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Male Sexual Dysfunction

Site: EHC | Egyptian Health Council
Course: Urology Surgery Guidelines
Book: Male Sexual Dysfunction
Printed by: Guest user
Date: Tuesday, 24 December 2024, 4:59 AM

Description

"last update: 15 Oct 2024"  

- Acknowledgement

Guidelines Development Group (GDG) of Male Sexual Dysfunction committee.

1.     Prof

Abdel Rahman M. Zahran, MD Faculty of Medicine, Alexandria University

2.     Prof

AbdelNasser El Gamasy, Tanta University

3.     Prof

Ahmed Aly Morsy, Cairo University

4.     Prof

Ahmed El Taher, MD Faculty of Medicine, Assuit University

5.     Prof

Ahmed I. El-Sakka, MD (Chief) Faculty of Medicine, Suez Canal University

6.     Prof

Ahmed M. Al Adl, MD Faculty of Medicine, Benha university

7.     Prof

Emad A. Salem, MD Faculty of Medicine, Zagazig University

8.     Prof

Hisham Hammouda, Assiut University

9.     Prof

Khaled Mohyelden, MD Faculty of Medicine, Fayoum University

10.  Prof

Magdy S. El-Bahnasawy, MD Faculty of Medicine, Mansoura University

11.  Prof

Mamdouh M. El-Hawy MD Faculty of Medicine, Minia University

12.  Prof

Mohamed Ahmed Shalaby, Assiut University

13.  Prof

Mohamed Rafik El Halaby, Ain Shams University

14.  Prof

Mohamed Sherif Mourad, Ain Shams University (Chair of Panel)

15.  Prof

Mohammed Abdel-Rassoul, MD Faculty of Medicine, Cairo University

16.  Prof

Raouf M. Seyam King Faisal specialist hospital, Saudi

 Funding:

- No funding resources for the development of the guidelines.


- List of Abbreviations

Abbreviation

Description

AIPE

Arabic Index of Premature Ejaculation

ART

Assisted reproductive technology

AUA

American Urological Association

BSSM

British Society for Sexual Medicine

CCH

Collagenase Clostridium histolyticum

CDU

Color duplex ultrasonography

DE

Delayed Ejaculation

DM

Diabetes mellitus

EAU

European Association of Urology

ED

Erectile dysfunction

EDV

End diastolic velocity

EE

Electo-ejaculation

EMA

European Medicines Agency

eNOS

Endothelial nitric oxide synthase

ESWT

Extracorporeal Shockwave Therapy

FDA

Food and drug administration

FSH

Follicular Stimulating Hormone

ICI

Intracavernous injection

ICSI

Intracytoplasmic sperm injection

IELT

Intravaginal ejaculation latency time

IHD

Ischaemic heart disease

IIEF

Iinternational Index of Erectile Function

iNOS

Inducible nitric oxide synthase

ISSM

International Society of Sexual Medicine

IVF

In-vetro fertilization

LH

Luteinizing Hormone

LUTS

Lower urinary tract symptoms

nNOS

Neuronal nitric oxide synthase

NPT

Nocturnal penile tumescence

PD

Peyronie’s disease

PDE5Is

Phosphodiesterase type 5 inhibitors

PE

Premature ejaculation

PEDT

Premature Ejaculation Diagnostic Tool

PGE1

Prostaglandin E 1

PP

Penile prosthesis

PSA

Prostate-specific antigen

PSV

Peak systolic velocity

PVS

Penile vibratory stimulation

QoL

Quality of life

RI

Resistive index

RP

Radical prostatectomy

SCD

Sickle cell disease

SCI

Spinal cord injury

SCs

Stem cells

SSRIs

Selective serotonin reuptake inhibitors

TA

Tunica albuginea

TGF-β1

Transforming growth factor beta 1

VED

Vacuum erection device

VOD

Veno-occlusive dysfunction


- Glossary


1- Erectile Dysfunction (ED): The persistent or recurrent inability to attain and maintain an erection sufficient to permit satisfactory sexual performance.

2- Premature Ejaculation: Ejaculation that always or nearly always occurs prior to or within about one minute of vaginal penetration (lifelong PE) or a clinically significant and bothersome reduction in latency time, often to about three minutes or less (acquired PE).

3- Delayed Ejaculation: Marked delay in ejaculation or marked infrequency or absence of ejaculation on almost all or all occasions (75-100% of the times) of partnered sexual activity without the individual desiring delay persisting for at least 6 months and causing significant distress to the individual.

4- Peyronie’s Disease (PD) is a symptomatic disorder characterized by a constellation of penile symptoms and signs, such as penile pain, curvature, shortening, narrowing, hinge deformity, and palpable plaque with subsequent ED.

5- Priapism is a persistent penile erection for more than four hours and not related to sexual stimulation or relieved by ejaculation. Priapism carries high risk of structural damage to the cavernosal tissue which may lead to permanent ED.

4- Anejaculation: The complete absence of ejaculation either antegrade or retrograde. Caused by failed seminal emission from the seminal vesicles, prostate, and ejaculatory ducts into the urethra. In true anejaculation, there is normal orgasmic sensation and is always associated with central or peripheral nervous system dysfunction or with drugs.

5- Painful Ejaculation: is a condition in which the patient may feel variable degrees of pain during or after ejaculation involving the penis, scrotum, and perineum.

6- Haemospermia: is the presence of blood in the seminal fluid ejaculate. The condition causes anxiety and may indicate underlying pathology in many cases.

 


- Executive Summary


 Scope of the guidelines

Sexual health-related issues are wide-ranging and of importance to the overall health and sense of well-being for couples and families, and to the social and economic development of communities and countries. Erectile dysfunction (ED) and disorders of ejaculation are frequent encounters in male sexual medicine in the Middle East with the association of different risk factors and medical comorbidities in Arab region countries. Pharmacological therapies have completely changed the diagnostic and therapeutic approach to ED. This article integrates recent international guidelines with local experience and highlights the apparent lack of congruency between available treatment and communication, cultural, and gender norms of Middle East populations that may inhibit treatment seeking.

The Egyptian Urological Association (EUA) Male Sexual Dysfunction Guidelines aims to present the contemporary evidence for medical practice in Egypt for the diagnosis and treatment of patients suffering from sexual dysfunction.

Recommendations of the Male Sexual Dysfunction

Recommendations of Erectile Dysfunction:

1.  Obtain a thorough medical and sexual history for all patients. (Strong)

2. Use a validated questionnaire especially Arabic version (if available) related to ED to assess all sexual function domains and the effect of a specific treatment modality. (Strong)

3. Perform physical examination in the initial assessment of men with ED to identify underlying medical conditions and comorbid genital disorders that may be associated with ED (Strong).

4. Assess routine laboratory tests, including glucose-lipid profile and total testosterone, to identify and treat any reversible risk factors and lifestyle factors that can be modified. (Strong).

5. Consider specific diagnostic tests in the initial evaluation only in the presence of “Indications for specific diagnostic tests” (Strong).

6. Ensure Including changes in diet, increased physical activity, stop smoking, improve overall health at or before treatment of erectile dysfunction. (Strong)

7. Inform patients regarding approved PDE5Is, including discussion of benefits and risks/burdens. (Strong).

8. Use PDE5Is as first-line therapy. The dose should be titrated to provide optimal efficacy. (Strong)

9. Consider early rehabilitation programs (use of PDE5I and VED) post-RP may improve erectile function (Strong).

10. Inform patients that PDE5Is may be more effective if combined with testosterone therapy when indicated. (Strong).

11. Assess patients for, inadequate/incorrect prescriptions, poor sexual stimulation, and fat meals when not advised (Conditional).

12. Discuss benefits and risks/burdens regarding the use of VED, especially in well-informed older patients with infrequent sexual intercourse and comorbidity requiring non-invasive, drug-free management of ED (Conditional)

13. Perform an in-office injection test. Home therapy after positive office ICI test (Conditional).

14. Alprostadil (PGE1) is the best agent however its cost is a limitation. (Conditional)

15. Use low intensity shockwave treatment (LI-SWT) in patients not candidate for oral vasoactive treatment or non-responders to PDE5Is (Conditional)

16. Intracavernosal stem cell therapy should be considered investigational for treatment of ED (Conditional)

17. Intracavernosal Platelet Rich Plasma should be considered investigational for ED treatment (Conditional)

18. Botulinum Neurotoxin A (BoNT-A): Should be considered investigational for treatment of ED (Conditional).

19. Surgery should be reserved for men in whom less invasive reversible treatment has not succeeded or is contraindicated or undesirable. Strong

20.  Arterial revascularization surgery is offered only to select patients with ED who meet strict clinical and radiographic criteria for surgical success. (Strong)

21. Vascular surgery for veno-occlusive dysfunction is no longer recommended. Strong

22.  Use implantation of a penile prosthesis as third-line therapy if other treatments fail or based upon patient preference Strong.

Recommendations of Premature Ejaculation (PE)

23. Obtain medical and sexual history to diagnose and classify PE, which should include assessment of intravaginal ejaculatory latency time (IELT) (self-estimated), perceived control, distress, and interpersonal difficulty due to the ejaculatory dysfunction. Strong

24. Perform physical examination in the initial assessment of PE to identify anatomical abnormalities that may be associated with PE or other sexual dysfunctions, particularly erectile dysfunction (ED). Strong.

25. Use the patient-reported outcomes tools: Premature Ejaculation Diagnostic Tool (PEDT) and Arabic Index of Premature Ejaculation (AIPE) in daily clinical practice. (Conditional)

26. Laboratory or neuro-physiological tests are not routine. They should only be directed by specific findings from history or physical examination. Strong.

27. Define the subtype of PE and discuss patient’s expectations thoroughly before starting any treatment. Strong.

28. Treat the underlying cause (e.g., ED, prostatitis, LUTS, anxiety, hyperthyroidism) as the initial goal for patients with acquired PE. Strong.

29. Consider pharmacotherapy as the first-line treatment for patients with lifelong PE i.e. dapoxetine Strong.

30. The use of off-label topical anaesthetic agents i.e. the lidocaine/prilocaine spray is suggested as a viable alternative to oral treatment with SSRIs. (Conditional)

31. Use psychological/behavioural therapies in combination with pharmacological treatment in the management of acquired PE. (Conditional).

32.  Use various behavioural techniques in treating variable and subjective PE (Strong).

33. The on-demand Tramadol is a weak alternative to SSRIs. (Conditional).

34. PDE5Is alone or in combination with other therapies in patients with PE (without ED) may be used. (Conditional).

Recommendations for Delayed Ejaculation (DE)

35. Perform a thorough analysis of the complaint to exclude misdiagnosed other sexual dysfunctions stressing on anorgasmia Strong.

36. Obtain a detailed medical and sexual history to exclude risk factors (medications especially SSRIs, antipsychotics, drug abuse, DM, depression, LUTS, etc) Strong.

37. Define if DE is lifelong or acquired, global or situational. Strong.

38. Assess intravaginal ejaculatory latency time (IELT) (self-estimated) (Conditional).

39. Include physical examination in the initial assessment of DE to identify hypogonadism or anatomical abnormalities that may be associated with DE or other sexual dysfunctions, particularly erectile dysfunction Strong.

40. Request post-coital first voided urine sample to exclude retrograde ejaculation Strong.

41. Use specific questionnaires, specialized laboratory tests and radiologic investigation when indicated only. (Conditional).

42. If acquired DE, consider stopping or modifying underlying incriminated drug regimen. Strong.

43. Improving erectile function and maximizing stimulation may trigger ejaculation. (Conditional).

44. Psychosexual therapy can be particularly helpful in primary DE. (Conditional)

45. Testosterone replacement in hypogonadal patients may improve DE. (Conditional)

46. Cabergoline and bupropion could be beneficial for some cases of delayed ejaculation. (Conditional).

47. Use PDE5I treatment significantly improved ejaculation and orgasm Strong.

48. Sympathetic α1 receptor agonists may help ejaculation with variable success rates in non-SCI patients. (Conditional)

49. Use penile vibratory stimulation or electro-ejaculation for sperm retrieval in patients with fertility issues and SCI. Strong.

Recommendations for Peyronie’s Disease (PD)

50. Obtain a detailed history with specific emphasis on various characteristics of PD, such as onset, duration, course, pain, deformity, and ED. (Strong)

51. Perform physical examination, include assessment of palpable plaques, penile length, extent of curvature (self-photograph, or pharmacological-induced erection). Strong.

52. Do not use specific PD questionnaire, ultrasound measurement of plaque size in everyday clinical practice. (Conditional).

53.  erform proper pre-operative counselling including the available treatment options and the known benefits and risks of each treatment, and the patient expectation will reduce post treatment patient dissatisfaction. (Strong)

54.  Use conservative treatment in patients not fit for surgery or when surgery is not acceptable to the patient. (Conditional).

55.  Consider that intralesional collagenase injection has shown some outcome benefits in PD management. (Strong).

56. Offer extracorporeal shockwave treatment in the active stage of the disease may alleviate penile pain. Do not use extracorporeal shockwave treatment to improve penile curvature and reduce plaque size. (Conditional).

57.  Offer penile traction devices and vacuum devices may reduce penile deformity and increase penile length. (Conditional).

58.  Do not use oral treatment with vitamin E and tamoxifen for signifiant reduction in penile curvature or plaque size. (Strong).

59.    Do not offer other oral treatments in chronic phase of PD (acetyl esters of carnitine, pentoxifylline, colchicine). (Conditional).

60.    Perform surgery only when PD has been stable for at least three months (without pain or deformity deterioration), which is usually the case after twelve months from the onset of symptoms. Strong.

61.    Assess penile length, curvature severity, erectile function (including response to pharmacotherapy in case of ED) and patients’ expectations prior to surgery. Strong.

62.    Use tunical shortening procedures, especially plication techniques as the first treatment option for PD with adequate penile length, curvature < 60°, absence of special deformities (hourglass, hinge) and adequate erection. Strong.

63.    Use grafting techniques for patients with PD with less than adequate penile length, curvature > 60º, presence of special deformities (hourglass, hinge) and adequate erection. (Strong).

64.    Use penile prosthesis implantation, with or without any additional procedure (modelling, plication, relaxing parallel incisions, grafting), in PD patients with ED not responding to pharmacotherapy. Strong.

Recommendations for Priapism

65.    Obtain thorough history, is important in making diagnosis, etiology and type of priapism. Strong

66.    Perform physical examination of the genitalia, the perineum and the abdomen. Strong.

67.    Include laboratory investigations, complete blood count, coagulation profile and arterial blood gases. Strong.

68.    Perform color duplex ultrasound of the penis and perineum for the differentiation between ischemic and non-ischemic priapism. Strong.

69.    Use magnetic resonance imaging of the penis to predict smooth muscle viability in prolonged ischemic priapism. (Strong).

70.    Perform selected pudendal arteriogram when embolization is planned for the management of non-ischemic priapism. Strong.

71.    Start management of ischaemic priapism as early as possible (within four to six hours) and follow a stepwise approach. Strong.

72.    First, decompress the corpora cavernosa by penile aspiration until fresh red blood is obtained. (Conditional).

73.    Proceed to the next step, which is ICI of a sympathomimetic drug, in priapism that persists despite aspiration. Strong.

74.    Repeat injections and aspiration for at least up to 1 hour prior to proceeding with surgical intervention in patients presenting with a priapism of less than 24 hours. Strong.

75.    Consider more immediate surgical intervention in ischemic priapism of extended durations (typically greater than 72h), is unlikely to resolve with ICI therapy alone. Strong.

76.    Perform distal shunt surgical procedures. Result of proximal procedures in case of failure is questionable. Strong.

77.    Consider insertion of a penile prosthesis only if priapism episode is > 36 hours, or in cases for which all other interventions have failed. Strong.

Recommendations for the treatment of non-ischemic priapism

78.    Non-ischaemic priapism is not an emergency, perform definitive management at the discretion of the treating physician. (Conditional)

79.    Perform superselective arterial embolization, using temporary material for recurrent nonischaemic priapism Strong

80.    Repeat the procedure with temporary or permanent material for recurrent nonischaemic priapism following selective arterial embolization. (Conditional)

81.    Reserve selective surgical ligation of a fistula as a final treatment option when embolization has failed. (Conditional).

Recommendations for the treatment of Stuttering priapism

82.    Treatment of Stuttering priapism, manage each acute episode similar to that for ischaemic priapism. (Conditional).

83.    Use hormonal therapies (mainly gonadotropin-receptor hormone agonists or antagonists) and/or anti-androgens for the prevention of future episodes in patients with frequent relapses of stuttering priapism. Do not use them before sexual maturation is reached. (Conditional)

84.    Initiate treatment with phosphodiesterase type 5 inhibitors in stuttering priapism only when the penis is in its flaccid state.  (Conditional).

85.    Use digoxin, α-adrenergic agonists, baclofen, gabapentin, or terbutaline only in patients with very frequent and uncontrolled relapses stuttering priapism. (Conditional).

86.    Use intracavernous self-injections at home of sympathomimetic drugs until ischaemic priapism has been alleviated. (Conditional).


- Introduction, purpose, scope, and audience

➡️Introduction

Strategies for diagnosis and treatment of male sexual problems should consider the sociocultural factors that influence diagnosis and treatment seeking and engagement behaviours necessary for successful outcomes. Specifically, the detrimental effects of sexual problems on quality of life and the potential benefits of proper diagnosis and treatment should be more widely communicated to diminish the social disgrace associated with sexual problems and their management.

Erectile dysfunction (ED) and premature ejaculation (PE) are the two main complaints in male sexual medicine in the Middle East (1-2). Pharmacological therapies have completely changed the diagnostic and therapeutic approach to ED (3,4). The prevalence of ED is 20–90% among patients with different risk factors and medical comorbidities in Arab region countries and severe ED in patients in this region could be attributed to: (1) the high prevalence of risk factors; (2) the poor control of those risk factors; (3) the delay in seeking medical advice; and (4) the non-compliance with treatment (1-2). Unfortunately, in Arab countries there are no firm data on the true prevalence of sexual dysfunction.  This prompted several investigators in the region to conduct research to identify the magnitude of the current problem (1-2).

This article integrates recent international guidelines with local experience and also highlights the apparent lack of congruency between available treatment and communication, cultural, and gender norms of Middle East populations that may inhibit treatment seeking. We clarified in our recent publication that strategies for diagnosis and treatment should consider the sociocultural factors that influence diagnosis and treatment seeking and engagement behaviours necessary for successful outcomes. Specifically, the detrimental effects of sexual problems on quality of life and the potential benefits of proper diagnosis and treatment should be more widely communicated to diminish the social disgrace associated with sexual problems and their management (5).

Sexual dysfunction issues unique to our region:

 Infertility and sexual dysfunction: Infertility is negatively linked to sexuality in couples seeking assisted reproductive technology (ART), suggesting the need for integrated management of psychosexual problems (6). Unique to infertile couples in Egypt, like the Arab and Muslim world, the option of donor insemination is not accepted. The challenge of unsuccessful fertility issues in Egyptians may even further have a detrimental effect on the couple's sexual function. Infertility and sexual dysfunction are associated (7). Lack of sexual awareness and education contribute to this problem. Psychosexual management is warrantied in these couples.

 Unconsummated marriage: A specific situation urologist face in our region is unconsummated marriage. It is a social challenge for the man to deal with his wife's virginity on the wedding night. Such stress may lead to performance anxiety and failure, accumulating into a full-blown ED situation in an otherwise healthy young man. Unconsummated marriage might occur in men with normal erection due to other causes as premature ejaculation, performance anxiety, lack of desire, hypogonadism, lack of knowledge, social pressure, and female factors (8,9). The most common female factor was vaginismus (10). Particular to our regions, male lack of sexual desire may be related to consanguinity (11).

Polygamy, motives, and sexual dysfunction: Egypt is among the countries where polygamy is legal (12). Polygamy has a psychosexual impact on the first wife, impacting intimacy with her husband and negatively affecting the dynamics of the family that is peculiar to these parts of the world (13). Non-monogamous female drive to sex includes coping mechanisms to keep the partner, maintain self-esteem, and seek higher levels of sexual pleasure (14). Men seek polygamy for a variety of reasons. For example, in a Turkish study, men reported that they had a second wife because of decreased satisfaction of sexual desires by a wife, falling in love with the second wife, and incompatibility with the first wife (15). In the Asian community, a prevalent polygamous practice has many underlying factors (16). These include prestige, economic advantage, social customs, and exposure to commercial sex. While polygamy may negatively affect wives and children, a couple of studies showed that polygamous men have less ED, less premature ejaculation, lower depression scores, and higher sexual satisfaction (15,17).

Other male sexual problems include Premature Ejaculation: Ejaculation that always or nearly always occurs prior to or within about one minute of vaginal penetration (lifelong PE) or a clinically significant and bothersome reduction in latency time, often to about three minutes or less (acquired PE). Delayed Ejaculation: Marked delay in ejaculation or marked infrequency or absence of ejaculation on almost all or all occasions (75-100% of the times) of partnered sexual activity without the individual desiring delay persisting for at least 6 months and causing significant distress to the individual. Peyronie’s Disease (PD) is a symptomatic disorder characterized by a constellation of penile symptoms and signs, such as penile pain, curvature, shortening, narrowing, hinge deformity, and palpable plaque with subsequent ED. Priapism is a persistent penile erection for more than four hours and not related to sexual stimulation or relieved by ejaculation. Priapism carries high risk of structural damage to the cavernosal tissue which may lead to permanent ED.

➡️Purpose

The Urologic Egyptian Guidelines on Male Sexual Dysfunction aim to present the contemporary evidence for medical practice in Egypt for the diagnosis and treatment of patients suffering from sexual dysfunction.

➡️Scope

The Urologic Egyptian Guidelines on Male Sexual Dysfunction help and guide clinical practitioners to have knowledge of the incidence, pathophysiology, and strategies for diagnosis and treatment of male sexual problems. This document integrates recent international guidelines with local experts’ opinions based on Egyptian healthcare and socioeconomic circumstances. It also reflects the opinions of experts in Sexual Dysfunction and represents state-of-the art references for all clinicians, as of the publication date.

➡️Target audience

The target audience refers to those that deliver or implement the recommendations as well as health policymakers and other stakeholders involved in the adoption, adaptation, and transfer of health policies. The target audience of the guideline should not be misunderstood with the beneficiaries of the interventions or target population described in the guideline.

·  Urologists

·  Dermatologists and Andrologists

·  Family medicine and general practitioners

·  Gynaecologists, psychiatrists and endocrinologists


- Methods

A comprehensive search for guidelines was undertaken to identify the most relevant guidelines to consider for adaptation.

Inclusion/exclusion criteria followed in the search and retrieval of guidelines to be adapted:

• Selecting only evidence-based guidelines (guideline must include a report on systematic literature searches and explicit links between individual recommendations and their supporting evidence)

• Selecting only national and/or international guidelines

• Specific range of dates for publication (using Guidelines published or updated 2015 and later)

•  Selecting peer reviewed publications only

•  Selecting guidelines written in English language

•  Excluding guidelines written by a single author not on behalf of an organization in order to be valid and comprehensive, a guideline ideally requires multidisciplinary input

• Excluding guidelines published without references as the panel needs to know whether a thorough literature review was conducted and whether current evidence was used in the preparation of the recommendations

The following characteristics of the retrieved guidelines were summarized in a table:

• Developing organisation/authors

• Date of publication, posting, and release

• Country/language of publication

• Date of posting and/or release

• Dates of the search used by the source guideline developers

All retrieved Guidelines were screened and appraised using AGREE II instrument (www.agreetrust.org) by at least two members. the panel decided a cut-off point or rank the guidelines (any guideline scoring above 50% on the rigour dimension was retained).

Evidence assessment.

According to WHO handbook for Guidelines we used the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach to assess the quality of a body of evidence, develop and report recommendations (18, 19). GRADE methods are used by WHO because these represent internationally agreed standards for making transparent recommendations. Detailed information on GRADE is available on the following sites:

• GRADE working group: http://www.gradeworkingroup.org

• GRADE online training modules: http://cebgrade.mcmaster.ca/ 

• GRADE profile software: http://ims.cochrane.org/revman/gradepro

Table 1 Quality of evidence in GRADE


Table 2 Significance of the four levels of evidence

Table 3: Factors that determine How to upgrade or downgrade the quality of evidence


The strength of the recommendation.

The strength of a recommendation communicates the importance of adherence to the recommendation.

Strong recommendations.

With strong recommendations, the guideline communicates the message that the desirable effects of adherence to the recommendation outweigh the undesirable effects. This means that in most situations the recommendation can be adopted as policy.

Conditional recommendations.

These are made when there is greater uncertainty about the four factors above or if local adaptation has to account for a greater variety in values and preferences, or when resource use makes the intervention suitable for some, but not for other locations. This means that there is a need for substantial debate and involvement of stakeholders before this recommendation can be adopted as policy.

When not to make recommendations.

When there is lack of evidence on the effectiveness of an intervention, it may be appropriate not to make a recommendation.

Databases searched included four resource categories:

1. Four international guidelines and recommendations, namely European Association of Urology [EAU], American Urological Association Guidelines [AUA], British Society for Sexual Medicine [BSSM], International Society of Sexual Medicine [ISSM] (20 – 24).

2. Review of several guides, reviews, statements, recommendations, and standards (23 – 25).

3. Relevant Egyptian publications.

4. A panel of 10 high-calibre urologists and andrologists representing different universities, institutions and private practice in Egypt.

Adaptation of the Egyptian cultural aspects, the level of urologists’ capabilities and the availability of well-equipped hospitals were considered in the methodology of diagnosis and different treatment modalities.

 


- Recommendations


Recommendations for the diagnosis of Erectile Dysfunction:

Recommendations (20-24, 28-41)

GRADE Level of certainty

Strength Rating

1- Obtain a thorough medical and sexual history for all patients.

High

(28-32)

(Strong)

2- Use a validated questionnaire especially Arabic version (if available) related to ED to assess all sexual function domains and the effect of a specific treatment modality.

High

(28- 30)

(Strong)

3- Perform physical examination in the initial assessment of men with ED to identify underlying medical conditions and comorbid genital disorders that may be associated with ED.

High

(33 – 34)

(Strong)

4- Assess routine laboratory tests, including glucose-lipid profile and total testosterone, to identify and treat any reversible risk factors and lifestyle factors that can be modified.

High

(35-39)

Strong)

5- Consider specific diagnostic tests in the initial evaluation only in the presence of “Indications for specific diagnostic tests”.

High

(20-24, 35-41)

(Strong)

Recommendations for treatment of ED

GRADE Level of certainty

Strength Rating

6-  Ensure Including changes in diet, increased physical activity, stop smoking, improve overall health at or before treatment of erectile dysfunction.

High

(5, 42,43)

Strong

7-  Inform patients regarding approved PDE5Is, including discussion of benefits and risks/burdens.

High

(20-24, 42, 44-48)

Strong

8- Use PDE5Is as first-line therapy. The dose should be titrated to provide optimal efficacy.

High (20-24, 42, 44-48)

Strong

9-  Consider early rehabilitation programs (use of PDE5I and VED) post-RP may improve erectile function.

Moderate

(20-24, 49-56)

Strong

10-   Erectile Dysfunction and hypogonadism: Inform patients that PDE5Is may be more effective if combined with testosterone therapy when indicated.

Moderate

(20-24, 57,58)

Strong

11-   PDE5Is failure in patients with ED: Assess patients for, inadequate/incorrect prescriptions, poor sexual stimulation, and fat meals when not advised.

Low

(20-24, 44-48, 59-61)

Conditional

12-   Discuss benefits and risks/burdens regarding the use of VED, especially in well-informed older patients with infrequent sexual intercourse and comorbidity requiring non-invasive, drug-free management of ED.

Low

(20-24, 62, 63)

Conditional

13-   Perform an in-office injection test. Home therapy after positive office ICI test

Low

(20-24, 57, 64)

Conditional

14-   Alprostadil (PGE1) is the best agent however its cost is a limitation.

Low (57)

Conditional

15- Use low intensity shockwave treatment (LI-SWT) in patients not candidate for oral vasoactive treatment or non-responders to PDE5Is.

Low

(20-24, 65-75)

Conditional

16- Intracavernosal stem cell therapy should be considered investigational for treatment of ED

Low

(20-24)

Conditional

17-   Intracavernosal Platelet Rich Plasma should be considered investigational for ED treatment

Low

(20, 76-83)

Conditional

18-   Botulinum Neurotoxin A (BoNT-A): Should be considered investigational for treatment of ED

Low

(20, 84-87)

Conditional

Recommendations for Surgical treatment

 

 

19-   Surgery should be reserved for men in whom less invasive reversible treatment has not succeeded or is contraindicated or undesirable.

High

(20-24)

Strong

20-   Arterial revascularization surgery is offered only to select patients with ED who meet strict clinical and radiographic criteria for surgical success.

Moderate (88-90)

Strong

21-   Vascular surgery for veno-occlusive dysfunction is no longer recommended.

High

(20-24, 91)

Strong

22-   Use implantation of a penile prosthesis as third-line therapy if other treatments fail or based upon patient preference.

High

(92-100)

Strong

 

Clinical Indicators for monitoring:

1. Thorough medical and sexual history using a validated questionnaire especially Arabic version.

2. Focused physical examination.

3. Testosterone and lipid profile.

4. Consider specific diagnostic tests when indicated.

 

Recommendation for assessment and management of Premature Ejaculation

Recommendation

GRADE Level of certainty

Strength Rating

23-   Obtain medical and sexual history to diagnose and classify PE, which should include assessment of intravaginal ejaculatory latency time (IELT) (self-estimated), perceived control, distress, and interpersonal difficulty due to the ejaculatory dysfunction.

High

(101-103)

Strong

24-   Perform physical examination in the initial assessment of PE to identify anatomical abnormalities that may be associated with PE or other sexual dysfunctions, particularly erectile dysfunction (ED).

High

(101-103)

Strong

25-   Use the patient-reported outcomes tools: Premature Ejaculation Diagnostic Tool (PEDT) and Arabic Index of Premature Ejaculation (AIPE) in daily clinical practice.

Low

(104)

Conditional 

26-   Laboratory or neuro-physiological tests are not routine. They should only be directed by specific findings from history or physical examination.

High

(101-103)

Strong

27-   Define the subtype of PE and discuss patient’s expectations thoroughly before starting any treatment.

High

(101-103)

Strong

28-   Treat the underlying cause (e.g., ED, prostatitis, LUTS, anxiety, hyperthyroidism) as the initial goal for patients with acquired PE

High

(104)

Strong

29-   Consider pharmacotherapy as the first-line treatment for patients with lifelong PE i.e. dapoxetine

High

(104-106)

Strong

30-   The use of off-label topical anesthetic agents i.e. the lidocaine/prilocaine spray is suggested as a viable alternative to oral treatment with SSRIs.

Moderate

(104-106)

Conditional  

31-   Use psychological/behavioural therapies in combination with pharmacological treatment in the management of acquired PE

Low (104-106)

Conditional

32-   Use various behavioural techniques in treating variable and subjective PE

Moderate

(104-106)

Strong

33-   The on-demand Tramadol is a weak alternative to SSRIs.

Low

(104-106)

Conditional

34-   PDE5Is alone or in combination with other therapies in patients with PE (without ED) may be used.

Low

(104-106)

Conditional

 

Clinical Indicators for monitoring:

1. Medical and sexual history to diagnose and classify PE, use the patient-reported outcomes tools.

2. Focused physical examination.

3. Routine laboratory with seminal fluid culture and sensitivity to exclude underlying cause in patients with acquired PE

 

Recommendations for assessment of Delayed Ejaculation (107-109)

Recommendation

GRADE Level of certainty

Strength Rating

35-   Perform a thorough analysis of the complaint to exclude misdiagnosed other sexual dysfunctions stressing on anorgasmia

High

107

Strong

36-   Obtain a detailed medical and sexual history to exclude risk factors (medications especially SSRIs, antipsychotics, drug abuse, DM, depression, LUTS, etc)

High 107

Strong

37-   Define if DE is lifelong or acquired, global or situational.

High

107

Strong

38-   Assess intravaginal ejaculatory latency time (IELT) (self-estimated)

Low

(108-109)

Conditional

39-   Include physical examination in the initial assessment of DE to identify hypogonadism or anatomical abnormalities that may be associated with DE or other sexual dysfunctions, particularly erectile dysfunction

High

(108-109)

Strong

40-   Request post-coital first voided urine sample to exclude retrograde ejaculation.

High

(108-109)

Strong

41-   Use specific questionnaires, specialized laboratory tests and radiologic investigation when indicated only.

Low

(108-109)

Conditional

42-   If acquired DE, consider stopping or modifying underlying incriminated drug regimen.

High

(108-109)

Strong

43-   Improving erectile function and maximizing stimulation may trigger ejaculation.

Low (108-109)

Conditional

44-   Psychosexual therapy can be particularly helpful in primary DE.

Low (108-109)

Conditional

45-   Testosterone replacement in hypogonadal patients may improve DE.

Low (108-109)

Conditional

46-   Cabergoline and bupropion could be beneficial for some cases of delayed ejaculation.

Low (108-109)

Conditional

47-   Use PDE5I treatment significantly improved ejaculation and orgasm.

High

(107-109)

Strong

48-   Sympathetic α1 receptor agonists may help ejaculation with variable success rates in non-SCI patients.

Low (108-109)

Conditional

49-   Use penile vibratory stimulation or electro-ejaculation for sperm retrieval in patients with fertility issues and SCI.

High (108-109)

Strong

 

Clinical Indicators for monitoring:

1. Medical and sexual history with intravaginal ejaculatory latency time (IELT).

2.  Focused physical examination.

3. Define if DE is lifelong or acquired, global or situational.

4. Specialized laboratory tests and radiologic investigation when indicated only. 

Recommendations for evaluation and management of Peyronie’s Disease (PD):

Recommendations

GRADE Level of certainty

Strength Rating

50.    There is currently no international standard evaluation and treatment for PD and a detailed history should be obtained with specific emphasis on various characteristics of PD, such as onset, duration, course, pain, deformity, ED.

Moderate (20-24, 110-113)

Strong

51.    Physical examination, include assessment of palpable plaques, penile length, extent of curvature (self-photograph, or pharmacological-induced erection).

High (20-24, 110-113)

Strong

52.    Do not use specific PD questionnaire, ultrasound measurement of plaque size in everyday clinical practice.

Low

114

Conditional

53.    Proper pre-operative counselling including the available treatment options and the known benefits and risks of each treatment, and the patient expectation will reduce post treatment patient dissatisfaction.

Moderate

(86,114,115,116)

Strong

54.    Use conservative treatment in patients not fit for surgery or when surgery is not acceptable to the patient.

Low (114,115,116)

Conditional

55.    Intralesional collagenase injection has shown some outcome benefits in PD management.

Moderate

(116)

Strong

56.    Extracorporeal shockwave treatment may only be offered in the active stage of the disease to alleviate penile pain. Do not use extracorporeal shockwave treatment to improve penile curvature and reduce plaque size.

Low

(115)

Conditional

57.    Use penile traction devices and vacuum devices to reduce penile deformity and increase penile length.

Low

(114)

Conditional

58.    Do not use oral treatment with vitamin E and tamoxifen for significant reduction in penile curvature or plaque size.

High

(20-24, 114)

Strong

59.    Do not offer other oral treatments in chronic phase of PD (acetyl esters of carnitine, pentoxifylline, colchicine).

Low (114)

Conditional

60.    Perform surgery only when PD has been stable for at least three months (without pain or deformity deterioration), which is usually the case after twelve months from the onset of symptoms.

High (20-24, 117,118)

Strong

61.    Prior to surgery, assess penile length, curvature severity, erectile function (including response to pharmacotherapy in case of ED) and patient expectations.

High

(20-24, 117,118)

Strong

62.    Use tunical shortening procedures, especially plication techniques as the first treatment option for PD with adequate penile length, curvature < 60°, absence of special deformities (hourglass, hinge) and adequate erection.

High

(20-24, 117,118)

Strong

63.    Use grafting techniques for patients with PD with less than adequate penile length, curvature > 60º, presence of special deformities (hourglass, hinge) and adequate erection.

Moderate

(20-24, 117,118)

Strong

64.    Use penile prosthesis implantation, with or without any additional procedure (modelling, plication, relaxing parallel incisions, grafting), in PD patients with ED not responding to pharmacotherapy.

High

(20-24, 117,118)

Strong

 

Clinical Indicators for monitoring:

1. Medical and sexual history.

2. Focused physical examination (self-photograph, or pharmacological-induced erection).

3. Penile length, curvature severity, and erectile function.

 

Recommendations for diagnosis of ischemic priapism

Recommendation

GRADE Level of certainty

Strength Rating

65.    Obtain thorough history, is important in making diagnosis, etiology and type of priapism.

High

(119-122)

Strong

66.    Perform physical examination of the genitalia, the perineum and the abdomen.

High (119-122)

Strong

67.    Include laboratory investigations, complete blood count, coagulation profile and arterial blood gases.

High

(119-122)

Strong

68.    Perform color duplex ultrasound of the penis and perineum for the differentiation between ischemic and non-ischemic priapism.

High (119-122)

Strong

69.    Use magnetic resonance imaging of the penis to predict smooth muscle viability in prolonged ischemic priapism.

Moderate (119-122)

Strong

70.    Perform selected pudendal arteriogram when embolization is planned for the management of non-ischemic priapism.

High (119-122)

Strong

 

 Recommendations for the treatment of ischemic priapism:

Recommendations

GRADE Level of certainty

Strength Rating

71.    Start management of ischaemic priapism as early as possible (within four to six hours) and follow a stepwise approach.

High (119-122)

Strong

72.    First, decompress the corpora cavernosa by penile aspiration until fresh red blood is obtained.

Low

(119)

Conditional

73.    Proceed to the next step, which is ICI of a sympathomimetic drug, in priapism that persists despite aspiration.

High (119-122)

Strong

74.    Repeat injections and aspiration for at least up to 1 hour prior to proceeding with surgical intervention in patients presenting with a priapism of less than 24 hours.

High (119-122)

Strong

75.    Consider more immediate surgical intervention in ischemic priapism of extended durations (typically greater than 72h), is unlikely to resolve with ICI therapy alone.

High

(119-122)

Strong

76.    Perform distal shunt surgical procedures. Result of proximal procedures in case of failure is questionable.

High (119-122)

Strong

77.    Consider insertion of a penile prosthesis only if priapism episode is > 36 hours, or in cases for which all other interventions have failed.

High

(119-122)

Strong

 

Recommendations for the treatment of non-ischemic priapism

Recommendations

GRADE Level of certainty

Strength Rating

78.    Perform definitive management at the discretion of the treating physician, because non-ischaemic priapism is not an emergency.

Low (123-126)

Conditional

79.    Perform superselective arterial embolization, using temporary material.

High

(20-24)

Strong

80.    Repeat the procedure with temporary or permanent material for recurrent nonischaemic priapism following selective arterial embolization.

Low (123-126)

Conditional

81.    Reserve selective surgical ligation of a fistula as a final treatment option when embolization has failed.

Low (123-126)

Conditional

 

 Recommendations for the treatment of Stuttering priapism

Recommendations

GRADE Level of certainty

Strength Rating

82.    Treatment of Stuttering priapism, manage each acute episode similar to that for ischaemic priapism.

Low (119-121)

Conditional

83.    Use hormonal therapies (mainly gonadotropin-receptor hormone agonists or antagonists) and/or anti-androgens for the prevention of future episodes in patients with frequent relapses of stuttering priapism. Do not use them before sexual maturation is reached.

Low (119-121)

Conditional

84.    Initiate treatment with phosphodiesterase type 5 inhibitors in stuttering priapism only when the penis is in its flaccid state.

High

(119)

Conditional

85.    Use digoxin, α-adrenergic agonists, baclofen, gabapentin, or terbutaline only in patients with very frequent and uncontrolled relapses stuttering priapism.

Low (119-121)

Conditional

86.    Use intracavernous self-injections at home of sympathomimetic drugs until ischaemic priapism has been alleviated.

Low (119-121)

Conditional

 

Clinical Indicators for monitoring:

1. Medical and sexual history.

2. Focused physical examination.

3. laboratory investigations, complete blood count, coagulation profile and arterial blood gases.

4. Color duplex ultrasound of the penis and perineum


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65-  Capogrosso P, Frey A, Jensen CFS, Rastrelli G, Russo GI, Torremade J, Albersen M, Gruenwald I, Reisman Y, Corona G. Low-Intensity Shock Wave Therapy in Sexual Medicine-Clinical Recommendations from the European Society of Sexual Medicine (ESSM). J Sex Med. 2019 Oct;16(10):1490-1505. doi: 10.1016/j.jsxm.2019.07.016. Epub 2019 Aug 22. PMID: 31447380.

66- Chung E, Cartmill R. Evaluation of clinical efficacy, safety and patient satisfaction rate after low-intensity extracorporeal shockwave therapy for the treatment of male erectile dysfunction: an Australian first open-label single-arm prospective clinical trial. BJU Int. 2015 Apr;115 Suppl 5:46-9. doi: 10.1111/bju.13035. PMID: 25828173.

67-  Young Academic Urologists Men's Health Group; Fode M, Hatzichristodoulou G, Serefoglu EC, Verze P, Albersen M. Low-intensity shockwave therapy for erectile dysfunction: is the evidence strong enough? Nat Rev Urol. 2017 Oct;14(10):593-606. doi: 10.1038/nrurol.2017.119. Epub 2017 Jul 25. PMID: 28741629.

68-  Sokolakis I, Hatzichristodoulou G. Clinical studies on low intensity extracorporeal shockwave therapy for erectile dysfunction: a systematic review and meta-analysis of randomised controlled trials. Int J Impot Res. 2019 May;31(3):177-194. doi: 10.1038/s41443-019-0117-z. Epub 2019 Jan 21. PMID: 30664671.

69- Kalyvianakis D, Hatzichristou D. Low-Intensity Shockwave Therapy Improves Hemodynamic Parameters in Patients With Vasculogenic Erectile Dysfunction: A Triplex Ultrasonography-Based Sham-Controlled Trial. J Sex Med. 2017 Jul;14(7):891-897. doi: 10.1016/j.jsxm.2017.05.012. Erratum in: J Sex Med. 2018 Feb;15(2):270. PMID: 28673433.

70-  Tao R, Chen J, Wang D, Li Y, Xiang J, Xiong L, Ji J, Wu J, Zhou S, Jia C, Lv J, Yang J, Tang Q. The Efficacy of Li-ESWT Combined With VED in Diabetic ED Patients Unresponsive to PDE5is: A Single-Center, Randomized Clinical Trial. Front Endocrinol (Lausanne). 2022 Jun 23;13:937958. doi: 10.3389/fendo.2022.937958. PMID: 35813628; PMCID: PMC9259797.

71- Mykoniatis I, Pyrgidis N, Zilotis F, Kapoteli P, Fournaraki A, Kalyvianakis D, Hatzichristou D. The Effect of Combination Treatment With Low-Intensity Shockwave Therapy and Tadalafil on Mild and Mild-To-Moderate Erectile Dysfunction: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial. J Sex Med. 2022 Jan;19(1):106-115. doi: 10.1016/j.jsxm.2021.10.007. Epub 2021 Dec 2. PMID: 34866029.

72-  Kalyvianakis D, Mykoniatis I, Pyrgidis N, Kapoteli P, Zilotis F, Fournaraki A, Hatzichristou D. The Effect of Low-Intensity Shock Wave Therapy on Moderate Erectile Dysfunction: A Double-Blind, Randomized, Sham-Controlled Clinical Trial. J Urol. 2022 Aug;208(2):388-395. doi: 10.1097/JU.0000000000002684. Epub 2022 May 6. PMID: 35830338.

73-  Kalyvianakis D, Mykoniatis I, Memmos E, Kapoteli P, Memmos D, Hatzichristou D. Low-intensity shockwave therapy (LiST) for erectile dysfunction: a randomized clinical trial assessing the impact of energy flux density (EFD) and frequency of sessions. Int J Impot Res. 2020 May;32(3):329-337. doi: 10.1038/s41443-019-0185-0. Epub 2019 Sep 2. PMID: 31474753.

74- Adeldaeim HM, Abouyoussif T, Gebaly OE, Assem A, Wahab MMA, Rashad H, Sakr M, Zahran AR. Prognostic Indicators for Successful Low-intensity Extracorporeal Shock Wave Therapy Treatment of Erectile Dysfunction. Urology. 2021 Mar;149:133-139. doi: 10.1016/j.urology.2020.12.019. Epub 2020 Dec 26. PMID: 33373703.

75-  Rho BY, Kim SH, Ryu JK, Kang DH, Kim JW, Chung DY. Efficacy of Low-Intensity Extracorporeal Shock Wave Treatment in Erectile Dysfunction Following Radical Prostatectomy: A Systematic Review and Meta-Analysis. J Clin Med. 2022 May 14;11(10):2775. doi: 10.3390/jcm11102775. PMID: 35628901; PMCID: PMC9145026.

76-  Towe M, Peta A, Saltzman RG, Balaji N, Chu K, Ramasamy R. The use of combination regenerative therapies for erectile dysfunction: rationale and current status. Int J Impot Res. 2022 Dec;34(8):735-738. doi: 10.1038/s41443-021-00456-1. Epub 2021 Jul 12. PMID: 34253869.

77-  Oudelaar BW, Peerbooms JC, Huis In 't Veld R, Vochteloo AJH. Concentrations of Blood Components in Commercial Platelet-Rich Plasma Separation Systems: A Review of the Literature. Am J Sports Med. 2019 Feb;47(2):479-487. doi: 10.1177/0363546517746112. Epub 2018 Jan 16. PMID: 29337592.

78- Poulios E, Mykoniatis I, Pyrgidis N, Zilotis F, Kapoteli P, Kotsiris D, Kalyvianakis D, Hatzichristou D. Platelet-Rich Plasma (PRP) Improves Erectile Function: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial. J Sex Med. 2021 May;18(5):926-935. doi: 10.1016/j.jsxm.2021.03.008. Epub 2021 Apr 24. PMID: 33906807.

79-  Zaghloul AS, El-Nashaar AM, Said SZ, Osman IA, Mostafa T. Assessment of the intracavernosal injection platelet-rich plasma in addition to daily oral tadalafil intake in diabetic patients with erectile dysfunction non-responding to on-demand oral PDE5 inhibitors. Andrologia. 2022 Jul;54(6):e14421. doi: 10.1111/and.14421. Epub 2022 Mar 17. PMID: 35301742.

80-  Alkandari MH, Touma N, Carrier S. Platelet-Rich Plasma Injections for Erectile Dysfunction and Peyronie's Disease: A Systematic Review of Evidence. Sex Med Rev. 2022 Apr;10(2):341-352. doi: 10.1016/j.sxmr.2020.12.004. Epub 2021 Jul 2. PMID: 34219010.

81- Panunzio A, Labate C, Zacheo F, Orlando R, Rizzo FL, Porcaro AB, Migliorini F, Pagliarulo V, Tafuri A. Platelet-rich plasma intracavernosal injections for the treatment of primary organic erectile dysfunction: a systematic review and meta-analysis of contemporary controlled studies. Int J Impot Res. 2023 Nov 22. doi: 10.1038/s41443-023-00798-y. Epub ahead of print. PMID: 37993601.

82- Fazekas D, Campbell K, Ledesma B, Masterson T. Platelet-rich plasma for erectile dysfunction: a review of the current research landscape. Sex Med Rev. 2023 Sep 27;11(4):369-374. doi: 10.1093/sxmrev/qead032. PMID: 37786350.

83-  Shaher H, Fathi A, Elbashir S, Abdelbaki SA, Soliman T. Is Platelet Rich Plasma Safe and Effective in Treatment of Erectile Dysfunction? Randomized Controlled Study. Urology. 2023 May;175:114-119. doi: 10.1016/j.urology.2023.01.028. Epub 2023 Feb 1. PMID: 36736914.

84- Reddy AG, Dick BP, Natale C, Akula KP, Yousif A, Hellstrom WJG. Application of Botulinum Neurotoxin in Male Sexual Dysfunction: Where Are We Now? Sex Med Rev. 2021 Apr;9(2):320-330. doi: 10.1016/j.sxmr.2020.05.004. Epub 2020 Jul 5. PMID: 32641225.

85-  Ghanem H, Raheem AA, Abdel Rahman IFS, Johnson M, Abdel- Raheem T. Botulinum neurotoxin and its potential role in the treatment of erectile dysfunction. Sex Med Rev 2018;6(1):135– 42. doi:10.1016/j.sxmr.2017.07.008.

86-   Abdelrahman IFS, Raheem AA, Elkhiat Y, Aburahma AA, Abdel-Raheem T, Ghanem H. Safety and efficacy of botulinum neurotoxin in the treatment of erectile dysfunction refractory to phosphodiesterase inhibitors: Results of a randomized controlled trial. Andrology. 2022 Feb;10(2):254-261. doi: 10.1111/andr.13104. Epub 2021 Oct 7. PMID: 34618409.

87-  El-Shaer W, Ghanem H, Diab T, Abo-Taleb A, Kandeel W. Intra-cavernous injection of BOTOX® (50 and 100 Units) for treatment of vasculogenic erectile dysfunction: Randomized controlled trial. Andrology. 2021 Jul;9(4):1166-1175. doi: 10.1111/andr.13010. Epub 2021 Apr 20. PMID: 33784020.

88-  Babaei, A.R., M.R. Safarinejad, and A.A. Kolahi, Penile revascularization for erectile dysfunction: a systematic review and meta-analysis of effectiveness and complications. Urol J, 2009. 6(1): p. 1-7.

89- Hellstrom, W.J., et al., Implants, mechanical devices, and vascular surgery for erectile dysfunction. J Sex Med, 2010. 7(1 Pt 2): p. 501-23.

90-  Kawanishi, Y., et al., Penile revascularization surgery for arteriogenic erectile dysfunction: the long-term efficacy rate calculated by survival analysis. BJU Int, 2004. 94(3): p. 361-8.

91-  Sohn, M., et al., Standard operating procedures for vascular surgery in erectile dysfunction: revascularization and venous procedures. J Sex Med, 2013. 10(1): p. 172-9.

92- Antonini, G., et al., Minimally invasive infrapubic inflatable penile prosthesis implant for erectile dysfunction: evaluation of efficacy, satisfaction profile and complications. Int J Impot Res, 2016. 28(1): p. 4-8.

93-  Kramer, A.C. and A. Schweber, Patient expectations prior to coloplast titan penile prosthesis implant predicts postoperative satisfaction. J Sex Med, 2010. 7(6): p. 2261-2266.

94-  Pisano F, Falcone M, Abbona A, Oderda M, Soria F, Peraldo F, Marson F, Barale M, Fiorito C, Gurioli A, Frea B, Gontero P. The importance of psychosexual counselling in the re-establishment of organic and erotic functions after penile prosthesis implantation. Int J Impot Res. 2015 Sep-Oct;27(5):197-200. doi: 10.1038/ijir.2015.17. Epub 2015 Aug 13. PMID: 26268774.

95-  Montague, D.K., Penile prosthesis implantation in the era of medical treatment for erectile dysfunction. Urol Clin North Am, 2011. 38(2): p. 217-25.

96- Mulcahy, J.J., et al., The penile implant for erectile dysfunction. J Sex Med, 2004. 1(1): p. 98-109.

97- Natali, A., R. Olianas, and M. Fisch, Penile implantation in Europe: successes and complications with 253 implants in Italy and Germany. J Sex Med, 2008. 5(6): p. 1503-12.

98- Akakpo, W., M.A. Pineda, and A.L. Burnett, Critical Analysis of Satisfaction Assessment After Penile Prosthesis Surgery. Sex Med Rev, 2017. 5(2): p. 244-251.

99-  Carson, C.C., J.J. Mulcahy, and F.E. Govier, Efficacy, safety and patient satisfaction outcomes of the AMS 700CX inflatable penile prosthesis: results of a long-term multicenter study. AMS 700CX Study Group. J Urol, 2000. 164(2): p. 376-80.

100- Henry, G.D., et al., An outcomes analysis of over 200 revision surgeries for penile prosthesis implantation: a multicenter study. J Sex Med, 2012. 9(1): p. 309-15.

101- Serefoglu EC, McMahon CG, Waldinger MD, Althof SE, Shindel A, Adaikan G, et al. An evidence-based unified definition of lifelong and acquired premature ejaculation: report of the second International Society for Sexual Medicine Ad Hoc Committee for the Definition of Premature Ejaculation. J Sex Med. 2014 Jun;11(6):1423-41. doi: 10.1111/jsm.12524. Epub 2014 May 22. PMID:24848805.

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- Annexes

Figure 1: Personalized Management Algorithm:

 

Figure 2: Management algorithm for



Table 4: Comparison of the properties of phosphodiesterase type 5 inhibitors (PDE5i) (42)

Property

Sildenafil

Tadalafil

Vardenafil

Avanafil

 

TMAX

30–120min

30–360min

30–120min

30–45min

 

Terminal half life

4h

17.5h

4h

6–17h

 

Available doses

25mg,50mg,100mg

5mg,10mg,20mg

5mg,10mg,20mg

50mg,100mh,200mg

 

Max dose

100mg

20mg

20mg

200mg

 

Efficacy

Each offer similar efficacy

Side effects

(5 most common)

Headache, flushing, dyspepsia, nasal congestion, alteration in color vision

Headache, dyspepsia, back pain, myalgia, nasal congestion

Headache, flushing, rhinitis, dyspepsia,

sinusitis

Headache, flushing, rhinitis,

dyspepsia, sinusitis

 

Use with α-blockers.

 

- Concomitant use of selective α-blockers does not present a risk for significant hypotension

- There is a risk of significant hypotension when using non-selective α-blockers

Contraindications

 

- Regularly or intermittent use of organic nitrates.

- Known hypersensitivity to any component of the tablet

Dose adjustments that may be needed

· Patients aged > 65 years.

· Hepatic impairment

· Renal impairment

· Concomitant use of potent cytochrome P450 3A4 inhibitors (e.g. ritonavir, cobicistat and erythromycin)

· Concomitant use of cimetidine with sildenafil

TMAX = time to maximum plasma concentration.


Table 5: Clinical History, Physical Examination, Laboratory Investigations and Radiologic Assessment in Different Types of Priapism (119,120).

 

Variant

History and clinical examination

Penile blood appearance

Penile blood gas

findings

Color Duplex

ultrasonography

findings

Ischemic priapism

Tender and rigid corpora cavernosa

Corpus cavernosum

testing: blood is hypoxic

and dark in color

pO2> 30 mmHg

pCO2>60 mmHg

pH<7.25

Minimal or absent blood

flow

Nonischemic priapism

Perineal or

penile trauma; non tender, partially tumescent corpora cavernosa

Corpus cavernosum

testing: blood is

oxygenated and red

pO2<90 mmHg

pCO2<40 mmHg

pH=7.4

similar to normal

arterial blood)

Blood flow is normal to

high in velocity

Stuttering (recurrent)

priapism

Similar attacks

Corpus cavernosum

testing: blood is hypoxic

and dark in color

Blood gases:

pO2<30 mmHg; pCO2>60 mmHg

pH <7.25

Minimal or absent

blood flow during acute

priapism; normal blood

flow otherwise

pCO2, partial pressure of carbon dioxide; pO2, partial pressure of oxygen.


Table 6: Percutaneous distal shunts, open distal shunts, open proximal shunts, and vein anastomoses/shunts

Distal shunts

 

Example

Technique

Percutaneous distal shunts

Winter (corporoglanular)

shunt large biopsy needle is inserted through glans

Ebbehoj (corporoglanular)

shunt #11 blade scalpel is percutaneously passed

T shunt (corporoglanular shunt)

Modified Ebbehoj using #10 blade scalpel and introducing the scalpel rotating it inside 90°

Open distal shunt

Al-Ghorab

 

A 1 cm incision is made distal to coronal sulcus with

excision of 5 × 5 mm cone segment of distal tunica

albuginea from each corporal body

Burnett ‘snake’ maneuver

 

Modification of Al-Ghorab shunt. A Hegar dilator is

used to evacuate ischemic blood through a distal

tunical window

Proximal shunts

Open proximal shunt

Quackels or Sacher (corporospongiosal) shunt

 

In lithotomy position, bulbocavernosus muscle

is dissected from corpus spongiosum and 1 cm

staggered ellipses of tissue are incised/excised

from spongiosal/corporal bodies, and the defects

anastomosed together

Corporo saphenous vein or superficial/deep dorsal vein shunts

Grayhack shunt

 

The saphenous vein is ligated and anastomosed

with corpora cavernosa

Barry shunt

 

The superficial or deep dorsal vein is ligated and

anastomosed to the corpora cavernosa