OPTIMIZE 5.5 - Optimizing Impella 5.5 Outcomes Through Advanced Data Science (OPTIMIZE)
Clinical Outcomes and Adverse Events Associated With Microaxial Flow Pump Support: An Explorative Retrospective Study
The main goal of this observational, study is to develop a clinical decision support tool utilizing Impella 5.5 pump parameters to predict native heart recovery and prevent adverse events, by leveraging data science and real-world clinical data of cardiogenic shock patients.
Therefore, secondary objectives are essential to consolidating a retrospective longitudinal analysis of Impella 5.5 pump data alongside ICU digital health record datasets to:
- Validate the Impella 5.5 placement signal by comparing it with ICU arterial line waveforms.
- Integrate pump data with ICU clinical data to identify patterns associated with therapy outcomes, including native heart recovery, heart replacement therapy, and mortality while on device support.
- Define clinical scenarios linked to hemolysis, HRAEs, and arrhythmias and develop predictive models to mitigate their occurrence.
調査の概要
詳細な説明
The clinical management of patients experiencing severe cardiogenic shock requires precise, real-time monitoring to optimize hemodynamic support and guide therapeutic transitions. The Impella 5.5 micro-axial flow pump provides left ventricular unloading, generating automated internal continuous parameters that reflect moving cardiac states. This study establishes a retrospective, longitudinal framework that integrates these high-frequency device metrics with corresponding clinical data housed within intensive care unit (ICU) digital health records (DHR). By synthesizing these disparate data streams, this research aims to build an advanced analytical framework to support clinical decisions in the cardiogenic shock landscape.
Signal Validation and Data Preprocessing:
The initial phase of the study validates the physiological fidelity of the continuous data stream. High-frequency digital logs generated by the pump console-specifically the optical placement signal-will undergo time-series alignment with standard physiological waveforms recorded in the ICU, using indwelling arterial line pressure data as the reference standard. This signal validation ensures that the longitudinal parameter data accurately capture mechanical positioning and true left ventricular dynamics prior to entering the downstream modeling pipeline.
Analytical Framework and Modeling Strategy:
Following data integration and signal validation, the consolidated dataset will be leveraged to develop predictive models aimed at distinguishing patient trajectories and forecasting complications. The computational pipeline is divided into two primary analytical pathways:
Endpoint Classification:
An artificial neural network will be developed to evaluate patient trajectories toward distinct clinical endpoints: native heart recovery, escalation to heart replacement therapy, or death. The modeling pipeline incorporates a rigorous framework to ensure generalizability and guard against overfitting. The complete dataset will be partitioned into an 80% development subset and a 20% independent testing subset. The development subset will undergo 5-fold cross-validation to drive comprehensive model architecture optimization, systematically testing structural variations to identify the highest-performing network configuration.
Adverse Event Forecasting:
Separate statistical and machine learning architectures will be constructed to evaluate risk patterns and clinical scenarios associated with severe on-device complications, specifically clinical hemolysis, new-onset arrhythmias, and hemocompatibility-related adverse events (HRAEs). These models focus on identifying early-warning clusters within the high-frequency pump log data to identify sub-clinical changes before manifest physiological degradation occurs.
Through these combined pathways, this observational study seeks to lay the foundational algorithmic groundwork for a real-time clinical decision support tool utilizing objective, automated device analytics to improve safety and personalization in mechanical circulatory support.
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Thomas Schlöglhofer, PhD, MSc
- 電話番号:+4314040027280
- メール:thomas.schloeglhofer@meduniwien.ac.at
研究連絡先のバックアップ
- 名前:Lukas Ruoff, MSc
- メール:lukas.ruoff@meduniwien.ac.at
研究場所
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Vienna、オーストリア
- 募集
- Medical University of Vienna
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コンタクト:
- Thomas Schlöglhofer, PhD, MSc
- 電話番号:+4314040027280
- メール:thomas.schloeglhofer@meduniwien.ac.at
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コンタクト:
- Lukas Ruoff, MSc
- メール:lukas.ruoff@meduniwien.ac.at
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Adult patients who were treated for cardiogenic shock and supported with an Impella 5.5 micro-axial flow pump
- Only patients with available high-resolution pump data (downloaded from the clinical console) and ICU digital health record datasets
Exclusion Criteria:
- Patients supported with an Impella 5.5 for indications other than cardiogenic shock (e.g., protected PCI or CABG)
- Patients younger than 18 years
- Patients with incomplete data, procedural records, or demographic information
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
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Native heart recovery
Patients supported with the Impella 5.5 device (J&J MedTech) achieving native heart recovery
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Temporary circulatory support using the Impella 5.5 micro-axial flow pump.
The device is surgically placed (typically via the axillary artery) across the aortic valve into the left ventricle to provide active forward flow, unloading the left ventricle and maintaining systemic perfusion during cardiogenic shock.
Management of the device includes the collection and analysis of continuous device-derived hemodynamic data and associated clinical parameters throughout the duration of support.
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Heart replacement therapy (durable MCS or HTX)
Patients supported with the Impella 5.5 device (J&J MedTech) transitioning to heart replacement therapy (durable mechanical circulatory support or heart transplantation
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Temporary circulatory support using the Impella 5.5 micro-axial flow pump.
The device is surgically placed (typically via the axillary artery) across the aortic valve into the left ventricle to provide active forward flow, unloading the left ventricle and maintaining systemic perfusion during cardiogenic shock.
Management of the device includes the collection and analysis of continuous device-derived hemodynamic data and associated clinical parameters throughout the duration of support.
|
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All-cause mortality
Patients supported with the Impella 5.5 device (J&J MedTech) suffering from all-cause mortality during mechanical circulatory support.
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Temporary circulatory support using the Impella 5.5 micro-axial flow pump.
The device is surgically placed (typically via the axillary artery) across the aortic valve into the left ventricle to provide active forward flow, unloading the left ventricle and maintaining systemic perfusion during cardiogenic shock.
Management of the device includes the collection and analysis of continuous device-derived hemodynamic data and associated clinical parameters throughout the duration of support.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Predictive Performance and Optimization of the Clinician Decision Support Tool
時間枠:From the time of Impella 5.5 insertion up to device explant (estimated average of 5 to 14 days).
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The predictive performance of the developed clinical decision support tool will be evaluated by its ability to classify patient trajectories toward native heart recovery versus adverse outcomes. The model will undergo comprehensive model architecture optimization to identify the structural configuration that yields optimal performance. Model training, validation, and testing will follow a standard data split: 80% of the dataset will be utilized for training and internal validation using 5-fold cross-validation, and the remaining 20% will be held out as a definitive testing dataset. Final classification performance will be quantified using specific metrics derived from Receiver Operating Characteristic (ROC) curve analysis, including: Area Under the Curve (AUC), Sensitivity, Specificity |
From the time of Impella 5.5 insertion up to device explant (estimated average of 5 to 14 days).
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Bias Between the Impella 5.5 Placement Signal and ICU Arterial Line Waveforms
時間枠:Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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The systematic difference (bias) between the automated Impella 5.5 optical placement signal and the gold-standard ICU indwelling arterial line pressure waveforms will be quantified using Bland-Altman analysis to evaluate signal alignment. Unit of Measure: Millimeters of mercury (mmHg) |
Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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Correlation Coefficient Between the Impella 5.5 Placement Signal and ICU Arterial Line Waveforms
時間枠:Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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The strength and direction of the linear relationship between the continuous time-series data of the Impella 5.5 optical placement signal and the ICU arterial line waveforms will be evaluated. Unit of Measure: Correlation coefficient (r) on a scale from -1.0 to 1.0. |
Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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Concordance Rate of Directional Trends Between the Impella 5.5 Placement Signal and ICU Arterial Line Waveforms
時間枠:Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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The trending ability of the placement signal will be assessed via concordance plots. The concordance rate represents the percentage of data points where the directional change (increase or decrease) matches between both signal streams over time, excluding zones of clinical noise. Unit of Measure: Percentage (%) of concordant data pairs. |
Continuously through the duration of active Impella 5.5 device support (from device insertion up to explant, estimated average of 5 to 14 days).
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Percentage of Participants Exhibiting Specific Device-Support Clinical Endpoints
時間枠:Through the duration of hospital stay (estimated average of 30 days).
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The final clinical trajectory of the cohort on device support will be categorized into one of three mutually exclusive outcomes:
Unit of Measure: Percentage (%) of participants within each categorical outcome category. |
Through the duration of hospital stay (estimated average of 30 days).
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Percentage of Participants Experiencing Device-Related Hemolysis
時間枠:From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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The incidence of clinically significant hemolysis on device support, defined by standard laboratory criteria (e.g., plasma free hemoglobin greater than 40 mg/dL or a doubling of lactate dehydrogenase alongside clinical signs). Unit of Measure: Percentage (%) of participants. |
From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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Percentage of Participants Experiencing New-Onset Clinically Significant Arrhythmias
時間枠:From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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The incidence of new-onset atrial or ventricular arrhythmias occurring during device support that require immediate pharmacological, electrical, or device-setting intervention. Unit of Measure: Percentage (%) of participants. |
From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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Number of Hemocompatibility-Related Adverse Events (HRAEs) Per Participant
時間枠:From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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The rate of hemocompatibility-related adverse events, including major bleeding episodes (requiring transfusion or reoperation) and thromboembolic events (e.g., ischemic stroke, peripheral arterial embolization) occurring during device support. Unit of Measure: Number of events per participant. |
From device insertion up to 30 days post-explant or hospital discharge, whichever occurs first.
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協力者と研究者
捜査官
- 主任研究者:Thomas Schlöglhofer, PhD, MSc、Medical University of Vienna
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- EK Nr: 1245/2026
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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