauren Komarow, Abinash Virk, Nipunie S Rajapakse, Audrey Schuetz, Brenda Dylla, Michelle Earley, Judith Lok, Peggy Kohner, Sherry Ihde, Nicolynn Cole, Lisa Hines, Katelyn Reed, Omai Garner, Sukantha Chandrasekaran, Annabelle M de St. Maurice, Meganne Kanatani, Jennifer Curello, Rubi Arias, William Swearingen, Sarah B Doernberg, and Robin Patel
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medicine.medical_specialty ,Palliative care ,Intention-to-treat analysis ,medicine.diagnostic_test ,business.industry ,medicine.drug_class ,Antibiotics ,Antimicrobial susceptibility ,law.invention ,Abstracts ,Infectious Diseases ,Oncology ,Randomized controlled trial ,law ,Internal medicine ,Poster Abstracts ,Gram-negative bacteremia ,Medicine ,Antimicrobial stewardship ,Blood culture ,business - Abstract
Background Rapid blood culture diagnostics increase cost and have unclear benefit for patients with Gram-negative bacilli (GNB) bloodstream infections (BSIs). We conducted a multicenter, prospective randomized controlled trial (RAPIDS-GN), comparing outcomes of patients with GNB BSI who had blood culture testing with standard of care (SOC) culture and antibiotic susceptibility testing (AST) vs. rapid organism identification (ID) and phenotypic AST using the Accelerate Pheno System (AXDX). Methods Subjects with blood culture Gram stain showing GNB were randomized to receive SOC testing with antimicrobial stewardship review (AS) or AXDX plus SOC testing with AS, at two academic medical centers between October 2017 and October 2018. SOC testing included rapid MALDI-TOF mass spectrometry ID and agar dilution or broth microdilution AST. In a modified intention to treat analysis, subjects were excluded if: Gram stain was erroneous, culture was positive during off-hours, blood culture in the prior week had GNB, they were deceased/on comfort care, or admitted to a nonparticipating hospital. The primary outcome was time to first antibiotic modification within 72 hours after randomization. Subjects without antibiotic modifications were assigned a time of 72 hours. No censoring was observed. T-tests and Wilcoxon rank-sum tests were used for statistical analyses. Results Of 500 randomized subjects, 448 were included (226 SOC, 222 AXDX). Groups did not differ in baseline characteristics (Table 1). Median (IQR) hours to first antibiotic modification was faster in the AXDX vs. SOC group [8.6 (2.6, 27.6) vs. 14.9 (3.3, 41.1)], P = 0.02 (Figure 1). Median (IQR) hours to first Gram-negative antibiotic modification (including escalation and de-escalation) was faster in the AXDX than SOC group [17.4 (4.9, 72) vs. 42.1 (10.1, 72)], P < 0.001 (Figure 2). Groups did not differ in clinical outcomes (Table 2). Mean (S.D.) time to results was faster for AXDX than SOC for organism ID [2.7 (1.2) h vs. 15.6 (20.3) h, P < 0.001] and AST [13 (55.7) h vs. 54.6 (45.5) h, P < 0.001]. Conclusion In the largest trial to evaluate the clinical impact of a blood culture diagnostic for GNB BSI, we found that rapid organism ID and phenotypic AST led to faster changes in antibiotic therapy for Gram-negative bacteremia. Disclosures Ritu Banerjee, MD, PhD, Accelerate Diagnostics: Grant/Research Support; BioFire: Research Grant; Biomerieux: Research Grant; Roche: Research Grant Robin Patel, MD, ASM and IDSA: Other Financial or Material Support, Travel reimbursement, editor’s stipends; CD Diagnostics, Merck, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, ContraFect, TenNor Therapeutics Limited, Shionogi: Grant/Research Support; Curetis, Specific Technologies, NextGen Diagnostics, PathoQuest, Qvella: Consultant; NBME, Up-to-Date, the Infectious Diseases Board Review Course: Honorarium recipient, Other Financial or Material Support; Patent on Bordetella pertussis/parapertussis PCR issued, a patent on a device/method for sonication with royalties paid by Samsung to Mayo Clinic, and a patent on an anti-biofilm substance issued: Other Financial or Material Support, Patents.
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- 2019
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8. 1108. Diagnostic Yield of the BioFire FilmArray Gastrointestinal Panel in Hospitalized Children at an Academic Children’s Center
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Nipunie S Rajapakse, Theresa Madigan, and Robin Patel
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medicine.medical_specialty ,Abstracts ,Infectious Diseases ,Oncology ,B. Poster Abstracts ,business.industry ,Hospitalized patients ,Pcr test ,Internal medicine ,Medicine ,business - Abstract
Background The BioFire FilmArray Gastrointestinal Panel (BioFire Diagnostics) (GIP) is a multiplex stool PCR test that detects 22 organisms. Studies in adults suggest that the diagnostic yield of the GIP in hospitalized patients is low. The utility of the GIP among hospitalized pediatric patients and indications for diagnostic stewardship of this test are not well described. Methods We conducted a retrospective chart review of hospitalized pediatric patients who had a GIP ordered between October 2015 and October 2017. Demographic, clinical, and laboratory information was extracted from the medical record. Statistical analysis was completed using JMP Pro 13.0.0 (SAS Institute Inc.). Results Over the 2-year study period, 193 GIPs were obtained on 155 individual pediatric patients. The mean patient age was 8 years and 59% were male. Forty-four percent of patients were immunocompromised and 21% had inflammatory bowel disease. The pediatric infectious disease (PID) team was consulted in 15% of patients at the time the test was ordered. The overall positivity rate of the GIP for one or more pathogens was 42% (Figure 1), with 76% of GIPs positive for one, 23% for two, and 1% for three pathogens. No parasitic infections were diagnosed. The GIP was more likely to be positive if GI symptom onset was prior to admission (48% vs. 24%, P = 0.004), if GI symptoms had been present for < 2 weeks vs. ≥2 weeks (52% vs. 20%, P = 0.0001), and if GI symptoms were the primary reason for the hospital admission (50% vs. 32%, P = 0.012). Only Clostridioides difficile or viral pathogens were detected in patients whose symptoms began in the hospital (Figure 2). Among patients with a positive test, 40% received treatment targeted at one or more of the detected pathogens (Figure 1). Enteropathogenic E.coli (EPEC) and Enteroaggregative E.coli (EAEC) were never treated (Figure 3). Conclusion The GIP was positive for one or more pathogens in 42% of hospitalized children for whom the test was ordered, and led to specific therapy in 40% of those with a positive test. EPEC and EAEC were not treated. The diagnostic yield of the GIP was higher if GI symptoms were present for Disclosures R. Patel, CD Diagnostics, BioFire, Curetis, Merck, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, Allergan, and The Medicines Company: Grant Investigator, Research grant – monies paid to Mayo Clinic. Curetis, Specific Technologies, Selux Dx, GenMark Diagnostics, PathoQuest and Genentech: Consultant and Scientific Advisor, Consulting fee – monies paid to Mayo Clinic. ASM and IDSA: Travel reimbursement and editor’s stipends, Travel reimbursement and editor’s stipends. NBME, Up-to-Date and the Infectious Diseases Board Review Course: Varies, Honoraria. Mayo Clinic: Employee, Salary.
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- 2018
9. 1304. From Information Bolus to Continuous Infusion: Resident Knowledge and Satisfaction With an 'Antibiotic of the Month' Educational Initiative at an Academic Children’s Hospital
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Luke C. Radel, Nipunie S Rajapakse, Yasaman Fatemi, and Theresa Madigan
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Abstracts ,medicine.medical_specialty ,Infectious Diseases ,Bolus (medicine) ,B. Poster Abstracts ,Oncology ,Continuous infusion ,business.industry ,medicine.drug_class ,Emergency medicine ,Antibiotics ,medicine ,business - Abstract
Background Medical trainees play a critical role in the prescribing of antimicrobials. Prescriber education is one of the CDC core elements of antimicrobial stewardship programs. Optimal strategies for educating residents about antimicrobials have not been identified; however, the common practice of teaching all classes of available antibiotics over a short period of time (usually a single 1–2 hour lecture or “bolus”) is generally not well received and likely ineffective. Methods We developed a novel antibiotic of the month (AOTM) education program (“continuous infusion”) for pediatric residents. It included a monthly 10-minute presentation by an infectious diseases physician or fellow about a single commonly prescribed antibiotic, a handout summarizing important aspects of the antibiotic and a display posted in the resident workroom. An anonymous survey was sent to all pediatric residents before and 6 months after implementation of the AOTM program. The survey consisted of questions on demographics, satisfaction with the program, and antibiotic knowledge. Responses were tabulated and analyzed using Microsoft Excel. Responses were summarized and reported as a proportion of total responses. Results Both pre- and post-implementation surveys were completed by 21 pediatric residents (51% response rate). Prior to the AOTM program, 55% of respondents felt very or somewhat uncomfortable about their current level of knowledge about antimicrobials and antimicrobial prescribing. Six months after initiation of the program, 86% and 76% agreed or strongly agreed that their knowledge of antimicrobials and antimicrobial resistance, respectively, had improved. After introduction of the program, 81% felt more comfortable or much more comfortable with antimicrobial prescribing. Fifty-seven percent had referenced the handout at some point after the teaching session and 100% agreed that the program was worthwhile continuing in the next academic year. Conclusion A continuous infusion of antimicrobial education in the form of an AOTM education program was well received among pediatric residents and increased their knowledge and comfort level with antimicrobial prescribing. Further studies to measure knowledge retention with this strategy are required. Disclosures All authors: No reported disclosures.
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- 2018
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