Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_959_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
29 Мб
Скачать
14 Challenging Concepts in Urological Surgery
https://t.me/med1917
Clinical diagnosis
of prostatic abscess
<1 cm >1 cm
TRUS
Conservative management
(ABx)
Reassess
Cured No response
Localized
to prostate
TUR drainage
Figure 2.3 Flowchart depicting an algorithm for management of a patient diagnosed with
prostatic abscess. ABx, antibiotics; TRUS, transrectal ultrasound; TUR, transurethral.
Adapted from Abdelmoteleb et al. Management of prostate abscess in absence of guidelines. Int Braz J Urol. 2017; 43:835– 40 under the Attribution 4.0 International (CC by 4.0) (https:// creativecommons.org/ licenses/ by/ 4.0/ ).
US drainage and
ABx
If no improvement
CT scan
Extraprostatic
extension
Open drainage
5
Figure 2.4 Cross- sectional imaging of the pelvis. (a) Coronal section, (b) sagittal section, and (c) transverse
section showing resolution of prostatic abscess following transurethral drainage.
The patient recovered thereafter and a CT scan done by the colorectal team sug-
gested resolution of the prostatic abscess as seen in Figure 2.4.
Learning point Classification of prostatitis
Prostatitis is one of the common urinary tract problems found especially in men younger than 50 years of age. It is a group of disorders with a wide spectrum of symptoms and ranges from a clinically straightforward entity to a more complex- to- treat presentation. The disease was traditionally classified into
acute bacterial, chronic bacterial, chronic non- bacterial, and prostatodynia.6 However, in 1995 the National
https://t.me/med1917
Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the US National Institutes of Health (NIH) adopted a new working definition7 which is currently applied in clinical practice (Table 2.1).
Table 2.1 NIH classification of prostatitis
Category Designation Status of infection
I Acute bacterial prostatitis Acute infection of prostatitis
II Chronic bacterial prostatitis Recurrent infection of prostate
III Chronic non- bacterial prostatitis/
chronic pelvic pain syndrome
IIIA Inflammatory WBC in semen/ EPS/ post- prostatic massage urine
IIIB Non- inflammatory No WBC in semen/ EPS/ post- prostatic massage urine
IV Asymptomatic inflammatory
prostatitis
EPS, expressed prostatic secretion; WBC, white blood cell.
Clinical tip Meares– Stamey test
Stamey et al. described a test in 1965 to help localize UTIs.8 It enables separation of voided urinary stream into urethral (voided bladder one or VB1), midstream urine (voided bladder two or VB2), and post- prostatic massage urine (voided bladder three or VB3) in order to distinguish urethral and prostatic infection in the presence of sterile midstream urine. In 1968, Meares and Stamey introduced the concept and value of direct culture of expressed prostatic secretions (EPS) when VB1 and VB3 were equivocal. In simpler terms, the VB1 is the first 10 mL of voided urine and represents the urethral specimen; the next 150– 200 mL is VB2 and represents the bladder specimen. EPS is collected while carrying out a vigorous prostatic massage and represents prostatic fluid. Finally, VB3 is the first 10 mL of urine after prostatic massage and represents EPS trapped in prostatic urethra. This information continues to be relevant with the new classification system of prostatitis as shown in Table 2.2 below.
Although the four- glass (specimen) Meares– Stamey test is the standard method of assessing men with symptoms of chronic pelvic pain syndrome (CPPS) or chronic prostatitis (CP), it can be quite cumbersome and thus a simplified two- glass pre- and post- massage test is being widely used. The results from a two- glass test have been shown to have a strong concordance with results from a four- glass Meares– Stamey test and thus offers a reasonable alternative that is simple and cost- effective.
Semen culture has also been proposed as a simpler test than the gold standard four- glass test. The sensitivity of semen cultures for diagnosing CBP is very variable, therefore the diagnostic value remains controversial and further studies are needed.
9
No demonstrable infection
Asymptomatic
15Case 2 Prostatitis
Table 2.2 Diagnostic criteria used for the classification of prostatitis
Type White blood cell count/
high- power field (400×)
I >10 + + X + II >10 + + IIIA >10 – IIIB <10 – IV >10
VBI VB2 EPS VB3
16 Challenging Concepts in Urological Surgery
https://t.me/med1917
Expert comment Bacterial prostatitis (types I and II)
Type 1 prostatitis presents acutely either in the outpatient or emergency setting. The diagnosis is mainly clinical and treatment with antibiotics usually resolves the problem. The symptoms initially are storage or voiding LUTS associated with suprapubic rectal or perineal pain. If untreated or inadequately treated, ABP can progress to prostatic abscess and one needs to have an index of suspicion for prostatic abscess if the patient has systemic symptoms like fever, chills, nausea, vomiting, and malaise. Some patients may develop urinary retention as a complication of prostatic abscess.
Ten per cent of patients diagnosed with ABP may progress to CBP and this diagnosis is made if the patient is symptomatic for at least 3 months or has recurrent prostatitis. The aetiology of the bacterial types of prostatitis has been described earlier and for successful treatment, use of appropriate antibiotics is important.
Antibiotic penetration into the prostate depends upon their lipid solubility, dissociation constant (pKa), and protein binding. Beta lactam antibiotics due to their low pKa and low lipid solubility penetrate poorly into prostate. However good to excellent penetration is seen with quinolones, tetracyclines, macrolides, sulphonamides, nitrofurantoin, and aminoglycosides like tobramycin and netilmicin.
In CBP, oral antibiotic therapy can achieve cure rates of 70– 90% at 6 months but a systematic review did not identify any randomized controlled trials to compare it with a placebo or no treatment.11 There are some studies showing the effectiveness of anal submucosal12 or prostatic antimicrobial injections,13 but the evidence is limited and such treatment is not standard and mostly experimental. Interventions like transurethral resection of the prostate (TURP) for treatment of CBP have not been studied in a randomized controlled setting but some retrospective studies have suggested a role for TURP in patients with CBP and obstructive symptoms.14 There are some reports of surgical options like TURP and radical prostatectomy performed in extreme cases of CBP.
10
Future directions
Treatment with phage therapy has been explored recently due to the role of phage strains in bacterial elimination and local immunomodulation.15 However, further research needs to be done to establish its effectiveness as a future tool in treatment of bacterial prostatitis.
Learning point Aetiology and symptoms in CP/ CPPS
CP/ CPPS is the most common form of prostatitis and also the most poorly understood one. Ten per cent of patients with CP progress to CP/ CPPS. However, the aetiology is unclear in most of the cases. Non- infectious factors that have been implicated include inflammation, autoimmunity, hormonal imbalances, pelvic floor tension myalgia, intraprostatic urinary reflux, and psychological disturbances.16 A case– control study by Pontari et al. showed that the lifetime prevalence of non- specific urethritis, cardiovascular disease, neurological disease, psychiatric conditions, and haematopoietic, lymphatic, and infectious disease was significantly greater in men with CP/ CPPS.17 CP/ CPPS shares multiple demographic, clinical, and psychosocial aspects with chronic pain conditions like fibromyalgia and chronic fatigue syndrome and thus may have a similar primary pathophysiology.
18
The patients experience chronic pelvic pain and LUTS but there may also be associated sexual dysfunction. Some patients may complain of unusual symptoms like the sensation of a foreign body in the rectum, rectal pain during and after defecation, premature ejaculation, spontaneous sexual stimulation, or alteration of orgasms.19 Owing to the heterogeneous nature of this condition, the diagnosis is based on symptoms; absence of any diagnostic biomarkers makes its diagnosis and treatment approaches variable and thus outcomes relatively poor. As a result of this, there is high disease burden and patient as well as physician dissatisfaction.
Clinical tip Clinical evaluation of CP/ CPPS
Clinical evaluation to assess the severity of CP/ CPPS can be carried out using the 13- point validated National Institute of Health Chronic Prostatitis Symptoms Index (NIH- CPSI) (Figure 2.5).20 An alternative classification system using the UPOINT system categorizes the severity of patients’ symptoms based on the predominant symptom group.21 This UPOINT system in CP/ CPPS originally encompassed Urinary, Psychosocial, Organ specific, Infective, Neurological, and Tenderness as different symptom phenotypes but the aspect of Sexual dysfunction was added later on (Table 2.3).
22
17Case 2 Prostatitis
https://t.me/med1917
Figure 2.5 The NIH- CPSI.
18 Challenging Concepts in Urological Surgery
https://t.me/med1917
Table 2.3 UPOINT classification phenotypes in CP/ CPPS
U Urinary NIH- CPSI score >4, obstructive and storage LUTS, high post- void residuals
P Psychosocial Clinical depression, anxiety, stress, maladaptive coping, etc.
O Organ specific Prostate tenderness, leucocytes in prostatic fluid, haematospermia,
prostatic calcification
I Infective Gram- negative bacilli or enterococci in prostatic fluid, documented
successful response to antimicrobial therapy
N Neurological Clinical evidence of central neuropathy, pain beyond pelvis, irritable bowel
syndrome, fibromyalgia, chronic fatigue syndrome, etc.
T Tenderness Painful tenderness and/ or painful muscle spasm or trigger points in
abdomen and/ or pelvic floor
S Sexual Sexual and ejaculatory dysfunction
Treatment is aimed to alleviate symptoms using strategies targeting the predominant phenotype of symptom. Interventions include identification and avoidance of risk factors23 which include aspects of lifestyle (sedentary, fatigue, high stress), diet (alcohol, coffee, pepper, spicy foods, excessive dieting), sexual habits (delaying ejaculation, extremes in frequency of sexual activity, coitus interruptus), and perineal trauma (sitting position, sports, tight clothing). Education and clear communication with the patient and his sexual partner providing information about the nature of disorder, chronic pain cycle, treatment options, and clinical outcomes is important.
24
Expert comment Patients with CP/ CPPS
CP/ CPPS is a complex and poorly understood condition with a huge impact on the quality of life of the affected person and treating the condition needs effective communication with the patient and a shift away from a traditional approach to management towards a more pragmatic multimodal approach. Communication not only between the physician and the patient but also between the multidisciplinary team looking after the patient, including their general practitioner, is the key element of this. Education of patients and their sexual partners to understand the current concepts, the chronic pain cycles, and the challenging nature of this disease can level expectations and help focus on achievable objectives. Social support helps gain the much- needed adjustments that might need to be made at work or elsewhere to help the patient manage his condition.
Learning point Therapeutic and evidence base in CP/ CPPS
A combined approach addressing risk factors, promoting a healthy lifestyle and diet, and pharmacological, psychological, and neuromodulatory interventions improve outcomes. Pharmacological interventions include the use of alpha blockers, antimicrobials, anti­inflammatory and other pain medications, antidepressants, and neuroleptics. By reducing voiding pressures and improving voiding flow patterns, alpha blockers alleviate discomfort. A randomized placebo- controlled study, however, did not show any benefit and hence these are reserved for the subset of patients with voiding symptoms. There is no clear- cut role for 5- alpha reductase inhibitors but they reduce NIH- CPSI scores; the same is true for phosphodiesterase type 5 inhibitors.
There is only moderate to low- quality evidence for benefit from short- term use of anti­inflammatory medications (non- steroidal anti- inflammatory drugs and steroids), antibiotics, and phytotherapy (quercetin, pollen extract (Cernilton®), cranberry, etc.). Intraprostatic botulinum toxin A has been shown to have benefit in improving NIH- CPSI scores and pain scores but the benefit is short term and treatment may need to be repeated. Pelvic floor botulinum toxin A did not show much benefit. In a recent Cochrane review, allopurinol, anticholinergics, antidepressants, pentosan polysulfate, pregabalin, and mepartricin were ineffective.
25
25
There is moderate quality evidence for non- pharmacological interventions like acupuncture,
https://t.me/med1917
extracorporeal shockwave therapy, circumcision, and tibial nerve stimulation in improving prostatitis symptoms, but the quality of evidence is weak for other interventions like lifestyle modifications, physical activity, prostatic massage, electromagnetic chair, thermotherapy, sonoelectromagnetic therapy, ultrasound therapy, biofeedback, external radiofrequency, laser therapy, myofascial trigger point release, osteopathy, trans- electrical nerve stimulation, transurethral needle ablation, and so on.26 However, lifestyle modifications and physical activity have an overall benefit on health and are frequently recommended.
Future directions
Further research to study the effect of various proven and unproven interventions on various different parameters of this symptom complex is needed as most studies have so far focused on urinary and pain symptoms. Cannabinoids such as N- palmitoylethanolamide and flavonoid polydatin are currently being studied.
Psychological distress evaluation should be carried out by a dedicated psychologist or mental health practitioner such that at- risk patients can be identified and interventions introduced as an integrative therapy and as part of a multimodal approach.28 Such evaluation would provide an insight into patients’ internal beliefs, perception of chronic pain, social support and interactions, relationships, and so on. This would not only help understand possible psychological causes of physical manifestations but also help plan adjustment and coping strategies.
Expert comment Asymptomatic inflammatory prostatitis
Asymptomatic inflammatory prostatitis is usually a histological diagnosis and is frequently an incidental finding in men undergoing investigations for prostate cancer or in men undergoing infertility investigations. Its prevalence ranges between 11% and 42%.29 As the name suggests, it is asymptomatic and only presents clinical issues in the context of unnecessary biopsies for raised prostate- specific antigen or abnormal findings on MRI related to it. There are suggestions of a role in development of benign prostate hyperplasia and prostate cancer30 but this unproven. It is usually left untreated but when seen in conjunction with leucocytospermia, it can be associated with male infertility.
27
19Case 2 Prostatitis
A final word from the expert
Inflammation of the prostate gland has been recognized as an entity for around two centuries but remains essentially a clinical diagnosis with the use of other investigations primarily to provide supportive evidence of either inflammation or infection localized to the prostate. The term ‘prostatitis’ itself can cover a wide range of clinical conditions and it is therefore important that, whenever possible, this is also qualified with type and the 1995 NIDDK/ NIH classification is useful for this purpose.
Acute prostatitis (category I) has the clearest treatment pathway, and the majority of patients have infection from Gram- negative bacteria which usually responds well to antibiotic treatment with only a small proportion developing an abscess which can be readily identified on imaging and drained via the transrectal or transurethral route. As for any acute infection, a high index of suspicion and early diagnosis is critical to avoid systemic involvement and improve outcomes.
Unfortunately, CP (categories II and III) is an altogether more difficult entity both to characterize and treat. The role of the Meares–Stamey test and/ or semen culture should not be underestimated as it is important to establish early on in the management whether bacteria are involved in causing symptoms. Where this is the case, that is, CBP (category II), treatment with extended courses of antibiotics can lead to a satisfactory resolution in much the same manner
20 Challenging Concepts in Urological Surgery
https://t.me/med1917
as acute prostatitis. However, it is more commonly the case that bacteria are not detected and chronic non- bacterial CP/ CPPS (category III) is therefore the most common form of prostatitis.
The treatment of CP/ CPPS is difficult, often unsatisfactory for patients, and should not be regarded as the purview of the urologist alone. Its effective management frequently requires the use of multiple modalities and multiple clinical disciplines with the primary focus being on symptomatic management. Early recognition of the need for a multimodality approach is perhaps the most important aspect of the modern- day management of this still very poorly understood condition.
References
1. Stamatiou K, Magri V, Perletti G, et al. Chronic prostatic infection: microbiological findings in two Mediterranean populations. Arch Ital Urol Androl. 2019;91(3):177– 181.
2. Barozzi L, Pavlica P, Menchi I, et al. Prostatic abscess: diagnosis and treatment. AJR Am J Roentgenol. 1998;170(3):753– 757.
3. Wen SC, Juan YS, Wang CJ, et al. Emphysematous prostatic abscess: case series study and review. Int J Infect Dis. 2012;16(5):e344– e349.
4. Papanicolaou N, Pfister RC, Stafford SA, Parkhurst EC. Prostatic abscess: imaging with transrectal sonography and MR. AJR Am J Roentgenol. 1987;149(5):981– 982.
5. Abdelmoteleb H, Rashed F, Hawary A. Management of prostate abscess in the absence of guidelines. Int Braz J Urol. 2017;43(5):835– 840.
6. Stamey TA. Prostatitis. J. R Soc Med. 1981;74(1):22– 40.
7. Krieger JN, Nyberg L Jr, Nickel JC. NIH consensus definition and classification of prostatitis. JAMA. 1999;282(3):236– 237.
8. Stamey TA, Govan DE, Palmer JM. The localisation and treatment of urinary tract infec­tions: the role of bactericidal urine levels as opposed to serum levels. Medicine (Baltimore). 1965;44:1– 36.
9. Nickel JC, Shoskes D, Wang Y, et al. How does the pre- massage and post- massage 2- glass test compare to the Meares- Stamey 4- glass test in men with chronic prostatitis/ chronic pelvic pain syndrome? J Urol. 2006;176(1):119– 124.
10. Charalabopoulos K, Karachalios G, Baltogiannis D, Charalabopoulos A, Giannakopoulos X, Sofikitis N. Penetration of antimicrobial agents into the prostate. Chemotherapy. 2003;49(6):269– 279.
11. Perletti G, Marras E, Wagenlehner FM, et al. Antimicrobial therapy for chronic bacterial prostatitis. Cochrane Database Syst Rev. 2013;8:CD009071.
12. Hu WL, Zhong SZ, He HX. Treatment of chronic bacterial prostatitis with amikacin through anal submucosal injection. Asian J Androl. 2002;4(3):163– 167.
13. Baert L, Leonard A. Chronic bacterial prostatitis: 10 years of experience with local anti­biotics. J Urol. 1988;140:755– 757.
14. Smart CJ, Jenkins JD, Lloyd RS. The painful prostate. Br J Urol. 1975;47(7):861– 869.
15. Górski A, Jońzyk- Matysiak E, Łusiak- Szelachowska M, et al. Phage therapy in prostatitis: re­cent prospects. Front Microbiol. 2018;9:1434.
16. Bowen DK, Dielubanza E, Schaeffer AJ. Chronic bacterial prostatitis and chronic pelvic pain syndrome. BMJ Clin Evid. 2015;2015:1802.
17. PontarI MA, Ruggieri MR. Mechanisms in prostatitis/ chronic pelvic pain syndrome. J Urol. 2004;172:839– 845.
18. Bullones Rodríguez MÁ, Afari N, Buchwald DS; National Institute of Diabetes and Digestive and Kidney Diseases Working Group on Urological Chronic Pelvic Pain. Evidence for overlap between urological and nonurological unexplained clinical conditions. J Urol. 2013;189(1 Suppl):S66– S74.
19. Roberts RO, Jacobson DJ, Girman CJ, Rhodes T, Lieber MM, Jacobsen SJ. Prevalence
https://t.me/med1917
of prostatitis- like symptoms in a community based cohort of older men. J Urol. 2002;168(6):2467– 2471.
20. Litwin MS, McNaughton- Collins M, Fowler FJ Jr, et al. The National Institutes of Health chronic prostatitis symptom index: development and validation of a new outcome measure. Chronic Prostatitis Collaborative Research Network. J Urol. 1999;162(2):369– 375.
21. Shoskes DA, Nickel JC, Dolinga R, Prots D. Clinical phenotyping of patients with chronic prostatitis/ chronic pelvic pain syndrome and correlation with symptom severity. Urology. 2009;73(3):538– 542.
22. Magri V, Wagenlehner F, Perletti G, et al. Use of the UPOINT chronic prostatitis/ chronic pelvic pain syndrome classification in European patient cohorts: sexual function domain improves correlations. J Urol. 2010;184(6):2339– 2345.
23. Gallo L. Effectiveness of diet, sexual habits and lifestyle modifications on treatment of chronic pelvic pain syndrome. Prostate Cancer Prostatic Dis. 2014;17(3):238– 245.
24. Rees J, Abrahams M, Doble A, Cooper A. Diagnosis and treatment of chronic bacterial pros­tatitis and chronic prostatitis/ chronic pelvic pain syndrome: a consensus guideline. BJU Int. 2015;116(4):509– 525.
25. Franco JVA, Turk T, Jung JH, et al. Pharmacological interventions for treating chronic prostatitis/ chronic pelvic pain syndrome: a Cochrane systematic review. BJU Int. 2020;125(4):490– 496.
26. Franco JV, Turk T, Jung JH, et al. Non- pharmacological interventions for treating chronic prostatitis/ chronic pelvic pain syndrome. Cochrane Database Syst Rev. 2018;5(5):CD012551.
27. Magri V, Boltri M, Cai T, et al. Multidisciplinary approach to prostatitis. Arch Ital Urol Androl. 2019;90(4):227– 248.
28. Nickel JC, Mullins C, Tripp DA. Development of an evidence- based cognitive behavioural treatment program for men with chronic prostatitis/ chronic pelvic pain syndrome. World J Urol. 2008;26(2):167– 172.
29. Wu C, Zhang Z, Lu Z, et al. Prevalence of and risk factors for asymptomatic inflammatory (NIH- IV) prostatitis in Chinese men. PLoS One. 2013;8(8):e71298.
30. Krušlin B, Tomas D, Džombeta T, Milković- Periša M, Ulamec M. Inflammation in prostatic hyperplasia and carcinoma— basic scientific approach. Front Oncol. 2017;7:77.
21Case 2 Prostatitis
https://t.me/med1917
https://t.me/med1917
SECTION 2
Urinary tract stones
Case 3 Renal stones
Case 4 Ureteric stones
Case 5 Bladder stone management