Kamis, 17 April 2008
LEPROSY
HOSPITAL OF LEPROSY Dr.RIVAI ABDULLAH PALEMBANG
Leprosy
www.searo.who.int/en/Section10/Section20/Section2293.htm
Cause
Leprosy is a chronic disease caused by a bacillus, Mycobacterium leprae (M. laprae).
M. leprae multiplies very slowly and the incubation period of the disease is considered to be about five years.
TRANSMISSION
Leprosy is transmitted by air through droplets from the nose and mouth, during close and frequent contacts with untreated cases.
Leprosy is one of the least infectious diseases, because:
Over 99% of the population has adequate natural immunity;
Over 85% of the clinical cases are non-infectious, and
An infectious case is rendered non-infectious within one week, most often after the very first dose of treatment.
SYMPTOMS
Leprosy mainly affects the skin and peripheral nerves.
If left untreated, it can lead to progressive and permanent damage of nerves, leading to loss of sensation and sweating in the extremities and paralysis of muscles in the hands, feet and face.
The disease is classified as paucibacillary (PB) or multibacillary (MB), depending on the bacillary load.
PB leprosy is a milder disease characterized by few (up to five) skin lesions (pale or reddish), whereas MB is associated with multiple (more than five) skin lesions, nodules, plaques, thickened dermis or skin infiltration.
HISTORY OF THE DISEASE
The first known written mention of leprosy is dated 600 BC.
Leprosy was recognized in the ancient civilizations of China, Egypt and India.
All countries of the South-East Asia Region were known to be endemic for leprosy.
Throughout history, the afflicted have often been ostracized by their communities and families. This situation has changed since leprosy is now completely curable and there is greater awareness about the disease.
HISTORY OF TREATMENT
The first breakthrough occurred in the 1940s with the development of the drug dapsone, which cured the disease. But the duration of the treatment of leprosy was many years, even a lifetime, making it difficult for patients to be regular in their treatment.
In the 1960s, M. leprae started to develop resistance to dapsone, the world’s only known anti-leprosy drug at that time.
TREATMENT TODAY
In 1981, a World Health Organization (WHO) Study Group recommended multi-drug therapy (MDT), a combination of three drugs.
MDT effectively kills the pathogen and cures the patient.
Treatment provided in the early stages averts disability.
With minimal training, leprosy can be easily diagnosed by clinical signs alone.
WHAT IS MDT
MDT comprises of three drugs, dapsone, rifampicin and clofazimine. Rifampicin and clofazimine were discovered in the early 1960s.
MDT is safe, effective and easily administered under field conditions.
MDT is available in convenient monthly calendar blister packs.
Since 1995, WHO has been providing free MDT for all patients in the world, initially through the drug fund provided by the Nippon Foundation and since 2000, through the MDT donation provided by Novartis and the Novartis Foundation for Sustainable Development.
Novartis has pledged free supply of MDT till 2010.
HIGH EFFECTIVENESS OF MULTIDRUG THERAPY
Transmission of leprosy is interrupted after the very first dose of MDT. In other words, patients are no longer infectious to others after being administered the first dose of the treatment regimen.
PB patients treated with MDT are cured within six months.
MB patients treated with MDT are cured within 12 months.
There are virtually no relapses, i.e. no recurrences of the disease after treatment is completed.
No resistance of the bacillus to MDT has been detected.
WHO estimates that early detection and treatment with MDT has prevented about four million people from becoming disabled.
MDT is very cost-effective as a health intervention, considering the economic and social losses averted.
THE ELIMINATION OF LEPROSY AS A PUBLIC HEALTH PROBLEM
In 1991 World Health Assembly passed a resolution to eliminate leprosy as a public health problem by the year 2000. Elimination of leprosy as a public health problem is defined as a prevalence rate of less than one case per 10,000 population.
Globally, the leprosy elimination goal was achieved in 2000.
The global disease burden reduced from 5.2 million in 1985 to 805,000 in 1995 to 753,000 at the end of 1999 to about 219,826 cases at the end of 2005.
The South-East Asia Region, including India, achieved the elimination goal in December 2005.
The Regional prevalence rate steadily declined from 4.6/10,000 population in 1996 to 0.82/10,000 population as of July 2006.
The Regional new case detection also declined from a peak of 47.8/100,000 in 1998 to 11.9/100,000 as of March 2006.
Between 1985 and 2005, more than 15 million leprosy cases were cured globally. Of these, about 12.8 million were from the SEA Region, of which India accounted for about 11.8 million.
The SEA Region has made substantial contribution to the achievement of leprosy elimination globally.
CURRENT LEPROSY SITUATION
At the beginning of 2006, about 219,826 cases were under MDT globally and the prevalence rate was about 0.2 per 10,000 population.
Globally, 296,499 new cases of leprosy were detected during 2005.
The top 10 countries in new case detection in 2005 are India, Brazil, Indonesia, DR Congo, Bangladesh, Nepal, Mozambique, Nigeria, Ethiopia and Tanzania. Together, they constitute about 96% of the 2005 global new case detection.
The SEA Region contributed to about 69% of the 2005 global new case detection.
Six countries (small countries with <1 million population excluded), Brazil, DR Congo, Madagascar, Mozambique, Nepal and Tanzania are yet to achieve the elimination goal.
In the SEA Region, two countries, Nepal and Timor-Leste (population of Timor-Leste is less than 1 million) are yet to achieve elimination.
As of December 2005, the PR in Nepal was 1.81/10,000 and Timor-Leste 1.89/10,000 population. These countries are expected to achieve elimination in 2006 or 2007.
REMAINING CHALLENGES
Achieving elimination in the remaining countries and sustaining elimination in the countries that have achieved the goal at the national level.
Sustaining political commitment and ensuring adequate resources in order to sustain elimination at national level, and progress towards further reducing the burden of leprosy.
Strengthening integration of leprosy services into the general health system through capacity building and skill development, in order to ensure and sustain quality leprosy services, including diagnosis and treatment and prevention/care of disabilities.
Ensuring a wider coverage of leprosy services, especially in currently under-served population groups such as remote rural areas, urban slums, migrant labour.
Increasing and sustaining community awareness through sustained advocacy and IEC activities to promote voluntary case detection and decrease the stigma.
Minimizing/preventing operational factors, such as:
Setting case detection targets and basing performance appraisal on target achievement
Over-diagnosis and re-registration of cases due to:
Non-adherence to WHO-recommended case definitions
Active search and surveys repeatedly targeting the same population groups
Repeated leprosy elimination campaigns in the same areas
Lack of “Quality” and “Accuracy” of diagnosis
Multiple registration
Wrong classification - PB cases recorded as MB (more frequent than vice-versa)
Delayed treatment completion due to:
Irregularity
Drug shortage at peripheral level
Delayed release from treatment
Over-treatment
Non-existent cases
Job insecurity among vertical staff leading to large number of suspect/doubtful cases being recorded as leprosy cases
Preventing discrimination and displacement of leprosy affected and ensuring community based rehabilitation and integration of cured/disabled leprosy persons into the community.
Streamlining the MDT supply and stock management at all levels, considering the low endemic situation.
Strengthening existing partnerships and identifying new partners to support leprosy activities.
THE STRATEGY FOR LEPROSY ELIMINATION
Sustain leprosy services and activities in all endemic countries.
Use annual new case detection and cure rates as the main indicator to monitor progress.
Ensure high-quality diagnosis, case management, recording and reporting in all endemic countries.
Strengthen routine and referral services.
Discontinue the campaign approach, since they are not cost-effective any more and lead to over-detection.
Develop tools and procedures that are home/community-based, integrated and locally appropriate for the prevention of disabilities/impairments and for the provision of rehabilitation services.
Promote operational research in order to improve implementation of a sustainable strategy.
Encourage supportive working arrangements with partners at all levels.
www.searo.who.int/en/Section10/Section20/Section2293.htm
Leprosy
www.searo.who.int/en/Section10/Section20/Section2293.htm
Cause
Leprosy is a chronic disease caused by a bacillus, Mycobacterium leprae (M. laprae).
M. leprae multiplies very slowly and the incubation period of the disease is considered to be about five years.
TRANSMISSION
Leprosy is transmitted by air through droplets from the nose and mouth, during close and frequent contacts with untreated cases.
Leprosy is one of the least infectious diseases, because:
Over 99% of the population has adequate natural immunity;
Over 85% of the clinical cases are non-infectious, and
An infectious case is rendered non-infectious within one week, most often after the very first dose of treatment.
SYMPTOMS
Leprosy mainly affects the skin and peripheral nerves.
If left untreated, it can lead to progressive and permanent damage of nerves, leading to loss of sensation and sweating in the extremities and paralysis of muscles in the hands, feet and face.
The disease is classified as paucibacillary (PB) or multibacillary (MB), depending on the bacillary load.
PB leprosy is a milder disease characterized by few (up to five) skin lesions (pale or reddish), whereas MB is associated with multiple (more than five) skin lesions, nodules, plaques, thickened dermis or skin infiltration.
HISTORY OF THE DISEASE
The first known written mention of leprosy is dated 600 BC.
Leprosy was recognized in the ancient civilizations of China, Egypt and India.
All countries of the South-East Asia Region were known to be endemic for leprosy.
Throughout history, the afflicted have often been ostracized by their communities and families. This situation has changed since leprosy is now completely curable and there is greater awareness about the disease.
HISTORY OF TREATMENT
The first breakthrough occurred in the 1940s with the development of the drug dapsone, which cured the disease. But the duration of the treatment of leprosy was many years, even a lifetime, making it difficult for patients to be regular in their treatment.
In the 1960s, M. leprae started to develop resistance to dapsone, the world’s only known anti-leprosy drug at that time.
TREATMENT TODAY
In 1981, a World Health Organization (WHO) Study Group recommended multi-drug therapy (MDT), a combination of three drugs.
MDT effectively kills the pathogen and cures the patient.
Treatment provided in the early stages averts disability.
With minimal training, leprosy can be easily diagnosed by clinical signs alone.
WHAT IS MDT
MDT comprises of three drugs, dapsone, rifampicin and clofazimine. Rifampicin and clofazimine were discovered in the early 1960s.
MDT is safe, effective and easily administered under field conditions.
MDT is available in convenient monthly calendar blister packs.
Since 1995, WHO has been providing free MDT for all patients in the world, initially through the drug fund provided by the Nippon Foundation and since 2000, through the MDT donation provided by Novartis and the Novartis Foundation for Sustainable Development.
Novartis has pledged free supply of MDT till 2010.
HIGH EFFECTIVENESS OF MULTIDRUG THERAPY
Transmission of leprosy is interrupted after the very first dose of MDT. In other words, patients are no longer infectious to others after being administered the first dose of the treatment regimen.
PB patients treated with MDT are cured within six months.
MB patients treated with MDT are cured within 12 months.
There are virtually no relapses, i.e. no recurrences of the disease after treatment is completed.
No resistance of the bacillus to MDT has been detected.
WHO estimates that early detection and treatment with MDT has prevented about four million people from becoming disabled.
MDT is very cost-effective as a health intervention, considering the economic and social losses averted.
THE ELIMINATION OF LEPROSY AS A PUBLIC HEALTH PROBLEM
In 1991 World Health Assembly passed a resolution to eliminate leprosy as a public health problem by the year 2000. Elimination of leprosy as a public health problem is defined as a prevalence rate of less than one case per 10,000 population.
Globally, the leprosy elimination goal was achieved in 2000.
The global disease burden reduced from 5.2 million in 1985 to 805,000 in 1995 to 753,000 at the end of 1999 to about 219,826 cases at the end of 2005.
The South-East Asia Region, including India, achieved the elimination goal in December 2005.
The Regional prevalence rate steadily declined from 4.6/10,000 population in 1996 to 0.82/10,000 population as of July 2006.
The Regional new case detection also declined from a peak of 47.8/100,000 in 1998 to 11.9/100,000 as of March 2006.
Between 1985 and 2005, more than 15 million leprosy cases were cured globally. Of these, about 12.8 million were from the SEA Region, of which India accounted for about 11.8 million.
The SEA Region has made substantial contribution to the achievement of leprosy elimination globally.
CURRENT LEPROSY SITUATION
At the beginning of 2006, about 219,826 cases were under MDT globally and the prevalence rate was about 0.2 per 10,000 population.
Globally, 296,499 new cases of leprosy were detected during 2005.
The top 10 countries in new case detection in 2005 are India, Brazil, Indonesia, DR Congo, Bangladesh, Nepal, Mozambique, Nigeria, Ethiopia and Tanzania. Together, they constitute about 96% of the 2005 global new case detection.
The SEA Region contributed to about 69% of the 2005 global new case detection.
Six countries (small countries with <1 million population excluded), Brazil, DR Congo, Madagascar, Mozambique, Nepal and Tanzania are yet to achieve the elimination goal.
In the SEA Region, two countries, Nepal and Timor-Leste (population of Timor-Leste is less than 1 million) are yet to achieve elimination.
As of December 2005, the PR in Nepal was 1.81/10,000 and Timor-Leste 1.89/10,000 population. These countries are expected to achieve elimination in 2006 or 2007.
REMAINING CHALLENGES
Achieving elimination in the remaining countries and sustaining elimination in the countries that have achieved the goal at the national level.
Sustaining political commitment and ensuring adequate resources in order to sustain elimination at national level, and progress towards further reducing the burden of leprosy.
Strengthening integration of leprosy services into the general health system through capacity building and skill development, in order to ensure and sustain quality leprosy services, including diagnosis and treatment and prevention/care of disabilities.
Ensuring a wider coverage of leprosy services, especially in currently under-served population groups such as remote rural areas, urban slums, migrant labour.
Increasing and sustaining community awareness through sustained advocacy and IEC activities to promote voluntary case detection and decrease the stigma.
Minimizing/preventing operational factors, such as:
Setting case detection targets and basing performance appraisal on target achievement
Over-diagnosis and re-registration of cases due to:
Non-adherence to WHO-recommended case definitions
Active search and surveys repeatedly targeting the same population groups
Repeated leprosy elimination campaigns in the same areas
Lack of “Quality” and “Accuracy” of diagnosis
Multiple registration
Wrong classification - PB cases recorded as MB (more frequent than vice-versa)
Delayed treatment completion due to:
Irregularity
Drug shortage at peripheral level
Delayed release from treatment
Over-treatment
Non-existent cases
Job insecurity among vertical staff leading to large number of suspect/doubtful cases being recorded as leprosy cases
Preventing discrimination and displacement of leprosy affected and ensuring community based rehabilitation and integration of cured/disabled leprosy persons into the community.
Streamlining the MDT supply and stock management at all levels, considering the low endemic situation.
Strengthening existing partnerships and identifying new partners to support leprosy activities.
THE STRATEGY FOR LEPROSY ELIMINATION
Sustain leprosy services and activities in all endemic countries.
Use annual new case detection and cure rates as the main indicator to monitor progress.
Ensure high-quality diagnosis, case management, recording and reporting in all endemic countries.
Strengthen routine and referral services.
Discontinue the campaign approach, since they are not cost-effective any more and lead to over-detection.
Develop tools and procedures that are home/community-based, integrated and locally appropriate for the prevention of disabilities/impairments and for the provision of rehabilitation services.
Promote operational research in order to improve implementation of a sustainable strategy.
Encourage supportive working arrangements with partners at all levels.
www.searo.who.int/en/Section10/Section20/Section2293.htm
ALAMAT
Jl. Sungai Kundur Kelurahan Mariana
Kecamatan Banyuasin I - Kabupaten Banyuasin
Provinsi Sumatera Selatan
Indonesia Kode Pos Mariana 30763
Kotak Pos 1364 Palembang 30000
Telp.0711-537201 - Fax : 0711-537204
Alamat Email : rsdr_rivaiadullah@yahoo.co.id
atau : rsrivaiabdullah@gmail.com
Hubungi Bagian Informasi
RUMAH SAKIT KUSTA Dr. RIVAI ABDULLAH PALEMBANG
Telp.(0711)537201 Ext. 220
Kecamatan Banyuasin I - Kabupaten Banyuasin
Provinsi Sumatera Selatan
Indonesia Kode Pos Mariana 30763
Kotak Pos 1364 Palembang 30000
Telp.0711-537201 - Fax : 0711-537204
Alamat Email : rsdr_rivaiadullah@yahoo.co.id
atau : rsrivaiabdullah@gmail.com
Hubungi Bagian Informasi
RUMAH SAKIT KUSTA Dr. RIVAI ABDULLAH PALEMBANG
Telp.(0711)537201 Ext. 220
FASILITAS UMUM
1. Sarana Sport Centre
2. Gedung Serba Guna
3. Penginapan/Guest House
4. Kolam pemancingan ikan
5. Hospital garden
2. Gedung Serba Guna
3. Penginapan/Guest House
4. Kolam pemancingan ikan
5. Hospital garden
PELAYANAN POLIKLINIK
Jam buka poliklinik adalah sbb :
1. Senin s.d Kamis : 08.00 s.d 13.00 WIB
2. Jum'at : 08.00 s.d 11.00 WIB
3. Sabtu : 08.00 s.d 12.00 WIB
1. Senin s.d Kamis : 08.00 s.d 13.00 WIB
2. Jum'at : 08.00 s.d 11.00 WIB
3. Sabtu : 08.00 s.d 12.00 WIB
FASILITAS PELAYANAN
I. IRD (IGD) 24 JAM
Instalasi rawat Darurat yang siap melayani 24 jam, ditunjang oleh sarana yang baik dan
dan tenaga yang profesional.
II.UNIT LAYANAN
*)Pelayanan pasien kusta terdiri dari :
- Rawat Jalan
- Rawat Inap
- Kamar Operasi/Bedah rekonstruksi
- Fisioterapi
- Okupasi terapi
- Protesa & Orthosa
- Laboratorium
- Rehabilitasi Karya
- Rehabiltasi Medis
- Rehabilitasi Sosial
- Farmasi
- Ambulance
- Radiologi
- Psikologi
- Gizi
*)Pelayanan Pasien Umum terdiri dari :
1. Rawat Jalan
a. Poliklinik Penyakit Dalam
b. Poliklinik Kebidanan, BKIA
c. Poliklinik Mata
d. Poliklinik Gigi
e. Poliklinik Anak
f. Poliklinik Bedah
g. Poliklinik THT
h. Poliklinik Kulit, Kelamin dan Kecantikan
i. Psikologi
j. Fisioterapi
k. Okupasi terapi
l. Protesa & Orthosa
m. Laboratorium 24 jam
n. Radiologi 24 jam
o. Farmasi 24 jam
p. Gizi
2. Rawat Inap
a. Ruang rawat inap umum terpisah dengan ruang rawat inap kusta.
b. Kapasitas tempat tidur 50 TT terdiri dari :
- Kelas I, sebanyak 5 tempat tidur
- Kelas II, sebanyak 10 tempat tidur
- Kelas III, sebanyak 35 tempat tidur
3. Instalasi Bedah
Pelayanan operasi/bedah meliputi bedah rekonstruksi, bedah umum, Sectio Caesarian (SC),
perasi mata, bedah kulit dan tindakan operasi kecil lainnya.
III. SARANA & PENUNJANG MEDIK
Untuk menunjang pelayanan, kami menyediakan :
1. USG Kebidanan
2. Ultrasound with imazing system
3. USG Fisioterapi
4. Diathermy
5. E K G
6. Laboratorium
7. Radiologi
8. Kamar Operasi
9. Konsultasi Gizi
10. Apotik 24 jam
11. Mobil Ambulance 118
12. Mobil Jenazah
13. Kolam Renang Rehabilitasi medik
14 Dermaga dan Poliklinik Terapung
Instalasi rawat Darurat yang siap melayani 24 jam, ditunjang oleh sarana yang baik dan
dan tenaga yang profesional.
II.UNIT LAYANAN
*)Pelayanan pasien kusta terdiri dari :
- Rawat Jalan
- Rawat Inap
- Kamar Operasi/Bedah rekonstruksi
- Fisioterapi
- Okupasi terapi
- Protesa & Orthosa
- Laboratorium
- Rehabilitasi Karya
- Rehabiltasi Medis
- Rehabilitasi Sosial
- Farmasi
- Ambulance
- Radiologi
- Psikologi
- Gizi
*)Pelayanan Pasien Umum terdiri dari :
1. Rawat Jalan
a. Poliklinik Penyakit Dalam
b. Poliklinik Kebidanan, BKIA
c. Poliklinik Mata
d. Poliklinik Gigi
e. Poliklinik Anak
f. Poliklinik Bedah
g. Poliklinik THT
h. Poliklinik Kulit, Kelamin dan Kecantikan
i. Psikologi
j. Fisioterapi
k. Okupasi terapi
l. Protesa & Orthosa
m. Laboratorium 24 jam
n. Radiologi 24 jam
o. Farmasi 24 jam
p. Gizi
2. Rawat Inap
a. Ruang rawat inap umum terpisah dengan ruang rawat inap kusta.
b. Kapasitas tempat tidur 50 TT terdiri dari :
- Kelas I, sebanyak 5 tempat tidur
- Kelas II, sebanyak 10 tempat tidur
- Kelas III, sebanyak 35 tempat tidur
3. Instalasi Bedah
Pelayanan operasi/bedah meliputi bedah rekonstruksi, bedah umum, Sectio Caesarian (SC),
perasi mata, bedah kulit dan tindakan operasi kecil lainnya.
III. SARANA & PENUNJANG MEDIK
Untuk menunjang pelayanan, kami menyediakan :
1. USG Kebidanan
2. Ultrasound with imazing system
3. USG Fisioterapi
4. Diathermy
5. E K G
6. Laboratorium
7. Radiologi
8. Kamar Operasi
9. Konsultasi Gizi
10. Apotik 24 jam
11. Mobil Ambulance 118
12. Mobil Jenazah
13. Kolam Renang Rehabilitasi medik
14 Dermaga dan Poliklinik Terapung
SUMBER DAYA MANUASIA(KETENAGAAN)
1. Dokter Spesialis Kulit & Kecantikan : 2 orang
2. Dokter Spsialis Obgin (Kebidanan) : 3 orang
3. Dokter Spesialis Mata : 2 orang
4. Dokter Spesialis Anaesthesi : 1 orang
5. Dokter Spesialis Penyakit Dalam : 2 orang
6. Dokter Spesialis Anak : 2 orang
7. Dokter Spesialis Gigi Anak : 1 orang
8. Dokter Gigi : 1 orang
9. Dokter Umum : 15 orang
10. Sarjana Farmasi/Apoteker : 3 orang
11. Psikolog : 1 orang
12. Paramedis Perawatan : 112 orang
13. Paramedis Non Perawatan : 46 orang
14. Non medis non Paramedis : 125 orang
2. Dokter Spsialis Obgin (Kebidanan) : 3 orang
3. Dokter Spesialis Mata : 2 orang
4. Dokter Spesialis Anaesthesi : 1 orang
5. Dokter Spesialis Penyakit Dalam : 2 orang
6. Dokter Spesialis Anak : 2 orang
7. Dokter Spesialis Gigi Anak : 1 orang
8. Dokter Gigi : 1 orang
9. Dokter Umum : 15 orang
10. Sarjana Farmasi/Apoteker : 3 orang
11. Psikolog : 1 orang
12. Paramedis Perawatan : 112 orang
13. Paramedis Non Perawatan : 46 orang
14. Non medis non Paramedis : 125 orang
MOTTO RSK Dr. RIVAI ABDULLAH
"MEMBERIKAN PELAYANAN YANG OPTIMAL AGAR ANDA DAPAT BERKARYA DAN LEBIH PRODUKTIF"
VISI DAN MISI RSK Dr.RIVAI ABDULLAH
VISI :
- Terwujudnya Pelayanan Kesehatan Masyarakat yang optimal dengan Unggulan Kusta dan Pelayanan Spesifik Spesialistik.
MISI :
1. Meningkatkan disiplin karyawan
2. Meningkatkan dan memenuhi kualitas dan kuantitas sumber daya manusia
3. Memenuhi dan membedayakan secara optimal sarana dan prasarana sesuai kebutuhan
4. Membuat kebijakan yang tepat sesuai Visi Rumah Sakit
5. Membina kerjasama lintas sektoral
6. Meningkatkan pembinaan di wilayah binaan
7. Menjadikan Rumah Sakit sebagai tujuan wisata medis dan wisata sosial
8. Menjadikan Rumah Sakit sebagai pusat riset dan pelayan rujukan penyakit tropis,
rawa dan perairan
- Terwujudnya Pelayanan Kesehatan Masyarakat yang optimal dengan Unggulan Kusta dan Pelayanan Spesifik Spesialistik.
MISI :
1. Meningkatkan disiplin karyawan
2. Meningkatkan dan memenuhi kualitas dan kuantitas sumber daya manusia
3. Memenuhi dan membedayakan secara optimal sarana dan prasarana sesuai kebutuhan
4. Membuat kebijakan yang tepat sesuai Visi Rumah Sakit
5. Membina kerjasama lintas sektoral
6. Meningkatkan pembinaan di wilayah binaan
7. Menjadikan Rumah Sakit sebagai tujuan wisata medis dan wisata sosial
8. Menjadikan Rumah Sakit sebagai pusat riset dan pelayan rujukan penyakit tropis,
rawa dan perairan
TUGAS POKOK RSK Dr.RIVAI ABDULLAH PALEMBANG
*Berdasarkan SK.Menkes.RI No.185/MENKES/SK/II/1993 tanggal 26 Februari 1993, Rumah Sakit Kusta Dr.Rivai abdullah Palembang merupakan Rumah Sakit Rujukan Kusta untuk wilayah Indonesia Bagian barat meliputi seluruh Sumatera dan Kalimantan Barat.
Tugas Pokok RS.Kusta Dr.Rivai Abdullah Palembang adalah :
"Melaksnakan pelayanan pasien penyakit kusta secara menyeluruh, terpadu dan berkesinambungan, kegiatan pendidikan, pelatihan, pengkajian, dan pengembangan di bidang kesehatan kusta sesuai dengan peraturan perundang-undangan yang berlaku"
SEJARAH SINGKAT RSK Dr.RIVAI ABDULLAH
*Pada mulanya hanya sebagai tempat penampungan/pengasingan penderita kusta bernama KEMBANG PUMPUNG yang berlokasi di daerah Kertapati-Palembang, pendiriannya atas prakarsa seorang nakhoda kapal Belanda pada tahun 1914.
*Selanjutnya dipindahkan ke lokasi sekarang yaitu di Sungai Kundur keluarahan Mariana Kecamatan Banyuasin I Kabupaten Banyuasin, jarak dari kota Palembang ke Mariana + 20 Km dan terletak di pinggir Sungai Musi.
*Sampai dengan tahun 1960 Rumah sakit ini dikelola oleh sebuah yayasan yang kegiatan internnya dilakukan oleh BALA KESELAMATAN.
*Dengan terbitnya SK.Menkes.RI Nomor : 95048/Hukum tanggal 9 Desember 1960, maka pada tanggal 1 April 1961 oleh BALA KESELAMATAN diserahkan kepada Departemen Kesehatan RI.
* Berdasarkan SK.Menkes.RI Nomor : 270/MENKES/SK/VI/1985 tanggal 4 Juni 1985, RS.Kusta Sungai Kundur Palembang menjadi RS.Kusta Pembina untuk wilayah Regional Barat, meliputi seluruh pulau Sumatera dan Kalimantan Barat.
*Berdasarkan SK.Menkes.RI Nomor : 185/MENKES/SK/II/1993 tanggal 26 Februari 1993, Organisasi dan Tata Kerja RS.Kusta Sungai Kundur Palembang meningkat dari eselon III.b menjadi eselon II.b.
*Berdasarkan Surat Direktur Jenderal Pelayanan Medik Dep.Kes.RI Nomor : BM.01.03.3.2.04929A tanggal 31 Desember 1995 tentang Izin Memberikan Pelayanan Umum, telah dirintis berbagai langkah hingga RS.Kusta Sungai Kundur Palembang dapat memberikan pelayanan kepada masyarakat umum, khususnya bagi masyarakat yang berdomisili di sekitar Rumah Sakit.
*Dilanjutkan dengan SK menkes.RI No.HK.00.06.1.4.3399 tanggal 26 Agustus 2002 tentang Penunjukan Uji Coba RS.Kusta Sungai Kundur Palembang untuk Melaksnakan Pelayanan Umum, dengan Unggulan Kusta, Rehabilitasi Medik dan Pusat Rehabilitasi Stroke.
*RS.Kusta Sungai Kundur Palembang berubah nama menjadi : " RUMAH SAKIT KUSTA
Dr. RIVAI ABDULLAH PALEMBANG", sesuai SK.Menkes.RI No.: 630/MENKES/SK/VIII/2006 tanggal 10 Agustus 2006. dDr. Rivai Abdullah adalah Direktur kedua RS.Kusta Sungai kundur Palembang dari tahun 1971 s.d tahun 1986, selama kepemimpinannya, beliau sangat berjasa dalam pengembangan fisik maupun pelayanan.
*Selanjutnya dipindahkan ke lokasi sekarang yaitu di Sungai Kundur keluarahan Mariana Kecamatan Banyuasin I Kabupaten Banyuasin, jarak dari kota Palembang ke Mariana +
*Sampai dengan tahun 1960 Rumah sakit ini dikelola oleh sebuah yayasan yang kegiatan internnya dilakukan oleh BALA KESELAMATAN.
*Dengan terbitnya SK.Menkes.RI Nomor : 95048/Hukum tanggal 9 Desember 1960, maka pada tanggal 1 April 1961 oleh BALA KESELAMATAN diserahkan kepada Departemen Kesehatan RI.
* Berdasarkan SK.Menkes.RI Nomor : 270/MENKES/SK/VI/1985 tanggal 4 Juni 1985, RS.Kusta Sungai Kundur Palembang menjadi RS.Kusta Pembina untuk wilayah Regional Barat, meliputi seluruh pulau Sumatera dan Kalimantan Barat.
*Berdasarkan SK.Menkes.RI Nomor : 185/MENKES/SK/II/1993 tanggal 26 Februari 1993, Organisasi dan Tata Kerja RS.Kusta Sungai Kundur Palembang meningkat dari eselon III.b menjadi eselon II.b.
*Berdasarkan Surat Direktur Jenderal Pelayanan Medik Dep.Kes.RI Nomor : BM.01.03.3.2.04929A tanggal 31 Desember 1995 tentang Izin Memberikan Pelayanan Umum, telah dirintis berbagai langkah hingga RS.Kusta Sungai Kundur Palembang dapat memberikan pelayanan kepada masyarakat umum, khususnya bagi masyarakat yang berdomisili di sekitar Rumah Sakit.
*Dilanjutkan dengan SK menkes.RI No.HK.00.06.1.4.3399 tanggal 26 Agustus 2002 tentang Penunjukan Uji Coba RS.Kusta Sungai Kundur Palembang untuk Melaksnakan Pelayanan Umum, dengan Unggulan Kusta, Rehabilitasi Medik dan Pusat Rehabilitasi Stroke.
*RS.Kusta Sungai Kundur Palembang berubah nama menjadi : " RUMAH SAKIT KUSTA
Dr. RIVAI ABDULLAH PALEMBANG", sesuai SK.Menkes.RI No.: 630/MENKES/SK/VIII/2006 tanggal 10 Agustus 2006. dDr. Rivai Abdullah adalah Direktur kedua RS.Kusta Sungai kundur Palembang dari tahun 1971 s.d tahun 1986, selama kepemimpinannya, beliau sangat berjasa dalam pengembangan fisik maupun pelayanan.
DIREKSI
1. DIREKTUR : Dr. H. Bayu Wahyudi, MPH.M, Sp.OG
2. WADIR ADM.UMUM & KEUANGAN : Dra.Hj. Kartini, MARS
3. WADIR PELAYANAN & REHABILITASI : Dr. H. Raden Pamudji, Sp.KK
4. Ketua Komite Medis : Dr. H. Mustofa Husin Syahab, Sp.OG
2. WADIR ADM.UMUM & KEUANGAN : Dra.Hj. Kartini, MARS
3. WADIR PELAYANAN & REHABILITASI : Dr. H. Raden Pamudji, Sp.KK
4. Ketua Komite Medis : Dr. H. Mustofa Husin Syahab, Sp.OG
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