TY - JOUR
T1 - A global point prevalence survey of antimicrobial use in neonatal intensive care units
T2 - The no-more-antibiotics and resistance (NO-MAS-R) study
AU - for the Global NEO-ASP Study Group
AU - Prusakov, Pavel
AU - Goff, Debra A.
AU - Wozniak, Phillip S.
AU - Cassim, Azraa
AU - Scipion, Catherine E.A.
AU - Urzúa, Soledad
AU - Ronchi, Andrea
AU - Zeng, Lingkong
AU - Ladipo-Ajayi, Oluwaseun
AU - Aviles-Otero, Noelia
AU - Udeigwe-Okeke, Chisom R.
AU - Melamed, Rimma
AU - Silveira, Rita C.
AU - Auriti, Cinzia
AU - Beltrán-Arroyave, Claudia
AU - Zamora-Flores, Elena
AU - Sanchez-Codez, Maria
AU - Donkor, Eric S.
AU - Kekomäki, Satu
AU - Mainini, Nicoletta
AU - Trochez, Rosalba Vivas
AU - Casey, Jamalyn
AU - Graus, Juan M.
AU - Muller, Mallory
AU - Singh, Sara
AU - Loeffen, Yvette
AU - Pérez, María Eulalia Tamayo
AU - Ferreyra, Gloria Isabel
AU - Lima-Rogel, Victoria
AU - Perrone, Barbara
AU - Izquierdo, Giannina
AU - Cernada, María
AU - Stoffella, Sylvia
AU - Ekenze, Sebastian Okwuchukwu
AU - de Alba-Romero, Concepción
AU - Tzialla, Chryssoula
AU - Pham, Jennifer T.
AU - Hosoi, Kenichiro
AU - Consuegra, Magdalena Cecilia Calero
AU - Betta, Pasqua
AU - Hoyos, O. Alvaro
AU - Roilides, Emmanuel
AU - Naranjo-Zuñiga, Gabriela
AU - Oshiro, Makoto
AU - Garay, Victor
AU - Mondì, Vito
AU - Mazzeo, Danila
AU - Stahl, James A.
AU - Cantey, Joseph B.
AU - Abdellatif, Mohamed
N1 - Funding Information:
Dr. Pablo J. Sánchez has received research grant support from Merck & Co. during the conduct of the study, and grant from MedImmune, Inc - AstraZeneca, outside of the submitted work.
Funding Information:
Mr. Wozniak received a Barnes Medical Student Research Scholarship grant from The Ohio State University College of Medicine.
Funding Information:
Dr. Pavel Prusakov has received research grant support from Merck & Co. and Pfizer.
Funding Information:
All data will be available upon reasonable request to the corresponding author, and it will be shared according to the standards of ethical policies regulating data sharing of human subjects. Merck & Co. (PJS, PP, DAG); The Ohio State University College of Medicine Barnes Medical Student Research Scholarship (PSW), Pavel Prusakov (PP), Debra A. Goff, and Pablo J. S?nchez (PJS) conceptualized and designed the study and analyzed the data set. PP wrote the first draft of the manuscript. All authors are members of the Global NEO-ASP Study Group and obtained the local data, contributed to the interpretation of the data, and made critical revision of the manuscript for important intellectual content. All authors have read and agreed to the final version of the manuscript. PJS as the corresponding author had full access to all of the data in the study and had final responsibility for the decision to submit for publication. Additional members of the Global NEO-ASP Study Group who contributed to the study: Uchechukwu Obiora Ezomike MBBS, University of Nigeria Teaching Hospital; Kenechukwu K Iloh MBBS, University of Nigeria Teaching Hospital; Carlos Fajardo MD, EpicLatino Neonatal Network; Alejandro Jordan-Villegas, MD, Arnold Palmer Hospital for Children; Ana A. Garcia Robles, PharmD, La Fe University and Polytechnic Hospital; Ana Ruth Mej?a-Elizondo MD, Hospital Central Dr. Ignacio Morones Prieto and Universidad Autonoma de San Luis Potosi; Angeliki Kontou, MD, Hippokration Hospital; Ashley Casper, PharmD, Norton Children's Hospital; Ayah Al Bizri MPH, American University of Beirut; Bel?n Fern?ndez Monteagudo MD, Gregorio Mara?on University Hospital; Benedict Nwomeh, MD, Nationwide Children's Hospital; Carlo Pietrasanta, MD, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Carlos Andr?s Espinosa Rivas MD, Hospital General San Francisco; Carolina Guerra, MD, Division of Neonatology Hospital Barros Luco Trudeau, Santiago, Chile; Claudia R. Hentges, MD, Universidade Federal do Rio Grande do Sul. Hospital de Clinicas de Porto Alegre; David A Kaufman, MD, University of Virginia School of Medicine; Diana Singh, MBBS, University of Guyana, School of Medicine; Efrain Gabriel Suarez Concha MD, Hospital General San Francisco; Eilon Shany, MD, Soroka University Medical Center; Elias Iosifidis, MD, Hippokration Hospital; Elisavet Chorafa, MD, Hippokration Hospital; Emmanuel A. Ameh, MBBS, National Hopital, Abuja, Nigeria; Felix Alakaloko, FMCS, Lagos University Teaching Hospital; Hilary White, DO, St. Vincent Women's Hospital; Imad Kassis MD, The Ruth Rappaport Children's Hospital; Jack Long MD, The Robert Larner College of Medicine at The University of Vermont; Jennifer Bowes, MSc, Children's Hospital of Eastern Ontario; Kosmas Sarafidis, MD, Hippokration Hospital; Laura Piedad Simba?a Guachamin MD, Hospital General San Francisco; Lorenza Pugni, MD, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Laszlo Markasz, MD, Uppsala University, Uppsala University Children's Hospital; Louis Bont, MD, Wilhelmina Children's Hospital; Mame Y. Nyarko, MBChB, Princess Marie Louise Children's Hospital; Maranatha Persaud MBBS, University of Guyana, School of Medicine; Mar?a L. Avila-Aguero MD, Hospital Nacional de Ni?os ?Dr Carlos S?enz Herrera? and Yale School of Public Health; Mariya Mukhtar-Yola. MBBS, National Hopital, Abuja, Nigeria; Meirav Sela MSc, The Ruth Rappaport Children's Hospital; Navjyot K. Vidwan, MD, Norton Children's Hospital; Pinky Lea Chirwa MBChB, Nelson Mandela Children's Hospital; Renato S. Procianoy MD, Universidade Federal do Rio Grande do Sul. Hospital de Clinicas de Porto Alegre; Roc?o Inojosa MD, Pontificia Universidad Catolica; Ulanda Kilanya Haynes MD, University of Guyana, School of Medicine; Valentina Favero MD, TrevisoHospital; Wilmer Orlando S?nchez Escalante, Hospital General San Francisco; Zaid Alhinai MD, Sultan Qaboos University Hospital, We thank the EpicLatino Neonatal Network for assistance in recruitment of study sites. The study was supported by a grant from Merck & Co. (PP, DAG, and PJS) and The Ohio State University College of Medicine Barnes Medical Student Research Scholarship (PSW). These sponsors had no role in the design and conduct of the study; collection, analysis, and interpretation of data; in the writing of the study; and in the decision to submit the paper for publication.
Publisher Copyright:
© 2021 The Authors
PY - 2021/2
Y1 - 2021/2
N2 - Background: Global assessment of antimicrobial agents prescribed to infants in the neonatal intensive care unit (NICU) may inform antimicrobial stewardship efforts. Methods: We conducted a one-day global point prevalence study of all antimicrobials provided to NICU infants. Demographic, clinical, and microbiologic data were obtained including NICU level, census, birth weight, gestational/chronologic age, diagnoses, antimicrobial therapy (reason for use; length of therapy), antimicrobial stewardship program (ASP), and 30-day in-hospital mortality. Findings: On July 1, 2019, 26% of infants (580/2,265; range, 0–100%; median gestational age, 33 weeks; median birth weight, 1800 g) in 84 NICUs (51, high-income; 33, low-to-middle income) from 29 countries (14, high-income; 15, low-to-middle income) in five continents received ≥1 antimicrobial agent (92%, antibacterial; 19%, antifungal; 4%, antiviral). The most common reasons for antibiotic therapy were “rule-out” sepsis (32%) and “culture-negative” sepsis (16%) with ampicillin (40%), gentamicin (35%), amikacin (19%), vancomycin (15%), and meropenem (9%) used most frequently. For definitive treatment of presumed/confirmed infection, vancomycin (26%), amikacin (20%), and meropenem (16%) were the most prescribed agents. Length of therapy for culture-positive and “culture-negative” infections was 12 days (median; IQR, 8–14) and 7 days (median; IQR, 5–10), respectively. Mortality was 6% (42%, infection-related). An NICU ASP was associated with lower rate of antibiotic utilization (p = 0·02). Interpretation: Global NICU antibiotic use was frequent and prolonged regardless of culture results. NICU-specific ASPs were associated with lower antibiotic utilization rates, suggesting the need for their implementation worldwide. Funding: Merck & Co.;
AB - Background: Global assessment of antimicrobial agents prescribed to infants in the neonatal intensive care unit (NICU) may inform antimicrobial stewardship efforts. Methods: We conducted a one-day global point prevalence study of all antimicrobials provided to NICU infants. Demographic, clinical, and microbiologic data were obtained including NICU level, census, birth weight, gestational/chronologic age, diagnoses, antimicrobial therapy (reason for use; length of therapy), antimicrobial stewardship program (ASP), and 30-day in-hospital mortality. Findings: On July 1, 2019, 26% of infants (580/2,265; range, 0–100%; median gestational age, 33 weeks; median birth weight, 1800 g) in 84 NICUs (51, high-income; 33, low-to-middle income) from 29 countries (14, high-income; 15, low-to-middle income) in five continents received ≥1 antimicrobial agent (92%, antibacterial; 19%, antifungal; 4%, antiviral). The most common reasons for antibiotic therapy were “rule-out” sepsis (32%) and “culture-negative” sepsis (16%) with ampicillin (40%), gentamicin (35%), amikacin (19%), vancomycin (15%), and meropenem (9%) used most frequently. For definitive treatment of presumed/confirmed infection, vancomycin (26%), amikacin (20%), and meropenem (16%) were the most prescribed agents. Length of therapy for culture-positive and “culture-negative” infections was 12 days (median; IQR, 8–14) and 7 days (median; IQR, 5–10), respectively. Mortality was 6% (42%, infection-related). An NICU ASP was associated with lower rate of antibiotic utilization (p = 0·02). Interpretation: Global NICU antibiotic use was frequent and prolonged regardless of culture results. NICU-specific ASPs were associated with lower antibiotic utilization rates, suggesting the need for their implementation worldwide. Funding: Merck & Co.;
KW - Antibiotics
KW - Antifungal
KW - Global point prevalence study
KW - Neonatal antimicrobial stewardship
KW - Neonatal infection
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U2 - 10.1016/j.eclinm.2021.100727
DO - 10.1016/j.eclinm.2021.100727
M3 - Article
C2 - 33554094
AN - SCOPUS:85100054626
SN - 2589-5370
VL - 32
JO - eClinicalMedicine
JF - eClinicalMedicine
M1 - 100727
ER -