OBS & GYN Flashcards

(284 cards)

1
Q

What is normal menstrual bleeding?

A

Normal Menstrual Bleeding:
• Avg 30mL lost with each menstrual period
• Upper limit is 80mL

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2
Q

Definition of abnormal uterine bleeding

A
  • Blood loss of more than 80mL (subjective by the patient)
  • Cycle length of < 24 days or > 35 days
  • Intermenstrual or postcoital bleeding
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3
Q

Definition of dysfunctional uterine bleeding

A

Excessive bleeding which is not due to pregnancy, pelvic pathology or systemic disease that can be cyclical (ovulatory) or non-cyclical (anovulatory). Anovulatory bleeding commonly occurs at the beginning and end of reproductive life
(adolescence and premenapause).

Diagnosis of exclusion

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4
Q

Definition of menorrhagia

A
  • Excessive or prolonged menstrual bleeding occurring at regular intervals
  • Note: both patient and doctor are unreliable at predicting amount of blood lost
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5
Q

Definition of inter-menstrual bleeding

A

Bleeding that occurs between regular menstrual cycles

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6
Q

Definition of post-coital bleeding

A

Bleeding up to 24 hours after intercourse

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7
Q

Definition of pre-menstrual spotting

A

Bleeding during the week prior to a period

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8
Q

Definition of Metrorrhagia

A

Bleeding of normal or less than normal volumes at irregular intervals

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9
Q

Definition of Menometrorrhagia

A

Prolonged or excessive bleeding at irregular intervals

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10
Q

Definition of Polymenorrhoea

A

Regular bleeding that occurs at intervals < 24 days

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11
Q

Aetiology of abnormal uterine bleeding

A
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12
Q

What History and Examination for abnormal uterine bleeding

A
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13
Q

Investigations for abnormal uterine bleeding

A
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14
Q

Investigation considerations according to patient group

A

Common to consider:
- BHCG
- Bloods: iron, FBC, folate, B12, coags ,TFTs, LFTs
- Imaging: Pelvic, abdominal or transvaginal US
- STI swab
- Pap smear
- Colposcopy
- Hysteroscopy
- biopsy

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15
Q

Management of abnormal uterine bleeding

A
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16
Q

Uterine blood flow

A
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17
Q

Causes of abnormal uterine bleeding

A
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18
Q

DDx of abnormal uterine bleeding

A
  • Ectopic pregnancy
  • Miscarriage
  • Placental abruption, placenta previa
  • Breakthrough bleeding
  • Benign structural abnormalities (adenomyosis, fibroids, polyps)
  • Gynaecological malignancies
  • Chlamydia
  • Hormonal changes – menopause/perimenopause
  • Prolapse
  • Trauma
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19
Q

Investigation for abnormal uterine bleeding (part 2)

A
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20
Q

Treatment for abnormal uterine bleeding

A
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21
Q

Definition of uterine fibroids (leiomyoma)

A

Benign tumours of the uterus composed of smooth muscle and fibrous connective tissue

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22
Q

Epidemiology of uterine fibroids

A

Epidemiology:
• Incidence increases with age
• Affects 20-50% of women > 30 years
• Prevalence may be as high as 80%

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23
Q

Aetiology and anatomical classification of uterine fibroids

A
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24
Q

Clinical features of uterine fibroids

A
  • Asymptomatic – most common
  • Menorrhagia (caused by submucosal fibroids)
  • Dysmenorrhoea (painful periods)
  • Pelvic pain/pressure
  • Bloating
  • Enlarged uterus – firm, asymmetric, non-tender
  • Usually slow growing but can be accelerated growth in pregnancy due to high oestrogen
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25
**Investigations for uterine fibroids**
* Pelvic U/S * Endometrial biopsy (via hysteroscopy) * DDx – clinically similar to adenomyosis and uterine polyps (require biopsy)
26
**Treatment for uterine fibroids**
27
**Complications and prognosis of Uterine fibroids**
28
Anatomy of uterus
29
**Definition and epidemiology of Antepartum Haemorrhage**
**Definition:** • Uterine bleeding that occurs after 20 weeks gestation that is unrelated to labour and delivery **Epidemiology:** • 6% of all pregnancies experience PV (per vagina) bleeding in the 3rd trimester
30
**Aetiology of antepartum haemorrhage**
31
**General management of antepartum haemorrhage**
32
**Definition and epidemiology of abruptio placenta (placenta abruption)**
**Definition:** • Premature separation of a normal implanted placenta from the decidual lining of the uterus after 20 weeks gestation **Epidemiology:** • Occurs in 1 in 200 pregnancies • Black women \> white women
33
**Aetiology and risk factors for placenta abruption**
Aetiology: • Exact cause is unknown
34
**Types of placenta abruption**
Types: • Apparent: Bleeding apparent • Concealed: Bleeding is not-apparent • Mixed: Bleeding with concealment
35
**Pathophysiology of placenta abruption**
**Pathophysiology:** * **Rupture of maternal vessels** in the decidua basalis at the interface of the anchoring villi * **Accumulating blood splits the decidua**, separating a thin layer of decidua with its placental attachment from the uterus * **The bleeding may be small and self-limited** or it can continue to separate the decidua leading to complete or near complete placental separation * The **detached portion is no longer able to exchange gases** and nutrients * **May lead to foetal compromise** if the remaining foeto-placental unit is unable to compensate for this loss of function
36
**Clinical features of antepartum haemorrhage**
37
**DDx for anterpartum haemorrhage**
DDx: * Preterm labour - can co-exist/caused by placental abruption * Placenta praevia * Chorioamnionitis - bleeding is uncommon
38
**Diagnosis and complications of antepartum haemorrhage**
**Diagnosis:** • Diagnosis of exclusion, based on clinical Hx and U/S **Complications:** • Hypovolaemic shock (medium) • DIC • Intra-uterine growth restriction • Preterm birth • Perinatal death
39
**Management of antepartum haemorrhage**
40
**Definition of Placenta Praevia**
Definition: * The presence of placental tissue that extends over or lies proximate to the internal cervical os * Should be suspected in any woman \> 20 weeks gestation that presents with painless vaginal bleeding
41
**Epidemiology and risk factors of placenta praevia**
**Epidemiology:** * Uncommon in 1st pregnancies (0.2% in nulliparous) * 0.5% in multiparous and a 4-8% recurrence **Risk Factors:** * Previous placenta praevia - 0.7% risk * Infertility treatments (IVF) - 2% risk • Endometrial scarring, (previous LSCS) - 0.6% * Impeded endometrial vascularisation e.g. HTN, diabetes, uterine tumour, drugs (cocaine) smoking and Advanced maternal age * Increased placental mass: ⁃ Multiparity
42
**Aetiology and classification of placenta praevia**
43
**Clinical features of Placenta Praevia**
44
**DDx for placenta praevia**
DDx: * Normal labour * Placental abruption * Placenta accreta * Miscarriage (more common in early pregnancy)
45
**Investigations for placenta praevia**
**Investigations:** * Transabdominal U/S - Assess placental position * Transvaginal U/S - Preferred * FBC - Assess Hb level in acute bleeds * Type and crossmatch
46
**Management of Placenta Praevia**
47
**Complications of placenta praevia**
Complications: * Anaemia (short-term high) - due to bleeding * Complications of C-section * Preterm birth * Abnormally adherent placenta
48
**Prognosis of placenta praevia**
49
**Definition of Placenta Accreta**
50
**Epidemiology and risk factors of Placenta Accreta**
**Epidemiology** * 5-10% risk in the presence of placenta praevia * 10-20% risk with previous LSCS **Risk Factors:** * Placenta praevia * Previous C-section or uterine surgery * Maternal age \> 35 years * Multiparity - increases after each childbirth * Uterine pathology like fibroids
51
**Aetiology and pathophysiology of placenta accreta**
**Aetiology:** * Unknown * Abnormality to the uterine lining **Pathophysiology:** * Defective decidualisation (thin, poorly formed or absent decidua) related to previous surgeries or anatomical pathologies or extra-villous trophoblastic invasion * Allows for the placenta to attach directly to the myometrium
52
**Clinical features, Investigations and Management of Placenta Accreta**
53
**For Vasa Previa what is the:** * **Definition** * **Epidemiology** * **Aetiology and pathophysiology** * **Clinical features** * **Diagnosis**
54
Assisted reprodutive tech cards to be filled - Gobi's incomplete - might have to check in Jims
55
**Common cancer of the vulva, epidemiology and symptoms**
The female external genitalia is called the vulva. Made up of 3 main parts: labia majora, labia minora and clitoris * Cancer of the vulva makes up around 4% of female genital tract cancers and is quite rare * Most are SCCs * Most commonly diagnosed in post-menopausal women, ~ 70 years * Symptoms include ulcerative sores that do not heal, itching, unusual vaginal bleeding and/or discharge
56
**Aetiology of cancer of the vulva**
57
**Sites of vulval cancer**
58
**Symptoms of vulval cancer**
59
**Risk factors of vulval cancer**
60
**Types of vulval cancer**
61
**Diagnosis and staging of vulval cancer**
62
**Treatment of vulval cancer**
63
**Definition of cervical cancer**
* Cervical cancer is a HPV-related malignancy of the uterine cervical mucosa * HPV is transmitted via sexual intercourse
64
**Epidemiology of cervical cancer**
**Epidemiology:** * Cervical cancer is the 2nd most common malignancy in women worldwide * Peak infection incidence is between 15-25 years, with the majority resolving in 12-18 months * Prevalence of HPV at age 35 is 5% * Effective screening programs have reduced mortality by 75% in the last 50 years * 60% of diagnoses occur in women who have never had screening or have not been screened in the last 5 years * Pap smears are a very successful cancer screening tool
65
**Aetiology and risk factors of cervical cancer**
66
**Pathophysiology of cervical cancer**
67
**Clinical features and staging of cervical cancer**
68
**Investigations for cervical cancer**
69
**Pap smear results in cervical cancer screening**
70
**Classification and staging of cervical cancer**
71
**Management of cervical cancer**
72
**Screening for cervical cancer**
- 25-74 years - Every 5 years - Test looks for HPV
73
**Prognosis for cervical cancer**
74
**Histology of the transformation zone and types of smears**
75
**Histology of cervical cancer**
76
Contraception cards - gobi's incomplete - please insert
77
**Epidemiology and factors enhancing risk of diabetes in pregnancy**
78
**Complications and maternal insulin requirements in T1DM and pregnancy**
79
**Management of T1DM in pregnancy and delivery**
80
**Considerations and management of T2DM in pregnancy**
81
**Definition and epidemiology of Gestational Diabetes Mellitus (GDM)**
**Definition:** * Any degree of glucose intolerance with onset or first recognition in pregnancy * Includes women that develop T1DM/T2DM during the pregnancy, hence need for retrospective classification **Epidemiology:** * Accounts for 70% of diabetes in pregnancy * Higher in asian and black populations * Rates of GDM are on the rise
82
**Aetiology of GDM**
83
**Pathophysiology of GDM**
84
**Clinical features of GDM**
85
**Investigations for GDM**
86
**Screening for GDM**
87
**Management for GDM**
88
**Complications of GDM**
89
**Prognosis for GDM**
90
**Role of prostaglandins in labour**
91
**Role of oxytocin in labour**
92
**Role of B2 agonists in labour**
93
**Role of tocolytics in labour**
94
**Induction of labour and myometrial contraction**
95
**Inhibition of labour and myometrial relaxation**
96
**Definition of ectopic pregnancy**
**Definition:** * A pregnancy resulting from the fertilised ovum implanting in a site other than the normal uterine cavity * Obstetric Emergency: If undiagnosed it can lead to maternal death due to rupture of the implantation site and intraperitoneal haemorrhage **Epidemiology:** * Incidence rate of 1-2% and rising * Recurrence rate is 15% after 1st and 25% after the 2nd * Accounts for 80% of 1st trimester maternal deaths. Mortality rates are declining
97
**Aetiology and risk factors of ectopic pregnancy**
98
**Classification of ectopic pregnancy**
99
**Pathophysiology of ectopic pregnancy**
100
**Clinical features of ectopic pregnancy**
101
**Investigations for ectopic pregnancy**
102
**Diagnosis of ectopic pregnancy**
**Diagnosis:** * Elevated β-hCG with no intrauterine gestation sac (\> 5 weeks is visible on TVS) * Detection of free-fluid in the peritoneal cavity * Laparoscopy rarely required for diagnostic purposes
103
**Differential diagnosis for ectopic pregnancy**
**DDx:** * Miscarriage * Acute appendicitis * Ovarian torsion * Ruptured corpus luteal cyst or follicle * Normal 1st trimester bleeding (20% of women have normal pregnancies) * UTI/PID
104
**Management of ectopic pregnancy**
105
**Complications and management of ectopic pregnancy**
106
**Normal B-Hcg and diagnosis of interuterine/normal pregnancy**
107
**Definition and epidemiology of endometrial cancer**
**Definition:** • Epithelial malignancy of the uterine corpus mucosa - usually adenocarcinoma **Epidemiology:** * Most common gynaecological malignancy in the developed world * 7th most common cancer in women overall * Incidence in western countries is 10x more than in developing
108
**Aetiology of endometrial cancer**
109
**Risk factors for endometrial cancer**
**Risk Factors:** * Obesity * Age \> 50 years * Endometrial hyperplasia * Unopposed exogenous/endogenous oestrogen exposure * FHx of endometrial cancer * FHx of breast or ovarian cancer * HNPCC * Tamoxifen use (oestrogen receptors antagonist) for Rx of breast Ca (7x) * DM * HTN
110
**Classification of endometrial cancer**
**Classification:** * Adenocarcinoma (90%) * SCC * Transitional cell carcinoma * Small cell * Undifferentiated
111
**Clinical features of endometrial cancer**
112
**Investigations for endometrial cancer**
113
**Differential diagnosis for endometrial cancer**
**DDx:** * Endometrial hyperplasia - commonly presents with abnormal uterine bleeding, irregular or heavy periods * Endometrial polyp - usually asymptomatic, but if symptomatic presents similarly * Endometriosis - More common in younger pre-menopausal women * Cervical cancer - Typically younger women; PV bleeding usually provoked (post-coital)
114
**Spread and management of endometrial cancer**
115
**Complications and prognosis of endometrial cancer**
116
**Definition and epidemiology of endometriosis**
**Definition:** • Ectopic endometrial glands and stroma growing outside the endometrial cavity and uterine musculature **Epidemiology:** * 3-10% of women aged 20-50 (women of reproductive age usually) * Average age at diagnosis is 25-28 years * Account for 25-35% of infertility * Severity of symptoms increases with age and peaks at 40yrs • Prevalence higher in white women and women with Lower BMIs • Adolescent endometriosis exists
117
**Aetiology + risk factors for endometriosis**
**Aetiology:** • Several theories exist + Genetic predisposition **Risk Factors:** * Reproductive Age * Family Hx * Nulliparity * Mullerian anomolies * Others: White, Low BMI, Autoimmune disease, Smoking
118
**Pathogenesis of endometriosis**
**1. Retrograde menstruation theory:** ⁃ Retrograde menstruation seeds in the abdominal cavity ⁃ Occurs in 70-90% of women **2. Coelomic metaplasia:** ⁃ Peritoneal mesothelium undergoes metaplastic transformation into endometrial tissue **3. Induction theory:** ⁃ Unknown biochemical substance induce undifferentiated peritoneal cells to form endometrial tissue **4. Immunological theory:** ⁃ Alterations in cell-mediated immunity leads to abnormal clearance of endometrial cells
119
**Pathophysiology of endometriosis**
1. Endometriosis and sub-fertility: Altered anatomy with tube/ovarian involvement and scarring and PG overproduction can also interfere with fertilisation 2. Dysmenorrhoea occurs due to reactive hormonal-tissue in the abdomen 3. Chronic pain may be due to fibrosis that occurs with chronic inflammation
120
**Types of lesions in endometriosis**
Three types of lesions in endometriosis: * superficial peritoneal endometriosis – powder burn lesions on ovaries, serosa and peritoneum, may also appear as white plaques, scarring, red implants, serous vesicles * ovarian cysts (endometrioma) – ‘chocolate cysts’ forming from menstrual bleeding in the ovaries * deep infiltrative endometriosis – nodules extending more than 5mm beneath the peritoneum involving the uterosacral ligaments, vagina, bowel, bladder, or ureters
121
**Signs and symptoms of endometriosis**
122
**Staging of endometriosis**
123
**Clinical presentation of endometriosis**
124
**Differential diagnosis of endometriosis**
* Adenomyosis – hyperplasia leading to growth of endometrial tissue within the myometrium, symptoms may be identical, and endometriosis is often concurrent * Pelvic inflammatory disease * Malignancy – ovarian, uterine, endometrial * Ovarian cyst * Irritable bowel syndrome
125
**Investigations and diagnosis of endometriosis**
**Investigations:** * TVS - may show ovarian endometrioma or deep pelvic endometriosis * Diagnostic laparoscopy **Diagnosis:** * Laparoscopy - _Gold Standard_. Finding of extra-uterine endometrial tissue on visualization and biopsy (histopathology) * Examination - Pouch of Douglas Pain with nodularity of the uterosacral ligament. Fixed in retroversion * TVS: Especially for endometrioma
126
**Management of endometriosis**
127
**Complications and prognosis of endometriosis**
128
**Definition of foetal malpresentation**
**Definitions:** * In normal pregnancies the foetus assumes a normal longitudinal (vertical) lie with a cephalic presentation and the head well flexed * 5% of all term pregnancies have a deviation from this lie
129
**Causative factors for foetal malpresentation**
130
**Types of foetal malpresentations**
Types of Malpresentations: 1. Unstable lie 2. Face presentation 3. Brow presentation 4. Compound presenation 5. Breech presentation
131
**Unstable or abnormal lie of foetal malpresentations**
132
Face presentation of foetal malpresentation
133
**Brow position of foetal malpresentation**
134
**Compound presentation of foetal malpresentation**
135
**Breech presentation of foetal malpresentation**
136
**Definition of gestational trophoblastic disease**
137
**Epidemiology and aetiology of gestational trophoblastic disease**
138
**Pathophysiology of gestational trophoblastic disease**
139
**Classification of gestational trophoblastic disease**
140
**Clinical features of gestational trophoblastic disease**
141
**Differential diagnosis of larger than stated uterus**
DDx of larger than stated uterus: * Wrong dates for LMP * Multiple gestation (twins) * Other intrauterine pathology (e.g. fibroids) * GTD
142
**Investigations for gestational trophoblastic disease**
143
**Differential diagnosis for gestational trophoblastic disease**
DDx: * Spontaneous abortion - can be differentiated on U/S * Multiple gestation - larger than normal uterus and elevated hCG * Pelvic tumour - may present with enlarged uterus, painless bleeding and adnexal mass
144
**Management of gestational trophoblastic disease**
145
**Complications and prognosis of gestational trophoblastic disease**
146
**Gynae Hx Taking**
147
**Abdomen and vaginal exam**
Antenal exam" - BP - void bladder and urine analysis - general inspection - Check for ankle oedema - fundal height - Foetal lie - Foetal doppler
148
**Vaginal examination**
149
**Definition of pre-eclampsia**
150
**Epidemiology, aetiology and risk factors for pre-eclampsia**
151
**Pathophysiology and types of pre-eclampsia**
152
**Clinical features of pre-eclampsia**
153
**Investigations for pre-eclampsia**
154
**Management of pre-eclampsia**
155
**Complications and prognosis of pre-eclampsia**
156
**Definition of eclampsia**
Definition: • Onset of convulsions during pregnancy or postpartum unrelated to other cerebral pathologies in women with pre-eclampsia
157
**Epidemiology of eclampsia**
158
**Clinical features of eclampsia**
159
**Management of eclampsia**
160
**Definition of induction of labour**
Definition: * The planned initiation of labour prior to its spontaneous onset. * It is an intervention designed to artificially initiate uterine contractions, resulting in progressive effacement and dilation of the cervix leading to birth of the baby * It is performed when the benefits of delivery outweigh the risks of continuing the pregnancy * Should be performed if the risk of the process to the mother and/or foetus is acceptable, otherwise proceed to a C-section * Occurs in 1 in 5 deliveries
161
**Aims for induction of labour**
**Aims:** * To stimulate regular uterine contractions * To generate progressive cervical dilation * To facilitate a subsequent vaginal delivery
162
**Indication for Induction of Labour**
**Indication for IOL: “When the benefits of delivery outweigh the potential risks of continuing pregnancy”** * Prolonged pregnancy (post-date pregnancy) \*\* most common cause * Foetal growth restriction * Pre-eclampsia or other maternal HTN disorders * Prelabour rupture of membranes * Chorioamnionitis - inflammation of the foetal membranes * Unexplained antepartum haemorrhage * Maternal medical problems - diabetes or renal disease * Logistics - distance from hospital
163
**Contraindications for induction of labour**
Contraindications: * Placenta previa or Vasa previa (placental cord running close to the os) * Transverse foetal lie * Previous classical uterine incision * Active genital herpes infection * Pelvic structural abnormalities
164
**Pre-induction of labour scoring system**
165
**Steps/Process involved in induction of labour**
166
**Complications and special cases in IOL**
167
Questions
168
**Definition of infertility**
169
Epidemiology and risk factors for infertility
**Epidemiology:** • Affects 1 in 12 couples **Risk Factors:** * Age \> 35 years * Hx of STIs * Very high BMI * Very low BMI * Cigarette smoking ⁃ Related to accelerated menopause and decreased cilia function in uterine tubes
170
**Aetiology of infertility**
171
**Pathophysiology of infertility**
172
**Fecundity to consider in infertility**
173
**History taking in infertility**
174
**Examination for infertility**
**Females:** ⁃ General Exam ⁃ Pelvic Exam ⁃ Cervical Smear ⁃ Swabs as appropriate **Male:** ⁃ General Exam ⁃ Testes, vas, varicocele ⁃ Prostate
175
**Investigations for infertility**
176
**Management of infertility**
177
**Prognosis for infertility**
178
**Notes on IVF**
179
**Infertility advice for couples**
180
**Definition of labour**
181
**Foetal and maternal anatomy in labour**
182
**The process of labour**
183
**Mechanism of labour**
184
Factors affecting the outcome of labour
185
Factors affecting the duration of labour
186
**Management of labour**
187
Investigations prior to hospital booking for antenatal care
188
**Schedule of routine visits for normal antenatal care**
**Schedule of Routine Visits:** * 11-12 weeks - booking Hx by hospital staff * 12-14 weeks - appointment with specialist & allocated a model of AN care * 16-24 weeks - 4 weekly appointments * 28-36 weeks - 2 weekly appointments * 36+ weeks - weekly appointments
189
**Checks on each visit for normal antenatal care**
190
**Dietary advice for normal antenatal care**
191
**Additional investigations in normal antenatal care**
192
**Post delivery date women in antenatal care**
193
Ovarian cancer epidemiology and introduction
* Ovarian cancer is the 2nd most common gynaecological malignancy and the major cause of death from gynaecological cancers * Mean age of presentation is 63 years * Patients with early-stage ovarian cancer are asymptomatic or have vague/non-specific symptoms * In late disease, patients present with abdominal pain or swelling * Survival rates for ovarian cancer remains poor due to late presentation of the disease
194
**Aetiology and risk factors for ovarian cancer**
195
Symptoms of Ovarian cancer
196
**Metastatic spread of ovarian cancer**
Metastatic Spread: * Direct: Spread to surrounding structures * Lymphatic: Spread to the pelvic and para-aortic nodes is common * Haematoganous: Distant mets are uncommon
197
**Types of ovarian cancer**
198
**Staging of ovarian cancer**
**Staging:** * _Stage 1_: Growth limited to the ovaries - * _Stage 2:_ Growth involving one or both ovaries with pelvic extension * _Stage 3_: Growth involving one or both ovaries with peritoneal implants outside the pelvis or positive retroperitoneal or inguinal nodes * _Stage 4_: Growth with distant metastases
199
**Investigations for ovarian cancer**
200
**Blood tests and markers for ovarian cancer**
201
**Management of ovarian cancer**
202
**Definition of pelvic mass**
**Definition:** * A mass arising from a pelvic organ * May originate from female reproductive organs (ovaries, uterus) or other pelvic organs (bladder, rectum, blood vessels)
203
**Clinical features of pelvic mass**
204
**Definition of pelvic organ prolapse**
205
**Epidemiology, risk factors and aetiology of pelvic organ prolapse**
206
**Pelvic anatomy and support in pelvic organ prolapse**
3 levels of pelvic support: - Level I has long mesenteric attachments (cardinal and uterosacral ligaments), - Level II has more direct connections to the pelvic walls (e.g. paravaginal attachments), - Level III has a direct fusion of the vagina with the levator ani muscles, perineal membrane and body
207
**Cystocele types, grading and treatment in pelvic organ prolapse**
208
**Rectocele and Enterocele description and treatment in pelvic organ prolapse**
209
**Uterine and vaginal wall description and treatment in pelvic organ prolapse**
210
**Staging and clinical features of pelvic organ prolapse**
211
**Investigations and complications of pelvic organ prolapse**
212
**Perineal tears description**
213
**Risk factors for 3rd and 4th degree perineal tears**
**Risk Factors for 3rd and 4th Degree Tears:** * Birth weight \> 4kg * Persistant occipitoposterior position * Nulliparity * Induction of labour * Epidural anaesthesia * 2nd stage labour \> 1 hour * Shoulder dystocia * Midline episiotomy * Forceps delivery
214
**Anatomy of perineum and classification of perineal tears**
215
Description of an episiotomy in perineal tears
216
**Perineal repair and prognosis**
217
**Definition of Polycystic Ovarian Syndrome**
According to the Rotterdam consensus,1 polycystic ovarian syndrome (PCOS) is defined by the presence of two of three of the following criteria: - oligo‐anovulation, - hyperandrogenism and polycystic ovaries (≥ 12 follicles measuring 2‐9 mm in diameter and/or an ovarian volume > 10 mL in at least one ovary). **Definition:** • Complex endocrine disorder characterised by hyper-androgenism, symptoms of hyper-androgenism, oligo/ anovulation, and polycycstic ovarian morphology on U/S
218
**Epidemiology, risk factors and aetiology of polycystic ovarian syndrome**
219
**Pathophysiology of polycystic ovarian syndrome**
220
**Clinical features of polycystic ovarian syndrome**
221
**Investigations for polycystic ovarian syndrome**
222
**Differential diagnosis for polycystic ovarian syndrome**
**DDx:** * 21-hydroxylase deficiency - Leads to accumulation of androgen precursors * Thyroid dysfunction - May lead to irregular menstruation but hyper-androgenism is absent * Hyperprolactinaemia - May lead to infrequent or absent menses. Galactorrhoea is usually present * Cushingʼs syndrome - Cortisol excess leading to obesity, HTN, hirsutism, acne and menstrual irregularities * Androgen secreting neoplasms - Of the adrenal gland or ovaries
223
**Diagnosis of polycystic ovarian syndrome**
Diagnosis: * Clinical features, elevated androgens and polycystic ovarian morphology on U/S * NOTE: Up to 25% of women have polycystic ovarian morphology, but do not have PCOS without symptoms
224
**Management of polycystic ovarian syndrome**
225
Complications and prognosis of polycystic ovarian syndrome
226
**Definition of post partum haemorrhage**
227
**Epidemiology of post partum haemorrhage**
228
**Aetiology of post partum haemorrhage**
229
**Antepartum risk factors for post partum haemorrhage**
230
**Intrapartum and post partum risk factors for post partum haemorrhage**
231
**Management of post partum haemorrhage**
232
**Reasons for foetal HR monitoring**
233
**CTG interpretations in foetal HR monitoring**
234
**Deceleration in detail on CTG for foetal HR monitoring**
235
**Management of Foetal HR in context of CTG readings**
236
**Interpret CTG**
237
**Interpret CTG**
238
**Interpret CTG**
239
**Interpret CTG**
240
**Interpret CTG**
241
**Interpret CTG**
242
**Interpret CTG**
243
**Interpret CTG**
244
**Interpret CTG**
245
**Definition of pre-term labour**
Definition: * Pre-term Labour = Labour that occurs between 20 weeks and 36 + 6 weeks * Term Labour = Labour that occurs between 37 weeks and 41 + 6 weeks
246
**Epidemiology of pre-term labour**
Epidemiology: * Leading cause of perinatal morbidity/mortality in developed countries * Morbidity/mortality inversely proportional to gestational age * Morbidity/mortality is uncommon \> 32 weeks getation * Incidence of 5-25% * 12.7% in Australia with \< 2% below 32 weeks * Increasing incidence (IVF, multiple pregnancies, elective)
247
**Aetiology of pre-term labour**
**Multifactorial:** ⁃ 50% - Spontaneous ⁃ 30% - PPROM (Pre-term prelabour rupture of membranes) = Rupture of membranes \< 37 weeks ⁃ 20% - Iatrogenic ⁃ \< 1% - Cervical incompetence
248
**Pathophysiology and classification of pre-term labour**
- inflammation (infection or autoimmune) - uterine stretch + cervical incompetence - antepartum hemorrhage - premature desidual activation - social stress - Genetics
249
**Risk factors of pre-term labour**
250
**Clinical features of pre-term labour**
251
**Management of pre-term labour**
252
**Definition of rhesus haemolytic disease**
253
**Causes of foetal anaemia**
**Causes of Foetal Anaemia:** * Rhesus disease * Transplacental viral infection (Parvovirus B16) * Placental foetal vessel rupture * Twin-twin transfusion
254
**Epidemiology of Rhesus Haemolytic Disease**
255
**Aetiology of foetal haemolytic disease**
256
**Pathophysiology of foetal haemolytic disease**
257
**Signs of foetal aneamia**
**Signs of Foetal Anaemia:** * Polyhydramnios * Enlarged foetal heart * Ascites and pericardial effusion * Hyperdynamic foetal circulation (detected on MCA flow doppler) * Reduced foetal movements * Abnormal CTG with reduced variability, eventually leading to a _sinusoidal trace_
258
**Investigations for foetal haemolytic disease**
259
**Management of Foetal Haemolytic Disease**
260
**Complications and prognosis of foetal haemolytic disease**
261
**Red cell Antigens**
262
**Definition of twin gestation**
**Definition:** * Multiple Gestation: Consists of two or more foetuses (twins make up 99% of this) * Monozygotic Twins: Arising from a single fertilised egg that divides * Dizygotic Twins: Arising from two separately fertilised eggs
263
**Epidemiology of twin gestation**
**Epidemiology:** * 1-2% of pregnancies have more than one foetus * The chance of miscarriage, foetal abnormalities, poor growth, preterm delivery and intrauterine or neonatal death are considerably higher in twin than singleton pregnancies * 2/3rds of twins are dizygotic (non-identical) & 1/3rd are monozygotic (identical) * Incidence is on the rise
264
**Risk factors of multiple gestations**
**Risk Factors for Multiple Gestations:** * Assisted reproduction techniques (ovulation induction and IVF) * ↑Maternal Age (35-39 years) * High parity * Black race * Maternal family Hx
265
**Aetiology of twin gestation**
266
**Classification of multiple gestations**
267
**Types of twin gestation**
268
Maternal physiological changes of twin gestation
269
**Complications of twin gestation**
270
**Medical management of twin gestation**
271
**Twin to twin transfusion syndrome:** * **Pathophysiology** * **Management** * **Complications** * **Prognosis**
272
**Twin Reversed Arterial Perfusion sequence:** * **Description** * **Management** * **Prognosis**
273
**Multifoetal reduction**
274
**Description/definition of vaginal cancer**
The vagina is a muscular canal ~7.5cm long that extends from the vulva to the cervix * Primary cancer of the vagina is one of the rarest gynaecological cancers (makes up around 2%) * Most commonly diagnosed in women \> 50 years who were exposed to the drug Diethylstilbestrol (DES) in the womb * Symptoms include abnormal vaginal bleeding, postcoital bleeding, vaginal discharge & pelvic pain * Most cases are detected in advanced stages and require radiation therapy or chemoradiation for treatment
275
**Aetiology of vaginal cancer**
276
**Symptoms of vaginal cancer**
**Symptoms of Vaginal Cancer:** * Early stages are asymptomatic * Painless vaginal bleeding not associated with menstruation * Postcoital bleeding * Smelly discharge * Pain on urinating or passing bowel motions (may indicate local spread) • Constant pelvic pain
277
**Metastatic spread of vaginal cancer**
278
**Risk factors for vaginal cancer**
**Risk Factors:** * Age - usually occurs in women \> 50 years * Previous Hx of gynaecological cancers * Previous treatment of dysplastic cells * HPV infection * Smoking * Prenatal exposure to DES * Vaginal adenosis (almost all DES daughters have vaginal adenosis)
279
**Types of vaginal cancers**
**Types of Vulval Cancers:** * Vaginal SCC - Accounts for 95% * Vaginal Adenocarcinoma - most are clear-cell carcinomas arising from DES daughters * Vaginal Melanoma - rare * Vaginal Sarcoma - arising from connective tissue or muscle cells of the vagina (rare)
280
**DES-related vaginal cancers**
**DES-related Vaginal Cancers:** * Diethylstilbestrol was used from 1938-1971 as a synthetic hormone that was mistakenly used to prevent miscarriage * DES exposure in utero alters the shape of the cervix and uterus and up to 30% have vaginal adenosis * There is a small risk (1 in 1000) of vaginal adenosis in DES-exposed women to develop into a clear-cell carcinoma of the vagina * Mean age of diagnosis is 19 years
281
**Investigations for vaginal cancer**
Investigations: * Colposcopy * Biopsy and staging * CXR, CT abdomen and pelvis or MRI/PET for mets
282
**Treatment for vaginal cancer**
283
**Other complications of vaginal cancer**
Other complications: • Rectovaginal or vesicovaginal fistula formation, which can be hard to treat palliatively
284
**Shoulder dystocia**