Printer Friendly

Mycobacterium bovis BCG-associated Osteomyelitis/Osteitis, Taiwan.

To the Editor: Thirty-eight patients with Mycobacterium bovis BCG-associated osteomyelitis/osteitis, including 8 who were previously reported (1), were identified during Taiwan's vaccine injury compensation program during 1989-2012; a total of 30 (79%) patients applied for compensation during 2009-2012 (Figure). In Taiwan, a laboratory program to differentiate BCG from other species of the M. tuberculosis complex, using a kit for the Tokyo-172 vaccine strain spoligotyping, was established in 2004 (1). Since 2008, the isolated extrapulmonary tuberculosis strains and pathologic specimens collected from children <5 years of age have been sent to the national reference mycobacterial laboratory for BCG detection (2). The detected incidence of BCG osteitis/osteomyelitis increased from 3.68 cases per million vaccinations during 2002-2006 to 30.1 per million during 2008-2012.

Parents or guardians signed written consent forms on behalf of the children when they submitted claims for the vaccine injury compensation program. After consent, children's hospital information was stored in the Taiwan Centers for Disease Control database and used for research.

Of the 38 compensated BCG osteomyelitis/osteitis patients, 18 were boys. According to chart review, no patients had immunodeficiency or other underlying conditions; however, 3 were premature babies (born at 34-36 weeks of gestation). Eighteen (47%) children had received BCG at [less than or equal to] 1 week of age, 12 (32%) at 1-4 weeks, 7 (18%) at 1-2 months, and 1 at >2 months. The average age at inoculation was 16.2 [+ or -] 16.6 days. Symptoms or signs began 3-32 months (average 12.4 [+ or -] 6.1 months) after BCG vaccination; for 68%, symptoms or signs developed 7-18 months after vaccination (online Technical Appendix Figure, http:// wwwnc.cdc.gov/EID/article/21/3/14-0789-Techapp1.pdf). Time from vaccination to onset of symptoms or signs did not differ for the 3 premature infants.

As in previous reports (3,4), extremity bones were more commonly involved than axial bones. For 30 (79%) children, extremity bones were involved: 14 right lower limbs, 7 left lower limbs, 6 left upper limbs, and 3 right upper limbs. The tibia was the most common site (9 patients), followed by ankle bones (8 patients), femur (4 patients), radius and thumb (3 patients each), humerus and knee (2 patients each), and ulna (1 patient). Of these, 2 patients had 2 bony lesions. In 8 (21%) children, axial bones were involved: 5 sternums, 2 thoracic vertebrae, and 1 right rib. Presentation included a mass (25 [66%] children), tenderness (22 [58%]), limping (19 [50%]), redness (14 [37%]), and heat (7 [18%]). Average time from first clinical visit to final surgical management was 1.6 [+ or -] 2.1 months.

Eight (53%) of 15 patients had positive tuberculin skin test results. No specific abnormalities were found with regard to blood cell counts and inflammation markers or to chest radiographs, except for 1 child with rib erosion. Pathologic diagnosis of Mycobacterium infection from bony specimens was recorded for 35 (92%) patients. For 29 (76%), diagnosis was conducted by molecular study, including 25 (66%) by the national reference mycobacterial laboratory. For 4 patients, diagnosis was confirmed by culture of M. bovis. Osteomyelitis/osteitis for 5 patients was considered BCG related according to pathologic diagnosis of Mycobacterium infection, BCG vaccination history, and lack of a history of contact with a person with tuberculosis.

Thirty-two (84%) children underwent surgery (excision, debridement, open biopsy), 4 children received arthrotomy (3 ankle and knee joint), and 2 children underwent only aspiration biopsy. All patients received isoniazid and rifampin therapy; 33 patients also received pyrazinamide, and 6 received additional ethambutol therapy. Medications were adjusted after diagnoses changed from tuberculosis to BCG infection. Two patients had major sequelae, both involving the thoracic spine and causing severe kyphosis.

Adverse reactions after BCG vaccination depend on the BCG dose, vaccine strain, vaccine administration method, injection technique, and recipient's underlying immune status (5). The vaccine strain and manufacturing process in Taiwan did not change during the study period. Findings were not associated with a specific batch of vaccine, inoculation age, underlying disease, or Salmonella spp. infection. Patients had no common birth place, hospital, or area of residence. We believe the increased number of cases resulted mainly from policy changes and laboratory facility improvements.

A surgical approach to obtain a specimen is indicated. However, because medical treatment usually yields a good outcome (6), extensive debridement should be avoided. Although some patients with lower extremity involvement initially limped, most were able to walk well later. Vertebral involvement is rare. Unlike previously reported cases (7,8), both patients reported here who had vertebral involvement had sequelae. For young children with suspected vertebral tuberculosis but no tuberculosis contact history, a biopsy specimen for BCG studies is preferable to spondylectomy. Although no definite immunologic deficit was found in these BCG osteomyelitis/osteitis patients, 2 other compensated infants with disseminated BCG during the same period in Taiwan had identified immunodeficiency (9). Studies are ongoing by the Taiwan Centers for Disease Control to evaluate medical treatment duration, long-term outcomes, and more detailed immune genetic tests.

DOI: http://dx.doi.org/10.3201/eid2103.140789

Acknowledgments

We thank the members of the Taiwan Vaccine Injury Compensation Program committee for their evaluation of the relation between BCG and possible adverse reactions in the patients of this study.

This research is approved and funded by Taiwan Centers for Disease Control, Ministry of Health and Welfare, Executive Yuan (project no. YY101015).

References

(1.) Jou R, Huang WL, Su WJ. Tokyo-172 BCG vaccination complications, Taiwan. Emerg Infect Dis. 2009; 15:1525-6. http://dx.doi.org/10.3201/eid1509.081336

(2.) Chan PC, Huang WL, Wang KF, Ma CY, Lu BY, Lin FT, et al. The active surveillance of BCG-related adverse events. Taiwan Epidemiology Bulletin. 2012; 28:13-21.

(3.) Koyama A, Toida I, Nakata S. Osteitis as a complication of BCG vaccination [in Japanese]. Kekkaku. 2009; 84:125-32.

(4.) Bottiger M, Romanus V, de Verdier C, Boman G. Osteitis and other complications caused by generalized BCG-itis. Experiences in Sweden. Acta Paediatr Scand. 1982; 71:471-8. http://dx.doi. org/10.1111/j.1651-2227.1982.tb09454.x

(5.) Lotte A, Wasz-Hockert O, Poisson N, Dumitrescu N, Verron M, Couvet E. A bibliography of the complications of BCG vaccination. A comprehensive list of the world literature since the introduction of BCG up to July 1982, supplemented by over 100 personal communications. Adv Tuberc Res. 1984; 21:194-245.

(6.) Kroger L, Korppi M, Brander E, Kroger H, Wasz-Hockert O, Backman A, et al. Osteitis caused by bacille Calmette-Guerin vaccination: a retrospective analysis of 222 cases. J Infect Dis. 1995; 172:574-6. http://dx.doi.org/10.1093/infdis/172.2.574

(7.) Moreno L, Gottrand F, Herbaux B, Savage C, Farriaux JP. Vertebral osteitis following BCG vaccination in a previously healthy child. Eur J Pediatr. 1990; 149:668. http://dx.doi.org/10.1007/BF02034763

(8.) Sandstrom S. Multifocal sclerotic BCG spondylitis in a 13-year-old girl. Pediatr Radiol. 1983; 13:239-40. http://dx.doi.org/10.1007/ BF00973166

(9.) Huang LH, Shyur SD, Weng JD. Shin-Chi, Tzen CY, Huang FY. Disseminated bacille Calmette-Guerin disease as the initial presentation of X-linked severe combined immunodeficiency--a case report. Asian Pac J Allergy Immunol. 2005; 23:221-6.

Nan-Chang Chiu, Meng-Chin Lin, Wen-Li Lin, Shin-Yi Wang, Hsin Chi, Li-Min Huang, Ren-Bin Tang, Yhu-Chering Huang, Ching-Chuan Liu, Fu-Yuan Huang, Tzou-Yien Lin

Author affiliations: Mackay Memorial Hospital, Taipei, Taiwan (N.-C. Chiu, M.-C. Lin, W.-L. Lin, H. Chi, F.-Y. Huang); Mackay Junior College of Medicine, Nursing and Management, Taipei (N.-C. Chiu, H. Chi); Taiwan Centers for Disease Control, Taipei (S.-Y. Wang); National Taiwan University Hospital, Taipei (L.-M. Huang); Cheng Hsin General Hospital, Taipei (R.-B. Tang); Chang Gung Memorial Hospital, Taoyuan, Taiwan (Y.-C. Huang, T.-Y. Lin); National Cheng Kung University Hospital, Tainan, Taiwan (C.-C. Liu); Ministry of Health and Welfare, Executive Yuan, Taipei (T.-Y. Lin)

Address for correspondence: Tzou-Yien Lin, Ministry of Health and Welfare, No. 36, Tacheng St, Datong District, Taipei 10341, Taiwan; email: alinpid@gmail.com
COPYRIGHT 2015 U.S. National Center for Infectious Diseases
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2015 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:LETTERS
Author:Chiu, Nan-Chang; Lin, Meng-Chin; Lin, Wen-Li; Wang, Shin-Yi; Chi, Hsin; Huang, Li-Min; Tang, Ren-Bin
Publication:Emerging Infectious Diseases
Article Type:Letter to the editor
Geographic Code:9TAIW
Date:Mar 1, 2015
Words:1328
Previous Article:Rickettsia rickettsii in Amblyomma patinoi Ticks, Colombia.
Next Article:High prevalence of hepatitis delta virus among persons who inject drugs, Vietnam.
Topics:

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters