ObjectivesCombined hormonal contraceptives (CHCs) are the most widely prescribed contraceptive methods in the UK; however, their use is associated with significant cardiovascular risk for women with some medical conditions and risk factors. The objective of this study was to assess the potential change in CHC prescribing among higher-risk women following publication of the UK Medical Eligibility Criteria for Contraceptive Use (UKMEC) in 2006.MethodsA cross-sectional study was conducted using the General Practice Research Database to analyse UK women aged 15–49 years who were prescribed CHCs during the period 2004–2010. Of women prescribed CHCs, those at higher risk of cardiovascular events (with UKMEC Category 3 or 4 risk factors) were identified. The percentage of higher-risk CHC users, among all CHC users, in 2005 (pre-UKMEC) was compared to that in 2010 (post-UKMEC).ResultsThe percentage of higher-risk CHC users significantly decreased by 0.8% (95% CI 0.68% to 1.02%) following publication of UKMEC [8.1% (95% CI 7.98% to 8.22%) in 2005 vs 7.3% (95% CI 7.14% to 7.38%) in 2010; p<0.001]. However, an estimated 1 74 472 women in the UK were prescribed CHCs in 2010 despite having Category 3 or 4 risk factors. The most common Category 3 or 4 risk factors were body mass index ≥35 kg/m2, hypertension and smoking in women aged ≥35 years.ConclusionsDespite the observed reduction in prescribing of CHCs to higher-risk women after publication of UKMEC, a large number of women with Category 3 or 4 risk factors are still prescribed CHCs. The increased risk of cardiovascular events is unnecessary for many of these women given the availability of alternative contraceptive methods.
Objectives: Cost is considered one of the major barriers to greater use of LARC (Long-Acting Reversible Contraceptive) methods, especially cost of treatment initiation. However, when considering their contraceptive efficacy alongside cost of pregnancy, LARC methods are deemed by NICE to be more cost-effective than combined oral contraceptive pills even at one year of use. (NICE LARC CG30 2005). MethOds: A 3 year time-horizon cost-benefit model was developed to assess budgetary impact of increasing LARC uptake (implant, IUD, IUS and injectable) compared to the oral contraceptive pill, in UK women aged 16-49 who currently use the following contraceptives of interest: non-LARC method (defined as contraceptive pill only) or LARC methods (IUD, IUS, injectable, implant). A weighted-average price based on current market shares was calculated, for all contraceptive pills currently available in the UK. Increased uptake of any LARC method was offset against a reduction in contraceptive pill usage. Unintended pregnancies, based on typical failure rate, occurring with all treatments considered was taken into account. Results: Of approximately 14,750,000 women aged 16-49 in the UK, official statistics confirm 37% use contraceptive methods of interest to our model. This proportion formed our cohort of approximately 5,500,000 UK women aged 16-49, which was followed over a 3 year time horizon. A 100% increase in uptake of each LARC method would lead to a 49% decrease in oral contraceptive pill uptake. Over a three year period this would save 374,794 unintended pregnancies, and elicit financial savings of £630,831,022, on which £54,098,847 is attributable to treatment costs (ingredient, consultations, removal/insertion costs) and £576,732,175 to the cost of unintended pregnancies (live birth, miscarriage, abortion, ectopic pregnancy). cOnclusiOns: The model projects that increasing LARC uptake will result in a significant reduction in the number of unintended pregnancies, with consequent savings to the NHS across the UK.Objectives: Our aim was to assess the costs and consequences of labour induction using misoprostol vaginal insert (MVI) compared with currently used technologies using a specifically developed user-friendly decision model developed and Slovakia. MethOds: The model was developed in Microsoft Office Excel and compares clinical and safety aspects like time to vaginal delivery, time to active labour, occurrence of cesarean delivery and adverse events of MVI with selected comparators. Efficacy and safety data were retrieved from targeted literature review, conducted in the main medical databases. Country-specific information about costs and resource use was incorporated into the model. Local data were collected for each country via a specifically developed questionnaire. The model considered the hospital and public payer perspectives. The model generated results as an incremental difference between the total costs related to labour induction with MVI or a comparator. The threshold price of MVI was also calculated. Resu...
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