Limited utility of repeated vital sign monitoring during initiation of oral propranolol for complicated infantile hemangioma.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
08 2021
Historique:
received: 11 07 2019
revised: 03 04 2020
accepted: 04 04 2020
pubmed: 15 4 2020
medline: 3 9 2021
entrez: 15 4 2020
Statut: ppublish

Résumé

Initial propranolol recommendations for infantile hemangioma published in 2013 were intended as provisional best practices to be updated as evidence-based data emerged. A retrospective multicenter study was performed to evaluate utility of prolonged monitoring after first propranolol dose and escalation(s). Inclusion criteria included diagnosis of hemangioma requiring propranolol of greater than or equal to 0.3 mg/kg per dose, younger than 2 years, and heart rate monitoring for greater than or equal to 1 hour. Data collected included demographics, dose, vital signs, and adverse events. A total of 783 subjects met inclusion criteria; median age at initiation was 112 days. None of the 1148 episodes of prolonged monitoring warranted immediate intervention or drug discontinuation. No symptomatic bradycardia or hypotension occurred during monitoring. Mean heart rate change from baseline to 1 hour was -8.19/min (±15.54/min) and baseline to 2 hours was -9.24/min (±15.84/min). Three preterm subjects had dose adjustments because of prescriber concerns about asymptomatic vital sign changes. No significant difference existed in pretreatment heart rate or in heart rate change between individuals with later adverse events during treatment and those without. Prolonged monitoring for initiation and escalation of oral propranolol rarely changed management and did not predict future adverse events. Few serious adverse events occurred during therapy; none were cardiovascular.

Sections du résumé

BACKGROUND
Initial propranolol recommendations for infantile hemangioma published in 2013 were intended as provisional best practices to be updated as evidence-based data emerged.
METHODS
A retrospective multicenter study was performed to evaluate utility of prolonged monitoring after first propranolol dose and escalation(s). Inclusion criteria included diagnosis of hemangioma requiring propranolol of greater than or equal to 0.3 mg/kg per dose, younger than 2 years, and heart rate monitoring for greater than or equal to 1 hour. Data collected included demographics, dose, vital signs, and adverse events.
RESULTS
A total of 783 subjects met inclusion criteria; median age at initiation was 112 days. None of the 1148 episodes of prolonged monitoring warranted immediate intervention or drug discontinuation. No symptomatic bradycardia or hypotension occurred during monitoring. Mean heart rate change from baseline to 1 hour was -8.19/min (±15.54/min) and baseline to 2 hours was -9.24/min (±15.84/min). Three preterm subjects had dose adjustments because of prescriber concerns about asymptomatic vital sign changes. No significant difference existed in pretreatment heart rate or in heart rate change between individuals with later adverse events during treatment and those without.
CONCLUSION
Prolonged monitoring for initiation and escalation of oral propranolol rarely changed management and did not predict future adverse events. Few serious adverse events occurred during therapy; none were cardiovascular.

Identifiants

pubmed: 32289387
pii: S0190-9622(20)30553-3
doi: 10.1016/j.jaad.2020.04.013
pii:
doi:

Substances chimiques

Propranolol 9Y8NXQ24VQ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

345-352

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Katherine B Püttgen (KB)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Leanna M Hansen (LM)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Christine Lauren (C)

Columbia University, New York, New York.

Nicole Stefanko (N)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Erin Mathes (E)

University of California-San Francisco, San Francisco, California.

Gerilyn M Olsen (GM)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Megha M Tollefson (MM)

Mayo Clinic, Rochester, Minnesota.

Denise Adams (D)

Harvard Medical School, Boston, Massachusetts.

Eulalia Baselga (E)

Universitat Autonoma de Barcelona, Barcelona, Spain.

Sarah Chamlin (S)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Kristen Corey (K)

Harvard Medical School, Boston, Massachusetts.

Flora F Frascari (FF)

University of California-San Francisco, San Francisco, California.

Ilona J Frieden (IJ)

University of California-San Francisco, San Francisco, California.

Eloise R Galligan (ER)

Columbia University, New York, New York.

Deepti Gupta (D)

Seattle Children's Hospital/University of Washington School of Medicine, Seattle, Washington.

Anita Haggstrom (A)

Indiana University, Indianapolis, Indiana.

Kimberly Horii (K)

University of Missouri, Kansas City, Missouri.

Christoph P Hornik (CP)

Duke University School of Medicine, Durham, North Carolina.

Justyna Klajn (J)

University of California-San Francisco, San Francisco, California.

Leonardo Liberman (L)

Columbia University, New York, New York.

Anthony Mancini (A)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Diana Mannschreck (D)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Anelah McGinness (A)

University of California-San Francisco, San Francisco, California.

Catherine McCuaig (C)

Sainte-Justine University Hospital Center, Montreal, Quebec, Canada.

Brandon Newell (B)

University of Missouri, Kansas City, Missouri.

Henry Nguyen (H)

Mayo Clinic, Rochester, Minnesota.

Amy Nopper (A)

University of Missouri, Kansas City, Missouri.

Tola Oyesanya (T)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Julie Powell (J)

Sainte-Justine University Hospital Center, Montreal, Quebec, Canada.

Megan Reynolds (M)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Monica Rios (M)

Universitat Autonoma de Barcelona, Barcelona, Spain.

Dawn H Siegel (DH)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Kendra Ward (K)

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Maria C Garzon (MC)

Columbia University, New York, New York.

Peter Frommelt (P)

Medical College of Wisconsin, Milwaukee, Wisconsin.

Beth A Drolet (BA)

School of Medicine and Public Health, University of Wisconsin, Milwaukee, Wisconsin. Electronic address: bdrolet@dermatology.wisc.edu.

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Classifications MeSH