VTE Protocol Presented by: Selina Baskins, RN Quality Coordinator 1 Each Risk Factor Represents 1 Point •Age 41-60 years •Minor surgery planned •Hx of prior major surgery (<1 month) •Varicose veins •Hx of inflammatory bowel disease •Swollen legs (current) •Obesity (BMI>25kg/m2) •AMI •CHF •Sepsis •Serious lung disease including pneumonia 2 Each Risk Factor Represents 1 Point Abnormal pulmonary function (COPD) Medical patient currently at bed rest Oral contraceptives Pregnancy or postpartum (<1month) Hx of unexplained stillborn infant, recurrent spontaneous abortion (>3), premature birth with toxemia, or growth-restricted infant 3 Each Risk Factor Represents 2 Points Age 61-74 years Arthroscopic surgery Malignancy (present or previous) Major surgery (over 45 minutes) Laparascopic surgery (over 45 minutes) Patient confined to bed (>72 hours) Immobilizing plaster cast (<1 month) Central venous access 4 Each Risk Factor Represents 3 Points Age ≥ 75 years Hx of VTE/PE Family Hx of thrombosis Blood/bone marrow dyscrasias * Thrombophilic condition ** Heparin induce thrombocytopenia 5 Each Risk Factor represents 5 Points Elective major lower extremity arthroplasty Hip, pelvis, or leg fracture Stroke Multiple trauma Acute spinal cord injury (paralysis 6 Contraindications Contraindications to pharmacologic prophylaxis i.e. active bleeding, current or history of heparin induced thrombocytopenia, platelet count < 100,000 Contraindications to sequential compression devices, i.e. severe peripheral arterial disease, CHF, acute/superficial VTE Other contraindications 7 Standard of Care for assessed Risk Score: IF INTERVENTIONS HAVE NOT BEEN ORDERED, CALL MD FOR ORDERS! 0-1 Low Risk = Early and aggressive ambulation 2 Moderate Risk Lovenox 40 mg subcutaneous daily (Choose one) Lovenox 30 mg subcutaneous daily if CrCl less than 30 Graduated compression stockings thigh, knee high Sequential compression device 3-4 High Risk Lovenox 40 mg subcutaneous daily AND Sequential compression device 8 Standard of Care for assessed Risk Score: IF INTERVENTIONS HAVE NOT BEEN ORDERED, CALL MD FOR ORDERS (Cont’d) (Choose one) Lovenox 30 mg subcutaneous daily AND Sequential compression device if CrCl less than 30 5 or more Very High Lovenox 40 mg subcutaneous daily, Sequential compression device AND graduated Risk compression stocking Lovenox 30 mg subcutaneous daily if CrCl less than 30, Sequential compression device AND graduated compression stocking 9 Other instructions If the patient received epidural anesthesia, do not start Lovenox until 24 hours after establishment of stable hemostasis If the patient has an epidural postoperatively, do not start Heparin/LMWH until epidural ha 10 QUESTIONS???? 11