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OPTIMIZE 5.5 - Optimizing Impella 5.5 Outcomes Through Advanced Data Science (OPTIMIZE)

2026年5月27日 更新者:Thomas Schlöglhofer, PhD, MSc、Medical University of Vienna

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:

  1. Validate the Impella 5.5 placement signal by comparing it with ICU arterial line waveforms.
  2. 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.
  3. 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

観察的

入学 (推定)

100

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

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

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

The study population comprises adult patients admitted to the intensive care unit (ICU) presenting with severe cardiogenic shock who required temporary mechanical circulatory support between January 2019 and March 2026, treated at the Medical University of Vienna, Austria. Eligible individuals are those who undergo clinical management utilizing the Impella 5.5 micro-axial flow pump as part of their standard of care. Only patients with available high-resolution pump data (downloaded from the clinical console) and ICU digital health record datasets extracted from ICCA (IntelliSpace Critical Care and Anesthesia, Philips Medical Systems Development and Manufacturing Centre, Hamburg, Germany) will be included for analysis.

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

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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
Native heart recovery
Patients supported with the Impella 5.5 device (J&J MedTech) achieving native heart recovery
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.
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
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.
All-cause mortality
Patients supported with the Impella 5.5 device (J&J MedTech) suffering from all-cause mortality during mechanical circulatory support.
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.

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
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).

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).

二次結果の測定

結果測定
メジャーの説明
時間枠
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).

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).
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).

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).
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).

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).
Percentage of Participants Exhibiting Specific Device-Support Clinical Endpoints
時間枠:Through the duration of hospital stay (estimated average of 30 days).

The final clinical trajectory of the cohort on device support will be categorized into one of three mutually exclusive outcomes:

  1. Native heart recovery (successful device weaning and explant)
  2. Escalation to heart replacement therapy (durable LVAD implantation or heart transplantation)
  3. All-cause mortality while on active device support.

Unit of Measure: Percentage (%) of participants within each categorical outcome category.

Through the duration of hospital stay (estimated average of 30 days).
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.

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.
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.

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.
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.

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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Thomas Schlöglhofer, PhD, MSc、Medical University of Vienna

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年5月8日

一次修了 (推定)

2029年1月8日

研究の完了 (推定)

2029年5月30日

試験登録日

最初に提出

2026年5月21日

QC基準を満たした最初の提出物

2026年5月27日

最初の投稿 (実際)

2026年6月1日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月1日

QC基準を満たした最後の更新が送信されました

2026年5月27日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

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?

いいえ

IPD プランの説明

IPD will not be shared because the dataset contains highly sensitive, high-frequency physiological data linked with intensive care health records. Further, IPD is currently not planned for public sharing as the dataset is being actively used to develop a proprietary clinical decision support tool and model architecture optimization.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

はい

米国で製造され、米国から輸出された製品。

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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