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Sample Adult Infectious Diseases Fellowship Practice Questions

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1A 54-year-old man with no prior cardiac history presents with 2 weeks of remittent fever, malaise, and a new holosystolic murmur at the apex radiating to the axilla. Blood cultures grow methicillin-susceptible Staphylococcus aureus (MSSA) in 4 of 4 bottles within 12 hours. Transesophageal echocardiography (TEE) demonstrates a 16-mm mobile vegetation on the anterior leaflet of the mitral valve with severe mitral regurgitation and mild pulmonary venous systolic flow reversal. On hospital day 2, while receiving intravenous cefazolin, he develops sudden-onset left hemiparesis. Brain MRI reveals a 12-mm non-hemorrhagic cortical ischemic infarct in the right middle cerebral artery territory. What is the most appropriate next step in the management of this patient?
A.Continue cefazolin monotherapy and delay any surgical consideration for at least 4 weeks to avoid hemorrhagic conversion
B.Proceed with urgent mitral valve repair or replacement within 24 to 72 hours
C.Switch cefazolin to daptomycin plus rifampin and gentamicin for bactericidal synergy
D.Discontinue intravenous antibiotics and administer intravenous recombinant tissue plasminogen activator (rtPA)
Explanation: According to the 2023 Duke-ISCVID criteria and both AHA and ESC guidelines for infective endocarditis, urgent valve surgery is indicated for native valve endocarditis presenting with severe acute valve regurgitation, heart failure, high embolic risk (vegetation >10 mm on the mitral valve), and persistent mobile mass after an embolic event. For non-hemorrhagic, small ischemic stroke without massive cerebral edema, valve surgery should not be delayed (recommended within 24-72 hours if no coma or severe neurological impairment is present) because the risk of recurrent recurrent embolization outweighs the risk of secondary hemorrhagic conversion.
2A 48-year-old previously healthy woman is brought to the emergency department with acute high-grade fever, severe headache, photophobia, and altered mental status. On examination, she is somnolent with marked nuchal rigidity and positive Kernig sign. Lumbar puncture demonstrates opening pressure of 290 mm H2O, WBC count of 3,800/mcL (92% neutrophils), glucose 18 mg/dL (serum glucose 110 mg/dL), and protein 240 mg/dL. Gram stain reveals lancet-shaped Gram-positive diplococci. What is the recommended strategy regarding adjunctive corticosteroid therapy in this patient?
A.Administer intravenous dexamethasone 10 mg prior to or concurrently with the first dose of antimicrobial therapy and continue for 4 days if Streptococcus pneumoniae is confirmed
B.Initiate dexamethasone only after Streptococcus pneumoniae susceptibility to ceftriaxone is finalized
C.Withhold dexamethasone because adjunctive corticosteroids increase neurological complications in adult pneumococcal meningitis
D.Administer dexamethasone for a full 14-day course concurrently with intravenous vancomycin and ceftriaxone
Explanation: In adult patients with suspected or proven acute bacterial meningitis, adjunctive dexamethasone (10 mg IV every 6 hours) should be administered prior to or concurrently with the first dose of empiric antibiotics. Pivotal trials have shown that dexamethasone significantly reduces hearing loss, neurological sequelae, and overall mortality in pneumococcal meningitis. If S. pneumoniae is identified, dexamethasone is continued for 4 days; if another pathogen is confirmed (except Haemophilus influenzae type b), corticosteroids should be discontinued.
3A 62-year-old man presents with persistent dull left shoulder pain and mild stiffness 14 months following a total shoulder arthroplasty. He has no fever or systemic symptoms, and the surgical scar is well-healed without sinus tract. Inflammatory markers show an ESR of 28 mm/hr and CRP of 14 mg/L (normal <5 mg/L). Fluoroscopy-guided glenohumeral joint aspiration yields synovial fluid with 2,400 WBCs/mcL (72% polymorphonuclear cells). Anaerobic cultures from the synovial fluid yield Cutibacterium acnes (formerly Propionibacterium acnes) on day 9 of incubation. What is the most appropriate management plan for this delayed prosthetic joint infection (PJI)?
A.Oral cephalexin monotherapy for 6 months with prosthesis retention
B.Arthroscopic joint washout and retention of all prosthetic components followed by 6 weeks of intravenous penicillin
C.One-stage or two-stage exchange arthroplasty combined with intravenous penicillin or ceftriaxone followed by oral rifampin-based combination therapy
D.Permanent resection arthroplasty without antimicrobial therapy because Cutibacterium acnes is a non-pathogenic skin commensal
Explanation: Cutibacterium acnes is a classic pathogen of indolent shoulder prosthetic joint infections, capable of forming persistent biofilms on implant surfaces. Debridement and implant retention (DAIR) has unacceptably high failure rates in chronic infections (>30 days post-implantation). Complete implant removal via one-stage or two-stage revision arthroplasty combined with high-dose intravenous beta-lactams (penicillin G or ceftriaxone) followed by oral switch (frequently incorporating rifampin with an active companion agent) is required for cure.
4A 65-year-old mechanically ventilated patient in the intensive care unit develops new purulent endotracheal secretions, worsening hypoxemia (PaO2/FiO2 ratio 160), and progressive bilateral lower lobe infiltrates on day 10 of hospitalization. Endotracheal aspirate culture yields >10^6 CFU/mL of Pseudomonas aeruginosa. Susceptibility testing reveals resistance to piperacillin-tazobactam, cefepime, meropenem, imipenem, ciprofloxacin, and tobramycin (difficult-to-treat resistance [DTR] phenotype). The isolate remains susceptible to ceftolozane-tazobactam and colistin. What is the preferred definitive antimicrobial therapy according to IDSA guidance on antimicrobial-resistant Gram-negative infections?
A.Intravenous colistin monotherapy with high-dose loading
B.Inhaled tobramycin monotherapy at standard cystic fibrosis doses
C.Intravenous meropenem extended infusion at 2 g every 8 hours combined with ciprofloxacin
D.Intravenous ceftolozane-tazobactam 3 g every 8 hours by extended infusion
Explanation: According to the IDSA guidance for the treatment of antimicrobial-resistant Gram-negative infections, ceftolozane-tazobactam (3 g IV every 8 hours infused over 3 hours for normal renal function) is the preferred first-line agent for DTR-Pseudomonas aeruginosa pneumonia when susceptible. It avoids the severe nephrotoxicity and neurotoxicity associated with polymyxins and achieves higher clinical cure and lower 30-day mortality compared to polymyxin-based regimens.
5A 71-year-old woman with chronic kidney disease presents with watery diarrhea (6 loose stools daily), lower abdominal cramping, and leukocytosis (WBC 14,200/mcL). Stool nucleic acid amplification test and toxin EIA are positive for Clostridioides difficile. She was treated 4 weeks ago for her initial episode of non-severe C. difficile infection with oral vancomycin 125 mg 4 times daily for 10 days, achieving complete symptom resolution. What is the most appropriate management for this first recurrence of C. difficile infection according to current IDSA/SHEA clinical guidelines?
A.Oral fidaxomicin 200 mg twice daily for 10 days (or twice daily for 5 days then every other day for 20 days)
B.Repeat the exact course of oral vancomycin 125 mg 4 times daily for 10 days
C.Immediate fecal microbiota transplantation (FMT) via colonoscopy
D.Oral metronidazole 500 mg 3 times daily for 14 days
Explanation: According to IDSA/SHEA guidelines, the preferred therapy for a first recurrence of C. difficile infection when oral vancomycin was used for the primary episode is oral fidaxomicin (200 mg twice daily for 10 days or an extended-pulsed regimen). Fidaxomicin achieves narrow-spectrum bactericidal activity against C. difficile with minimal disruption of the protective fecal Bacteroidetes and Firmicutes microbiota, significantly reducing subsequent recurrence rates.
6A 52-year-old man with decompensated alcohol-related cirrhosis (Child-Pugh class C, MELD-Na 24) presents with worsening abdominal distension, fever (38.4 C), and mild diffuse abdominal tenderness without rigidity. Diagnostic paracentesis yields cloudy ascitic fluid with an absolute neutrophil count of 420 cells/mcL. What is the most appropriate immediate medical management?
A.Withhold antimicrobials until ascitic fluid bacterial culture results are finalized in 48 hours
B.Initiate intravenous ceftriaxone (or cefotaxime) plus intravenous 20% albumin infusion (1.5 g/kg on day 1 and 1.0 g/kg on day 3)
C.Administer oral ciprofloxacin 500 mg twice daily as outpatient monotherapy
D.Perform emergency laparotomy for presumed hollow viscus perforation
Explanation: Spontaneous bacterial peritonitis (SBP) is defined by an ascitic fluid absolute polymorphonuclear neutrophil (PMN) count >= 250 cells/mcL in the absence of an intra-abdominal surgically treatable source. Immediate empiric therapy with a third-generation cephalosporin (e.g., ceftriaxone 2 g IV daily) is indicated. In addition, intravenous albumin (1.5 g/kg at diagnosis and 1.0 g/kg on day 3) reduces the incidence of hepatorenal syndrome from 30% to 10% and significantly decreases inpatient mortality.
7A 59-year-old man with well-controlled type 2 diabetes presents with progressive mid-lumbar back pain and low-grade fever for 3 weeks. Spinal MRI demonstrates T1 hypointensity, T2 hyperintensity, and post-contrast enhancement of the L3-L4 intervertebral disc and adjacent vertebral endplates with minimal non-compressive epidural phlegmon. CT-guided disc biopsy yields methicillin-susceptible Staphylococcus aureus (MSSA). Neurological examination is completely normal. He receives IV cefazolin with rapid defervescence and normalization of pain. What is the evidence-based recommendation regarding total duration and oral step-down therapy according to the OVIVA trial and IDSA guidelines?
A.Mandatory 12 weeks of intravenous cefazolin via peripherally inserted central catheter (PICC) without oral step-down
B.A total of 2 weeks of IV antibiotics followed by immediate cessation if follow-up MRI shows stable discitis
C.A total course of 6 weeks of antimicrobial therapy, with high-bioavailability oral therapy (e.g., oral cefalexin or fluoroquinolone/clindamycin) shown to be non-inferior to continued IV therapy once clinically stable
D.Immediate surgical decompression and disc fusion regardless of neurological status
Explanation: According to IDSA guidelines and the landmark OVIVA (Oral versus Intravenous Antibiotics for Bone and Joint Infection) trial, 6 weeks of total antimicrobial therapy is the standard duration for uncomplicated native vertebral osteomyelitis. In patients who achieve clinical stability, defervescence, and declining inflammatory markers, transition to a regimen of highly bioavailable oral antibiotics is non-inferior to a full 6-week intravenous regimen, avoiding vascular catheter-associated bloodstream and thrombotic complications.
8A 36-year-old previously healthy man presents with excruciating right lower extremity pain out of proportion to physical exam findings following a minor skin abrasion sustained 24 hours earlier. Within 4 hours of arrival, the leg develops dusky violaceous bullae, cutaneous anesthesia, and crepitus. Blood pressure drops to 78/46 mmHg and heart rate is 135 bpm. Urgent operative exploration reveals greyish dishwater fluid and lack of bleeding along the deep fascia. Intraoperative Gram stain shows chains of Gram-positive cocci. What antimicrobial regimen should be initiated immediately alongside emergent surgical debridement?
A.Intravenous penicillin G plus intravenous clindamycin
B.Intravenous vancomycin monotherapy
C.Intravenous ciprofloxacin plus metronidazole
D.Intravenous piperacillin-tazobactam monotherapy
Explanation: Necrotizing fasciitis caused by Streptococcus pyogenes (Group A Streptococcus, GAS) is a medical and surgical emergency. High-dose IV penicillin G (4 million units every 4 hours) targets the pathogen cell wall. Clindamycin (900 mg IV every 8 hours) is critically added because of the Eagle effect (penicillins lose efficacy in stationary growth phase high-inoculum deep infections) and because clindamycin acts on the 50S ribosomal subunit to suppress bacterial protein synthesis and toxin production (streptococcal pyrogenic exotoxins A, B, and C).
9A 61-year-old woman undergoing induction chemotherapy for acute myeloid leukemia via a tunneled subclavian central venous catheter (Hickman line) develops rigors and fever to 39.2 C. Two sets of blood cultures (one peripheral and one from the catheter hub) turn positive for Staphylococcus aureus at 14 hours and 8 hours of incubation, respectively. She has no erythema or purulence along the subcutaneous tunnel. In addition to initiating IV daptomycin, what is the mandatory recommendation regarding the catheter?
A.Attempt catheter salvage using antibiotic lock therapy with vancomycin and heparin for 14 days
B.Exchange the catheter over a guidewire under sterile conditions
C.Leave the catheter in place and re-evaluate with repeat blood cultures in 7 days
D.Promptly remove the central venous catheter
Explanation: According to IDSA guidelines for the management of intravascular catheter-related infections, prompt catheter removal is mandatory for catheter-related bloodstream infection (CRBSI) caused by Staphylococcus aureus, Pseudomonas aeruginosa, fungi (Candida species), or mycobacteria. Retaining the catheter in S. aureus CRBSI is associated with recurrent bacteremia, metastatic seeded complications (endocarditis, vertebral osteomyelitis), and significantly higher mortality. Antibiotic lock therapy is never recommended for S. aureus catheter infections.
10A 50-year-old man presents with acute perforated appendicitis with a 4-cm retrocecal abscess. Percutaneous drainage is performed, and peritoneal fluid cultures grow Escherichia coli producing an extended-spectrum beta-lactamase (ESBL). The isolate tests susceptible in vitro to piperacillin-tazobactam (MIC 4 mcg/mL), ertapenem (MIC <= 0.25 mcg/mL), and meropenem (MIC <= 0.25 mcg/mL). Blood cultures are negative, and the patient is clinically improving. Based on evidence from randomized clinical trials (e.g., the MERINO trial) and current IDSA guidance, what is the preferred definitive antimicrobial therapy?
A.Intravenous piperacillin-tazobactam 4.5 g every 6 hours
B.Intravenous ertapenem 1 g once daily
C.Intravenous cefepime 2 g every 8 hours
D.Oral amoxicillin-clavulanate 875/125 mg twice daily
Explanation: According to IDSA guidance for ESBL-producing Enterobacterales and the findings of the MERINO trial, carbapenems remain the drugs of choice for invasive infections caused by ESBL-producing pathogens. For non-pseudomonal, community-onset intra-abdominal infections, once-daily ertapenem is highly effective, convenient, and spares antipseudomonal carbapenems (meropenem/imipenem). The MERINO trial established that piperacillin-tazobactam was associated with significantly higher 30-day mortality compared to meropenem in ESBL bacteremia.

About the Adult Infectious Diseases Fellowship Exam

Independent English-language MCQ study adaptation by OpenExamPrep. Independent practice question bank by OpenExamPrep for fellows preparing for the Saudi Fellowship Final Written Examination in Adult Infectious Diseases administered by the Saudi Commission for Health Specialties (SCFHS). This practice resource covers bacterial, viral, fungal, mycobacterial, parasitic, and tropical infections, immunocompromised host care, clinical microbiology, stewardship, and antimicrobial pharmacology. It is an independent MCQ study aid for the written final exam and does not simulate the clinical, OSCE, or structured oral examination.

Exam sponsor: Saudi Commission for Health Specialties (SCFHS). The requirements and fees below concern the certification or admission exam, separate from our free practice resources.

Assessment

One paper of 80–120 single-best-answer MCQs. Up to 10% additional unscored items may be added. Duration is not stated in the written blueprint.

Time Limit

Not published by SCFHS

Passing Score

70% (lowered to minimum 65% if pass rate under 70%)

Exam / Certification Fees

Not published by SCFHS

Exam sponsor website

Reported exam pass rate: Not published by SCFHS. SCFHS publishes no candidate pass rate. The blueprint instead sets the passing score at 70% and, if fewer than 70% of candidates pass before final approval, lowers that score one mark at a time until a 70% pass rate is reached or the score reaches 65%, whichever comes first; it is never lowered below 65%. Exam sponsor website

Fees, eligibility, and exam policies can change. Confirm them with the exam sponsor before applying or paying.

Our practice resources: topics covered

We aim to reflect publicly available exam outlines and topic information in our study resources. Coverage, format, and difficulty may differ from the actual exam, and we cannot guarantee that every detail is accurate or current. Confirm exam requirements, fees, and policies with the official exam sponsor.

23%

Bacterial Diseases

Bacteremia, infective endocarditis, CNS infections, bone and joint infections, SSTIs, intra-abdominal infections, and MDR pathogens.

10%

Clinical Microbiology

Diagnostic microbiology, Gram stain and culture interpretation, susceptibility testing methodologies, molecular diagnostics, and mass spectrometry.

10%

Viral Diseases

HIV/AIDS diagnosis and management, viral hepatitis (HBV, HCV, HDV), herpesviruses, respiratory viruses, arboviruses, and emerging viral pathogens.

10%

Mycobacterial Infections

Pulmonary and extrapulmonary tuberculosis, drug-resistant TB (MDR/XDR), latent TB infection, and non-tuberculous mycobacteria (NTM).

10%

Parasites, Tropical and Zoonotic Infections

Malaria, leishmaniasis, schistosomiasis, echinococcosis, brucellosis, MERS-CoV, dengue, rabies, and regional travel/zoonotic infections.

5%

Immunology and Vaccination

Primary and secondary immunodeficiencies, adult immunization schedules, pre-travel vaccines, post-exposure prophylaxis, and vaccine safety.

15%

Immunocompromised Host and Fungal Infections

Infections in solid organ and hematopoietic stem cell transplant recipients, neutropenic fever, candidiasis, invasive aspergillosis, and mucormycosis.

10%

Antimicrobial Stewardship and Infection Control

Stewardship metrics, formulary restriction, antibiograms, healthcare-associated infections (CAUTI, CLABSI, SSI), outbreak response, and isolation precautions.

7%

Pharmacology and Therapeutics

Antimicrobial pharmacokinetics and pharmacodynamics (PK/PD), therapeutic drug monitoring, adverse drug reactions, drug-drug interactions, and organ dose adjustments.

Preparing for the Adult Infectious Diseases Fellowship Exam

What You Need to Know

  • Passing score: 70% (lowered to minimum 65% if pass rate under 70%)
  • Assessment: One paper of 80–120 single-best-answer MCQs. Up to 10% additional unscored items may be added. Duration is not stated in the written blueprint.
  • Time limit: Not published by SCFHS
  • Exam / certification fees: Not published by SCFHS Official sources

Using Our Practice Resources

  • Work through all 100 available questions
  • Review every answer and explanation
  • Track weak areas and revisit them
  • Use our AI tutor for tough concepts

Frequently Asked Questions

What is the structure of the Saudi Fellowship Final Written Examination in Adult Infectious Diseases?

One paper of 80–120 single-best-answer MCQs. Up to 10% additional unscored items may be added. Duration is not stated in the written blueprint.

What is the passing score for the Saudi Fellowship Adult Infectious Diseases written examination?

The standard passing score is 70%. If the overall candidate pass rate falls below 70%, the passing score is adjusted downward one percentage mark at a time to target a 70% pass rate, but it is never lowered below 65%.

Does this practice bank include clinical or oral exam preparation?

This bank is an independent English-language MCQ study adaptation for the written examination. It does not simulate or replace the separate mandatory final clinical/practical assessment. Consult the specialty clinical blueprint for its station formats and any structured oral or OSCE components.

Is OpenExamPrep affiliated with the Saudi Commission for Health Specialties (SCFHS)?

No. OpenExamPrep is an independent educational platform. This practice resource is not endorsed by, sponsored by, or affiliated with the Saudi Commission for Health Specialties.