1990
DOI: 10.1016/0002-9378(90)90594-w
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Hemostasis profile in women taking low-dose oral contraceptives

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Cited by 56 publications
(20 citation statements)
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“…There are anecdotal reports of the disappearance of bleeding symptoms during treatment, with normalization of vWF and FVIII levels in several cases [48]. A significant increase in FVIII and vWF levels in normal women on oral contraception has been shown in some but not all studies [31,[49][50][51]. However, the hemostatic effects are variable with markedly elevated clotting factor levels in some individuals [50].…”
Section: Oral Contraceptivesmentioning
confidence: 99%
See 1 more Smart Citation
“…There are anecdotal reports of the disappearance of bleeding symptoms during treatment, with normalization of vWF and FVIII levels in several cases [48]. A significant increase in FVIII and vWF levels in normal women on oral contraception has been shown in some but not all studies [31,[49][50][51]. However, the hemostatic effects are variable with markedly elevated clotting factor levels in some individuals [50].…”
Section: Oral Contraceptivesmentioning
confidence: 99%
“…A significant increase in FVIII and vWF levels in normal women on oral contraception has been shown in some but not all studies [31,[49][50][51]. However, the hemostatic effects are variable with markedly elevated clotting factor levels in some individuals [50]. Estrogens also inhibit endometrial proliferation, which explains their benefit in women with type 3 disease, in whom FVIII and vWF levels are unchanged.…”
Section: Oral Contraceptivesmentioning
confidence: 99%
“…Combined oral contraceptive pill (COCP) use causes a small rise in the level of VWF:Ag and VWF:RCo. In 36 women who did not have VWD the VWF:Ag and VWF:RCo rose from 88 ± 29 (IU dL −1 , mean ± SD) and 103 ± 31 to 92 ± 38 and 107 ± 46 respectively after 6 months treatment with low dose COCP [23].…”
Section: Combined Oral Contraceptive Pillmentioning
confidence: 99%
“…As for testing on OC, present preparations do not contain supraphysiological doses of oestrogen [44] and so are unlikely to affect the laboratory diagnosis of VWD. This is because the majority of studies in normal women exposed to much lower doses of oestrogen as contained in the second and third generation OC preparations have shown no significant increase in the VWF levels [39,45–48] with only a few exceptions [49]. Interestingly, in two of these studies, there was a decrease noted in the VWF levels [39,47], although this was not statistically significant.…”
Section: The Laboratory Diagnosis Of Vwd: Does Testing In Relation Tomentioning
confidence: 99%