Human immunodeficiency virus (HIV) infection: Clinical sciences

Last updated: February 03, 2025

Human immunodeficiency virus (HIV) infection: Clinical sciences

STAGE DE PÉDIATRIE

STAGE DE PÉDIATRIE

Henoch-Schonlein purpura: Clinical sciences
Approach to inborn errors of metabolism (progressive or chronic): Clinical sciences
Meningitis (pediatrics): Clinical sciences
Approach to anemia in the newborn and infant (destruction and blood loss): Clinical sciences
Approach to anemia in the newborn and infant (underproduction): Clinical sciences
Approach to anemia (destruction and sequestration): Clinical sciences
Approach to anemia (underproduction): Clinical sciences
Sickle cell disease: Clinical sciences
Sepsis (pediatrics): Clinical sciences
Approach to constipation (pediatrics): Clinical sciences
Approach to a cough (pediatrics): Clinical sciences
Bronchiolitis: Clinical sciences
Pneumonia (pediatrics): Clinical sciences
Upper respiratory tract infections: Clinical sciences
Influenza: Clinical sciences
Croup and epiglottitis: Clinical sciences
Congestive heart failure: Clinical sciences
Asthma: Clinical sciences
Approach to diarrhea (pediatrics): Clinical sciences
Infectious gastroenteritis (acute) (pediatrics): Clinical sciences
Infectious gastroenteritis (subacute) (pediatrics): Clinical sciences
Approach to a fever (over 2 months): Clinical sciences
Osteomyelitis (pediatrics): Clinical sciences
Pharyngitis, peritonsillar abscess, and retropharyngeal abscess (pediatrics): Clinical sciences
Otitis media and externa (pediatrics): Clinical sciences
Septic arthritis and transient synovitis (pediatrics): Clinical sciences
Stevens-Johnson syndrome and toxic epidermal necrolysis: Clinical sciences
Urinary tract infection (pediatrics): Clinical sciences
Approach to viral exanthems (pediatrics): Clinical sciences
Approach to bacterial causes of fever and rash (pediatrics): Clinical sciences
Juvenile idiopathic arthritis: Clinical sciences
Kawasaki disease: Clinical sciences
Acute group A streptococcal infections and sequelae (pediatrics): Clinical sciences
Approach to congenital infections: Clinical sciences
Staphylococcal scalded skin syndrome and impetigo: Clinical sciences
Approach to head and neck masses (pediatrics): Clinical sciences
Periorbital and orbital cellulitis (pediatrics): Clinical sciences
Approach to a murmur (pediatrics): Clinical sciences
Approach to congenital heart diseases (cyanotic): Clinical sciences
Approach to hematuria (pediatrics): Clinical sciences
Nephritic syndromes (pediatrics): Clinical sciences
Approach to leukocoria (pediatrics): Clinical sciences
Hepatitis B: Clinical sciences
Approach to a limp (pediatrics): Clinical sciences
Approach to common musculoskeletal injuries (pediatrics): Clinical sciences
Developmental dysplasia of the hip: Clinical sciences
Legg-Calve-Perthes disease and slipped capital femoral epiphysis: Clinical sciences
Human immunodeficiency virus (HIV) infection: Clinical sciences
Approach to proteinuria (pediatrics): Clinical sciences
Approach to a red eye: Clinical sciences
Conjunctival disorders: Clinical sciences
Eyelid disorders: Clinical sciences
Approach to vomiting (newborn and infant): Clinical sciences
Approach to vomiting (pediatrics): Clinical sciences
Gastroesophageal reflux disease (pediatrics): Clinical sciences
Approach to increased intracranial pressure: Clinical sciences
Peptic ulcers, gastritis, and duodenitis (pediatrics): Clinical sciences
Large bowel obstruction: Clinical sciences
Small bowel obstruction: Clinical sciences
Approach to acid-base disorders: Clinical sciences
Approach to metabolic acidosis: Clinical sciences
Approach to metabolic alkalosis: Clinical sciences
Approach to respiratory acidosis: Clinical sciences
Approach to respiratory alkalosis: Clinical sciences
Approach to hypocalcemia (pediatrics): Clinical sciences
Approach to hypoglycemia (pediatrics): Clinical sciences
Approach to hypernatremia (pediatrics): Clinical sciences
Approach to hyponatremia (pediatrics): Clinical sciences
Adrenal insufficiency: Clinical sciences
Syndrome of inappropriate antidiuretic hormone secretion: Clinical sciences
Approach to a fever (0-60 days): Clinical sciences
Approach to hypotonia (newborn and infant): Clinical sciences
Approach to jaundice (newborn and infant): Clinical sciences
Approach to poor feeding (newborn and infant): Clinical sciences
Approach to complications of prematurity (early): Clinical sciences
Approach to complications of prematurity (late): Clinical sciences
Necrotizing enterocolitis: Clinical sciences
Neonatal respiratory distress syndrome: Clinical sciences
Approach to prenatal teratogen exposure: Clinical sciences
Respiratory failure (pediatrics): Clinical sciences
Foreign body aspiration and ingestion (pediatrics): Clinical sciences
Approach to upper airway obstruction (pediatrics): Clinical sciences
Anaphylaxis: Clinical sciences
Approach to epilepsy: Clinical sciences
Approach to a first unprovoked seizure (pediatrics): Clinical sciences
Febrile seizure (pediatrics): Clinical sciences
Diabetes mellitus (pediatrics): Clinical sciences
Dehydration (pediatrics): Clinical sciences
Brief, resolved, unexplained event (BRUE): Clinical sciences
Approach to bradycardia: Clinical sciences
Approach to tachycardia: Clinical sciences
Approach to melena and hematemesis (pediatrics): Clinical sciences
Burns: Clinical sciences
Approach to trauma (pediatrics): Clinical sciences
Approach to a child with Down syndrome (trisomy 21): Clinical sciences
Cystic fibrosis and primary ciliary dyskinesia: Clinical sciences
Approach to delay or regression in developmental milestones: Clinical sciences
Approach to growth faltering: Clinical sciences
Approach to neurodevelopmental disorders: Clinical sciences
Approach to short stature: Clinical sciences
Approach to feeding and eating disorders: Clinical sciences
Allergic rhinitis: Clinical sciences
Essential hypertension: Clinical sciences
Approach to a rash in the well newborn and infant: Clinical sciences
Immunizations (pediatrics): Clinical sciences
Well-child visit (newborn and infant): Clinical sciences
Well-child visit (toddler and child): Clinical sciences
Well-child visit (adolescent): Clinical sciences
Bacterial and viral skin infections: Pathology review
Nasal, oral and pharyngeal diseases: Pathology review
Pediatric musculoskeletal disorders: Pathology review
Viral exanthems of childhood: Pathology review
Seizures: Pathology review
Congenital TORCH infections: Pathology review
Central nervous system infections: Pathology review
Developmental and learning disorders: Pathology review
Breastfeeding
Anatomy clinical correlates: Eye

Decision-Making Tree

Transcript

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Human immunodeficiency virus, or HIV for short, is a single-stranded RNA retrovirus that targets the body’s immune system. HIV is transmitted by contact with infected body fluids, such as blood, semen, and vaginal fluids. There are two types of HIV: HIV-1 and HIV-2; but generally, when we talk about HIV infection, we usually mean HIV-1 because it's the most widespread.

Now, HIV causes immunosuppression by targeting and infecting CD4 T cells, which are a type of white blood cell that helps coordinate the immune response to infection. The acute phase of HIV infection is called acute retroviral syndrome, after which the individual can be asymptomatic for as long as a couple of years. However, without appropriate medical management, HIV infection can progress to acquired immunodeficiency syndrome, or AIDS.

Now, if your patient presents with chief concerns suggesting an HIV infection, first perform a focused history and physical examination. These patients typically have nonspecific symptoms, such as fever, fatigue, night sweats and unintentional weight loss. Additionally, your patient might report myalgias, arthralgias, or gastrointestinal manifestations, like nausea, vomiting, and diarrhea. Your patient could also report a sore throat.

Other historical findings may include high-risk sexual behavior such as unprotected sexual activities or multiple sexual partners; intravenous substance use; or occupational risk factors such as accidental needlestick injury.

Physical examination might reveal a rash, lymphadenopathy, or signs of sexually transmitted infections, such as purulent urethral discharge or painful fluid-filled blisters around the genitals. You might also find needle marks on the skin overlying veins in individuals who have used intravenous drugs. Finally, distinctive but rare manifestations of HIV infection include mucocutaneous ulcers, which typically affect oral and genital regions.

Here’s a clinical pearl! In some cases, patients with undiagnosed HIV infection may present with opportunistic infections like Pneumocystis jirovecii pneumonia, or opportunistic neoplasms, such as Kaposi sarcoma, which presents as dark, reddish-purple or brown skin lesions. Unfortunately, these are also considered AIDS-defining illnesses, which occur at a CD4 count less than 200 per microliter. So, if you encounter a patient with an opportunistic disease, without a known immunocompromising condition, remember to perform HIV testing!

With these findings, you should suspect an HIV infection, and order a combined HIV antibody and p24 antigen immunoassay.

Here’s a clinical pearl to keep in mind! It’s also recommended to screen for HIV during pre-pregnancy planning and as early in pregnancy as possible. Individuals with certain risk factors, such as more than one sexual partner, should be screened more often.

Okay, first let’s focus on patients with a non-reactive HIV antibody and p24 antigen immunoassay. This means both HIV antibodies and p24 antigen were not detected. Your next step is to assess for HIV exposure within the past month. If your patient reports no known recent HIV exposure, you can exclude HIV infection and consider an alternative diagnosis.

On the other hand, if your patient reports a known HIV exposure, order an HIV-1 nucleic acid test, or HIV-1 NAT for short, which detects levels of HIV-1 RNA in the blood. This test can help you rule out HIV infection because HIV antibodies and the p24 antigen can take up to 6 weeks to appear in the blood and be detected, while the NAT can usually detect HIV 10 to 33 days after exposure! So, if the HIV-1 NAT is negative, you should consider an alternative diagnosis. However, if the HIV-1 NAT is positive, diagnose HIV-1 infection.

Sources

  1. "Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents with HIV" ClinicalInfoHIV.gov (2023)
  2. "Antiretroviral Drugs for Treatment and Prevention of HIV Infection in Adults: 2022 Recommendations of the International Antiviral Society-USA Panel" JAMA (2023)
  3. "Division of HIV/AIDS Prevention. 2018 Quick reference guide: Recommended laboratory HIV testing algorithm for serum or plasma specimens" CDC (2018)
  4. "Trends in HIV-2 Diagnoses and Use of the HIV-1/HIV-2 Differentiation Test - United States, 2010-2017" MMWR Morb Mortal Wkly Rep (2020)