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Clinical Utility of Postoperative Hemoglobin Testing

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TriHealth

Status

Completed

Conditions

Anaemia Postoperative

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to evaluate how many patients have hemoglobin less than 10 g/dL at post-operative day 1

Full description

Obtaining a complete blood count (CBC) on post-operative day 1 to assess postoperative hemoglobin levels is routine practice at Cincinnati Urogynecology Associates, TriHealth Inc. after pelvic reconstructive surgery.

There is minimal data supporting this practice. Multiple studies throughout the gynecology literature suggest that this is not a necessary or cost effective strategy to assess for postoperative anemia. Most patients who require blood transfusion or reoperation for bleeding will show clinical signs of anemia.

The investigators aim to determine if checking a routine CBC results in clinically relevant changes to patient care in women undergoing pelvic reconstructive surgery with vaginal hysterectomy for treatment of pelvic organ prolapse.

Enrollment

664 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Total vaginal hysterectomy with or without bilateral salpingectomy/oophorectomy (CPT 58260, 58262, 58263, 58270, 58290, 58291, 58292, 58294)

  • At least one of the following vaginal native tissue prolapse repairs

    • Apical repair with uterosacral ligament suspension (CPT 57283)
    • Apical repair with sacrospinous ligament fixation (CPT 57282)
    • Anterior repair (CPT 57240, 57260, 57284, 57285, 57250)
    • Posterior repair (CPT 45560, 56800, 56810, 57200, 57210, 57250)
  • Surgery by one of four fellowship trained urogynecologists at TriHealth

Exclusion criteria

  • Concomitant surgical procedure by a second surgeon
  • Malignancy identified at the time of surgery or active malignancy
  • Cases converted to open hysterectomy or prolapse repairs
  • Prolapse repair completed robotically
  • Prolapse repair completed with mesh
  • Known coagulopathy
  • Patient on long term preoperative anticoagulant medication (Arixtra, Coumadin, Eliquis, Heparin, Lovenox, Pradaxa, Savaysa, Xarelto)

Trial design

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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