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Heparin-Induced Thrombocytopenia - Retrospective Analysis of Data on Incidence and Outcomes Study

Completed
Conditions
Heparin Induced Thrombocytopenia
Registration Number
NCT01178333
Lead Sponsor
Carelon Research
Brief Summary

HIT-RADIO is a study of patients who had a positive heparin PF-4 antibody test between 1/21/2008 and 9/25/2008 at selected hospitals. The study will collect and analyse information that is already in the patients' medical records. Information about laboratory values (such as platelet counts), treatments (such as medications), and outcomes (such as blood clots, amputation, and death) will be included.

Detailed Description

HIT-RADIO is a retrospective chart-review study of patients who had a positive heparin PF-4 antibody test between 1/21/2008 and 9/25/2008 at selected hospitals associated with the Transfusion Medicine/Hemostasis Clinical Trials Network .

Heparin-induced thrombocytopenia (HIT) is a major complication of the administration of heparin and can result in life-threatening thrombosis with or without thrombocytopenia (HIT-T) or can produce thrombocytopenia without clinically symptomatic thrombosis ("isolated" HIT). Isolated heparin-induced thrombocytopenia is defined as a fall in platelet count associated with a positive heparin PF-4 antibody test, in the absence of clinically overt thrombosis. While the treatment of HIT-T (HIT with thrombosis) with anticoagulation is well established, the risks and treatment of isolated HIT are unclear.

It is anticipated that this data analysis will provide a current overview of the implications of a positive heparin PF-4 antibody test in clinical practice. It should determine the percentage of positive heparin PF-4 antibody tests that are associated with thrombocytopenia and thrombosis (HIT-T) or "isolated" HIT at diagnosis and the subsequent major clinical outcomes of death, limb amputation/gangrene, and new thrombosis. No "snapshot" of such HIT patients has been conducted in the past decade and the results will be important in assessing the impact of HIT in current medical care as well as documenting current treatment strategies.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
668
Inclusion Criteria
  • All subjects with a positive heparin PF-4 antibody test occurring between 1/21/2008 and 9/25/2008
  • Medical record available for the admission during which the positive heparin PF-4 antibody test was obtained
Exclusion Criteria
  • None

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to Occurrence of a Composite Triple Endpoint Consisting of Death, Limb Amputation/Gangrene, and New ThrombosisFrom the time that the positive heparin PF-4 antibody test was drawn until hospital discharge or day 45, whichever occurred first.

The median survival time is reported by each group for the time to occurrence of a composite triple endpoint consisting of death, limb amputation/gangrene, and new thrombosis.

Secondary Outcome Measures
NameTimeMethod
Time to DeathFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

The median survival time is reported by each group for the time to death.

Time to Occurrence of Limb Amputation or Limb GangreneFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

Due to the small number of events, the median or mean survival time could not be defined. Therefore, the number of subjects with limb amputation or limb gangrene was reported in "Outcome Measure Data Table".

Time to Occurrence of Radiographically Confirmed ThromboembolismFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

The mean time to an event is estimated by the area under the survival function. If the largest time is an event time, then the survival function goes to zero at that time, and the mean survival estimate is finite. Otherwise, the mean time cannot be estimated and may lead to a bias. However, the median survival times could not be defined for all three groups, so the mean time was reported in "Outcome Measure Data Table".

Time to Occurrence of Major BleedingFrom the time that the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

The median survival time is reported by each group for the time to occurrence of major bleeding.

Proportion of Subjects With HIT With Thrombosis (HIT-T) and Isolated HITFrom the date 5 days before the positive heparin PF-4 antibody test was drawn to the date it was drawn

Proportion of subjects who, at the time the positive heparin PF-4 antibody test was drawn, were in each of the following categories:

* Group 1: Those with thrombosis and or without thrombocytopenia (HIT-T): 16% of 442 subjects.

* Group 2: Those with thrombocytopenia but not thrombosis (Isolated HIT): 64% of 442 subjects.

* Group 3: Those with neither thrombocytopenia nor thrombosis (Neither HIT-T nor Isolated HIT): 20% of 442 subjects.

Type of Heparin Exposure - Unfractionated Heparin (UFH)Hospital admission to date the positive heparin PF-4 antibody test was drawn, or 28 days prior to the date it was drawn, whichever is later, through the date it was drawn

Two types of heparins are commonly used as anticoagulants - unfractionated heparin (UFH) and low-molecular-weight heparin (LMWH). UFH has been used for the prevention and treatment of thrombosis for several decades.

Type of Heparin Exposure - Low Molecular Weight Heparin (LMWH)Hospital admission to date the positive heparin PF-4 antibody test was drawn, or 28 days prior to the date it was drawn, whichever is later, through the date it was drawn

Two types of heparins are commonly used as anticoagulants - unfractionated heparin (UFH) and low-molecular-weight heparin (LMWH). LMWHs are derived from UFH by depolymerization. Each LMWH product has a specific molecular weight distribution that determines its anticoagulant activity and duration of action.

Relationship of the Heparin PF-4 (Platelet Factor 4) Antibody Titer to the Clinical DiagnosisFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

Heparin PF-4 (platelet factor 4) optical density (OD) test results were the dichotomous outcome (\<1.0 vs. \>=1.0). Clinical diagnosis was three groups (HIT-T, Isolated HIT and No HIT). The Heparin PF-4 optical density test looks for antibodies to complexes of heparin combined with platelet factor 4. Higher optical density indicates higher antibody concentration. We could say that generally OD values above 0.4 are considered a positive result, and that the higher the OD, the greater the concentration of antibodies in the patient's blood.

Relationship of the Heparin PF-4 Antibody Titer to the Degree of ThrombocytopeniaFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

Heparin PF-4 optical density (OD) test results were the dichotomous outcome (\<1.0 vs. \>=1.0). Nadir Platelet Count (x10\^9 / L) was used for the degree of thrombocytopenia. The Heparin PF-4 optical density test looks for antibodies to complexes of heparin combined with platelet factor 4. Higher optical density indicates higher antibody concentration. We could say that generally OD values above 0.4 are considered a positive result, and that the higher the OD, the greater the concentration of antibodies in the patient's blood.

Relationship of the Heparin PF-4 Antibody Titer to the Primary EndpointFrom the time the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

Heparin PF-4 OD test results were the dichotomous outcome (\<1.0 vs. \>=1.0). Primary endpoint was the composite endpoint of death, limb amputation/gangrene, or new thrombosis.

Use of Treatment (Non-heparin Anticoagulant) Used in HospitalFrom the time that the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first

Types of treatment (direct thrombin inhibitor, fondaparinux, warfarin, no treatment) provided to subjects in hospital

Use of Treatment (Non-heparin Anticoagulant) Used at the Time of DischargeFrom the time that the positive heparin PF-4 antibody test was drawn until hospital discharge, death, or day 45, whichever occurred first
Time to Platelet Recovery, Among Subjects With a Low Platelet Count When the Positive PF4 Antibody Test Was DrawnFrom the time that the nadir platelet count was drawn until hospital discharge, death, or day 45, whichever occurred first

Trial Locations

Locations (21)

University of Iowa

🇺🇸

Iowa City, Iowa, United States

Children's Hospital, Boston

🇺🇸

Boston, Massachusetts, United States

Brigham and Women's Hospital

🇺🇸

Boston, Massachusetts, United States

Case Western Reserve University School of Medicine

🇺🇸

Cleveland, Ohio, United States

Cleveland Clinic

🇺🇸

Cleveland, Ohio, United States

Johns Hopkins

🇺🇸

Baltimore, Maryland, United States

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

Tulane University

🇺🇸

New Orleans, Louisiana, United States

University of Pittsburgh

🇺🇸

Pittsburgh, Pennsylvania, United States

Cornell University

🇺🇸

New York, New York, United States

University of North Carolina, Chapel Hill

🇺🇸

Chapel Hill, North Carolina, United States

University of Wisconsin Comprehensive Cancer Center

🇺🇸

Madison, Wisconsin, United States

Froedtert

🇺🇸

Milwaukee, Wisconsin, United States

St. Luke's Medical Center

🇺🇸

Milwaukee, Wisconsin, United States

University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

Gunderson Clinic

🇺🇸

LaCrosse, Wisconsin, United States

Duke University Medical Center

🇺🇸

Durham, North Carolina, United States

Fred Hutchinson Cancer Research Center

🇺🇸

Seattle, Washington, United States

University of Maryland Greenebaum Cancer Center

🇺🇸

Baltimore, Maryland, United States

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

University of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

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