The Obstetrician & Gynaecologist 2007;9:4:276-279
doi: 10.1576/toag.9.4.276.27359
Copyright © 2007 by the Royal College of Obstetricians and Gynaecologists.
Answers to questions for volume 9, number 2
Numbered references correspond with the citations in the original article and so are not listed here. Discussions are not provided for questions relating to the clinical (Green-top) guidelines. All recent guidelines produced by the RCOG can be found on the RCOG website (www.rcog.org.uk).
The current management of vaginal birth after previous caesarean delivery
In the UK
| 1 |
the relative risk of uterine rupture during vaginal birth after caesarean section is under 3%. |
True |
| 2 |
a countrywide audit has reported a caesarean section rate of 26%. |
False |
| 3 |
over 50% of women attempt vaginal birth after one caesarean section. |
True |
| 4 |
over 30% of women with a previous caesarean section achieve a vaginal delivery. |
True |
| Discussion |
| In the UK, 21.5% of births are currently by caesarean section and 56% of women attempt vaginal birth after one caesarean section, with 66.7% of them succeeding. |
|
With regard to caesarean section,
| 5 |
there are no overall cost savings from VBAC compared with elective repeat caesarean. |
False |
| 6 |
there is a higher risk of caesarean hysterectomy associated with VBAC compared with caesarean section. |
False |
| 7 |
endometritis is more common after failed than successful VBAC. |
True |
| Discussion |
| There are cost savings from VBAC if success rates of 60–75% are achieved.3 The risk of hysterectomy in VBAC appears to be reduced or unchanged,5,7,8 but the rate of hysterectomy for uterine rupture is increased by 3.4/10 000.17 |
|
With regard to the risks of VBAC,
| 8 |
epidural anaesthesia masks the pain associated with scar dehiscence. |
False |
| 9 |
a baby of more than 4000 g predisposes to failed VBAC, but not to uterine rupture. |
True |
| 10 |
the rate of uterine rupture where there is a classical caesarean scar is over 20%. |
False |
| 11 |
the maternal mortality rate is 0.02 per 1000. |
True |
| Discussion |
| Epidural anaesthesia rarely masks scar pain but signs and symptoms of uterine rupture can be confused with acute placental abruption.24 A previous classical caesarean or T-shaped scar has been linked to scar rupture in 4–9% of VBACs.21 |
|
With regard to research into VBAC,
| 12 |
most of the evidence available today is based on large randomised controlled trials. |
False |
| 13 |
a recent statistical model includes antenatal findings to predict the likelihood of success. |
True |
| 14 |
one aim of the Caesarean Section Surgical Techniques (CAESAR) trial is to evaluate the effect of uterine closure on future pregnancies. |
True |
| Discussion |
| The available evidence on VBAC stems from case control or retrospective observational studies, with inherent problems of selection bias and limited comparability between study groups. |
|
Regarding the diagnosis of uterine rupture,
| 15 |
cardiotocography (CTG) changes are present in more than 90% of cases. |
False |
| 16 |
CTG changes include tachycardia, late decelerations and the disappearance of contractions. |
True |
| 17 |
uterine rupture usually leads to fetal death. |
False |
| Discussion |
| Cardiotocography heralds uterine rupture in 50–70% of cases.21 Uterine rupture is associated with a neonatal death rate of 1.8%.8 |
|
With regard to induction in cases of VBAC,
| 18 |
the use of oxytocin is associated with rupture precisely at the site of the previous scar. |
False |
| 19 |
recent evidence suggests that sequential use of prostaglandin and oxytocin is more hazardous than oxytocin after amniotomy. |
True |
| 20 |
one study has reported a >15% increase in risk of uterine rupture with prostaglandin induction. |
True |
| Discussion |
| Oxytocin is more usually associated with defects remote from the old scar.43 |
|
Cardiac disease in pregnancy. Part 2: acquired heart disease
Regarding the management of acute myocardial infarction during pregnancy and the puerperium,
| 21 |
coronary angiography is safe. |
True |
| 22 |
most deaths occur within 2 weeks of treatment. |
False |
| 23 |
thrombolysis is contraindicated. |
False |
| Discussion |
| Maternal mortality rates of 37–50% have been reported, with most deaths occurring at the time of infarction.15 Thrombolysis can cause bleeding from the placental site but is still indicated in the management of acute myocardial infarction. |
|
In a woman with mitral stenosis,
| 24 |
pregnancy increases the risk of atrial fibrillation. |
True |
| 25 |
pregnancy is associated with an approximately 10% maternal mortality rate. |
False |
| 26 |
pregnancy should be delayed until surgical correction where the symptoms or the stenosis are severe. |
True |
| 27 |
treatment with balloon mitral valvuloplasty is required in those with refractory symptoms. |
True |
| Discussion |
| Mortality among pregnant women with minimal symptoms is less than 1%. |
|
During pregnancy, open heart surgery with cardiac bypass is
| 28 |
best avoided. |
True |
| 29 |
associated with a 25% maternal mortality rate. |
False |
| 30 |
associated with a 16–33% risk of fetal mortality. |
True |
| Discussion |
| Open heart surgery with cardiac bypass carries a 1.5–5% risk of maternal mortality.11 |
|
With regards to peripartum cardiomyopathy,
| 31 |
the diagnosis is usually one of exclusion. |
True |
| 32 |
the mortality is approximately 20%. |
True |
| 33 |
subsequent pregnancies do not carry a risk of relapse if left ventricular systolic function has recovered completely. |
False |
| Discussion |
| Subsequent pregnancy carries a higher risk if left ventricular systolic function is not fully recovered first and, even with full recovery, some additional risk of relapse remains.24 |
|
Cardiac arrhythmias
| 34 |
should be treated with amiodarone during pregnancy. |
False |
| 35 |
should not be treated with cardioversion during pregnancy. |
False |
| Discussion |
| Amiodarone is contraindicated, as it is associated with fetal hypothyroidism, growth restriction and prematurity. Electrical cardioversion is safe in pregnancy and necessary in all women with tachyarrhythmias who are haemodynamically unstable. |
|
In pregnant women with mechanical heart valves
| 36 |
oral anticoagulation during pregnancy is associated with a rate of maternal thromboembolism of less than 5%. |
True |
| 37 |
the use of low molecular weight heparin during the first trimester carries a high risk of fetal embryopathy compared with use in the second trimester. |
False |
| 38 |
the fetal mortality rate is approximately 1 in 3. |
True |
| Discussion |
| Effective anticoagulation is critical and the risks to the mother and fetus need to be carefully balanced; several approaches are available. Substituting low molecular weight heparin for warfarin during the period of organogenesis (6–12 weeks of gestation) abolishes the risk of warfarin embryopathy but doubles the maternal thromboembolism risk to 9%. |
|
With regard to maternal mortality rates in the United Kingdom,
| 39 |
valvular disease following rheumatic fever has recently become one of the major causes. |
True |
| Discussion |
| With increasing immigration from countries where rheumatic fever remains prevalent, valvular heart disease is set to become a significant problem in the UK. |
|
During pregnancy
| 40 |
all women with heart valve lesions should be given antibiotics to prevent endocarditis. |
False |
| Discussion |
| Antibiotic prophylaxis should be given during labour and delivery to all women with valvular lesions except mitral valve prolapse without regurgitation. |
|
Uterine leiomyosarcomas: a review of the diagnostic and therapeutic pitfalls
Uterine leiomyosarcomas
| 41 |
are associated with exposure to tamoxifen. |
True |
| 42 |
are the commonest uterine sarcomas. |
True |
| 43 |
belong to the subgroup of mixed mesodermal tumours. |
False |
| 44 |
originate from leiomyomas. |
False |
| 45 |
most commonly metastasise to the bones. |
False |
| Discussion |
| Leiomyosarcomas belong to the uterine sarcomas group. Uterine fibroids are not generally thought to develop into malignant leiomyomas. Leiomyosarcomas commonly metastasise to the lungs. |
|
Regarding the diagnosis of uterine leiomyosarcoma,
| 46 |
a frozen section is not beneficial if a leiomyosarcoma is suspected intraoperatively. |
True |
| 47 |
the presence of coagulative necrosis is indicative of leiomyosarcoma. |
True |
| 48 |
the presence of coagulative tumour cell necrosis is a more accurate diagnostic criterion than mitotic count. |
True |
| Discussion |
| Intraoperative frozen sections performed for suspicious fibroids are often inaccurate.6 |
|
Concerning adjuvant therapy for uterine leiomyosarcomas,
| 49 |
adjuvant pelvic radiotherapy has a significant impact on survival. |
False |
| 50 |
anthracycline-based chemotherapy has a role in treatment. |
True |
| Discussion |
| Despite the possible benefit of adjuvant pelvic radiotherapy in reducing local recurrence rates, there has not been a proven significant impact on overall survival.7 |
|
With regard to surgical treatment of uterine leiomyosarcomas,
| 51 |
bilateral salpingo-oophorectomy is mandatory. |
False |
| 52 |
myomectomy is contraindicated. |
False |
| 53 |
the role of pelvic lymphadenectomy is unclear. |
True |
| 54 |
if the pelvic disease is controlled, resection of a single metastasis may be indicated. |
True |
| Discussion |
| It may be reasonable to consider ovarian conservation in young women with early-stage disease. A therapeutic dilemma in treating younger women is the discovery of a leiomyosarcoma during histological examination of a myomectomy specimen. Total hysterectomy has been established as the safest surgical procedure for these cases. A conservative approach following myomectomy should only be taken for specific and accurately selected women who strongly desire pregnancy and who are well counselled about the risks involved. |
|
With regard to treatment for uterine leiomyosarcomas,
| 55 |
palliative radiotherapy is preferred for advanced unresectable disease. |
False |
| 56 |
aggressive surgical cytoreduction at initial operation offers the best long-term prognosis. |
True |
|
In women with recurrent uterine leiomyosarcomas,
| 57 |
more than half have been shown to respond to gemcitabine combined with docetaxel. |
True |
|
Concerning the prognosis of uterine leiomyosarcomas,
| 58 |
the most important factor is tumour size. |
False |
| 59 |
staging is similar to that of endometrial carcinoma. |
True |
| 60 |
there is a direct relationship between high levels of Ki67 and rapid tumour growth. |
True |
| Discussion |
| Overall, tumour stage has been confirmed as the strongest prognostic variable. |
|
Obstetric management of women with female genital mutilation
The following statements about female genital mutilation are true:
| 61 |
The World Health Organization is working towards its recognition as a violation of human rights. |
False |
| 62 |
Under the Female Genital Mutilation Act 2003, it is illegal to perform the procedure in the UK, but a health worker can perform it abroad. |
False |
| Discussion |
| The World Health Organization has outlawed female genital mutilation.4 Under the Female Genital Mutilation Act 2003 it is an offence for any person to carry out the procedure abroad. |
|
In the UK,
| 63 |
the incidence of female genital mutilation has fallen since the introduction of the Female Circumcision Act 1985. |
True |
| 64 |
around 7 000 women are still at risk of having genital mutilation. |
True |
|
Regarding female genital mutilation,
| 65 |
girls are being mutilated at increasingly younger ages. |
True |
| Discussion |
| As the campaign against female genital mutilation in the West increases, parents are bringing down the age of mutilation and are increasingly taking girls abroad for the procedure. |
|
With regards to the practice of female genital mutilation in African countries,
| 66 |
it is performed in 28 to 30 countries in Sub-Saharan Africa. |
True |
| 67 |
approximately 500 procedures are carried out per day. |
False |
| Discussion |
| Six thousand girls a day are at risk of having the procedure. |
|
The following are acute complications of female genital mutilation:
| 68 |
Retention of urine resulting from pelvic haematoma. |
False |
| 69 |
Haematocolpos from retention of menstrual blood. |
False |
| 70 |
Faecal incontinence. |
True |
| Discussion |
| Retention of urine from pain and direct mechanical obstruction is an acute complication; haematocolpos from retention of menstrual blood is a long-term complication. |
|
Regarding obstetric complications from the procedure,
| 71 |
there is a significant increase in the rate of infant morbidity from fetal hypoxia. |
True |
| 72 |
there is an increased incidence of postpartum haemorrhage. |
True |
|
In women with type III female genital mutilation, the defibulation procedure
| 73 |
should be left until the second stage of labour if it is not performed at 20 weeks of gestation. |
False |
| 74 |
should preferably be performed under general anaesthesia to avoid evoking painful memories of the past. |
False |
| Discussion |
| Defibulation should be offered and performed early in pregnancy, before 20 weeks of gestation, according to the RCOG guidelines.31 The procedure can be performed under local or spinal anaesthesia. |
|
In women with type III mutilation,
| 75 |
the labia minora are absent. |
True |
| 76 |
difficulty in bladder catheterisation during labour can lead to a prolonged second stage. |
False |
| Discussion |
| A full bladder can prolong the first stage because of difficulties in catheterising the bladder. |
|
Recent research shows that, where indicated, many pregnant women with genital mutilation
| 77 |
prefer to undergo defibulation between 34 and 38 weeks of gestation. |
False |
| Discussion |
| A recent study shows that a significant number of women prefer to wait until the onset of labour.26 |
|
Healthcare professionals caring for women with genital mutilation during pregnancy,
| 78 |
should ensure that women have a pelvic examination at the first antenatal visit. |
False |
| Discussion |
| Digital assessment is not always needed as physical appearance may provide the reassurance that is needed. |
|
Regarding female genital mutilation,
| 79 |
defibulation may be necessary if urinary tract infections keep recurring. |
True |
|
One way in which obstetric services could be improved,
| 80 |
would be to ensure that midwives are trained in performing an anterior episiotomy. |
True |
|
Modern management of miscarriage
In women with threatened miscarriage,
| 81 |
the therapeutic role of progesterone in prevention and treatment has not been established. |
True |
| 82 |
the use of uterine muscle relaxant drugs improves outcome. |
False |
| Discussion |
| There is insufficient evidence to support the use of uterine muscle relaxant drugs13 in women with threatened miscarriage. |
|
Regarding non-viable pregnancy,
| 83 |
approximately 30% of women will choose expectant management if given the choice. |
False |
| 84 |
use of biochemical markers is not a practical consideration when considering the best treatment option. |
True |
| 85 |
the incidence of diarrhoea is significantly higher with the use of vaginal misoprostol when compared with oral misoprostol. |
False |
| 86 |
nulliparity is a factor that predicts success with misoprostol. |
True |
| Discussion |
| Up to 70% of women will choose expectant management if given the choice.16 While biochemical markers can predict the likelihood of successful expectant management, they would increase costs. Vaginal misoprostol is as effective as oral misoprostol, with a significant reduction in the incidence of diarrhoea.23 |
|
Regarding treatment of miscarriage,
| 87 |
the risk of infection is higher with medical treatment than with surgical treatment. |
False |
| 88 |
about 50% of women would opt for the same management in the future. |
True |
| 89 |
expectant management appears to be the least costly alternative. |
True |
| 90 |
filmy intrauterine adhesions may develop following surgical evacuation but not after conservative or medical management. |
True |
| 91 |
anti-D should be given to all women with a confirmed miscarriage <12 weeks of gestation. |
False |
| 92 |
women who choose their own treatment have been shown to have the best health-related quality of life over time. |
True |
| Discussion |
| The MIST trial36 showed that the risk of infection is low (2–3%), regardless of treatment modality. Regarding anti-D prophylaxis for Rh-negative women, see Figure 1 in the article. |
|
Regarding early pregnancy assessment units,
| 93 |
one of the benefits is a reduction in inpatient admission by an average of 1 day for women requiring no treatment. |
False |
| Discussion |
| Admission time is reduced from 1.5 days (range 0.5–3.0) to 2 hours for women requiring no treatment.2 |
|
Regarding viable intrauterine pregnancy,
| 94 |
miscarriage is likely to occur in about 1 in 10 pregnancies where a fetal heartbeat is present. |
True |
|
Regarding treatment of miscarriage,
| 95 |
the duration of expectant management can be up to approximately 2 months. |
True |
| 96 |
the low levels of progesterone present in non-viable pregnancy means that prostaglandins can be administered on their own. |
True |
| 97 |
research has shown that treatment with vaginal misoprostol can lead to heavy bleeding for about 2 weeks afterwards. |
False |
| 98 |
a benefit of using vacuum aspiration is that there is no need for analgesia. |
False |
| 99 |
metronidazole may be given as part of a prophylactic antibiotic regime in women with Chlamydia trachomatis before undergoing surgical evacuation. |
True |
| 100 |
there are no differences between treatments with regard to long-term conception rates and pregnancy outcomes. |
True |
| Discussion |
| Following treatment with vaginal misoprostol, mild–moderate bleeding lasts 4–6 days. Analgesia and sedation should be provided as needed for vacuum aspiration. |
|