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1.
Int J Tuberc Lung Dis ; 27(6): 458-464, 2023 06 01.
Article in English | MEDLINE | ID: mdl-37231600

ABSTRACT

BACKGROUND: Twelve weeks of weekly isoniazid and rifapentine (3HP) prevents TB disease among people with HIV (PWH), but the costs to people of taking TB preventive treatment is not well described.METHODS: We surveyed PWH who initiated 3HP at a large urban HIV/AIDS clinic in Kampala, Uganda, as part of a larger trial. We estimated the cost of one 3HP visit from the patient perspective, including both out-of-pocket costs and estimated lost wages. Costs were reported in 2021 Ugandan shillings (UGX) and US dollars (USD; USD1 = UGX3,587)RESULTS: The survey included 1,655 PWH. The median participant cost of one clinic visit was UGX19,200 (USD5.36), or 38.5% of the median weekly income. Per visit, the cost of transportation was the largest component (median: UGX10,000/USD2.79), followed by lost income (median: UGX4,200/USD1.16) and food (median: UGX2,000/USD0.56). Men reported greater income loss than women (median: UGX6,400/USD1.79 vs. UGX3,300/USD0.93), and participants who lived further than a 30-minute drive to the clinic had higher transportation costs than others (median: UGX14,000/USD3.90 vs. UGX8,000/USD2.23).CONCLUSION: Patient-level costs to receive 3HP accounted for over one-third of weekly income. Patient-centered approaches to averting or defraying these costs are needed.


Subject(s)
Acquired Immunodeficiency Syndrome , Latent Tuberculosis , Tuberculosis , Male , Humans , Female , Isoniazid/therapeutic use , Antitubercular Agents/therapeutic use , Uganda , Tuberculosis/drug therapy , Latent Tuberculosis/drug therapy , Drug Therapy, Combination , Acquired Immunodeficiency Syndrome/drug therapy
2.
Infect Immun ; 37(1): 378-81, 1982 Jul.
Article in English | MEDLINE | ID: mdl-6809634

ABSTRACT

The resistance of Pseudomonas aeruginosa to phagocytosis by polymorphonuclear leukocytes was overcome by opsonization with antibody to slime glycolipoprotein or, to a lesser extent, with complement. Resistance was most effectively overcome in the presence of both. Protection against viable-cell challenge conferred by anti-glycolipoprotein serum in experimental infection is discussed briefly in the light of these findings.


Subject(s)
Bacterial Proteins/immunology , Glycoproteins/immunology , Neutrophils/immunology , Phagocytosis , Pseudomonas aeruginosa/immunology , Animals , Complement System Proteins , Glycolipids/immunology , Immune Sera , Mice , Opsonin Proteins
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