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Efficacy of Antibiotic Regimens for Pneumonia in Young Infants Aged 0-59 Days: A Systematic Review.
North, Krysten; Frade Garcia, Alejandro; Crouch, Mark; Kimsen, Spencer; Hoey, Amber; Wade, Carrie; Kim, Yumin; Chou, Roger; Edmond, Karen M; Lee, Anne C C; Rees, Chris A.
Affiliation
  • North K; Department of Pediatrics, Brigham and Women's Hospital, Boston, Massachusetts.
  • Frade Garcia A; Harvard Medical School, Boston, Massachusetts.
  • Crouch M; Centro Médico ABC, Mexico City, Mexico.
  • Kimsen S; Nazarene General Hospital, Kudjip and University of Papua New Guinea, Port Moresby, Papua New Guinea.
  • Hoey A; Nazarene General Hospital, Kudjip and University of Papua New Guinea, Port Moresby, Papua New Guinea.
  • Wade C; Bryn Mawr College, Bryn Mawr, Pennsylvania.
  • Kim Y; Harvard Medical School, Boston, Massachusetts.
  • Chou R; Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
  • Edmond KM; Departments of Medicine and Medical Informatics & Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon.
  • Lee ACC; World Health Organization, Geneva, Switzerland.
  • Rees CA; Department of Pediatrics, Brigham and Women's Hospital, Boston, Massachusetts.
Pediatrics ; 154(Suppl 1)2024 Aug 01.
Article de En | MEDLINE | ID: mdl-39087803
ABSTRACT
CONTEXT Pneumonia is a leading cause of death in young infants.

OBJECTIVES:

To evaluate the efficacy of different antibiotic regimens to treat young infant pneumonia on critical clinical outcomes. DATA SOURCES MEDLINE, Embase, CINAHL, World Health Organization (WHO) Global Index Medicus, Cochrane Central Registry of Trials. STUDY SELECTION We included randomized controlled trials of young infants aged 0 to 59 days with pneumonia (population) comparing the efficacy of antibiotic regimens (intervention) with alternate regimens or management (control) on clinical outcomes. DATA EXTRACTION We extracted data and assessed risk of bias in duplicate. We used Grading of Recommendations, Assessment, Development, and Evaluation to assess certainty of evidence.

LIMITATIONS:

Trials were heterogeneous, which precluded data pooling.

RESULTS:

Of 2601 publications screened, 10 randomized controlled trials were included. Seven trials were hospital-based (n = 869) and 3 were nonhospital-based (n = 4329). No hospital-based trials evaluated WHO-recommended first-choice regimens. One trial found the WHO-recommended second-choice antibiotic, cefotaxime, to have similar rates of treatment success as non-WHO-recommended regimens of either amoxicillin-clavulanate (RR 0.99, 95% confidence interval 0.82-1.10) or amoxicillin-clavulanate/cefotaxime (RR 1.02, 95% confidence interval 0.86-1.12). Among 3 nonhospital-based trials comparing oral amoxicillin to alternate regimens to treat isolated tachypnea among infants aged 7-59 days, there were no differences in treatment failure between amoxicillin and alternate regimens. Certainty of evidence was low or very low for all primary outcomes.

CONCLUSIONS:

We found limited evidence to support the superiority of any single antibiotic regimen over alternate regimens to treat young infant pneumonia.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antibactériens Limites: Humans / Infant / Newborn Langue: En Journal: Pediatrics Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Antibactériens Limites: Humans / Infant / Newborn Langue: En Journal: Pediatrics Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique