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Systematic Evaluation by an Intensivist of Hematological Malignancy Patients Presenting With Acute Respiratory or Hemodynamic Failure (CAREHEMA)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Completed

Conditions

Hematologic Malignancy
Respiratory Insufficiency

Treatments

Other: Systematic evaluation by an intensivist

Study type

Observational

Funder types

Other

Identifiers

NCT03399149
2017-A00411-52 (Other Identifier)
CARE HEMA (38RC16.238)

Details and patient eligibility

About

Over the last two decades, the number of patients with hematological malignancies (HMs) admitted to the ICU increased and their mortality has dropped sharply. Patients with HMs increasingly require admission to the intensive care unit (ICU) for life-threatening events related to the malignancy and/or treatments, with immunosuppression being a major contributor. Whether the increase in ICU admissions is related to increased referrals by hematologists and/or to increased admissions by intensivists is unknown. The criteria used for ICU referral and admission decisions have not been extensively evaluated. Finally, the links between admission policies and treatment-limitation decisions are unclear, but ICUs with broad admission policies may change the treatment goals based on the response to several days of full-code management.

The aim of this study is to evaluate the impact of a systematic evaluation by an intensivist of HMs patients presenting with acute respiratory and/or hemodynamic failure.

Enrollment

221 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients hospitalized in a hematology unit

  • Patients presenting with criteria for critical respiratory and/or hemodynamic condition and worsening during the next 4 hours

    1. Respiratory : oxygen saturation <90 % and/or O2 >3l/min, with either a worsening of saturation or increased oxygen needs within 4h
    2. Hemodynamic : systolic blood pressure < 90 mmHg and remaining < 90 mmHg within 4h despite ≥ 1l of crystalloid administration, or becoming < 80 mmHg no matter the quantity of fluid (even if no fluid administration).

Exclusion criteria

  • therapeutic limitations decided hematological investigators (moribund patients, uncontrolled allogenic graft,...)
  • Do-not-reanimate directives
  • Pregnant or breastfeeding women

Trial design

221 participants in 2 patient groups

"Before phase"
Description:
Retrospective study of ICU admissions of hematology patients for respiratory and hemodynamic reasons Time period: January 2012 to March 2017
"After Phase": Systematic evaluation by an intensivist
Description:
Corresponding to the period after the implementation of a systematic intensivist evaluation Daily screening of systolic blood pressure, oxygen saturation and oxygen requirements of all patients hospitalized in hematology wards. Systematic evaluation of any patient presenting the inclusion criteria by an intensivist and collegial care planning. Time period: From March 2017 to end of study
Treatment:
Other: Systematic evaluation by an intensivist

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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