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Efficacy of glucocorticoids for the treatment of macrolide refractory mycoplasma pneumonia in children: meta-analysis of randomized controlled trials

BMC Pulmonary Medicine volume 19, Article number: 251 (2019) Cite this article

Abstract

Background

Mycoplasma pneumoniae is one of the most common pathogens causing community acquired pneumonia in children. Although the rate of macrolide-refractory Mycoplasma pneumoniae (MRMP) has increased, systemic glucocorticoids as a treatment option has not been validated yet. The purpose of this study was to assess the efficacy of glucocorticoids add-on in the treatment of MRMP in children through systematic review and meta-analysis.

Methods

Data sources

A systematic literature search was conducted using ten electronic bibliographic databases including English, Korean, Chinese and Japanese languages, up to March 8, 2018.

Study selection

The study was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist and selected randomized control trials which compared the efficacy of glucocorticoids add-on to macrolide in the treatment of MRMP in children.

Data extraction

Two independent reviewers extracted: primary outcomes as hospital days, fever duration, and change in C-reactive protein (CRP) and main analysis was performed through meta-analysis with random effects model.

Results

Twenty-four unique randomized controlled trials met the inclusion criteria. The mean length of hospital stay in glucocorticoids treatment group was significantly shorter than that in conventional macrolide-treatment group (Weighted mean difference (WMD) = − 4.03 days). The mean length of fever duration was significantly shorter in the glucocorticoid treatment group in comparison with the conventional treatment group (WMD = -3.32 days). Level of CRP after treatment was significantly lower in the glucocorticoid treatment group than that in the conventional treatment group (WMD = -16.03). Sensitivity analysis and subgroup analysis showed no significant improvement in heterogeneity. As limitations of the study, most of the studies included were from a single country and we were unable to control for heterogeneity across interventions, lack of standardized measures, and different time points of assessments across studies.

Conclusions

Glucocorticoid add-on treatment for MRMP can significantly shorten the duration of fever and hospital stay and decrease the level of CRP. These results should be confirmed by adequately powered studies in the future.

Peer Review reports

Background

Mycoplasma pneumoniae (M. pneumoniae) is one of the major pathogens causing community acquired pneumonia and bronchitis in children. Treatment of M. pneumoniae-related respiratory infection is based on symptomatic treatment with antibiotics. Macrolides have been used as first line treatment. However, macrolide-refractory M. pneumoniae (MRMP) strains are increasing abruptly, particularly in East Asian countries including Korea, Japan, and China [1,2,3].

Most patients with MRMP do not show improvement of fever when they are treated with macrolides. Some may develop refractory or severe clinical course that requires additional treatment. Treatment for MRMP includes tetracyclines, fluoroquinolones, and systemic glucocorticoids [4].

Secondary antibiotics such as tetracyclines and fluoroquinolones are considered as effective alternatives in the treatment of MRMP. However, they are of limited use due to safety-concerns of teeth discoloration and musculoskeletal toxicity, particularly in children. Glucocorticoids can be also considered as alternative treatment options due to two reason. First, the pathogenesis of M. pneumoniae infection is associated with amplified host immune response and virulence of M. pneumoniae [5]. Second, adverse effects of glucocorticoids have been well established. Further risk is not likely to be added in the treatment of MRMP. However, previous studies on the effect of glucocorticoids have shown conflicting results [6,7,8].

The objective of this study was to assess the efficacy of glucocorticoids for treatment of MRMP in children through systematic review and meta-analysis.

Methods

Systematic Review and Meta-Analysis Protocols (PRISMA-P) 2015 were used for this systematic review and meta-analysis [9]. The Population-Intervention-Comparison-Outcome (PICO) question used for our search strategy was: “Does use of glucocorticoids help improve the outcome of MRMP in children?”

Search strategy

We performed a systematic search utilizing a protocol designed by two independent medical librarians (D.W.S. and M.L) specifically for this study with 10 electronic databases: PubMed, EMBASE, Cochrane Library, and Core journal (Korean, Japanese, and Chinese Journal) Full-text Database. The search encompassed articles published from January, 1990 to March 8, 2018. We used search terms listed in Additional file 1 to search PubMed, Cochrane, EMBASE, and database of core countries. We imposed no language or publication restrictions.

The first screening was executed by two independent reviewers (H.S.K. and I.S.S.) who evaluated the titles and abstracts obtained from the search. Records were managed using Endnote (version X8; Clarivate Analytics, Philadelphia, PA, USA). From this initial screening, articles that did not focus on glucocorticoid use in MRMP and review articles were immediately excluded. After initial exclusion process, full texts of the remaining articles were reviewed independently by two authors (H.S.K. and I.S.S.) to determine whether any articles met the predetermined eligibility criteria described in the next section. Disagreements between the two reviewers regarding the inclusion or exclusion of particular studies were settled by consultation with a third reviewer (Y.J.L.).

Eligibility

The following inclusion criteria were applied: (1) randomized control trial (RCT) which compare the efficacy of glucocorticoids add-on to macrolide alone in children with MRMP, (2) MRMP which was diagnosed with serology or polymerase chain reaction, and that refractories were defined clinically, (3) only included children < 18 years of age, and (4) outcome measures with hospital days, fever duration, and level of C-reactive protein (CRP) change. Review articles, published abstracts without full-text publications, and case-study reports with 10 participants or less were excluded. Our search strategy included non-English articles in our initial search results. Non-English articles were then translated and included for evaluation.

Study selection

Two reviewers (H.S.K. and I.S.S.) independently screened titles and abstracts of the studies identified in our systematic search. Studies focusing on MRMP were included after review of abstracts. Full texts from included studies were reviewed to evaluate for eligibility. Reference lists of selected studies and previous reviews were also examined to determine any relevant publications overlooked by the electronic search. Disagreements between the two reviewers in the selection of particular studies were settled after discussion with a third reviewer (Y.J.L.).

Risk of bias assessment

Cochrane Collaboration Risk of Bias Tool was used by the two reviewers (H.S.K. and I.S.S.) who independently evaluated the risk of bias in included studies [10]. Risk of bias was determined as hi, low or unclear by evaluating random sequence generation, blinding of participants and personnel, incomplete outcome data, and selective reporting. Disagreements between the two reviewers regarding the risk of bias assessment of particular studies were settled after discussion with a third reviewer (Y.J.L.).

Data extraction

Two reviewers (H.S.K. and I.S.S.) used a structured form to extract data from each eligible study. Data extracted from each study could be characterized as characteristics of the sample, intervention details, and measurement of outcomes. Disagreements between the two reviewers regarding the data extraction of particular studies were settled by consultation with a third reviewer (Y.J.L.). Primary outcomes of the current study were hospital days, fever duration, and change in CRP.

Statistical analysis

The estimated mean effect of glucocorticoid add-on treatment on hospital days, fever duration, and change in C-reactive protein (CRP) and the associated 95% confidence intervals (CIs) were extracted or calculated for the 24 studies included in the meta-analysis with Review Manager 5.3 (The Cochrane Collaboration, London, United Kingdom). Random-effects model was used for studies included in the analysis.

Heterogeneity was calculated using I2 statistic. The I2 statistic threshold should always be interpreted with care. A rough estimate of 25% denotes low heterogeneity while 50% denotes moderate heterogeneity, and 75% denotes high heterogeneity [11]. We conducted sensitivity analyses when heterogeneity was noted. This was performed by removing a study from the analysis to determine changes in I2 values and assess which studies play a significant role resulting in heterogeneity [11]. To assess the risk of publication bias, we used funnel plots for visual inspection, and Egger test and trim-and-fill method were performed for statistical identifying. All statistical analyses were performed using R (version 3·3·3) and Review Manager 5.3.

Results

Systematic literature search results

A total of 1829 citations were identified initially. Of these, 1773 studies were discarded after reviewing titles and abstracts, leaving 56 articles for full text review (Fig. 1). A total of 32 studies were excluded after full text review due to no proper subject, inadequate study protocol, review article, or no relevant outcome. A total of 24 studies were included in our systematic review and meta-analysis [12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35]. All studies were RCTs. (Additional file 1 for search strategies for database, Additional file 2 for PRISMA checklist).

Fig. 1
figure 1

Preferred Reporting Items for Systematic Reviews and Meta-Analyses flowchart

Full size image

Sample characteristics

Participants of studies enrolled in our meta-analysis was a total of 2365 patients. All these studies examined fever duration. Fifteen studies examined hospital days while 14 studies examined CRP level after treatment (Table 1).

Table 1 Characteristics of studies included in the meta-analysis
Full size table

Fever duration

The mean length of total duration of fever was significantly shorter in the glucocorticoid add-on group than that in the conventional treatment group (weighted mean difference, WMD = − 3.32, 95%CI: − 4.16 – -2.48, Z = 7.72, P < 0.00001). However, there was a high between-study heterogeneity of this effect (I2 = 98%; Fig. 2).

Fig. 2
figure 2

Comparison of fever duration between glucocorticoid therapy and macrolide therapy

Full size image

Hospital days

The mean length of hospital stays in the glucocorticoid add-on treatment group was significantly shorter than that in the conventional treatment group (WMD = − 4.03, 95% CI: − 4.89 - -3.18, Z = 9.26, P < 0.00001). However, there was a high between-study heterogeneity of this effect (I2 = 90%; Fig. 3).

Fig. 3
figure 3

Comparison of hospital days between glucocorticoid therapy and macrolide therapy

Full size image

Reduction of CRP level after treatment

The level of CRP after treatment was significantly lower in the glucocorticoid add-on treatment group than that in the conventional treatment group (WMD = − 16.03, 95%CI: − 22.56 – -9.50, Z = 4.81, P < 0.00001). However, there was a high between-study heterogeneity of this effect (I2 = 100%; Fig. 4).

Fig. 4
figure 4

Comparison of C-reactive protein level after treatment between glucocorticoid therapy and macrolide therapy

Full size image

Sensitivity analyses was performed because of high level of heterogeneity. We removed a study from the analysis to determine which studies contributed most significantly to the heterogeneity by determining the changes in I2 values. We found that I2 values of fever duration, hospital days, and CRP level did not change.

Subgroup analysis

Use of glucocorticoids included the use of any type of glucocorticoids (e.g., methylprednisolone, dexamethasone, and prednisolone). The use of different types of glucocorticoids was different across studies. This might have contributed to the heterogeneity in the overall use of glucocorticoids. Thus, we stratified the meta-analysis by subgroup analyses. In subgroup meta-analysis for use of methylprednisolone compared with the use of other glucocorticoids for the length of hospital stay, the use of other steroids did not show any significant subgroup differences (Figs. 5, 6 and 7).

Fig. 5
figure 5

Forest plot for hospital days in subgroup analysis with use of methylprednisolone and other steroids

Full size image
Fig. 6
figure 6

Forest plot for fever duration in subgroup analysis with use of methylprednisolone and other steroids

Full size image
Fig. 7
figure 7

Forest plot for C-reactive protein level in subgroup analysis with use of methylprednisolone and other steroids

Full size image

Publication bias

All funnel plots were symmetric, indicating an absence of significant publication bias within these studies except for CRP outcome. Egger test results were − 1.73 (P = 0.09) for fever duration, 0.59 (P = 0.56) for hospital days, and − 3.19 (P = 0.008) for CRP. Trim-and-fill method for adjusting publication bias on CRP outcome was performed. The mean difference changed from – 3.27 (P = 0.35) to − 16.03 (P < 0.001). These results indicated that there was substantial evidence of publication bias in CRP outcome (Fig. 8).

Fig. 8
figure 8

Funnel plots showing WMDs and 95% CIs for the efficacy of glucocorticoid therapy on the length of hospital stays (a), fever duration (b), and level of change of C reactive protein (c). Tests of asymmetry showed no significant deviation from the symmetry assumption (a, P = 0.56; b, P = 0.06). However, significant asymmetry was found in the level of change of CRP (c, P = 0.008). Trim-and-fill method for adjusting publication bias was used. Results showed substantial evidence of publication bias in CRP outcome (d)

Full size image

Discussion

This systematic review and meta-analysis identified and assessed RCTs on the use of glucocorticoids in children with MRMP. We specifically investigated effects of glucocorticoids on fever duration, length of hospital stay, and CRP level after treatment in comparison with conventional macrolide therapy. Results revealed positive effects of glucocorticoid treatment on all outcome measures.

M. pneumoniae is a common pathogen causing community acquired pneumonia. The clinical course of M. pneumoniae infection is diverse, ranging from self-limiting to severe pneumonia with extra-pulmonary complications [36]. Macrolide is considered the first-line treatment for M. pneumoniae infection [37]. In adults, one study reported that prednisone treatment for 7 days in patients with community-acquired pneumonia admitted to hospital can shorten time to clinical stability without increase in complications [38]. However, another study reported that glucocorticoid use did not show any benefits in children [8]. Pulmonary injury associated with severe mycoplasma pneumonia could be caused by host immune response rather than by direct microbial damage [39, 40]. Overly active cell-mediated immunity and cytokine responses play a significant role in MRMP [41]. Severe M. pneumoniae infections and MRMP show similar laboratory findings with severe acute respiratory syndrome such as increased levels of non-specific markers of inflammation such as serum CRP, lactate dehydrogenase, and D-dimer [42]. Since MRMP can be considered as an immune-mediated disease, use of immune modulatory therapy could seem rational. For cases with MRMP infection, secondary treatment options are limited due to adverse effects of tetracycline or fluoroquinolones, especially in children [43]. The use of systemic steroids, in addition to antimicrobial therapy, to diminish host immune response in MRMP has been used in children and demonstrated satisfactory effects [7, 8, 14]. Glucocorticoids have shown to improve clinical features and reduce lung injury in children and adults [5, 44, 45]. The use of glucocorticoids in M. pneumoniae infection showed reduced lung histopathologic score by reducing cytokines and decreasing inflammatory response ultimately leading to lower mortality [5, 44, 45]. Therefore, glucocorticoids have been considered suitable as adjunctive therapy to macrolide therapy. Although previous studies have reported the efficacy of glucocorticoids in the treatment of severe MRMP, treatment protocols varied from oral prednisolone of 1 mg/kg/day to intravenous methylprednisolone 30 mg/kg/day for 3 days [7, 17]. These variable treatment protocols are due to the lack of guidelines for glucocorticoids treatment in severe MRMP to date [7, 46].

In our study, the mean length of total duration of fever, mean length of hospital stay, and level of CRP after treatment in the glucocorticoid treatment group were significantly shorter or lower than that those in the conventional treatment group. However, heterogeneity in all outcome measures was high and sensitivity analysis resulted in no significant difference. Subgroup analysis showed no significant decrease in heterogeneity. In spite of high level of heterogeneity, all studies reported favorable outcomes of hospital stays and fever duration after the use of glucocorticoids in MRMP. For CRP level, only one study reported unfavorable result after the use of glucocorticoids in MRMP. Therefore, we could consider that the use of glucocorticoids has significantly favorable effects on outcomes of MRMP.

The strength of this review is that it summarized the current evidence on the efficacy of glucocorticoids from RCT. Conducting RCTs offers the potential to produce the most definitive evidence to confirm or refute whether glucocorticoids can help improve outcomes of MRMP.

This review has some limitations. Firstly, almost all studies included in this review had at least one methodological flaw. Secondly, publication bias was significant for change in CRP level. It might be due to small sample sizes in most studies and the fact that most studies were conducted in a single country. As a result, the robustness of these outcomes should be explored with future studies. Thirdly, most of the studies included were from a single country. Lastly, we could not evaluate other outcomes such as improvement in chest x-ray infiltration or other symptoms such as cough because these data were not available in each study.

Despite these limitations, with our review and meta-analysis, this is the first study to date to synthesize the efficacy of glucocorticoids in MRMP.

Conclusions

In conclusion, even though some studies have reported the efficacy and effectiveness of systemic glucocorticoids in the treatment of MRMP [12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35], this is the first systematic review and meta-analysis to investigate the effectiveness of glucocorticoids in MRMP. We found that the use of glucocorticoids could shorten hospital days, shorten fever duration, and lower CRP levels after treatment.

However, these results should be interpreted cautiously, and future studies should also assess other outcomes to clarify the effect of glucocorticoids in MRMP.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CI:

Confidence interval

CRP:

C-reactive protein

M. pneumoniae :

Mycoplasma pneumoniae

MRMP:

Macrolide-refractory M. pneumoniae

PICO:

Population-Intervention-Comparison-Outcome

PRISMA-P:

Systematic Review and Meta-Analysis Protocols

RCT:

Randomized control trial

WMD:

weighted mean difference

References

  1. Lee E, Cho HJ, Hong SJ, Lee J, Sung H, Yu J. Prevalence and clinical manifestations of macrolide resistant mycoplasma pneumoniae pneumonia in Korean children. Korean J Pediatr. 2017;60:151–7.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Meyer Sauteur PM, Unger WW, Nadal D, Berger C, Vink C, van Rossum AM. Infection with and carriage of mycoplasma pneumoniae in children. Front Microbiol. 2016;7:329.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Yamazaki T, Kenri T. Epidemiology of mycoplasma pneumoniae infections in Japan and therapeutic strategies for macrolide-resistant M pneumoniae. Front Microbiol. 2016;7:693.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Yang HJ, Song DJ, Shim JY. Mechanism of resistance acquisition and treatment of macrolide-resistant mycoplasma pneumoniae pneumonia in children. Korean J Pediatr. 2017;60:167–74.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Youn YS, Lee KY. Mycoplasma pneumoniae pneumonia in children. Korean J Pediatr. 2012;55:42–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Meijvis SC, Hardeman H, Remmelts HH, Heijligenberg R, Rijkers GT, van Velzen-Blad H, et al. Dexamethasone and length of hospital stay in patients with community-acquired pneumonia: a randomised, double-blind, placebo-controlled trial. Lancet. 2011;377:2023–30.

    Article  CAS  PubMed  Google Scholar 

  7. You SY, Jwa HJ, Yang EA, Kil HR, Lee JH. Effects of methylprednisolone pulse therapy on refractory mycoplasma pneumoniae pneumonia in children. Allergy Asthma Immunol Res. 2014;6:22–6.

    Article  CAS  PubMed  Google Scholar 

  8. Okubo Y, Michihata N, Morisaki N, Uda K, Miyairi I, Ogawa Y, et al. Recent trends in practice patterns and impact of corticosteroid use on pediatric mycoplasma pneumoniae-related respiratory infections. Respir Investig. 2018;56:158–65.

    Article  PubMed  Google Scholar 

  9. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6:e1000097.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ. 2011;343:d5928.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327:557–60.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Shao X-L, Liu S-M, Lou W-Y, Zhu G-Z. Methylprednisolone in adjunctive treatment of refractory mycoplasma pneumonia. Chin Gen Pract. 2011;14:186–7.

    CAS  Google Scholar 

  13. Xu-yun T, Hong-yu Q. Clinical effect and safety of small-dose methylprednisolone triple therapy on refractory lobar mycoplasma pneumoniae pneumonia in children. Pract J Card Cerebral Pneumal Vasc Dis. 2015;23:74–6.

    Google Scholar 

  14. Ling L. The effect of low-dose methylprednisolone in the treatment of children with refractory mycoplasma pneumoniae pneumonia. J Pediatr Pharm. 2015;21:18–21.

    Google Scholar 

  15. Ming L, Ye-qing H. Small doses of methyl prednisolone sodium succinate and prednisone combined treatment the curative effect of children refractory mycoplasma pneumoniae pneumonia. Medical Innovation of China. 2015;12:10–3.

    Google Scholar 

  16. Jianqin L. Evaluation clinical curative effect of methylprednisolone in treatment of 42 case children with refractory mycoplasma pneumonia. China Contin Med Educ. 2015;7:148–9.

    Google Scholar 

  17. Yan L, Wei L. Effect of low-dose glucocorticoid in the treatment of children with refractory mycoplasma pneumonia. China Mod Med. 2015;22:82–4.

    Google Scholar 

  18. Xuwei F. Methylprednisolone combined with azithromycin in treatment of children with refractory mycoplasma pneumonia (RMPP) efficacy and safety. Prog Biomed Eng. 2015;36:246–8.

    Google Scholar 

  19. Lijun Y. Clinical curative effect analysis of methyl prednisolone auxiliary treatment of refractory mycoplasma pneumonia. China Contin Med Educ. 2015;7:142–3.

    Google Scholar 

  20. Ming-xing R, Guochang X, Linna S, Huan X, Yuejuan S, Li C. Efficacy and safety of methylprednisolone combined with azithromycin on refractory mycoplasma pneumonia in children. Chin Gen Pract. 2015;18:588–91.

    Google Scholar 

  21. Zhang X. Clinical study of glucocorticoid in the treatment of refractory mycoplasma pneumoniae pneumonia. J Clin Pulm Med. 2015;20:1472–5.

    Google Scholar 

  22. Qing L, Hu L, Ling Z, Yajun H. Effect of therapy with glucocorticoids in children with refractory mycoplasma pneumoniae pneumonia. J Pediatr Pharm. 2016;22:25–7.

    Google Scholar 

  23. Jianjun W. Study on the effect of azithromycin and methylprednisolone in the treatment of children with refractory mycoplasma pneumonia. Chin Community Dr. 2016;32:31–3.

    Google Scholar 

  24. Hao W, Jingrong Y, Jinglin O. Clinical effect of methylprednisolone combined with azithromycin in the treatment of children with RMPP. Med Sci J Cent South China. 2016;44:442–6.

    Google Scholar 

  25. Xuan Z, Juanjuan Z, Huichao J, Yang Z. Observation on efficacy of methylprednisolone in treatment of children with refractory mycoplasma pneumoniae. Eval Anal Drug-Use Hosp China. 2016;16:1351–3.

    Google Scholar 

  26. Xiaoqiang F, Chunyan G, Xiaohong H, Shiping L. Clinical analysis of the effects of methylprednisolone on the treatment of refractory mycoplasma pneumoniae pneumonia in children. Transl Med J. 2016;5:92–5.

    Google Scholar 

  27. Hai-yan Q. To observe the curative effect of small dose of glucocorticoid combined with Pulmicort inhalation in the treatment of refractory mycoplasma pneumonia. Contemp Med. 2017;23:37–9.

    Google Scholar 

  28. Chaoyu J, Rongfang M. Hormone refractory mycoplasma pneumonia lavage cytokines. Shaanxi Med J. 2017;46:22–4.

    Google Scholar 

  29. Xiaoyun L, Jinping F, Qiaoziang X. Intravenous methylprednisolone combined with azithromycin in treatment of children with refractory mycoplasma pneumonia and influence on relevant laboratory parameters. J Pediatr Pharm. 2017;23:14–6.

    Google Scholar 

  30. Chun-yan L, Ling-zhi C. Clinical effect of methylprednisolone pluse therapy in treatment of refractory mycoplasma pneumoniae in children. Syst Med. 2017;2:70–87.

    Google Scholar 

  31. Jia-li X, Ying W, Peng C. Clinical effect of methylprednisolone combined with azithromycin sequential therapy in treating children with mycoplasma pneumonia and the impact on serum levels CRP and sTREM-1. Pract J Card Cereb Pneumal Vasc Dis. 2017;25:155–7.

    Google Scholar 

  32. Yu J, Wang X, Wu C. Clinical analysis of methylprednisolone in the treatment of children refractory mycoplasma pneumoniae pneumonia. China Pract Med. 2017;12:7–9.

    Article  CAS  Google Scholar 

  33. Wu X. Analysis of the effect of combined use of methylprednisolone and azithromycin on refractory mycoplasma pneumonia in children. Contemp Med Symp. 2017;15:133–4.

    Google Scholar 

  34. Shuqing Z, Yanrong Z. Effect of small doses of methylprednisolone treatment of children with refractory mycoplasma. Med Recapitulate. 2017;23:798–801.

    Google Scholar 

  35. Shan LS, Liu X, Kang XY, Wang F, Han XH, Shang YX. Effects of methylprednisolone or immunoglobulin when added to standard treatment with intravenous azithromycin for refractory mycoplasma pneumoniae pneumonia in children. World J Pediatr. 2017;13:321–7.

    Article  CAS  PubMed  Google Scholar 

  36. Defilippi A, Silvestri M, Tacchella A, Giacchino R, Melioli G, Di Marco E, et al. Epidemiology and clinical features of mycoplasma pneumoniae infection in children. Respir Med. 2008;102:1762–8.

    Article  PubMed  Google Scholar 

  37. Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, et al. Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44(Suppl 2):S27–72.

    Article  CAS  PubMed  Google Scholar 

  38. Blum CA, Nigro N, Briel M, Schuetz P, Ullmer E, Suter-Widmer I, et al. Adjunct prednisone therapy for patients with community-acquired pneumonia: a multicentre, double-blind, randomised, placebo-controlled trial. Lancet. 2015;385:1511–8.

    Article  CAS  PubMed  Google Scholar 

  39. Waites KB, Talkington DF. Mycoplasma pneumoniae and its role as a human pathogen. Clin Microbiol Rev. 2004;17:697–728.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Tanaka H, Narita M, Teramoto S, Saikai T, Oashi K, Igarashi T, et al. Role of interleukin-18 and T-helper type 1 cytokines in the development of mycoplasma pneumoniae pneumonia in adults. Chest. 2002;121:1493–7.

    Article  CAS  PubMed  Google Scholar 

  41. Shimizu T, Kida Y, Kuwano K. Cytoadherence-dependent induction of inflammatory responses by mycoplasma pneumoniae. Immunology. 2011;133:51–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Wang JY, Lee CH, Cheng SL, Chang HT, Hsu YL, Wang HC, et al. Comparison of the clinical manifestations of severe acute respiratory syndrome and mycoplasma pneumoniae pneumonia. J Formos Med Assoc. 2004;103:894–9.

    PubMed  Google Scholar 

  43. Principi N, Esposito S. Macrolide-resistant mycoplasma pneumoniae: its role in respiratory infection. J Antimicrob Chemother. 2013;68:506–11.

    Article  CAS  PubMed  Google Scholar 

  44. Tamura A, Matsubara K, Tanaka T, Nigami H, Yura K, Fukaya T. Methylprednisolone pulse therapy for refractory mycoplasma pneumoniae pneumonia in children. J Inf Secur. 2008;57:223–8.

    Google Scholar 

  45. Tagliabue C, Salvatore CM, Techasaensiri C, Mejias A, Torres JP, Katz K, et al. The impact of steroids given with macrolide therapy on experimental mycoplasma pneumoniae respiratory infection. J Infect Dis. 2008;198:1180–8.

    Article  CAS  PubMed  Google Scholar 

  46. Luo Z, Luo J, Liu E, Xu X, Liu Y, Zeng F, et al. Effects of prednisolone on refractory mycoplasma pneumoniae pneumonia in children. Pediatr Pulmonol. 2014;49:377–80.

    Article  PubMed  Google Scholar 

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Acknowledgements

We thank Misoon Lim and Dong Won Shin for providing assistance and support for the systematic search.

Funding

This research was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HI16C2300). It was also supported by the Soonchunhyang University Research Fund. The funding source had no role in study design, data collection, data analysis, data interpretation, or writing of the report.

Author information

Author notes

  1. Hwan Soo Kim and In Suk Sol are co-first authors.

Authors and Affiliations

  1. Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, South Korea

    Hwan Soo Kim & Hyun Hee Kim

  2. Department of Pediatrics, Hallym University Chuncheon Sacred Heart Hospital, Chuncheon, Korea

    In Suk Sol

  3. Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea

    In Suk Sol

  4. Interdisciplinary Program of Bioinformatics, Seoul National University, Seoul, South Korea

    Donghe Li

  5. Division of Health Technology Assessment Research, National Evidence-based Healthcare Collaborating Agency (NECA), Seoul, South Korea

    Miyoung Choi

  6. Department of Pediatrics, Seoul National University Hospital, Seoul, Korea

    Yun Jung Choi

  7. Department of Pediatrics, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, South Korea

    Kyung Suk Lee

  8. Department of Pediatrics, Dankook University Hospital, Cheonan, South Korea

    Ju Hee Seo

  9. Department of Pediatrics, Hallym University Kangnam Sacred Heart Hospital, Hallym University College of Medicine, 1 Singil-ro, Yeongdeungpo-gu, Seoul, 07441, South Korea

    Yong Ju Lee

  10. Pediatric Allergy and Respiratory Center, Department of Pediatrics, SCH Biomedical Informatics Research Unit, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul, 04401, South Korea

    Hyeon-Jong Yang

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Contributions

Study conception and design: HJY, YJL, HHK. Acquisition of data: HJY, YJL, DHL, MC, JHS. Analysis and interpretation of data: HSK, ISS, MC, HJY, YJL. Drafting of manuscript: HSK, DHL, YJC, KSL, JHS. Critical revision: HSK, ISS, KSL, HHK. All authors read and approved the final manuscript.

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Correspondence to Yong Ju Lee or Hyeon-Jong Yang.

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Hyeon-Jong Yang and Yong Ju Lee are co-corresponding authors.

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Kim, H.S., Sol, I.S., Li, D. et al. Efficacy of glucocorticoids for the treatment of macrolide refractory mycoplasma pneumonia in children: meta-analysis of randomized controlled trials. BMC Pulm Med 19, 251 (2019). https://doi.org/10.1186/s12890-019-0990-8

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Keywords

BMC Pulmonary Medicine

ISSN: 1471-2466

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