What is robotic aortic valve replacement, its purpose, and associated care?

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Robotic Aortic Valve Replacement (RAVR): Comprehensive Clinical Overview

System Classification

Robotic aortic valve replacement is a cardiovascular surgical procedure utilizing the da Vinci robotic surgical system (Intuitive Surgical) to perform aortic valve replacement through a minimally invasive right lateral thoracotomy approach. 1, 2, 3

  • System: Cardiovascular/Cardiac Surgery 1, 2
  • Robotic Platform: da Vinci Si or Xi robotic system with 3-4 port configuration 1, 2, 3
  • Approach: Right lateral mini-thoracotomy (3-4 cm incision) with 3-port technique 3, 4

Purpose and Clinical Indications

RAVR provides a minimally invasive alternative to traditional surgical aortic valve replacement (SAVR) for patients requiring durable valve replacement who desire to avoid sternotomy, particularly addressing gaps left by transcatheter approaches. 5, 3

Primary Indications:

  • Bicuspid aortic stenosis (56% of cases in recent series) where TAVR outcomes remain uncertain 3
  • Severe aortic insufficiency (16% of cases) where TAVR is contraindicated 3, 4
  • Young patients requiring mechanical valves (32% of cases) for lifelong durability without anticoagulation concerns from TAVR 3
  • Patients requiring concomitant procedures (Cox maze, mitral repair, root enlargement) that cannot be addressed transcatheter 3, 4
  • Low-risk patients preferring minimally invasive approach over sternotomy 5, 3
  • Horizontal valve position making TAVR technically challenging 5

Required Supplies and Equipment

Robotic System Components:

  • da Vinci Si or Xi robotic surgical system with patient-side cart 1, 2
  • Three robotic ports: 1 endoscopic camera port (8-12mm) and 2 instrument arm ports 1, 2
  • 3-4 cm right lateral working incision in 4th intercostal space 3
  • Robotic instruments: needle drivers, forceps, scissors 1, 2

Cardiopulmonary Bypass Equipment:

  • Peripheral cannulation supplies: femoral arterial and venous cannulas 1, 2
  • Transthoracic aortic cross-clamp inserted through 2nd intercostal space stab wound 6
  • Cardioplegia delivery system: antegrade cold crystalloid or blood cardioplegia catheter placed in ascending aorta 1, 2
  • Vent cannula for placement through right superior pulmonary vein 1
  • Vacuum-assisted venous drainage system 6

Valve Prostheses:

  • Conventional SAVR prostheses: mechanical or bioprosthetic valves with interrupted braided sutures 3
  • Sutureless valves (Perceval S) for facilitated deployment 1
  • Valve sizers and deployment instruments 1

Additional Instruments:

  • Long scissors for bedside surgeon assistance with calcified valve excision 1
  • Decalcification instruments for annular preparation 1
  • Defibrillator pads positioned outside operative field 6
  • Transesophageal echocardiography (TEE) probe 6

Pre-Procedure Steps

Patient Selection and Evaluation:

  • Multidisciplinary Heart Team evaluation involving cardiac surgery, interventional cardiology, imaging specialists, and anesthesia 6, 7
  • Comprehensive echocardiographic assessment including valve morphology, annular size, and ventricular function 7
  • CT angiography to evaluate chest anatomy, pleural adhesions, and peripheral vascular access 6
  • Assessment for contraindications: significant right pleural adhesions, peripheral vascular disease precluding femoral access, porcelain aorta 6

Anesthesia Preparation:

  • Dedicated anesthesia team with expertise in TEE and robotic cardiac surgery 6
  • Single lung ventilation setup: double lumen endotracheal tube or single lumen with bronchial blocker 6
  • Monitoring lines: arterial line, central venous access, pulmonary artery catheter (optional), percutaneous pulmonary artery vent 6

Patient Positioning:

  • Supine position with right hemithorax elevated 30 degrees, hips flat 6
  • Right arm tucked with shoulder slightly extended, elbow flexed, arm hanging supported below table 6
  • Small pillow placed inferior to scapula 6
  • Defibrillator pads applied outside operative field with consideration for potential sternotomy conversion 6

Surgical Field Preparation:

  • Sterile prep and drape from neck to groin, including entire right chest and both groins for peripheral access 6
  • Positioning verification to avoid robotic arm collision with head, endotracheal tube, abdomen, or pelvis 6

Procedure Steps

Phase 1: Access and Cannulation (Time: 30-45 minutes)

  1. Peripheral vascular access: femoral artery and vein cannulation for cardiopulmonary bypass 1, 2
  2. Port placement:
    • Camera port in medial aspect of 4th intercostal space 6
    • Robotic arm ports in 2nd-3rd intercostal space (anterior axillary line) and 5th-6th intercostal space 6
    • 3-4 cm working incision in 4th intercostal space 3
  3. Robot docking: patient-side cart positioned and instruments inserted 1, 2

Phase 2: Cardiopulmonary Bypass Initiation (Time: 15-20 minutes)

  1. Vent cannula placement through right superior pulmonary vein 1
  2. Cardioplegia cannula insertion in ascending aorta with robotic purse-string suture 1, 2
  3. Transthoracic aortic cross-clamp inserted through 2nd intercostal space stab wound, 8-10 cm posterior to left robotic arm 6
  4. Cardiopulmonary bypass initiation with mild-moderate hypothermia (28-33°C) 6
  5. Cardioplegic arrest following aortic cross-clamping 1, 2

Phase 3: Aortic Valve Exposure (Time: 10-15 minutes)

  1. Clam shell aortotomy performed robotically with excellent exposure 1
  2. Valve visualization under direct camera view 1, 2

Phase 4: Valvectomy and Annular Preparation (Median: 4 minutes)

  1. Native valve excision using robotic instruments 3
  2. Calcified cusp removal with assistance from bedside surgeon using long scissors for severely calcified valves 1
  3. Annular decalcification to ensure proper prosthesis seating 1
  4. Annular sizing to determine appropriate prosthesis size 1

Phase 5: Prosthesis Implantation (Median: 20 minutes for sutures, 31 minutes for aortotomy closure)

  1. Interrupted braided sutures placed circumferentially around annulus robotically (for conventional valves) 3
  2. Prosthesis parachuting and seating:
    • Conventional valves: sutures passed through sewing ring, valve lowered and tied 3
    • Sutureless valves: 3 guiding sutures placed, Perceval S valve parachuted and deployed 1
  3. Valve position confirmation via direct visualization and TEE 1

Phase 6: Closure and De-airing (Time: 30-40 minutes)

  1. Aortotomy closure with running polypropylene or polytetrafluoroethylene suture 6, 3
  2. De-airing maneuvers: ascending aortic vent, left ventricular vent, Trendelenburg positioning 6
  3. Cross-clamp removal after adequate de-airing 2, 3
  4. Rhythm management: defibrillation if needed (only after removing robotic instruments and re-expanding lungs) 6

Phase 7: Separation from Bypass and Closure (Time: 20-30 minutes)

  1. Weaning from cardiopulmonary bypass with TEE confirmation of valve function 3
  2. Decannulation and hemostasis 2
  3. Port site inspection for bleeding 6
  4. Chest tube placement: 1-2 tubes through robotic arm ports (one high pleural, one pericardial soft drain) 6
  5. Port closure with absorbable suture 6

Median procedural times: Total procedure 166-231 minutes, CPB 121-166 minutes, cross-clamp 98-117 minutes 1, 2, 3

Post-Procedure Care

Immediate Post-Operative (0-4 hours):

  • Operating room extubation in 84% of patients; remaining 16% extubated within 4 hours 3
  • ICU admission with continuous hemodynamic monitoring 3
  • TEE or transthoracic echo to confirm valve function and rule out perivalvular leak 3

Early Recovery (4-24 hours):

  • Chest tube output monitoring: expect <100 mL/hour initially, decreasing progressively 6
  • Hemodynamic stability assessment: maintain adequate preload, avoid excessive vasodilation 6
  • Rhythm monitoring: atrial fibrillation occurs in approximately 20% (1 in 5 patients in reported series) 1
  • Pain management: multimodal analgesia with reduced opioid requirements compared to sternotomy 5

Hospital Course (1-5 days):

  • Chest tube removal when output <200 mL/24 hours and no air leak 6
  • Early mobilization facilitated by minimal incision 5, 3
  • 30-day echocardiography to document valve function (no valvular or perivalvular abnormalities in reported series) 3
  • Anticoagulation initiation for mechanical valves; aspirin for bioprosthetic valves 8

Discharge Planning:

  • Typical length of stay: 3-5 days (shorter than traditional sternotomy) 5, 3
  • Wound care instructions for small incisions 3
  • Activity restrictions: avoid heavy lifting >10 lbs for 6 weeks 5
  • Follow-up echocardiography at 30 days, 6 months, and annually 7, 8

Nursing Responsibilities

Pre-Operative:

  • Verify informed consent including discussion of potential conversion to sternotomy 6
  • Ensure availability of conversion equipment: sternotomy tray immediately accessible 6
  • Coordinate with perfusion team for peripheral cannulation setup 6
  • Position patient according to protocol with pressure point padding 6

Intra-Operative:

  • Assist with robotic system setup and port placement 1, 2
  • Monitor for robotic arm conflicts with patient anatomy or external equipment 6
  • Maintain sterile field around working incision and port sites 6
  • Communicate with surgical team regarding suture management and instrument needs 6
  • Prepare for potential emergencies: rapid conversion to sternotomy, bleeding control 6

Post-Operative:

  • Continuous hemodynamic monitoring: arterial pressure, central venous pressure, cardiac output 6
  • Chest tube assessment: output volume, character, air leak 6
  • Respiratory support: incentive spirometry, early mobilization to prevent pneumonia 1
  • Pain assessment and management: multimodal analgesia protocol 5
  • Cardiac rhythm monitoring: detect and manage atrial fibrillation 1
  • Anticoagulation management for mechanical valves (INR goal 2.5-3.5) 8
  • Wound assessment: monitor port sites and working incision for infection or bleeding 6

Normal Parameters

Hemodynamic:

  • Mean arterial pressure: 65-90 mmHg 6
  • Central venous pressure: 8-12 mmHg 6
  • Cardiac index: >2.2 L/min/m² 6
  • Heart rate: 60-100 bpm (may require temporary pacing) 6

Valve Function (Post-Operative Echo):

  • Peak gradient: <20 mmHg for appropriately sized prosthesis 7
  • Mean gradient: <10 mmHg 7
  • No perivalvular leak or trace only 3
  • Normal leaflet/disc motion 3

Laboratory:

  • Hemoglobin: >8 g/dL (transfusion threshold) 6
  • INR: 2.5-3.5 for mechanical valves (once therapeutic) 8
  • Creatinine: return to baseline within 48-72 hours 6

Chest Tube Output:

  • First 4 hours: <100 mL/hour 6
  • 24 hours: <200 mL total 6
  • Character: serosanguinous, not bright red 6

Alarms and Troubleshooting

Intra-Operative Complications:

Robotic System Malfunction:

  • Alarm: Loss of instrument control, system error messages 6
  • Action: Immediately undock robot, convert to direct visualization through working incision or sternotomy 6

Inadequate Exposure:

  • Problem: Cannot visualize valve adequately 1
  • Action: Reposition camera, adjust retraction, consider enlarging working incision 6, 1

Severe Annular Calcification:

  • Problem: Difficulty with decalcification using robotic instruments 1
  • Action: Bedside surgeon assists with long instruments through working incision 1

Bleeding from Aortotomy:

  • Alarm: Excessive bleeding obscuring field 6
  • Action: Increase suction, verify cross-clamp position, consider additional sutures, prepare for conversion 6

Endoaortic Balloon Migration:

  • Problem: Balloon migrates distally (obstructs arch vessels) or proximally (impairs exposure) 6
  • Action: Reposition under TEE guidance, consider conversion to transthoracic clamp 6

Inadequate Venous Drainage:

  • Problem: Right heart distention, poor myocardial protection 6
  • Action: Increase vacuum-assisted drainage, verify cannula position, consider bicaval cannulation 6

Post-Operative Complications:

Excessive Chest Tube Output (>100 mL/hour):

  • Action: Check coagulation parameters, consider re-exploration if >200 mL/hour for 2 consecutive hours 6
  • Escalation threshold: Hemodynamic instability, >500 mL in first hour 6

Hemodynamic Instability:

  • Hypotension with low filling pressures: Volume resuscitation, rule out bleeding 6
  • Hypotension with high filling pressures: Inotropic support, rule out tamponade 6
  • Action: Urgent echocardiography to assess valve function and pericardial effusion 6

New Murmur or Abnormal Echo:

  • Problem: Perivalvular leak, prosthetic dysfunction 3
  • Action: Immediate cardiology consultation, consider re-exploration if severe 3

Atrial Fibrillation:

  • Incidence: ~20% of patients 1
  • Action: Rate control, anticoagulation, consider cardioversion if hemodynamically unstable 1

Pneumonia:

  • Risk factor: Single lung ventilation, elderly patients 1, 2
  • Action: Aggressive pulmonary toilet, early mobilization, antibiotics if indicated 1

Red Flags and Escalation Criteria

Immediate Surgical Re-Exploration Required:

  • Cardiac tamponade: hypotension, elevated CVP, equalization of pressures, echo confirmation 6
  • Massive bleeding: chest tube output >500 mL in first hour or >200 mL/hour for 2+ hours 6
  • Acute prosthetic valve dysfunction: severe perivalvular leak, leaflet/disc immobility 3
  • Acute myocardial ischemia: ST elevation, new wall motion abnormalities suggesting coronary ostial obstruction 6

Urgent Cardiology/Cardiac Surgery Consultation:

  • New stroke symptoms: focal neurological deficits (stroke rate 0% in recent series but remains risk) 6, 3
  • Hemodynamic instability not responding to initial resuscitation 6
  • New significant perivalvular leak on echocardiography 3
  • Prosthetic valve endocarditis: fever, positive blood cultures, new murmur 8

Conversion to Sternotomy (Intra-Operative):

  • Unexpected right chest adhesions preventing safe dissection 6
  • Inability to achieve adequate exposure of aortic valve 6, 1
  • Uncontrolled bleeding from aorta or cardiac structures 6
  • Aortic dissection during cannulation or clamping 6
  • Inability to wean from cardiopulmonary bypass requiring mechanical support 6
  • Robotic system failure that cannot be immediately resolved 6

Critical Monitoring Thresholds:

  • STS-PROM >8%: High-risk patients require intensive monitoring 6, 7
  • LVEF <40%: Increased risk of post-operative heart failure 6
  • Frailty indicators: Prolonged recovery, increased complication risk 6

Documentation Requirements

Pre-Operative:

  • Heart Team consensus on RAVR as optimal approach 6, 7
  • Informed consent including risks of conversion to sternotomy, stroke, bleeding, valve dysfunction 6
  • STS-PROM score and risk stratification 6, 7
  • Echocardiographic measurements: valve area, gradients, LVEF, annular size 7
  • CT findings: chest anatomy, vascular access suitability 6

Intra-Operative:

  • Procedural times: total procedure, CPB, cross-clamp, valvectomy, suturing, closure 1, 2, 3
  • Valve details: type (mechanical vs. bioprosthetic), size, manufacturer, lot number 3
  • Complications: bleeding, conversion, technical difficulties 6, 1
  • Concomitant procedures: Cox maze, root enlargement, mitral repair 3, 4
  • De-airing maneuvers performed 6
  • TEE findings: valve function, perivalvular leak assessment 3

Post-Operative:

  • 30-day echocardiography: valve gradients, perivalvular leak, ventricular function 3
  • Complications: mortality, stroke, bleeding requiring re-exploration, pneumonia, atrial fibrillation, pacemaker requirement 6, 1, 3
  • Length of stay and discharge disposition 5, 3
  • Anticoagulation plan for mechanical valves 8
  • Follow-up schedule: 30 days, 6 months, annually with echocardiography 7, 8

Registry Reporting:

  • STS Database submission for all SAVR procedures including RAVR 6
  • Device-specific registry participation if required by manufacturer 6
  • Outcomes tracking: mortality, stroke, valve dysfunction, reoperation rates 6, 3

References

Research

Early experience with robotic aortic valve replacement.

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery, 2005

Research

Robotic Aortic Valve Replacement: First 50 Cases.

The Annals of thoracic surgery, 2022

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

TAVR Indications and Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Surgical Management of Severe Aortic Regurgitation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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