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ARCHIVES OF LEPROSY MAILING LIST
Archives of recent messages from Leprosy Mailing List (LML) managed by Dr Salvatore Noto.

Over the past few years, LML moderated by Dr Noto has become one of the most important online resource for promoting discussions about leprosy. For joining this mailing list kindly send an email to Dr. Salvatore Noto: salvatore.notoathsanmartino.it  (substitute at with @ in the email address)

Leprosy Mailing List – December 3rd, 2006

 

Ref.:     How valid are any of these figures?”

From:   Ryan T J., Al Wakeel Y., Oxford, UK


  

 

 

Dear Salvatore,

 

I have noted the question posed by several of your correspondents “How valid are any of these figures?”

 

One reason for writing to you is that reliable figures are very hard to come by.  May be it should in itself be a field for study, and hopefully the following comments will indicate why.  It must be a major concern that there are clearly large numbers of new cases of leprosy that never become National statistics.

 

Dr Yasir Al Wakeel and I have collected the following data in India.  I would welcome opinion on their accuracy because if true the answer to the question “How accurate?” must be “Not at All!” The Government sector is not attractive and it is likely in my view that a majority of persons affected by leprosy will think twice and may well choose an alternative.

 

Number of public Hospitals                         17,000

Number of primary health centres                24,000

Percentage adequately staffed                      38%

(This consequently is reflected in short consultations, in uncompassionate and unwelcoming surroundings)

India lies at 171st place out of 175 for health spending

0.2% 0f the population have health insurance.

24% of villagers cannot afford health care.

 

I agree with Dr Baniprasad and spoke about this at the 2006 Annual meeting of the Association of Dermatology Venereology and Leprosy in Hyderabad and found a high level of agreement about the following.

 

The Dermatology Private Sector

The Indian Association of Dermatology Venereology and Leprosy which provides a full training, examination accreditation and CME in leprosy has a Membership of 4000.  There are lesser qualified (diplomatists) Dermatologists in the order of 6000.  My impression is that the private sector is quite generous to the poor and skin camps are commonly done with no charge.  The last one I attended picked up 4 new cases of leprosy and did refer to he National programme but did not make sure that they attended. 

 

Leprosy new cases detected annually per dermatologist very approximately are 24 to 240.  The average number of such cases referred to the National programme is unclear but many are not referred and of those that are, an instruction to report is usually done verbally to a bemused patient, and few are confirmed as registered.

 

Indian Systems of Medicine (Ayurveda, Siddha and Unani)

Ayurveda is the most popular system of health.  There are over 600,000 practitioners that have had 6 years training in up to 300 colleges or 26 universities.  Almost 8000 students graduate each year. Many take a further 2years course in postgraduate medicine inclusive of Biomedicine.  In addition there are more than 6000 ayurvedic, 346 Siddha and 375 Unani pharmacies.

The skin signs of leprosy are of less interest to these practitioners than the constitution of their clients.  Therapy for imbalances may alter immunosurveillance and be of benefit to the control of leprosy.  Postgraduates will usually diagnose leprosy.  Referral to the National programme will usually be delayed or will not happen. The number of new cases of leprosy seen each year is unknown but I would guess it is large.

 

Non-governmental organisations

The society for participatory research in Asia states that there are 1.2 million NGOs in India.  One study of 12,265 NGOs found 91.5% in the social sector of which 52% were for rural development.  In 1991 there were 250 concerned with leprosy but recent figures for “leprosy centres” records 700! Questioning several of these it is clear that many new cases are never referred to the National Programme.  Furthermore some well known centres receive patients from far distances and refer them back to their home district without having a system for confirming registration.  I have noted that several NGOs purchase MDT “to avoid bureaucracy”.

 

Our full report of our findings and our plea for integrated approaches can be found on

<< http://www.leprosyhistory.org/englishbulletin/discussion.htm >>

<< http://www.leprosyhistory.org/english/englishhome.htm >>

 

Best regards,

 

Terence J Ryan and Yasir Al Wakeel

 

 

 

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