The correct statement is that unopposed oestrogen increases the risk of endometrial cancer. Combined oestrogen and progesterone HRT can reduce the risk of endometrial cancer in patients with a uterus, while patients without a uterus should be prescribed oestrogen-only HRT as combined HRT is less well tolerated. The statement that unopposed oestrogen increases the risk of breast cancer is incorrect, as both types of HRT can increase the risk of breast cancer, with combined HRT potentially increasing the risk more than oestrogen-only. Additionally, the statement that unopposed oestrogen increases the risk of heart disease is incorrect, as oestrogen has a protective role in inhibiting the development of atherosclerosis, which can reduce the risk of heart disease. Finally, the statement that unopposed oestrogen increases the risk of osteoporosis is also incorrect, as HRT can be prescribed to prevent or treat osteoporosis in some patients and can reduce the risk of fracture instead of increasing it.

Adverse Effects of Hormone Replacement Therapy

Hormone replacement therapy (HRT) is a treatment that involves the use of a small dose of oestrogen, often combined with a progesterone in women with a uterus, to alleviate menopausal symptoms. While it can be effective in reducing symptoms such as hot flashes and vaginal dryness, HRT can also have adverse effects and potential complications.

Some common side-effects of HRT include nausea, breast tenderness, fluid retention, and weight gain. However, there are also more serious potential complications associated with HRT. For example, the use of HRT has been linked to an increased risk of breast cancer, particularly when a progesterone is added. The Women’s Health Initiative study found a relative risk of 1.26 at 5 years of developing breast cancer with HRT use. The risk of breast cancer is also related to the duration of use, and it begins to decline when HRT is stopped.

Another potential complication of HRT is an increased risk of endometrial cancer. Oestrogen by itself should not be given as HRT to women with a womb, as this can increase the risk of endometrial cancer. The addition of a progesterone can reduce this risk, but it is not eliminated completely. The British National Formulary states that the additional risk is eliminated if a progesterone is given continuously.

HRT has also been associated with an increased risk of venous thromboembolism (VTE), particularly when a progesterone is added. However, transdermal HRT does not appear to increase the risk of VTE. Women who are at high risk for VTE should be referred to haematology before starting any treatment, even transdermal, according to the National Institute for Health and Care Excellence (NICE).

Finally, HRT has been linked to an increased risk of stroke and ischaemic heart disease if taken more than 10 years after menopause. It is important for women considering HRT to discuss the potential risks and benefits with their healthcare provider and make an informed decision based on their individual circumstances.

No additional contraception is needed when switching from an IUD to COCP if it is removed on days 1-5 of the menstrual cycle. The COCP is effective immediately if started on these days, but if started from day 6 onwards, barrier contraception is required for 7 days. There is no need to delay starting the COCP after IUD removal. If the patient had recently taken ulipristal as an emergency contraceptive, she would need to wait for 5 days before starting hormonal contraception.

Intrauterine contraceptive devices include copper IUDs and levonorgestrel-releasing IUS. Both are over 99% effective. The IUD prevents fertilization by decreasing sperm motility, while the IUS prevents endometrial proliferation and thickens cervical mucous. Potential problems include heavier periods with IUDs and initial bleeding with the IUS. There is a small risk of uterine perforation, ectopic pregnancy, and infection. New IUS systems, such as Jaydess® and Kyleena®, have smaller frames and less levonorgestrel, resulting in lower serum levels and different rates of amenorrhea.

This question involves two components. Firstly, the lady in question is seven weeks postpartum and has had unprotected intercourse after day 21, putting her at risk of pregnancy. Therefore, she must have a pregnancy test before receiving any form of contraception. Secondly, the safety of the combined oral contraceptive pill (COCP) at 7 weeks postpartum is being considered. While the COCP is contraindicated for breastfeeding women less than 6 weeks postpartum, this lady falls into the 6 weeks – 6 months postpartum category where the benefits of prescribing the COCP generally outweigh the risks. Therefore, it would be suitable to prescribe the COCP for her. It is important to note that even if a woman is exclusively breastfeeding, the lactational amenorrhea method (LAM) is only effective for up to 6 months postpartum. Additionally, while the progesterone only pill is a good form of contraception, it is not necessary to recommend it over the COCP in this case.

After giving birth, women need to use contraception after 21 days. The progesterone-only pill (POP) can be started at any time postpartum, according to the FSRH. Additional contraception should be used for the first two days after day 21. A small amount of progesterone enters breast milk, but it is not harmful to the infant. On the other hand, the combined oral contraceptive pill (COCP) is absolutely contraindicated (UKMEC 4) if breastfeeding is less than six weeks post-partum. If breastfeeding is between six weeks and six months postpartum, it is a UKMEC 2. The COCP may reduce breast milk production in lactating mothers. It should not be used in the first 21 days due to the increased venous thromboembolism risk post-partum. After day 21, additional contraception should be used for the first seven days. The intrauterine device or intrauterine system can be inserted within 48 hours of childbirth or after four weeks.

The lactational amenorrhoea method (LAM) is 98% effective if the woman is fully breastfeeding (no supplementary feeds), amenorrhoeic, and less than six months post-partum. It is important to note that an inter-pregnancy interval of less than 12 months between childbirth and conceiving again is associated with an increased risk of preterm birth, low birth weight, and small for gestational age babies.

If a woman has a suspected or personal history of breast cancer or a confirmed BRCA mutation, the safest form of contraception for her is the copper coil. The UK Medical Eligibility Criteria for Contraceptive Use (UKMEC) provides guidelines for the choice of contraception, grading non-barrier contraceptives on a scale of 1-4 based on a woman’s personal circumstances. Contraceptive methods that fall under category 1 or 2 are generally considered safe for use in primary care. In this case, all forms of contraception except the combined pill (category 3) can be offered, with the copper coil being the safest option as it falls under category 1.

Understanding Contraception: A Basic Overview

Contraception has come a long way in the past 50 years, with the development of effective methods being one of the most significant advancements in medicine. There are various types of contraception available, including barrier methods, daily methods, and long-acting methods of reversible contraception (LARCs).

Barrier methods, such as condoms, physically block sperm from reaching the egg. While they can help protect against sexually transmitted infections (STIs), their success rate is relatively low, particularly when used by young people.

Daily methods include the combined oral contraceptive pill, which inhibits ovulation, and the progesterone-only pill, which thickens cervical mucous. However, the combined pill increases the risk of venous thromboembolism and breast and cervical cancer.

LARCs include implantable contraceptives and injectable contraceptives, which both inhibit ovulation and thicken cervical mucous. The implantable contraceptive lasts for three years, while the injectable contraceptive lasts for 12 weeks. The intrauterine system (IUS) and intrauterine device (IUD) are also LARCs, with the IUS preventing endometrial proliferation and thickening cervical mucous, and the IUD decreasing sperm motility and survival.

It is important to note that each method of contraception has its own set of benefits and risks, and it is essential to consult with a healthcare provider to determine the best option for individual needs and circumstances.

The contraceptive patch regime involves wearing one patch per week for three weeks, followed by a patch-free week. This method is gaining popularity due to its flexibility, as the patch can be changed up to 48 hours late without the need for backup contraception. Additionally, the patch’s transdermal absorption eliminates the need for extra precautions during episodes of vomiting or diarrhea. Similar to the pill, this method involves three weeks of contraceptive use followed by a one-week break, during which the woman will experience a withdrawal bleed.

The Evra patch is the only contraceptive patch that is approved for use in the UK. The patch cycle lasts for four weeks, during which the patch is worn every day for the first three weeks and changed weekly. During the fourth week, the patch is not worn, and a withdrawal bleed occurs.

If a woman delays changing the patch at the end of week one or two, she should change it immediately. If the delay is less than 48 hours, no further precautions are necessary. However, if the delay is more than 48 hours, she should change the patch immediately and use a barrier method of contraception for the next seven days. If she has had unprotected sex during this extended patch-free interval or in the last five days, emergency contraception should be considered.

If the patch removal is delayed at the end of week three, the woman should remove the patch as soon as possible and apply a new patch on the usual cycle start day for the next cycle, even if withdrawal bleeding is occurring. No additional contraception is needed.

If patch application is delayed at the end of a patch-free week, additional barrier contraception should be used for seven days following any delay at the start of a new patch cycle. For more information, please refer to the NICE Clinical Knowledge Summary on combined hormonal methods of contraception.

Possible Causes of Abdominal Pain and Signs of Shock in Women: Differential Diagnosis

When a woman presents with abdominal pain and signs of shock, it is important to consider several possible causes. One of the most urgent and life-threatening conditions is ectopic pregnancy, which should be suspected until proven otherwise. A positive pregnancy test and pain localized to one side, especially with evidence of shock, are key indicators. The patient should be given intravenous access, blood tests, serum β-HCG, group and save, and a transvaginal ultrasound scan if stable. If necessary, she may need to undergo a laparoscopy urgently.

Other conditions that may cause abdominal pain in women include urinary tract infection, acute appendicitis, pelvic inflammatory disease, and miscarriage. However, these conditions are less likely to present with signs of shock. Urinary tract infection would show leukocytes, nitrites, and protein on dipstick. Acute appendicitis would cause pain in the right iliac fossa, but cervical excitation and signs of shock would be rare unless the patient is severely septic. Pelvic inflammatory disease would give rise to pain in the right iliac fossa and cervical excitation, but signs of shock would not be present on examination. Miscarriage rarely presents with signs of shock, unless it is a septic miscarriage, and the cervical os would be open with a history of passing some products of conception recently.

In summary, when a woman presents with abdominal pain and signs of shock, ectopic pregnancy should be considered as the most likely cause until proven otherwise. Other conditions may also cause abdominal pain, but they are less likely to present with signs of shock. A thorough differential diagnosis and appropriate diagnostic tests are necessary to determine the underlying cause and provide timely and effective treatment.

Investigations for Abdominal Pain in Women of Childbearing Age

When a woman of childbearing age presents with abdominal pain, it is important to consider the possibility of gynaecological problems, including ectopic pregnancy. The first step in investigation should be to ask about the patient’s last menstrual period and sexual history, and to perform a pregnancy test measuring β-human chorionic gonadotrophin (β-hCG) levels in urine or serum.

Proctoscopy is unlikely to be beneficial in the absence of specific gastrointestinal symptoms. Ultrasonography may be useful at a later stage to assess the location and severity of an ectopic pregnancy, but transvaginal ultrasound is preferable to transcutaneous abdominal ultrasound.

Specialist gynaecological opinion should only be sought once there is a high index of suspicion for a particular diagnosis. Laparoscopy is not indicated at this point, as less invasive tests are likely to yield the diagnosis. Exploratory laparoscopy may be considered if other investigations are inconclusive.

Investigating Abdominal Pain in Women of Childbearing Age

Patients with stress incontinence who do not respond to pelvic floor muscle exercises and decline surgical intervention may be prescribed duloxetine, a serotonin-norepinephrine re-uptake inhibitor. This drug increases sphincter tone during the filling phase of urinary bladder function. However, before starting drug therapy, patients should try pelvic floor exercises and consider surgical intervention. Oxybutynin, an anticholinergic drug, is used to treat urge incontinence or symptoms of detrusor overactivity, but it is not recommended for frail, older women at risk of health deterioration. Desmopressin is the preferred drug treatment for children with nocturnal enuresis and may also be used for women with nocturia. Mirabegron is prescribed for patients with urge incontinence who cannot tolerate antimuscarinic/anticholinergic drugs. It is a beta-3 adrenergic agonist that relaxes the bladder.

Understanding Urinary Incontinence: Causes, Classification, and Management

Urinary incontinence (UI) is a common condition that affects around 4-5% of the population, with elderly females being more susceptible. Several risk factors contribute to UI, including advancing age, previous pregnancy and childbirth, high body mass index, hysterectomy, and family history. UI can be classified into different types, such as overactive bladder (OAB)/urge incontinence, stress incontinence, mixed incontinence, overflow incontinence, and functional incontinence.

Initial investigation of UI involves completing bladder diaries for at least three days, vaginal examination, urine dipstick and culture, and urodynamic studies. Management of UI depends on the predominant type of incontinence. For urge incontinence, bladder retraining and bladder stabilizing drugs such as antimuscarinics are recommended. For stress incontinence, pelvic floor muscle training and surgical procedures such as retropubic mid-urethral tape procedures may be offered. Duloxetine, a combined noradrenaline and serotonin reuptake inhibitor, may also be used as an alternative to surgery.

In summary, understanding the causes, classification, and management of UI is crucial in providing appropriate care for patients. Early diagnosis and intervention can significantly improve the quality of life for those affected by this condition.

Causes of postmenopausal Bleeding: Understanding the Different Aetiologies

postmenopausal bleeding (PMB) can be a concerning symptom for women, and it is important to understand the different causes that may be responsible. One of the most common causes is vaginal atrophy, which occurs due to a decrease in oestrogen levels after menopause. This can lead to thinning and drying of the vaginal mucosa, as well as other symptoms such as vaginal dryness and an increased risk of urinary tract infections. Treatment options include non-hormonal approaches such as lubricants and moisturisers, as well as hormonal treatments like topical preparations or systemic oestrogen replacement.

Another potential cause of PMB is endometrial hyperplasia, which involves abnormal proliferation of the endometrium and is associated with an increased risk of endometrial cancer. While this is not the most common cause of PMB, ruling it out is important in order to identify any potential issues. Endometrial cancer itself is also a significant concern, with a 10% probability of being the cause of PMB. Urgent referral to a gynaecology outpatient is necessary to exclude this possibility.

Cervical cancer is not typically the cause of PMB, but it is important to discuss the cervical cancer screening programme with patients and any history of abnormal smears. Finally, the use of hormone replacement therapy (HRT) can also trigger menstruation and lead to PMB, although this is not the most common cause. By understanding these different aetiologies, healthcare providers can better diagnose and treat PMB in their patients.

Cervical ectropions are frequently observed in young women who are on COCP and experience post-coital bleeding. Although cervical cancer should be taken into account, the probability of it being the cause is reduced if the woman has had a recent normal smear. In such cases, ectropion is more probable.

Understanding Cervical Ectropion

Cervical ectropion is a condition that occurs when the columnar epithelium of the cervical canal extends onto the ectocervix, where the stratified squamous epithelium is located. This happens due to elevated levels of estrogen, which can occur during the ovulatory phase, pregnancy, or with the use of combined oral contraceptive pills. The term cervical erosion is no longer commonly used to describe this condition.

Cervical ectropion can cause symptoms such as vaginal discharge and post-coital bleeding. However, ablative treatments such as cold coagulation are only recommended for those experiencing troublesome symptoms. It is important to understand this condition and its symptoms in order to seek appropriate medical attention if necessary.