Background
Tuberculosis (TB) now exceeds human immunodeficiency virus (HIV) as the infectious disease responsible for the greatest number of deaths globally [
1]. In addition, multidrug-resistant tuberculosis (MDR-TB), patients resistant to rifampicin (INH) and isoniazid (RMP), hampers the prevention and control of tuberculosis. Due to poor effectiveness and elevated costs in treatment of MDR-TB patients, they may endure longer infectious periods than those with drug-susceptible TB [
2]. Early identification and diagnosis of MDR-TB patients are essential to further prevent the spread of MDR-TB and provide comprehensive and successful treatment.
Sputum culture plays an important role in monitoring treatment response in MDR-TB patients [
3]. Sputum culture conversion is a clinical tool used to predict therapeutic efficacy in MDR-TB patients. Non-conversion of sputum culture at the end of the intensive phase of treatment tends to yield unfavorable outcomes, more specifically with failure and death [
4,
5].
Evidence exists suggesting that sputum culture conversion after the first 2 months may be an early predictor of treatment success in MDR-TB patients [
6‐
8]. Lung cavitation at baseline chest X-ray and resistance to ofloxacin (Ofx) or streptomycin have been associated with a delay in sputum culture conversion in prior studies [
6]. Although sputum culture conversion has been used substantially in clinical settings, few prospective cohort studies have been performed in China and India, two countries with almost half of the global burden of drug resistant tuberculosis [
9,
10]. In addition, factors affecting the time of the culture conversion throughout the whole course of the treatment have rarely been investigated.
Through a prospective cohort study design in urban China, we analyzed secondary factors that influenced sputum culture conversion in the process of treatment of MDR-TB disease.
Discussion
To our knowledge, there is no similar study in China, to investigate factors that influenced sputum culture conversion in the process of treatment of MDR-TB disease. In this setting with a high burden of drug resistant tuberculosis, we further validated that time to sputum culture conversion is a useful prognostic tool to predict end-of-treatment outcomes in MDR-TB patients but that results differ substantially depending on the month of treatment in which conversion occurs [
5,
6]. The median time of sputum smear conversion was 91.5 days, which was similar with a recent study by B. Velayutham and longer than it reported in earlier studies [
14‐
17]. This might because during the time waiting for the DST results, clinicians usually give the anti-TB drugs according to their experience and previous medication history of the patients, which could results in the culture conversion of the patients before the initiation of the standardized treatment, who were then were excluded before the initiation of the treatments.
After multivariable analysis, we further assessed factors associated with increased delay in culture conversion. We found that resistance to Ofx, smoking, drinking, and a high sputum smear grade were risk factors affecting culture conversion. Yuen et al. suggested that MDR-TB regimens including more potentially effective drugs are likely to improve treatment response in MDR-TB patients [
18]. To evaluate the association between regimen composition and treatment response, we made a comparison between individualized and standardized drug regimens and treatment outcomes. We found no statistically significant differences however this may be due to statistical power during stratification.
Substantial evidence exists indicating that smoking delays culture conversion and adversely affects end-of-treatment outcomes in drug-susceptible TB patients [
19‐
22]. For example, Maciel et al. found that TB patients that smoked were approximately three times less likely to convert their sputum culture after two months compared to non-smoking TB patients. Leung CC et al. also found that approximately one in six treatment failures were due to patient smoking habits [
20]. A recent study conducted in Brazil demonstrated that tobacco smoking delayed culture conversion during treatment for pulmonary tuberculosis and that this relationship was dose-dependent [
21]. Whether smoking also delays culture conversion in MDR-TB patients has not been investigated previously and we were able to extend these previous findings in drug-susceptible TB patients [
19‐
21] to MDR-TB patients. In this study, we found that smokers had a higher risk for persistent culture-positivity compared with nonsmokers after adjustment for potential confounders. MDR-TB patients may have ceased smoking after hospital admission and this could have led to misclassification of patient smoking status. However, this bias, if present, likely brings the association between smoking and delayed culture conversion among MDR-TB patients towards the null. Smoking cessation programs in an attempt to reduce poor treatment outcomes may be an important supplementary control measure for TB programs dealing with a high-burden of drug resistance TB, such as China.
A few studies have shown that sputum culture conversion can be delayed in patients who have infecting isolates resistant to second line anti-TB drugs [
6,
22,
23]. After adjustment for confounders, we found that participants resistant to Ofx were significantly less likely to have sputum culture conversion. Fluoroquinolones are amongst the most effective medications for patients not susceptible to first line drugs and therefore play an important role in treating drug resistant tuberculosis [
24,
25]. Nevertheless, excessive and irregular medication were leading causes for fluoroquinolone resistance in Pakistan [
26,
27]. We found that, patients resistant to Ofx were over two times more likely to have continuous culture-positive laboratory tests by the end of multidrug-resistant TB treatment. Fluoroquinolone resistance is a potential critical threat to the control of drug resistant TB globally and efforts to prevent resistance through high medication compliance in high-burden settings are essential.
Rie Kanda et al. reported the time of the sputum culture conversion was prolonged by high smear grade [
28], consistent with the results of F. Qazi et al. in 2011 [
22] and Caetano Mota et al. in 2012 [
29]. Also, patients with a high colony count were less likely to convert than those who had a low smear grade. In our study, patients with a smear grade > + 1 had a lower likelihood of sputum smear conversion compared with those with a smear grade ≤ + 1. It might be natural that MDR-TB patients who had a higher colony count take a longer time for sputum culture conversion. This result highlights the importance of early detection and treatment of drug resistant TB patients.
There are several limitations of this study. First, all patients ceased smoking and drinking during treatment, which may have led to nondifferential misclassification driving our results toward the null. Moreover, we did not quantify smoking or drinking in more detail which may have led to a lack of an effect on culture conversion. Second, missing information was present among some of our variables of interest. To account for this, we attempted to retrieve any missing information by revisiting participants and checking the infectious disease reporting system. Third, this survey did not collect information on HIV infection status and this may potentially be an important confounder. Patients with tuberculosis in China are not routinely tested for HIV and, due to this we were unable to assess the influence of HIV coinfection.
Conclusions
In conclusion, we present a prospective cohort study of MDR-TB patients from urban China and we found MDR-TB patients that smoke, drink, have ofloxacin resistance, or a high smear grade are less likely to respond to treatment and should be meticulously followed up. A multidimensional approach is needed to effectively control TB, including early detection and treatment, and proper interventions to lower the drinking rate and cigarette smoking rate.