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Table 2 Treatment characteristics

From: A retrospective evaluation of fondaparinux for confirmed or suspected heparin-induced thrombocytopenia in left-ventricular-assist device patients

Patient

CKD

Fondaparinux dose

Duration of fondaparinux (days)

Transitioned and discharged on warfarin (Y/N)

Concurrent aspirin dosage

New thrombosis after fondaparinux*

Major bleeding after fondaparinux

1

Y

2.5 mg

5

Y

81 mg

No

No

2

N

2.5 mg

22

N

81 mg

LVAD thrombosis

No

3

N

5 mg

14

Y

325 mg

No

No

4

N

5 mg

4

Y

325 mg

No

No

5

N

5 mg

3

Y

81 mg

PE

No

6

N

7.5 mg

10

Y

81 mg

DVT

Overt bleed**

7

N

7.5 mg

3

N

81 mg

No

Blood transfusion***

8

Y

10 mg

2

Y

81 mg

No

Blood transfusion***

  1. *All thrombotic events occurred prior to discharge on the admission in which HIT was diagnosed.
  2. **Overt bleeding = ≥ 2 gram g/dL decrease in any 24 hr period.
  3. ***Believed to be related to clinical course and unrelated to anticoagulation therapy.
  4. CKD = chronic kidney disease; defined as estimated glomerular filtration rate (GFR) < 60 mL/min/1.73 m2 for > 3 months.
  5. DVT = deep vein thrombosis.
  6. PE = pulmonary embolism.