Treatment
Leprosy is curable with a combination of drugs known as multidrug therapy (MDT), as the treatment of leprosy with only one anti-leprosy drug (monotherapy) will result in development of drug resistance to that drug.
Access to treatment
MDT, first recommended by WHO study group on chemotherapy of leprosy for control programmes 1982, rapidly became the standard treatment of leprosy and has been supplied by WHO free of charge to all endemic countries since 1995.
WHO works closely with donors and manufacturers to plan the manufacture, procurement and shipment of the MDT drugs having the maximum available shelf life, at the time most appropriate for each national programme. WHO also arranges independent laboratory testing of the drugs at the manufacturer's own expense in order to ensure that the finished WHO product is the best available for national programmes. Such testing is considered essential to maintain the confidence of national programmes in the donated product.
In order to meet emergency requests for MDT, WHO maintains at the donor's expense, substantial buffer stocks at the manufacturing plant. Currently these buffer stocks are equivalent to around 40% of global annual requirements but vary depending on perceived need. To ensure a rapid response to requests for smaller emergency supplies, WHO maintains additional buffer stocks at its headquarters in Geneva and Regional Office in Manila. Response times from WHO Geneva are typically 48 hours and most dispatches are made via courier.
WHO recommended multidrug therapy (MDT) regimens
The Guidelines for the diagnosis, treatment and prevention of leprosy (WHO, 2018), recommends the same 3-drug regimen with rifampicin, dapsone and clofazimine for all leprosy patients, with a duration of treatment of 6 months for PB leprosy and of 12 months for MB leprosy.
Rifampicin is given once a month. No toxic effects have been reported in the case of monthly administration. The urine may be coloured slightly reddish for a few hours after its intake, this should be explained to the patient while starting MDT.
Clofazimine is most active when administered daily. The drug is well tolerated and virtually non-toxic in the dosage used for MDT. The drug causes brownish black discoloration and dryness of skin. However, this disappears within few months after stopping treatment. This should be explained to patients starting MDT regimen.
Dapsone is very safe in the dosage used in MDT and side effects are rare. The main side effect is allergic reaction, causing itchy skin rashes and exfoliative dermatitis. Patients known to be allergic to any of the sulpha drugs should not be given dapsone.
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