Phys Vivas · general-medicine
Perioperative Medicine — Viva Defence
Structured DCE viva for physician-level perioperative medicine: long-case defence of a complex elderly patient with atrial fibrillation on a DOAC, insulin-treated diabetes, COPD, and a recent coronary stent facing major cancer surgery, and short-case discussion of cardiac risk stratification, perioperative diabetes, anticoagulation bridging and reversal, and VTE prophylaxis.
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Perioperative Medicine — Viva
Long Case Viva Defence
Candidate's opening statement (model answer)
"Mr Henare is a 74-year-old retired farmer referred two weeks before an elective anterior resection for a stage II rectal adenocarcinoma. He has atrial fibrillation on apixaban 5 milligrams twice daily; type 2 diabetes for 20 years on insulin glargine 30 units nocte and rapid-acting 12 units with meals, plus empagliflozin 10 milligrams; COPD with an FEV1 of 55 per cent predicted on tiotropium and budesonide-formoterol; ischaemic heart disease with a drug-eluting stent inserted eight months ago, on aspirin and clopidogrel; hypertension on perindopril and bisoprolol; and stage 3 chronic kidney disease with an eGFR of 45. He smokes ten cigarettes a day. His HbA1c is 64. He can walk on the flat but stops after one flight of stairs with breathlessness." [1]
"His main problems are:
- High perioperative cardiac risk — a Revised Cardiac Risk Index of at least three, with poor functional capacity, and a recent coronary stent.
- Perioperative diabetes needing an SGLT2 inhibitor hold and an insulin infusion plan.
- A complex anticoagulation and antiplatelet strategy — apixaban for AF, dual antiplatelet therapy with a recent stent, all needing to be reconciled around major cancer surgery.
- COPD optimisation and smoking cessation.
- Very high VTE risk requiring pharmacological and mechanical prophylaxis. [1]
"My immediate priorities are to risk-stratify his heart and decide on functional testing, to make a written perioperative medication and anticoagulation plan, to optimise his COPD, and to enrol him in an enhanced recovery pathway." [1]
Examiner probing questions and model answers
Examiner: "His RCRI is high and his functional capacity is poor. What is the role of a dobutamine stress echo here?" [1]
"By the guideline rule, non-invasive cardiac testing is reserved for a patient with elevated clinical risk AND poor or unknown functional capacity in whom the result will change management. He meets both — his RCRI is at least three and he cannot climb a flight of stairs. So a dobutamine stress echocardiogram is appropriate, because if it shows significant inducible ischaemia I would involve cardiology to consider whether he has a flow-limiting lesion that needs intervention for an independent cardiac indication. What I would not do is revascularise him purely to clear him for surgery — the CARP trial showed that prophylactic revascularisation before vascular surgery did not improve survival or reduce cardiac events in stable disease. I would also not initiate a beta-blocker acutely — the POISE trial showed that starting metoprolol just before surgery increased mortality and stroke, driven by hypotension and bradycardia. He should continue his bisoprolol, and I would make sure he is on a statin." [1]
Examiner: "How will you manage his apixaban around the surgery?" [1]
"Apixaban does not need bridging because it reaches full effect within hours of a dose, unlike warfarin. I would stop it 48 hours before surgery — two missed doses — for this major intra-abdominal procedure. His eGFR is 45, and because apixaban is only about 27 per cent renally cleared, 48 hours is adequate and I do not need to extend it the way I would for dabigatran, which is largely renally cleared. I would restart it once haemostasis is secure, typically 24 to 72 hours after a major resection. His CHA2DS2-VASc is high — age, hypertension, diabetes and vascular disease — so I would not interrupt anticoagulation any longer than necessary. If I needed to reverse apixaban in an emergency bleed, andexanet alfa is the specific reversal agent; if that were unavailable, four-factor PCC at 25 to 50 units per kilogram is the alternative." [1]
Examiner: "He is eight months out from a drug-eluting stent. How does that affect your plan?" [1]
"This is the single most dangerous part of his perioperative management. The minimum stent period for a drug-eluting stent is six months — or three to six months in selected stable patients — so he is just past the conservative floor for elective surgery, which is reassuring. The plan, which I would agree with cardiology, is to continue his aspirin through the surgery and to stop the clopidogrel five days before, for this moderate-to-high bleeding-risk cancer resection, restarting it as soon as haemostasis is secure and completing the full intended twelve-month dual antiplatelet course. The reason aspirin continues is that stent thrombosis carries a mortality of 30 to 50 per cent, and the bleeding risk of continuing aspirin alone is generally acceptable. I would not stop both agents, and I would not stop aspirin and continue the P2Y12 inhibitor — the logic is to keep one platelet blocker on board. POISE-2 showed aspirin did not reduce events in unselected surgical patients, but the coronary-stent population is the recognised exception." [1]
Examiner: "Walk me through his diabetes plan for the day of surgery." [1]
"First, I would stop his empagliflozin three days before surgery. The reason is the risk of euglycaemic diabetic ketoacidosis, which is precipitated by the combination of the SGLT2 inhibitor, fasting, surgical stress and dehydration, and which is frequently missed because the glucose may be only mildly elevated. On the day of surgery I would place him first on the list. I would continue his glargine — his basal insulin — at about 75 per cent of his usual dose on the night before and the morning of surgery, and omit the meal-time rapid-acting insulin while he is fasting. Because he is insulin-treated and facing a major resection with prolonged fasting, I would start a variable-rate intravenous insulin infusion with a glucose substrate fluid and hourly capillary glucose monitoring, targeting 6 to 10 millimoles per litre. The VRIII replaces the obsolete sliding scale, which produces erratic control with no basal cover. Once he is eating, I would overlap his first subcutaneous basal-bolus dose with the infusion and then stop the infusion, and restart the empagliflozin only when he is eating and drinking normally and clinically stable." [1]
Examiner: "His eGFR is 45. How does that change your LMWH prophylaxis?" [1]
"He is very high VTE risk by Caprini — active cancer, major abdominal surgery, age, obesity, immobility — so he absolutely needs pharmacological prophylaxis. Enoxaparin 40 milligrams once daily is acceptable down to a creatinine clearance of about 30, so at 45 I would use the standard 40 milligrams daily dose without reduction, given six to twelve hours postoperatively once haemostasis is secure. If his renal function were to deteriorate postoperatively, I would reassess — below a CrCl of 30 I would reduce to 20 milligrams daily or switch to unfractionated heparin. I would add mechanical prophylaxis with compression stockings and intermittent pneumatic compression during and after surgery, after checking his arterial circulation, and I would continue prophylaxis for the full hospital stay and consider extended prophylaxis for four weeks because this is cancer surgery." [1]
Examiner: "What is the most dangerous error a registrar could make in this patient?" [1]
"Stopping his aspirin around the surgery because of bleeding concerns, while he is within the stent period. Acute stent thrombosis is a frequently fatal event and the aspirin is the single most protective continuation in his regimen. The second most dangerous error is continuing the empagliflozin into the fasting and surgical-stress period, which risks euglycaemic DKA. The third is using a sliding-scale insulin regimen instead of a variable-rate intravenous insulin infusion." [1]
You have read the opening of this viva. The complete unit — every section and its primary-source references — is part of the Physician Medicine fellowship atlas.
References3Show ledgerHide ledger
- [1]Lee TH, Marcantonio ER, Mangione CM, et al. Derivation and prospective validation of a simple index for prediction of cardiac risk of major noncardiac surgery Circulation, 1999.PMID 10477528
- [2]Devereaux PJ, Yang H, Yusuf S, et al. Effects of extended-release metoprolol succinate in patients undergoing non-cardiac surgery (POISE trial): a randomised controlled trial Lancet, 2008.PMID 18479744
- [3]Sarode R, Milling TJ Jr, Refaai MA, et al. Efficacy and safety of a 4-factor prothrombin complex concentrate in patients on vitamin K antagonists presenting with major bleeding: a randomized, plasma-controlled, phase IIIb study Circulation, 2013.PMID 23935011