Journal List > Allergy Asthma Respir Dis > v.5(1) > 1059300

Wy, Min, Kim, Park, Shim, Jung, and Shim: Clinical characteristics of Mycoplasma pneumoniae pneumonia in Korean children during the recent 3 epidemics

Abstract

Purpose

Mycoplasma pneumoniae (MP) is a major cause of community-acquired pneumonia in children. Since 2000, emerging macrolide-resistant MP has been reported. Three epidemics of MP pneumonia have occurred in Korea during the past 10 years: 2006–2007, 2011, and 2015. We investigated the differences in MP pneumonia of each epidemic in terms of clinical, laboratory, and radiologic perspectives.

Methods

We retrospectively analyzed 529 medical records of children (1–18 years of age) who were admitted and diagnosed with MP pneumonia at Kangbuk Samsung Hospital during the past 3 epidemic periods. We compared the clinical, laboratory, and radiologic characteristics of MP pneumonia among individual epidemics and between children younger and older than 6 years of age.

Results

The mean age of the patients was 5.7 years old, which had increased by each epidemic and showed the highest (6.3 years old) in 2015 compared to previous epidemics. Among 3 epidemics, there were no sex differences. The duration of fever after admission and hospitalization, and the percentage of lobar pneumonia and use of systemic steroids increased significantly in 2015 epidemic. Since 2006, the mean levels of erythrocyte sedimentation rate and lactate dehydrogenase had increased and in 2015 it marked the highest. Children older than 6 years showed a higher proportion of lobar pneumonia and pleural effusion as well as longer duration of fever (before and after admission) and hospitalization days than those younger than 6 years.

Conclusion

This study suggests an increasing incidence of refractory MP pneumonia which required a more frequent use of systemic steroids over the past 10 years, and children older than 6 years were found to have more severe pneumonia than those younger than 6 years.

Figures and Tables

Fig. 1

Age distribution of total Mycoplasma pneumoniae pneumonia patients (n=529).

aard-5-8-g001
Fig. 2

Percentage of patients with steroid treatment in each epidemic.

aard-5-8-g002
Table 1

Comparison of demographic data, duration of fever and hospitalization among 3 recent epidemics

aard-5-8-i001
Variable 2007 (n = 84) 2011 (n = 268) 2015 (n = 177) P for trend
Age (yr) 5.2 ± 3.0 5.4 ± 3.1 6.3 ± 3.2*,† < 0.01
Male sex 34 (40.5) 138 (51.5) 85 (48.0) 0.68
Fever duration before admission (day) 5.7 ± 3.6 5.6 ± 3.3 4.8 ± 2.7* 0.02
Fever duration after admission (day) 1.8 ± 2.3 2.3 ± 2.3 2.9 ± 2.5* < 0.01
Fever duration (day) 7.5 ± 4.3 7.9 ± 3.9 7.7 ± 3.3 0.89
Duration of hospitalization (day) 7.7 ± 3.5 5.6 ± 2.5* 6.8 ± 2.3*,† 0.44

Values are presented as mean±standard deviation or number (%).

*P<0.05, compared to 2007. P<0.05, compared to 2011. Multiple linear regression analysis adjusted for age.

Table 2

Comparison of the type of pneumonia and complications among 3 recent epidemics

aard-5-8-i002
Pneumonia and complication 2007 (n = 84) 2011 (n = 268) 2015 (n = 177) P-value
Type of pneumonia
 Bronchopneumonia 32 (38.1) 111 (41.4) 47 (26.6) 0.01
 Lobar pneumonia 52 (61.9) 157 (58.6) 130 (73.4)
Effusion 23 (27.4) 24 (9.0)* 8 (4.5)*,† < 0.01
Chest tube 7 (8.3) 5 (1.9)* 2 (1.1)*,† 0.01
Oxygen use 6 (7.1) 10 (3.7) 13 (7.4) 0.19

Values are presented as number (%).

*P<0.05, compared to 2007. P<0.05, compared to 2011.

Table 3

Multiple linear regression analysis of laboratory findings among 3 recent epidemics

aard-5-8-i003
Variable 2007 (n = 84) 2011 (n = 268) 2015 (n = 177) P for trend
Lymphocyte (/mm3) 2,750 ± 1,626 2,638 ± 1,459 2,235 ± 1,240 0.08
White blood cell count (/mm3) 10,300 ± 5,797 9,047 ± 4,366* 8,810 ± 3,554* 0.15
LogTEC (/mm3) 5.15 ± 1.26 4.79 ± 1.18* 4.48 ± 1.30* < 0.01
LogCRP (mg/dL) 0.46 ± 1.31 0.53 ± 0.91 0.68 ± 0.89 0.53
Erythrocyte sedimentation rate (mm/hr) 18.8 ± 9.7 36.1 ± 16.4* 42.0 ± 24.4* < 0.01
Platelet count (× 103/mm3) 365 ± 136 334 ± 123* 283 ± 93* < 0.01
Hemoglobin (g/dL) 12.5 ± 1.0 12.4 ± 0.9 12.3 ± 0.9 0.08
Lactate dehydrogenase (IU/L) 256 ± 75 207 ± 63* 314 ± 70* < 0.01

Values are presented as mean±standard deviation. Adjusted for age and the duration of fever before admission.

LogTEC, logarithmic transformation of blood total eosinophil count; LogCRP, logarithmic transformation of C-reactive protein.

*P<0.05, compared to 2007.

Table 4

Comparison of clinical characteristics by the age of 6 years

aard-5-8-i004
Variable < 6 Years (n = 276) ≥ 6 Years (n = 253) P-value
Age (yr) 3.2 ± 1.3 8.3 ± 2.3 < 0.01
Male sex 138 (50.0) 119 (47.0) 0.49
Type of pneumonia
 Broncho pneumonia 129 (46.7) 61 (24.1) < 0.01
 Lobar pneumonia 147 (53.3) 192 (75.9)
Effusion 19 (6.9) 36 (14.2) 0.01
Oxygen use 13 (4.7) 16 (6.3) 0.42
Fever duration before admission (day) 5.1 ± 3.4 5.8 ± 2.8 0.01
Fever duration after admission (day) 2.0 ± 2.1 2.9 ± 2.6 < 0.01
Fever duration (day) 7.1 ± 3.9 8.6 ± 3.3 < 0.01
Duration of hospitalization (day) 6.1 ± 2.4 6.6 ± 3.0 0.01

Values are presented as mean±standard deviation or number (%).

References

1. Waites KB, Talkington DF. Mycoplasma pneumoniae and its role as a human pathogen. Clin Microbiol Rev. 2004; 17:697–728.
crossref
2. Foy HM, Kenny GE, Cooney MK, Allan ID. Long-term epidemiology of infections with Mycoplasma pneumoniae. J Infect Dis. 1979; 139:681–687.
crossref
3. Hauksdottir GS, Love A, Sigurdardottir V, Jonsson T. Outbreaks of Mycoplasma pneumoniae infections in Iceland 1987 to 1997: a ten and a half years review. Eur J Epidemiol. 1999; 15:95–96.
4. Ito I, Ishida T, Osawa M, Arita M, Hashimoto T, Hongo T, et al. Culturally verified Mycoplasma pneumoniae pneumonia in Japan: a long-term observation from 1979-99. Epidemiol Infect. 2001; 127:365–367.
crossref
5. Lind K, Jensen JS, Clyde WA Jr. A seroepidemiological study of Mycoplasma pneumoniae infections in Denmark over the 50-year period 1946-1995. Eur J Epidemiol. 1997; 13:581–586.
6. Pönkä A. Occurrence of serologically verified Mycoplasma pneumoniae infections in Finland and in Scandinavia in 1970-1977. Scand J Infect Dis. 1980; 12:27–31.
crossref
7. Rastawicki W, Kałuzewski S, Jagielski M. Occurrence of serologically verified Mycoplasma pneumoniae infections in Poland in 1970-1995. Eur J Epidemiol. 1998; 14:37–40.
8. Ma YJ, Wang SM, Cho YH, Shen CF, Liu CC, Chi H, et al. Clinical and epidemiological characteristics in children with community-acquired mycoplasma pneumonia in Taiwan: a nationwide surveillance. J Microbiol Immunol Infect. 2015; 48:632–638.
crossref
9. Sztrymf B, Jacobs F, Fichet J, Hamzaoui O, Prat D, Avenel A, et al. Mycoplasma-related pneumonia: a rare cause of acute respiratory distress syndrome (ARDS) and of potential antibiotic resistance. Rev Mal Respir. 2013; 30:77–80.
10. Wang RS, Wang SY, Hsieh KS, Chiou YH, Huang IF, Cheng MF, et al. Necrotizing pneumonitis caused by Mycoplasma pneumoniae in pediatric patients: report of five cases and review of literature. Pediatr Infect Dis J. 2004; 23:564–567.
crossref
11. Shen Y, Zhang J, Hu Y, Shen K. Combination therapy with immune-modulators and moxifloxacin on fulminant macrolide-resistant Mycoplasma pneumoniae infection: a case report. Pediatr Pulmonol. 2013; 48:519–522.
crossref
12. Katsushima Y, Katsushima F, Suzuki Y, Seto J, Mizuta K, Nishimura H, et al. Characteristics of Mycoplasma pneumoniae infection identified on culture in a pediatric clinic. Pediatr Int. 2015; 57:247–252.
crossref
13. Liu Y, Ye X, Zhang H, Xu X, Li W, Zhu D, et al. Antimicrobial susceptibility of Mycoplasma pneumoniae isolates and molecular analysis of macrolide-resistant strains from Shanghai, China. Antimicrob Agents Chemother. 2009; 53:2160–2162.
crossref
14. Xin D, Mi Z, Han X, Qin L, Li J, Wei T, et al. Molecular mechanisms of macrolide resistance in clinical isolates of Mycoplasma pneumoniae from China. Antimicrob Agents Chemother. 2009; 53:2158–2159.
crossref
15. Hong KB, Choi EH, Lee HJ, Lee SY, Cho EY, Choi JH, et al. Macrolide resistance of Mycoplasma pneumoniae, South Korea, 2000-2011. Emerg Infect Dis. 2013; 19:1281–1284.
16. Hsieh YC, Tsao KC, Huang CG, Tong S, Winchell JM, Huang YC, et al. pneumoniae. Pediatr Infect Dis J. 2012; 31:208–209.
17. Lee KY, Lee HS, Hong JH, Lee MH, Lee JS, Burgner D, et al. Role of prednisolone treatment in severe Mycoplasma pneumoniae pneumonia in children. Pediatr Pulmonol. 2006; 41:263–268.
crossref
18. 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; 49:377–380.
crossref
19. Wang M, Wang Y, Yan Y, Zhu C, Huang L, Shao X, et al. Clinical and laboratory profiles of refractory Mycoplasma pneumoniae pneumonia in children. Int J Infect Dis. 2014; 29:18–23.
crossref
20. Eun BW, Kim NH, Choi EH, Lee HJ. Mycoplasma pneumoniae in Korean children: the epidemiology of pneumonia over an 18-year period. J Infect. 2008; 56:326–331.
crossref
21. Kim EK, Youn YS, Rhim JW, Shin MS, Kang JH, Lee KY. Epidemiological comparison of three Mycoplasma pneumoniae pneumonia epidemics in a single hospital over 10 years. Korean J Pediatr. 2015; 58:172–177.
crossref
22. Kim NH, Lee JA, Eun BW, Shin SH, Chung EH, Park KW, et al. Comparison of polymerase chain reaction and the indirect particle agglutination antibody test for the diagnosis of Mycoplasma pneumoniae pneumonia in children during two outbreaks. Pediatr Infect Dis J. 2007; 26:897–903.
crossref
23. Yoo SJ, Oh HJ, Shin BM. Evaluation of four commercial IgG- and IgM-specific enzyme immunoassays for detecting Mycoplasma pneumoniae antibody: comparison with particle agglutination assay. J Korean Med Sci. 2007; 22:795–801.
crossref
24. 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; 102:1762–1768.
crossref
25. Miyashita N, Kawai Y, Inamura N, Tanaka T, Akaike H, Teranishi H, et al. Setting a standard for the initiation of steroid therapy in refractory or severe Mycoplasma pneumoniae pneumonia in adolescents and adults. J Infect Chemother. 2015; 21:153–160.
crossref
26. Zhang Y, Zhou Y, Li S, Yang D, Wu X, Chen Z. The clinical characteristics and predictors of refractory Mycoplasma pneumoniae pneumonia in children. PLoS One. 2016; 11:e0156465.
crossref
27. Kawamata R, Yokoyama K, Sato M, Goto M, Nozaki Y, Takagi T, et al. Utility of serum ferritin and lactate dehydrogenase as surrogate markers for steroid therapy for Mycoplasma pneumoniae pneumonia. J Infect Chemother. 2015; 21:783–789.
crossref
28. Choi SH, Park EY, Jung HL, Shim JW, Kim DS, Park MS, et al. Serum vascular endothelial growth factor in pediatric patients with community-acquired pneumonia and pleural effusion. J Korean Med Sci. 2006; 21:608–613.
crossref
29. Shin JH, Shim JW, Kim DS, Shim JY. TGF-beta effects on airway smooth muscle cell proliferation, VEGF release and signal transduction pathways. Respirology. 2009; 14:347–353.
crossref
30. Yamazaki T, Kenri T. Epidemiology of Mycoplasma pneumoniae infections in Japan and therapeutic strategies for macrolide-resistant M. pneumoniae. Front Microbiol. 2016; 7:693.
crossref
31. Maroushek SR. Principles of antimycobacterial therapy. In : Kliegman RM, Stanton BF, St Geme JW, Schor NF, Behrman RE, editors. Nelson textbook of pediatrics. 20th ed. Philadelphia: Elsevier;2015. p. 1439–1444.
TOOLS
ORCID iDs

Jung Yeon Shim
https://orcid.org/http://orcid.org/0000-0001-9367-2233

Similar articles