Recent trends in treatment and management of filariasis.

Filariasis is the name for a group of tropical diseases caused by various thread-like parasitic round worms (nematodes) and their larvae. The larvae transmit the disease to humans through a mosquito bite. Filariasis is characterized by fever, chills, headache, and skin lesions in the early stages and, if untreated, can progress to include gross enlargement of the limbs and genitalia in a condition called elephantiasis. While filariasis is rarely fatal, it is the second leading cause of permanent and long-term disability in the world. The World Health Organization (WHO) has named filariasis one of only six "potentially eradicable" infectious diseases and has embarked upon a 20-year campaign to eradicate the disease. These infections have a significant economic and psychosocial impact in endemic areas, disfiguring and/or incapacitating more than 40 million individuals. Studies from the Indian subcontinent have shown that infected patients lose significant time from work because of the disease costing the national treasury a minimum of $842 million per year. The treatment of filariasis consists of using medicines that kill the worms combined with the treatment to relieve the symptoms. Filariasis may be treated in early, mild cases with a three-week course of antifilarial drugs. This medication usually cures the infection, but may cause a reaction marked by fever, illness, and muscle or joint pains. Treatment for symptomatic relief includes bed rest, antibiotic use for secondary infections, elastic stockings and pressure bandages to reduce swelling and fluid accumulation, and suspensory bandaging for swollen testicles or breasts. Chronic infections are more difficult to treat effectively. Small accumulations of fluid may benefit from local injection of sclerosing (condensing) agents. Surgery may be required. Mass accumulations may be managed using shunt procedures combined with removal of excess fatty and fibrous tissue, drainage and physical therapy.

[1]  A. Hoerauf Filariasis: new drugs and new opportunities for lymphatic filariasis and onchocerciasis , 2008, Current opinion in infectious diseases.

[2]  Fengfei Wang,et al.  Confirmation of elimination of lymphatic filariasis by an IgG4 enzyme-linked immunosorbent assay with urine samples in Yongjia, Zhejiang Province and Gaoan, Jiangxi Province, People's Republic of China. , 2007, The American journal of tropical medicine and hygiene.

[3]  J. Critchley,et al.  Diethylcarbamazine (DEC)-medicated salt for community-based control of lymphatic filariasis. , 2007, The Cochrane database of systematic reviews.

[4]  J. Kazura,et al.  Mass chemotherapy options to control lymphatic filariasis: a systematic review. , 2005, The Lancet. Infectious diseases.

[5]  P. Vanamail,et al.  Comparison of an immunochromatographic card test with night blood smear examination for detection of Wuchereria bancrofti microfilaria carriers. , 2004, The National medical journal of India.

[6]  Achim Hoerauf,et al.  Reliable and frequent detection of adult Wuchereria bancrofti in Ghanaian women by ultrasonography , 2004, Tropical medicine & international health : TM & IH.

[7]  E. Pearlman,et al.  The role of endosymbiotic Wolbachia bacteria in filarial disease , 2004, Cellular microbiology.

[8]  M. Itoh,et al.  Sensitive and specific enzyme-linked immunosorbent assay for the diagnosis of Wuchereria bancrofti infection in urine samples. , 2001, The American journal of tropical medicine and hygiene.

[9]  Mark J. Taylor,et al.  Inflammatory Responses Induced by the Filarial Nematode Brugia malayi Are Mediated by Lipopolysaccharide-like Activity from Endosymbiotic Wolbachia Bacteria , 2000, The Journal of experimental medicine.

[10]  D. Addiss,et al.  Evaluation of the whole blood filariasis ICT test for short-term monitoring after antifilarial treatment. , 2000, The American journal of tropical medicine and hygiene.

[11]  F. Abath,et al.  Diagnosis of Wuchereria bancrofti infection by the polymerase chain reaction using urine and day blood samples from amicrofilaraemic patients. , 1998, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[12]  A. Hightower,et al.  Randomised placebo-controlled comparison of ivermectin and albendazole alone and in combination for Wuchereria bancrofti microfilaraemia in Haitian children , 1997, The Lancet.

[13]  J. Habbema,et al.  Ivermectin for the chemotherapy of bancroftian filariasis: a meta‐analysis of the effect of single treatment , 1997, Tropical medicine & international health : TM & IH.

[14]  S. Williams,et al.  A polymerase chain reaction-based assay for detection of Wuchereria bancrofti in human blood and Culex pipiens. , 1997, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[15]  L. Nicolas,et al.  Reduction of Wuchereria bancrofti adult worm circulating antigen after annual treatments of diethylcarbamazine combined with ivermectin in French Polynesia. , 1997, The Journal of infectious diseases.

[16]  J. D. Smyth,et al.  The mechanisms of action of antiprotozoal and anthelmintic drugs in man. , 1997, General pharmacology.

[17]  D. Addiss,et al.  Assessment of the efficacy of diethylcarbamazine on adult Wuchereria bancrofti in vivo. , 1997, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[18]  D. Addiss,et al.  Evaluation of the Og4C3 ELISA in Wuchereria bancrofti infection: infected persons with undetectable or ultra‐low microfilarial densities , 1996, Tropical medicine & international health : TM & IH.

[19]  D. Meyrowitsch,et al.  Mass diethylcarbamazine chemotherapy for control of bancroftian filariasis through community participation: comparative efficacy of a low monthly dose and medicated salt. , 1996, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[20]  J. McCarthy,et al.  Clearance of circulating filarial antigen as a measure of the macrofilaricidal activity of diethylcarbamazine in Wuchereria bancrofti infection. , 1995, The Journal of infectious diseases.

[21]  G Dreyer,et al.  Direct assessment of the adulticidal efficacy of a single dose of ivermectin in bancroftian filariasis. , 1995, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[22]  J. Chodakewitz Ivermectin and lymphatic filariasis: a clinical update , 1995 .

[23]  D. Freedman,et al.  Lymphoscintigraphic analysis of lymphatic abnormalities in symptomatic and asymptomatic human filariasis. , 1994, The Journal of infectious diseases.

[24]  W. Campbell,et al.  Ivermectin in human medicine. , 1994, The Journal of antimicrobial chemotherapy.

[25]  T. Nutman,et al.  Effectiveness of diethylcarbamazine in treating loiasis acquired by expatriate visitors to endemic regions: long-term follow-up. , 1994, The Journal of infectious diseases.

[26]  R. Maizels,et al.  Immunological modulation and evasion by helminth parasites in human populations , 1993, Nature.

[27]  R. Speare,et al.  A comparison of the Og4C3 antigen capture ELISA, the Knott test, an IgG4 assay and clinical signs, in the diagnosis of Bancroftian filariasis. , 1993, Tropical medicine and parasitology : official organ of Deutsche Tropenmedizinische Gesellschaft and of Deutsche Gesellschaft fur Technische Zusammenarbeit.

[28]  G. Weil,et al.  Changes in circulating parasite antigen levels after treatment of bancroftian filariasis with diethylcarbamazine and ivermectin. , 1991, The Journal of infectious diseases.

[29]  A. Sadanandam,et al.  A controlled trial of ivermectin and diethylcarbamazine in lymphatic filariasis. , 1990, The New England journal of medicine.