[Adherence to antiretroviral therapy measured by pill count and drug serum concentrations. Variables associated with

Melcior Riera1, Laura de La Fuente Ld, Bartomeu Castanyer

  • 1Unidad de Enfermedades Infecciosas, Servicio de Medicina Interna, Hospital Universitario Son Dureta, Palma de Mallorca, Spain. mriera@hsd.es

Medicina Clinica
|September 19, 2002
PubMed

Insights

Adherence to highly active antiretroviral therapy (HAART) was 58.8%. Factors like female sex, methadone programs, psychiatric issues, and adverse effects were linked to lower adherence in HIV patients.

Area of Science:

  • Infectious Diseases
  • Pharmacology
  • Public Health

Context:

  • Highly active antiretroviral therapy (HAART) is crucial for managing HIV infection.
  • Measuring adherence to HAART is essential for treatment efficacy and preventing drug resistance.
  • Suboptimal adherence to HAART is a significant challenge in HIV care.

Purpose:

  • To measure adherence to HAART using pill counts and drug plasma levels.
  • To identify factors associated with suboptimal adherence to HAART in HIV-infected patients.
  • To determine the prevalence of adherence to antiretroviral treatment.

Summary:

  • A prospective observational study followed 202 HIV patients for 9 months, assessing adherence via monthly pill counts and quarterly drug plasma levels.
  • Overall adherence to HAART was 58.8%. Non-adherence was associated with younger age, female sex, methadone maintenance, psychiatric treatment, depression, adverse effects, and prior treatment withdrawal.
  • Independent risk factors for non-adherence included female sex, methadone programs, adverse drug effects, and previous voluntary withdrawal. Men who have sex with men showed higher adherence.

Impact:

  • Findings highlight specific patient groups at higher risk for non-adherence, enabling targeted interventions.
  • Understanding risk factors can inform the development of strategies to improve HAART adherence.
  • The study provides insights into the management of chronic diseases, comparing HIV adherence to other conditions.
Abstract

Related Concept Videos

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Drug Concentrations: Measurements01:23

Drug Concentrations: Measurements

Drug concentration is the quantity of a drug present in a biological sample. Measuring drug amounts in biological samples allows the clinician to understand how a drug is absorbed, distributed, metabolized, and excreted. Samples can be obtained through invasive or non-invasive methods. Invasive techniques involve surgical or parenteral interventions to gather blood, cerebrospinal fluid, or tissue biopsy. Conversely, non-invasive approaches provide samples like urine, feces, and saliva.
Plasma —...
Factors Affecting Protein-Drug Binding: Patient-Related Factors01:29

Factors Affecting Protein-Drug Binding: Patient-Related Factors

Protein-drug binding, a pivotal aspect of pharmacokinetics, is subject to considerable variability influenced by an array of patient-related factors. The intricate interplay of age, individual differences, and pathological conditions significantly impact the binding dynamics and subsequent pharmacological effects.
Age stands as a key determinant in protein-drug binding. Neonates, characterized by low albumin content, experience heightened concentrations of unbound drugs such as phenytoin and...
Bioavailability: Influencing Factors01:22

Bioavailability: Influencing Factors

Bioavailability refers to the extent and rate at which a drug reaches systemic circulation in its active form. Extent refers to the amount of the drug that makes it into circulation, while rate is the speed at which it enters circulation. It is influenced by several factors critical for optimizing drug formulations, dosing regimens, and therapeutic outcomes.Physicochemical properties of drugs and formulationsThe solubility, stability, and dissolution rate of a drug significantly impact its...
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.