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  • Title: Evaluation of the present dengue situation and control strategies against Aedes aegypti in Cebu City, Philippines.
    Author: Mahilum MM, Ludwig M, Madon MB, Becker N.
    Journal: J Vector Ecol; 2005 Dec; 30(2):277-83. PubMed ID: 16599163.
    Abstract:
    The present dengue situation and methods to control Aedes aegypti larvae in Cebu City, Philippines, were evaluated for the development of an integrated community-based dengue control program. The study included the detection of dengue infection among Filipino patients, surveying mosquito breeding sites to determine larval population density of Aedes aegypti, an evaluation of public knowledge, attitude, and personal protection practices against dengue, and an evaluation of the efficacy of VectoBac DT/Culinex Tab tablets based on Bacillus thuringiensis israelensis against Ae. aegypti larvae. Of the 173 human sera samples that were assayed for dengue viruses, 94.9% were positive, 2.2% negative and 2.8% equivocal. Thirty households were randomly chosen per Barangay "Villages" (lowest level of formal local administration). Of the 489 breeding sites surveyed, 29.4% were infested with Ae. aegypti larvae, with discarded tires having the highest infestation rate (69.4%). A survey of people's knowledge, attitude, and practices for integrated community-based dengue control showed that 68.7% of the interviewees were aware that dengue is transmitted by mosquitoes, but only 4.3% knew that a virus was the cause of the disease. The efficacy of one and two tablets of VectoBac DT/Culinex Tab, based on Bacillus thuringiensis israelensis, was assessed against the larvae of Ae. aegypti exposed to sunshine and shaded water containers in semi-field and field tests. In semi-field tests, 100% mortality was achieved until the 18th and 30th day after the application of one and two tablets, respectively, in sun-exposed containers. In shaded containers, 100% mortality was observed until the 30th and 36th day after the application of one and two tablets, respectively. In field tests, the tablets were effective for approximately 3 weeks.
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