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

2026년 5월 27일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

관찰

등록 (추정된)

100

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
개입 / 치료
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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Predictive Performance and Optimization of the Clinician Decision Support Tool
기간: 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).

2차 결과 측정

결과 측정
측정값 설명
기간
Bias Between the Impella 5.5 Placement Signal and ICU Arterial Line Waveforms
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Thomas Schlöglhofer, PhD, MSc, Medical University of Vienna

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 5월 8일

기본 완료 (추정된)

2029년 1월 8일

연구 완료 (추정된)

2029년 5월 30일

연구 등록 날짜

최초 제출

2026년 5월 21일

QC 기준을 충족하는 최초 제출

2026년 5월 27일

처음 게시됨 (실제)

2026년 6월 1일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 1일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 27일

마지막으로 확인됨

2026년 5월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

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.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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