Disease
Leprosy (Hansen's disease, Hanseniasis) is a chronic Mycobacterial disease caused by Mycobacterium leprae primarily affecting the peripheral nervous system and secondarily involving skin and certain other tissues.
Leprosy is a chronic infectious disease caused by Mycobacterium leprae affecting mainly peripheral nerves & skin, known for its potential to cause permanent and progressive Physical disability.
Leprosy has predominant psycho-social aspects/Social Stigma due to misconceptions/misbeliefs/Taboos/Ignorance.
Man is the only host reservoir.
Incubation period ranges from 6 months to 30 years with average of 2 to 5 years.
It is transmitted from untreated MB patient to healthy person via respiratory tract.
The major sites from which bacilli escape from the body of an infectious patient are nose and mouth.
Wide spectrum of host resistance, ranging from effective immunity to absence of resistance leads to varied presentation of the disease manifestations.
Extremely slow generation time of the organisms results in :a) Long incubation period,
b) A very slow development of pathology,
c) A slow and insidious clinical evolution,
d) An unclear epidemiological pattern,
e) Low infectivity.
There is no potent anti leprosy vaccine.
INTRODUCTION
Leprosy, once considered to be a dreadful disease especially because of the disfigurement & deformities associated with it, has lost its dreadful nature, thanks to the wonders of Multi Drug Therapy (MDT). The number of leprosy cases that was in millions has now come down to few thousands and the day is not far away when leprosy, like smallpox would be a disease of history. But this is possible only when people discard the apprehension and come forward to report the disease on their own and start the treatment early, as early diagnosis and prompt MDT is the key to leprosy elimination.
The target of elimination has been fixed at 1 or less than 1 case per 10,000 population as the scientific studies indicate that leprosy as a disease gets naturally eliminated at such a low prevalence.
It is therefore necessary that concepts of isolation and discrimination associated with leprosy are removed from the social milleau and leprosy is regarded as an ordinary disease like any other diseases afflicting mankind.
History
From the old records, it is evident that LEPROSY is a very ancient disease dating back many centuries. In India, leprosy was referred to as "KUSHTHA" in the ancient vedic literature as far back as 1400 B.C. The laws of Manu mention the instructions for the prevention of leprosy. A good description of this disease and its treatment is given in "SUSHRUTA SAMHITA" a book on surgery written in 600 B.C. by the eminent Indian surgeon SUSHRUTA. He regarded this disease as a contagious disease carried from a person suffering from this disease to a healthy person. There is strong evidence to show that leprosy was common as far back as 1400 B.C.
The word Leprosy is a translation of the Hebrew word "ZARAATH" and is mentioned in the Bible. The term included not only leprosy but also a number of other skin diseases. In ' LEVITICUS' clear instructions are given to the priests about the preventive measures against the spread of disease from persons suffering from leprosy. Some reference is made to Leprosy in Chinese literature dating back to 600 B.C. But there is no conclusive evidence to prove that it existed before.
The earliest description of the disease in Europe was given by Aractus a contemporary of Galen. Galen also referred to Leprosy as Elephantiasis Graecorum. Galen lived about A.D. 150. Hippocrates who lived in 450 B.C. did not mention Leprosy. The returning Greek and Roman armies probably introduced the disease into Europe. Prof. Moller Christensen through his studies of cranial bones found evidence of Leprosy in Great Britanin, France, and Egypt during the period A.D. 500-700. The disease was at its height in Europe between 1000 A.D and 1400A.D. Anderson in his thesis (1969) reviewed all the literature available about the spread and decline of Leprosy in Europe. The literature reveals that the authors believed Leprosy to be highly contagious. This known fact was probably responsible for the inhuman measures taken to contain the disease during that period.
During the 18th and early 19th century, before Hansen discovered the leprosy bacillus, the hereditary theory of leprosy became very popular in Europe. It was strongly supported by the Norwegian scientists but in view of the new epidemiological evidence in favour of the contagiousness of the disease, the hereditary theory lost its ground. Few authentic outbreaks of leprosy in Nuaru, Cape Breton, Louisiana and other places confirmed the contagiousness of the disease.
The patients during that time were confined in Lazar houses. Leprosy declined form this period and was completely eradicated during the 19th century in Europe due to : 1.Isolation of the patients & 2.Improvement of the socio-economic conditions in the continent, better housing, improved economic conditions, good nutrition, better sanitation have reduced the other factors responsible for the transmission of the disease.
Literature on the origin and spread of Leprosy in Africa is inadequate but the prevalence of disease in states like Nigeria, Uganda, Zaire was very high.
Leprosy was introduced into the Americas by the soldiers of Columbus first & later through the slave trade from the endemic areas of West Africa. Immigrants from Europe & China also introduced the disease into the continent.
The germ causing Leprosy is called Mycobacterium leprae and was discovered by G.H. Armauer Hansen (1841-1912) from Norway in 1873. Therefore, the organism is commonly known as Hansen's bacillus.
Historical Background / Periodical Development
Prior to formation of Separate state, Maharashtra was the part
of Bombay Province till 1960. Post of State Leprosy Officer was
in existence since 1943 and was filled in 1949, the main duty then
included advising the Govt. on leprosy services based on sample
surveys conducted by him. Then the available leprosy services included
leprosy asyla run by missionaries to provide sheltered segregation
and treatment with hydnocarpus oil. In 1951 treatment with sulphones
was initiated.
1942
Leprosy Hospital at Kondhawa taken over by Govt.
from the " Mission to Lepers".
1944
Leprosy Hospital Ratnagiri taken over by Govt.
from District Local Board.
1950
Scheme for Leprosy Control Work in a limited area
under Hind Kushtha Nivaran Sangh.
1953
Leprosy Control Centre established at Ambewadi
in district Sangali. Pilot projects for leprosy control started
at Vairag dist. Solapur, Mul dist. Chandrapur, Sevagram dist.
Wardha.
1955
Treatment with DDS tablets introduced in all local
bodies and Govt. hospitals, 1st documentary film on leprosy
prepared by Directorate of Publicity. Greater Bombay Leprosy
Control Scheme of Bombay Municipal Corporation in collaboration
with Gandhi Memorial Leprosy Foundation and State Govt.
1955- 56
Launch of National Leprosy Control Program throughout
the country including state with following principles
i) Detection of all cases especially those of the infectious
type at as early as possible
ii) Provision of treatment facilities to all patients so detected
and
iii) Health Education to create a favorable atmosphere which
will help both in case detection as well as case holding program.
1958
SET centre attached to existing dispensaries and
centres started. Thereafter with every 5 year plan SET centres,
leprosy control units and urban leprosy centres were established
in the entire state.
Post of state leprosy officer was upgraded to
Deputy Director (Health) in 1965 and further upgraded to Joint
Director (Health) in 1981
Milestones of NLEP in Maharashtra
1955- 1956
launch of National Leprosy Control Programme.
1970s
Definite cure through MDT was identified
1983
launching of National Leprosy Eradication Programme.,
Multi Drug Therapy introduced in selected urban area & Wardha
district.
1983- 1997
Remaining districts brought under MDT in phased
manner.
1993 - 2000
World Bank Assisted NLEP Project Phase- I
Objectives
1.
To support vertical programme structure for endemic
dists.
Jan. 1997: Implementation of National Leprosy Elimination.
2.
Establishment of Mobile Leprosy Treatment Unit
(MLTU) in moderate & low endemic dists.
3.
Formation of district leprosy societies.
Jan. 1997: Implementation of National Leprosy Elimination
Strategy
Main Activities-Programme renamed as National
Leprosy Elimination Programme with an objective to bring down
the P R of leprosy to below 1 per 10,000 population.
1998
Introduction of ROM in the state.
30 Jan 98-5 Feb 98
1st Modified Leprosy Elimination Campaign
Main Activities - Programme renamed as National Leprosy Elimination Programme with an objective to bring down the P R of leprosy to below 1 per 10,000 population.
30 Jan 99 - 5 Feb 99
Additional M L E C (1998-99) GOM
30 Jan 2000-6 Feb 2000
II M L E C (1999-2000) GOI
30 & 31 Jan 2000
V R C
Oct 2000 - Mar 2004
World Bank Assisted NLEP Phase-II
2001 - 2002
III M L E C, V R C - 30th &31st Oct.2001
2002 - 2003
IV Modified Leprosy Elimination Campaign.
2003 - 2004
V Modified Leprosy Elimination.
2004 - 2005
Block Leprosy Awareness Campaign
2005 - 2006
Block Leprosy Awareness Campaign II
2005 - 2007
Extended Leprosy Eradication Programme
2007-2008
Implementetion of DPMR Plan
2007-2008
Block Leprosy Awareness Campaign IV
2007-2012
Programme aims for eradication i.e. zero endemicity of leprosy, as the ultimate gaol, sustained control measures need to continue even during the 11th Plan period.