IDS Malaria, Salmonella, Rabies, HIV, COVID 19 Flashcards

Malaria, Salmonella, Rabies, HIV, COVID 19

1
Q

What is the pathognomonic histopathologic finding in rabies?

A

Negri bodies (basophilic cytoplasmic inclusions in brain neurons).

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2
Q

Where are Negri bodies most commonly found?

A

Purkinje cells of the cerebellum & pyramidal cells of the hippocampus.

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3
Q

Do all infected neurons show Negri bodies?

A

No, Negri bodies occur in only a minority of infected neurons.

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4
Q

What is the best antemortem test for rabies diagnosis?

A

RT-PCR from saliva, CSF, or nuchal skin biopsy.

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5
Q

What is the most common cause of death in rabies?

A

Respiratory failure due to brainstem dysfunction.

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6
Q

What is the primary mode of rabies transmission?

A

Bite or saliva exposure from an infected animal (e.g., dog, bat).

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7
Q

What is the incubation period of rabies?

A

Typically 1-3 months (range: 5 days to 1 year).

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8
Q

What are the two major clinical types of rabies?

A
  1. Encephalitic (Furious) Rabies, 2. Paralytic Rabies.
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9
Q

What are the key features of Encephalitic (Furious) Rabies?

A

Hydrophobia, aerophobia, hypersalivation, agitation, autonomic instability.

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10
Q

What are the key features of Paralytic Rabies?

A

Flaccid, ascending paralysis (resembles Guillain-Barré Syndrome).

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11
Q

What is the recommended post-exposure prophylaxis (PEP) for Category III rabies exposure?

A

Rabies vaccine + Rabies Immunoglobulin (RIG).

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12
Q

What should be done immediately after a rabies-exposure bite?

A

Thorough wound washing with soap & water for at least 15 minutes.

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13
Q

Which histopathologic finding is specific to rabies?

A

Negri bodies in a minority of infected neurons.

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14
Q

Why are Negri bodies not reliable for antemortem diagnosis?

A

Because they occur in only a minority of infected neurons and are seen postmortem.

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15
Q

What is the most characteristic sign of rabies prodrome?

A

Paresthesia at the bite site (pathognomonic early symptom).

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16
Q

What is the etiologic agent of HIV?

A

HIV is caused by the Human Immunodeficiency Virus, a retrovirus that targets CD4+ T cells.

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17
Q

What are the two types of HIV?

A

HIV-1 (most common worldwide, highly virulent) and HIV-2 (less virulent, primarily in West Africa).

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18
Q

How is HIV transmitted?

A

Sexual contact, blood exposure (IV drug use, transfusions), perinatal transmission (mother-to-child), occupational exposure.

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19
Q

What is the pathophysiology of HIV?

A

HIV binds to CD4 receptors and CCR5/CXCR4 co-receptors, integrates into host DNA via reverse transcriptase, leading to progressive CD4+ T-cell depletion.

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20
Q

What are the clinical stages of HIV according to WHO classification?

A

Stage 1: Acute HIV (flu-like symptoms, high viral load), Stage 2: Chronic HIV (asymptomatic or mild symptoms), Stage 3: AIDS (CD4 <200 or AIDS-defining illness).

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21
Q

What are common opportunistic infections at CD4 <500?

A

TB, Kaposi sarcoma (HHV-8), Candida oral thrush, Herpes zoster, bacterial pneumonia.

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22
Q

What are common opportunistic infections at CD4 <200?

A

PCP (Pneumocystis jirovecii pneumonia), PML (Progressive multifocal leukoencephalopathy), Cryptosporidiosis.

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23
Q

What are common opportunistic infections at CD4 <100?

A

Toxoplasmosis, Cryptococcal meningitis, Chronic diarrhea due to Cryptosporidium.

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24
Q

What are common opportunistic infections at CD4 <50?

A

CMV retinitis, Mycobacterium avium complex (MAC) infection.

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25
Q

What is the gold standard test for HIV diagnosis?

A

Western Blot (historical) and HIV RNA PCR; however, 4th Generation HIV Ag/Ab Test is now the standard confirmatory test.

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26
Q

What is the first-line screening test for HIV?

A

4th Generation HIV Ag/Ab Combo Test (Detects p24 antigen and HIV antibodies).

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27
Q

Which test detects HIV in the earliest stage?

A

HIV RNA PCR (NAT – Nucleic Acid Test), detects HIV within 1-2 weeks post-exposure.

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28
Q

What is the AIDS-defining CD4 count and key illnesses?

A

AIDS is defined as CD4 <200 or an AIDS-defining illness such as PCP, CNS lymphoma, Cryptococcus, CMV, or Kaposi Sarcoma.

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29
Q

What is the first-line ART regimen recommended by WHO?

A

First-line regimen: Tenofovir + Lamivudine (or Emtricitabine) + Dolutegravir (TLD regimen).

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30
Q

When should ART be initiated in an HIV patient?

A

ART should be initiated immediately in all HIV patients, regardless of CD4 count.

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31
Q

What is the goal of ART in terms of viral load?

A

Undetectable viral load (<50 copies/mL); U=U (Undetectable = Untransmittable).

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32
Q

What is the post-exposure prophylaxis (PEP) regimen for HIV?

A

PEP should be started within 72 hours of exposure and consists of Tenofovir + Lamivudine + Dolutegravir for 28 days.

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33
Q

What is the pre-exposure prophylaxis (PrEP) regimen for HIV?

A

PrEP is used for high-risk individuals (MSM, discordant partners) and consists of daily Tenofovir + Emtricitabine (Truvada).

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34
Q

What are the key side effects of Tenofovir?

A

Tenofovir can cause nephrotoxicity (Fanconi syndrome) and decreased bone mineral density.

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35
Q

What are the key side effects of Efavirenz?

A

Efavirenz is associated with neuropsychiatric effects (vivid dreams, depression, dizziness).

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36
Q

What are the key side effects of Protease inhibitors (PIs)?

A

Protease inhibitors (PIs) can cause hyperlipidemia, insulin resistance, and lipodystrophy.

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37
Q

What is immune reconstitution inflammatory syndrome (IRIS)?

A

IRIS is a paradoxical worsening of infections after starting ART, due to immune recovery.

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38
Q

How is HIV-related tuberculosis managed?

A

HIV increases TB risk; Start ART after 2 weeks of TB treatment if CD4 <50, otherwise after 8 weeks.

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39
Q

What is the preferred ART regimen for pregnant HIV patients?

A

Preferred regimen: Tenofovir + Lamivudine + Dolutegravir; avoid Efavirenz due to teratogenicity.

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40
Q

What is the recommended neonatal prophylaxis for an HIV-exposed infant?

A

Neonates should receive Zidovudine for 4-6 weeks, with additional prophylaxis for high-risk cases.

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41
Q

What vaccines should be avoided in HIV patients with CD4 <200?

A

Live vaccines should be avoided in CD4 <200 patients, including BCG, MMR, Varicella, and Yellow Fever vaccines.

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42
Q

What are the two types of HIV?

A

HIV-1 (most common worldwide, highly virulent) and HIV-2 (less virulent, primarily in West Africa).

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43
Q

How is HIV transmitted?

A

Sexual contact, blood exposure (IV drug use, transfusions), perinatal transmission (mother-to-child), occupational exposure.

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44
Q

What is the pathophysiology of HIV?

A

HIV binds to CD4 receptors and CCR5/CXCR4 co-receptors, integrates into host DNA via reverse transcriptase, leading to progressive CD4+ T-cell depletion.

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45
Q

What are the clinical stages of HIV according to WHO classification?

A

Stage 1: Acute HIV (flu-like symptoms, high viral load), Stage 2: Chronic HIV (asymptomatic or mild symptoms), Stage 3: AIDS (CD4 <200 or AIDS-defining illness).

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46
Q

What are common opportunistic infections at CD4 <500?

A

TB, Kaposi sarcoma (HHV-8), Candida oral thrush, Herpes zoster, bacterial pneumonia.

How well did you know this?
1
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2
3
4
5
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47
Q

What are common opportunistic infections at CD4 <200?

A

PCP (Pneumocystis jirovecii pneumonia), PML (Progressive multifocal leukoencephalopathy), Cryptosporidiosis.

How well did you know this?
1
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2
3
4
5
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48
Q

What are common opportunistic infections at CD4 <100?

A

Toxoplasmosis, Cryptococcal meningitis, Chronic diarrhea due to Cryptosporidium.

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2
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49
Q

What are common opportunistic infections at CD4 <50?

A

CMV retinitis, Mycobacterium avium complex (MAC) infection.

How well did you know this?
1
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2
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50
Q

What is the gold standard test for HIV diagnosis?

A

Western Blot (historical) and HIV RNA PCR; however, 4th Generation HIV Ag/Ab Test is now the standard confirmatory test.

How well did you know this?
1
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2
3
4
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51
Q

What is the first-line screening test for HIV?

A

4th Generation HIV Ag/Ab Combo Test (Detects p24 antigen and HIV antibodies).

How well did you know this?
1
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2
3
4
5
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52
Q

Which test detects HIV in the earliest stage?

A

HIV RNA PCR (NAT – Nucleic Acid Test), detects HIV within 1-2 weeks post-exposure.

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53
Q

What is the AIDS-defining CD4 count and key illnesses?

A

AIDS is defined as CD4 <200 or an AIDS-defining illness such as PCP, CNS lymphoma, Cryptococcus, CMV, or Kaposi Sarcoma.

How well did you know this?
1
Not at all
2
3
4
5
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54
Q

What is the first-line ART regimen recommended by WHO?

A

First-line regimen: Tenofovir + Lamivudine (or Emtricitabine) + Dolutegravir (TLD regimen).

How well did you know this?
1
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55
Q

When should ART be initiated in an HIV patient?

A

ART should be initiated immediately in all HIV patients, regardless of CD4 count.

How well did you know this?
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56
Q

What is the goal of ART in terms of viral load?

A

Undetectable viral load (<50 copies/mL); U=U (Undetectable = Untransmittable).

57
Q

What is the post-exposure prophylaxis (PEP) regimen for HIV?

A

PEP should be started within 72 hours of exposure and consists of Tenofovir + Lamivudine + Dolutegravir for 28 days.

58
Q

What is the pre-exposure prophylaxis (PrEP) regimen for HIV?

A

PrEP is used for high-risk individuals (MSM, discordant partners) and consists of daily Tenofovir + Emtricitabine (Truvada).

59
Q

What are the key side effects of Tenofovir?

A

Tenofovir can cause nephrotoxicity (Fanconi syndrome) and decreased bone mineral density.

60
Q

What are the key side effects of Efavirenz?

A

Efavirenz is associated with neuropsychiatric effects (vivid dreams, depression, dizziness).

61
Q

What are the key side effects of Protease inhibitors (PIs)?

A

Protease inhibitors (PIs) can cause hyperlipidemia, insulin resistance, and lipodystrophy.

62
Q

What is immune reconstitution inflammatory syndrome (IRIS)?

A

IRIS is a paradoxical worsening of infections after starting ART, due to immune recovery.

63
Q

How is HIV-related tuberculosis managed?

A

HIV increases TB risk; Start ART after 2 weeks of TB treatment if CD4 <50, otherwise after 8 weeks.

64
Q

What is the etiologic agent of Salmonella infections?

A

Salmonella enterica, a Gram-negative facultative anaerobic bacillus.

65
Q

What are the two major types of Salmonella infections?

A

Typhoidal Salmonella (S. Typhi, S. Paratyphi) causing enteric fever, and Nontyphoidal Salmonella (NTS) (S. enteritidis, S. typhimurium) causing gastroenteritis and bacteremia.

66
Q

How is Salmonella transmitted?

A

Fecal-oral route via contaminated food, water, and person-to-person contact.

67
Q

What is the pathophysiology of Salmonella infection?

A

Invades intestinal M cells, enters macrophages, spreads through the bloodstream, causing systemic illness.

68
Q

What are the key clinical features of typhoid fever?

A

Stepwise fever progression, relative bradycardia, rose spots, hepatosplenomegaly, constipation > diarrhea.

69
Q

What are the key clinical features of nontyphoidal Salmonella infection?

A

Nausea, vomiting, non-bloody diarrhea, usually self-limited but can cause bacteremia in immunocompromised patients.

70
Q

What are the complications of typhoid fever?

A

Intestinal perforation, encephalopathy, myocarditis, chronic carrier state.

71
Q

What are the complications of nontyphoidal Salmonella?

A

Sepsis, osteomyelitis (especially in sickle cell disease), endovascular infections.

72
Q

What is the gold standard for diagnosing typhoid fever?

A

Blood culture (gold standard, ~60% sensitivity).

73
Q

Which diagnostic test has the highest sensitivity for typhoid fever?

A

Bone marrow culture (>80% sensitivity, remains positive despite prior antibiotics).

74
Q

What is the role of culture of intestinal secretions in Salmonella diagnosis?

A

Culture of intestinal secretions (via duodenal string test) may be positive even when blood and bone marrow cultures are negative.

75
Q

What are the first-line treatments for typhoid fever?

A

Fluoroquinolones (Ciprofloxacin or Levofloxacin) for 7-14 days, Azithromycin (for fluoroquinolone-resistant strains), Ceftriaxone IV (severe cases).

76
Q

When should antibiotics be used for nontyphoidal Salmonella infection?

A

Only for severe cases or in immunocompromised patients (Fluoroquinolones or Ceftriaxone).

77
Q

How can Salmonella infections be prevented?

A

Hand hygiene, proper food handling, improved sanitation, typhoid vaccination for at-risk individuals.

78
Q

What are special considerations for treating Salmonella in pregnancy?

A

Avoid fluoroquinolones; Ceftriaxone is preferred during pregnancy.

79
Q

Name the four species of Plasmodium that cause human malaria.

A
  1. P. falciparum – most severe, cerebral malaria
  2. P. vivax – relapses, tertian fever
  3. P. ovale – relapses, tertian fever
  4. P. malariae – quartan fever, chronic infection
    (+ P. knowlesi – zoonotic, severe, daily fever)
80
Q

How is malaria transmitted?

A
  • Bite of an infected female Anopheles mosquito
  • Blood transfusion
  • Congenital transmission
  • Needle sharing
81
Q

What is the key pathogenic mechanism of P. falciparum malaria?

A
  • Cytoadherence and sequestration of infected RBCs
  • Leads to microvascular obstruction → severe malaria (cerebral malaria, multi-organ failure)
82
Q

What are the hallmark symptoms of malaria?

A
  1. Fever, chills, sweats (paroxysmal)
  2. Headache, myalgia
  3. Anemia, jaundice
  4. Hepatosplenomegaly

Severe Malaria Signs (P. falciparum):
- Cerebral malaria (seizures, coma)
- Severe anemia
- ARDS, pulmonary edema
- Acute kidney injury
- Shock, metabolic acidosis

83
Q

Match the Plasmodium species with their fever pattern.

A
  • P. falciparum → Irregular fever (malignant tertian)
  • P. vivax/ovale → Tertian fever (every 48 hours)
  • P. malariae → Quartan fever (every 72 hours)
  • P. knowlesi → Daily fevers (24-hour cycle)
84
Q

What are the gold standard and rapid tests for malaria?

A
  1. Gold Standard: Thick and thin blood smear (Giemsa stain)
    • Thick: Detects parasites
    • Thin: Identifies species
  2. Rapid Diagnostic Tests (RDTs): Detects Plasmodium antigens (HRP2, pLDH)
  3. PCR (Polymerase Chain Reaction): High sensitivity but not routinely used
  4. Serology: Not useful for acute infection
85
Q

What is the treatment for uncomplicated malaria?

A
  • P. falciparum (chloroquine-resistant):
    • Artemisinin-based combination therapy (ACT) (e.g., artemether-lumefantrine)
  • P. falciparum (chloroquine-sensitive):
    • Chloroquine
  • P. vivax/ovale:
    • Chloroquine + Primaquine (to eradicate hypnozoites)
  • P. malariae/P. knowlesi:
    • Chloroquine

🔴 Check for G6PD deficiency before giving Primaquine!

86
Q

What is the treatment for severe malaria?

A
  1. IV Artesunate (preferred)
  2. IV Quinine (if artesunate unavailable)
  3. Supportive care: Fluids, glucose, transfusion, seizure control

💡 Switch to oral ACT when stable.

87
Q

What are the chemoprophylaxis options for malaria?

A
  • Chloroquine-sensitive areas: Chloroquine
  • Chloroquine-resistant areas:
    • Mefloquine (neuropsych SEs)
    • Doxycycline (not for pregnancy, photosensitivity)
    • Atovaquone-proguanil (short half-life)
88
Q

How do you prevent relapses in P. vivax and P. ovale?

A
  • Primaquine (eradicates liver hypnozoites)
  • Test for G6PD deficiency first!
89
Q

What is the most common cause of native valve infective endocarditis (IE)?

A

Staphylococcus aureus (acute) and Viridans streptococci (subacute).

90
Q

What is the most common cause of prosthetic valve endocarditis (PVE) within the first 2 months post-surgery?

A

Staphylococcus epidermidis (coagulase-negative Staphylococcus).

91
Q

What is the most common organism in IV drug users with infective endocarditis?

A

Staphylococcus aureus, often affecting the tricuspid valve.

92
Q

Which valve is most commonly affected in infective endocarditis?

A

Mitral valve (except in IV drug users, where the tricuspid valve is most commonly affected).

93
Q

What are the major Duke criteria for diagnosing infective endocarditis?

A
  1. Positive blood cultures for typical organisms, 2. Evidence of endocardial involvement (vegetation on echocardiography, new valvular regurgitation).
94
Q

What are the minor Duke criteria for infective endocarditis?

A
  1. Predisposing condition (e.g., prosthetic valve, IV drug use), 2. Fever ≥38°C, 3. Vascular phenomena (e.g., Janeway lesions, emboli), 4. Immunologic phenomena (e.g., Roth spots, Osler nodes), 5. Positive blood culture not meeting major criteria.
95
Q

What is required to establish a definite diagnosis of infective endocarditis using Duke criteria?

A

2 major criteria, or 1 major + 3 minor, or 5 minor criteria.

96
Q

What are Janeway lesions?

A

Painless, erythematous macules on the palms and soles caused by septic emboli.

97
Q

What are Osler nodes?

A

Painful, tender nodules on the fingers and toes due to immune complex deposition.

98
Q

What are Roth spots?

A

Retinal hemorrhages with a pale center, seen in infective endocarditis.

99
Q

What is the most sensitive imaging modality for detecting infective endocarditis?

A

Transesophageal echocardiography (TEE).

100
Q

What is the initial empiric antibiotic treatment for native valve infective endocarditis?

A

Vancomycin + Ceftriaxone or Vancomycin + Gentamicin (to cover MRSA, Strep, and Enterococcus).

101
Q

What is the initial treatment for prosthetic valve endocarditis?

A

Vancomycin + Gentamicin + Rifampin (covers MRSA and biofilm-forming organisms).

102
Q

When is surgery indicated in infective endocarditis?

A
  1. Heart failure due to valve dysfunction, 2. Uncontrolled infection despite antibiotics, 3. Large vegetations (>10 mm) with embolic risk, 4. Prosthetic valve involvement.
103
Q

What is the most common complication of infective endocarditis?

A

Heart failure due to valvular destruction.

104
Q

What are the most common embolic complications of infective endocarditis?

A

Stroke, renal infarcts, splenic infarcts, and septic pulmonary emboli (especially in right-sided endocarditis).

105
Q

Which patients require prophylactic antibiotics for infective endocarditis?

A

Patients with prosthetic heart valves, prior IE, congenital heart disease, or cardiac transplant recipients undergoing dental procedures.

106
Q

What is the recommended prophylactic antibiotic regimen for high-risk patients before dental procedures?

A

Amoxicillin 2g PO 30-60 minutes before procedure (Clindamycin or Azithromycin if allergic).

107
Q

What is the most common cause of culture-negative infective endocarditis?

A

HACEK organisms (Haemophilus, Aggregatibacter, Cardiobacterium, Eikenella, Kingella) and prior antibiotic use.

108
Q

What is the pathophysiology of infective endocarditis?

A

Bacteria adhere to damaged endocardium, form vegetations with platelets and fibrin, leading to persistent bacteremia and embolization.

110
Q

What is the causative agent of COVID-19?

A

SARS-CoV-2 (a novel coronavirus, from the Coronaviridae family).

111
Q

What is the primary mode of transmission?

A

Respiratory droplets and aerosols.

112
Q

What is the incubation period of COVID-19?

A

2-14 days (average: 5 days).

113
Q

Which populations are at highest risk for severe COVID-19?

A

Elderly (≥60 y/o), immunocompromised, pregnant women, patients with comorbidities (DM, CKD, COPD, CVD).

114
Q

What are the 4 clinical categories of COVID-19?

A
  1. Mild, 2. Moderate, 3. Severe, 4. Critical.
115
Q

What defines mild COVID-19?

A

Symptoms (fever, cough, anosmia, sore throat) WITHOUT pneumonia or hypoxia.

116
Q

What defines moderate COVID-19?

A

Pneumonia WITHOUT hypoxia (SpO₂ ≥94%).

117
Q

What defines severe COVID-19?

A

Pneumonia WITH hypoxia (SpO₂ <94%, RR ≥30, or PaO₂/FiO₂ <300).

118
Q

What defines critical COVID-19?

A

ARDS, respiratory failure, septic shock, or multi-organ dysfunction (MODS).

119
Q

What is the gold standard test for COVID-19 diagnosis?

A

RT-PCR (Nasopharyngeal swab).

120
Q

When is rapid antigen testing (RAT) useful?

A

Best used within the first 5-7 days of symptoms in symptomatic cases.

121
Q

What is the characteristic finding on chest CT in severe COVID-19?

A

Bilateral ground-glass opacities (GGO) and crazy paving pattern.

122
Q

What chest X-ray findings are seen in severe COVID-19?

A

Bilateral interstitial infiltrates, patchy opacities.

123
Q

What is the first-line treatment for mild COVID-19?

A

Supportive care: hydration, antipyretics, NO antibiotics or antivirals.

124
Q

Which antiviral is recommended for high-risk outpatients with mild COVID-19?

A

Paxlovid (Nirmatrelvir-Ritonavir) within 5 days of symptom onset.

125
Q

What is the treatment for moderate COVID-19 requiring hospitalization?

A

Oxygen therapy (SpO₂ >94%) + Remdesivir in high-risk cases.

126
Q

What is the first-line steroid for severe COVID-19?

A

Dexamethasone 6 mg/day for 10 days.

127
Q

Which immunomodulator is recommended for severe COVID-19?

A

Tocilizumab (IL-6 inhibitor) for rapid progression cases.

128
Q

When is mechanical ventilation indicated in COVID-19?

A

For refractory hypoxemia (ARDS) despite oxygen support.

129
Q

What are the four main types of COVID-19 vaccines?

A
  1. mRNA vaccines, 2. Viral vector vaccines, 3. Inactivated virus vaccines, 4. Protein subunit vaccines.
130
Q

What are the mRNA vaccines for COVID-19?

A

Pfizer-BioNTech (Comirnaty) and Moderna (Spikevax).

131
Q

What are the viral vector vaccines for COVID-19?

A

AstraZeneca (Vaxzevria), Janssen (J&J), Sputnik V.

132
Q

What are the inactivated virus vaccines for COVID-19?

A

Sinovac (CoronaVac), Sinopharm (BBIBP-CorV).

133
Q

What is the protein subunit vaccine for COVID-19?

A

Novavax (Nuvaxovid).

134
Q

Which COVID-19 vaccine has the highest efficacy?

A

mRNA vaccines (Pfizer & Moderna) ~95% against severe disease.

135
Q

Which COVID-19 vaccine is single-dose?

A

Janssen (J&J).

136
Q

Which COVID-19 vaccines require storage at ultra-low temperatures?

A

Pfizer (-80°C to -20°C) and Moderna (-20°C).

137
Q

What are the key preventive measures for COVID-19?

A

Face masks, hand hygiene, ventilation, vaccination, avoiding crowded places.

138
Q

Who should receive a COVID-19 booster dose?

A

Elderly (≥60 y/o), immunocompromised, healthcare workers, pregnant women.

139
Q

Can COVID-19 vaccines be mixed for booster doses?

A

Yes, heterologous boosting is recommended.