Skip to main content

Main menu

  • Home
  • Current issue
  • ERJ Early View
  • Past issues
  • ERS Guidelines
  • Authors/reviewers
    • Instructions for authors
    • Submit a manuscript
    • Open access
    • Peer reviewer login
  • Alerts
  • Subscriptions
  • ERS Publications
    • European Respiratory Journal
    • ERJ Open Research
    • European Respiratory Review
    • Breathe
    • ERS Books
    • ERS publications home

User menu

  • Log in
  • Subscribe
  • Contact Us
  • My Cart

Search

  • Advanced search
  • ERS Publications
    • European Respiratory Journal
    • ERJ Open Research
    • European Respiratory Review
    • Breathe
    • ERS Books
    • ERS publications home

Login

European Respiratory Society

Advanced Search

  • Home
  • Current issue
  • ERJ Early View
  • Past issues
  • ERS Guidelines
  • Authors/reviewers
    • Instructions for authors
    • Submit a manuscript
    • Open access
    • Peer reviewer login
  • Alerts
  • Subscriptions

Prognostic factors for surgical resection in patients with multidrug-resistant tuberculosis

H. J. Kim, C. H. Kang, Y. T. Kim, S-W. Sung, J. H. Kim, S. M. Lee, C-G. Yoo, C-T. Lee, Y. W. Kim, S. K. Han, Y-S. Shim, J-J. Yim
European Respiratory Journal 2006 28: 576-580; DOI: 10.1183/09031936.06.00023006
H. J. Kim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
C. H. Kang
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Y. T. Kim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S-W. Sung
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
J. H. Kim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S. M. Lee
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
C-G. Yoo
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
C-T. Lee
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Y. W. Kim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S. K. Han
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Y-S. Shim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
J-J. Yim
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

Although surgical lung resection could improve prognosis in some patients with multidrug-resistant tuberculosis (MDR-TB), there are no reports on the optimal candidates for this surgery. The aim of the present study was to elucidate the prognostic factors for surgery in patients with MDR-TB.

Patients who underwent lung resection for the treatment of MDR-TB between March 1993 and December 2004 were included in the present study. Treatment failure was defined as greater than or equal to two of the five cultures recorded in the final 12 months of treatment being positive, any one of the final three cultures being positive, or the patient having died during treatment. The variables that affected treatment outcomes were identified through univariate and multivariate logistic regression analysis.

In total, 79 patients with MDR-TB were included in the present study. The treatment outcomes of 22 (27.8%) patients were classified as failure. A body mass index <18.5 kg·m-2, primary resistance, resistance to ofloxacin and the presence of a cavitary lesion beyond the range of the surgical resection were associated with treatment failure.

Low body mass index, primary resistance, resistance to ofloxacin and cavitary lesions beyond the range of resection are possible poor prognostic factors for surgical lung resection in multidrug-resistant tuberculosis patients.

  • Multidrug-resistant
  • prognosis
  • surgery
  • tuberculosis

Multidrug-resistant tuberculosis (MDR-TB), resistant to at least both isoniazid and rifampicin, poses a serious threat to global health because it requires treatment for a long duration and frequent hospitalisation, and results in a considerable number of mortalities 1. According to a World Health Organization (WHO) report in 2000, 3.2% of all new tuberculosis (TB) cases are multidrug resistant (MDR). In Estonia and Latvia, MDR was observed in 14 and 9% of new TB cases, respectively 2.

The treatment of MDR-TB is difficult as second-line drugs must be used; these are less potent than first-line drugs and are not as well tolerated. Early publications on the treatment response of MDR-TB reported considerable mortality, sometimes as high as 37% 3. After the successful introduction of surgical resection of the diseased lung in patients with refractory MDR-TB 4, favourable results among patients with MDR-TB ensued 5–12. The rates of sputum conversion or of patients who remained negative after surgical resection are as high as 80–98% 5–12. Recently, surgical resection, along with the use of new quinolones, has been widely accepted to improve the results of MDR-TB treatment 13, 14.

Although surgical resection has been tried and favourable outcomes have been increasingly reported in patients with MDR-TB 5–12, there is no consensus as to which patients should undergo surgical resection. The aim of the current study was to elucidate prognostic factors in patients with MDR-TB refractory to medical treatment who had undergone surgical resection of the diseased lung.

METHODS

Inclusion criteria and data collection

The subjects included in the present study were patients who had undergone surgical lung resection for the treatment of MDR-TB at Seoul National University Hospital (Seoul, Republic of Korea), a university-affiliated tertiary referral hospital, between March 1993 and December 2004. Although the decision to perform surgical resection was made by individual physicians, the general indication for surgical resection used in the Seoul National University Hospital was MDR-TB refractory to at least 6 months of medical treatment with a main localised lesion. The medical records, microbiology results, other laboratory results, and radiographic examinations of the enrolled patients were reviewed. The protocol of the current study was approved by the Ethical Review Committee of Seoul National University Hospital.

Definitions

The type of resistance was classified according to the definitions of the WHO 15. MDR-TB patients without prior treatment with anti-TB drugs were classified as having primary resistance. If the patients had a history of previous anti-TB treatment, they were classified as having an acquired resistance 15. Body mass index (BMI; kg·m-2), measured just before the operation, was used in the analysis. The treatment outcomes were classified in accordance with the suggested criteria of Laserson et al. 16. Cure was defined as an MDR-TB patient who completed treatment according to the country's protocol and had been consistently culture negative (with at least five results) during the final 12 months of treatment. If only one positive culture was reported during that time, and there was no concomitant clinical evidence of deterioration, a patient may still be considered cured, provided that this positive culture was followed by a minimum of three consecutive negative cultures, taken at least 30 days apart. Treatment failure was defined as greater than or equal to two of the five cultures recorded in the final 12 months being positive, or any one of the final three cultures being positive, as recently suggested. In addition, on analysing treatment outcomes, a patient who died during the course of MDR-TB treatment was included in the treatment failure group.

Statistical analysis

Data are presented as median values or mean±sd. Chi-squared test for comparison of categorical variables and unpaired t-test for comparison of continuous variables were applied. Variables analysed include clinical characteristics (age, sex, BMI, type of resistance and drugs used), laboratory results (drug-susceptibility tests, liver-function tests, serum creatinine level and lung function) and radiographic findings. To identify the predictors for the treatment failure after surgical lung resection, multivariate logistic regression models were constructed including age, sex and any variables with a p-value <0.20 through univariate analysis. Statistical significance was determined by a p-value <0.05.

RESULTS

Annual number of surgeries and patient baseline characteristics

Between March 1993 and December 2004, 88 surgical lung resections were carried out at Seoul National University Hospital in 79 patients with MDR-TB refractory to medical treatment. Resections had been performed twice in seven patients and three times in one patient because of persistently positive acid-fast bacilli smear and/or Mycobacterium tuberculosis culture. In 1993, one patient with refractory MDR-TB underwent surgery. The number of surgeries increased to five in 1994 and peaked with 14 surgeries in 2002 (fig. 1⇓). The clinical data of 27 out of the 79 patients were included in an article published in 1999 9. All patients were Korean. Among the 79 cases, 48 were male and 31 female. Their median (range) age was 29 (19–60) yrs. The mean BMI was 21.5 and 19.8 kg·m-2 in the male and female patients, respectively. A total of 24 (30.4%) patients had other underlying diseases. None of the enrolled patients were anti-HIV antibody seropositive. The patients had received a median (range) of six (4–8) anti-TB drugs during a median (range) of 14.5 (9–112) months before the surgery. The M. tuberculosis isolates from these patients were resistant to a median (range) of five (2–11) drugs. Drug resistance rates among the 79 patients are summarised in table 1⇓. At the time of operation, 77 (97.5%) patients were M. tuberculosis culture positive. Cavitary lesions were evident in the chest radiographs of 77 (97.5%) patients. Among them, 28 (35.4%) patients had other cavitary lesions beyond the range of the resection. These were as follows: 25 patients had cavitary lesions in the contralateral side to the resected lung and three patients had lesions ipsilateral to the resected lung. In the latter three patients, the cavities could not be completely resected because of limited lung function.

Fig. 1—
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 1—

Annual numbers of lung resection surgeries in patients with multidrug-resistant tuberculosis (MDR-TB) and their results. A total of 88 operations in 79 patients with MDR-TB took place. □: successful results; ░: failure.

View this table:
  • View inline
  • View popup
Table 1—

Demographic and clinical characteristics of the 79 patients

Results of surgical lung resection and subsequent anti-TB chemotherapy

Among the 79 patients who underwent surgical lung resection, lobectomy was the most common procedure, performed in 44 (55.7%) patients. Surgical complications developed in 18 (22.8%) patients (table 2⇓). Anti-TB medications were continued for a median (range) of 18 (9–48) months after the surgery. The treatment results were as follows: cure in 57 (72.2%) patients, treatment failure in 21 (26.6%) patients, and death in one (1.2%) patient. The cause of death in the patient in whom right pneumonectomy was performed was respiratory failure caused by worsening TB in the left lung.

View this table:
  • View inline
  • View popup
Table 2—

Types of surgery and results of subsequent anti-tuberculosis (TB) chemotherapy in the 79 patients with multidrug-resistant TB

Predictors of treatment outcomes

Several variables were screened for any association with the results of treatment, including surgical lung resection. The variables evaluated included clinical characteristics (age, sex, BMI, type of resistance and drugs used), the results of microbiological tests and the radiographic findings (table 3⇓). Among them, primary resistance (p<0.001), resistance to ofloxacin (p = 0.015), and the presence of cavities beyond the range of resection were associated with treatment failure (p<0.001). Multivariate logistic regression analysis involving the variables age, sex and BMI was carried out for association with the results of surgery (table 4⇓). BMI <18.5 kg·m-2 (p = 0.043), primary resistance (p<0.001), resistance to ofloxacin (p = 0.048) and the presence of a cavitary lesion beyond the range of the surgical resection (p<0.001) were associated with treatment failure despite surgical lung resection.

View this table:
  • View inline
  • View popup
Table 3—

Individual predictors for treatment outcomes in multidrug-resistant patients who underwent surgical lung resection

View this table:
  • View inline
  • View popup
Table 4—

Predictors by multivariate logistic analysis for treatment failure in multidrug-resistant tuberculosis patients who underwent surgical lung resection

DISCUSSION

Through the current, retrospective, cohort study, it was demonstrated that lower BMI (p = 0.043), primary resistance (p<0.001), resistance to ofloxacin (p = 0.048), and the presence of a cavitary lesion beyond the range of the resection (p<0.001) were independently associated with poor treatment outcomes, including surgical resection for treatment of MDR-TB. A lower BMI and the presence of cavities have been reported to be associated with poor outcomes in patients with MDR-TB 17–19. In addition, use of new quinolones along with surgical resection has been widely accepted to improve the results of MDR-TB treatment 13, 14. However, there have been no previous reports of a primary resistance as a poor prognostic factor.

Drug-resistant TB bacilli have been reported as being generally less viable than drug-sensitive bacilli both in vitro and in vivo 20, and have lower transmissibility in most cases 21, 22, although some exceptions have been reported 23, 24. In this context, the hypothesis that transmitted bacilli with resistance to multidrugs (strains with primary resistance) are phenotypically more virulent than bacilli without definite evidence of transmissibility (strains with acquired resistance), is possible. The report of fatal outcomes from MDR-TB transmitted among family members without definite immune defects supports this hypothesis 25. However, the observed association between primary resistance and poor prognosis in the current study should be confirmed by future studies enrolling larger numbers of patients with MDR-TB, regardless of surgical resection.

The failure rate of 27.8% seen in the current study for treatments, including surgical resection, is relatively high compared with other reports 5–12, and could be explained by several factors. First, most patients (n = 77; 97.5%) included in the present study showed positive sputum culture for M. tuberculosis at the time of operation. This rate is much higher than the 50% positive sputum cultures reported among the patients in the study by Pomerantz et al. 7, which showed a 2% failure rate. Secondly, surgical resection was used aggressively, even in patients with bilateral cavities, because no other treatment options were available. These cases increased the failure rate and showed association with unfavourable outcomes. Thirdly, because all patients with MDR-TB included in the present study had undergone surgical resection because of refractoriness to medical treatment, the results could be unfavourable when compared with those from studies involving various indications, for example, prevention of treatment failure or relapse, or haemoptysis 8.

In conclusion, although the surgical resection of diseased lungs in patients with multidrug-resistant tuberculosis refractory to medical treatment has been accepted as a rescue therapy, clinicians should carefully select the patients for this treatment, giving consideration to possible poor prognostic factors, such as a low body mass index, primary resistance, resistance to ofloxacin, and the presence of cavitary lesions beyond the range of the resection.

Acknowledgments

The authors would like to thank C-H. Lee (Division of HIV and TB control, Korea Center for Disease Control and Prevention, Seoul, Republic of Korea) for his insightful opinion on the manuscript.

  • Received February 13, 2006.
  • Accepted April 21, 2006.
  • © ERS Journals Ltd

References

  1. ↵
    Iseman MD. Treatment of multidrug-resistant tuberculosis. N Engl J Med 1993;329:784–791.
    OpenUrlCrossRefPubMedWeb of Science
  2. ↵
    Dye C, Espinal MA, Watt CJ, Mbiaga C, Williams BG. Worldwide incidence of multidrug-resistant tuberculosis. J Infect Dis 2002;185:1197–1202.
    OpenUrlAbstract/FREE Full Text
  3. ↵
    Goble M, Iseman MD, Madsen LA, Waite D, Ackerson L, Horsburgh CR Jr. Treatment of 171 patients with pulmonary tuberculosis resistant to isoniazid and rifampin. N Engl J Med 1993;328:527–532.
    OpenUrlCrossRefPubMedWeb of Science
  4. ↵
    Pomerantz M, Madsen L, Goble M, Iseman M. Surgical management of resistant mycobacterial tuberculosis and other mycobacterial pulmonary infections. Ann Thorac Surg 1991;52:1108–1111.
    OpenUrlCrossRefPubMedWeb of Science
  5. ↵
    Shiraishi Y, Nakajima Y, Katsuragi N, Kurai M, Takahashi N. Resectional surgery combined with chemotherapy remains the treatment of choice for multidrug-resistant tuberculosis. J Thorac Cardiovasc Surg 2004;128:523–528.
    OpenUrlCrossRefPubMedWeb of Science
  6. Park SK, Lee CM, Heu JP, Song SD. A retrospective study for the outcome of pulmonary resection in 49 patients with multidrug-resistant tuberculosis. Int J Tuberc Lung Dis 2002;6:143–149.
    OpenUrlPubMedWeb of Science
  7. ↵
    Pomerantz BJ, Cleveland JC Jr, Olson HK, Pomerantz M. Pulmonary resection for multi-drug resistant tuberculosis. J Thorac Cardiovasc Surg 2001;121:448–453.
    OpenUrlCrossRefPubMedWeb of Science
  8. ↵
    Chiang CY, Yu MC, Bai KJ, Suo J, Lin TP, Lee YC. Pulmonary resection in the treatment of patients with pulmonary multidrug-resistant tuberculosis in Taiwan. Int J Tuberc Lung Dis 2001;5:272–277.
    OpenUrlPubMedWeb of Science
  9. ↵
    Sung SW, Kang CH, Kim YT, Han SK, Shim YS, Kim JH. Surgery increased the chance of cure in multi-drug resistant pulmonary tuberculosis. Eur J Cardiothorac Surg 1999;16:187–193.
    OpenUrlAbstract/FREE Full Text
  10. van Leuven M, De Groot M, Shean KP, von Oppell UO, Willcox PA. Pulmonary resection as an adjunct in the treatment of multiple drug-resistant tuberculosis. Ann Thorac Surg 1997;63:1368–1372.
    OpenUrlCrossRefPubMedWeb of Science
  11. Kir A, Tahaoglu K, Okur E, Hatipoglu T. Role of surgery in multi-drug-resistant tuberculosis: results of 27 cases. Eur J Cardiothorac Surg 1997;12:531–534.
    OpenUrlAbstract/FREE Full Text
  12. ↵
    Treasure RL, Seaworth BJ. Current role of surgery in Mycobacterium tuberculosis. Ann Thorac Surg 1995;59:1405–1407.
    OpenUrlCrossRefPubMedWeb of Science
  13. ↵
    Chan ED, Laurel V, Strand MJ, et al. Treatment and outcome analysis of 205 patients with multidrug-resistant tuberculosis. Am J Respir Crit Care Med 2004;169:1103–1109.
    OpenUrlCrossRefPubMedWeb of Science
  14. ↵
    Tahaoglu K, Torun T, Sevim T, et al. The treatment of multidrug-resistant tuberculosis in Turkey. N Engl J Med 2001;345:170–174.
    OpenUrlCrossRefPubMedWeb of Science
  15. ↵
    World Health Organization. Guidelines for the management of drug-resistant tuberculosis. Geneva, World Health Organization, 1997
  16. ↵
    Laserson KF, Thorpe LE, Leimane V, et al. Speaking the same language: treatment outcome definitions for multidrug-resistant tuberculosis. Int J Tuberc Lung Dis 2005;9:640–645.
    OpenUrlPubMedWeb of Science
  17. ↵
    Yew WW, Chan CK, Chau CH, et al. Outcomes of patients with multidrug-resistant pulmonary tuberculosis treated with ofloxacin/levofloxacin-containing regimens. Chest 2000;117:744–751.
    OpenUrlCrossRefPubMedWeb of Science
  18. Leimane V, Riekstina V, Holtz TH, et al. Clinical outcome of individualised treatment of multidrug-resistant tuberculosis in Latvia: a retrospective cohort study. Lancet 2005;365:318–326.
    OpenUrlCrossRefPubMedWeb of Science
  19. ↵
    Mitnick C, Bayona J, Palacios E, et al. Community-based therapy for multidrug-resistant tuberculosis in Lima, Peru. N Engl J Med 2003;348:119–128.
    OpenUrlCrossRefPubMedWeb of Science
  20. ↵
    Ordway DJ, Sonnenberg MG, Donahue SA, Belisle JT, Orme IM. Drug-resistant strains of Mycobacterium tuberculosis exhibit a range of virulence for mice. Infect Immun 1995;63:741–743.
    OpenUrlAbstract/FREE Full Text
  21. ↵
    Godfrey-Faussett P, Sonnenberg P, Shearer SC, et al. Tuberculosis control and molecular epidemiology in a South African gold-mining community. Lancet 2000;356:1066–1071.
    OpenUrlCrossRefPubMedWeb of Science
  22. ↵
    Garcia-Garcia ML, Ponce de Leon A, Jimenez-Corona ME, et al. Clinical consequences and transmissibility of drug-resistant tuberculosis in southern Mexico. Arch Intern Med 2000;160:630–636.
    OpenUrlCrossRefPubMedWeb of Science
  23. ↵
    Kruuner A, Hoffner SE, Sillastu H, et al. Spread of drug-resistant pulmonary tuberculosis in Estonia. J Clin Microbiol 2001;39:3339–3345.
    OpenUrlAbstract/FREE Full Text
  24. ↵
    Teixeira L, Perkins MD, Johnson JL, et al. Infection and disease among household contacts of patients with multidrug-resistant tuberculosis. Int J Tuberc Lung Dis 2001;5:321–328.
    OpenUrlPubMedWeb of Science
  25. ↵
    Sofia M, Maniscalco M, Honore N, et al. Familial outbreak of disseminated multidrug-resistant tuberculosis and meningitis. Int J Tuberc Lung Dis 2001;5:551–558.
    OpenUrlPubMedWeb of Science
PreviousNext
Back to top
View this article with LENS
Vol 28 Issue 3 Table of Contents
European Respiratory Journal: 28 (3)
  • Table of Contents
  • Index by author
Email

Thank you for your interest in spreading the word on European Respiratory Society .

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Prognostic factors for surgical resection in patients with multidrug-resistant tuberculosis
(Your Name) has sent you a message from European Respiratory Society
(Your Name) thought you would like to see the European Respiratory Society web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
Citation Tools
Prognostic factors for surgical resection in patients with multidrug-resistant tuberculosis
H. J. Kim, C. H. Kang, Y. T. Kim, S-W. Sung, J. H. Kim, S. M. Lee, C-G. Yoo, C-T. Lee, Y. W. Kim, S. K. Han, Y-S. Shim, J-J. Yim
European Respiratory Journal Sep 2006, 28 (3) 576-580; DOI: 10.1183/09031936.06.00023006

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
Prognostic factors for surgical resection in patients with multidrug-resistant tuberculosis
H. J. Kim, C. H. Kang, Y. T. Kim, S-W. Sung, J. H. Kim, S. M. Lee, C-G. Yoo, C-T. Lee, Y. W. Kim, S. K. Han, Y-S. Shim, J-J. Yim
European Respiratory Journal Sep 2006, 28 (3) 576-580; DOI: 10.1183/09031936.06.00023006
del.icio.us logo Digg logo Reddit logo Technorati logo Twitter logo CiteULike logo Connotea logo Facebook logo Google logo Mendeley logo
Full Text (PDF)

Jump To

  • Article
    • Abstract
    • METHODS
    • RESULTS
    • DISCUSSION
    • Acknowledgments
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
  • Tweet Widget
  • Facebook Like
  • Google Plus One

More in this TOC Section

  • Determinants of community-acquired pneumonia in children and young adults in primary care
  • Oral versus i.v. antibiotics for community-acquired pneumonia in children: a cost-minimisation analysis
  • Incidence, characteristics and outcomes of patients with severe community acquired-MRSA pneumonia
Show more Original Articles: Respiratory Infections

Related Articles

Navigate

  • Home
  • Current issue
  • Archive

About the ERJ

  • Journal information
  • Editorial board
  • Press
  • Permissions and reprints
  • Advertising

The European Respiratory Society

  • Society home
  • myERS
  • Privacy policy
  • Accessibility

ERS publications

  • European Respiratory Journal
  • ERJ Open Research
  • European Respiratory Review
  • Breathe
  • ERS books online
  • ERS Bookshop

Help

  • Feedback

For authors

  • Instructions for authors
  • Publication ethics and malpractice
  • Submit a manuscript

For readers

  • Alerts
  • Subjects
  • Podcasts
  • RSS

Subscriptions

  • Accessing the ERS publications

Contact us

European Respiratory Society
442 Glossop Road
Sheffield S10 2PX
United Kingdom
Tel: +44 114 2672860
Email: journals@ersnet.org

ISSN

Print ISSN:  0903-1936
Online ISSN: 1399-3003

Copyright © 2023 by the European Respiratory Society