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Deep Vein ThrombosisNCT00550082

3 Screen Electronic Alert

An observational study of Deep Vein Thrombosis and Pulmonary Embolism, run by Brigham and Women's Hospital at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Evaluation of physician responses to BICS-Clinical Information 3-screen alerts that informs the clinician that his/her patient may be eligible for thromboprophylaxis. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Deep Vein Thrombosis, Pulmonary Embolism, Cancer
How many people
880 participants
Where
1 siteUnited States
Study dates
Jul 2007to Nov 2009
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Hospitalized patients at Brigham and Women's Hospital from medical and surgical services who are 18 yrs old or older and are at a moderate to high risk for venous thromboembolism (VTE)

Who may be able to join

  • Hospitalized patients at Brigham and Women's Hospital from medical and surgical services who are 18 yrs old or older and are at a moderate to high risk for venous thromboembolism (VTE)

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02115

Other trials in United States

About this study

Official title: Multi-Screen Electronic Alert for Venous Thromboembolism Prevention

Evaluation of physician responses to BICS-Clinical Information 3-screen alerts that informs the clinician that his/her patient may be eligible for thromboprophylaxis.

Read the detailed description

Background and Significance:

Scope of the Problem: VTE is the third most common cardiovascular disease (heart attack and stroke are more common) but is the most preventable medical problem among patients hospitalized with other illnesses. DVT often causes chronic venous insufficiency, a potentially disabling and painful condition that lowers the quality of life. Acute PE may cause death or disabling chronic thromboembolic pulmonary hypertension. After discharge from a short-term hospital stay, one study reported that the incidence of DVT was 48 per 100,000 and the incidence of PE (with or without DVT) was 23 per 100,000.9 In addition, the incidence of VTE increases dramatically with age.10-11 Clinical manifestations of DVT often include swelling, pain, and extremity discoloration and may lead to PE. Manifestations of PE may include dyspnea, pleuritic pain, cough, and hemoptysis or may be asymptomatic.12-13 The 28-day mortality rate for a first VTE event is alarmingly high, approximately 11%.14 In addition, 3-month mortality rates for PE have been reported as high as 17%.15 However, appropriate prophylaxis-using anticoagulants, mechanical measures, or both anticoagulants plus mechanical measures-can prevent most episodes of VTE16. For example, mechanical measures as simple as "low tech" and inexpensive graduated compression stockings can reduce VTE rates.16a, 16b, 16c

Burden to Patients: VTE is associated with complications including recurrence of DVT or PE, chronic thromboembolic pulmonary hypertension, death, or the subsequent development of post-thrombotic syndrome. The risk of VTE recurrence is greatest within 6-12 months after the first event and continues for at least 10 years,17 and is a risk factor for death after PE.18 The post-thrombotic syndrome can have devastating effects on the patients' quality of life and is associated with venous hypertension that may cause pain, edema, skin changes, varicose veins, and skin ulcers. Valve dysfunction, which can lead to venous hypertension, is most often caused by a previous DVT.19 The cumulative incidence of the development of postthrombotic syndrome after a VTE event is high: 17% at one year, 23% at 2 years, and 29% at 8 years, with 30% of these cases classified as severe.20

Burden to Society: Direct medical costs to the United States health care system related to VTE events and complications approximate at least $600 million annually. Bullano and colleagues21 estimate that managed care plans pay a median of $3,131 per incident DVT, $6,424 per incident PE, and $12,200 for a DVT plus PE combination event. A 2004 registry of 5,451 patients with ultrasound-confirmed DVT at 183 institutions in the United States revealed that DVT led to hospitalization in 80% of those diagnosed as outpatients. Those initially diagnosed with DVT as inpatients remained hospitalized for a median of 12 days.7

Role of computerized healthcare delivery systems:

The use of computerized physician order entry (CPOE) is growing and is currently utilized in about 10% of U.S. Hospitals.22 When linked with clinical decision support, it provides a unique and important tool to improve ordering decisions, thereby reducing medication errors, transcribing errors, decreasing the frequency of adverse drug events, and increasing compliance with evidence-based clinical guidelines.23 This leads to overall improved patient care. There is growing recognition of the importance and utility of CPOE technology, and currently, there is a concerted effort nation-wide to implement it in all hospitals and private practices. CPOE programs provide an excellent platform to increase the implementation of clinical practice guidelines, thereby changing physician behavior.

At Brigham and Women's Hospital, we have developed an electronic alert system, which is integrated with the CPOE system but functions independently. We have created risk score criteria by which the system determines the risk of DVT or PE for a particular patient. All the information needed to accomplish this risk assessment is stored in the computer system, allowing the process to run in an automated fashion. The system according to present criteria determines whether to generate an alert. To do this, the system checks for the existence of current orders for prophylaxis, using the Brigham and Women's Hospital CPOE system. The presence of medication class orders for anticoagulants or general care orders for mechanical prophylaxis prevents the computer from issuing an alert. We will enhance this computerized system to produce a series of alerts that provide more information related to prescription or omission of thromboprophylaxis. We aim to test this new system in our proposed study.

At Brigham and Women's Hospital, we also leverage the use of the multiple outpatient electronic medical records and inpatient CPOE systems to facilitate the process of medication reconciliation before, during, and after the hospital stay. This system aggregates medication data from electronic medical records (EMR) and CPOE systems so that clinicians can efficiently generate an accurate pre-admission medication list. Information collected with the use of this application subsequently supports the writing of admission and discharge orders by physicians, performance of admission assessment by nurses, and reconciliation of inpatient orders by pharmacists. Medication histories are thus seamlessly transferred during transition of care from inpatient admission to discharge to home, rehabilitation, or skilled nursing facilities. This efficient system will allow us to carefully document the use or omission of thromboprophylaxis orders. Furthermore, for 90 day follow-up, we will be able to track thromboprophylaxis prescriptions after hospital discharge by using a combination of the Brigham and Women's Hospital's pharmacy's electronic outpatient prescription reconciliation program and Partners' internally developed EMR, the Longitudinal Medical Record.

The Longitudinal Medical Record is used by our outpatient clinics to record clinical visit information such as history, notes, problems, medications, and allergies, and provides inpatient and outpatient test results, including imaging tests and laboratory blood tests, from 7 Partners-affiliated institutions: Brigham and Women's Hospital, Massachusetts General Hospital, Dana Farber Cancer Institute, Newton Wellesley Hospital, North Shore Medical Center, Faulkner Hospital, and Spaulding Rehabilitation Hospital. The Longitudinal Medical Record is especially useful for following patients who might undergo evaluation for a new problem, such as sudden onset of shortness of breath, at a suburban hospital such as Newton Wellesley Hospital, after a prior hospitalization at Brigham and Women's Hospital for treatment of a complicated medical illness with a high risk of VTE. In our 2005 randomized trial of electronic alerts for VTE prophylaxis,8 we relied upon the Longitudinal Medical Record to achieve 94% follow-up at 90 days of all patients enrolled at Brigham and Women's Hospital.

Between 2000 and 2004, we developed a computer generated alert system for VTE prophylaxis and tested it in a large randomized controlled trial at Brigham and Women's Hospital. The system was linked to the patient database, identifying patients at high risk for VTE (defined as ≥ 4 score points and shown in Table 1) who were not receiving prophylaxis. High-risk patients not receiving VTE prophylaxis were randomized to an intervention group in which their physicians received an electronic alert or a control group in which physicians were not alerted. Patients in the intervention group experienced a 41% reduction in the incidence of symptomatic VTE events within 90 days, without an increase in the risk of major or minor bleeding. However, prophylactic measures were prescribed for only 33.5% of the patients in the intervention group. For the remaining patients (66.5%), we were surprised that physicians declined to implement the suggested intervention, initiation of VTE prophylaxis.

There is still considerable scope for electronic methodology and technology to increase prophylaxis rates and reduce the rates of VTE. Therefore, we will focus these new study initiatives on improving our current methods and strategies to further reduce the incidence of VTE.

Significance of our proposed studies:

Our projects will address several gaps in our understanding of the issues related to implementation of VTE prophylaxis in hospitalized patients. We aim to identify subgroups in the hospitalized population that are at especially high risk for VTE. An improved and novel automated electronic alerting system will facilitate this identification. Our new alert system will be much more rigorous than our prior protocol. The new alert will have three sequential screens rather than the single alert screen that we had in the prior version.

This computerized system will identify hospitalized patients at high risk for VTE and will analyze their records to determine whether they have received thromboprophylaxis orders. If the system identifies any high-risk patient who does not have orders for thromboprophylaxis, then a series of prompts will be issued to the ordering physician. The physician whose patient is at risk for VTE will be requested to institute prophylaxis. If the automated request is not followed, a series of alerts will query reasons for withholding preventive measures. Further prompts will lead to centralized computer-generated ordering of graduated compression stockings, unless the physician opts out and unselects this order. Important elements in the alerts include an up-to-date selection of pharmacological agents, doses based on renal clearance, and the documentation of reasons for withholding prophylaxis by the ordering physician.

We will follow all high-risk patients whose physicians received an alert. We will determine whether within 90 days, the patient has developed symptomatic DVT or PE. The Longitudinal Medical Record will facilitate follow-up after hospital discharge.

Through the use of this novel alert system, we will identify patients at high risk for VTE, maximize the implementation of VTE prophylaxis, learn the rationale for physicians' withholding anticoagulant or mechanical prophylaxis in some high-risk patients, and test whether this novel electronic intervention reduces clinically important episodes of PE and DVT. The success of this program will provide a useful model for dissemination of VTE preventive strategies nationwide and worldwide.

Keywords
Anticoagulation, High-Risk, Deep Vein Thrombosis, Pulmonary Embolism, Surgery
Medical subject headings
Venous Thrombosis, Pulmonary Embolism, Neoplasms

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Venous Thromboembolism and Bleeding Events

    Measured: 90 Days

Secondary outcomes (2)
  1. Re-hospitalization

    Measured: 90 Days

  2. Mortality

    Measured: 30 Days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Oct 2007 (estimated)
  2. Study startJul 2007
  3. Primary completionNov 2009
  4. Study completionNov 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
880 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00550082
Sponsor's protocol ID
2006-P-002346
Status last verified
Feb 2012
First submitted
24 Oct 2007
Last updated
10 Feb 2012
Results posted
No
Data monitoring committee
No

Publications

  • Parasuraman S, Goldhaber SZ. Venous thromboembolism in children. Circulation. 2006 Jan 17;113(2):e12-6. doi: 10.1161/CIRCULATIONAHA.105.583773. No abstract available.

    PubMed 16418440
  • Piazza G, Goldhaber SZ. Acute pulmonary embolism: part II: treatment and prophylaxis. Circulation. 2006 Jul 18;114(3):e42-7. doi: 10.1161/CIRCULATIONAHA.106.620880. No abstract available.

    PubMed 16847156
  • Piazza G, Goldhaber SZ. Acute pulmonary embolism: part I: epidemiology and diagnosis. Circulation. 2006 Jul 11;114(2):e28-32. doi: 10.1161/CIRCULATIONAHA.106.620872. No abstract available.

    PubMed 16831989
  • Geerts WH, Pineo GF, Heit JA, Bergqvist D, Lassen MR, Colwell CW, Ray JG. Prevention of venous thromboembolism: the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy. Chest. 2004 Sep;126(3 Suppl):338S-400S. doi: 10.1378/chest.126.3_suppl.338S.

    PubMed 15383478
  • Paterno MD, Cina JL, Goldhaber SZ, Kucher N. Preventing DVT and PE in hospitalized patients: improving a successful electronic alert. AMIA Annu Symp Proc. 2006;2006:1058.

    PubMed 17238677
  • Kucher N, Goldhaber SZ. Risk stratification of acute pulmonary embolism. Semin Thromb Hemost. 2006 Nov;32(8):838-47. doi: 10.1055/s-2006-955466.

    PubMed 17171598
  • Kucher N, Koo S, Quiroz R, Cooper JM, Paterno MD, Soukonnikov B, Goldhaber SZ. Electronic alerts to prevent venous thromboembolism among hospitalized patients. N Engl J Med. 2005 Mar 10;352(10):969-77. doi: 10.1056/NEJMoa041533.

    PubMed 15758007
  • Goldhaber SZ, Dunn K, MacDougall RC. New onset of venous thromboembolism among hospitalized patients at Brigham and Women's Hospital is caused more often by prophylaxis failure than by withholding treatment. Chest. 2000 Dec;118(6):1680-4. doi: 10.1378/chest.118.6.1680.

    PubMed 11115458
  • Goldhaber SZ, Turpie AG. Prevention of venous thromboembolism among hospitalized medical patients. Circulation. 2005 Jan 4;111(1):e1-3. doi: 10.1161/01.CIR.0000150393.51958.54. No abstract available.

    PubMed 15630031
  • Goldhaber SZ, Tapson VF; DVT FREE Steering Committee. A prospective registry of 5,451 patients with ultrasound-confirmed deep vein thrombosis. Am J Cardiol. 2004 Jan 15;93(2):259-62. doi: 10.1016/j.amjcard.2003.09.057.

    PubMed 14715365
  • Cushman M, Tsai AW, White RH, Heckbert SR, Rosamond WD, Enright P, Folsom AR. Deep vein thrombosis and pulmonary embolism in two cohorts: the longitudinal investigation of thromboembolism etiology. Am J Med. 2004 Jul 1;117(1):19-25. doi: 10.1016/j.amjmed.2004.01.018.

    PubMed 15210384
  • Anderson FA Jr, Wheeler HB, Goldberg RJ, Hosmer DW, Patwardhan NA, Jovanovic B, Forcier A, Dalen JE. A population-based perspective of the hospital incidence and case-fatality rates of deep vein thrombosis and pulmonary embolism. The Worcester DVT Study. Arch Intern Med. 1991 May;151(5):933-8.

    PubMed 2025141

Questions about this trial

What is this clinical trial studying?

An observational study of Deep Vein Thrombosis and Pulmonary Embolism, run by Brigham and Women's Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Feb 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Venous Thromboembolism and Bleeding Events (time frame: 90 Days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00550082, which also lists 12 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2012; AzTrials last refreshed its copy on 28 Oct 2026.

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