Intravenous Magnesium and Hospital Outcomes in Children Hospitalized With Asthma.


Journal

Hospital pediatrics
ISSN: 2154-1671
Titre abrégé: Hosp Pediatr
Pays: United States
ID NLM: 101585349

Informations de publication

Date de publication:
08 2021
Historique:
pubmed: 3 7 2021
medline: 30 10 2021
entrez: 2 7 2021
Statut: ppublish

Résumé

Use of intravenous magnesium (IVMg) for childhood asthma exacerbations has increased significantly in the last decade. Emergency department administration of IVMg has been shown to reduce asthma hospitalization, yet most children receiving IVMg in the emergency department are subsequently hospitalized. Our objective with the study was to examine hospital outcomes of children given IVMg for asthma exacerbations. We conducted a retrospective cohort study using data from the Pediatric Health Information System. We used propensity score matching to compare children who received IVMg on the first day of hospitalization with those who did not. Primary outcomes were initiation and duration of noninvasive positive pressure ventilation. Secondary outcomes included mechanical ventilation (MV) initiation, duration of MV, length of stay, and subsequent tertiary medication use. Primary analysis was restricted to children admitted to nonintensive care inpatient units. Overall, 91 309 hospitalizations met inclusion criteria. IVMg was administered in 25 882 (28.4%) children. After propensity score matching, IVMg was not significantly associated with lower initiation (adjusted odds ratio 0.88; 95% confidence interval [CI] 0.74-1.05) or shorter duration of noninvasive positive pressure ventilation (rate ratio 0.94; 95% CI 0.87-1.02). Similarly, no significant associations were seen for MV initiation, MV duration, or length of stay. IVMg was associated with lower subsequent tertiary medication use (adjusted odds ratio 0.66; 95% CI 0.60-0.72). However, the association was lost when ipratropium was removed from the tertiary medication definition. IVMg administration was not significantly associated with improved hospital outcomes. Further study is needed to inform the optimal indications and timing of magnesium use during hospitalization.

Sections du résumé

BACKGROUND
Use of intravenous magnesium (IVMg) for childhood asthma exacerbations has increased significantly in the last decade. Emergency department administration of IVMg has been shown to reduce asthma hospitalization, yet most children receiving IVMg in the emergency department are subsequently hospitalized. Our objective with the study was to examine hospital outcomes of children given IVMg for asthma exacerbations.
METHODS
We conducted a retrospective cohort study using data from the Pediatric Health Information System. We used propensity score matching to compare children who received IVMg on the first day of hospitalization with those who did not. Primary outcomes were initiation and duration of noninvasive positive pressure ventilation. Secondary outcomes included mechanical ventilation (MV) initiation, duration of MV, length of stay, and subsequent tertiary medication use. Primary analysis was restricted to children admitted to nonintensive care inpatient units.
RESULTS
Overall, 91 309 hospitalizations met inclusion criteria. IVMg was administered in 25 882 (28.4%) children. After propensity score matching, IVMg was not significantly associated with lower initiation (adjusted odds ratio 0.88; 95% confidence interval [CI] 0.74-1.05) or shorter duration of noninvasive positive pressure ventilation (rate ratio 0.94; 95% CI 0.87-1.02). Similarly, no significant associations were seen for MV initiation, MV duration, or length of stay. IVMg was associated with lower subsequent tertiary medication use (adjusted odds ratio 0.66; 95% CI 0.60-0.72). However, the association was lost when ipratropium was removed from the tertiary medication definition.
CONCLUSIONS
IVMg administration was not significantly associated with improved hospital outcomes. Further study is needed to inform the optimal indications and timing of magnesium use during hospitalization.

Identifiants

pubmed: 34210764
pii: hpeds.2020-004770
doi: 10.1542/hpeds.2020-004770
pmc: PMC8591772
mid: NIHMS1749893
doi:

Substances chimiques

Ipratropium GR88G0I6UL
Magnesium I38ZP9992A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

785-793

Subventions

Organisme : NHLBI NIH HHS
ID : K12 HL137943
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL136842
Pays : United States

Informations de copyright

Copyright © 2021 by the American Academy of Pediatrics.

Déclaration de conflit d'intérêts

POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

Références

Pediatr Pulmonol. 2018 Jul;53(7):866-871
pubmed: 29660840
Pediatr Pulmonol. 2016 Dec;51(12):1414-1421
pubmed: 27218606
J Pediatr. 2020 May;220:165-174.e2
pubmed: 32147221
Acad Emerg Med. 2010 Nov;17(11):1189-96
pubmed: 21175517
JAMA Pediatr. 2016 Sep 1;170(9):878-86
pubmed: 27398908
Pediatr Crit Care Med. 2016 Feb;17(2):e29-33
pubmed: 26649938
Am J Emerg Med. 2007 Jan;25(1):6-9
pubmed: 17157675
Stat Med. 2009 Nov 10;28(25):3083-107
pubmed: 19757444
Am J Clin Nutr. 2016 Aug;104(2):247-58
pubmed: 27413128
Lancet Respir Med. 2013 Jun;1(4):301-8
pubmed: 24429155
Cochrane Database Syst Rev. 2016 Apr 29;4:CD011050
pubmed: 27126744
J Hosp Med. 2020 Jun 17;15(7):403-406
pubmed: 32584247
J Pediatr. 1996 Dec;129(6):809-14
pubmed: 8969721

Auteurs

James W Antoon (JW)

Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee james.antoon@vumc.org.
Department of Pediatrics, School of Medicine, Vanderbilt University, Nashville, Tennessee.

Matt Hall (M)

Children's Hospital Association, Lenexa, Kansas.

Vineeta Mittal (V)

Division of Pediatric Hospital Medicine, Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, Texas.

Kavita Parikh (K)

Hospitalist Division, Children's National Medical Center and School of Medicine, George Washington University, Washington, District of Columbia.

Rustin B Morse (RB)

Children's Health, Dallas, Texas.

Ronald J Teufel (RJ)

Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina.

Alexander H Hogan (AH)

Department of Pediatrics, Connecticut Children's Medical Center, Hartford, Connecticut.

Samir S Shah (SS)

Division of Hospital Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Chén C Kenyon (CC)

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia and School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH