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 Filariasis is a major parasitic infection, which 
continues to be a public health problem in the 
Philippines. It was first discovered in the Philippines in 
1907 by foreign workers. Consolidated field reports 
showed a prevalence rate of 9.7% per 1000 
population in 1998. It is the second leading cause of 
permanent and long-term disability. The disease 
affects mostly the poorest municipalities in the country 
about 71% of the case live in the 4th-6th class type of 
municipalities.
 The World Health Assembly in 1997 declared 
“Filariasis Elimination as a priority” and followed by 
WHO’s call for global elimination. A sign of the DOH’s 
commitment to eliminate the disease, the program’s 
official shift from control to elimination strategies was 
evident in an Administrative Order #25-A,s 1998 
disseminated to endemic regions. In support to the 
program, an Administrative Order declaring 
“November as Filariasis Mass Treatment Month was 
signed by the Secretary of Health last July 2004 and 
was disseminated to all endemic regions.
 Vision: Healthy and productive individuals and 
families for Filariasis-free Philippines 
 Mission: Elimination of Filariasis as a public 
health problem thru a comprehensive approach 
and universal access to quality health services
 Goal: To eliminate Lymphatic Filariasis as a 
public health problem in the Philippines by year 
2017 
 General Objectives: To decrease Prevalence 
Rate of filariasis in endemic municipalities to 
<1/1000 population.
Specific Objectives: 
The National Filariasis Elimination Program 
specifically aims to: 
1. Reduce the Prevalence Rate to elimination level 
of <1%; 
2. Perform Mass treatment in all established 
endemic areas; 
3. Develop a Filariasis disability prevention program 
in established endemic areas; 
4. Continue surveillance of established endemic 
areas 5 years after mass treatment.
 Human Lymphatic Filariasis is a chronic parasitic 
infection caused by nematode parasites known as 
wuchereria bancrofti, brugia malayi or brugia 
timori.The young and adult worms live in 
lymphatic vessels and lymph nodes while the 
microfilariae are usually found in blood. The life-span 
of the adult parasites is about 10 years ( but 
a 40-year life- span has been reported)while 
microfilariae live for about a year at the most.
 The disease is transmitted to a person through 
bites from a infected female mosquito primarily 
Aedes poecillius that bites at night.
 The filarial life cycle, like that of all nematodes, 
consists of 5 developmental (larval) stages in a 
vertebral host and an arthropod intermediate host and 
vector. Adult female worms produce thousands of first-stage 
larvae, or microfilariae, which are ingested by a 
feeding insect vector. Some microfilariae have a 
unique daily circadian periodicity in the peripheral 
circulation. The arthropod vectors (mosquitoes and 
flies) also have a circadian rhythm in which they obtain 
blood meals. The highest concentration of 
microfilariae usually occurs when the local vector is 
feeding most actively.
 Microfilariae undergo 2 developmental changes in 
the insect. Third-stage larvae then are inoculated 
back into the vertebral host during the act of 
feeding for the final 2 stages of development. 
These larvae travel through the dermis and enter 
regional lymphatic vessels. During the next 9 
months, the larvae develop into mature worms 
(20-100 mm in length). An average parasite can 
survive for about 5 years.
 The prepatent period is defined as the interval 
between a vector bite and the appearance of 
microfilariae in blood, with an estimated duration 
of about 12 months.
 The quantity of accumulating adult worm antigen 
in the lymphatics 
 The duration and level of exposure to infective 
insect bites 
 The number of secondary bacterial and fungal 
infections 
 The degree of host immune response
 Filarial infection generates significant 
inflammatory immune responses that participate in 
the development of symptomatic lymphatic 
obstruction. Increased levels of immunoglobulin E 
(IgE) and immunoglobulin G4 (IgG4) secondary to 
antigenic (from dead worms) stimulation of Th2- 
type immune response have been demonstrated.
 Studies have shown that there is a familial tendency to 
lymphatic obstruction, providing support for the 
hypothesis that host genes influence lymphedema 
susceptibility. Studies also suggest that microfilaremia 
may be increased in individuals with low levels of 
mannose-binding lectin, suggesting a genetic 
predisposition.Further, a propensity to develop chronic 
disease has been demonstrated in patients with 
polymorphisms of endothelin-1 and tumor necrosis 
factor receptor II.
 Prenatal exposure seems to be an important 
determinant in conferring greater immune 
tolerance to parasite antigen. Thus, individuals 
from endemic areas are often asymptomatic until 
late in the disease when they have high worm 
burden, whereas nonimmune expatriates tend to 
have brisk immune responses and more severe 
early clinical symptoms, even in light infections.
 Studies have shown that lymphatic filarial 
parasites contain rickettsialike Wolbachia 
endosymbiotic bacteria. This association has been 
recognized as contributing to the inflammatory 
reaction seen in filariasis.
 The incubation period which starts from the entry 
of the infective larvae to the development of 
clinical manifestation is variable. Nevertheless, it 
ranges from 8-16 months.
ASYMPTOMATIC STAGE: 
 Characterized by the presence of microfilariae in the 
peripheral blood 
 No clinical signs and symptoms of the disease 
 Some remain asymptomatic for years and in some 
instances for life 
 Others progress to acute and chronic stages 
 Microfilariae rate increases with age and then levels off 
 In most endemic areas including the Philippines the 
Philippines, men have higher microlariae rate than 
women.
Starts when there are already manifestation such 
as: 
 Lymphadenitis ( Inflammation of lymph nodes) 
 Lymphangitis ( inflammation of lymph vessels) 
 In some cases, the male genitalia is affected 
leading to funiculitis, epidydimitis, or orchitis 
( redness, painful and tender scrotum)
 Develop 10-15 years from the onset of the first 
attack 
 Immigrants from areas where filariasis is not 
endemic tend to develop this stage more often 
and much sooner (1-2 years) than do the 
indigenous population of endemic areas.
 Hydrocoele (swelling of the scrotum) 
 Lymphedema ( temporary swelling of the upper 
and lower extremities) 
 Elephantiasis ( enlargement and thickening of the 
skin of the lower and/or upper extremeties, 
scrotum, breast)
 Physical examination is done in the main health 
center or during scheduled survey bites in the 
community 
 History taking 
 Observation of the major and minor signs ang 
symptoms
 STRATEGY 1. Endemic Mapping 
 STRATEGY 2. Capability Building 
 STRATEGY 3. Mass Treatment (integrated with 
other existing parasitic programs) 
 STRATEGY 4. Support Control 
 STRATEGY 5. Monitoring and Supervision 
 STRATEGY 6. Evaluation 
 STRATEGY 7. National Certification 
 STRATEGY 8. International Certification
 Nocturnal Blood Examination (NBE)- blood are 
taken from the patient at the patient’s residence or 
in the hospital after 8:00 pm 
 Immunochromatographic Test (ICT)- it is the rapid 
assessment method. It is an antigen test that can 
be done at daytime.
 1. Selective Treatment – treating individuals found 
to be positive for microfilariae in nocturnal blood 
examination. 
Drug: Diethylcarbamazine Citrate 
Dosage: 6 mg/kg body weight in 3 divided doses for 
12 consecutive days (usually given after meals)
2. Mass Treatment – giving the drugs to all 
population from aged 2 years and above in all 
established endemic areas. 
 Drug: Diethlcarbamazine Citrate (single dose 
based on 6 mg/kg body wt) plus Albendazole 
400mg given single dose given once annually to 
people 2 yrs & above living in established 
endemic areas
 3. Disability Prevention thru home-based or 
community-based care for lymphedema & 
elephantiasis cases. Surgical management for 
hydrocele patients.
 PROVINCES THAT REACHED ELIMINATION 
STAGE: Southern Leyte, Sorsogon, Biliran, 
Bukidnon, Romblon, Agusan Sur, Dinagat island, 
Cotabato Province and COMVAL
 1. Assist low performing areas to increase the MDA 
coverage in order to interrupt the transmission of the LF. 
 2. Assist implementing Units to reach the goal of 
elimination. 
 3. Strengthen integration with other NTD programs. 
 4. Strengthen the disability prevention strategy thru 
community-based or home –based care & thru integration 
with leprosy. 
 5. Implement an integrated vector management 
 6. Implement a sustainability plan for provinces that 
have reached elimination level.
Basic Components 
1. Hygiene 
2. Prevention & cure 
of entry lesions 
3. Exercise 
4. Elevation of foot 
5. Use of proper 
footwares 
Lymphoedema 
management helps 
 to eliminate the bad odour 
 to prevent & heal entry 
lesion 
 to help patients self-confident 
 to reduce the size of the 
lyphoedema 
 to prevent disability 
 to prevent economic loss
 Filariasis patients are advised to observe personal 
hygiene by washing the affected areas with soap 
and water at least twice a day or prescribed 
antibiotics or anti- fungals for super infection.
A.Measures aimed to control the vector 
 Environmental sanitation such as proper drainage 
and cleanliness of surroundings 
 Spraying with insecticides may also produce 
harmful effects)
B. Measures aimed to protect the individual and 
families in endemic areas 
 Use of mosquito nets 
 Use of long sleeves, long pants and socks 
 Application of insect repellants screening of 
houses 
 Health education
 The prognosis in filariasis is good if infection is 
recognized and treated early. Filarial diseases are 
rarely fatal, but the consequences of infection can 
cause significant personal and socioeconomic 
hardship for those who are affected.
 The morbidity of human filariasis results mainly 
from the host reaction to microfilariae or 
developing adult worms in different areas of the 
body. The WHO has identified lymphatic filariasis 
as the second leading cause of permanent and 
long-term disability in the world.
References: 
 Cuevas, Frances Prescilla L.et al;2007 Public 
Health Nursing in the Philippines 10th 
edition,pp257-260 
 www.chd7.gov.ph
Lymphatic Filariasis

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Lymphatic Filariasis

  • 1.
  • 2.  Filariasis is a major parasitic infection, which continues to be a public health problem in the Philippines. It was first discovered in the Philippines in 1907 by foreign workers. Consolidated field reports showed a prevalence rate of 9.7% per 1000 population in 1998. It is the second leading cause of permanent and long-term disability. The disease affects mostly the poorest municipalities in the country about 71% of the case live in the 4th-6th class type of municipalities.
  • 3.  The World Health Assembly in 1997 declared “Filariasis Elimination as a priority” and followed by WHO’s call for global elimination. A sign of the DOH’s commitment to eliminate the disease, the program’s official shift from control to elimination strategies was evident in an Administrative Order #25-A,s 1998 disseminated to endemic regions. In support to the program, an Administrative Order declaring “November as Filariasis Mass Treatment Month was signed by the Secretary of Health last July 2004 and was disseminated to all endemic regions.
  • 4.  Vision: Healthy and productive individuals and families for Filariasis-free Philippines  Mission: Elimination of Filariasis as a public health problem thru a comprehensive approach and universal access to quality health services
  • 5.  Goal: To eliminate Lymphatic Filariasis as a public health problem in the Philippines by year 2017  General Objectives: To decrease Prevalence Rate of filariasis in endemic municipalities to <1/1000 population.
  • 6. Specific Objectives: The National Filariasis Elimination Program specifically aims to: 1. Reduce the Prevalence Rate to elimination level of <1%; 2. Perform Mass treatment in all established endemic areas; 3. Develop a Filariasis disability prevention program in established endemic areas; 4. Continue surveillance of established endemic areas 5 years after mass treatment.
  • 7.  Human Lymphatic Filariasis is a chronic parasitic infection caused by nematode parasites known as wuchereria bancrofti, brugia malayi or brugia timori.The young and adult worms live in lymphatic vessels and lymph nodes while the microfilariae are usually found in blood. The life-span of the adult parasites is about 10 years ( but a 40-year life- span has been reported)while microfilariae live for about a year at the most.
  • 8.  The disease is transmitted to a person through bites from a infected female mosquito primarily Aedes poecillius that bites at night.
  • 9.  The filarial life cycle, like that of all nematodes, consists of 5 developmental (larval) stages in a vertebral host and an arthropod intermediate host and vector. Adult female worms produce thousands of first-stage larvae, or microfilariae, which are ingested by a feeding insect vector. Some microfilariae have a unique daily circadian periodicity in the peripheral circulation. The arthropod vectors (mosquitoes and flies) also have a circadian rhythm in which they obtain blood meals. The highest concentration of microfilariae usually occurs when the local vector is feeding most actively.
  • 10.  Microfilariae undergo 2 developmental changes in the insect. Third-stage larvae then are inoculated back into the vertebral host during the act of feeding for the final 2 stages of development. These larvae travel through the dermis and enter regional lymphatic vessels. During the next 9 months, the larvae develop into mature worms (20-100 mm in length). An average parasite can survive for about 5 years.
  • 11.  The prepatent period is defined as the interval between a vector bite and the appearance of microfilariae in blood, with an estimated duration of about 12 months.
  • 12.  The quantity of accumulating adult worm antigen in the lymphatics  The duration and level of exposure to infective insect bites  The number of secondary bacterial and fungal infections  The degree of host immune response
  • 13.  Filarial infection generates significant inflammatory immune responses that participate in the development of symptomatic lymphatic obstruction. Increased levels of immunoglobulin E (IgE) and immunoglobulin G4 (IgG4) secondary to antigenic (from dead worms) stimulation of Th2- type immune response have been demonstrated.
  • 14.  Studies have shown that there is a familial tendency to lymphatic obstruction, providing support for the hypothesis that host genes influence lymphedema susceptibility. Studies also suggest that microfilaremia may be increased in individuals with low levels of mannose-binding lectin, suggesting a genetic predisposition.Further, a propensity to develop chronic disease has been demonstrated in patients with polymorphisms of endothelin-1 and tumor necrosis factor receptor II.
  • 15.  Prenatal exposure seems to be an important determinant in conferring greater immune tolerance to parasite antigen. Thus, individuals from endemic areas are often asymptomatic until late in the disease when they have high worm burden, whereas nonimmune expatriates tend to have brisk immune responses and more severe early clinical symptoms, even in light infections.
  • 16.  Studies have shown that lymphatic filarial parasites contain rickettsialike Wolbachia endosymbiotic bacteria. This association has been recognized as contributing to the inflammatory reaction seen in filariasis.
  • 17.  The incubation period which starts from the entry of the infective larvae to the development of clinical manifestation is variable. Nevertheless, it ranges from 8-16 months.
  • 18. ASYMPTOMATIC STAGE:  Characterized by the presence of microfilariae in the peripheral blood  No clinical signs and symptoms of the disease  Some remain asymptomatic for years and in some instances for life  Others progress to acute and chronic stages  Microfilariae rate increases with age and then levels off  In most endemic areas including the Philippines the Philippines, men have higher microlariae rate than women.
  • 19. Starts when there are already manifestation such as:  Lymphadenitis ( Inflammation of lymph nodes)  Lymphangitis ( inflammation of lymph vessels)  In some cases, the male genitalia is affected leading to funiculitis, epidydimitis, or orchitis ( redness, painful and tender scrotum)
  • 20.  Develop 10-15 years from the onset of the first attack  Immigrants from areas where filariasis is not endemic tend to develop this stage more often and much sooner (1-2 years) than do the indigenous population of endemic areas.
  • 21.  Hydrocoele (swelling of the scrotum)  Lymphedema ( temporary swelling of the upper and lower extremities)  Elephantiasis ( enlargement and thickening of the skin of the lower and/or upper extremeties, scrotum, breast)
  • 22.  Physical examination is done in the main health center or during scheduled survey bites in the community  History taking  Observation of the major and minor signs ang symptoms
  • 23.  STRATEGY 1. Endemic Mapping  STRATEGY 2. Capability Building  STRATEGY 3. Mass Treatment (integrated with other existing parasitic programs)  STRATEGY 4. Support Control  STRATEGY 5. Monitoring and Supervision  STRATEGY 6. Evaluation  STRATEGY 7. National Certification  STRATEGY 8. International Certification
  • 24.  Nocturnal Blood Examination (NBE)- blood are taken from the patient at the patient’s residence or in the hospital after 8:00 pm  Immunochromatographic Test (ICT)- it is the rapid assessment method. It is an antigen test that can be done at daytime.
  • 25.  1. Selective Treatment – treating individuals found to be positive for microfilariae in nocturnal blood examination. Drug: Diethylcarbamazine Citrate Dosage: 6 mg/kg body weight in 3 divided doses for 12 consecutive days (usually given after meals)
  • 26. 2. Mass Treatment – giving the drugs to all population from aged 2 years and above in all established endemic areas.  Drug: Diethlcarbamazine Citrate (single dose based on 6 mg/kg body wt) plus Albendazole 400mg given single dose given once annually to people 2 yrs & above living in established endemic areas
  • 27.  3. Disability Prevention thru home-based or community-based care for lymphedema & elephantiasis cases. Surgical management for hydrocele patients.
  • 28.  PROVINCES THAT REACHED ELIMINATION STAGE: Southern Leyte, Sorsogon, Biliran, Bukidnon, Romblon, Agusan Sur, Dinagat island, Cotabato Province and COMVAL
  • 29.  1. Assist low performing areas to increase the MDA coverage in order to interrupt the transmission of the LF.  2. Assist implementing Units to reach the goal of elimination.  3. Strengthen integration with other NTD programs.  4. Strengthen the disability prevention strategy thru community-based or home –based care & thru integration with leprosy.  5. Implement an integrated vector management  6. Implement a sustainability plan for provinces that have reached elimination level.
  • 30. Basic Components 1. Hygiene 2. Prevention & cure of entry lesions 3. Exercise 4. Elevation of foot 5. Use of proper footwares Lymphoedema management helps  to eliminate the bad odour  to prevent & heal entry lesion  to help patients self-confident  to reduce the size of the lyphoedema  to prevent disability  to prevent economic loss
  • 31.
  • 32.  Filariasis patients are advised to observe personal hygiene by washing the affected areas with soap and water at least twice a day or prescribed antibiotics or anti- fungals for super infection.
  • 33. A.Measures aimed to control the vector  Environmental sanitation such as proper drainage and cleanliness of surroundings  Spraying with insecticides may also produce harmful effects)
  • 34. B. Measures aimed to protect the individual and families in endemic areas  Use of mosquito nets  Use of long sleeves, long pants and socks  Application of insect repellants screening of houses  Health education
  • 35.  The prognosis in filariasis is good if infection is recognized and treated early. Filarial diseases are rarely fatal, but the consequences of infection can cause significant personal and socioeconomic hardship for those who are affected.
  • 36.  The morbidity of human filariasis results mainly from the host reaction to microfilariae or developing adult worms in different areas of the body. The WHO has identified lymphatic filariasis as the second leading cause of permanent and long-term disability in the world.
  • 37. References:  Cuevas, Frances Prescilla L.et al;2007 Public Health Nursing in the Philippines 10th edition,pp257-260  www.chd7.gov.ph