Recent Advances in Obstetrics & Gynaecology 25 William Ledger, Justin Clark
INDEX
Note: Page numbers in bold or italic refer to tables or figures, respectively.
A
Abnormal uterine bleeding (AUB) 20
Acupuncture, as adjuvant to ART 134135
Acute myocardial infarction (AMI) 6971, 70, 71
Adenomyosis 4
and chronic pelvic pain 2
laparoscopy in, role of 2, 4
Adhesions
and chronic pelvic pain 2
laparoscopy in, role of 2, 4
Adjuvants, use of, in ART 131135
acupuncture and herbal medicine 134135
androgens and androgen modulating agents 132
corticosteroids 133134
endometrial biopsy 133
growth hormone 131132
intralipid 134
intravenous immunoglobulin 134
low-molecular-weight heparin 132133
psychological intervention 135
vasodilators and muscle relaxants 133
Amenorrhoea, hypothalamic 142
AMI see Acute myocardial infarction (AMI)
Anastrozole 132
Androgen-modulating agents 132
Androgens 132
APTIMA HPV assay 105, 106
ART see Assisted reproductive technology (ART)
Aspirin 93
Assisted reproductive technology (ART) 87, 131 see also In vitro fertilisation (IVF)
adjuvant treatment with 131135
Atypical squamous cells of unknown significance (ASCUS) 101
B
β-human chorionic gonadotropin (β-hCG)
ectopic pregnancy and 30, 3233, 33, 34, 3738, 39
Beta-blockers 71, 73
Bethesda classification, of cervical cytology 100, 101
Bipolar resectoscopes 25
Bladder pain syndrome (BPS) 45
American Association of Urology (AUA) on 5
classification of 5, 5
cystoscopy in, role of 5, 56
International Society for the Study of 5
prevalence of 5
BPS see Bladder pain syndrome (BPS)
BRCA1 77, 78
BRCA2 77, 78
BRCA testing, in cancer patients 79
Breast cancer 77 see also Breast cancer susceptibility genes
asymptomatic carriers in, management of 82
BRCA mutation and 7879
BRCA-related 79
genes with risk of 7778
hormone replacement treatment in 84
mammographic screening for 82
MRI as screening tool for 82
predictive testing 82
pregnancy and 84
risk reducing surgery in carriers with 84
Breast cancer susceptibility genes
BRCA1 77, 78
BRCA2 77, 78
and endometrial cancer 86
mutations in 7779
predictive testing 82
preimplantation genetic diagnosis 8586
testing in cancer patients 79
Bromocriptine 72
C
Cardiac disease, in pregnancy 65
acute myocardial infarction 6971, 70, 71
cardiovascular changes and 66
congenital heart disease 6669, 68
maternal death rates 65, 66
peripartum cardiomyopathy 7173, 72
pre-pregnancy counselling 66
Cardiac enzymes 69
Cardiac output (CO) 66
Cervarix 112
Cervical cancer 99
cervical intraepithelial neoplasia 100, 101, 102
cytology in, use of 99100, 100
human papillomavirus and (see Human papillomavirus (HPV))
screening for 102103
squamous intraepithelial lesion 101
Cervical intraepithelial neoplasia (CIN) 100
CIN1 101
CIN2 101
CIN3 102
Cervista HPV HR 105
Cervista HPV 16/18 test 105
Child health and nutrition research initiative (CHNRI) 58
Chronic pelvic pain (CPP) 1
definition of 1
gynaecological causes of 2, 2
laparoscopy in, role of 2, 24
non-gynaecological causes of 2
prevalence of 12
Chronic pelvic pain syndrome (CPPS) 4
CIN see Cervical intraepithelial neoplasia (CIN)
Clopidogrel 71
Cobas 4800 HPV 105, 106
Colposcopy 102103
Combined oral contraceptive pill (COC) 84
Congenital heart disease (CHD), in pregnancy 6669, 68
Corticosteroids, use of, during ART 133134
CPP see Chronic pelvic pain (CPP)
Cyanosis 66
Cystoscopy
in bladder pain syndrome 5, 56
uncertainties of 6
D
Digene Hybrid Capture 2 (HC2) 105
Digital analysis of selected regions (DANSR) technique 4647
Dysfunctional uterine bleeding (DUB) 20, 22
Dyskaryosis 100
E
ECLIPSE study 24
Ectopic pregnancy 2930
biochemistry in diagnosis of 3233, 33, 34
clinical diagnosis of 30
definition of 29
expectant management of 3638, 37
in fallopian tube 29
incidence of 29
management of, overview of 39
medical treatment for 3536
operative procedure for diagnosis of 3334
surgical treatment for 3435
ultrasound diagnosis of 3032, 31
Egg donation (ED) 87, 88 see also In vitro fertilisation with egg donation
Eicosanoids 117, 118
arachidonic acid-derived 117, 118
biological functionality 121
biosynthesis and regulation 117121
diagnostic ability of 123125, 124, 125
endocannabinoid converter 117120, 118, 119
in labour onset 122123
low/no FAAH and 122
miscarriage and 121
and preterm labour 127
Electrocardiogram (ECG) 69, 70
Endometrial ablation, in heavy menstrual bleeding 25
Endometrial biopsy (EB) 20, 21, 133
Endometrial cancer 85
and heavy menstrual bleeding 20
Endometrial hyperplasia, and heavy menstrual bleeding 20
Endometrial polyps, and heavy menstrual bleeding 20
Endometriosis 3
and chronic pelvic pain 2
laparoscopy in, role of 2, 3
Enhanced recovery (ER) 9
discharge criteria 13
elements of 11
evidence to benefits of 14
future developments 14
and gynaecology 10
implementation of 14
non-surgical intervention in 11
patient feedback on 13
postoperative 13
primary care in 10
principles of 1013
quality and cost of 13
secondary care in 1011
surgical and anaesthetic intervention in 1112
Enhanced recovery partnership programme 9
ER see Enhanced recovery (ER)
F
FAAH see Fatty acid amide hydrolase (FAAH)
Familial breast/ovarian cancer syndrome 7779, 78
Fatty acid amide hydrolase (FAAH) 117, 122, 126
Fetal aneuploidy, non-invasive prenatal testing for 4448, 45
clinical use of 4748
fetal cfDNA enrichment 4445
and intellectual property issues 47
massively parallel sequencing 45
shotgun MPS approach 4546
targeted MPS approach 46, 4647
Fetal cell-free DNA (cfDNA) 42 see also Prenatal testing, non-invasive
Fetal growth restriction (FGR), and stillbirth 56, 59, 60, 61
Fetal sex determination 4243
Fibroids 2
G
Gardasil 112
GnRH see Gonadotropin-releasing hormone (GnRH)
Goal directed fluid therapy (GDFT) 12
Gonadotropin-releasing hormone (GnRH) 132
kisspeptins and 140145 (see also Kisspeptins)
Growth hormone (GH), use of, on IVF patients 131132
H
Heavy menstrual bleeding (HMB) 19
causes of 20, 20
cost-effectiveness of diagnosis in 2224
definition of 1920
endometrial ablation 25
hysterectomy for 2526
hysteroscopic surgery for 2425
medical treatment of 24
tests for diagnosis of 2022, 21
training programmes and 24
Heparin, use of, in ART patients 132133
HMB see Heavy menstrual bleeding (HMB)
Hormone replacement treatment (HRT) 84
HPV see Human papillomavirus (HPV)
Human chorionic gonadotropin (hCG) 147
Human papillomavirus (HPV) 103
aetiological factors associated with 104105, 105
ARTISTIC trial 109
ASCUS/LSIL triage study 106107
and cervical cancer, development of 104, 104
emerging markers for 111
genotyping 111
and glandular abnormalities 110111
and men 105
prevalence of 103, 103
as primary screening test for cervical cancer 106, 107
in resolution of uncertainties 110
self-sampling testing 111
sentinel site project 109110
subtypes and pathogenesis 103
techniques for detection of 105106
as test of cure post treatment 110
therapeutic vaccination 112
triage 106110, 108
vaccination 112
Hunner's ulcers 5
Hypogonadotrophic hypogonadism 143
Hysterectomy 10
in heavy menstrual bleeding 2526
Hysteroscopic myomectomy 25
Hysteroscopic surgery, in heavy menstrual bleeding 2425
I
Intracytoplasmic sperm injection (ICSI) 88, 94
Intralipid, in ART patients 134
Intravenous immunoglobulin (IVIG), in ART patients 134
In vitro fertilisation (IVF) 69, 87
with egg donation (ED) 8796 (see also In vitro fertilisation with egg donation)
In vitro fertilisation with egg donation 8788
early pregnancy in 93
ethical issues in 96
first trimester in 9394
indications for 8890, 89
maternal age and 90
postnatal thromboprophylaxis 9596
pregnancy outcomes in 9192
pregnancy with, considerations in 9091
pre-pregnancy counselling and medical evaluation 88, 9293
screening prior to 90
second trimester in 94
single embryo transfer 93
technique of 88
third trimester in 95
women with Turner's syndrome and 9091
IVF see In vitro fertilisation (IVF)
K
Kick-counting, use of 59
KISS1 (kisspeptin gene) 139 see also Kisspeptins
Kisspeptin neurones 140
Kisspeptin receptor (KISS1R) 139
Kisspeptin receptor antagonist 147
Kisspeptins 139140
adulthood and 141143
clinical uses of 145, 147
and gonadotrophin-releasing hormone 140145
hyperprolactinaemia and 143
lactation and 143
pituitary gonadotrophs, hormonal regulation of 145, 146
postmenopausal women and 144145
puberty and 140141
undernutrition and overnutrition and 143144
Kleihauer test 57
L
Laparoscopy, for ectopic pregnancy 3435
Laparoscopy, in chronic pelvic pain 2, 24 see also Chronic pelvic pain (CPP)
benefits of 2, 23
uncertainties of 4
Leptin 143144
Letrozole 132
Levonorgesterol-releasing intrauterine system (LNG-IUS) 21, 22, 24
Liquid based cytology (LBC) 99100
Low-molecular-weight heparin (LMWH) 93
use of, in ART patients 132133
M
Marfan syndrome (MFS), in pregnancy 73
Massively parallel sequencing (MPS) approaches 4547
Metal stents 71
Methotrexate, for ectopic pregnancy 3536
MI see Myocardial infarction (MI)
Morcellators 25
Mothers and babies: reducing risk through audits and confidential enquiries (MBRRACE) collaboration 56, 61
Myocardial infarction (MI) 6971, 70, 71
N
Nucleic acid amplification techniques (NATs) 105
O
Olaparib 8182
Outpatient hysteroscopy (OPH), for uterine pathology 21
Ovarian cancer 77 see also Breast cancer; Breast cancer susceptibility genes
BRCA1/2-deficient 80
BRCA mutation and 80
chemotherapy for 80
combined oral contraceptive pill and 84
poly ADP-ribose polymerase inhibitors for 8082, 81
pregnancy and 84
risk-reducing salpingo-oophorectomy in 83
risk reducing surgery in carriers with 84
screening for 83
Ovarian cancer cluster region (OCCR) 78
Ovarian cysts 2
Ovarian hyperstimulation syndrome (OHSS) 147
P
PAH see Pulmonary arterial hypertension (PAH)
Papanicolaou (Pap) smear 99
Pelvic congestion syndrome 2
Pelvic inflammatory disease 2
Pelvic pain, chronic see Chronic pelvic pain (CPP)
Percutaneous coronary intervention (PCI) 71
Perinatal audit
definition of 56
role of, in stillbirth prevention 5657
Peripartum cardiomyopathy (PPCM) 7173, 72
PGD see Pre-implantation genetic diagnosis (PGD)
PGs see Prostaglandins (PGs)
Physiological cardiac hypertrophy 66
Pituitary gonadotrophs, hormonal regulation of 145, 146
Placental mosaicism 47
Platinum-based chemotherapy
for BRCA-mutant breast cancer 79
for epithelial ovarian cancer 80
Poly ADP-ribose polymerase (PARP) inhibitors 8082, 81
PPCM see Peripartum cardiomyopathy (PPCM)
Pre-eclampsia, risk of, in IVF-ED pregnancies 92, 93, 95
Pregnancy of unknown location (PUL) 3233, 33, 34, 36
Pre-implantation genetic diagnosis (PGD) 8485
Prenatal testing, non-invasive 4142
aneuploidy detection 4448
ethical considerations in 49
fetal cell-free DNA (cfDNA) and 42
fetal sex determination 4243
rhesus determination 4344
of single gene disorders 48
Progesterone 33
16 kDa prolactin (16-kDa PRL) 7172
Prolactin and kisspeptin, relationship between 143
Prostacyclin synthase (PGES) 119
and cyclo-oxygenase-2 120
and thromboxane synthase (TXAS) 120121
Prostaglandin D2 (PGD2) 121
Prostaglandin F2 alpha synthase (PGFS) 120
Prostaglandin H synthase (PGHS) 117, 118, 127
Prostaglandin I2 (PGI2) 120121
Prostaglandins (PGs) 119, 122123, 126 see also Eicosanoids
Puberty, kisspeptins and 140141
PUL see Pregnancy of unknown location (PUL)
Pulmonary arterial hypertension (PAH)
causes of 74
definition of 73
management of 74
in pregnancy 7374
Q
Qiagen hybrid capture II 105
R
Raloxifene 83
Rectus sheath catheters 13
Reduced fetal movements (RFM), and stillbirth 58, 61
Relative mutation dosage (RMD) 48
Rhesus determination 4344
Risk reducing bilateral mastectomy (RRBM) 8384
Risk-reducting salpingo-oophorectomy (RRSO) 83
RRBM see Risk reducing bilateral mastectomy (RRBM)
RRSO see Risk-reducting salpingo-oophorectomy (RRSO)
S
Saline infusion ultrasound, for uterine pathology 21
Salpingectomy, for tubal ectopic pregnancy 35
Salpingotomy, for ectopic pregnancy 35
Selective oestrogen receptor modulators (SERM) 83
Sildafenil 74
Single embryo transfer (SET) 93
Single gene disorders, non-invasive prenatal diagnosis for 48
Stillbirth 53
antenatal care and 6061
causes of 53
challenges in prevention of 5559
definition of 53
fetal growth restriction and 61
impact of 5455
perinatal audit in, role of 5657
preconception care and 60
prevention of 55, 5961, 60
rate of 5354, 54
reduced fetal movements and 61
research on, role of 5759
science of implementing change and 59
smoking and 61
SurePath 100
T
TAK-448 (kisspeptin receptor analogue) 147
Tamoxifen 83
ThinPrep 100
Thrombolytic therapy 71
Total vascular resistance (TVR) 66
Transvaginal ultrasound (TVS)
for ectopic pregnancy 29, 30
for uterine pathology 21
‘Trial embryo transfer’ 133
Triple negative tumours 78
TS see Turner's syndrome (TS)
Turner's syndrome (TS) 9091
TVS see Transvaginal ultrasound (TVS)
U
Ulipristal acetate 24
Ultrasound, for ectopic pregnancy 3032, 31
Uterine fibroids, and heavy menstrual bleeding 20
Uterine relaxing agents 133
V
Valvular egurgitation 66
Vasodilators, use of 133
Venous thromboembolism (VTE), risk of, in ART 9394
W
Warfarin 96
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Chapter Notes

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The role of laparoscopy and cystoscopy in the diagnosis and management of chronic pelvic and bladder painChapter 1

Seema A Tirlapur,
Khalid S Khan,
Elizabeth Ball
 
BACKGROUND
Chronic pelvic pain (CPP) in women has prevalence rates comparable to that of lower back pain and asthma, causing a huge impact on the quality of life of the individual patient and a large burden on the economy [1]. In this chapter, we explore the role of laparoscopy as a diagnostic and therapeutic tool in the management of CPP. We investigate bladder pain syndrome (BPS) as a manifestation of CPP and the role cystoscopy plays in its diagnosis and treatment. We also explore the causes of CPP and evaluate the most effective methods of diagnosis.
 
WHAT IS CHRONIC PELVIC PAIN?
Chronic pelvic pain is an intermittent or constant pain in the lower abdomen for at least 6 months, not associated with pregnancy and not occurring exclusively with menstruation or sexual intercourse [2]. The International Association for the Study of Pain and the European Association of Urology revised definition of CPP includes both men and women, with pain perceived in structures related to the pelvis, acknowledging its negative impact on cognition, behaviour, sexual and emotional well-being and noting the possible association with urinary, bowel, sexual, pelvic floor or gynaecological dysfunction [3, 4].
There is difficulty in delineating causes behind CPP as there are many possible causes for the pain and several pathologies may co-exist, making a single diagnosis sometimes impossible. A recent systematic review estimated the prevalence of CPP to range between 8–81% worldwide [5].
___________________
Seema A Tirlapur MBChB, Women's Health Research Unit, Queen Mary, University of London, London, UK. Email: s.a.tirlapur@qmul.ac.uk (for correspondence)
Khalid S Khan MRCOG MMed MSc, Women's Health Research Unit, Queen Mary, University of London, London, UK.
Elizabeth Ball MD PhD MRCOG, Barts Health NHS Trust, The Royal London Hospital, London, UK.2
The range of causes for CPP is extensive and the methods of diagnosis for each vary in terms of diagnostic accuracy and patient acceptability. The causes of CPP may be classified as gynaecological versus non-gynaecological or structural and non-structural. Gynaecological causes include endometriosis, adenomyosis, ovarian cysts, uterine fibroids, pelvic congestion syndrome, chronic pelvic inflammatory disease (PID) and adhesions, which may be gynaecological, secondary to endometriosis or PID or non-gynaecological after previous surgery or infection. Non-gynaecological causes include irritable bowel syndrome and BPS as well as musculoskeletal, neuropathic and psychological conditions.
 
THE ROLE OF LAPAROSCOPY
More than 250,000 laparoscopies are performed annually in the United Kingdom. Diagnostic laparoscopy has been regarded as the ‘gold standard’ investigation for CPP, after a careful preoperative work-up, which involves a thorough history, physical examination and imaging in the form of pelvic ultrasound or pelvic magnetic resonance imaging, if necessary [2]. However, depending on the preceding work-up, up to 40% of diagnostic laparoscopies fail to show any pathological cause for the patient's pain [6].
Table 1.1 shows the gynaecological causes of CPP and the accuracy of laparoscopy as a diagnostic tool. Laparoscopy can successfully diagnose adhesions and several types of endometriosis [6, 7], but its accuracy in diagnosing other pathologies associated with CPP is unproven. Nevertheless, diagnostic laparoscopy remains a popular test in the work-up of CPP and this may reflect its additional benefits. These include assessment of fertility by examining tubal patency, and evaluating the severity of disease to plan appropriate treatment, e.g. identifying the presence of severe endometriosis necessitating management in an experienced endometriosis centre.
Table 1.1   Gynaecological causes of chronic pelvic pain and the accuracy of laparoscopy as a diagnostic tool
Target condition
Diagnostic criteria
Role of laparoscopy
Adenomyosis
Presence of islands of ectopic endometrial tissue within the myometrium confirmed histologically
Uncertain value – appearance bulky ‘boggy’ uterus
Adhesions
Visual inspection during laparoscopy, or by absence of movement between adjacent organs
Gold standard – visual inspection
Endometriosis
Visual inspection during laparoscopy, noting appearance, size and depth of endometrial implants
Gold standard – negative laparoscopy can exclude disease but positive findings cannot accurately confirm disease [13]
Fibroids
Size and location noted during pelvic ultrasound
Uncertain – visual inspection of size and location of subserosal fibroids
Ovarian cysts
Pelvic ultrasound or magnetic resonance imaging to define size, location and nature of cyst, confirmed histologically
Uncertain value – visual inspection of size and location of cyst
Pelvic congestion syndrome
Definitive diagnosis on catheter-directed venography, showing uterine venous engorgement and ovarian complex congestion [29]
Uncertain value – appearance of pelvic varicosities
Pelvic inflammatory disease
Visual inspection during laparoscopy or histology from fimbrial biopsy [30]
Uncertain value – may identify salpingitis, adhesions and Fitz-Hugh-Curtis syndrome
3
Laparoscopy requires insertion of instruments into the peritoneal cavity and is not without risk, highlighted by the fact that up to 57% of gynaecologists have reported major bowel and vascular injures, regardless of the entry technique used [8]. Whilst laparoscopy is more invasive than other testing modalities in CPP, the technique allows surgical treatments to be effected enhanced by advances in instrumentation. Thus, in an attempt to avoid multiple operations and their associated surgical and anaesthetic risks, ‘see and treat’ therapeutic laparoscopies are considered preferable [9]. To successfully achieve such an efficient approach to managing CPP requires good prior diagnostic work up. For example, in addition to thorough clinical assessment, a rigorously performed pelvic ultrasound scan may be useful. Feature suggestive of endometriosis or adhesions can be detected such as site-specific pain of the uterosacral ligaments, decreased ovarian mobility, presence of endometriomas and hydrosalpinges [10]. The surgeon can then more effectively plan the site and setting for surgery and ensure that the patient is well informed and that suitably skilled staff and surgical instruments are available [9].
 
Endometriosis
Endometriosis often affects areas of the pelvis, such as the uterosacral ligaments, pouch of Douglas and rectovaginal septum, which are difficult to assess clinically [11]. Laparoscopy can improve diagnostic accuracy but has limitations. One observational study noted that 42% of general gynaecologists failed to recognise rectovaginal endometriosis on visual inspection at primary laparoscopy [12]. A systematic review of the accuracy of laparoscopic visual inspection in the diagnosis of peritoneal endometriosis showed that a negative laparoscopy could accurately exclude endometriosis, whilst a positive laparoscopy needed to be followed by histological confirmation [13]. The technique of diagnostic laparoscopy is important such that a careful, systematic inspection of the abdomen and pelvis is undertaken and importantly adequate anteversion and anteflexion of the uterus is achieved to allow for thorough inspection of the pouch of Douglas. Despite these limitations, most gynaecologists view visual inspection at laparoscopy as the ‘gold standard’ method of diagnosing superficial endometriosis.
Superficial peritoneal endometriosis can be treated by cautery or excision. There is much debate over the optimal method of treating superficial endometriosis and often depends on the surgeons preference. Whilst excision is effective and enables a histological biopsy to be obtained for disease confirmation, it requires dissection skills and knowledge of underlying structures to avoid trauma. Excision also allows visualisation of possible invasion below diseased areas, especially of uterosacral ligament endometriosis. In contrast, ablative treatments may be inadequate due to the risk of thermal injury to nearby structures. A small randomised controlled trial (RCT) of 24 patients, compared ablation using monopolar diathermy versus excision using monopolar diathermy scissors in patients with mild endometriosis (stage 1 or 2 revised American Fertility Score). Both methods of treatment produced symptomatic relief with no difference between the treatments with regard to 6-month symptom questionnaire scores [14]. A large randomised trial is needed to compare diathermy versus excision to obtain more reliable results.4
 
Adhesions
Adhesions may be caused by endometriosis, exposure to infection or previous surgery and can cause pain by organ distension or stretching [2]. They can range from fine filmy adhesions to dense, vascular ones. The symptomatic benefits of laparoscopic adhesiolysis are uncertain. Whilst there is no clear evidence to support adhesiolysis in women with CPP, an RCT of 100 patients treated with adhesiolysis compared to no treatment during diagnostic laparoscopy for chronic abdominal pain, showed both groups reported substantial pain relief with no difference between the groups 1 year after surgery [15]. Similar results were noted in a small observational study, with 45% of patients reporting on-going symptomatic relief 2 years after laparoscopic adhesiolysis [16]. From these results, it can be argued that there may be a psychologically beneficial effect to surgery and the perceived improvement in pain [17].
 
Adenomyosis
Adenomyosis is a common benign gynaecological condition, often reported on imaging or identified during laparoscopy. It is defined by the presence of islands of ectopic endometrial tissue within the myometrium, causing smooth muscle hypertrophy [18A]. It can be associated with endometriosis and endometrial hyperplasia and is known to cause heavy menstrual bleeding and dysmenorrhoea. On laparoscopy, the clinician may observe the classical appearance of a bulky ‘boggy’ uterus, although the accuracy of laparoscopic diagnosis is unproven and final diagnosis rests upon histological confirmation, usually after hysterectomy. Imaging in the form of pelvic ultrasound or magnetic resonance imaging (MRI) may identify the condition with good accuracy (72% sensitivity for transvaginal ultrasound and 77% for MRI, compared against histology), allowing medical treatment to be initiated without the need for surgery [18B].
 
UNCERTAINTIES OF LAPAROSCOPY
A diagnostic laparoscopy can be a useful tool for evaluating the causes of CPP, but 40% of laparoscopies may show no pathology. Clinicians should therefore carefully weigh up the perceived surgical benefits of laparoscopy against the risks of surgery. Patients need to be informed about the limitations of this investigation and the implications of a ‘negative’ laparoscopy. CPP has many non-gynaecological and non-structural causes, which may not be identified by laparoscopy, e.g. functional and psychosomatic conditions which may benefit from alternative complementary therapies. The term chronic pelvic pain syndrome (CPPS) has been introduced by the International Association for the Study of Pain to describe the occurrence of CPP where pain may be focused around a single organ or multiple pelvic organs, and where there is no proven infection or other obvious local pathology to account for the pain [4]. Whilst a laparoscopy may not always be able to identify any cause of pain, sometimes this can have a beneficial, reassuring effect on the patient [19].
 
WHAT IS BLADDER PAIN SYNDROME?
Patients suffering from BPS may present with CPP. BPS is the condition formerly known as interstitial cystitis and painful bladder syndrome. It is defined as CPP, pressure or discomfort 5related to the bladder along with at least one other urinary symptom, such as urgency or frequency, in the absence of any other pathology [20]. The prevalence of BPS is estimated to be between 2 and 306 per 100,000 of the population, with lower prevalence in the Japanese population compared to European and American patients [21]. There is variation in the method of diagnosing BPS because patients may present with a wide spectrum of pain and urinary symptoms, which makes accurate prevalence rates difficult to record.
In 2008, The International Society for the Study of BPS suggested that BPS may be classified according to the findings at cystoscopy, hydrodistension and bladder biopsies with a normal cystoscopy equating to BPS grade 1, glomerulations (pin point sized areas of bleeding) equating to grade 2 and Hunner's lesions (distinctive areas of inflammation) were grade 3 with sub-classification a, b, or c depending on biopsy results [20]. Table 1.2 shows the classification of BPS according to cystoscopy and biopsy findings. In some previous guidelines, BPS has traditionally been defined and diagnosed through cystoscopy findings alone [21]. In 2011, the American Association of Urology (AUA) published guidelines on the diagnosis and management of BPS, which recommend that initial assessments should include a careful history, physical examination and laboratory tests to exclude infection. An important recommendation is that cystoscopy may be used as an aid in complex cases but it is not necessary to make a diagnosis or commence treatment [22]. Conservative first-line treatments, such as stress and pain management, patient education and and lifestyle modifications such as change in diet, avoidance of caffeine and limiting evening fluid intake, should be initiated without delays.
 
THE ROLE OF CYSTOSCOPY
Cystoscopy is often thought of as the investigation of choice to diagnose BPS. It can differentiate between BPS with normal bladder mucosal appearance from grade 2 and 3 disease with the presence of petechial bleeds, glomerulations and Hunner's lesions/ulcers [23]. The presence of Hunner's ulcers may lead the clinician to offer alternative treatments such as fulguration at an early stage, rather than persevering with conservative treatments. Hydrodistension during cystoscopy can allow visualisation of petechial haemorrhages. It can also provoke petechial bleeds that are thought to be pathognomonic.
Table 1.2   Classification of bladder pain syndrome according to cystoscopy and biopsy findings [20]
Cystoscopy with hydrodistension
Not done
Normal
Glomerulations b
Hunner's lesions c
Biopsy:
Not done
XX
1X
2X
3X
Normal
XA
1A
2A
3A
Inconclusive
XB
1B
2B
3B
Positive a
XC
1C
2C
3C
a Histology showing inflammatory infiltrates and/or detrusor mastocytosis and/or granulation tissue and/or intrafasicular fibrosis.
b Glomerulations: grade 2 (several areas of submucosal bleeding) and grade 3 (diffuse bleeding of bladder mucosa).
c With or without glomerulations.
6
Cystoscopy with hydrodistension has a therapeutic effect. The hydropressure is believed to degenerate afferent nerves, leading to reduced bladder pain and increased bladder capacity [21]. If brief hydrodistension is performed, using 80–100 cm of water for 2–10 minutes, studies have shown variable symptomatic improvement but the effects decreased after 6 months post treatment [24]. Prolonged periods of hydrodistension are not recommended due to the adverse effect of bladder rupture [22].
 
THE UNCERTAINTIES OF CYSTOSCOPY
Cystoscopy and bladder biopsies have traditionally been used as the ‘gold standard’ to diagnose and classify BPS [20]. However, some studies show poor correlation between cystoscopy findings and diagnosis, because glomerulations may be seen in asymptomatic patients and bladder biopsies may not confirm disease in the presence of glomerulations [21, 25]. This has resulted in uncertainties in the diagnosis and management of the BPS. Some guidance ranks diagnosis by cystoscopy ahead of bladder biopsy when recommending evidence-based treatments [23]. Guidance from the AUA recognises the limitations of cystoscopy and bladder biopsy. It supports a clinical diagnosis, based upon symptoms and signs derived from the patient history and examination, on which to recommend treatment [22].
 
CONCLUSION
There are many causes for CPP. Several risk factors, such as a history of drug, alcohol and sexual abuse, PID, anxiety and depression have been associated with CPP [26]. In order to fully investigate a patient and possibly diagnose the cause of pain, invasive procedures like a laparoscopy and cystoscopy may be useful and can have therapeutic effects. The degree of sensitivity of each test varies with the target condition, and these procedures may not yield a cause of pain, which may reassure some patients but equally may cause distress if no obvious cause of pain can be identified [19]. Prior to surgery, a careful work-up of the patient with thorough history, examination and imaging is essential to correctly plan management. When a laparoscopy is performed, a ‘see and treat’ therapeutic laparoscopy is recommended rather than a purely diagnostic procedure, provided the surgeon is suitably trained and equipped.
CPP and BPS affect large numbers of people across the world, often with unknown etiology and overlapping symptoms and possibly co-existing disease pathology, which makes the management of such patients difficult [27, 28]. Both conditions may have non-specific symptoms with pain as the main complaint. In light of these considerations, it may be prudent to perform both laparoscopy and cystoscopy in cases of persistent CPP.7
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