Nk. Reed et al., PROGRESS OF IMPAIRMENT SCORES FOLLOWING COMMENCEMENT OF CHEMOTHERAPY IN MULTIBACILLARY LEPROSY PATIENTS, International journal of leprosy and other mycobacterial diseases, 65(3), 1997, pp. 328-336
Study aim: To investigate the progress of impairment over time in mult
ibacillary (MB) leprosy patients. Study design: Retrospective cohort s
tudy. Study population: One-thousand-eighty-two MB patients newly regi
stered in nine field clinics in the Western Region of Nepal between 19
80 and 1993. Methods: Data on impairment at diagnosis and at yearly in
tervals afterward were collected from patient records of MB patients a
lready released from multidrug therapy (MDT). The World Health Organiz
ation (WHO) 1988 ''disability'' grading scale (0-2, for both eyes, han
ds and feet-six sites) was used as a measure of impairment. For the an
alysis we summed the WHO grading for the six sites into an eyes-hands-
feet (EHF) sum score (minimum 0, maximum 12). The EHF score at 2 years
of follow up was used to compute the main outcome measures: impairmen
t at 2 years, yes or no, and deterioration of impairment compared with
diagnosis. The combined effect of age, sex, classification and impair
ment status at diagnosis on the outcome was examined with logistic reg
ression. Results: At diagnosis, 55.8% of the patients had some impairm
ent. This proportion decreased over 2 years to 43.9%. Among patients w
ithout initial impairment, 31/310 (10%) developed impairment during th
e study period. This was 81/396 (20.5%) among patients with impairment
at diagnosis. The adjusted odds ratio (OR) for developing impairment
was 1.87 [95% confidence interval (CI) 1.06-3.32] for patients with in
itial sensory impairment (WHO grade 1) and 1.98 (95% CT 1.15-3.4) for
those with initial visible deformity (WHO grade 2). Among patients wit
h impairment at diagnosis, 195/396 (49.2%) had improved after 2 years.
Conclusions: The proportion of patients with impairment after 2 years
of antileprosy treatment was 12% less than at diagnosis. Among patien
ts without initial impairment, 10% had developed some impairment after
2 years. The risk of developing impairment was almost double for thos
e with sensory impairment or visible deformity at diagnosis. For purpo
ses of monitoring, evaluation and planning, both the proportion of pat
ients with sensory impairment (WHO grade 1) and the proportion with vi
sible deformity (WHO grade 2) should be reported at diagnosis and at r
elease from treatment.