Late Identification of Perinatal Transmission of HIV in an Infant at High Risk.
Thomas J O'GradySuzanne KaufmanAmanda StolzLinda M StyerLisa HaskinPrapitha SureshNko L RymanDipal ShahTimothy J SullivanLucia TorianCharles GonzalezMonica M ParkerCarol-Ann SwainPublished in: Journal of public health management and practice : JPHMP (2024)
The focus of this case study is the delayed diagnosis of a perinatal HIV transmission, which was identified when the infant reached 4 months of age, and the social conditions and structural determinants that contributed to the increased transmission risk. Despite adhering to the diagnostic testing protocols and neonatal antiretroviral (ARV) guidelines of the New York State Department of Health, this transmission still occurred. This transmission event prompted strategies to address criminalization of substance use during pregnancy and a reevaluation of the HIV testing and treatment protocols, including the timing of testing. Obtaining a diagnostic specimen at birth before initiating prophylactic or presumptive therapy, without causing delays in therapy, and incorporating HIV-1 DNA or RNA testing 2 to 6 weeks after discontinuing ARV therapy might have facilitated earlier detection and a quicker resumption of ARV therapy for this high-risk infant. Subsequently, the New York State HIV perinatal testing guidelines were updated. These changes included the recommendation to obtain a diagnostic specimen at birth before initiating ARV medications, whenever feasible, without causing delays in ARV initiation. Additionally, an extra virologic diagnostic test is recommended at 2 to 6 weeks after discontinuing ARVs for infants at high risk of perinatal HIV transmission, especially those with possible DNA or RNA suppression due to ARV prophylaxis or presumptive HIV therapy.
Keyphrases
- hiv testing
- men who have sex with men
- antiretroviral therapy
- hiv positive
- hiv infected
- human immunodeficiency virus
- hiv aids
- hepatitis c virus
- hiv infected patients
- healthcare
- pregnant women
- public health
- gestational age
- mental health
- stem cells
- clinical practice
- single molecule
- nucleic acid
- mesenchymal stem cells
- bone marrow
- preterm birth
- cell therapy
- human health
- combination therapy
- bioinformatics analysis