Share your insights

Help us by sharing what content you've recieved in your exams


Human immunodeficiency virus

Background knowledge 🧠

Definition

  • Human immunodeficiency virus (HIV) is a retrovirus that targets the immune system, specifically CD4+ T cells, leading to immunodeficiency.
  • If untreated, HIV infection can progress to acquired immunodeficiency syndrome (AIDS), characterised by severe immune suppressionΒ and opportunistic infections.
  • Transmission occurs via blood, sexual contact, and from mother to child during childbirth or breastfeeding.
  • Effective antiretroviral therapy (ART) can control the virus and prevent progression to AIDS.
  • HIV remains a global public health issue, with significant efforts directed towards prevention, treatment, and research.

Epidemiology

  • Global prevalence: approximately 38 million people living with HIV (2020).
  • UK prevalence: around 106,000 people living with HIV (2020).
  • Higher prevalence in certain groups: men who have sex with men (MSM),Β Black African communities,Β and individuals with multiple sexual partners.
  • Incidence declining due to effective prevention and treatment strategies.
  • Late diagnosis remains a challenge, with around 42% diagnosed late in the UK (2020).
  • Universal testing and early initiation of ART are key public health strategies.

Aetiology and pathophysiology

  • HIV is caused by two types: HIV-1 and HIV-2, with HIV-1 being more common and virulent.
  • Virus targets CD4+ T cells, macrophages, and dendritic cells.
  • Integration of viral DNA into host genome leads to chronic infection.
  • Progressive depletion of CD4+ T cells results in immunodeficiency.
  • Opportunistic infections and malignancies develop as immune system weakens.
  • Chronic inflammation and immune activation contribute to morbidity and mortality.
  • ART suppresses viral replication, preserves immune function,Β and reduces transmission risk.

Types

  • HIV-1: most common and widespread type, responsible for the majority of global HIV infections.
  • HIV-2: less transmissible,Β predominantly found in West Africa,Β slower progression to AIDS.

Clinical Features 🌑️

Symptoms

  • Acute retroviral syndrome: flu-like symptoms 2-4 weeks post-exposure (fever, sore throat, rash).
  • Asymptomatic phase: lasts for several years with no or minimal symptoms.
  • Persistent generalised lymphadenopathy: enlarged lymph nodes.
  • Constitutional symptoms: fever, night sweats, weight loss, fatigue.
  • Opportunistic infections: oral thrush, tuberculosis, PCP pneumonia.
  • AIDS-defining illnesses: Kaposi’s sarcoma, CNS lymphoma, recurrent bacterial infections.
  • Neurological symptoms: cognitive impairment, peripheral neuropathy, HIV-associated dementia.
  • Gastrointestinal symptoms: chronic diarrhoea, oesophageal candidiasis.
  • Dermatological manifestations: seborrheic dermatitis, molluscum contagiosum.

Signs

  • Fever and night sweats
  • Lymphadenopathy
  • Oral thrush
  • Weight loss and muscle wasting
  • Skin lesions (Kaposi’s sarcoma, molluscum contagiosum)
  • Chronic diarrhoea and dehydration
  • Neurological deficits (cognitive impairment, peripheral neuropathy)
  • Signs of opportunistic infections (e.g., tachypnea in PCP pneumonia)
  • Hepatosplenomegaly
  • Recurrent bacterial infections

Investigations πŸ§ͺ

Tests

  • HIV serology: ELISA for HIV antibodies and p24 antigen, confirmatory Western blot.
  • HIV RNA PCR: viral load testing for diagnosis and monitoring.
  • CD4 count: to assess immune function and disease progression.
  • Complete blood count: to detect anaemia, leukopenia,Β thrombocytopenia.
  • Liver function tests: monitor ART toxicity.
  • Screening for opportunistic infections: TB testing, CMV serology, Toxoplasma serology.
  • Genotypic resistance testing: to guide ART regimen selection.
  • Hepatitis B and C serology: co-infections.
  • Sexually transmitted infection (STI) screening: syphilis, gonorrhoea, chlamydia.
  • Urinalysis: to detect renal involvement.
  • Baseline and follow-up metabolic panels: to monitor ART side effects and complications.

Management πŸ₯Ό

Management

  • Antiretroviral therapy (ART): combination regimens (e.g., NRTIs, NNRTIs, IIs, PIs, INSTIs).
  • Prophylaxis and treatment of opportunistic infections (e.g., TMP-SMX for PCP).
  • Monitoring and managing ART side effects: liver toxicity, renal dysfunction, lipid abnormalities.
  • Regular follow-up: CD4 count, viral load testing, clinical assessment.
  • Vaccinations: pneumococcal, influenza, hepatitis B.
  • Psychosocial support: counselling, mental health services.
  • Education on safe sex practices and reducing transmission risk.
  • Nutritional support: to address weight loss and malnutrition.
  • Pre-exposure prophylaxis (PrEP) and post-exposure prophylaxis (PEP) for high-risk individuals.
  • Substance abuse treatment: if applicable.
  • Regular dental and ophthalmologic evaluations.
  • Comprehensive, multidisciplinary approach involving primary care, infectious disease specialists, and support services.

Complications

  • Opportunistic infections: PCP, TB, CMV retinitis, toxoplasmosis.
  • Malignancies: Kaposi’s sarcoma, non-Hodgkin lymphoma, cervical cancer.
  • Neurological complications: HIV-associated neurocognitive disorder, peripheral neuropathy.
  • Metabolic complications: lipodystrophy, insulin resistance, hyperlipidemia.
  • Cardiovascular disease: increased risk of myocardial infarction and stroke.
  • Chronic kidney disease: HIV-associated nephropathy.
  • Liver disease: from ART toxicity or co-infection with hepatitis B/C.
  • Psychosocial issues: stigma, depression, anxiety.
  • Drug resistance: due to non-adherence or inadequate ART.
  • Persistent immune activation and inflammation despite ART.
  • Increased susceptibility to common infections.
  • Bone disorders: osteoporosis, osteopenia.

Prognosis

  • With effective ART, life expectancy approaches that of the general population.
  • Early diagnosis and treatment initiation are critical for better outcomes.
  • Prognosis poorer with late diagnosis, low CD4 count, and high viral load.
  • Regular monitoring and adherence to ART improve prognosis.
  • Management of comorbidities and complications essential for quality of life.
  • Continued research and development of new treatments improve long-term outlook.
  • Psychosocial support enhances adherence and coping with chronic illness.
  • Public health interventions reduce transmission and support affected individuals.
  • Comprehensive, multidisciplinary care essential for optimal outcomes.
  • Prognosis affected by co-infections, particularly hepatitis B and C.

Key points

  • HIV is a chronic, manageable condition with effective ART.
  • Early diagnosis and treatment are critical for preventing complications.
  • Regular monitoring and adherence to ART are essential for maintaining health.
  • Comprehensive care includes managing comorbidities and psychosocial support.
  • Prevention strategies include safe sex practices, PrEP, and PEP.
  • Continued research and public health efforts are crucial to control the epidemic.
  • Patient education on transmission risk and ART adherence is vital.
  • Reducing stigma and supporting affected individuals improves quality of life.
  • Multidisciplinary approach is key to comprehensive HIV care.
  • Addressing global health disparities is essential for effective HIV control.

No comments yet πŸ˜‰

Leave a Reply