Rana F. Hamdy
Children's National Medical Center
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Featured researches published by Rana F. Hamdy.
Pediatrics | 2017
Rana F. Hamdy; Alice J. Hsu; Chris Stockmann; Jared Olson; Matthew Bryan; Adam L. Hersh; Pranita D. Tamma; Jeffrey S. Gerber
This multicenter retrospective cohort study evaluates the clinical epidemiology and outcomes of children with MRSA bacteremia and determines risk factors for treatment failure. BACKGROUND: Methicillin-resistant Staphylococcus aureus (MRSA) bacteremia is associated with high rates of treatment failure in adults. The epidemiology, clinical outcomes, and risk factors for treatment failure associated with MRSA bacteremia in children are poorly understood. METHODS: Multicenter, retrospective cohort study of children ≤18 years hospitalized with MRSA bacteremia across 3 tertiary care children’s hospitals from 2007 to 2014. Treatment failure was defined as persistent bacteremia >3 days, recurrence of bacteremia within 30 days, or attributable 30-day mortality. Potential risk factors for treatment failure, including the site of infection, vancomycin trough concentration, critical illness, and need for source control, were collected via manual chart review and evaluated using multivariable logistic regression. RESULTS: Of 232 episodes of MRSA bacteremia, 72 (31%) experienced treatment failure and 23% developed complications, whereas 5 (2%) died within 30 days. Multivariable analysis of 174 children treated with vancomycin with steady-state vancomycin concentrations obtained found that catheter-related infections (odds ratio [OR], 0.36; 95% confidence interval [CI]: 0.13–0.94) and endovascular infections (OR, 4.35; 95% CI: 1.07–17.7) were associated with lower and higher odds of treatment failure, respectively, whereas a first vancomycin serum trough concentration <10 μg/mL was not associated with treatment failure (OR, 1.34; 95% CI, 0.49–3.66). Each additional day of bacteremia was associated with a 50% (95% CI: 26%–79%) increased odds of bacteremia-related complications. CONCLUSIONS: Hospitalized children with MRSA bacteremia frequently suffered treatment failure and complications, but mortality was low. The odds of bacteremia-related complications increased with each additional day of bacteremia, emphasizing the importance of achieving rapid sterilization.
PLOS ONE | 2018
Daniele Dona; Silvia Zingarella; Andrea Gastaldi; Rebecca Lundin; Giorgio Perilongo; Anna Chiara Frigo; Rana F. Hamdy; Theoklis E. Zaoutis; Liviana Da Dalt; Carlo Giaquinto
BACKGROUNDnItalian pediatric antimicrobial prescription rates are among the highest in Europe. As a first step in an Antimicrobial Stewardship Program, we implemented a Clinical Pathway (CP) for Community Acquired Pneumonia with the aim of decreasing overall prescription of antibiotics, especially broad-spectrum.nnnMATERIALS AND METHODSnThe CP was implemented on 10/01/2015. We collected antibiotic prescribing and outcomes data from children aged 3 months-15 years diagnosed with CAP from 10/15/2014 to 04/15/2015 (pre-intervention period) and from 10/15/2015 to 04/15/2016 (post-intervention period). We assessed antibiotic prescription differences pre- and post-CP, including rates, breadth of spectrum, and duration of therapy. We also compared length of hospital stay for inpatients and treatment failure for inpatients and outpatients. Chi-square and Fishers exact test were used to compare categorical variables and Wilcoxon rank sum test was used to compare quantitative outcomes.nnnRESULTSn120 pre- and 86 post-intervention clinic visits were identified with a diagnosis of CAP. In outpatients, we observed a decrease in broad-spectrum regimens (50% pre-CP vs. 26.8% post-CP, p = 0.02), in particular macrolides, and an increase in narrow-spectrum (amoxicillin) post-CP. Post-CP children received fewer antibiotic courses (median DOT from 10 pre-CP to 8 post-CP, p<0.0001) for fewer days (median LOT from 10 pre-CP to 8 post-CP, p<0.0001) than their pre-CP counterparts. Physicians prescribed narrow-spectrum monotherapy more frequently than broad-spectrum combination therapy (DOT/LOT ratio 1.157 pre-CP vs. 1.065 post-CP). No difference in treatment failure was reported before and after implementation (2.3% pre-CP vs. 11.8% post-CP, p = 0.29). Among inpatients we also noted a decrease in broad-spectrum regimens (100% pre-CP vs. 66.7% post-CP, p = 0.02) and the introduction of narrow-spectrum regimens (0% pre-CP vs. 33.3% post-CP, p = 0.02) post-CP. Hospitalized patients received fewer antibiotic courses post-CP (median DOT from 18.5 pre-CP to 10 post-CP, p = 0.004), while there was no statistical difference in length of therapy (median LOT from 11 pre-CP to 10 post-CP, p = 0.06). Days of broad spectrum therapy were notably lower post-CP (median bsDOT from 17 pre-CP to 4.5 post-CP, p <0.0001). No difference in treatment failure was reported before and after CP implementation (16.7% pre-CP vs. 15.4% post-CP, p = 1).nnnCONCLUSIONSnIntroduction of a CP for CAP in a Pediatric Emergency Department led to reduction of broad-spectrum antibiotic prescriptions, of combination therapy and of duration of treatment both for outpatients and inpatients.
Journal of the Pediatric Infectious Diseases Society | 2017
Alice J. Hsu; Rana F. Hamdy; Yanjie Huang; Jared Olson; Shahira Ghobrial; Jeffrey S. Gerber; Adam L. Hersh; Pranita D. Tamma
In a multicenter retrospective study, we sought to determine the optimal vancomycin trough concentration that would impact the duration of methicillin-resistant Staphylococcus aureus bacteremia in children. We found that a median vancomycin trough concentration of <10 µg/mL within the first 72 hours may be associated with a longer duration of bacteremia compared to a median trough concentration of ≥10 µg/mL.
Pediatric Infectious Disease Journal | 2018
Daniele Donà; Maura Baraldi; Giulia Brigadoi; Rebecca Lundin; Giorgio Perilongo; Rana F. Hamdy; Theoklis E. Zaoutis; Liviana Da Dalt; Carlo Giaquinto
Open Forum Infectious Diseases | 2017
Amol Purandare; Madan Kumar; Rana F. Hamdy
Open Forum Infectious Diseases | 2017
Rana F. Hamdy; Daniele Dona; Jeffrey S. Gerber
Open Forum Infectious Diseases | 2017
Daniele Dona; Rana F. Hamdy; Theoklis E. Zaoutis; Jeffrey S. Gerber
Open Forum Infectious Diseases | 2016
Lori Handy; Rana F. Hamdy; Matthew Bryan; Daniele Dona; Evangelos Spyridakis; Areti Kyriakousi; Talene A. Metjian; Jeffrey S. Gerber
Open Forum Infectious Diseases | 2016
Rana F. Hamdy; Lori Handy; Evangelos Spyridakis; Daniele Dona; Matthew Bryan; Areti Kyriakousi; Jeffrey S. Gerber
Open Forum Infectious Diseases | 2016
Daniele Dona; Maura Baraldi; Giulia Brigadoi; Silvia Zingarella; Rebecca Lundin; Rana F. Hamdy; Theoklis E. Zaoutis; Liviana Da Dalt; Carlo Giaquinto