Nebulized Terbutaline and Ipratropium Bromide Versus Terbutaline Alone in Acute Exacerbation of Chronic Obstructive Pulmonary Disease Requiring Noninvasive Ventilation: A Randomized Double-blind Controlled Trial.


Journal

Academic emergency medicine : official journal of the Society for Academic Emergency Medicine
ISSN: 1553-2712
Titre abrégé: Acad Emerg Med
Pays: United States
ID NLM: 9418450

Informations de publication

Date de publication:
04 2019
Historique:
received: 16 04 2018
revised: 10 07 2018
accepted: 14 07 2018
pubmed: 30 8 2018
medline: 18 2 2020
entrez: 30 8 2018
Statut: ppublish

Résumé

Short-acting β The objective was to evaluate whether combining ipratropium bromide (IB) to terbutaline reduces hospital and intensive care unit (ICU) admission rates compared to terbutaline alone in AECOPD hypercapnic patients. In this double-blind controlled trial, patients who were admitted to the ED for AECOPD requiring noninvasive ventilation (NIV) were randomized to receive either 5 mg of nebulized terbutaline combined to 0.5 mg of IB (terbutaline/IB group, n = 115) or 5 mg of terbutaline sulfate (terbutaline group, n = 117). Nebulization was repeated every 20 minutes for the first hour and every 4 hours within the first day. Primary outcomes were the rate of hospital admission and need for endotracheal intubation within the first 24 hours of the start of the experimental treatment. Secondary outcomes included changes from baseline of dyspnea, physiologic variables, length of hospital stay, ICU admission rate, and 7-day mortality. The two groups were similar regarding baseline demographic and clinical characteristics. Hospital admission was observed in 70 patients (59.8%) in the terbutaline/IB group and in 75 patients (65.2%) in the terbutaline group (respiratory rate [RR] = 1.09, 95% confidence interval [CI] = 0.93 to 1.27, p = 0.39). ICU admission was required in 37 (32.2%) patients in the terbutaline/IB group and 30 patients (25.6%) in terbutaline group (RR = 1.25, 95% CI = 1.02 to 1.54, p = 0.27). There were no significant differences in dyspnea score, blood gas parameters changes, vital signs improvement, and 7-day death rate between both groups. In patients admitted to the ED for AECOPD requiring NIV, combination of nebulized IB and terbutaline did not reduce hospital admission and need to ICU care.

Sections du résumé

BACKGROUND
Short-acting β
OBJECTIVE
The objective was to evaluate whether combining ipratropium bromide (IB) to terbutaline reduces hospital and intensive care unit (ICU) admission rates compared to terbutaline alone in AECOPD hypercapnic patients.
METHODS
In this double-blind controlled trial, patients who were admitted to the ED for AECOPD requiring noninvasive ventilation (NIV) were randomized to receive either 5 mg of nebulized terbutaline combined to 0.5 mg of IB (terbutaline/IB group, n = 115) or 5 mg of terbutaline sulfate (terbutaline group, n = 117). Nebulization was repeated every 20 minutes for the first hour and every 4 hours within the first day. Primary outcomes were the rate of hospital admission and need for endotracheal intubation within the first 24 hours of the start of the experimental treatment. Secondary outcomes included changes from baseline of dyspnea, physiologic variables, length of hospital stay, ICU admission rate, and 7-day mortality.
RESULTS
The two groups were similar regarding baseline demographic and clinical characteristics. Hospital admission was observed in 70 patients (59.8%) in the terbutaline/IB group and in 75 patients (65.2%) in the terbutaline group (respiratory rate [RR] = 1.09, 95% confidence interval [CI] = 0.93 to 1.27, p = 0.39). ICU admission was required in 37 (32.2%) patients in the terbutaline/IB group and 30 patients (25.6%) in terbutaline group (RR = 1.25, 95% CI = 1.02 to 1.54, p = 0.27). There were no significant differences in dyspnea score, blood gas parameters changes, vital signs improvement, and 7-day death rate between both groups.
CONCLUSION
In patients admitted to the ED for AECOPD requiring NIV, combination of nebulized IB and terbutaline did not reduce hospital admission and need to ICU care.

Identifiants

pubmed: 30156361
doi: 10.1111/acem.13560
doi:

Substances chimiques

Bronchodilator Agents 0
Ipratropium GR88G0I6UL
Terbutaline N8ONU3L3PG

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

434-442

Informations de copyright

© 2018 by the Society for Academic Emergency Medicine.

Auteurs

Kaouthar Beltaief (K)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Mohamed Amine Msolli (MA)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Asma Zorgati (A)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.

Adel Sekma (A)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Marwen Fakhfakh (M)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Maryem Ben Marzouk (MB)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Hamdi Boubaker (H)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Mohamed Habib Grissa (MH)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Mehdi Methamem (M)

Emergency Department, Farhat Hached University Hospital, Sousse, Tunisia.

Riadh Boukef (R)

Emergency Department, Sahloul University Hospital, Sousse, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Asma Belguith (A)

Department of Preventive Medicine, Fattouma Bourguiba University Hospital, Monastir, Tunisia.

Wahid Bouida (W)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

Semir Nouira (S)

Emergency Department, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
Research Laboratory LR12SP18, University of Monastir, Monastir, Tunisia.

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Classifications MeSH