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Original Investigation
°¿³¦³Ù´Ç²ú±ð°ùÌý28, 2024

Inhaled Reliever Therapies for Asthma: A Systematic Review and Meta-Analysis

Daniel G.ÌýRayner,ÌýMSc1; Dario M.ÌýFerri,ÌýMD2; Gordon H.ÌýGuyatt,ÌýMD1; et al Paul M.ÌýO’Byrne,ÌýMD2; ¸é´Ç³¾¾±²Ô²¹Ìýµþ°ù¾±²µ²Ô²¹°ù»å±ð±ô±ô´Ç-±Ê±ð³Ù±ð°ù²õ±ð²Ô,Ìý±Ê³ó¶Ù1; ¹ó²¹°ù¾±»åÌý¹ó´Ç°ù´Ç³Ü³Ù²¹²Ô,Ìý±Ê³ó¶Ù1; µþ°ù²¹»å±ô±ð²âÌý°ä³ó¾±±è±è²õ,Ìý²Ñ¶Ù3; °­²¹³ó²¹°ù³ÜÌý³§³Ü³¾¾±²Ô´Ç,Ìý²Ñ¶Ù4; Tamara T.ÌýPerry,ÌýMD5; ³§³ó²¹°ù³¾¾±±ô±ð±ðÌý±·²â±ð²Ô³ó³Ü¾±²õ,Ìý²Ñ¶Ù6; ´³´Ç³ó²ÔÌý°¿±è±è±ð²Ô³ó±ð¾±³¾±ð°ù,Ìý²Ñ¶Ù7; ·¡±ô±ô¾±´Ç³ÙÌý±õ²õ°ù²¹±ð±ô,Ìý²Ñ¶Ù8; ¹ó±ô²¹±¹¾±²¹Ìý±á´Ç²â³Ù±ð,Ìý²Ñ¶Ù9; °­²¹³Ù³ó±ð°ù¾±²Ô±ðÌý¸é¾±±¹±ð°ù²¹-³§±è´Ç±ôÂá²¹°ù¾±³¦,Ìý²Ñ¶Ù10; ·¡±ô±ô±ð²ÔÌý²Ñ³¦°ä²¹²ú±ð,Ìý±Ê³ó¶Ù11; ³§³Ü²õ²¹²Ô²¹Ìý¸é²¹²Ô²µ±ð±ô,Ìý²Ñ³§±·12; Lindsay E.ÌýShade,ÌýPA13; Valerie G.ÌýPress,ÌýMD14; ³¢¾±²õ²¹Ìý±á²¹±ô±ô15; ¶Ù¾±²¹Ìý³§³Ü±ð-°Â²¹³ó-³§¾±²Ô²µ,Ìý²Ñ³§16; ´¡²Ô²µ±ð±ôÌý²Ñ±ð±ô±ð²Ô»å±ð³ú,Ìý²Ñ±á³¢17; ±á¾±±ô²¹°ù°ù²âÌý°¿°ù°ù,Ìýµþ³§·¡18; °Õ´Ç²Ô²â²¹Ìý°Â¾±²Ô»å±ð°ù²õ,Ìý²Ñµþ´¡19; Donna D.ÌýGardner,ÌýDrPH20; °­²¹³Ù³ó²â°ù²ÔÌý±Ê°ù³ú²â·É²¹°ù²¹,Ìýµþ³§·¡21; Matthew A.ÌýRank,ÌýMD22; Leonard B.ÌýBacharier,ÌýMD23; ³Ò¾±²õ±ð±ô±ô±ðÌý²Ñ´Ç²õ²Ô²¹¾±³¾,Ìý²Ñ¶Ù24; Derek K.ÌýChu,ÌýMD, PhD1,2
Author Affiliations
  • 1Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada
  • 2Department of Medicine, McMaster University, Hamilton, Ontario, Canada
  • 3Capital Allergy & Respiratory Disease Center, Sacramento, California
  • 4Department of Medicine, Washington University School of Medicine in St Louis, St Louis, Missouri
  • 5Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock
  • 6Department of Pediatrics, The University of Chicago, Chicago, Illinois
  • 7Department of Internal Medicine, University of Medicine and Dentistry of New Jersey/Rutgers New Jersey Medical School, Newark
  • 8Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts
  • 9Department of Medicine, National Jewish Health, Denver, Colorado
  • 10Division of Allergy, Immunology, and Pulmonary Medicine, Washington University School of Medicine in St Louis, St Louis, Missouri
  • 11Hunter-Bellevue School of Nursing, Hunter College, New York, New York
  • 12Los Angeles General Medical Center, Los Angeles, California
  • 13Wake Forest University School of Medicine, Winston-Salem, North Carolina
  • 14Department of Medicine, The University of Chicago, Chicago, Illinois
  • 15Bertha, Minnesota
  • 16Canadian Severe Asthma Network, Toronto, Ontario, Canada
  • 17El Paso, Texas
  • 18New Philadelphia, Ohio
  • 19Global Allergy & Airways Patient Platform, Vienna, Austria
  • 20Allergy & Asthma Network, Fairfax, Virginia
  • 21Asthma and Allergy Foundation of America, Arlington, Virginia
  • 22Department of Internal Medicine, Mayo Clinic, Phoenix, Arizona
  • 23Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee
  • 24Department of Medicine, Endeavor Health, Evanston, Illinois
JAMA. Published online October 28, 2024. doi:10.1001/jama.2024.22700
Key Points

QuestionÌý In people with asthma, compared with short-acting β agonists (SABA) alone, is the combination of SABA with inhaled corticosteroids (ICS-SABA) and the combination of formoterol with inhaled corticosteroids (ICS-formoterol) associated with better asthma outcomes?

FindingsÌý In this systematic review and network meta-analysis that included 27 randomized clinical trials (50 496 adult and pediatric patients), compared with SABA alone, ICS-SABA was associated with a 4.7% reduction in risk of severe exacerbations and ICS-formoterol was associated with a 10.3% reduction in severe exacerbations, without an increase in adverse events.

MeaningÌý Both combined ICS with SABA and ICS with formoterol were associated with lower risks of severe asthma exacerbations compared with SABA alone.

Abstract

ImportanceÌý The optimal inhaled reliever therapy for asthma remains unclear.

ObjectiveÌý To compare short-acting β agonists (SABA) alone with SABA combined with inhaled corticosteroids (ICS) and with the fast-onset, long-acting β agonist formoterol combined with ICS for asthma.

Data SourcesÌý The MEDLINE, Embase, and CENTRAL databases were searched from January 1, 2020, to September 27, 2024, without language restrictions.

Study SelectionÌý Pairs of reviewers independently selected randomized clinical trials evaluating (1) SABA alone, (2) ICS with formoterol, and (3) ICS with SABA (combined or separate inhalers).

Data Extraction and SynthesisÌý Two reviewers independently extracted data and assessed risk of bias. Random-effects meta-analyses synthesized outcomes. GRADE (Grading of Recommendations Assessment, Development, and Evaluation) was used to evaluate the certainty of evidence.

Main Outcomes and MeasuresÌý Asthma symptom control (5-item Asthma Control Questionnaire; range, 0-6, lower scores indicate better asthma control; minimum important difference [MID], 0.5 points), asthma-related quality of life (Asthma Quality of Life Questionnaire; range, 1-7, higher scores indicate better quality of life; MID, 0.5 points), risk of severe exacerbations, and risk of serious adverse events.

ResultsÌý A total of 27 randomized clinical trials (N = 50 496 adult and pediatric patients; mean age, 41.0 years; 20 288 male [40%]) were included. Compared with SABA alone, both ICS-containing relievers were associated with fewer severe exacerbations (ICS-formoterol risk ratio [RR], 0.65 [95% CI, 0.60-0.72]; risk difference [RD], −10.3% [95% CI, −11.8% to −8.3%]; ICS-SABA RR, 0.84 [95% CI, 0.73-0.95]; RD, −4.7% [95% CI, −8.0% to −1.5%]) with high certainty. Compared with SABA alone, both ICS-containing relievers were associated with improved asthma control (ICS-formoterol RR improvement [MID] in total score, 1.07 [95% CI, 1.04-1.10]; RD, 4.1% [95% CI, 2.3%-5.9%]; ICS-SABA RR, 1.09 [95% CI, 1.03-1.15]; RD, 5.4% [95% CI, 1.8%-8.5%]) with high certainty. In an indirect comparison with ICS-SABA, ICS-formoterol was associated with fewer severe exacerbations (RR, 0.78 [95% CI, 0.66-0.92]; RD, −5.5% [95% CI, −8.4% to −2.0%]) with moderate certainty. Compared with SABA alone, ICS-formoterol (RD, −0.6% [95% CI, −1.3% to 0%]) was not associated with increased risk of serious adverse events (high certainty) and ICS-SABA (RD, 0% [95% CI, −1.1% to 1.2%]) was not associated with increased risk of serious adverse events (moderate certainty).

Conclusions and RelevanceÌý In this network meta-analysis of patients with asthma, ICS combined with formoterol and ICS combined with SABA were each associated with reduced asthma exacerbations and improved asthma control compared with SABA alone.

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