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Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.

Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.

期刊: Cardiovascular journal of Africa 日期: 2026-05-15 PMID: 42345562 DOI: 10.5830/CVJA-2026-008 浏览: 40
作者: Mohamed AG, Alsheikh H, Elshahat MF
AG, M., H, A., & MF, E. (2026). Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.. Cardiovascular journal of Africa. https://doi.org/10.5830/CVJA-2026-008
AG M, H A, MF E. Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.. Cardiovascular journal of Africa. 2026; doi: 10.5830/CVJA-2026-008
AG M, H A, MF E. Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.[J]. Cardiovascular journal of Africa. 2026. DOI: 10.5830/CVJA-2026-008.
@article{ag2026,
  author = {Mohamed AG and Alsheikh H and Elshahat MF},
  title = {Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.},
  journal = {Cardiovascular journal of Africa},
  year = {2026},
  doi = {10.5830/CVJA-2026-008},
  note = {PMID: 42345562},
}
TY  - JOUR
AU  - Mohamed AG
AU  - Alsheikh H
AU  - Elshahat MF
TI  - Efficacy of using 50 mL syringe manual thrombectomy catheter in patients with heavy thrombus burden undergoing primary percutaneous coronary intervention.
T2  - Cardiovascular journal of Africa
PY  - 2026
DO  - 10.5830/CVJA-2026-008
AN  - PMID:42345562
ER  - 

摘要

BACKGROUND: Patients with ST-segment elevation myocardial infarction (STEMI) and heavy thrombus burden are at increased risk of distal embolisation and impaired reperfusion during primary percutaneous coronary intervention (PPCI). Conventional manual aspiration thrombectomy with a 30 mL syringe has shown limited benefit in large randomised trials. Increasing syringe volume to 50 mL may enhance suction efficiency and clot retrieval, offering a simple and cost-effective strategy to optimise reperfusion. METHODS: In this prospective cohort study, 88 consecutive STEMI patients with angiographic thrombus burden grade 4-5 undergoing PPCI were included. Group I (n = 44) underwent thrombectomy with a 30 mL syringe, while Group II (n = 44) underwent thrombectomy with a 50 mL syringe using an Export Advance catheter. Primary endpoints were post-procedural thrombolysis in myocardial infarction (TIMI) 3 flow and myocardial blush grade (MBG). Secondary endpoints included ST-segment resolution, echocardiography recovery (wall motion score index [WMSI] and left ventricular ejection fraction [LVEF]), and 30-day adverse cardiovascular events. RESULTS: Baseline clinical and laboratory characteristics were comparable between groups. The 50 mL syringe group achieved higher rates of complete reperfusion (TIMI 3 flow: 77% vs. 59%, p = 0.04; MBG 3: 59% vs. 45%, p = 0.05). The primary composite endpoint of TIMI 3 flow plus MBG 3 was significantly greater in Group II (59% vs. 41%, p = 0.04). ST-segment resolution (68 % 15% vs. 55 ± 12%, p = 0.01), immediate post-PCI WMSI (1.7 ± 0.4 vs. 2.1 ± 0.5, p = 0.002), one-month WMSI (1.5 ± 0.3 vs. 1.8 ± 0.4, p = 0.001), and LVEF (54 ± 5% vs. 49 ± 6%, p = 0.002) were all superior in the 50 mL group. At 30 days, cardiovascular events were numerically lower with the 50 mL syringe (2.3% vs. 4.1%, p = 0.17), with no increase in procedural complications. CONCLUSION: In STEMI patients with high thrombus burden undergoing PPCI, manual thrombectomy with a 50 mL syringe improved reperfusion, myocardial recovery, and procedural outcomes compared with the conventional 30 mL syringe, without added risk. This low-cost, accessible modification may represent a practical alternative to mechanical aspiration systems, warranting validation in larger randomised trials.

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