Mitral clips

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"MitraClip" AND "mitral regurgitation"

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Mitral Clips (Transcatheter Edge-to-Edge Repair / TEER)

What is a Mitral Clip?

The MitraClip (Abbott Vascular) is a percutaneous device that mimics the Alfieri edge-to-edge surgical repair - it clips the free edges of the anterior and posterior mitral leaflets together to create a double-orifice mitral valve, reducing mitral regurgitation (MR) without open-heart surgery.
  • Delivered via a transfemoral transseptal approach under general anesthesia with TEE guidance
  • The clip grasps both leaflets on the ventricular side to create leaflet apposition
  • The effect on MR is evaluated in real time by echocardiography (unlike open surgery, which is assessed after cardiopulmonary bypass is discontinued)
  • Multiple clips can be placed if the initial result is suboptimal
  • Classic clip position: between the A2 and P2 scallops, creating a double orifice
- Barash Clinical Anesthesia 9e, p. 2687; Braunwald's Heart Disease, p. 809

3D Echo View After MitraClip Placement

Here is an intraoperative 3D TEE "surgeon's view" showing the MitraClip in position between the A2/P2 scallops, with the double orifice visible on either side:
3D en face TEE of mitral valve after MitraClip placement showing double orifice
3D en face (surgeon's view) TEE showing MitraClip between anterior leaflet (AL) and posterior leaflet (PL), with the aortic valve (AoV) visible superiorly. - Miller's Anesthesia 10e, Fig. 33.30

Indications

Type of MRIndication
Primary (degenerative) MRHigh surgical risk patients with symptomatic moderately-severe to severe MR (e.g., flail leaflet, prolapse)
Secondary (functional) MRHeart failure patients with secondary MR who remain symptomatic despite optimal guideline-directed medical therapy (GDMT)
Contraindications/unfavorable features (per Fuster & Hurst):
  • LVEF <30%
  • Extreme NT-proBNP >10,000 pg/mL
  • Significant RV dysfunction (TAPSE <15 mm)
  • Severe pulmonary hypertension or severe TR
  • Major comorbidities (significant renal dysfunction)
  • Excessive LV dilatation (LVESD >70 mm per COAPT)
- Fuster & Hurst's The Heart 15e, p. 969

Key Clinical Trials

Primary MR - EVEREST II

  • 184 MitraClip vs. 95 surgical repair/replacement
  • 30-day major adverse events: 9.6% vs. 57% (surgery) - largely driven by transfusion requirement
  • Freedom from death/MV surgery/MR >2+ at 12 months: 55% (clip) vs. 73% (surgery) - surgery superior for durability
  • BUT: MitraClip showed greater benefit than surgery in higher-risk patients
  • Durable results at follow-up in patients with acute procedural success

Secondary MR - COAPT Trial (US/Canada, n=614)

  • Symptomatic HF + moderate-severe secondary MR; all on optimal GDMT
  • LVEF 20-50%, LVESD ≤69 mm, MR grade 3-4+
  • Primary endpoint (HF hospitalization at 24 months): 35.8 vs 67.9 per 100 patient-years (NNT = 3.1) - P<0.001
  • All-cause mortality at 24 months: 29.1% vs 46.1% (NNT = 5.9) - P<0.001
  • Benefits even more pronounced at 3 years

Secondary MR - MITRA-FR Trial (France, n=304)

  • No significant difference in all-cause death + HF hospitalization at 12 months (54.6% vs 51.3%, P=NS)
  • No change at 24-month follow-up either

Why did COAPT and MITRA-FR conflict?

FeatureMITRA-FRCOAPT
MR severity criteriaERO >20 mm²MR grade 3-4+ (AHA)
LV size exclusionNoneLVESD >70 mm
RV dysfunction exclusionNoneModerate/severe excluded
Follow-up endpoint1 year2 years (recurrent events)
GDMT intensityLess strictMore intensive
Post-hoc analysis: COAPT enrolled patients with proportionally more severe MR relative to LV size (more "valve-driven" rather than "ventricle-driven" disease), hence more potential for benefit. Patients most likely to benefit: ERO ≥0.30 cm² + no excessive LV dilatation + after intensive GDMT has failed.
- Fuster & Hurst's The Heart 15e, p. 972; Braunwald's Heart Disease, p. 810

Procedure - Anesthetic Considerations

  • General anesthesia with invasive monitoring is standard
  • TEE is mandatory - guides transseptal puncture, clip positioning, and real-time MR assessment
  • Transseptal puncture target: superior and posterior in the fossa ovalis (to allow adequate working height above the mitral valve)
  • Mortality is lower with MitraClip vs. surgery using standard surgical risk prediction models
- Barash Clinical Anesthesia 9e, p. 2687; Miller's Anesthesia 10e, p. 5057

Next-Generation Devices

DeviceKey Feature
MitraClip NTR/XTR (Abbott)Newer iterations with better grasping; EXPAND registry showed improved outcomes with experience
PASCAL (Edwards Lifesciences)Wider paddles + central spacer to fill regurgitant orifice; independent leaflet capture; 98% success in early series
DRAGONFLY (Hangzhou Valgen, China)Early clinical development

Tricuspid Extension

Both MitraClip and PASCAL are also being used in the tricuspid position (anterior + septal leaflet clipping):
  • Trivalve Registry (n=249): 96% technical success; TR ≥3+ reduced from 97% to 23% at discharge; 1-year mortality 20.3%
  • TRILUMINATE trial: Prospective multicenter study ongoing
- Braunwald's Heart Disease, p. 811

Recent Evidence (2023-2026)


Summary Points

  1. MitraClip = percutaneous edge-to-edge repair; mimics Alfieri technique; creates double-orifice MV
  2. Main indications: high-surgical-risk primary MR; secondary MR with HF after adequate GDMT
  3. EVEREST II: less durable than surgery overall, but better for high-risk patients
  4. COAPT: landmark benefit for secondary MR (NNT 3.1 for HF hospitalization, NNT 5.9 for mortality)
  5. MITRA-FR: negative trial - key lesson is patient selection (proportionate vs. disproportionate MR)
  6. TEE guidance is essential throughout the procedure
  7. Expanding to tricuspid valve repair and newer devices (PASCAL)
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