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Intramuskuläre versus orale Kortikosteroide bei akutem Asthma zur Verminderung von Rückfällen nach Entlassung aus der Notaufnahme

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Background

Acute asthma is a common cause of presentations to acute care centres, such as the emergency department (ED), and while the majority of patients can be discharged, relapse requiring additional medical care is common. Systemic corticosteroids are a major part in the treatment of moderate to severe acute asthma; however, there is no clear evidence regarding the most effective route of administration for improving outcomes in patients discharged from acute care.

Objectives

To examine the effectiveness and safety of a single dose of intramuscular (IM) corticosteroids provided prior to discharge compared to a short course of oral corticosteroids in the treatment of acute asthma patients discharged from an ED or equivalent acute care setting.

Search methods

The Cochrane Airways Group conducted searches of the Cochrane Airways Group Register of Trials, most recently on 14 March 2018. In addition in April 2017 we completed an extensive search of nine electronic databases including Medline, Embase, EBM ALL, Global Health, International Pharmaceutical Abstracts, CINAHL, SCOPUS, Proquest Dissertations and Theses Global, and LILACS. Furthermore, we searched the grey literature to identify any additional studies.

Selection criteria

We included randomized controlled trials or controlled clinical trials if they compared the effectiveness of intramuscular (IM) versus oral corticosteroids to treat paediatric or adult patients presenting with acute asthma to an ED or equivalent acute care setting. Two independent reviewers assessed study eligibility and study quality. We resolved disagreements via a third party and assessed risk of bias using the Cochrane 'Risk of bias' tool. We assessed the quality of the evidence using GRADE.

Data collection and analysis

For dichotomous outcomes, we calculated individual and pooled statistics as risk ratios (RRs) with 95% confidence intervals (CIs) using a random‐effects model. We reported continuous outcomes using mean difference (MD) or standardised mean difference (SMD) with 95% CIs using a random‐effects model. We reported heterogeneity using I² and Cochran Q statistics. We used standard procedures recommended by Cochrane.

Main results

Nine studies involving 804 participants (IM = 402 participants; oral = 402 participants) met our review inclusion criteria. Four studies enrolled children (n = 245 participants), while five studies enrolled adults (n = 559 participants). All of the studies recruited participants presenting to an ED, except one study which recruited participants attending a primary care clinic. All of the paediatric studies compared intramuscular (IM) dexamethasone to oral prednisone/prednisolone. In the adult studies, the IM corticosteroid provided ranged from methylprednisolone, betamethasone, dexamethasone, or triamcinolone, while the regimen of oral corticosteroids provided consisted of prednisone, methylprednisolone, or dexamethasone. Only five studies were placebo controlled. For the purposes of this review, we did not take corticosteroid dose equivalency into account in the analysis. The most common co‐intervention provided to participants during the acute care visit included short‐acting beta₂‐agonists (SABA), methylxanthines, and ipratropium bromide. In some instances, some studies reported providing some participants with supplemental oral or IV corticosteroids during their stay in the ED. Co‐interventions provided to participants at discharge consisted primarily of SABA, methylxanthine, long‐acting beta₂‐agonists (LABA), and ipratropium bromide. The risk of bias of the included studies ranged from unclear to high across various domains. The primary outcome of interest was relapse to additional care defined as an unscheduled visit to a health practitioner for worsening asthma symptoms, or requiring subsequent treatment with corticosteroids which may have occurred at any time point after discharge from the ED.

We found intramuscular and oral corticosteroids to be similarly effective in reducing the risk for relapse (RR 0.94, 95% CI 0.72 to 1.24; 9 studies, 804 participants; I² = 0%; low‐quality evidence). We found no subgroup differences in relapse rates between paediatric and adult participants (P = 0.71), relapse occurring within or after 10 days post‐discharge (P = 0.22), or participants with mild/moderate or severe exacerbations (P = 0.35). While we found no statistical difference between participants receiving IM versus oral corticosteroids regarding the risk for adverse events (RR 0.83, 95% CI 0.64 to 1.07; 5 studies, 404 participants; I² = 0%; moderate‐quality evidence), an estimated 50 fewer patients per 1000 receiving IM corticosteroids reported experiencing adverse events (95% from 106 fewer to 21 more). We found inconsistent reporting of specific adverse events across the studies. There were no differences in the frequency of specific adverse events including nausea and vomiting, pain, swelling, redness, insomnia, or personality changes. We did not seek additional adverse events data.

Participants receiving IM corticosteroids or oral corticosteroids both reported decreases in peak expiratory flow (MD −7.78 L/min, 95% CI −38.83 L/min to 23.28 L/min; 4 studies, 272 participants; I² = 33%; moderate‐quality evidence), similar symptom persistence (RR 0.41, 95% CI 0.14 to 1.20; 3 studies, 80 participants; I² = 44%; low‐quality evidence), and 24‐hour beta‐agonist use (RR 0.54, 95% CI 0.21 to 1.37; 2 studies, 48 participants; I² = 0%; low‐quality evidence).

Authors' conclusions

There is insufficient evidence to identify whether IM corticosteroids are more effective in reducing relapse compared to oral corticosteroids among children or adults discharged from an ED or equivalent acute care setting for acute asthma. While we found no statistical differences, patients receiving IM corticosteroids reported fewer adverse events. Additional studies comparing the effectiveness of IM versus oral corticosteroids could provide further evidence clarity. Furthermore, there is a need for studies comparing different IM corticosteroids (e.g. IM dexamethasone versus IM methylprednisone) and different oral corticosteroids (e.g. oral dexamethasone versus oral prednisone), with consideration for dosing and pharmacokinetic properties, to better identify the optimal IM or oral corticosteroid regimens to improve patient outcomes. Other factors, such as patient preference and potential issues with adherence, may dictate practitioner prescribing.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Intramuskuläre versus orale Kortikosteroide bei akutem Asthma

Fragestellung

Wir untersuchten die Wirksamkeit einer Injektion von Kortikosteroiden im Vergleich zu oral eingenommenen Kortikosteroiden, um Ergebnisse bei den Patienten, die eine Notaufnahme oder ähnliche Akutversorgungen wegen akutem Asthma aufsuchen mussten, zu verbessern.

Hintergrund

Asthmaanfälle entstehen durch Verengung der Atemwege zur Lunge aufgrund einer Entzündung, welche Keuchen, Husten und Atembeschwerden erzeugt. Menschen mit Asthmaanfällen gehen oft zu Notaufnahmen. Kortikosteroide, stark entzündungshemmende Wirkstoffe, sind die Eckpfeiler der Behandlung von Asthmaverschlechterungen und nachweislich wirksam bei der Verbesserung der Lungenfunktion und der Verringerung von Krankenhauseinweisungen bei Patienten mit Asthma. Bei der Entlassung erhalten Patienten häufig Kortikosteroide, die die Wahrscheinlichkeit vermindern, aufgrund einer Verschlechterung von Asthmasymptomen in die Notaufnahme zurückzukehren. Kortikosteroide können über eine einzige Injektion unter die Haut in den Muskel (intramuskulär) oder als Tabletten für zuhause bereitgestellt werden. Derzeit ist unklar, welche Form von Kortikosteroiden wirksamer bei der Verbesserung der Ergebnisse für Patienten nach Entlassung aus der Notaufnahme ist.

Recherchedatum

Wir haben unsere letzte Suche im März 2018 durchgeführt.

Studienmerkmale

Wir schlossen neun Studien ein, die die Wirksamkeit einer intramuskulären Injektion mit Kortikosteroid‐Tabletten bei Patienten, die eine Notaufnahme oder ähnliche Akutversorgungen mit akutem Asthma aufsuchten, verglichen. Die Studien nahmen insgesamt 804 Teilnehmer, sowohl Erwachsene als auch Kinder, auf. Die meisten Studien untersuchten die injizierbaren Kortikosteroide Dexamethason oder Methylprednisolon im Vergleich zu den Kortikosteroid‐Tabletten Prednison oder Methylprednisolon.

Quellen der Studienfinanzierung

Die meisten Studien berichteten nicht über ihre Finanzierungsquellen (5 Studien). Zwei Studien wurden mit Fördermitteln der allgemeinen Gesundheitsforschung finanziert. Eine Studie wurde von einem Pharmaunternehmen (Pfizer) finanziert; allerdings wurde berichtet, dass das Unternehmen an keinem Aspekt der Studie oder der Vorbereitung des Manuskripts beteiligt war. Eine Studie berichtete, dass sie nicht gefördert wurde.

Hauptergebnisse

Intramuskuläre Injektionen von Kortikosteroiden scheinen so wirksam wie Kortikosteroid‐Tabletten bei der Verhinderung von Rückfällen zu sein. Wir fanden keine Unterschiede im Risiko eines Rückfalls zwischen Teilnehmern, die Injektionen und Tabletten erhielten. Obwohl nicht alle Studien über unerwünschte Wirkungen in ihren Studiengruppen berichteten, fanden wir keine Unterschiede zwischen den Teilnehmern, die intramuskuläre Injektionen und Kortikosteroid‐Tabletten erhielten. Bei der Nachbeobachtung fanden wir keine Unterschiede in den Lungenfunktionstests der Teilnehmer, die eine intramuskuläre Injektion oder Kortikosteroid‐Tabletten erhalten hatten. In den Studien, die Symptomscores und ‐dauer berichteten, konnten wir keine Unterschiede zwischen den Teilnehmern, die Kortikosteroide per Injektion oder Tabletten erhielten, feststellen.

Qualität der Evidenz

Die Qualität der Evidenz für die Wirksamkeit intramuskulärer Injektionen von Kortikosteroiden bei der Verbesserung der gesundheitsbezogenen Endpunkte reichte von niedrig bis moderat. Wir hatten nur mäßiges Vertrauen in die geschätzten Wirkungen der intramuskulären Steroide auf Krankenhauseinweisungen, Verbesserung der Atemfunktion und Rückfälle aufgrund des Risikos für Bias in den eingeschlossenen Studien.

Authors' conclusions

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Implications for practice

For adults and children who have presented to the ED or equivalent acute care settings and who are suitable for discharge, a single dose of IM corticosteroids or a short dose of oral corticosteroids are both effective treatments to mitigate relapse events. We noted no differences with regards to pulmonary function, symptom persistence, or beta‐agonist use following treatment with either IM or oral corticosteroids. This review did not control for corticosteroid equivalency in the analysis; however, both arms used a moderate to high dose of intermediate‐duration agents. The review is also unable to reach conclusions regarding specific IM or oral corticosteroid treatments based on dosing or pharmacokinetic properties.

There is some evidence to suggest IM corticosteroids may decrease the risk of adverse events by as much as 36%, compared to a 7% potential increase; however, IM delivery is painful and can cause inflammation or infection (or both) at the site of injection.

Implications for research

Additional comparative effectiveness studies of IM versus oral corticosteroids to improve patient outcomes are needed to better inform clinicians and patients about how best to optimise patient care. In particular, we recommend additional studies enrolling school‐aged children to better understand the effectiveness of IM versus oral corticosteroids in this age group.

Additional comparative effectiveness studies using different IM corticosteroids (e.g. IM dexamethasone versus IM methylprednisone) and different oral corticosteroids (e.g. oral dexamethasone versus oral prednisone), with consideration for dosing and pharmacokinetic properties, are needed to explore the optimal IM or oral corticosteroid regimens to improve patient outcomes.

We strongly recommend comprehensive and standardized outcome reporting including clearly defined criteria and adjudication of health services outcomes (e.g. relapses resulting in primary care or ED visits, hospitalisation, death), side effects, pulmonary function, and symptom prevalence in future studies.

Compliance with the provided oral corticosteroid regimens was infrequently documented across the studies, and compliance, or lack thereof, could have impacted the results of this review. It is important that future comparative studies document compliance with oral corticosteroid regimens.

Future research needs to consider and address potential sources of bias, including randomisation, concealment of allocation, blinded outcome assessment, placebo‐controlled, avoidance of selective outcome reporting, and complete documentation of follow‐up.

Future research needs to better document the occurrence of adverse events associated with IM and oral corticosteroids, in particular adverse events associated with IM corticosteroids, which have been reported less extensively than those associated with oral corticosteroids, and range from pain, redness and swelling to rarer adverse events including avascular necrosis and hypothalamic/pituitary axis suppression.

Future research needs to examine the effects of repeat treatments of IM or oral corticosteroids among paediatric or adult patients with frequent exacerbations.

Given the importance of ICS agents in the chronic treatment of asthma, either alone or in combination with other agents, it is important that future research clearly documents the co‐interventions (e.g. ICS, ICS/LABA, monoclonal antibodies, etc.) provided to patients either in the ED, or at discharge, so that researchers may better understand the impact of these co‐interventions on the efficacy of IM or oral corticosteroids' reports on the pre‐ED and post‐ED use of all other anti‐inflammatory treatments (e.g. ICS, ICS/LABA, monoclonal antibodies, etc.).

Summary of findings

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Summary of findings for the main comparison. Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma

Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma

Patient or population: patients with acute asthma
Settings: Acute care settings
Intervention: Intramuscular corticosteroids
Comparison: Oral corticosteroids

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Assumed risk

Corresponding risk

Oral corticosteroids

Intramuscular corticosteroids

Relapse

201 per 1000

12 fewer per 1000
(from 56 fewer to 48 more)

RR 0.94
(0.72 to 1.24)

804
(9 studies)

⊕⊕⊝⊝
low1,2

Relapse within 10 days postdischarge

154 per 1000

40 fewer per 1000

(from 75 fewer to 11 more)

RR 0.74
(0.51 to 1.07)

742
(7 studies)

⊕⊕⊕⊝
moderate1

Relapse occurring after 10 days postdischarge

245 per 1000

2 fewer per 1000
(from 64 fewer to 81 more)

RR 0.99
(0.74 to 1.33)

556
(5 studies)

⊕⊕⊝⊝
low1,2

Adverse events

294 per 1000

50 fewer per 1000
(from 106 fewer to 21 more)

RR 0.83
(0.64 to 1.07)

404
(5 studies)

⊕⊕⊝⊝
low1,3

Pulmonary function: Peak expiratory flow

The mean pulmonary function: peak expiratory flow ranged across control groups from
304 to 419 litres/min

The mean pulmonary function: peak expiratory flow in the intervention groups was
7.78 liters/min lower
(38.83 lower to 23.28 higher)

272
(4 studies)

⊕⊕⊕⊝
moderate2

Symptom persistence

537 per 1000

317 fewer per 1000
(from 461 fewer to 107 more)

RR 0.41
(0.14 to 1.2)

80
(3 studies)

⊕⊕⊝⊝
low1,3

24hour beta agonist use

375 per 1000

172 fewer per 1000
(from 296 fewer to 139 more)

RR 0.54
(0.21 to 1.37)

48
(2 studies)

⊕⊕⊝⊝
low1,3

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: Risk ratio;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 Downgraded 1 level for risk of bias. Majority of studies received an unclear risk of bias for random sequence generation and selective outcome reporting
2 Downgraded 1 level for imprecision including wide confidence intervals (including both benefit, harm, and no effect)
3 Downgraded 1 level for Imprecision including wide confidence intervals (including both benefit, harm, and no effect) and few events

Background

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Description of the condition

Asthma is a chronic inflammatory disease of the airways of the lungs that affects both children and adults. It is estimated that 300 million people worldwide have asthma (Croisant 2014). In the United States, the prevalence of asthma has increased from 7.3% to 8.2% from 2001 to 2009 (Croisant 2014). Acute asthma, characterised by worsening cough, wheezing, shortness of breath, or chest tightness, is a common cause of presentation to the hospital emergency department (ED) or similar acute care settings. Most patients with acute asthma presenting to the ED can be safely managed with interventions including systemic corticosteroids, anticholinergics, or beta₂‐agonists, and discharged home (Rowe 2009). However, approximately 10% to 18% (Emerman 1999; Emerman 2001; Rowe 2015; Topal 2014), and up to 31% (Ducharme 1993), of patients will relapse and return to the ED or other acute care settings with acute exacerbations of asthma within the following four weeks. In the US, it is estimated that the economic cost of asthma in 2007 was approximately USD 56 billion due to medical costs and missed work and school days (CDC 2011). Identifying effective treatment options to help patients manage their symptoms after discharge from acute care and reducing the proportion of patients who relapse are important management issues designed to improve health outcomes for patients with asthma.

Description of the intervention

Systemic corticosteroids are potent general anti‐inflammatory agents for the treatment of asthma (Alangari 2014). When given in the ED, systemic corticosteroids can reduce hospitalisations and improve lung function in patients with acute asthma (Rowe 2001). A Cochrane Review reported significant decreases in symptom scores when patients were given systemic corticosteroids at or following discharge from the ED (i.e. an IM injection at discharge, or oral corticosteroids to be taken at home over the subsequent 3 to 8 days). Heterogeneity in outcome reporting prohibited meaningful pooling (Rowe 2007a). Treatment with systemic corticosteroids at discharge has also been shown to prevent relapse (Rowe 2007a). Current guidelines recommend systemic corticosteroids at ED discharge for all but the mildest presentations of acute asthma in an effort to reduce future relapse (GINA 2017). While systemic corticosteroids can effectively mitigate asthma relapses, the optimal route of administration is less clear.

How the intervention might work

At discharge from the ED or acute care setting, systemic corticosteroids may be administered via intramuscular (IM) or oral routes. A single dose of IM corticosteroids has long‐acting pharmacokinetic properties with fewer side effects associated with nausea/vomiting; however, adverse events associated with the IM injection (i.e. pain and swelling around the injection site) are well known to occur (Lahn 2004). Oral corticosteroids have short‐acting properties, and patients are typically provided with a short course of oral corticosteroids for five to seven days (GINA 2017). While no injection is needed, side effects associated with oral corticosteroids often include nausea and vomiting, and adherence/compliance with oral corticosteroid regimens is often sub‐optimal (Ducharme 2011). Although IM corticosteroids represent an alternative treatment option for patients with intolerance to oral agents or patients where adherence/compliance concerns exist, it is unclear whether IM corticosteroids are as effective as oral corticosteroids in mitigating relapse.

Why it is important to do this review

The effectiveness of systemic corticosteroids is known (Rowe 2007a), and widely accepted by clinicians; however, whether patients benefit more or less from IM or oral corticosteroids is less clear. This review provides supplemental information with another review of different oral corticosteroid regimens for acute asthma (Normansell 2016). An umbrella review reported no differences in relapse events in adults after treatment with IM or oral corticosteroids for acute asthma (Krishnan 2009); however, this review was limited to English‐language studies, and since its publication no other systematic reviews have been conducted that have used an extensive literature search to synthesize all of the available evidence from studies that have compared IM to oral corticosteroids.

Objectives

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To examine the effectiveness and safety of a single dose of intramuscular (IM) corticosteroids provided prior to discharge compared to a short course of oral corticosteroids in the treatment of acute asthma patients discharged from an ED or equivalent acute care setting.

Methods

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Criteria for considering studies for this review

Types of studies

We included randomised controlled trials (RCT) in this systematic review. We also included studies reported in full text, those published as an abstract only, and unpublished data in our search criteria.

Types of participants

We considered for inclusion in the review studies that included children or adults presenting to a hospital ED or other equivalent acute care setting with an uncomplicated exacerbation of asthma. For the purposes of this review, we defined 'uncomplicated exacerbations' as patients whose acute exacerbation of asthma was the primary reason for presentation to the ED, with no coexisting complications (e.g. no evidence of pneumonia, pneumothorax, etc.). The asthma diagnosis had to be made either using international/national clinical guidelines, or spirometric criteria, or both. We excluded from this review studies that focused on corticosteroid treatment in hospitalised participants. We only included studies that assessed patients with acute asthma who were treated and discharged from the ED or other urgent care/acute care setting. None of the included studies enrolled participants with both chronic obstructive pulmonary disease (COPD) and asthma; however, we had determined a priori that if this were to be the case, we would only include these studies if they provided results of asthma participants separately from COPD participants, or if the study population of COPD participants consisted of less than 20% of the total population.

Types of interventions

We included studies that compared a single dose of IM corticosteroids given prior to discharge versus a short course (one to 14 days) of oral corticosteroids. There were no restrictions on the IM or oral corticosteroids used, or the dosage. The single dose of IM corticosteroids may have been administered to participants at any point prior to discharge from the ED or other equivalent acute care setting. The short course of oral corticosteroids may have been started at any point prior to discharge or have been provided to participants to be taken over a period of a few days (one to 14 days) post‐discharge. We did not set any restrictions on the type of co‐interventions participants could receive (e.g. beta₂‐agonists, systemic or inhaled corticosteroids (ICS), anticholinergics, theophylline compounds, or antihistamines) during their stay in the ED/acute care setting; however, we did not permit other prescriptions of corticosteroids.

Types of outcome measures

Primary outcomes

The primary dichotomous outcome was relapse to additional care defined as an unscheduled visit to a health practitioner for worsening asthma symptoms, or requiring subsequent treatment with corticosteroids, which may have occurred at any time point after discharge from the ED. We also accepted the occurrence of relapse at any point as well as whether the occurrence of relapse was reported via self‐report or verification via health records.

Secondary outcomes

  1. The occurrence of serious adverse events (e.g. hospitalisation; intensive care unit (ICU) admission; death; relapse for visits other than worsening symptoms of asthma).

  2. Adverse events (e.g. pain, cellulitis/abscess, gastrointestinal bleeding, vomiting, behavioural/mental health exacerbations, abdominal pain, insomnia, hyperphagia/weight gain, skin eruptions, etc.).

  3. Continuous data from pulmonary function testing (including peak expiratory flow (PEF), absolute/per cent change in PEF from baseline; forced expiratory volume in one second (FEV₁), and absolute/per cent change in FEV₁ from baseline).

  4. Continuous data from symptom scores, measured via validated scales.

  5. Duration of symptoms (days until symptom free).

  6. Descriptive analysis of compliance/adherence with oral (corticosteroid or placebo) treatment.

  7. Quality of life measures measured via validated scale.

  8. The number of beta₂‐agonists doses taken by participants within a 24‐hour period of discharge.

Reporting one or more of the outcomes listed here was not an inclusion criterion for the review.

Search methods for identification of studies

Electronic searches

We identified studies from the Cochrane Airways Trials Register (CATR), which is maintained by the Information Specialist for the Cochrane Airways Group. The CATR contains studies identified from several sources.

  1. Monthly searches of the Cochrane Central Register of Controlled Trials (CENTRAL) in the Cochrane Library, through the Cochrane Register of Studies Online (http://crso.cochrane.org/).

  2. Weekly searches of MEDLINE Ovid SP.

  3. Weekly searches of Embase Ovid SP.

  4. Monthly searches of PsycINFO Ovid SP.

  5. Monthly searches of CINAHL EBSCO (Cumulative Index to Nursing and Allied Health Literature).

  6. Monthly searches of AMED EBSCO (Allied and Complementary Medicine).

  7. Handsearches of the proceedings of major respiratory conferences.

Studies contained in the CATR are identified through search strategies based on the scope of the Cochrane Airways Group. Details of these strategies, as well as a list of handsearched conference proceedings, are in Appendix 1. See Appendix 2 for search terms used to identify studies for this review. This search was completed on 14 March 2018.

In addition, an expert medical librarian (SC) conducted a supplemental search of nine electronic databases including MEDLINE (Appendix 3), Embase (Appendix 4), CINAHL (Appendix 5), Proquest Dissertation Abstracts and Theses Global (Appendix 6), SCOPUS (Appendix 7), PROSPERO (Appendix 8), the Cochrane Library (Appendix 9), and LILACS (Appendix 10) using controlled vocabulary and key words.

We also conducted an extensive search of the grey literature including ClinicalTrials.gov, the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP), Google Scholar, bibliographies of included studies and relevant reviews, and SCOPUS forward search of a sentinel paper; and a handsearch of medical conference abstracts from 2008 to 2017 including the Canadian Journal of Emergency Medicine, Academic Emergency Medicine, and Annals of Emergency Medicine.

We conducted all searches without any restrictions on language or publication status.

Searching other resources

We checked the reference lists of all primary studies and review articles for additional references. We also searched relevant manufacturers' web sites for study information.

We searched for errata or retractions from included studies published in full text on PubMed and planned to report the date this was done within the review.

Data collection and analysis

Selection of studies

Two review authors (SWK and EC) screened the titles and abstracts of the search results independently and coded them as either potentially eligible or ineligible. We then retrieved the full‐text study reports of all potentially eligible studies and two review authors (SWK and EC) independently screened them for inclusion and recorded the reasons for exclusion of ineligible studies. We resolved any disagreement through discussion or, if required, we consulted a third review author (CVR or BHR). We identified and excluded duplicates and collated multiple reports of the same study so that each study, rather than each report, was the unit of interest in the review. We recorded the selection process in sufficient detail to complete a PRISMA flow diagram and 'Characteristics of excluded studies' table (Moher 2009).

Data extraction and management

We used a data collection form for study characteristics and outcome data, which we piloted on at least one included study in the review. Two review authors (SWK and EC) independently extracted the following study characteristics from the included studies.

  1. Methods: study design, total duration of study, details of any 'run‐in' period, number of study centres and location, study setting, withdrawals, and date of study.

  2. Participants: number, mean age, age range, sex, severity of condition, diagnostic criteria, baseline lung function, smoking history, inclusion criteria, and exclusion criteria.

  3. Interventions: intervention, comparison, concomitant medications, and excluded medications.

  4. Outcomes: primary and secondary outcomes specified and collected, and time points reported.

  5. Notes: funding for studies and notable conflicts of interest of study authors.

Two review authors (SWK and EC) independently extracted outcome data from included studies. We noted in the 'Characteristics of included studies' table if an included study did not report outcome data in a usable way. We resolved disagreements by consensus or by involving a third review author (CVR or BHR). One review author (SWK) transferred data into the Review Manager 5 (RevMan 5) file (Review Manager 2014). To ensure that the data was entered correctly, a second review author (EC) verified the extracted data for accuracy against the study report.

Assessment of risk of bias in included studies

Two review authors (SWK and EC) assessed risk of bias independently for each included study using the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). We resolved any disagreements by discussion or by involving a third review author (CVR or BHR). We assessed the risk of bias according to the following domains.

  1. Random sequence generation.

  2. Allocation concealment.

  3. Blinding of participants and personnel.

  4. Blinding of outcome assessment.

  5. Incomplete outcome data.

  6. Selective outcome reporting.

  7. Other bias.

We judged each potential source of bias as high risk, low risk, or unclear risk and provided a quote from the study report together with a justification for our judgement in the 'Risk of bias' table. We summarised the 'Risk of bias' judgements across different studies for each of the domains listed. We considered blinding separately for different key outcomes where necessary. Where information on risk of bias relates to unpublished data or correspondence with an author, we noted this in the 'Risk of bias' table.

When considering treatment effects, we took into account the risk of bias for the studies that may have contributed to that outcome.

Assessment of bias in conducting the systematic review

We conducted the review according to the published protocol and justify any deviations from it in the 'Differences between protocol and review' section of the systematic review.

Measures of treatment effect

Dichotomous data are reported as relative risk (RR) values and continuous data are reported as mean difference (MD) or standardised mean difference (SMD), as appropriate. If we combined data from rating scales in a meta‐analysis, we ensured we entered them with a consistent direction of effect (e.g. lower scores always indicate improvement).

We undertook meta‐analyses only when meaningful; that is, if the treatments, participants, outcomes and the underlying interventions were similar enough for pooling to make sense.

We provided a narrative description of skewed data reported as medians and interquartile ranges (IQR).

In individual studies with multiple arms, we included only the study arms assessing IM and oral corticosteroids. If we combined two comparison groups (e.g. IM corticosteroids versus different regimens of oral corticosteroids) in the same meta‐analysis, we either combined the active study arms or halved the control group to avoid double‐counting.

If a study reported outcomes at multiple time points, we used the last time point measured.

We conducted an 'as reported' and intention‐to‐treat (ITT) analysis of the primary outcome. We assessed the secondary outcomes using an 'as reported' analysis.

Unit of analysis issues

For dichotomous outcomes, we used participants, rather than events, as the unit of analysis (i.e. number of individuals who relapsed rather than number of relapses per individual).

Dealing with missing data

We contacted investigators or study sponsors in order to verify key study characteristics and obtain missing numerical outcome data where possible (e.g. if we identified a study as an abstract only). Where this was not possible and the missing data had the potential to introduce serious bias, we took this into consideration in the GRADE rating for affected outcomes.

Assessment of heterogeneity

We used the I² statistic to measure heterogeneity among the studies in each analysis. If we identified substantial heterogeneity we reported it and explored the possible causes by prespecified subgroup analysis. 

Assessment of reporting biases

We were unable to pool more than 10 studies, so we were unable to create a funnel plot to explore possible small study and publication biases.

Data synthesis

We used a random‐effects model and performed a sensitivity analysis with a fixed‐effect model.

'Summary of findings' table

We created a 'Summary of findings' table using the following outcomes including: all relapse, relapse within 10 days post‐discharge, relapse after 10 days post‐discharge, adverse events, PEF/FEV₁, symptom scores, and beta₂‐agonist use in a 24‐hour period. We used the five GRADE considerations (i.e. risk of bias, consistency of effect, imprecision, indirectness, and publication bias) to assess the quality of a body of evidence as it related to the studies that contributed data for the prespecified outcomes. We used the methods and recommendations described in Section 8.5 and Chapter 12 of the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011), and used GRADEpro software (GRADEpro GDT). We justified all decisions to downgrade the quality of studies using footnotes and we made comments to aid the reader's understanding of the review where necessary.

Subgroup analysis and investigation of heterogeneity

We examined potential sources of heterogeneity in the primary outcome in the following subgroup analyses.

  1. Children (zero to 18 years of age) versus adults (18 years of age and older) to examine any potential age‐specific treatment effects of IM or oral corticosteroids.

  2. Relapse occurring within 10 days and over 10 days post‐discharge.

  3. Low versus moderate versus high exacerbation severity based on the pulmonary function taken at the time of the participant's presentation to the ED, prior to treatment with a bronchodilator.

  4. Co‐interventions received (ICS versus ICS corticosteroids/long‐acting beta₂‐agonists (LABA)).

We used the formal test for subgroup interactions in RevMan 5 (Review Manager 2014). We restricted the subgroup analysis to relapse.

Sensitivity analysis

We carried out the following sensitivity analyses, by removing the following types of studies from the primary outcome analyses.

  1. Studies that we consider to be at high risk of bias based on the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011).

  2. Studies in which the duration of oral corticosteroid treatment was less than five days.

  3. The results from fixed‐effect models were compared with the random‐effects models for the main outcome.

  4. Studies in which supplemental corticosteroids were provided to the patients in the ED as a co‐intervention.

Results

Description of studies

Please see Characteristics of included studies for additional information on the included studies.

Results of the search

The literature searches identified 912 studies (see Figure 1). Removing duplicates resulted in 685 potentially eligible studies overall. We selected 20 studies for full‐text review, while we excluded the remaining 665 studies, based on lack of relevance. We excluded 11 studies after full‐text review (see Excluded studies). We included the remaining nine studies in the review. We identified one of the eligible studies by grey literature search (Al‐Wahadneh 2006). A search of errata or retractions in September 2017 did not identify any retracted publications. We included insufficient studies in this review for an assessment of publication bias (i.e. by a funnel plot). We made every effort to locate all available studies through an extensive search of the literature, with no limitations set on year of publication or language of publication.


Study flow diagram.

Study flow diagram.

Included studies

Publication

The first study to compare the effectiveness of IM versus oral corticosteroids in participants with acute asthma discharged from an acute care setting was published in 1988 (Hoffman 1988) while the most recent study was published in 2007 (Gordon 2007). The majority of studies were published in the United States (Gordon 2007; Gries 2000; Hoffman 1988; Klig 1997; Lahn 2004; Schuckman 1998), while the remaining studies were published in Canada (Chan 2001), Jordan (Al‐Wahadneh 2006), and Taiwan (Lee 1993). All of the studies were RCTs published in peer‐reviewed journals.

Participants/Setting

The nine studies enrolled a total of 804 participants. Overall, the studies were small clinical trials, with a range of 17 to 187 participants across the studies. Five of the studies enrolled fewer than 90 participants each (Al‐Wahadneh 2006; Gries 2000; Hoffman 1988; Klig 1997; Lee 1993). Five of the included studies enrolled adults (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998), while the remaining four enrolled children (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). The age of eligible children included in the studies ranged from 9 months to 14 years (Al‐Wahadneh 2006), 18 months to 7 years (Gordon 2007), 6 months to 7 years (Gries 2000), and 3 to 16 years (Klig 1997). Among the adult studies, the mean ages of participants ranged from 31 to 42 years old (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998), while the mean age of children ranged from 3 to 6.8 years old (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). Most of the included studies recruited more male participants, except in three studies where women comprised over 50% of participants (Chan 2001; Lahn 2004; Schuckman 1998). Only three studies reported smoking history (Chan 2001; Lahn 2004; Schuckman 1998). Chan 2001 reported that current smokers made up 31% to 33% of the participants in the IM and oral corticosteroid groups respectively. Tobacco use ranged from 35% to 38% of participants randomised to the IM and oral corticosteroid groups respectively in Lahn 2004, while Schuckman 1998 reported a range of 64% to 74% of participants randomised to receive IM or oral corticosteroids had ever smoked. All of the studies recruited participants with acute asthma presenting to an ED, except one study which recruited participants with acute asthma attending a primary care clinic (Gries 2000). We attempted to estimate and categorize exacerbation severity among the included studies based on the reported baseline pulmonary function of the included studies (Table 1). We considered studies that reported a baseline average PEF of greater than 200 L/min of the groups to be mild/moderate (Chan 2001; Lahn 2004; Lee 1993; Schuckman 1998). We considered the exacerbation severity of patients enrolled in Hoffman 1988 to be severe, as the baseline PEF of included patients was less than 150 L/min. Four studies did not report baseline pulmonary function and so exacerbation severity could not be estimated (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997).

Open in table viewer
Table 1. Exacerbation severity

Studies

Pulmonary function: Eligibility criteria

Exacerbation severity

Al‐Wahadneh 2006

Severity estimated using modified scoring system based on GINA guidelines. Reported to enrolling patients with mild‐moderate exacerbations, however baseline pulmonary function of the groups was not reported.

Unable to assess

Chan 2001

Reported mean baseline PEF greater than 200 L/min: IM group: 270 L/min (SD: 103); oral group: 261 L/min (SD: 104).

Mild/moderate

Gordon 2007

Reported to enrolling patients identified as moderate exacerbations, however baseline pulmonary function was not reported.

Unable to assess

Gries 2000

Applied adapted exacerbation severity score (unspecified). Reported to enrolling patients rated as mild/moderate, however baseline pulmonary function of the groups was not reported.

Unable to assess

Hoffman 1988

Reported baseline mean PEF of enrolled patients of less than 150 L/min: IM group: 129 L/min (SD:14); oral group: 141 L/min (SD: 14).

Severe

Klig 1997

Exacerbation severity estimated via pulmonary index score. Study reported to enrolling patients with mild/moderate exacerbations, however baseline pulmonary function was not reported.

Unable to assess

Lahn 2004

Eligibility criteria required patients to have a PEFR of ≤ 70% predicted with a minimum PEFR of ≥ 40%. Reported PEF of enrolled patients was ≥ 200 L/min: IM group: 205 L/min (SD: 70); oral group: 209 L/min (SD: 72).

Mild/moderate

Lee 1993

Reported mean baseline PEF of ≥ 200 L/min: IM group: 210 L/min (SD: 30); oral group: 208 L/min (SD: 26).

Mild/moderate

Schuckman 1998

Reported mean baseline PEF of ≥ 200 L/min: IM group: 243.6 L/min (SD: 64); oral group: 244.7 L/min (SD: 83).

Mild/moderate

Abbreviations:

GINA = Global Initiative for Asthma; PEF = Peak expiratory flow; PEFR = Peak expiratory flow rate; IM = intramuscular; SD = standard deviation

Intervention

All of the paediatric studies provided their participants with a single dose of IM dexamethasone (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997), while the IM corticosteroid provided in adult studies ranged from methylprednisolone (Hoffman 1988; Lahn 2004), to betamethasone (Chan 2001), dexamethasone (Lee 1993), and triamcinolone (Schuckman 1998). All of the participants randomised to receive IM corticosteroids received a single dose of IM corticosteroids prior to discharge. Only five studies were placebo controlled, in which all participants receiving IM corticosteroids were also provided with a course of oral placebo tablets (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998). There was significant variation between the IM corticosteroid used, as well as the dosing. We provide additional information on the IM corticosteroids used in Characteristics of included studies and Table 2. We estimated corticosteroid equivalency to methylprednisolone using an equivalence converter (www.medcalc.com/steroid.html). Overall, the median dose was 78 mg with a range of 40 mg to 120 mg (Table 2).

Open in table viewer
Table 2. Study characteristics of included studies

Studies

Location/setting

Co‐interventions

Corticosteroid doses and durations

Methyprednisolone equivalency

Relapse outcome

Al‐Wahadneh 2006

Jordan, ED

Provided in ED: not stated

Provided at discharge: SABA

Dexamethasone (IM)

1.7 mg/kg

Mean dose: 24 mg

Single dose

Prednisolone (oral)

2 mg/kg/day for 5 days

Mean dose: 19.2 mg per day

Total dose: 96 mg

IM

Methylprednisone equivalency: 120 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

76.8 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

1/16

Day 21

Oral group

3/14

Day 21

Chan 2001

Canada, ED

Provided in ED: SABA, methylxanthines, supplemental oral/IV corticosteroids

Provided at discharge: Methylxanthines, unspecified inhaled beta₂‐agonists, and ICS

Betamethasone (IM)

12 mg

Single dose. Received placebo capsules over 7 days.

Prednisone (oral)

50 mg a day for 7 days. Received a single placebo injection

Total dose: 350 mg

IM

Methylprednisone equivalency:

72 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

280 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

12/86

Day 7

Oral group

19/82

Day 7

Gordon 2007

United States, Pediatric ED

Provided in ED: SABA, ipratropium bromide. IV corticosteroids for patients who vomited oral corticosteroids.

Provided at discharge: Inhaled beta₂‐agonists and ICS

Dexamethasone (IM)

0.6 mg/kg (max 16 mg)

Single dose

Prednisolone (oral)

2 mg/kg (max 50 mg) daily for 5 days

Total: 250 mg

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12‐36 hours)

Oral

Methylprednisone equivalency:

200 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

8/69

Day 4

Oral group

11/73

Day 4

IM group

15/68

Day 14

Oral group

16/73

Day 14

Gries 2000

United States, Tertiary medical center

Provided in ED: SABA

Provided at discharge: SABA

Dexamethasone (IM)

Patients 6 to 12 months old received 16 mg.

Patients 13 to 35 months old received 24 mg.

Children ≥ 36 months received 36 mg.

Single dose

Prednisone (oral)

2 mg/kg a day for 5 days

Total dose: unclear

IM

Methylprednisone equivalency:

Unable to assess

Oral

Methylprednisone equivalency:

Unable to assess

IM group

1/15

Day 28

Oral group

3/17

Day 28

Hoffman 1988

United States, ED

Provided in ED: SABA, epinephrine, methylxanthines, IV corticosteroids

Provided at discharge: Methylxanthine and inhaled beta₂‐agonists

Methylprednisonlone (IM)

80 mg

Single dose. Received placebo capsules for 7 days

Methylprednisolone (oral)

Tapering dose over 7 days.

Total dose: 216 mg

Received placebo injection

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

216 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

0/8 day

Day 7

Oral group

2/10

Day 7

Klig 1997

United States, Pediatric ED

Provided in ED: SABA

Provided at discharge: SABA

Dexamethasone (IM)

0.3 mg/kg

Total dose: 15 mg

Single dose

Prednisone (oral)

2 mg/kg a day for 3 days

Total dose: 100 mg

IM

Methylprednisone equivalency:

75 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

0/21

Day 5

Oral group

0/21

Day 5

Lahn 2004

United States, ED

Provided in ED: inhaled beta₂‐agonists, IV corticosteroids

Provided at discharge: SABA

Methylprednisolone (IM)

160 mg

Single dose. Received placebo capsules for 8 days

Methylprednisolone (oral)

Tapering dose over 8 days.

Total dose: 160 mg (tapering dose 32 mg day 1).

Received placebo injection

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

13/92

Day 10

Oral group

12/88

Day 10

IM group

17/92

Day 21

Oral group

20/88

Day 21

Lee 1993

Taiwan, ED

Provided in ED: SABA, methylxanthines

Provided at discharge: Methylxanthine and inhaled beta₂‐agonists

Dexamethasone (IM)

10 mg

Single dose. Received placebo capsules for 7 days

Dexamethasone (oral)

Tapering dose over 7 days.

11.75 mg total. Received placebo injection

IM

Methylprednisone equivalency:

50 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

58.8 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

1/17

Day 7

Oral group

0/19

Day 7

Schuckman 1998

United States, ED

Provided in ED: SABA, oral/IV corticosteroids

Provided at discharge: SABA, antibiotics, ICS, cromolyn sodium, ipratropium bromide

Triamcinolone (IM)

40 mg

Single dose. Received placebo capsules for 5 days

Prednisone (oral)

40 mg a day for 5 days.

Total dose: 160 mg

Received placebo injection

IM

Methylprednisone equivalency:

40 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

160 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

7/78

Day 7

Oral group

11/76

Day 7

ED = emergency department; SABA = short‐acting beta₂‐agonists; LABA = long‐acting beta₂‐agonists; IV = intravenous; IM = intramuscular; ICS = inhaled corticosteroids

Comparison

All of the paediatric studies compared IM dexamethasone to oral prednisone/prednisolone (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). The oral corticosteroid regimen provided in the adult studies consisted of either prednisone (Chan 2001; Schuckman 1998), methylprednisolone (Hoffman 1988; Lahn 2004), or dexamethasone (Lee 1993). The paediatric studies tended to provide participants a shorter course of oral corticosteroids, lasting from three (Klig 1997) to five days (Al‐Wahadneh 2006; Gordon 2007; Gries 2000). The course of oral corticosteroids tended to last slightly longer in the adult studies, ranging from five (Schuckman 1998), seven (Hoffman 1988; Lee 1993), to eight days (Lahn 2004). Six studies provided a consistent dose of oral corticosteroids (Al‐Wahadneh 2006; Chan 2001; Gordon 2007; Gries 2000; Klig 1997; Schuckman 1998) while three studies provided a tapering dose (Hoffman 1988; Lahn 2004; Lee 1993). All participants randomised to receive oral corticosteroids were provided with their medications prior to discharge which was to be taken at home over the next 3 to 8 days. Only five studies were placebo controlled, in which all participants receiving oral corticosteroids were provided with IM placebo (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998). We present additional information on the oral corticosteroids provided in Characteristics of included studies and Table 2. We estimated corticosteroid equivalency to methylprednisolone using an equivalence converter (www.medcalc.com/steroid.html). Overall, the median dose was 116 mg with a range of 58.8 mg to 280 mg (Table 2).

Co‐interventions

The co‐interventions provided varied among the included studies (see Characteristics of included studies and Table 2). In some cases, all participants received standardised co‐interventions (Al‐Wahadneh 2006; Gordon 2007; Hoffman 1988; Gries 2000; Klig 1997; Lee 1993; Schuckman 1998), while another study reported that participants received non‐standardized co‐interventions at the discretion of the attending physicians (Chan 2001). The most common co‐interventions provided to participants during the acute care visit included: SABA (Chan 2001; Gordon 2007; Gries 2000; Hoffman 1988; Klig 1997; Lahn 2004; Lee 1993; Schuckman 1998), methylxanthines (Chan 2001; Hoffman 1988; Lee 1993), and ipratropium bromide (Gordon 2007). In some instances, some studies reported providing participants with supplemental oral (Chan 2001; Schuckman 1998) or IV (Chan 2001; Hoffman 1988; Schuckman 1998) corticosteroids during their stay in the ED. Gordon 2007 provided participants with IV corticosteroids if they vomited the oral corticosteroids while in the ED. Co‐interventions provided to participants at discharge consisted primarily of SABA (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997; Lahn 2004; Schuckman 1998), methylxanthine (Chan 2001; Hoffman 1988; Lee 1993), LABA (Chan 2001), and unspecified inhaled beta₂‐agonists (Hoffman 1988). Supplemental corticosteroids provided at discharge were limited across the included studies. Chan 2001 and Gordon 2007 reported that the attending ED physician decided whether or not to provide participants with ICS at discharge. Participants in Lahn 2004 received ICS at discharge if they were using them previously.

Outcomes

All included studies reported relapse to additional care, with a measurement range of four to 28 days after discharge. Seven studies assessed relapse within 10 days post‐discharge (Chan 2001; Gordon 2007; Hoffman 1988; Klig 1997; Lahn 2004; Lee 1993; Schuckman 1998), while five studies measured relapse occurring more than 10 days post‐discharge (Al‐Wahadneh 2006; Chan 2001; Gordon 2007; Gries 2000; Lahn 2004). Three studies assessed relapse at two different time points after discharge (Chan 2001; Gordon 2007; Lahn 2004). In comparison to relapse, we found infrequent reporting and inconsistent measurement of our proposed secondary outcomes.

Excluded studies

We excluded 11 studies from this review, mostly due to inappropriate study design (not an RCT) (Andrews 2012; Droszcz 1981; Droszcz 1985; Ducharme 2004; Green 1995; Hofmann 2008; Kelso 2014; Ozpenpe 2011; Razi 2006; Watnick 2016; White 2010) (See Characteristics of excluded studies).

Risk of bias in included studies

Overall, the risk of bias of the included studies ranged from unclear to high and none of the studies had an overall low risk of bias (see Figure 2; Figure 3). Of the nine studies assessed, we rated four as having high risk of bias (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997), while we assessed the remaining studies as having an unclear risk of bias (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998).


Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.


Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Allocation

Three studies provided adequate information on randomisation to allow for an assessment of low risk of bias for sequence generation (Lahn 2004; Lee 1993; Schuckman 1998). We considered the remaining studies to be at unclear risk of bias due to missing information on randomisation of participants (Al‐Wahadneh 2006; Chan 2001; Gordon 2007; Gries 2000; Hoffman 1988; Klig 1997). Five studies had a low risk of bias with regard to allocation concealment (Chan 2001; Gordon 2007; Klig 1997; Lahn 2004; Schuckman 1998), while the remaining studies did not provide enough information to make a clear judgement on the risk of bias on allocation concealment (Al‐Wahadneh 2006; Gries 2000; Hoffman 1988; Lee 1993).

Blinding

Given the feasibility of employing a placebo‐controlled study design, and that many outcomes of interest were collected via participant self‐report, we considered the primary and secondary outcomes of interest may have been susceptible to potential performance and detection bias. We considered three studies to have adequately blinded participants and personnel (Chan 2001; Lahn 2004; Schuckman 1998). Four studies did not blind participants or personnel, and we judged them to be at high risk of bias (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). We considered two studies to be at unclear risk of bias due to a lack of information provided (Hoffman 1988; Lee 1993). Five studies reported adequate blinding of outcome assessors (Chan 2001; Gordon 2007; Gries 2000; Klig 1997; Schuckman 1998). We considered one study to be at high risk of bias because they did not blind outcome assessors (Al‐Wahadneh 2006), while we considered three studies to be at unclear risk of bias due to a lack of available information on the blinding of outcome assessors (Hoffman 1988; Lahn 2004; Lee 1993).

Incomplete outcome data

We assessed two studies as having an unclear risk of bias due to a lack of information on attrition (Al‐Wahadneh 2006; Lee 1993). We assessed the remaining studies as having a low risk of bias (Chan 2001; Gordon 2007; Gries 2000; Hoffman 1988; Klig 1997; Lahn 2004; Schuckman 1998).

Selective reporting

We considered only one study to be at low risk of bias for reporting bias; we received a study protocol upon request from the study authors (Chan 2001). We considered the remaining studies at be at unclear risk of reporting bias due to the lack of an available protocol (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Hoffman 1988; Klig 1997; Lahn 2004; Lee 1993; Schuckman 1998).

Other potential sources of bias

We considered four studies to be at low risk of bias for other potential sources of bias (Chan 2001; Klig 1997; Lahn 2004; Schuckman 1998). Three studies reported their source of funding in the included article (Chan 2001; Lahn 2004; Schuckman 1998), while we found additional information regarding study funding in one study (Klig 1997). Two studies received funding from general health research grants (Chan 2001; Schuckman 1998). One study received pharmaceutical company (Pfizer) sponsorship but reported that Pfizer was not involved in any aspect of the study or manuscript preparation (Lahn 2004). One study was unfunded (Klig 1997). We considered five studies to be at unclear risk of bias because the studies did not state their source of funding (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Hoffman 1988; Lee 1993). We did not consider any study to be at high risk of bias for other potential sources of bias.

Effects of interventions

See: Summary of findings for the main comparison Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma

See summary of findings Table for the main comparison for a summary of the main comparisons. Insufficient reporting prevented meaningful meta‐analysis of several proposed secondary outcomes, including symptom scores; relapse requiring hospitalisation; and quality of life; and specific adverse events such as pain; swelling; redness/bruising; personality changes; and insomnia.

Primary Outcome

Relapse

We detected no difference in the proportion of patients who relapsed between participants receiving IM versus oral corticosteroids (RR 0.94, 95% CI 0.72 to 1.24; 9 studies, 804 participants = 804; I² = 0%; Analysis 1.1) with low heterogeneity (I² = 0%). An ITT analysis revealed similar results (RR 0.95, 95% CI 0.72 to 1.26; 9 studies, 821 participants; I² = 0%; Analysis 1.2).

Subgroup analysis

A subgroup analysis comparing the effectiveness of IM versus oral corticosteroids to reduce relapse in paediatric (RR 0.86, 95% CI 0.48 to 1.53; 4 studies, 245 participants; I² = 0%) or adult (RR 0.97, 95% CI 0.71 to 1.33; 5 studies, 559 participants; I² = 0%) participants revealed no subgroup differences (P = 0.71; Analysis 1.3). In addition, we found no subgroup differences between studies assessing relapse within 10 days (RR 0.74, 95% CI 0.51 to 1.07; 7 studies, 742 participants; I² = 0%) or greater than 10 days post‐discharge (RR 0.99, 95% CI 0.74 to 1.33; 5 studies, 556 participants; I² = 0%) (P = 0.22; Analysis 1.4). It is important to note, however, that for the relapse greater than 10 days post‐discharge subgroup, it is unclear whether this includes relapses occurring within 10 days. We found no subgroup differences (P = 0.35; Analysis 1.5) in relapse between studies estimated to have enrolled participants with mild/moderate (RR 0.98, 95% CI 0.71 to 1.34; 4 studies, 539 participants; I² = 0%) versus severe exacerbations (RR 0.24, 95% CI 0.01 to 4.47; 1 study, 18 participants; I² = 100%). We could not complete the proposed co‐interventions subgroup comparing the effects of ICS versus ICS/LABA on relapse as planned due to a lack of studies providing information on the use of ICS and ICS/LABA agents as co‐interventions.

Sensitivity analysis

We conducted a sensitivity analysis in which we removed from the meta‐analysis the four studies considered to be at high risk of bias (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). We identified no difference in relapse proportions between participants receiving IM or oral corticosteroids (RR 0.97, 95% CI 0.71 to 1.33; 5 studies, 559 participants; I² = 0%; Analysis 1.6). An additional sensitivity analysis, in which studies providing participants with an oral corticosteroid regimen of less than five days (Klig 1997), revealed no difference in relapse rates between participants receiving IM or oral corticosteroids (RR 0.94, 95% CI 0.72 to 1.24; 8 studies, 762 participants; I² = 0%; Analysis 1.7). Finally, fixed effects revealed similar findings to that of random effects (RR 0.91, 95% CI 0.69 to 1.19; 9 studies, 804 participants; I² = 0%; Analysis 1.8). Removing studies in which patients received additional corticosteroids as a co‐intervention during the patients' stay in the ED revealed no differences in relapse rates between participants receiving IM or oral corticosteroids (RR 0.76, 95% CI 0.45 to 1.29; 5 studies, 320 participants; I² = 0%; Analysis 1.9).

Secondary outcomes

Serious adverse effects

Insufficient reporting of serious adverse events prohibited any meaningful meta‐analysis. Only one study reported on participants relapsing and requiring hospitalisation or ICU admission by 14‐day follow‐up; however, the effect estimate is imprecise (RR 1.43, 95% CI 0.33 to 6.16; 1 study, 141 participants; Analysis 1.10) (Gordon 2007).

Adverse events

Across the included studies we found poor documentation and inconsistent measurement of adverse events associated with the use of IM and oral corticosteroids, resulting in few meaningful comparisons. Overall, a meta‐analysis did not reveal whether participants receiving IM corticosteroids are more or less likely to experience any adverse events compared to participants receiving oral corticosteroids (RR 0.83, 95% CI 0.64 to 1.07; 5 studies, 404 participants; I² = 0%; Analysis 1.11). In some cases, the occurrence of specific adverse events was reported in greater detail. We found no differences in the frequency of nausea and vomiting among participants receiving either IM or oral corticosteroids (RR 0.56, 95% CI 0.09 to 3.59; 3 studies, 320 participants; I² = 58%; Analysis 1.12). We found insufficient evidence to conclusively state whether there is a difference in the occurrence of insomnia (RR 1.74, 95% CI 0.61 to 4.97; 1 study, 171 participants; I² = 0%; Analysis 1.13) or personality changes (RR 0.82, 95% CI 0.56 to 1.19; 1 study, 30 participants; I² = 0%; Analysis 1.14) among participants receiving IM or oral corticosteroids. Some studies reported the occurrence of side effects associated with the IM corticosteroid injection. Two studies strictly reported on the occurrence of pain, swelling, and redness at the injection site among participants receiving IM corticosteroids only, as these studies did not utilize a IM placebo control group (Gordon 2007; Gries 2000). Gordon 2007 reported the proportion of paediatric participants experiencing discomfort, swelling, and redness following the IM corticosteroid injection was 1.6%, 6.5%, and 1.6% respectively. Gries 2000 reported that no paediatric participants receiving IM corticosteroids experienced any other side effects besides personality changes. Two placebo‐controlled studies compared the occurrence of pain, swelling, and redness between participants receiving IM corticosteroids compared to participants receiving oral corticosteroids who received an IM placebo injection. Overall, the imprecision of the estimate precluded identifying a difference in the occurrence of pain (RR 1.75, 95% CI 0.32 to 9.66; 2 studies, 181 participants; I² = 8%; Analysis 1.15), swelling (RR 4.76, 95% CI 0.57 to 39.84; 2 studies, 180 participants; I² = 0%; Analysis 1.16), or redness (RR 13.50, 95% CI 0.77 to 235.63; 2 studies, 175 participants; I² = 0%; Analysis 1.17) between participants receiving IM corticosteroids versus IM placebo.

Pulmonary function

None of the included studies assessing a paediatric population collected PEF or FEV₁ measures. Four studies assessed PEF among an adult population following discharge from the ED. We found no differences in PEF between participants receiving IM versus oral corticosteroids at follow‐up (MD −7.78 L/min, 95% CI −38.83 L/min to 23.28 L/min; 4 studies, 272 participants; I² = 33%; Analysis 1.18). Only one study reported on FEV₁/FVC (%), and it reported no significant differences between participants receiving IM versus oral corticosteroids (MD −1.00, 95% CI −12.44 to 10.44; 1 study, 36 participants; I² = 0%; Analysis 1.19). No studies assessed per cent change in baseline PEF following discharge from the ED.

Symptom scores

None of the included studies assessed symptom scores following discharge from the ED using validated scales. One study reported symptom scores for shortness of breath, cough, wheeze, activity limitation, and sleep disturbance at days 7 and 21 post‐discharge using an unspecified tool, in which participants were asked to give a score between 1 (indicating 'not present') to 10 (indicating 'most severe') for each symptom (Chan 2001). At day 21 post‐discharge, symptom scores between participants receiving IM versus oral corticosteroids were similar for each symptom including: shortness of breath (IM 3.8 (SD 2.4) n = 48; oral: 3.8 (SD 2.4) n = 58), cough (IM 2.8 (SD 2.2) n = 48; oral 3.4 (SD 2.4) n = 58), wheeze (IM 3.4 (SD 2.5) n = 48; oral 3.4 (SD 2.3) n = 58), activity limitation (IM 2.1 (SD 2.3) n = 48; oral 2.2 (SD 2.1) n = 58), and sleep disturbance (IM 2.9 (SD 2.7) n = 48; oral 2.8 (SD 2.7) n = 58). The study reported no significant differences in symptoms' scores between patients receiving IM or oral corticosteroids (P value not reported).

Duration of symptoms

None of the included studies reported the duration for which symptoms occurred following discharge from the ED. Three studies reported whether participants were still experiencing non‐specific symptoms at the time of follow‐up, which was assessed at day 5 (Al‐Wahadneh 2006; Gries 2000) and between 5 to 7 days post‐discharge (Hoffman 1988). We found no significant differences in the presence of symptoms at follow‐up between participants receiving IM or oral corticosteroids (RR 0.41, 95% CI 0.14 to 1.20; 3 studies, 80 participants; I² = 44%; Analysis 1.20). Three studies reported whether participants were still experiencing cough (RR 0.69, 95% CI 0.17 to 2.73; 3 studies, 178 participants; I² = 50%; Analysis 1.21) or wheezing (RR 0.59, 95% CI 0.14 to 2.52; 3 studies, 177 participants; I² = 53%; Analysis 1.22) at the time of follow‐up but no differences between participants receiving IM versus oral corticosteroids were found. As previously noted, while Chan 2001 reported symptom scores for shortness of breath, cough, wheeze, activity limitation, and sleep disturbances at days 7 and 21 post‐discharge, the study did not assess whether there was a significant difference in symptom scores between the IM and oral corticosteroid groups at days 7 and 21.

Compliance with oral medications

Three adult studies reported compliance with the oral corticosteroid treatment regimens. Although the overall compliance with the prescribed oral corticosteroid regimen varied, the reported adherence was high, with a low of 66.7% (n = 6/9; Hoffman 1988), to 94% (n = 64/68; Schuckman 1998), and 100% (n = 84/84; Chan 2001). Only two paediatric studies examined compliance with oral corticosteroids. Al‐Wahadneh 2006 reported that eight parents reported difficulties in providing their children with the oral corticosteroid tablets and four children (n = 4/14) missed between 50% and 75% of their doses. Gries 2000 reported that 41% (n = 7/17) of patients did not comply with their prescribed oral prednisone regimen, with three participants missing more than 75% of their oral prednisone doses, while another four children did not take one‐third of their medication.

Beta agonist use

Two studies reported the use of beta₂‐agonists among participants 24 hours after discharge from the ED. We found no differences in beta₂‐agonists use 24 hours after discharge from the ED among participants receiving either IM or oral corticosteroids (RR 0.54, 95% CI 0.21 to 1.37; 2 studies, 48 participants; I² = 0%; Analysis 1.23).

Discussion

available in

Summary of main results

Systemic corticosteroids are an effective treatment in reducing relapses in patients with acute asthma after discharge from an emergency department (ED) or equivalent acute care setting (Krishnan 2009; Rowe 2007a). While systemic corticosteroids are commonly provided to prevent admission and reduce the risk of relapse, the optimal route of administration is unclear.

This systematic review set out to compare the effectiveness of a single dose of intramuscular (IM) corticosteroids to a regimen of oral corticosteroids to prevent relapse among children and adult patients discharged from an ED or equivalent acute care setting for acute asthma. Utilizing methods to reduce publication and selection bias, we identified nine trials involving 804 participants comparing a single dose of IM to oral corticosteroids in adult and paediatric participants with acute asthma.

Overall, this review could not identify a statistically significant difference in relapses among participants receiving IM versus oral corticosteroids. Furthermore, we identified no subgroup differences between children and adults, relapse occurring within or after 10 days post‐discharge, or participants presenting to the ED with a mild/moderate versus severe exacerbation. The effectiveness of IM versus oral corticosteroids to mitigate relapse remained consistent following several sensitivity analyses, including fixed versus random effects, variations in study quality, and variations in duration of oral corticosteroid regimens. Regarding other important clinical outcomes, the risk for adverse events among participants receiving IM corticosteroids ranged from a 36% decrease up to a 7% increase. Neither corticosteroid regimen demonstrated superiority with respect to pulmonary function measures, symptom persistence, or need for beta₂‐agonists following discharge.

With a similar risk for relapse, the decision to provide patients with either IM or oral corticosteroids at discharge will likely involve other considerations such as patient preference, palatability, socio‐economic conditions, ability to afford prescriptions, side‐effect profile, and clinician estimation of patient adherence. This may vary between paediatric and adult patients. For patients who may have difficulties complying with an oral corticosteroid or patients who have previously experienced nausea or vomiting with oral corticosteroids, IM corticosteroids appear to provide physicians with an effective alternative. Unfortunately, a lack of reporting of many secondary outcomes of interest severely limited the number of studies that could be included in each meta‐analysis. While all of the included studies reported on relapse outcomes, the majority of secondary outcomes were reported sparingly across the included studies, and this limited the ability of this review to make any meaningful conclusions regarding the overall effectiveness of IM corticosteroids.

Overall completeness and applicability of evidence

We believe the overall completeness of the review to be moderate. We conducted an extensive search of the literature which identified nine studies including 804 participants. Among the nine studies, five enrolled adults (n = 559) (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998) while four studies involved children (n = 245) (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997).

Overall, the paediatric studies tended to focus on young children, with the mean ages of the IM and oral corticosteroid groups ranging from 3 to 7 years old. The age of eligible children included in the studies ranged from 9 months to 14 years (Al‐Wahadneh 2006), 18 months to 7 years (Gordon 2007), 6 months to 7 years (Gries 2000), and 3 to 16 years (Klig 1997). It is important for future studies assessing the effectiveness of corticosteroids in children with acute asthma to attempt to ensure that the included patients had a true diagnosis of asthma: among the included children studies, only two of the studies reported only enrolling children with prior episodes of respiratory illness treated with bronchodilators (Gordon 2007; Klig 1997).

Within the paediatric studies, there is a paucity of studies on systemic corticosteroids in children aged 7 to 17 years old. Given the evidence that pre‐school‐aged children with acute asthma/wheezing may not respond to corticosteroids due to fewer airway eosinophils (Castro‐Rodriguez 2016), it is possible that the effectiveness of the IM or oral corticosteroid treatments may have been impacted by the age of the enrolled patients, which would affect the generalisability of this review. To our knowledge, efforts were made to avoid the inclusion of patients with a diagnosis of bronchiolitis in the included paediatric studies. This contamination, however, would have a conservative effect by decreasing the chance of detecting a difference.

In the adult studies, the age of eligible participants ranged from over the age of 18 (Chan 2001), 15 to 55 (Hoffman 1988), 18 to 45 (Lahn 2004), 16 to 60 (Lee 1993), and 18 to 50 years old (Schuckman 1998). While the majority of studies included young and middle‐aged adults, only one study included patients over the age of 60 (Chan 2001). As a result, the results of this review may not be applicable to the teenage (up to age 14) and older (> 60 years) patients with acute asthma. In addition, the effectiveness of corticosteroids in the paediatric studies may be underestimated due to the age of the participants included in the paediatric studies. All of the included studies enrolled patients presenting with acute asthma to the ED, except Gries 2000 which enrolled patients in an paediatric medical clinic. Overall, the applicability of our review focuses primarily on very young (0 to 7 years old) and young/middle‐aged adults with acute asthma presenting to the ED with acute asthma in North America (United States/Canada). More research is needed in acute care centres across the world. In particular, additional paediatric (enrolling school aged children) or elderly studies are needed to better understand the effectiveness of IM versus oral corticosteroids in those patient populations.

The type of IM agents used, as well as the doses employed, varied considerably across studies. For example, IM agents included methylprednisolone (Hoffman 1988; Lahn 2004), betamethasone (Chan 2001), dexamethasone (Lee 1993), and triamcinolone (Schuckman 1998); they also varied in dose. It is possible that the variation in the dosing and IM agents used could have impacted the effectiveness of this corticosteroid comparison. Moreover, the co‐interventions were poorly reported; and, given the age of some of the studies, the use of these agents in clinical practice likely has been stopped (e.g. metaproterenol, aminophylline, etc.).

Some newer agents, which are now the mainstay of chronic asthma treatment such as ICS and ICS/LABA agents, were either not prescribed or not reported in sufficient detail among the included studies. A recent study found that patients receiving ICS/LABA at presentation to the ED were at the highest risk of relapse following discharge (Rowe 2015) and there is evidence that ICS agents, when added to oral (and presumably IM) systemic corticosteroids at discharge, may reduce relapse (Rowe 1999). Among patients presenting with acute asthma who are already receiving ICS agents, fewer relapses occurred when ICS/LABA was substituted for ICS agents in addition to oral (and presumably IM) systemic corticosteroids at discharge (Rowe 2007b). A lack of reporting on the use of ICS and ICS/LABA agents limited the ability of this review to estimate the impact of these agents on the efficacy of IM or oral corticosteroids.

This review did not attempt to control for corticosteroid equivalency of the varying corticosteroids regimens used across the studies. It is possible that the dose and pharmacokinetic properties of various prescribed corticosteroids could have impacted the effectiveness of the IM or oral corticosteroids. Other studies have compared the effectiveness of oral prednisone compared to oral dexamethasone (which has a longer half‐life) to improve outcomes in children with acute asthma (Paniagua 2017; Normansell 2016). A recently published Cochrane Review reported insufficient evidence to identify whether lower or shorter doses of oral corticosteroids were any less effective than longer or higher doses and recommended additional large high‐quality clinical trials (Normansell 2016). Additional studies comparing the effectiveness of varying IM corticosteroids (e.g. IM dexamethasone versus IM methylprednisone) and the impact of dosing/pharmacokinetics are needed.

Quality of the evidence

The overall risk of bias of the included studies ranged from unclear to high, with no studies being assessed as having a low risk of bias. Four high risk of bias studies were not placebo controlled trials (Al‐Wahadneh 2006; Gordon 2007; Gries 2000; Klig 1997). The remaining studies had an overall unclear risk of bias (Chan 2001; Hoffman 1988; Lahn 2004; Lee 1993; Schuckman 1998). The majority of studies did not adequately describe their method of randomisation and all but Chan 2001 had an unclear risk of bias for selective outcome reporting due to a lack of an available protocol. Using GRADE, the overall quality of the outcomes ranged from low to moderate. We reduced to low quality the primary outcomes of relapse as well as relapse after 10 days due to overall unclear to high risk of bias of the studies, and imprecision due to wide confidence intervals including both benefit, harm, and no effect. We assessed the quality of the subgroup analyses for relapse to be low due to the low number of available patients and wide confidence intervals. We judged the quality of the outcome adverse events to be low quality due to the overall unclear to high risk of bias of the included studies and imprecision due to few events. We considered both 'symptom persistence' and '24 hour beta₂‐agonists use' to be low quality due the overall unclear to high risk of bias of the included studies, as well as few events. We assessed the 'outcome of relapse within 10 days' as being of moderate quality due to the overall unclear to high risk of bias of the studies. We reduced 'peak expiratory flow' to moderate quality due to imprecision of the results.

Potential biases in the review process

While there is always a potential for screening and study selection bias, we took several steps to attenuate this risk. An expert health sciences librarian conducted a comprehensive search of the literature, including the CATR, a separate search of nine electronic databases, and a detailed search of the grey literature. Indeed, we identified one study from the grey literature (Al‐Wahadneh 2006). We placed no limits with regard to language, date of publication, or status of publication on any of the searches. We translated and screened all foreign language articles identified. If the information provided in the text did not allow for a clear inclusion/exclusion decision, we attempted to contact study authors to clarify the information provided in the text. Two review authors independently completed study selection, including both title and abstract screening and full‐text review. Despite our efforts, we recognize that some studies could have been missed. Unfortunately, due to an insufficient number of included studies, publication bias could not be assessed as planned (Higgins 2011). As such, the risk of publication bias should be considered unclear.

Agreements and disagreements with other studies or reviews

Only two reviews have been published comparing the effectiveness of IM versus oral corticosteroids in patients presenting to an acute care centre with acute asthma (Krishnan 2009; Rowe 2017). The results of this review are similar to a previously published umbrella review which compared the effectiveness of IM versus oral corticosteroids in adults (Krishnan 2009). The review identified five adult studies (all five of which were included in this review) and reported no significant difference in relapse rates in adult participants receiving IM versus oral corticosteroids for acute asthma after discharge from an ED. Unlike the current review, Krishnan 2009 did not include paediatric studies. In addition, a recently published review compared the effectiveness of various regimens of systemic corticosteroids to reduce relapse in adults with acute asthma (Rowe 2017). Unlike the current review which strictly included studies comparing IM versus oral corticosteroids, Rowe 2017 included any studies comparing IM or oral corticosteroids to other oral corticosteroid or placebo regimens and conducted indirect comparisons using a Bayesian network analysis. The review reported that both IM and long‐course oral corticosteroids were effective in reducing relapse, with a risk of bias ability of best analysis identifying IM corticosteroids as having the highest risk of bias of being the most effective treatment option compared to short‐course or long‐course oral corticosteroids. Unlike the current review, Rowe 2017 did not exclusively compare the effectiveness of IM versus oral corticosteroids to mitigate relapse.

Study flow diagram.
Figures and Tables -
Figure 1

Study flow diagram.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figures and Tables -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figures and Tables -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 1 Relapse.
Figures and Tables -
Analysis 1.1

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 1 Relapse.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 2 Relapse intention to treat.
Figures and Tables -
Analysis 1.2

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 2 Relapse intention to treat.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 3 Subgroup analysis: children versus adults.
Figures and Tables -
Analysis 1.3

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 3 Subgroup analysis: children versus adults.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 4 Subgroup analysis: relapse within 10 days and over 10 days post‐discharge.
Figures and Tables -
Analysis 1.4

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 4 Subgroup analysis: relapse within 10 days and over 10 days post‐discharge.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 5 Subgroup analysis: mild/moderate versus severe exacerbations.
Figures and Tables -
Analysis 1.5

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 5 Subgroup analysis: mild/moderate versus severe exacerbations.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 6 Sensitivity analysis: risk of bias.
Figures and Tables -
Analysis 1.6

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 6 Sensitivity analysis: risk of bias.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 7 Sensitivity analysis: oral corticosteroid prescriptions greater than 5 days.
Figures and Tables -
Analysis 1.7

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 7 Sensitivity analysis: oral corticosteroid prescriptions greater than 5 days.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 8 Sensitivity analysis: fixed effects.
Figures and Tables -
Analysis 1.8

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 8 Sensitivity analysis: fixed effects.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 9 Sensitivity analysis: corticosteroids in ED.
Figures and Tables -
Analysis 1.9

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 9 Sensitivity analysis: corticosteroids in ED.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 10 Serious adverse events; hospitalization following discharge.
Figures and Tables -
Analysis 1.10

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 10 Serious adverse events; hospitalization following discharge.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 11 Adverse events.
Figures and Tables -
Analysis 1.11

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 11 Adverse events.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 12 Adverse events: nausea/vomiting/GI distress.
Figures and Tables -
Analysis 1.12

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 12 Adverse events: nausea/vomiting/GI distress.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 13 Adverse events: insomnia.
Figures and Tables -
Analysis 1.13

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 13 Adverse events: insomnia.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 14 Adverse events: personality changes.
Figures and Tables -
Analysis 1.14

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 14 Adverse events: personality changes.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 15 Adverse events: pain.
Figures and Tables -
Analysis 1.15

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 15 Adverse events: pain.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 16 Adverse events: swelling.
Figures and Tables -
Analysis 1.16

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 16 Adverse events: swelling.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 17 Adverse events: redness.
Figures and Tables -
Analysis 1.17

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 17 Adverse events: redness.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 18 Pulmonary function: peak expiratory flow (L/min).
Figures and Tables -
Analysis 1.18

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 18 Pulmonary function: peak expiratory flow (L/min).

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 19 Pulmonary function: FEV₁/FVC (%).
Figures and Tables -
Analysis 1.19

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 19 Pulmonary function: FEV₁/FVC (%).

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 20 Symptom persistence.
Figures and Tables -
Analysis 1.20

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 20 Symptom persistence.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 21 Symptom persistence: cough.
Figures and Tables -
Analysis 1.21

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 21 Symptom persistence: cough.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 22 Symptom persistence: wheezing.
Figures and Tables -
Analysis 1.22

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 22 Symptom persistence: wheezing.

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 23 24‐hour beta agonist use.
Figures and Tables -
Analysis 1.23

Comparison 1 Intramuscular versus oral corticosteroids, Outcome 23 24‐hour beta agonist use.

Summary of findings for the main comparison. Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma

Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma

Patient or population: patients with acute asthma
Settings: Acute care settings
Intervention: Intramuscular corticosteroids
Comparison: Oral corticosteroids

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Assumed risk

Corresponding risk

Oral corticosteroids

Intramuscular corticosteroids

Relapse

201 per 1000

12 fewer per 1000
(from 56 fewer to 48 more)

RR 0.94
(0.72 to 1.24)

804
(9 studies)

⊕⊕⊝⊝
low1,2

Relapse within 10 days postdischarge

154 per 1000

40 fewer per 1000

(from 75 fewer to 11 more)

RR 0.74
(0.51 to 1.07)

742
(7 studies)

⊕⊕⊕⊝
moderate1

Relapse occurring after 10 days postdischarge

245 per 1000

2 fewer per 1000
(from 64 fewer to 81 more)

RR 0.99
(0.74 to 1.33)

556
(5 studies)

⊕⊕⊝⊝
low1,2

Adverse events

294 per 1000

50 fewer per 1000
(from 106 fewer to 21 more)

RR 0.83
(0.64 to 1.07)

404
(5 studies)

⊕⊕⊝⊝
low1,3

Pulmonary function: Peak expiratory flow

The mean pulmonary function: peak expiratory flow ranged across control groups from
304 to 419 litres/min

The mean pulmonary function: peak expiratory flow in the intervention groups was
7.78 liters/min lower
(38.83 lower to 23.28 higher)

272
(4 studies)

⊕⊕⊕⊝
moderate2

Symptom persistence

537 per 1000

317 fewer per 1000
(from 461 fewer to 107 more)

RR 0.41
(0.14 to 1.2)

80
(3 studies)

⊕⊕⊝⊝
low1,3

24hour beta agonist use

375 per 1000

172 fewer per 1000
(from 296 fewer to 139 more)

RR 0.54
(0.21 to 1.37)

48
(2 studies)

⊕⊕⊝⊝
low1,3

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: Confidence interval; RR: Risk ratio;

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 Downgraded 1 level for risk of bias. Majority of studies received an unclear risk of bias for random sequence generation and selective outcome reporting
2 Downgraded 1 level for imprecision including wide confidence intervals (including both benefit, harm, and no effect)
3 Downgraded 1 level for Imprecision including wide confidence intervals (including both benefit, harm, and no effect) and few events

Figures and Tables -
Summary of findings for the main comparison. Intramuscular corticosteroids compared to Oral corticosteroids for acute asthma
Table 1. Exacerbation severity

Studies

Pulmonary function: Eligibility criteria

Exacerbation severity

Al‐Wahadneh 2006

Severity estimated using modified scoring system based on GINA guidelines. Reported to enrolling patients with mild‐moderate exacerbations, however baseline pulmonary function of the groups was not reported.

Unable to assess

Chan 2001

Reported mean baseline PEF greater than 200 L/min: IM group: 270 L/min (SD: 103); oral group: 261 L/min (SD: 104).

Mild/moderate

Gordon 2007

Reported to enrolling patients identified as moderate exacerbations, however baseline pulmonary function was not reported.

Unable to assess

Gries 2000

Applied adapted exacerbation severity score (unspecified). Reported to enrolling patients rated as mild/moderate, however baseline pulmonary function of the groups was not reported.

Unable to assess

Hoffman 1988

Reported baseline mean PEF of enrolled patients of less than 150 L/min: IM group: 129 L/min (SD:14); oral group: 141 L/min (SD: 14).

Severe

Klig 1997

Exacerbation severity estimated via pulmonary index score. Study reported to enrolling patients with mild/moderate exacerbations, however baseline pulmonary function was not reported.

Unable to assess

Lahn 2004

Eligibility criteria required patients to have a PEFR of ≤ 70% predicted with a minimum PEFR of ≥ 40%. Reported PEF of enrolled patients was ≥ 200 L/min: IM group: 205 L/min (SD: 70); oral group: 209 L/min (SD: 72).

Mild/moderate

Lee 1993

Reported mean baseline PEF of ≥ 200 L/min: IM group: 210 L/min (SD: 30); oral group: 208 L/min (SD: 26).

Mild/moderate

Schuckman 1998

Reported mean baseline PEF of ≥ 200 L/min: IM group: 243.6 L/min (SD: 64); oral group: 244.7 L/min (SD: 83).

Mild/moderate

Abbreviations:

GINA = Global Initiative for Asthma; PEF = Peak expiratory flow; PEFR = Peak expiratory flow rate; IM = intramuscular; SD = standard deviation

Figures and Tables -
Table 1. Exacerbation severity
Table 2. Study characteristics of included studies

Studies

Location/setting

Co‐interventions

Corticosteroid doses and durations

Methyprednisolone equivalency

Relapse outcome

Al‐Wahadneh 2006

Jordan, ED

Provided in ED: not stated

Provided at discharge: SABA

Dexamethasone (IM)

1.7 mg/kg

Mean dose: 24 mg

Single dose

Prednisolone (oral)

2 mg/kg/day for 5 days

Mean dose: 19.2 mg per day

Total dose: 96 mg

IM

Methylprednisone equivalency: 120 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

76.8 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

1/16

Day 21

Oral group

3/14

Day 21

Chan 2001

Canada, ED

Provided in ED: SABA, methylxanthines, supplemental oral/IV corticosteroids

Provided at discharge: Methylxanthines, unspecified inhaled beta₂‐agonists, and ICS

Betamethasone (IM)

12 mg

Single dose. Received placebo capsules over 7 days.

Prednisone (oral)

50 mg a day for 7 days. Received a single placebo injection

Total dose: 350 mg

IM

Methylprednisone equivalency:

72 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

280 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

12/86

Day 7

Oral group

19/82

Day 7

Gordon 2007

United States, Pediatric ED

Provided in ED: SABA, ipratropium bromide. IV corticosteroids for patients who vomited oral corticosteroids.

Provided at discharge: Inhaled beta₂‐agonists and ICS

Dexamethasone (IM)

0.6 mg/kg (max 16 mg)

Single dose

Prednisolone (oral)

2 mg/kg (max 50 mg) daily for 5 days

Total: 250 mg

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12‐36 hours)

Oral

Methylprednisone equivalency:

200 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

8/69

Day 4

Oral group

11/73

Day 4

IM group

15/68

Day 14

Oral group

16/73

Day 14

Gries 2000

United States, Tertiary medical center

Provided in ED: SABA

Provided at discharge: SABA

Dexamethasone (IM)

Patients 6 to 12 months old received 16 mg.

Patients 13 to 35 months old received 24 mg.

Children ≥ 36 months received 36 mg.

Single dose

Prednisone (oral)

2 mg/kg a day for 5 days

Total dose: unclear

IM

Methylprednisone equivalency:

Unable to assess

Oral

Methylprednisone equivalency:

Unable to assess

IM group

1/15

Day 28

Oral group

3/17

Day 28

Hoffman 1988

United States, ED

Provided in ED: SABA, epinephrine, methylxanthines, IV corticosteroids

Provided at discharge: Methylxanthine and inhaled beta₂‐agonists

Methylprednisonlone (IM)

80 mg

Single dose. Received placebo capsules for 7 days

Methylprednisolone (oral)

Tapering dose over 7 days.

Total dose: 216 mg

Received placebo injection

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

216 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

0/8 day

Day 7

Oral group

2/10

Day 7

Klig 1997

United States, Pediatric ED

Provided in ED: SABA

Provided at discharge: SABA

Dexamethasone (IM)

0.3 mg/kg

Total dose: 15 mg

Single dose

Prednisone (oral)

2 mg/kg a day for 3 days

Total dose: 100 mg

IM

Methylprednisone equivalency:

75 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

0/21

Day 5

Oral group

0/21

Day 5

Lahn 2004

United States, ED

Provided in ED: inhaled beta₂‐agonists, IV corticosteroids

Provided at discharge: SABA

Methylprednisolone (IM)

160 mg

Single dose. Received placebo capsules for 8 days

Methylprednisolone (oral)

Tapering dose over 8 days.

Total dose: 160 mg (tapering dose 32 mg day 1).

Received placebo injection

IM

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

80 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

13/92

Day 10

Oral group

12/88

Day 10

IM group

17/92

Day 21

Oral group

20/88

Day 21

Lee 1993

Taiwan, ED

Provided in ED: SABA, methylxanthines

Provided at discharge: Methylxanthine and inhaled beta₂‐agonists

Dexamethasone (IM)

10 mg

Single dose. Received placebo capsules for 7 days

Dexamethasone (oral)

Tapering dose over 7 days.

11.75 mg total. Received placebo injection

IM

Methylprednisone equivalency:

50 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

58.8 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

1/17

Day 7

Oral group

0/19

Day 7

Schuckman 1998

United States, ED

Provided in ED: SABA, oral/IV corticosteroids

Provided at discharge: SABA, antibiotics, ICS, cromolyn sodium, ipratropium bromide

Triamcinolone (IM)

40 mg

Single dose. Received placebo capsules for 5 days

Prednisone (oral)

40 mg a day for 5 days.

Total dose: 160 mg

Received placebo injection

IM

Methylprednisone equivalency:

40 mg

Duration: intermediate half‐life (12 to 36 hours)

Oral

Methylprednisone equivalency:

160 mg

Duration: intermediate half‐life (12 to 36 hours)

IM group

7/78

Day 7

Oral group

11/76

Day 7

ED = emergency department; SABA = short‐acting beta₂‐agonists; LABA = long‐acting beta₂‐agonists; IV = intravenous; IM = intramuscular; ICS = inhaled corticosteroids

Figures and Tables -
Table 2. Study characteristics of included studies
Comparison 1. Intramuscular versus oral corticosteroids

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Relapse Show forest plot

9

804

Risk Ratio (M‐H, Random, 95% CI)

0.94 [0.72, 1.24]

2 Relapse intention to treat Show forest plot

9

821

Risk Ratio (M‐H, Random, 95% CI)

0.95 [0.72, 1.26]

3 Subgroup analysis: children versus adults Show forest plot

9

804

Risk Ratio (M‐H, Random, 95% CI)

0.94 [0.72, 1.24]

3.1 Children

4

245

Risk Ratio (M‐H, Random, 95% CI)

0.86 [0.48, 1.53]

3.2 Adults

5

559

Risk Ratio (M‐H, Random, 95% CI)

0.97 [0.71, 1.33]

4 Subgroup analysis: relapse within 10 days and over 10 days post‐discharge Show forest plot

9

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

4.1 Within 10 days post‐discharge

7

742

Risk Ratio (M‐H, Random, 95% CI)

0.74 [0.51, 1.07]

4.2 Greater than 10 days post‐discharge

5

556

Risk Ratio (M‐H, Random, 95% CI)

0.99 [0.74, 1.33]

5 Subgroup analysis: mild/moderate versus severe exacerbations Show forest plot

5

557

Risk Ratio (M‐H, Random, 95% CI)

0.96 [0.70, 1.32]

5.1 Mild/moderate exacerbations

4

539

Risk Ratio (M‐H, Random, 95% CI)

0.98 [0.71, 1.34]

5.2 Severe exacerbations

1

18

Risk Ratio (M‐H, Random, 95% CI)

0.24 [0.01, 4.47]

6 Sensitivity analysis: risk of bias Show forest plot

5

559

Risk Ratio (M‐H, Random, 95% CI)

0.97 [0.71, 1.33]

7 Sensitivity analysis: oral corticosteroid prescriptions greater than 5 days Show forest plot

8

762

Risk Ratio (M‐H, Random, 95% CI)

0.94 [0.72, 1.24]

8 Sensitivity analysis: fixed effects Show forest plot

9

804

Risk Ratio (M‐H, Fixed, 95% CI)

0.91 [0.69, 1.19]

9 Sensitivity analysis: corticosteroids in ED Show forest plot

5

320

Risk Ratio (M‐H, Random, 95% CI)

0.76 [0.45, 1.29]

10 Serious adverse events; hospitalization following discharge Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

11 Adverse events Show forest plot

5

404

Risk Ratio (M‐H, Random, 95% CI)

0.83 [0.64, 1.07]

12 Adverse events: nausea/vomiting/GI distress Show forest plot

3

320

Risk Ratio (M‐H, Random, 95% CI)

0.56 [0.09, 3.59]

13 Adverse events: insomnia Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

14 Adverse events: personality changes Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

15 Adverse events: pain Show forest plot

2

181

Risk Ratio (M‐H, Random, 95% CI)

1.75 [0.32, 9.66]

16 Adverse events: swelling Show forest plot

2

180

Risk Ratio (M‐H, Random, 95% CI)

4.76 [0.57, 39.84]

17 Adverse events: redness Show forest plot

2

175

Risk Ratio (M‐H, Random, 95% CI)

13.5 [0.77, 235.63]

18 Pulmonary function: peak expiratory flow (L/min) Show forest plot

4

272

Mean Difference (IV, Random, 95% CI)

‐7.78 [‐38.83, 23.28]

19 Pulmonary function: FEV₁/FVC (%) Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Totals not selected

20 Symptom persistence Show forest plot

3

80

Risk Ratio (M‐H, Random, 95% CI)

0.41 [0.14, 1.20]

21 Symptom persistence: cough Show forest plot

3

178

Risk Ratio (M‐H, Random, 95% CI)

0.69 [0.17, 2.73]

22 Symptom persistence: wheezing Show forest plot

3

177

Risk Ratio (M‐H, Random, 95% CI)

0.59 [0.14, 2.52]

23 24‐hour beta agonist use Show forest plot

2

48

Risk Ratio (M‐H, Random, 95% CI)

0.54 [0.21, 1.37]

Figures and Tables -
Comparison 1. Intramuscular versus oral corticosteroids