HIV Flashcards

1
Q

The laboratory test generally accepted as the best indicator of the immediate state of immunologic competence of the patient with HIV infection.

A

CD4 count

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2
Q

Patients with CD4+ T-cell counts ______ are at high risk of disease from P. jirovecii

A

<200/μL

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3
Q

Patients with CD4+ T-cell counts _____ are also at high risk of disease from CMV, mycobacteria of the M. avium complex (MAC), and/or T. gondii

A

<50/ μL

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4
Q

Patients with HIV infection should have CD4+ T-cell measurements performed at ______ and ______ thereafter

A

the time of diagnosis, every 3–6 months

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5
Q

CDC HIV Infection Stage 3 in patients more than 5 years old is defined as CD4 count of?

A

<200

*Stage 1 - >500
Stage 2 - 200-499
Stage 3 - <200

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6
Q

The most common cause of HIV disease throughout the world

A

HIV 1

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7
Q

When should the plasma HIV RNA level be measured?

A

at the time of HIV diagnosis and every 3–6 months thereafter in the untreated patient.

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8
Q

The average length of time from HIV initial infection to the development of clinical disease

A

10 years

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9
Q

TRUE OR FALSE: A diagnosis of AIDS is made in any individual age 6 years and older with HIV infection and a CD4+ T-cell count <200/μL and in anyone with HIV infection who develops one of the HIV-associated diseases considered to be indicative of a severe defect in cell-mediated immunity

A

TRUE

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10
Q

It is the single most common cause of pneumonia in patients with HIV infection in the United States and can be identified as a likely etiologic agent in 25% of cases of pneumonia in patients with HIV infection

A

P. jirovecii

*Pneumocystis pneumonia (PCP) is caused by the fungus P. jirovecii and was once the hallmark of AIDS

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11
Q

The risk of PCP is greatest among those who have experienced a previous bout of PCP and those who have CD4+ T-cell counts of ______

A

<200/μL

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12
Q

The standard treatment for PCP or disseminated pneumocystosis

A

trimethoprim-sulfamethoxazole (TMP-SMX).

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13
Q

The treatment of choice for severe disease in the patient unable to tolerate TMP-SMX.

A

IV Pentamidine

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14
Q

What additional medication can be given for patients with a Pao2 <70 mmHg or with an a–a gradient >35 mmHg

A

Glucocorticoid

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15
Q

The preferred regimen for PCP prophylaxis.

A

TMP-SMX, one double-strength tablet daily

  • This regimen also provides protection against toxoplasmosis and some bacterial respiratory pathogens
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16
Q

When is prophylaxis for PCP indicated for any HIV-infected individual?

A

1) HIV-infected individual who has experienced a prior bout of PCP
2) any patient with a CD4+ T-cell count of <200/μL or a CD4 percentage <15
3) any patient with unexplained fever for >2 weeks
4) any patient with a recent history of oropharyngeal candidiasis

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17
Q

Indications to discontinue PCP prophylaxis

A

patients treated with ART who maintain good suppression of HIV (<50 copies/mL) and CD4+ T-cell counts >200/μL for at least 3 months.

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18
Q

AIDS pandemic is primarily caused by the ____

A

HIV-1 M group viruses.

19
Q

Two major envelope proteins if the HIV virion

A
  • the external gp120
    • the transmembrane gp41
20
Q

Two major co-receptors for HIV-1

A

CCR5 and CXCR4

21
Q

Among the parenteral type of exposure in HIV, which carries the highest risk of exposure?

A

Blood transfusion

22
Q

TRUE OR FALSE: Receptive anal intercourse carries the highest risk of HIV transmission

A

TRUE

23
Q

When should HIV testing be repeated if the patient’s HIV 1 western blot showed indeterminate result?

A

4-6 weeks

24
Q

the leading infectious cause of meningitis in patients with AIDS

A

Fungal meningitis

  • vast majority of these are due to C. neoformans
25
Q

TRUE OR FALSE: The diagnosis of cryptococcal meningitis is made by identification of organisms in spinal fluid with india ink examination or by the detection of cryptococcal antigen.

A

TRUE

26
Q

The diagnosis of this disease is usually suspected on the basis of MRI findings of multiple lesions in multiple locations

A

Cerebral Toxoplasmosis

27
Q

Initial treatment regimen for cryptococcal meningitis

A

Initial treatment is with IV amphotericin B 0.7 mg/kg daily, or liposomal amphotericin 4–6 mg/kg daily, with flucytosine 25 mg/kg 4x a day for at least 2 weeks if possible

28
Q

Standard regimen for toxoplasmosis

A

Standard treatment is sulfadiazine and pyrimethamine with leucovorin as needed for a minimum of 4–6 weeks

29
Q

It is one of the most devastating consequences of HIV infection that usually presents as a painless, progressive loss of vision

A

CMV retinitis

30
Q

What is the standard therapy for CMV retinitis ?

A

oral valganciclovir, IV ganciclovir, or IV foscarnet,

  • A 3-week induction course is followed by maintenance therapy with oral valganciclovir.
  • Maintenance therapy is continued until the CD4+ T-cell count remains >100 μL for >6 months
31
Q

Which of the following best describes Stage 3 (AIDS) in the CDC classification system for HIV?
A) CD4+ T-cell count between 500-1000/μL
B) Presence of any opportunistic infection regardless of CD4+ count
C) CD4+ T-cell count <200/μL or diagnosis of an AIDS-defining illness
D) Presence of HIV RNA but no detectable antibodies

A

Answer: C) CD4+ T-cell count <200/μL or diagnosis of an AIDS-defining illness
Rationale: Stage 3 (AIDS) is classified by either a CD4+ count below 200/μL or the presence of one or more opportunistic infections, regardless of CD4+ levels.

32
Q

What is the primary mode of HIV transmission worldwide?
A) Injection drug use
B) Blood transfusions
C) Heterosexual contact
D) Mother-to-child transmission

A

Answer: C) Heterosexual contact
Rationale: While injection drug use and blood transfusions can transmit HIV, the most common mode of transmission globally is heterosexual contact, especially in developing countries.

33
Q

Which of the following HIV proteins is responsible for binding to the CD4 receptor on host cells?
A) gp41
B) gp120
C) Reverse transcriptase
D) Integrase

A

Answer: B) gp120
Rationale: gp120 is the external envelope protein of HIV that binds to the CD4 receptor on host cells, initiating viral entry.

34
Q

What is the most important factor in determining the risk of sexual transmission of HIV?
A) The presence of STIs
B) The HIV-positive partner’s viral load
C) The type of sexual contact
D) The use of oral contraceptives

A

Answer: B) The HIV-positive partner’s viral load
Rationale: Viral load is the strongest predictor of HIV transmission risk, with the highest risk occurring during acute infection and late-stage disease.

35
Q

Which of the following is TRUE regarding “Undetectable = Untransmittable” (U=U)?
A) People with undetectable HIV RNA cannot transmit the virus sexually
B) People with undetectable HIV RNA are cured of HIV
C) Antiretroviral therapy (ART) eliminates HIV from the body completely
D) Having an undetectable viral load means HIV cannot be transmitted by any means

A

Answer: A) People with undetectable HIV RNA cannot transmit the virus sexually
Rationale: Studies have confirmed that when HIV viral load is suppressed below detectable levels with ART, the risk of sexual transmission is effectively zero.

36
Q

Which opportunistic infection is most commonly associated with a CD4+ T-cell count <50/μL?
A) Pneumocystis jirovecii pneumonia (PCP)
B) Cryptococcal meningitis
C) Mycobacterium avium complex (MAC)
D) Kaposi’s sarcoma

A

Answer: C) Mycobacterium avium complex (MAC)
Rationale: MAC infection is a major concern in patients with CD4+ counts below 50/μL, and primary prophylaxis is recommended unless ART is immediately initiated.

37
Q

What is the preferred first-line prophylaxis for Pneumocystis jirovecii pneumonia (PCP)?
A) Azithromycin
B) Trimethoprim-sulfamethoxazole (TMP-SMX)
C) Isoniazid
D) Amphotericin B

A

Answer: B) Trimethoprim-sulfamethoxazole (TMP-SMX)
Rationale: TMP-SMX is the preferred prophylactic treatment for PCP in HIV patients with CD4+ counts <200/μL.

38
Q

Which of the following describes a paradoxical immune reconstitution inflammatory syndrome (IRIS)?
A) Worsening of pre-existing opportunistic infection after starting ART
B) Development of new opportunistic infections after starting ART
C) Immediate clearance of opportunistic infections following ART initiation
D) Resistance to antiretroviral drugs leading to treatment failure

A

Answer: A) Worsening of pre-existing opportunistic infection after starting ART
Rationale: Paradoxical IRIS occurs when the immune system recovers rapidly after ART initiation, leading to an exaggerated inflammatory response against a known infection.

39
Q

What is the standard initial regimen for HIV treatment?
A) Single-drug therapy with a protease inhibitor
B) Two nucleoside/nucleotide reverse transcriptase inhibitors + a third agent
C) A combination of three protease inhibitors
D) Monotherapy with a non-nucleoside reverse transcriptase inhibitor

A

Answer: B) Two nucleoside/nucleotide reverse transcriptase inhibitors + a third agent
Rationale: The standard first-line HIV regimen includes two NRTIs plus either an NNRTI, integrase inhibitor, or a boosted protease inhibitor.

40
Q

When should ART be initiated in HIV-positive, antiretroviral-naive patients with a CD4 count >50 cells/μL and newly diagnosed TB?
A) Immediately
B) After 1 week of TB treatment
C) 2–4 weeks after starting TB treatment
D) After completing TB treatment

A

Answer: C) 2–4 weeks after starting TB treatment
Rationale: For patients with CD4 counts >50 cells/μL, delaying ART for 2–4 weeks reduces the risk of immune reconstitution inflammatory syndrome (IRIS) while allowing TB therapy to begin.

41
Q

How should ART be managed in patients with HIV and CD4 counts <50 cells/μL who are diagnosed with TB?
A) ART should be delayed until TB treatment is completed
B) ART should be started as soon as possible
C) ART should only be initiated if TB treatment fails
D) ART should be given only after a CD4+ count increase

A

Answer: B) ART should be started as soon as possible
Rationale: For patients with very low CD4 counts (<50 cells/μL), the benefits of immediate ART outweigh the risks of IRIS, so ART should be initiated promptly.

42
Q

What is unmasking IRIS?
A) A reaction to ART causing hypersensitivity
B) IRIS related to a previously undiagnosed infection
C) IRIS occurring only in patients with high CD4+ counts
D) A false positive result for an opportunistic infection

A

Answer: B) IRIS related to a previously undiagnosed infection
Rationale: Unmasking IRIS occurs when ART leads to an inflammatory response against a previously unrecognized infection.

43
Q

Which group is most at risk for developing IRIS after starting ART?
A) Patients with CD4+ counts >500 cells/μL
B) Patients with undetectable HIV RNA before ART
C) Patients with CD4+ counts <50 cells/μL and a rapid drop in HIV RNA
D) Patients with stable HIV viral loads

A

Answer: C) Patients with CD4+ counts <50 cells/μL and a rapid drop in HIV RNA
Rationale: IRIS is most common in severely immunosuppressed patients who experience a rapid decrease in HIV RNA after starting ART.