Title page for ETD etd-08012007-152157


Type of Document MD Thesis
Author Andrews, Jason Randolph
Author's Email Address jason.andrews@yale.edu
URN etd-08012007-152157
Title Clinical Predictors of Drug Resistance and Mortality Among Tuberculosis Patients in a Rural South African Hospital: A Case-Control Study
Degree MD
Department Medicine
Advisory Committee
Advisor Name Title
Gerald H. Friedland Committee Chair
Keywords
  • tuberculosis
  • drug therapy
  • South Africa
  • drug resistance
  • mortality
  • MDR-TB
  • XDR-TB
Date of Defense 0000-00-00
Availability restricted
Abstract
The recent discovery of a high prevalence of multidrug-resistant (MDR-TB) and

extensively drug-resistant tuberculosis (XDR-TB) in rural South Africa, where HIV is rampant,

has provoked alarms about the future of tuberculosis control in the region. Little is known about

the clinical manifestations of MDR-TB in general, and XDR-TB in particular, in the high HIV

prevalence settings of Sub-Saharan Africa.

We performed a retrospective, case-control study of patients diagnosed with tuberculosis

at a rural hospital in KwaZulu Natal, South Africa, where large numbers of MDR-TB and XDRTB

cases have been identified. All MDR-TB and XDR-TB patients who began treatment for TB

between June 1, 2005 and August 31, 2006 and whose charts were available were included in the

study. A comparison group of patients without resistance to both isoniazid and rifampicin (non-

MDR-TB), matched 1:1 with the size of the MDR-TB and XDR-TB groups, was created.

Clinical and laboratory data were obtained through review of hospital records, clinic registers,

and the laboratory system. We compared clinical characteristics to identify risk factors for MDRTB,

XDR-TB, and mortality. Bivariate and multivariate analyses were performed.

A total of 170 patients were enrolled in the study: 52 MDR-TB, 61 XDR-TB and 57 non-

MDR-TB. Greater than 75% of patients from all groups were tested for HIV; HIV prevalence

among those tested was 94% in the non-MDR group, 93% in the MDR group, and 100% in the

XDR-TB group (P=1.000 for MDR versus non-MDR; p=0.089 for XDR versus non-MDR).

Forty percent of MDR-TB patients and 57% of XDR-TB patients had no previous history of TB

treatment, strongly suggesting transmitted drug resistance.

Significant associations and risk factors for MDR-TB and XDR-TB in bivariate analysis

included positive sputum smear (P=0.015, P=0.005), TB treatment in the past year (P<0.0001,

P<0.001), and hospitalization in the past two years (P=0.007, P=0.004). In multivariate logistic

regression, positive sputum smear remained a significant risk factor for XDR-TB (adjusted odds

ratio (AOR) 2.79, 1.20-6.47), and TB treatment in the past year remained a risk factor for both

MDR-TB and XDR-TB (AOR 8.33, 95% CI 1.64-42.33; AOR 7.19, 95% CI 1.35-38.17).

Mortality for the non-MDR, MDR and XDR groups was 36.8%, 73.1% and 85.3%,

respectively (P= 0.0001 for MDR versus non MDR; P<0.0001 for XDR versus non-MDR;

P=0.109 for XDR versus MDR); median survival from TB diagnosis was 199 days, 103 days, and

92 days, respectively (P<0.001). In Cox Proportional Hazards model, positive sputum smear

(P=0.003), MDR-TB (P=0.028), XDR-TB (P=0.002), and CD4 cell count less than 200

cells/mm3 (P=0.037) were significant risk factors for mortality.

Forty of the 170 patients had sputum isolates with differing resistance patterns, and 18

moved from a lower to a higher resistance category; this increasing drug resistance appeared to be

more likely the result of super-infection than amplification.

A significant proportion of MDR-TB and all XDR-TB appear to be due to primary

resistance, with nosocomial transmission playing a critical role. MDR-TB and XDR-TB carry

extraordinarily high mortality rates in this setting; previous hospitalization, previous TB

treatment, positive sputum smear and low CD4 count may be used to target drug susceptibility

testing for patients at high risk of drug resistant TB and mortality.

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