See also:
All DVT prophylaxis clinical trials
All clinical trials of LMWH
All clinical trials of enoxaparin
|
|
Treatments
| Studied treatment |
Enoxaparin, 20 mg/d subcutaneously 18-24 hours postoperatively for 10 days
|
| Control treatment |
placebo
|
Patients
| Patients |
Neurosurgery, adult, 45-90 kg of weight, without excess bleeding risk |
| Baseline characteristics |
| Endpoint assessment |
Venography |
|
Method and design
| Randomized effectives |
67 / 63 (studied vs. control) |
| Follow-up duration |
NA |
Results
Endpoint
Studied treat. n/N
Control treat. n/N
Graph
RR [95% CI]
Bleeding
0 / 67
0 / 63
classic
0,94 [0,00;237,81]
Major bleeding
0 / 67
0 / 63
classic
0,94 [0,00;237,81]
0
2
1.0
|
Relative risks
|
| Endpoint |
Events (%) |
Relative Risk |
95% CI |
Endpoint definition in the trial |
Ref |
| Studied treat. |
Control treat. |
|
Major bleeding
|
0 / 67 (0,7%) |
0 / 63 (0,8%) |
0,94 |
[0,02;46,68] |
|
|
|
Bleeding
|
0 / 67 (0,7%) |
0 / 63 (0,8%) |
0,94 |
[0,02;46,68] |
|
|
|
The primary endpoint (if exists) appears in blod characters
|
|
Reference(s) used for data extraction:
|
| Endpoint |
studied treat. |
control treat. |
mean diff |
|
Absolute risk reduction
|
| Endpoint |
Events rate |
Absolute risk reduction (ARR) |
| Studied treat. |
Control treat. |
Reference(s)
-
Melon E, Keravel Y, Gaston A, Huet Y, Combes S, and the NEURONOX groupj.
Deep venous thrombosis prophylaxis by low molecular weight heparin in neurosurgical
patients [abstract.
Anesthesiology. 1987;75:A214
Pubmed
|
Hubmed
| Fulltext
|