About Me

THIS IS ONLY A COLLEGIUM OF PUBLIC HEALTH INTERESTED PERSONS WHO ARE OFFICIALLY DESIGNATED AS HEALTH SUPERVISORS IN KERALAHEALTH SERVICES NOT AN ORGANISATION OR A UNION OF EMPLOYEES TO FIGHT BUT TO SHARE THE IDEAS& INNOVATIONS THAT CAN BE USED FOR THE WELFARE OF PUBLIC.ALL HEALTH SUPERVISORS ARE APPEALED TO SHARE THIS PLATFORM WITHOUT DISTURBING THEIR OWN POLITICAL AND SOCIAL VIEWS.LET US THINK TOGETHER ACT TOGETHER TO CONFIRM A SPACE FOR PUBLIC HEALTH STAFF

Friday, 25 April 2014

KYASANUR FOREST     DISEASE

    Kyasanur forest disease is an arthropod borne viral disease
discovered in shimoga district of Karnataka state during March-1957.(
The disease first manifested as anepizootic outbreak among monkeys killing several of them in the year 1957. Hence the disease is also locally known as Monkey Disease or Monkey Fever.)
ETIOLOGY:- The disease is caused by " B"  group Arbo Virus. The agent
KFD Virus is a RNA Genome Virus of the genus flavi virus, Family flavi
viride. It is antigenicaly related to  Langat, DHF and westnile
viruses.

GEOGRAPHICAL DISTRIBUTION;-
    KFD was persisting only in 5 Districts of Karnataka namely Shimoga,
Chickmagalur, Dakshina Kannada, Uttara Kannada and Udupi till 2012. In
December -2012 incidences of KFD  was confirmed in monkeys, Ticks and
Human in Chamarajanagara District. Incidence of KFD in Monkey was
confirmed in Mysore district in January-2013. Later incidences of KFD
in monkey was also confirmed in Nilgiris district of Tamilnadu. One
incidence of Human was confirmed In Kerala State also.

EPIDEMIOLOGY:- The disease affects all ages in both sexes .  But it is
common in young people who are more exposed to forest. This is a
seasonal disease usually from December to May. During this period,
nymphal stage of Tick is very active, the exposure of Human is also
more in the forest.
MODE OF TRANSMISSION;- The disease is transmitted by the bite of
infected ticks.(
The vector for disease transmission is Haemaphysalis spinigera, a forest tick. Humans contract infection from the bite of nymphs of the tick.) The nymphal  stage of tick is primarily responsible for the transmission of the disease. The ticks once infected remains
infective through out their life. The tick belongs to genus
Heamophysalis and speices spinigera which is the commonest vector.
Incubation period is 3 - 8 days.

CLINICAL SIGNS AND SYMPTOMS:-  The onset is sudden with high fever,
severe headache, Nausea and Severe bodypain more in back and legs. The
viremia is upto 12 days maximum between 3 - 6 days. Persons with above
symptoms may be treated in the nearest Primary Health Centre. I E C
activities to be carried out for the local people.
HAEMATOLOGICAL MANIFESTATION:- There may be bleeding from nose, gums,
rectum, urethra person may become hypotensive leading to shock.
NEUROLOGICAL SYMPTOMS;- Drowsiness, twitching of muscles, tremors,
convulsions and neck stiffness.
TREATMENT FOR THE KFD PATIENTS;- There is no specific treatment for
KFD. Hence, all the  patients are treated symptomatically. Correction
severe dehydration by infusion of I.V. Fluids, use of antipyretics to
control fever help in recovery of patients. There is no special drug
for KFD, therefore following steps are adopted for treating the
patients.
a)    Early hospitalization.
b)    Absolute bedrest.
c)    Administration of oral and I.V.Fluids.
d)    Vitamin C and K.
e)    Antibiotics.
f)    Eye ointment.
g)    Injection perinorm.
h)    If there is cerebral edema 10% Dextrose I.V or Manitol should be
administered.
i)    Inj. Batrophase and blood transfusion in case of haemorraghic symptoms.

SURVEILLANCE PROGRAMME;-  Active and intensive surveillance should be
carried out. The following preventive measures are to be taken in KFD
epidemic area.
1)    People should be advised not  to go to the forest where monkey
deaths are reported.
2)    Persons whose visit to the forest is inevitable should be advised
to cover the body with thick cloths and Gum boots.
3)    Application of D.M.P Oil (Insect repellent) to expose parts before
going to forest.
4)    Washing clothes and body with hotwater and soap, after returning
from the forest.
5)    Incidences of human fever cases and unnatural monkey deaths
occurred KFD epidemic area to be monitored and detail information be
communicated to health authorities.
6)    Monkey death should be reported to the nearest PHC/PHU/CSC/GH.
Samples of brain, Lungs, Heart, Kidney and Lever may be collected from
dead monkey (Fresh) in Sterile plastic vials by Health workers with
the co-operation of local Veterinarians and transported in cold chain
to VDL, Shimoga. Carcass of the dead monkey should be burnt after
collection of samples. Hot spot dusting with Malathion powder in the
areas were monkey death have been reported with in 50 meter radius
around the spot of monkey death besides the endemic foci.
7)    Haemaphysalis spinigera, H.Turturis, H.Kinneri and H.Kyasanurensis,
are the commonest vector of KFD. Collection of ticks, larvae, nymphs
are carriedout by flag dragging method. Some of the ticks are
collected from domestic animals and body of the forest workers and
arround Hot spots where unnatural monkey deaths have occurred by
plucking method. Ticks samples are labled and sent in cold-chain to
VDL.Shimoga.
8)    The surveillance programme includes detection of Human fever cases.
Collection of suspected human blood samples for diagnosis is
necessary.  3 - 5 ml of serum is to be collected aseptically labled
and sent in cold-chain to VDL Shimoga.
KFD VACCINATION PROGRAMME;- KFD vaccination is the Key for the whole
programme. The timing of vaccination should be linked to the
transmission cycle so that people can be protected. Population at risk
should immunized.
a)    Population at risk
1)    Previously affected villages.
2)    Surrounding villages of 5 kms radius around monkey deaths, Tick
positives and Human positives.
b)    Planning of vaccination:-
1)    Population at risk are to be identified.
2)    Estimation of doses of vaccine required.
3)    Emphasis should be on I.E.C. activities to create awareness about
vaccination in the community.
    C) Vaccination schedule:-
          1) Two doses at an interval of one month.
          2) Age group  6 - 14 years -  0.5 ml S C route.
                                  15 - 65 years - 1.0 ml S C route.
4)    Booster dose is administered after  6 - 9 months.
            Warning: Vaccine should not be administered to pregnant
women, person allergic to Gentamycin, Crystaline pencilin and Egg
protein, and also to person with symptoms of  Jaundice and Cardiac
complaints.
            There will be irritation at the site of inoculation for 2
- 8 minutes.
  D) Storage of Vaccine:-
        1) Vaccine should be stored at + 2 C to + 4 C temperature.
Vaccine should not be frozen at any cost, if frozen discard

Sunday, 18 August 2013

tIcf tÌäv sl¯v C³kvs]IvtSgvkv bqWnb³
                        eb\ kt½f\w:kzmKXkwLw P\d I¬ho\റുടെ                                                                അഭ്യര്‍ത്ഥന
kplrt¯,
BtcmKyhIp¸nse sl¯vC³kvs]IvSÀ hn`mKw Poh\¡mcpsS aq¶p kwLS\IÄ ebn¨v ""tIcf tÌäv sl¯v C³kvs]IvtSgvkv bqWnb³'' F¶ Hä kwLS\bmbn {]hÀ¯n¡m³ Xocpam\n¨ hnhcw Adnªncn¡patÃm? kwLS\bpsS eb\kt½f\w 2013 sk]väw_À 7þmw XobXn tIm«b¯ph¨v \S¯m³ Xocpam\n¨ncn¡pIbmWv.
sl¯vC³kvs]IvSÀ hn`mK¯n\v GI kwLS\ aXnsb¶ Xocpam\¯nsâ {]kàn DÄs¡mÅpsa¶v {]Xo£n¡s«. s]mXphmb Bhiy§Ä t\SnsbSp¡p¶Xnt\msSm¸w sl¯v kq¸ÀsshkÀamcptSXmb {]tXyI {]iv\§Ä¡p ]cnlmcw ImWp¶Xn\pw GIkwLS\bpsS ¹mävt^mw BhiyamWv. Cu kmlNcy¯n eb\kt½f\w hnPbn¸nt¡ണ്ടXv \½psS D¯chmZn¯ambn ]cnKWn¨v ആവശ്യമായ സഹായ  klIcW§Ä D­­ണ്ടmIWsa¶v A`yÀ°nച്ചുകൊള്ളു¶p. eb\ kt½f\¯n എല്ലാവരെയും പങ്കെടുപ്പിക്കുന്നതിനും അനുബന്ധ പ്രവര്‍ത്തനങ്ങള്‍ക്കും ap³ssIs¿Sp¡patÃm?


kt½f\¯n ]s¦Spക്കുവാന്‍ ഏവരേയും A£c\Kcnbnte¡v ഹാര്‍ദ്ദമായി kzmKXw sNയ്തുകൊള്ളുന്നു.

     sI.Fw.km_p¡p«n
    (sl¯vkq¸ÀsshkÀ)
kzmKX kwLwP\d I¬ho\À                    
                     

Tuesday, 13 August 2013

                              AN IMPORTANT ANNOUNCEMENT

DEAR  FRIENDS,


A STATE LEVEL DISUSSION MEETING  OF OUR COLLEGIUM  IS DECIDED TO BE HELD  ON 22 AUGUST 2013 AT THE  RED CROSS HALL,GENERAL HOSPITAL COMPOUND , ERNAKULAM AT  10am.KINDLY MAKE  IT CONVENIENT  TO  PARTICIPATE   THE MEETING IN TIME.  THREE REPRESENTATIVES FROM EACH DISTRICT INCLUDING THE DISTRICT CONVENER  OF OUR COLLEGIUM ARE  EXPECTED TO  PARTICIPATE THE MEETING.KINDLY  CONDUCT A DISTRICT LEVEL  DISCUSSION  MEETING AMONG HEALTH SUPERVISORS IN YOUR DISTRICT  BEFORE  22-8-2013 AND PREPARE  PRIORITISED LIST OF MEASURES AND STEPS TO BE CONSIDERED FOR THE STATE LEVEL SITTING   AS THIS IS OUR FIRST DETAILED MEETING  TO FINALISE OUR FUTURE PLANS.PLEASE DO CONTRIBUTE BY OFFERING YOUR  ESTEEMED (REPRESENTED OR SELF) PRESENCE.

Thursday, 18 July 2013







കേരളഹെല്‍ത്ത്‌ ഇന്‍സ്പെക്ടഴ്സ് യൂണിയന്‍റെയും കേരള പബ്ലിക്ഹെല്‍ത്ത്‌ സ്റ്റാഫ് 
ആക്ഷന്‍കൌണ്‍സിലിന്‍റെയും സംസ്ഥാന അധ്യക്ഷനെന്ന നിലയിൽ നിസ്വാര്‍ത്ഥ സേവനമനുഷ്ഠിച്ച് സര്‍വ്വീസിൽനിന്ന് വിരമിച്ച ശ്രി.എം.എം.അഷ്‌റഫിന് ആരോഗ്യപ്രവര്‍ത്തകരുടെ അഭിവാദ്യങ്ങൾ.



എം.എം. അഷ്‌റഫിന് യാത്രയയപ്പ്   കൊച്ചി: സര്‍വീസിൽ നിന്ന് വിരമിച്ച കേരള ഹെല്‍ത്ത് ഇന്‍സ്‌പെക്ടേഴ്‌സ് യൂണിയൻ സംസ്ഥാന പ്രസിഡന്റും കേരള പബ്ലിക് ഹെല്‍ത്ത് സ്റ്റാഫ് ആക്ഷൻ കൗണ്‍സില്‍ സംസ്ഥാന ചെയര്‍മാനുമായ എം.എം. അഷ്‌റഫിന് യാത്രയയപ്പ് നല്‍കി. യാത്രയയപ്പ് സമ്മേളനം മന്ത്രി കെ. ബാബു ഉദ്ഘാടനം ചെയ്തു.സംസ്ഥാന ജനറൽ സെക്രട്ടറി കെ. സത്യൻ അധ്യക്ഷത വഹിച്ചു. എറണാകുളം ജില്ലാ പഞ്ചായത്ത് പ്രസിഡന്റ് അഡ്വ. എല്‍ദോസ് കുന്നപ്പിള്ളി, മരട് നഗരസഭാ ചെയര്‍മാൻ അഡ്വ. ടി.കെ. ദേവരാജൻ, എന്‍.ജി.ഒ. അസോസിയേഷൻ സംസ്ഥാന ജനറൽ സെക്രട്ടറി കെ.വി. മുരളി, ജോയിന്റ് കൗണ്‍സിൽ ജില്ലാ സെക്രട്ടറി പോള്‍ വര്‍ഗീസ്, എന്‍.ജി.ഒ. സംഘ് ജില്ലാ സെക്രട്ടറി പി.ആര്‍. സുനില്‍കുമാർ, കേരള ഗവ. മെഡിക്കൽ ഓഫീസേഴ്‌സ് അസോസിയേഷൻ ജില്ലാ വൈസ് പ്രസിഡന്റ് ഡോ. കെ.എം. മുഹമ്മദ് സലിം, കേരള ഗവ. ഫാര്‍മസിസ്റ്റ് അസോസിയേഷൻ ജനറൽ സെക്രട്ടറി ഇ.വി. രാജേന്ദ്രൻ, കേരള ഹെല്‍ത്ത് സര്‍വീസസ് മിനിസ്റ്റീരിയൻ സ്റ്റാഫ് അസോസിയേഷൻ ജില്ലാ പ്രസിഡന്റ് റെജി മാത്യു, കേരള പബ്ലിക് ഹെല്‍ത്ത് സ്റ്റാഫ് ആക്ഷൻ കൗണ്‍സിൽ സംസ്ഥാന കണ്‍വീനർ എസ്. ലെസിത, കേരള ഹെല്‍ത്ത് ഇന്‍സ്‌പെക്ടേഴ്‌സ് യൂണിയൻ സംസ്ഥാന വൈസ് പ്രസിഡന്റ് ടി. ബൈജുകുമാർ, സെക്രട്ടറി കെ.എൽ. സെബാസ്റ്റ്യൻ, ട്രഷറർ പവിത്രേശ്വരം രവികുമാർ തുടങ്ങിയവർ പ്രസംഗിച്ചു. ജില്ലാ സെക്രട്ടറി എം.എം. സക്കീർ സ്വാഗതവും ജില്ലാ പ്രസിഡന്റ് സി.എം. ജോണി നന്ദിയും പറഞ്ഞു. എം.എം. അഷ്‌റഫ് മറുപടി പ്രസംഗം നടത്തി.

Thursday, 11 July 2013



CHOLERA REPORTED  FROM KOTTAYAM DISTRICT !!!


TWO CASES OF CHOLERA HAS BEEN REPORTED FROM KOTTAYAM DISTRICT. ONE CASE AT ETTUMANOOR AND ONE CASE AT ATHIRAMPUZHA. EPIDEMIC ALERT AND EPIDEMIC PREDICTION HAS BEEN ALREADY GIVEN TO ALL INSTITUTIONS.


THIS IS A WARNING SIGNAL SO EVERYBODY SHOULD TAKE CARE AND INITIATE ALL POSSIBLE MEASURES TO PREVENT OCCURRENCE OF FURTHER CASES.

Cholera is an acute enteric infection caused by the ingestion of bacterium Vibrio cholerae present in faecally contaminated water or food. Primarily linked to insufficient access to safe water and proper sanitation.Cholera is characterized in its most severe form by a sudden onset of acute watery diarrhoea that can lead to death by severe dehydration. The extremely short incubation period - two hours to five days - enhances the potentially explosive pattern of outbreaks, as the number of cases can rise very quickly. About 75% of people infected with cholera do not develop any symptoms. However, the pathogens stay in their faeces for 7 to 14 days and are shed back into the environment, possibly infecting other individuals. Cholera is an extremely virulent disease that affects both children and adults. Unlike other diarrhoeal diseases, it can kill healthy adults within hours. Individuals with lower immunity, such as malnourished children or people living with HIV, are at greater risk of death if infected by cholera.

Diagnosis

The presence of V. cholerae in stools is confirmed through laboratory procedures. However, a new rapid diagnostic test (RDT), now available, allows quick testing at the patient's bedside.
Measures for the prevention of cholera mostly consist of providing clean water and proper sanitation.Communities should be reminded of basic hygienic behaviours, including the necessity of systematic hand-washing with soap after defecation and before handling food or eating, as well as safe preparation and conservation of food.
Among people developing symptoms, 80% of episodes are of mild or moderate severity. The remaining 10%-20% of cases develop severe watery diarrhoea with signs of dehydration. Once an outbreak is detected, the usual intervention strategy aims to reduce mortality - ideally below 1% - by ensuring access to treatment and controlling the spread of disease.

Case management

Efficient treatment resides in prompt rehydration through the administration of oral rehydration salts (ORS) or intravenous fluids, depending of the severity of cases. Up to 80% of patients can be treated adequately through the administration of ORS (WHO/UNICEF ORS standard sachet). Very severely dehydrated patients are treated through the administration of intravenous fluids, preferably Ringer lactate. Appropriate antibiotics can be given to severe cases to diminish the duration of diarrhoea, reduce the volume of rehydration fluids needed and shorten the duration of V. cholerae excretion. For children up to five years, supplementary administration of zinc2 has a proven effective in reducing duration of diarrhoea as well as reduction in successive diarrhoea episodes.
Cholera vaccines
The use of the parenteral cholera vaccine has never been recommended by WHO due to its low protective efficacy and the high occurrence of severe adverse reactions. An internationally licensed oral cholera vaccine (OCV) is currently available on the market in limited stocks and is suitable for travellers. This vaccine was proven safe and effective and is available for individuals aged two years and above. It is administered in two doses 10-15 days apart.

Tuesday, 9 July 2013







A CIRCULAR REGARDING THE D&O INSPECTIONS
IS PUBLISHED FROM THE LOCAL SELF GOVERNMENT DEPARTMENT,AFTER THE SO CALLED  GOVERNMENT ORDER  "SEVANAVAKAASANIYAMAM"

CHP BREAKING NEWS!!!

CHP BREAKING NEWS!!!

 It is brought to the attention of Govt and has finally revised the following exhisting
Micro Sector Codes
No 645, 647 stands modified by excluding the word Consumables" to make the spectrum more wide. 

New Micro Sctor Codes 965,966,967 for  relief and support to HIV patients,Prevention of Diseases;related activities and Medical camp in coastal areas respectively.

Hence it is requested to bring this matter to the notice of all implementing officers and Health staff at the earliest.The last date for including LSGD projects was on 15,06.2013 midnight. However, the date is likely to be extended further. Hence our initiatives to take up Health projects in LSGD Plan May be continued.It is also advisable to include projects for migrants health care,communicable diseases control,NCD primary prevention projects,good quality drinking water and waste management facility for hospitals etc and other innovative projects. It is further expected that model projects included in the LSG plan are likely to be supported financially to a certain % by NRHM as when it is decided by the  authorities.