Perioperative & Surgical Care
Preoperative antibiotic prophylaxis: SCIP measures
— SCIP Inf-1: Prophylactic antibiotic received within 1 hour before incision (2 hours for vancomycin or fluoroquinolones)
— SCIP Inf-2: Appropriate antibiotic selection for the specific surgery
— SCIP Inf-3: Prophylactic antibiotic discontinued within 24 hours after surgery end (48 hours for cardiothoracic)
— SCIP Inf-4: Cardiac surgery patients with 6 AM postop glucose <180 mg/dL on POD 1 and 2
— SCIP Inf-9: Urinary catheter removed by POD 2
— SCIP Inf-10: Perioperative normothermia (≥36°C) for colorectal surgery
— Any clean procedure with prosthetic implant (joint, mesh, vascular graft, valve)
— All clean-contaminated cases (GI, GU, GYN, head/neck entering aerodigestive mucosa)
— Contaminated cases (treatment, not just prophylaxis)
— High-risk clean cases: cardiac, breast with implant, neurosurgery
Board pearl: The single most-tested SCIP metric is antibiotic timing — within 60 minutes of incision (120 min for vanco/FQ). Earlier than 60 min or after incision = SCIP failure, even if the "right" drug was given.
Step 3 management: On CCS, when you "Order surgery," also order "prophylactic antibiotic" and document time relative to incision — the simulator credits proper timing.

— "A 68-year-old man is scheduled for elective total knee arthroplasty at 0800. At 0600 he receives 2 g cefazolin IV. Incision is made at 0815. Is timing appropriate?" → Yes if within 60 min; here 135 min before incision = failure.
— "Patient with MRSA nasal colonization going for CABG" → add vancomycin to cefazolin, do not replace it.
— "Patient reports penicillin allergy with rash as a child" → clarify reaction; non-severe rash ≠ contraindication to cefazolin (cross-reactivity <1%).
— "Anaphylaxis to penicillin" → use clindamycin or vancomycin depending on procedure.
— Allergy details: specific drug, reaction type, timing, severity, prior tolerance of cephalosporins
— MRSA status: prior infection, colonization, healthcare exposure, nursing home residence
— Recent antibiotic use (last 90 days) — affects resistance risk
— Weight — dosing is weight-based; cefazolin 2 g if <120 kg, 3 g if ≥120 kg
— Renal function — affects vancomycin and aminoglycoside dosing
— Diabetes and glycemic control — links to SCIP Inf-4
— Procedure type, duration, expected blood loss — drives redosing
— Colorectal: bowel prep status, mechanical + oral antibiotic prep (neomycin/metronidazole) reduces SSI
— Cardiac: sternal wound risk factors (DM, obesity, smoking, BIMA harvest)
— Ortho implant: prior joint infection, skin condition at incision site
Key distinction: Prophylaxis ≠ treatment. A patient with active cellulitis at the surgical site needs therapeutic antibiotics and case delay/redirection — not a single preop dose. Stem clues like "erythema, warmth, purulent drainage" demand you postpone elective surgery.
Board pearl: Always ask about β-lactam allergy nature before defaulting to vancomycin — overuse of vanco prophylaxis increases SSI from gram-negatives and is a tested pitfall.

— Skin at incision site: check for active dermatitis, cellulitis, open wounds, recent shaving abrasions. Clipping > shaving; razor shaving the night before doubles SSI rates.
— Nasal exam / MRSA swab result for cardiac and orthopedic implant cases — decolonization with mupirocin × 5 days + chlorhexidine baths reduces S. aureus SSI.
— Dentition: poor oral hygiene before cardiac valve or prosthetic joint surgery raises bacteremia risk.
— BMI and body habitus: obese patients need higher cefazolin dose (3 g) and may need redosing sooner.
— Indwelling devices: existing Foley, central line, drains — sources of contamination.
— Fever or tachycardia preop → delay elective surgery, work up source
— Hyperglycemia (random glucose >200) → optimize before elective case; cardiac surgery requires tight intraop/postop control
— Hypothermia risk: assess for thin habitus, long case duration → plan forced-air warming (SCIP Inf-10)
— Antibiotic ordered, dose appropriate for weight, scheduled to infuse within 60 min of incision
— Allergy verified and reconciled
— Hair management plan (clip in OR)
— Glucose check if diabetic
— Foley necessity assessed; if placed, plan for removal by POD 2
Step 3 management: If the vignette shows a patient shaved at home the night before for hernia repair, document and proceed — but on CCS, order chlorhexidine skin prep and counsel the patient that this is a modifiable risk for next time.
CCS pearl: Always order "chlorhexidine-alcohol skin prep" (superior to povidone-iodine for most clean and clean-contaminated cases per NEJM 2010 trial) when setting up a surgical case in the simulator — it's a credited intervention.
Board pearl: Normothermia, normoglycemia, and supplemental O₂ are the "triple S" SSI bundle beyond antibiotics.

— CBC: baseline WBC; leukocytosis preop suggests occult infection, delay elective case
— BMP: creatinine/eGFR required before vancomycin or aminoglycoside dosing
— Glucose / HbA1c: A1c >8% predicts SSI; cardiac surgery target preop A1c <7%. POD 1 and 2 glucose <180 mg/dL is the SCIP cardiac target.
— Albumin <3.5 g/dL and prealbumin: nutritional marker predicting SSI and dehiscence
— Coags if regional anesthesia planned (affects timing of antibiotic and block)
— MRSA nares PCR or culture — standard before cardiac, orthopedic implant, neurosurgical implant cases at most US institutions
— Urinalysis before urologic procedures, prosthetic joint, or vascular surgery; treat asymptomatic bacteriuria only if instrumentation of GU tract or implant placement
— Stool screening is not routine
— CXR if pulmonary symptoms, smoker, or thoracic case
— Dental panoramic before cardiac valve replacement at some centers
Key distinction: Asymptomatic bacteriuria generally does not warrant treatment except in pregnancy, prior to urologic procedure with mucosal trauma, or before prosthetic joint/heart valve implantation. Treating it otherwise is a tested pitfall (drives resistance, C. difficile, no SSI reduction).
Board pearl: A preop MRSA-positive nasal swab in a CABG patient mandates vancomycin + cefazolin (dual coverage), mupirocin nasal × 5 days, and chlorhexidine baths × 5 days — all three are tested as a bundle.
Step 3 management: Don't cancel surgery for mild anemia or stable CKD — but do delay elective surgery for uncontrolled hyperglycemia, untreated UTI before urologic instrumentation, or active skin infection at incision site.

— MRSA nasal PCR: rapid (1–2 hr); positive → add vancomycin and decolonize. Negative predictive value ~96% for S. aureus SSI.
— Wound or tissue culture if revising prior surgical site (e.g., revision arthroplasty for suspected indolent infection) — guides directed prophylaxis
— Synovial fluid analysis (cell count, alpha-defensin, culture) before revision joint surgery to rule out periprosthetic infection masquerading as aseptic loosening
— C. difficile PCR if recent diarrhea — affects choice and risk
— Local antibiogram — institutional gram-negative resistance rates may shift first-line choice (e.g., cefazolin failure rates for E. coli in colorectal cases)
— Prior culture data in the chart — if the patient grew ESBL E. coli from a recent UTI, urologic prophylaxis may require ertapenem
— Pre-infusion serum creatinine
— Weight-based dose (15 mg/kg, max ~2 g for prophylaxis)
— Infuse over ≥60 minutes (faster → red man syndrome — histamine release, not allergy)
— Start infusion 120 minutes before incision to complete on time
— Renal function and ideal body weight for dosing
— Single preop dose for prophylaxis avoids cumulative toxicity
Key distinction: Red man syndrome (flushing, pruritus during vanco infusion) is not an allergy — slow the rate, premedicate with antihistamine, continue use. Anaphylaxis (hypotension, bronchospasm, urticaria after dose) is a true allergy — switch agents.
Board pearl: A revision arthroplasty stem with elevated ESR/CRP and synovial WBC >3000 with PMN predominance signals chronic prosthetic joint infection — these patients need culture-directed therapy and possibly two-stage revision, not standard cefazolin prophylaxis.
CCS pearl: Order vancomycin trough only for therapeutic dosing, not single-dose prophylaxis — overordering wastes credit.

— Class I (clean): prophylaxis only if implant, high-risk host, or high-morbidity infection (cardiac, neuro, ortho implant, breast with implant, vascular)
— Class II (clean-contaminated): always prophylax (GI, biliary, GU with mucosal entry, head/neck, gyn, thoracic entering airway)
— Class III (contaminated): prophylaxis + often extended therapy (gross spillage, fresh trauma <4 hr, acute non-purulent inflammation)
— Class IV (dirty/infected): therapy, not prophylaxis (perforated viscus, abscess, devitalized tissue)
— Age >65, DM, obesity, smoking, malnutrition, immunosuppression, prior SSI, prolonged preop hospitalization, ASA ≥3
— Goal: therapeutic tissue concentration at incision and throughout case
— Cefazolin, cefuroxime, ampicillin-sulbactam, clindamycin: infuse within 60 min before incision
— Vancomycin, fluoroquinolones: within 120 min because of longer infusion
— Tourniquet cases (ortho): complete antibiotic infusion before tourniquet inflation
— Procedure duration exceeds 2 half-lives of the drug (cefazolin: redose at 4 hours)
— Blood loss >1500 mL or massive fluid resuscitation
— Adult cardiopulmonary bypass run
Step 3 management: A 5-hour open AAA repair with 2 L blood loss given a single 2 g cefazolin at induction is a SCIP failure — the correct answer is redose cefazolin at hour 4 and again if bleeding ongoing.
Board pearl: Dirty wounds get treatment, not prophylaxis. A vignette of perforated diverticulitis going to OR receives piperacillin-tazobactam or ceftriaxone + metronidazole as therapy, continued postop, not a single dose.
Key distinction: Postop antibiotic continuation beyond 24 hours (48 for cardiac) does not reduce SSI and increases C. difficile and resistance — a SCIP Inf-3 failure.

— Cardiac, vascular, orthopedic (including hip/knee arthroplasty), neurosurgery, head/neck (clean), thoracic (non-esophageal), plastic with implant, hernia with mesh, hysterectomy (with metronidazole), C-section
— Covers skin flora (S. aureus MSSA, S. epidermidis, streptococci) and some gram-negatives
— Colorectal: cefazolin + metronidazole OR cefoxitin OR ceftriaxone + metronidazole; add oral neomycin + metronidazole or erythromycin with mechanical bowel prep the day before
— Appendectomy (uncomplicated): cefoxitin or cefazolin + metronidazole, single dose
— Hysterectomy (vaginal or abdominal): cefazolin (some add metronidazole)
— C-section: cefazolin within 60 min before skin incision (changed from "after cord clamp" — reduces endometritis and SSI; add azithromycin for non-elective/laboring)
— Cholecystectomy (high-risk): cefazolin; low-risk elective lap chole — no prophylaxis needed
— GU with bowel involvement (cystectomy): cefoxitin or cef + metronidazole
— Transurethral prostate procedures: ciprofloxacin or TMP-SMX (treat preop bacteriuria first)
— Head/neck cancer with mucosal incision: ampicillin-sulbactam or cefazolin + metronidazole (covers oral anaerobes)
— Known MRSA colonization/infection
— High institutional MRSA rate
— Prosthetic implant + recent healthcare exposure
— Always co-administered with cefazolin (vanco has poor MSSA and gram-negative coverage)
Board pearl: The 2010 ACOG change: give cefazolin BEFORE skin incision for C-section, not after cord clamp. Tested repeatedly.
Step 3 management: Never substitute vancomycin alone for cefazolin in routine prophylaxis — vanco is inferior to cefazolin against MSSA and has narrower gram-negative coverage. Dual therapy if MRSA risk.
Key distinction: Cefoxitin (2nd-gen with anaerobic activity) is preferred where anaerobes matter and you want single-agent simplicity (colorectal, appy).

— Non-severe reaction (rash, GI upset, family history, unknown): cefazolin is safe — true cross-reactivity with penicillin is <1% (older 10% figure was overstated, contamination-driven). Use cefazolin.
— Severe IgE-mediated reaction (anaphylaxis, angioedema, bronchospasm, hypotension) or severe delayed (SJS/TEN, DRESS, AGEP, interstitial nephritis): avoid all β-lactams
— Alternative agents by procedure:
– Cardiac, vascular, ortho, neuro: vancomycin (± aztreonam or gentamicin if gram-negative coverage needed)
– Colorectal, GYN, GI: clindamycin + (gentamicin or aztreonam or ciprofloxacin) or metronidazole + (gent/aztreonam/cipro)
– Head/neck: clindamycin alone
— Cefazolin: 4 h
— Cefoxitin: 2 h
— Ampicillin-sulbactam: 2 h
— Clindamycin: 6 h
— Vancomycin: 8–12 h (rarely needed in single-dose prophylaxis)
— Metronidazole: not redosed in standard cases
— ≤24 hours post-op for most procedures
— ≤48 hours for cardiothoracic surgery
— Drains, catheters, packing are not indications to extend prophylaxis
— Intranasal mupirocin × 5 days + chlorhexidine bathing × 5 days for S. aureus decolonization in cardiac/ortho
— Vancomycin powder in wound in some spine cases (controversial, not standard)
— Wound irrigation with saline standard; antibiotic irrigation not routinely recommended
Board pearl: Continuing prophylactic antibiotics "until the drain comes out" is a classic SCIP failure — does not reduce SSI, increases C. difficile and resistance.
CCS pearl: On the simulator, after an uncomplicated colectomy, write "discontinue antibiotics" at 24 hours postop — credited stewardship action.
Step 3 management: A patient with "penicillin allergy — hives as a child, never tested" going for hip arthroplasty: order cefazolin, document shared decision and absence of severe reaction history.

— Same prophylaxis agents and timing apply; no age-based dose reduction for cefazolin
— Higher baseline SSI risk → strict adherence to bundle (timing, normothermia, glucose, hair clipping)
— Greater C. difficile susceptibility → strict SCIP Inf-3 discontinuation
— Polypharmacy: review for QT-prolonging agents before fluoroquinolone use
— Delirium risk with anticholinergic adjuncts
— Cefazolin: standard 2 g preop dose unchanged; redosing interval extended (eGFR 10–50: every 8 h instead of 4 h; eGFR <10: typically no redose needed in single-day case)
— Vancomycin: dose by actual body weight, no preop dose reduction for single use, but avoid redosing if eGFR <30; check trough if therapy continues
— Aminoglycosides: single preop dose generally safe; avoid in eGFR <30 when alternatives exist
— Fluoroquinolones: dose-adjust for eGFR <50
— Aztreonam: adjust for eGFR <30
— Metronidazole: reduce dose by 50% in severe (Child-Pugh C) cirrhosis
— Clindamycin: caution; monitor LFTs in prolonged use, single dose usually fine
— Ceftriaxone: caution in combined hepatic + renal failure (biliary sludge, displaces bilirubin)
— Albumin <3 g/dL predicts SSI; defer elective surgery for nutritional optimization when feasible
— Pressure injury risk → SCIP-adjacent: skin assessment, padding, positioning
Board pearl: Cefazolin is renally cleared but is rarely the culprit in AKI — most "renal" concerns in cefazolin use are about redosing frequency, not dose reduction of the preop dose itself.
Step 3 management: An 82-year-old with eGFR 35 going for total hip arthroplasty: give standard cefazolin 2 g preop; if case >4 hours, redose at 6–8 hours instead of 4. No need to substitute vancomycin unless MRSA risk.
Key distinction: Vancomycin nephrotoxicity is dose- and trough-dependent — a single prophylactic dose rarely causes AKI; avoid prolonged empiric use postop.

— C-section: cefazolin 2 g IV (3 g if ≥120 kg) within 60 minutes BEFORE skin incision — single most-tested OB prophylaxis fact
— Add azithromycin 500 mg IV for non-elective (laboring or ruptured membranes) C-section — reduces endometritis, wound infection
— β-lactam severe allergy: clindamycin + gentamicin
— Avoid: fluoroquinolones, tetracyclines, sulfonamides near term, aminoglycosides when alternatives exist
— Postpartum tubal ligation, D&C for retained products, cerclage: case-specific, often cefazolin
— Cefazolin 30 mg/kg (max 2 g) within 60 min of incision; redose every 4 h
— Vancomycin 15 mg/kg
— Clindamycin 10 mg/kg
— Weight-based dosing critical; underdosing common pitfall
— Cefazolin 3 g (some recommend 2 g if <120 kg, 3 g if ≥120 kg, with adult literature supporting up to 3 g for morbid obesity)
— Adequate dosing matters more than agent choice — underdosing predicts SSI
— Higher SSI baseline → strict bundle adherence
— Standard agents, but threshold to extend coverage for gram-negatives or fungi if indicated by surgery type
— Coordinate with transplant or oncology team for biologic timing (hold TNF-α inhibitors perioperatively per ACR/AAOS guidance)
— Maintain prophylaxis duration per SCIP — do not extend "just because immunocompromised" unless contamination
— Tight perioperative glucose (<180 mg/dL); SCIP Inf-4 for cardiac
— Hold SGLT2 inhibitors 3–4 days preop (DKA risk)
Board pearl: Cefazolin before skin incision in C-section is a near-guaranteed exam point — paired with azithromycin for non-elective cases.
Step 3 management: A 145 kg patient for ventral hernia repair with mesh: order cefazolin 3 g (not 2 g) within 60 min of incision; redose at 4 h if case extends.

— Superficial incisional: skin/subcutaneous, within 30 days
— Deep incisional: fascia/muscle, within 30–90 days
— Organ/space: within 30–90 days (or 1 year if implant)
— Most common organisms: S. aureus (MSSA > MRSA), coagulase-negative staph, E. coli, Enterococcus, Pseudomonas (procedure-dependent)
— C. difficile infection (CDI): risk rises with each unnecessary postop day of antibiotics — primary reason for SCIP Inf-3
— Allergic reactions: anaphylaxis, urticaria, rash; red man syndrome (vanco infusion rate) is non-allergic
— Nephrotoxicity: vancomycin, aminoglycosides
— AKI: vancomycin + piperacillin-tazobactam combination carries elevated AKI risk
— QT prolongation: fluoroquinolones, macrolides
— Tendinopathy and aortic dissection risk: fluoroquinolones (especially in elderly, steroid users)
— Antimicrobial resistance: selection of MDR organisms
— Wrong drug (e.g., vanco alone for clean cardiac in non-MRSA patient → MSSA breakthrough)
— Wrong dose (under-dosed obese patient)
— Wrong timing (>60 min preop, or after incision)
— Missed redose in long case
— Continued beyond 24/48 h
— Hypothermia → coagulopathy, increased SSI, cardiac events
— Hyperglycemia → impaired neutrophil function, sternal wound infection
— CAUTI from delayed Foley removal (SCIP Inf-9)
— VTE from missed prophylaxis (separate SCIP VTE measures)
Board pearl: A postop fever pattern: POD 0–1 atelectasis or drug fever, POD 3–5 UTI or pneumonia, POD 5–7 wound infection, POD >7 DVT/PE or abscess — the "5 Ws" mnemonic remains testable.
Key distinction: C. difficile presenting as postop diarrhea after "routine" prophylaxis extended to 5 days = iatrogenic, SCIP-preventable.
Step 3 management: Suspected SSI → open and drain, culture, then targeted antibiotics — don't escalate empirically without source control.

— Anaphylaxis during antibiotic infusion → stop infusion, epinephrine IM, IV fluids, secure airway, consider postponing elective surgery; allergy consult before next exposure
— Severe red man syndrome → slow infusion, antihistamines; not an escalation unless airway involvement
— Suspected SJS/TEN, DRESS → ICU or burn unit, dermatology, discontinue agent, no rechallenge ever
— Massive bleeding during long case → anesthesia communicates need for antibiotic redose; surgical team responsibility to track
— Sepsis from SSI or anastomotic leak: ICU admit, broad-spectrum empiric therapy (often piperacillin-tazobactam or meropenem + vancomycin), urgent source control (IR drainage or reoperation), surgical consult
— Mediastinitis after cardiac surgery: cardiac surgery consult, ICU, broad gram-positive + gram-negative coverage, washout
— Necrotizing soft tissue infection at wound: immediate surgical debridement, piperacillin-tazobactam + vancomycin + clindamycin (anti-toxin), ICU
— C. difficile fulminant (ileus, megacolon, shock): ICU, IV metronidazole + PO/PR vancomycin, surgical consult for colectomy
— Infectious disease for resistant organisms, prosthetic joint/valve infection, recurrent SSI
— Antimicrobial stewardship — institutional resource for de-escalation
— Allergy/immunology for verified severe β-lactam allergy needing future surgery (consider skin testing or graded challenge)
CCS pearl: When a postop patient spikes a fever and you suspect SSI, on the simulator: examine wound, open and culture if fluctuant, obtain blood cultures × 2, start empiric antibiotics based on local antibiogram, consult surgery — sequence credited.
Step 3 management: A patient develops hypotension and diffuse urticaria 5 minutes into vancomycin infusion → stop infusion, IM epinephrine 0.3–0.5 mg, IV fluids, diphenhydramine, methylprednisolone, secure airway, defer elective surgery, document true vancomycin allergy for future avoidance.
Board pearl: Always document and reconcile allergy events in the chart and EHR allergy list — transition-of-care failures kill.

— Superficial SSI: erythema, warmth, tenderness, purulent drainage from incision, fever; within 30 days. Treat with open-and-drain ± oral antibiotics if cellulitis surrounds.
— Deep incisional SSI: fascial dehiscence risk, deeper drainage; often requires OR washout.
— Organ/space SSI: intra-abdominal abscess after colorectal; CT + IR drainage + IV antibiotics.
— Anastomotic leak (POD 3–7): tachycardia, fever, leukocytosis, peritonitis or rising drain output that changes character. CT with oral/rectal contrast or surgery. Antibiotics alone don't substitute for source control.
— Seroma: painless, fluctuant, clear fluid; aspirate if symptomatic; no antibiotics
— Hematoma: painful, ecchymotic, expanding; evacuate if large; no antibiotics unless infected
— Suture reaction / stitch abscess: local, sterile; remove offending suture
— Fat necrosis: firm, indurated, slow resolution
— Wound dehiscence: mechanical failure; may or may not be infected — rule out fascial dehiscence (salmon-colored fluid = "pink fluid sign" → emergent OR)
— CLABSI, CAUTI, ventilator-associated pneumonia — different bundles, different antibiotics, but they masquerade as "SSI" in early postop fever
— Sternal wound infection / mediastinitis post-cardiac
— Periprosthetic joint infection — acute (<3 mo) vs chronic (>3 mo) → different surgical strategy (DAIR vs two-stage revision)
— Mesh infection after hernia repair — often requires mesh removal
Key distinction: Cellulitis vs. abscess: cellulitis = nonpurulent → β-lactam (cephalexin, dicloxacillin); abscess = purulent → I&D first, then antibiotics if surrounding cellulitis, immunocompromise, or systemic signs.
Board pearl: Salmon-colored "pink" serosanguinous drainage from a clean abdominal incision = impending fascial dehiscence, not infection — go to OR.
Step 3 management: Don't treat a postop seroma with antibiotics — aspirate and observe.

— Atelectasis (controversial as a fever cause but classically taught)
— Drug fever / transfusion reaction
— Malignant hyperthermia (intraop/immediate postop, masseter rigidity, hypercarbia) — dantrolene
— Pre-existing infection (UTI, pneumonia)
— UTI (especially if Foley in place — SCIP Inf-9 emphasizes removal by POD 2)
— Pneumonia / aspiration
— IV line-related phlebitis or CLABSI
— Early SSI (especially streptococcal or clostridial — onset <48 h with severe pain, crepitus, hypotension demands emergent debridement)
— Wound infection (typical SSI window)
— Anastomotic leak
— Intra-abdominal abscess
— C. difficile colitis from antibiotic exposure
— DVT / PE — fever, tachycardia, hypoxia
— Deep abscess, late SSI
— Drug-induced hepatitis, transfusion-associated infections
— Acalculous cholecystitis in critically ill
— Adrenal insufficiency in chronic steroid users without stress dosing
— Withdrawal syndromes (alcohol, benzodiazepine)
— Pancreatitis from medications or hypoperfusion
— Thyroid storm in undiagnosed Graves
Key distinction: Early-onset severe pain at the wound (POD 1–2) with crepitus and systemic toxicity → necrotizing fasciitis or clostridial myonecrosis, not routine SSI — emergent surgical debridement + broad antibiotics + ICU. Antibiotic prophylaxis would not have reliably prevented this in a contaminated case.
Board pearl: The 5 Ws of postop fever: Wind (POD 1–2 atelectasis/pneumonia), Water (POD 3 UTI), Walking (POD 4–5 DVT), Wound (POD 5–7 SSI), Wonder drugs (POD 7+ drug fever, C. diff).
Step 3 management: Postop fever without localizing signs on POD 1 → exam, basic labs, avoid reflex broadening of antibiotics; reassess in 24 h.

— Most procedures: stop within 24 h of surgery end
— Cardiothoracic: stop within 48 h
— Do not continue for drains, packing, catheters, or "just in case"
— Most clean and clean-contaminated cases: no antibiotic on discharge
— Contaminated/dirty cases or established infection: continue per source-specific guidelines (e.g., 4–7 days for perforated appendicitis with source control)
— Wound care instructions, infection warning signs (fever, increasing pain, drainage, opening of wound)
— Glycemic management for diabetics
— Mupirocin and chlorhexidine bath protocols ended preop unless prior known recurrent S. aureus infections — coordinate with ID
— Patients with prosthetic joints no longer require routine antibiotic prophylaxis for dental procedures per AAOS/ADA 2015 — case-by-case for immunocompromised
— Patients with prosthetic heart valves, prior IE, congenital cyanotic heart disease, cardiac transplant with valvulopathy still require endocarditis prophylaxis before high-risk dental/respiratory mucosal procedures per AHA
— Amoxicillin 2 g PO 30–60 min before dental work (clindamycin no longer first-line allergy alternative per 2021 update — use azithromycin or doxycycline)
— Document indication, agent, duration in discharge summary
— Flag any allergies developed perioperatively in EHR
— Communicate any positive cultures and follow-up plan to primary care
Key distinction: Surgical prophylaxis ≠ endocarditis prophylaxis. A patient with a mechanical mitral valve undergoing colonoscopy with biopsy needs no antibiotics (GI/GU procedures not in 2007/2021 AHA endocarditis prophylaxis indications).
Board pearl: Clindamycin is no longer recommended for endocarditis prophylaxis in penicillin-allergic patients (2021 AHA) due to C. difficile risk — use cephalexin (non-severe allergy), azithromycin, or doxycycline.
Step 3 management: Discharge summary must specify antibiotic stop date — transition-of-care safety issue.

— Vital signs, wound check on rounds
— Daily WBC trend not mandatory; check if clinical concern
— Glucose checks for diabetics and all cardiac surgery patients (target <180 mg/dL — SCIP Inf-4)
— Foley assessment daily; remove by POD 2 unless documented indication (urology, strict I/O for hemodynamics, sacral wound, comfort care)
— Drain output character and volume
— Temperature curve interpretation per "5 Ws"
— Postop visit 1–2 weeks with surgeon for wound check, suture/staple removal
— Longer-term visit per procedure (6 weeks for joint replacement rehab milestone, 30 days for SSI surveillance, 90 days for organ/space SSI in implant procedures)
— Primary care reconciliation within 1–2 weeks for chronic disease optimization
— Warning signs: fever >38.3°C, increasing pain or redness, wound drainage, opening, systemic symptoms
— Diabetes: continued tight glucose, A1c follow-up
— Smoking cessation: strongly tied to wound healing; offer pharmacotherapy
— Nutrition: protein intake, supplements if malnourished
— Activity: procedure-specific weight-bearing and lifting restrictions
— Catheter care if any indwelling device remains
— Institutions track 30-day SSI rates (NSQIP), readmissions for SSI, CDI rates
— Surgeon-level outcome feedback is part of value-based purchasing
Step 3 management: Postop wound check at 2 weeks reveals a 2 cm area of erythema without fluctuance, fever, or systemic symptoms in an otherwise healthy patient — mark borders, oral cephalexin × 5–7 days, return in 48 h or sooner if worsening — outpatient management appropriate.
Board pearl: Smoking cessation ≥4 weeks preop measurably reduces SSI and pulmonary complications — counsel and refer at every visit.
CCS pearl: On the simulator, order "smoking cessation counseling" and "nicotine replacement" during preop visits — both credit.

— Antibiotic administration is usually covered under broad surgical consent, but allergy disclosure and shared decision-making matter when using an agent with elevated risk (vancomycin in patient with renal disease, fluoroquinolone in elderly with QT prolongation)
— If a patient refuses prophylaxis, document capacity assessment, risks discussed (increased SSI), alternative non-pharmacologic measures, and proceed with their informed choice
— EHR allergy fields must specify drug, reaction, severity, date; vague "PCN allergy" entries lead to unnecessary vancomycin, more C. difficile, and higher SSI rates
— When a vague allergy is clarified preop (e.g., "rash as a child"), update the chart to reduce future overuse
— Handoffs between OR → PACU → floor → home are high-risk for missed antibiotic discontinuation orders (perpetuating beyond 24 h)
— Discharge summary must specify antibiotic stop date and any pending cultures
— Failure to communicate a positive MRSA swab or intraoperative culture to outpatient providers is a sentinel-event-level safety lapse
— Wrong-site surgery (time-out)
— Retained foreign object
— Mediastinitis after CABG — CMS non-payment trigger; reinforces glucose, decolonization, prophylaxis bundle
— CAUTI and CLABSI after hospital admission
— Inappropriate prophylaxis harms future patients via resistance — collective harm
— Stewardship programs are required by Joint Commission accreditation
— SSI rates publicly reported via NHSN/CMS Hospital Compare
— Adverse drug events to FDA MedWatch when serious
Step 3 management: A patient signed out from the OR team to the floor team with "continue antibiotics" but no stop date — the receiving team's responsibility is to review indication, check SCIP timing, write a stop order at 24 h unless documented reason to continue. Transition-of-care safety mandates closing this loop.
Board pearl: "PCN allergy" carries real morbidity — relabeling/de-labeling programs reduce SSI and C. difficile.

Board pearl: If the question gives a time for antibiotic infusion start, calculate whether it lands within 60 min (or 120 for vanco) of incision — this is the single most-tested SCIP fact.

Board pearl: Stems with explicit clock times are almost always testing timing of prophylaxis — calculate the interval before reading answer choices.

Give the right antibiotic, at the right dose, within 60 minutes of incision (120 for vancomycin/fluoroquinolones), redose for long cases or blood loss, and stop within 24 hours (48 for cardiothoracic) — that is the heart of SCIP-aligned surgical antibiotic prophylaxis.
Board pearl: When in doubt on a Step 3 surgical vignette — check the clock, the drug, the dose, the duration, and the allergy chart. Those five anchors capture nearly every testable SCIP point.

