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Risk of nonsteroidal anti-inflammatory drug-associated renal dysfunction among neonates diagnosed with patent ductus arteriosus and treated with gentamicin.
Constance, J E; Reith, D; Ward, R M; Balch, A; Stockmann, C; Korgenski, E K; Thorell, E A; Sherwin, C M T.
Afiliação
  • Constance JE; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Reith D; Section of Paediatrics and Child Health, Dunedin School of Medicine, University of Otago, Dunedin, Otago, New Zealand.
  • Ward RM; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Balch A; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Stockmann C; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Korgenski EK; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Thorell EA; Intermountain Healthcare, Pediatric Clinical Program, Salt Lake City, UT, USA.
  • Sherwin CMT; Division of Clinical Pharmacology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
J Perinatol ; 37(10): 1093-1102, 2017 10.
Article em En | MEDLINE | ID: mdl-28594394
ABSTRACT

OBJECTIVE:

To evaluate the risk of nonsteroidal anti-inflammatory drug (NSAID) therapy-associated acute kidney injury (AKI) among neonates diagnosed with patent ductus arteriosus (PDA) who are treated with gentamicin. STUDY

DESIGN:

Multicenter retrospective observational study of patients ⩽44 postmenstrual weeks of age diagnosed with PDA who received gentamicin during hospitalization between January 2006 and December 2014. Patients with and without NSAID exposure were matched on covariates associated with AKI and NSAID therapy. The primary end point, AKI, was defined according to Kidney Disease Improving Global Outcomes neonatal criteria.

RESULTS:

The rate of AKI for the entire cohort (n=594) was 12% (n=71). Among neonates receiving NSAIDS, 14.8% (n=44) experienced an AKI as compared to 9.1% (n=27) for those who were not exposed (relative risk, 1.6; 95% confidence interval, 1.0 to 2.6). Therefore, the attributable risk of NSAID use was 5.7% (95% confidence interval, 0.5 to 11.0).

CONCLUSION:

Among neonates with PDA and receiving gentamicin, NSAID therapy increases the risk of AKI by about 6%.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gentamicinas / Anti-Inflamatórios não Esteroides / Permeabilidade do Canal Arterial / Injúria Renal Aguda / Antibacterianos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gentamicinas / Anti-Inflamatórios não Esteroides / Permeabilidade do Canal Arterial / Injúria Renal Aguda / Antibacterianos Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2017 Tipo de documento: Article