Sickle cell disease: depo-provera contraceptive reduced painful crises.
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Clinical bottom line (level 1b)
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Women with sickle cell disease who were given depo-provera had fewer painful episodes than those given placebo
(NNT =
3
at 14
months)
.
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Women given depo-provera were less likely to experience bone pain
(NNT =
4
at 14
months)
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de Ceulaer et al:
Lancet
1982;
2:
229-231
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Expires
February 2003
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The study
Single-blinded ?concealed randomised cross-over
trial
without
intention-to-treat
Setting: university hospital, Jamaica
25 patients
(aged
range 20 to 41 years,
100%
female)
homozygous sickle cell disease diagnosed by 'standard criteria'
Note: Women were advised to continue with forms of contraception other than anything steroidal, during the study.
Control Group: (n = 23, 23 analysed):
saline im once every three months for nine months, followed by six month washout
Experimental Group: (n = 23, 23 analysed):
the contraceptive
depo-provera
(medroxyprogesterone) 150 mg im every three months for nine months, followed by six month washout period
100% followed for
14
months
The evidence
| Outcome |
Time to outcome |
CER | EER | RRR (95% CI) | ARR (95% CI) | NNT (95% CI) |
| bone pain
|
14
months |
20 (87.0%) |
14 (60.9%) |
30.0% (-1.00% to
51.0%) |
26.1% (1.85% to
50.3%) |
4
(2 to
54)
|
| increase in painful crises
|
14
months |
13 (56.5%) |
4 (17.4%) |
69.0% (20.0% to
88.0%) |
39.1% (13.6% to
64.6%) |
3
(2 to
7)
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Severity per episode of painful crises was worse in the depo-provera phase (2 on a severity scale of 1-3), compared with 1.8 with placebo.
26% of women had heavier than normal uterine bleeding- otherwise no other side effects.
Citation
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de Ceulaer
K,
Gruber
C,
Hayes
R, et al:
medroxyprogesterone acetate and homozygous sickle-cell disease.
Lancet
1982;
2:
229-231
Contributor: Chris Ball and CLare Wotton,
February 2000
Reviewer:
Clinical Question.
| Patient |
sickle cell disease |
| Intervention or Exposure |
depo-povera |
| Comparison |
saline |
| Outcome |
bone pain |
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