9.2
Leprosy
Malawi Standard Treatment Guidelines, 6th Edition, 2023. Chapter 9, Infectious Diseases.
Clinical Description
Leprosy is a chronic infection usually caused by the acid-fast bacilli mycobacterium leprae which has a unique tropism for peripheral nerves, skin and mucus membranes of the upper respiratory tract. Leprosy is classified into Paucibacillary (tuberculoid) and Multibacillary (lepromatous).
Signs and Symptoms
Paucibacillary (PB) Leprosy is characterized by:
- 5 lesions or less
- lesions that are asymmetrically distributed
- Definite loss of sensation on the lesions
- Only ONE nerve trunk is enlarged and Negative Slit Skin Smear (SSS).
Multibacillary (MB) is characterized by
- More than 5 lesions
- Symmetrically distributed lesion
- Some degree of loss of sensation on the lesions
- Many nerve trunks are enlarged and Positive Slit Skin Smear.
Treatment Objective
- To cure the patient (using multi drug therapy)
- To render patient non-infectious and thus control the spread of leprosy
- To prevent the development of multi drug resistant leprosy
Drugs used in leprosy as recommended by WHO are a combination of rifampicin, clofazimine and dapsone (MDT). The duration of treatment for PB leprosy is 6 months and 12 months for MB leprosy.
Recommended leprosy treatment regimens
Age group Medicine Dosage and frequency
Duration (Months)
MB PB
Adult Rifampicin 600mg once a month 12 6
Clofazamine 300 mg once a month and 50 mg daily
Dapsone 100 mg daily
Children 10 to 14 Years
Rifampicin 450 mg once a month 12 6
Clofazamine 150 mg once a month and 50 mg daily
Dapsone 50 mg daily
Children <10
years old or <40kg
Rifampicin 10 mg/kg once month 12 6
Clofazamine 100 mg once a month, 50 mg twice weekly
Dapsone 2 mg/kg daily
Treatment for drug-resistant leprosy
- Leprosy patients with rifampicin resistance are treated using at least two of the following second-line drugs: clarithromycin, minocycline, or a quinolone (oxfloxacin, levofloxacin or moxifloxacin), plus clofazimine daily for 6 months, followed by clofazimine plus one of the second-line drugs daily for an additional 18 months. In case of rifampicin plus oxfloxacin resistance, a quinolone should not be chosen; therefore, the recommended regimen is clarithromycin, minocycline and clofazimine for 6 months followed by clarithromycin or minocycline plus clofazimine for an additional 18 months.
Recommended Drug Resistant Leprosy regimens
Resistance Type Treatment
First 6 months (daily) Next 18 months (daily)
Rifampicin Resistance Oxfloxacin 400 mg* + minocycline 100 mg + clofazimine 50 mg
Oxfloxacin 400 mg OR minocycline 100 mg + clofazimine 50 mg
Oxfloxacin 400 mg* + clarithromycin 500 mg + clofazimine 50 mg
Oxfloxacin 400 mg* + clofazimine 50 mg
Rifampicin and oxfloxacin resistance
Clarithromycin 500 mg + minocycline 100 mg + clofazimine 50 mg
Clarithromycin 500 mg OR minocycline 100 mg + clofazimine 50 mg
Treatment of reactions
The term reaction is used to describe the appearance of signs and symptoms of acute inflammation in the lesions of a patient with leprosy.
Treatment for mild reactions
- Continue anti-leprosy treatment, do not lower the dosage.
- Give an analgesic (e.g Aspirin).
- If there is nerve tenderness, rest the affected limb (sling or splint the arm)
- See the patient again after 1-2 weeks and tell him to return at once should the reaction become more severe.
Treatment of severe Reaction
- Continue anti-leprosy treatment.
- Start treatment with steroids (prednisolone)- no other drugs are effective.
40mg daily for 2 weeks, 30mg daily for 2 weeks, 20mg daily for 2 weeks, 15mg daily for 2 weeks, 10mg daily for 2 weeks, 5mg daily for 2 weeks.
Acute Dapsone Allergic Reaction
Symptoms/Signs:
- Itching, rash, exfoliative dermatitis or Stevens- Johnson syndrome
- Refer urgently to Leprosy Control Assistant
- Stop Dapsone
- Then observe
Treatment
- Give Antihistamines, steroids or hospitalize depending on severity.
Check doses against the printed guideline and your clinical judgement before treating a patient. Spotted an error? Report it from the contact links below.
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