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The role of oral magnesium supplements for the management of stable bronchial asthma: a systematic review and meta-analysis

npj Primary Care Respiratory Medicinevolume 29, Article number: 4 (2019) | Download Citation

Abstract

Asthma is a chronic lung disease characterized by airway inflammation and hyper-responsiveness of airway smooth muscles. There is growing evidence that magnesium may have a role in managing asthma through its dual effect as an anti-inflammatory and bronchodilating agent. To assess the efficacy of oral magnesium supplements in chronic asthmatic patients. In addition to searching through Clinicaltrials.gov/ and references for oral magnesium supplement studies, we performed a database search in Medline, CINAHL, CENTRAL, and Embase. We contacted the authors of the included trials to ask for additional information. We included randomized controlled trials that compared oral magnesium supplements versus placebo, in addition to standard asthma treatment in mild-moderate asthmatic adults and children (older than 6 years). Two reviewers independently performed the study selection, data abstraction, and the assessment of the risk of bias. Eight trials at moderate risk of bias enrolling a total of 917 patients were included. Oral magnesium improved FEV1 at week 8 (5.69 (L/min); 95% CI: 1.92, 9.46; I2: 45%). There was no significant improvement in FEV1 at other follow up periods. There was no significant change in FVC, Methacholine challenge test, the frequency of bronchodilator use, or symptoms score. There were no data on mortality or quality of life. Oral magnesium supplements may lead to improvement in FEV1 that was only demonstrated at eight weeks; but no effect on any other outcome. Until future evidence emerges, oral magnesium cannot be recommended as adjuvants to standard treatment for mild to moderate asthmatic individuals.

Introduction

Asthma is a chronic inflammatory disease that affects ~300 million people worldwide,1 reaching up to 18% of the population in certain countries.1,2

Symptoms of asthma include coughing, wheezing, chest tightness, and other respiratory complaints. Most of the time these symptoms are mild and can be controlled with inhalers and avoidance of known allergens, but other times they can lead to exacerbations that can be life threatening. An estimated annual 300,000 deaths worldwide are attributed to asthma.3,4

The mainstay of management is a beta-agonist and corticosteroids inhaler. However, new investigations into the pathogenesis of the disease are emerging. For example, many reports have observed that low blood levels and low dietary intake of magnesium are factors that possibly contribute to the development of asthma.5,6,7,8,9 In addition, low levels of magnesium have been detected in asthmatics compared with non-asthmatics, especially those that have presented to the emergency department with exacerbations.8,9,10,11,12

Magnesium deficiency has a role in many diseases in addition to asthma, including migraines, depression, and epilepsy.6,7,13,14,15 Although the exact role magnesium has in asthma is not completely understood, it is known that it functions as an anti-inflammatory agent in addition to its role in inhibiting the effect of calcium to contract smooth muscle.6,16,17,18,19

Previous trials showed that magnesium use through intravenous or inhaled routes does have a role in managing asthma in acute exacerbations.20,21,22,23,24,25,26,27,28,29,30,31 However, studies published on the benefits of oral supplements have reported unclear conclusions.7,32,33,34,35,36 Major problems with these trials regarding randomization, placebo use, intervention duration, outcome measurements, and baseline level of serum magnesium may explain the conflicting results.

The role of intravenous and inhaled magnesium in the management of acute asthma has been extensively studied and the guidelines are well established.37,38 IV or inhaled routes can be used as a last resort for severe, persistent asthma that fails to respond to conventional treatment.39,40 Nevertheless, oral magnesium is not included in these guidelines.

Our aim in this study was to conduct a meta-analysis of all published reports on the effect of oral magnesium for the management of chronic asthma.

Results

Search results

A total of 5353 citations were identified by searching the databases; a manual search of the references and ongoing trials revealed an additional 24 articles. After screening the titles and abstracts and removing duplicates, 13 trials met our criteria. Full articles were retrieved and a further five articles were excluded, including crossover trials,33,41 on-going RCTs with no published results,4,42 and a narrative review.43 A total of eight trials were included in the present report.32,34,35,36,44,45,46,47 Figure 1 shows a flowchart depicting the process of selection and exclusion.48

Fig. 1
Fig. 1

PRISMA study selection flowchart

Study description

Of the eight enrolled articles, six were in English, one in Persian, and one in Russian.45,47 The trials were conducted in, Hungary, UK, USA, Brazil, Iran, and Russia. The total population was 917; four trials included adults and children, the other four only children, with age groups ranging from 4 to 60 years old. The enrolled subjects were labeled with either mild or moderate asthma. Type and dose of magnesium supplements were different across each trial; 200–290 mg Mg-citrate was used in three RCTs,44,45,46 two trials used 340 mg Mg-citrate,36,47 450 mg Mg amino-chelate was utilized in two trials,32,35 and one study chose 300 mg Mg-glycine.34 Durations of treatment were 4–26 weeks. Measured outcomes included changes in FEV132,34,36,44,46,47 and FVC32,34,36,47, frequency of bronchodilator use,32,34,44,45,46 asthma symptom scores,32,44,45,46 and methacholine challenge test.32,34,36 A summary of the characteristics is provided in Table 1.

Table 1 Evidence table: study description and characteristics

Risk of bias

The Cochrane ROB assessment tool was used to evaluate the eight included trials (Supplementary Figures S1 & S2). We identified a low ROB in the assessed sequence generation in three articles,32,35,36 whereas the ROB was unclear in the remaining articles. Allocation concealment was unclear across all trials. Five trials displayed a low ROB regarding blinding,32,34,35,36,47 whereas the ROB was unclear in two trials,44,46 and high-risk in one study.45 No dropouts were reported in four trials,34,44,45,46 whereas the remaining trials reported dropouts with a variety of reasons provided.32,35,36,47 None of the articles provided their study protocol; therefore, selective outcome reporting could not be assessed.

Outcomes

FVC

Three trials reported FVC (Fig. 2a).34,36,47 A fourth study was excluded because it reported the change in FVC using a different unit.32 There was no statistically significant difference in FVC at 8 weeks, 26 weeks, or overall.

Fig. 2
Fig. 2

a FCV comparison of Mg supplements vs. placebo, b FEV1 comparison of Mg supplements vs. placebo, c bronchodilator use comparison of Mg supplements vs. placebo

FEV1

Five trials reported FEV1 results (Fig. 2b).34,36,44,46,47 A sixth study was excluded from the analysis because it used different units.32 Data were available to assess the effect at weeks 4, 8, 12, and 26. The mean difference in FEV1 was only statistically significant at week 8 (5.69; 95% CI: 1.92, 9.46) with moderate heterogeneity (I2: 45%).

Bronchodilator use

Four trials included bronchodilator use (Fig. 2c).32,44,45,46 A fifth study was excluded due to the results that were reported as number of days rather than number of puffs as recorded in the other trials.34 Subgroup analysis was used according to duration at 4, 8, 12, 16, and 24 weeks. There was no statistically significant difference at any follow up period.

Symptoms scores

Both Bede et al.46 and Petrov et al.45 showed significant improvement in daytime symptoms after 12 weeks in the intervention group but not in other measures. Kazaks et al.36 on the other hand used two questionnaires (AQLQ and ACQ) to assess subjective measures, statistically significant improvements were noted after 6.5 months in the AQLQ.

PD20 inhaled methacholine challenge test

Three trials performed a PD20 inhaled methacholine challenge test.32,34,36 Subgroup analysis was used at weeks 8, 16, and 24 (Supplementary Figure S3). The mean difference was not significant at week 8 but reached statistical significance at week 16 (−0.14; 95% CI: −0.28, −0.0).

Supplementary Table 1 presents GRADE summary of finding for all outcomes.

Quality of evidence

The quality of evidence (i.e., certainty in the estimates) was low, reduced because of risk of bias (lack of clear allocation concealment) and imprecision (mostly nonsignificant results and small sample size). The outcomes available in the trials were surrogate outcomes except for symptoms score and possibly bronchodilators use.

Discussion

This systematic review and meta-analysis was performed to evaluate the effects of oral magnesium on chronic asthma. The results of the measured outcomes was overall precise and nonsignificant (except for FEV1 at week 8). None of the trials reported on mortality or adverse events. Certainty in these estimates is low. There was some high heterogeneity, which could be explained by different type, dose, or duration of the intervention across the experimental groups in the involved RCTs. We excluded crossover RCTs due to uncertainty over washout periods of magnesium. We have identified ongoing trials registered in Clinicaltrials.gov, which might have future implications on the conclusion reached in this study.4,42

The role of magnesium in bronchial asthma has been discussed in the recent GINA guidelines. The evidence supports the use of intravenous magnesium in acute situations, especially with asthmatics that do not respond to initial management. However, the routine use of intravenous magnesium in acute or chronic asthma is not supported by evidence.49 Nevertheless, the use of oral magnesium for the prevention of asthma exacerbations or to improve control has not been discussed in the GINA report. Other supplements, such as vitamin D, were mentioned in GINA.4 In the present study, only FEV1 was shown to be significantly improved with oral magnesium.

However, encouraging findings were found especially in Kazak’s study including a significant increase in the concentration of methacholine required to cause a 20% drop in FEV1 at 6 months, and a 5.8% improvement in PEFR and an improvement in subjective measures (AQLQ, ACQ) all noticed at 6.5 months in subjects who were in the treatment group. Therefore, there is a need for future large, high quality RCTs to reliably determine the role of oral magnesium in asthma management. To our knowledge, this is the first systematic review and meta-analyses evaluating the use of magnesium supplements as an adjunct treatment to inhalers for asthmatics.

There are several limitations to this study. First, sample sizes are considered relatively small for a common disease like asthma, some trials recruited less than fifty participants.34,44,45 Second, important data were missing in some of the trials; strategies we used to overcome this problem were discussed in the methodology above. Additionally, we were not able to assess the effect of the intervention on reducing the dose of inhaled steroid, because it was only reported in a single study which showed no benefit.35

Furthermore, GINA guidelines defined adults as those 6 years old and above. This dichotomy is not used in many of the available studies. Clearer details regarding trial methodology, particularly about sequence generation and allocation concealment would help future systematic reviewers appraise the literature more properly. Additionally, clear stratification by oral magnesium dose and duration of therapy can help produce more precise and useful estimates. Finally, none of the RCTs provided their research protocol.

The use of magnesium supplements as an adjuvant to standard asthma treatment in mild to moderate asthmatic patients is not supported by high quality evidence. Apart from one point at week 8 where the FEV1 had significantly improved, no other benefits from oral magnesium supplements were seen. Until future higher quality evidence emerges, oral magnesium cannot be recommended for mild to moderate asthma.

Methods

Search strategy

A medical librarian (MVN) performed a comprehensive literature search on April 2016. Searched databases were as follows: Medline, CINAHL, Cochrane Central Register of Controlled Trials (CENTRAL), Embase, and on-going clinical trials (https://clinicaltrials.gov/). The main search concepts were asthma and oral magnesium; Boolean operators: OR (for combining synonyms), AND (to combine concepts), and truncations were used when appropriate. A review of references and a manual search of relevant articles was completed. Additionally, we contacted the authors of the trials to minimize chances of missed articles. The search was updated on May 2017. No restrictions to study type, time, or language were applied.

Inclusion and exclusion criteria

We included RCTs that investigated the use of oral magnesium as an adjunct to asthma inhalers. Asthma was defined in accordance with the authors of the included trials, which were either clinically, objectively (spirometry), or both. All trials fulfilled the inclusion criteria as follows: (1) Population: mild and moderate asthmatic older than 6 years [6 years was the cut-off based on the global initiative for asthma (GINA) guidelines];4 (2) Intervention: all preparations of oral magnesium, regardless of name or dosage; (3) Comparisons: placebo or no treatment; (4) Outcomes: frequency of rescue asthma exacerbation, ER visits or hospital admissions, objective measures: FEV1, FVC, and PEF, daytime symptoms, daytime activity, night-time symptoms, frequency of bronchodilator use, use of oral or inhaled steroids, side effects, and mortality; (5) Timing: treatment for any duration was included; (6) Study type: RCTs, blinded or open-labeled. Crossover trials were excluded.

Study selection

Two reviewers (AA and FA) separately scanned the titles and abstracts of all articles, and when needed, the full text was retrieved and reviewed to identify all relevant articles. A third author (MF) resolved any disagreements.

Data extraction

Important data were extracted using a piloted form, which incorporated all attributes of the studies, including author, publication year, country, setting, design, sample size, intervention (dose and type), placebo, patient’s age and sex, severity, study duration, inclusion and exclusion criteria, outcomes, and limitations. Data was extracted by AA and FA and reviewed by MF. We contacted the author of the study in question for any missing information.

Methodological quality assessment

The risk of bias (ROB) was assessed using the Cochrane ROB assessment tool;38 this was done independently by AA and FA and disagreements were resolved by MF.

Statistical analysis

We combined the results using RevMan 5.3.5. There were five outcomes, which included FVC, FEV1, methacholine challenge test, bronchodilator use, and symptoms score. All outcomes were considered continuous data; therefore, we used the weighted mean difference (WMD).44,45 A random-effects model was used to pool the results because of anticipated high heterogeneity due to the different characteristics and qualities of the included studies. Subgroup analysis was used according to the duration of the intervention. Subgrouping was not performed based on severity because the included RCTs did not separate data based on severity except for one,44 which data were combined. To assess for heterogeneity, we used the I2 level of 50% or above, and Cochrane Q test which was considered significant if the p-value < 0.05.

Symptoms were considered an important clinical outcome. Symptom scores were reported differently in each trial, therefore it was not feasible to combine across trials in meta-analysis. Therefore, symptom scores were reported narratively and separately in the results section.

Four RCTs were available for analysis.32,44,45,46

Missing data

The standard deviations (SD) of the mean difference before and after treatment was missing in select trials. Therefore, we contacted the authors of each study and received no response, thus we recalculated the data whenever the p-value was available, and when neither the p-value nor SD was available, we used the SD of similar studies.44,46 In addition, the FEV1 and FVC units were not defined in one study, we contacted the author with no response, and thus we excluded these outcomes.32 The present study was approved by King Abdullah International Medical Research Center IRB committee on November 15, 2016 (research number RC16/084/R).

Additional information

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References

  1. 1.

    Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention. Online Appendix (2016).

  2. 2.

    Lai, C. K. et al. Global variation in the prevalence and severity of asthma symptoms: phase three of the International Study of Asthma and Allergies in Childhood (ISAAC). Thorax 64, 476–483 (2009).

  3. 3.

    Lozano, R. et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 380, 2095–2128 (2013).

  4. 4.

    Stern, J. S. Magnesium and Asthma - Clinical Trials (NCCIH, Bethesda, MD, 2006).

  5. 5.

    Rosanoff, A., Weaver, C. & Rude, R. K. Suboptimal magnesium status in the United States: are the health consequences underestimated? Nutr. Rev. 70, 153–164 (2012).

  6. 6.

    de Baaij, J. H., Hoenderop, J. G. & Bindels, R. J. Magnesium in man: implications for health and disease. Physiol. Rev. 95, 1–46 (2015).

  7. 7.

    Britton, J. et al. Dietary magnesium, lung function, wheezing, and airway hyperreactivity in a random adult population sample. Lancet 344, 357–362 (1994).

  8. 8.

    Sedighi, M. et al. Low magnesium concentration in erythrocytes of children with acute asthma. Iran. J. Allergy, Asthma Immunol. 5, 183–186 (2006).

  9. 9.

    Mircetic, R. N., Dodig, S., Raos, M., Petres, B. & Cepelak, I. Magnesium concentration in plasma, leukocytes and urine of children with intermittent asthma. Int. J. Clin. Chem. 312, 197–203 (2001).

  10. 10.

    Maha, Amin, Mohammed, A.-F. & Zaghloul, S. S. Magnesium concentration in acute asthmatic children. Iran. J. Pediatr. 22, 463–467 (2012).

  11. 11.

    Hashimoto, Y., Nishimura, Y., Maeda, H. & Yokoyama, M. Assessment of magnesium status in patients with bronchial asthma. J. Asthma 37, 489–496 (2000).

  12. 12.

    Emelyanov, A., Gleb, F. & Barnes, P. J. Reduced intracellular magnesium concentrations in asthmatic patients. Eur. Respir. J. 19, 38–40 (1999).

  13. 13.

    Cheungpasitporn, W. et al. Hypomagnesaemia linked to depression: a systematic review and meta-analysis. Intern. Med. J. 45, 436–440 (2015).

  14. 14.

    Chiu, H. Y., Yeh, T. H., Huang, Y. C. & Chen, P. Y. Effects of intravenous and oral magnesium on reducing migraine: a meta-analysis of randomized controlled trials. Pain Physician 19, E97–e112 (2016).

  15. 15.

    Gilliland, F. D., Berhane, K., Li, Y. F., Kim, D. H. & Margolis, H. G. Dietary magnesium, potassium, sodium, and children’s lung function. Am. J. Epidemiol. 155, 125–131 (2002).

  16. 16.

    Landon, R. A. & Young, E. A. Role of magnesium in regulation of lung function. J. Am. Diet. Assoc. 93, 674–677 (1993).

  17. 17.

    Kumasaka, D. et al. MgSO4 relaxes porcine airway smooth muscle by reducing Ca2+ entry. Am. J. Physiol. 270, L469–L474 (1996).

  18. 18.

    Spivey, W. H., S. E. & Levin, R. M. Effect of magnesium chloride on rabbit bronchial smooth muscle. Ann. Emerg. Med. 19, 1107–1112 (1990).

  19. 19.

    Okayama, H. et al. Bronchodilating effect of intravenous magnesium sulfate in bronchial asthma. JAMA 257, 1076–1078 (1987).

  20. 20.

    Skobeloff, E. M., Spivey, W. H., McNamara, R. M. & Greenspon, L. Intravenous magnesium sulfate for the treatment of acute asthma in the emergency department. JAMA 262, 1210–1213 (1989).

  21. 21.

    Silverman, R. A. et al. IV magnesium sulfate in the treatment of acute severe asthma: a multicenter randomized controlled trial. Chest 122, 489–497 (2002).

  22. 22.

    Hirashima, J., Yamana, H., Matsui, H., Fushimi, K. & Yasunaga, H. Effect of intravenous magnesium sulfate on mortality in patients with severe acute asthma. Respirology 21, 668–673 (2016).

  23. 23.

    Hossein, S. et al. The effect of nebulized magnesium sulfate in the treatment of moderate to severe asthma attacks: a randomized clinical trial. Am. J. Emerg. Med. 34, 883–886 (2016).

  24. 24.

    Griffiths, B. & Kew, K. M. Intravenous magnesium sulfate for treating children with acute asthma in the emergency department. Cochrane Database Syst. Rev. 4, CD011050 (2016).

  25. 25.

    Castro-Rodriguez, J. A., Gustavo, J. R. & Carlos, E. R.-M. Principal findings of systematic reviews of acute asthma treatment in childhood. J. Asthma 52, 1038–1045 (2015).

  26. 26.

    Alansari, K. et al. Nebulized magnesium for moderate and severe pediatric asthma: a randomized trial. Pediatr. Pulmonol. 50, 1191–1199 (2015).

  27. 27.

    Singhi, S., Grover, S., Bansal, A. & Chopra, K. Randomised comparison of intravenous magnesium sulphate, terbutaline and aminophylline for children with acute severe asthma. Acta Paediatr. 103, 1301–1306 (2014).

  28. 28.

    Shan, Z. et al. Intravenous and nebulized magnesium sulfate for treating acute asthma in adults and children: a systematic review and meta-analysis. Respir. Med. 107, 321–330 (2013).

  29. 29.

    Noppen, M., Vanmaele, L., Impens, N. & Schandevyl, W. Bronchodilating effect of intravenous magnesium sulfate in acute severe bronchial asthma. Chest 97, 373–376 (1990).

  30. 30.

    Ciarallo, L., Sauer, A. H. & Shannon, M. W. Intravenous magnesium therapy for moderate to severe pediatric asthma: results of a randomized, placebo-controlled trial. J. Pediatr. 129, 809–814 (1996).

  31. 31.

    Song, W. J. & Chang, Y. S. Magnesium sulfate for acute asthma in adults: a systematic literature review. Asia Pac. Allergy 2, 76–85 (2012).

  32. 32.

    Fogarty, A. et al. Oral magnesium and vitamin C supplements in asthma: a parallel group randomized placebo-controlled trial. Clin. Exp. Allergy. 33, 1355–1359 (2003).

  33. 33.

    Hill, J., Micklewright, A., Lewis, S. & Britton, J. Investigation of the effect of short-term change in dietary magnesium intake in asthma. Eur. Respir. J. 10, 2225–2229 (1997).

  34. 34.

    Gontijo-Amaral, C., Ribeiro, M. A., Gontijo, L. S., Condino-Neto, A. & Ribeiro, J. D. Oral magnesium supplementation in asthmatic children: a double-blind randomized placebo-controlled trial. Eur. J. Clin. Nutr. 61, 54–60 (2007).

  35. 35.

    Fogarty, A. et al. Corticosteroid sparing effects of vitamin C and magnesium in asthma: a randomised trial. Respir. Med. 100, 174–179 (2006).

  36. 36.

    Kazaks, A. G., Uriu-Adams, J. Y., Albertson, T. E., Shenoy, S. F. & Stern, J. S. Effect of oral magnesium supplementation on measures of airway resistance and subjective assessment of asthma control and quality of life in men and women with mild to moderate asthma: a randomized placebo controlled trial. J. Asthma 47, 83–92 (2010).

  37. 37.

    Al-Moamary, M. S. et al. The Saudi initiative for asthma - 2016 update: guidelines for the diagnosis and management of asthma in adults and children. Ann. Thorac. Med 11, 3–42 (2016).

  38. 38.

    Higgins, J. P. T., G. S. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 [updated March 2011]. The Cochrane Collaboration. (2011).

  39. 39.

    Rowe, B. H. et al. Magnesium sulfate for treating exacerbations of acute asthma in the emergency department. Cochrane Database of Syst. Rev. (2), CD001490 (2000).

  40. 40.

    Gallegos-Solorzano, M. C., Rogelio, P.-P. & Hernandez-Zenteno, R. J. Usefulness of inhaled magnesium sulfate in the coadjuvant management of severe asthma crisis in an emergency department. Pulm. Pharmacol. Ther. 23, 432–437 (2010).

  41. 41.

    Bernstein, W. K. et al. Lack of effectiveness of magnesium in chronic stable asthma. A prospective, randomized, double-blind, placebo-controlled, crossover trial in normal subjects and in patients with chronic stable asthma. Arch. Intern. Med. 155, 271–276 (1995).

  42. 42.

    Dahl, R. Daily Magnesium Supplement with Mablet for Steroid-resistant, Severe Asthmatics (University of Aarhus, Aarhus, Denmark, 2013).

  43. 43.

    Beckstrand, R. L. Beneficial effects of magnesium supplementation. J. Evid. Based Complement. Altern. Med. 16, 181–189 (2011).

  44. 44.

    Bede, O., Suranyi, A., Pinter, K., Szlavik, M. & Gyurkovits, K. Urinary magnesium excretion in asthmatic children receiving magnesium supplementation: a randomized, placebo-controlled, double-blind study. Magnes. Res. 16, 262–270 (2003).

  45. 45.

    Petrov, V. I., Shishimorov, I. N., Perminov, A. A. & Nefedov, I. V. Influence of magnesium deficiency correction on the effectiveness of bronchial asthma pharmacotherapy in children. Eksp. Klin. Farmakol. 77, 23–27 (2014).

  46. 46.

    Bede, O. et al. Effects of magnesium supplementation on the glutathione redox system in atopic asthmatic children. Inflamm. Res. 57, 279–286 (2008).

  47. 47.

    Fathi, N., Hosseini, S., Tavakkol, H., Khodadady, A. & Tabesh, H. Effect of oral magnesium citrate supplement on lung function and magnesium level in patients with asthma. J. Mazandaran Univ. Med. Sci. 24, 44–51 (2014).

  48. 48.

    Moher D., Liberati A., Tetzlaff J., Altman D. G., & ThePRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann. Intern. Med. 151, 264–269, W64 (2009).

  49. 49.

    Rowe, B., Bretzlaff, J., Bourdon, C., Bota, G., & Camargo, C. Magnesium sulfate is effective for severe acute asthma treated in the emergency department. West J. Med. 172, 96 (2000).

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Acknowledgements

We would like to express our gratitude to Mr.Muhammed Najeeb Vattamannathodi librarian for his assistance in the comprehensive search.

Author information

Affiliations

  1. Family Medicine Residency Program, King Abdulaziz Medical City, National Guard Health Affairs, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

    • Faisal Abuabat
    •  & Abdulaziz AlAlwan
  2. Department of Medical Education, King Saud bin Abdulaziz University for Health Sciences, King Abdullah International Medical Research Center, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh, Saudi Arabia

    • Emad Masuadi
  3. Evidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA

    • Mohammad Hassan Murad
  4. King Saud bin Abdulaziz University for Health Sciences, King Adulaziz Medical City, National Guard Health Affairs, King Abdullah International Medical Research Center, Riyadh, 11665, Saudi Arabia

    • Hamdan Al Jahdali
  5. King Saud bin Abdul-Aziz University for Health Sciences; National & Gulf Center for Evidence Based Health Practice, King Abdullah International Medical Research Center, Family Medicine & Primary Healthcare Department, King Abdul-Aziz Medical City, Ministry of National Guard – Health Affairs, Riyadh, Saudi Arabia

    • Mazen Saleh Ferwana

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Contributions

Research idea by F.A., comprehensive search by M.N.V., Abstraction, selections articles and ROB by F.A. and A.A. Any conflict in each step M.S.F., analysis by E.M. and M.H.M. Writing the manuscript F.A., A.A., M.S.F. GRADE summary by M.S.F. Critical review and editing H.J. and M.H.M.

Competing interests

The authors declare no competing interests.

Corresponding author

Correspondence to Mazen Saleh Ferwana.

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https://doi.org/10.1038/s41533-019-0116-z