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Edwards Lifesciences Presents 5-Year Follow Up Data From PARTNER Trials Showing Clinical Outcomes For Female And Small Annulus Patients With Transcatheter Aortic Valve Replacement At The New York Valves 2024: The Structural Heart Summit

Edwards Lifesciences Presents 5-Year Follow Up Data From PARTNER Trials Showing Clinical Outcomes For Female And Small Annulus Patients With Transcatheter Aortic Valve Replacement At The New York Valves 2024: The Structural Heart Summit

愛德華生命科學在紐約2024:結構性心臟峯會上發表了PARTNER試驗的五年追蹤數據,顯示結構性主動脈瓣置換對於女性和小主動脈瓣患者的臨牀效果。
Benzinga ·  06/05 23:48

Edwards Lifesciences (NYSE:EW) today announced the results from an analysis of data from the PARTNER Trials examining outcomes of transcatheter aortic valve replacement (TAVR) patients with a small annulus. Through five-year follow up of more than 1,300 low and intermediate risk SAPIEN 3 valve patients there were excellent clinical outcomes and valve durability irrespective of the patient's annulus size or sex. These data were presented during the late-breaking clinical sessions at New York Valves 2024: The Structural Heart Summit.

愛德華生命科學(紐交所:EW)今天宣佈了從PARTNER試驗數據分析中得出的結果,研究了具有小環形動脈瓣替換(TAVR)患者的結果。通過對超過1,300名低風險和中等風險SAPIEN 3瓣膜患者的五年隨訪,無論患者瓣環大小或性別如何,都有良好的臨床效果和瓣膜耐久性。這些數據在紐約瓣膜2024年:結構性心臟峯會的後期臨床會議上進行了介紹。

As part of this analysis, contemporary patient data with long-term follow up from the PARTNER 3 randomized controlled trial and PARTNER 2 S3i Trial were examined to determine if higher 30-day mean gradients and rates of prothesis-patient mismatch (PPM) translated to poorer long-term outcomes of death, disabling stroke or heart failure related hospitalization. The analysis revealed no association between clinical outcomes or valve durability and severe PPM or higher mean gradients (i.e., >20 mmHg.) Overall, this cohort of patients had extremely low rates of reintervention and high survival out to five years. As previously presented, the PARTNER 3 Trial demonstrated the highest reported survival rate in low-risk patients seen in any pivotal trial.

作爲該分析的一部分,對PARTNER 3隨機對照試驗和PARTNER 2 S3i試驗的現代患者數據進行了長期隨訪,以確定較高的30天平均梯度和假體-患者不匹配率(PPM)是否會導致更差的死亡率、致殘性卒中或與心力衰竭有關的住院率的長期結果。分析結果表明,嚴重PPM或較高的平均梯度(即>20 mmHg)與臨床結果或瓣膜耐久性無關。總體而言,這些患者的再手術率極低,且存活率高達五年。正如之前報道的那樣,PARTNER 3試驗在任何關鍵性試驗中看到低風險患者的最高報告存活率。

譯文內容由第三人軟體翻譯。


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