Mortality rates and recurrent rates of tuberculosis in patients with smear-negative pulmonary tuberculosis and tuberculous pleural effusion who have completed treatment
H. Banda et al., Mortality rates and recurrent rates of tuberculosis in patients with smear-negative pulmonary tuberculosis and tuberculous pleural effusion who have completed treatment, INT J TUBE, 4(10), 2000, pp. 968-974
Citations number
25
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE
SETTING: Queen Elizabeth Central Hospital, Blantyre, and Zomba Central Hosp
ital, Zomba, Malawi.
OBJECTIVE: Th follow-up human immunodeficiency virus (HIV) seropositive and
HIV-seronegative patients with smear-negative pulmonary tuberculosis (PTB)
and pleural TB who had completed treatment with two different regimens in
Blantyre and Zomba, and to assess rates of mortality and recurrent TB. DESI
GN: patients with smear-negative and pleural TB who had completed 8 months
ambulatory treatment in Blantyre or 12 months standard treatment in Zomba a
nd who were smear and culture negative for acid-fast bacilli at the complet
ion of treatment were actively followed every 4 months for a total of 20 mo
nths.
RESULTS: Of 248 patients, 150 with smear-negative PTR and 98 with pleural T
B, who completed treatment and were enrolled, 205 (83%) were HIV-positive.
At 20 months, 145 (58%) patients were alive, 85 (34%) had died and IS (7%)
had transferred out of the district. The mortality rate was 25.7 per 100 pe
rson-years, with increased rates strongly associated with HIV infection and
age >45 years. Forty-nine patients developed recurrent TB. The recurrence
rate of TB was 16.1 per 100 person-years, with increased rates strongly ass
ociated with HIV infection, having smear-negative PTB and having received '
standard treatment'.
CONCLUSION: High rates of mortality and recurrent TB were found in patients
with smear-negative PTB and pleural effusion during 20 months of follow-up
. TB programmes in sub-Saharan Africa must consider appropriate interventio
ns, such as co-trimoxazole and secondary isoniazid prophylaxis, to reduce t
hese adverse outcomes.