Advantages and limitations of current premature ejaculation assessment and diagnostic methods: a review
Introduction
Premature ejaculation (PE) is one of the most common male sexual dysfunction worldwide (1). Its estimated prevalence rate is 20–40% in the Asia-Pacific and continental regions (1,2). In some areas of China, the latest survey revealed that prevalence rates range from 10.98% to 21.39%, and the total complaint rate was 34.62% (3). The characteristic symptoms of PE are unexpected, rapid, and inability to delay ejaculation. It also causes persistent psychological stress to both sexual partners and negatively impacts their mental state and sexual experiences.
The initially classification of PE was as primary (lifelong) or secondary (acquired), and this classification was expanded by McMahon et al. to include lifelong PE (LPE), acquired PE (APE), variable PE (VPE), and subjective PE (SPE) (4). This classification system describes the particular characteristics of each PE category, but it was believed that this system failed in the elucidation of this complicated condition (5). Additionally, despite different domains of distress, such as sexual distress, interpersonal difficulties, inability to delay or withhold ejaculatory impulses as described in this classification system, current PE type and diagnosis were increasingly relying solely on the calculation of the duration from vaginal penetration to ejaculation or the intravaginal estimated latency time (IELT) (4). This trend makes the IELT the most important parameter for PE determination and diagnosis.
PE was also believed to be a psychological problem (5). Nevertheless, the classification of PE patients was firstly based on doctors’ impressions and their evaluation. The initial assessment of patients includes a medical history, physical examination, questionnaires, and other diagnostic tools. Overall, these assessment methods were less subjective (6). Thus, it would be essential to develop a quantitative and systematic measuring scheme to establish an objective approach for the diagnosis of PE, which could be used in the treatment of this condition.
To date, several measures have been applied for the evaluation of PE. These methods include history enquiry/physical examination (7), patients-reported outcome (PRO)-questionnaires (8-10), IELT evaluations (11), penile biothesiometry (12), and penile electrophysiologicaltest (13). The features, advantages, and limitations of these methods are listed in Table 1. Based on a comprehensive review of the literature, our study summarizes the main methods in order to elucidate the advantages and disadvantages associated with each.
Full table
History inquiry
A patient history inquiry regarding issues with ejaculation can be a difficult endeavour. The act of avoidance or an unwillingness to discuss sexual issues in clinical practice, either by patient or consultant, may aggravate any pre-existing misunderstanding over ejaculatory-related issues (1,14). In a survey of 12,113 men diagnosed with PE, Porst et al. demonstrated that the concomitance of PE with psychological disturbances is 23%, which is higher than it is in individuals without PE in the United States, Germany, and Italy (14). Regarding the outpatient PE visiting rate, Lee et al. reported that most men are reluctant to seek professional advice (15). He suggests that this is probably due to historical culture, reasons related to social psychology, and ignorance of the prevalence and diagnostic criteria of this condition (15). Similar social psychology, historical, and cultural effects are more evident in Asia, which may explain why the self-reported rate of ejaculatory abnormality is only 2% in these regions, while in Europe and the United States, it can reach 81.9% (14,16).
Furthermore, Shechter et al. pointed out that factors such as clinical practice, educational background, and the own sexual experiences of the physicians may constitute reasons for an underlying biased diagnosis of PE (17). These findings suggest that the misconceptions regarding the subjective ejaculatory symptoms and clinical history may lead to a biased patient history regarding PE and erroneous diagnosis in clinical practice. In these cases, the patient history must be rectified before reaching a diagnosis.
Physical examination
Physical examination of patients who experience PE is often unremarkable. Considering that PE may co-exist with other sexual dysfunctions, especially erectile dysfunction (18), the International Society for Sexual Medicine (ISSM) strongly recommends performing a physical examination in these cases (7). For lifelong PE, some patients found it reassuring for the physician to examine them. Regarding acquired PE, a targeted physical examination helps to rule out any acute or chronic illness or injury that may contribute to ejaculation dysfunction. These illnesses include urinary and reproductive tract infections, Peyronie’s disease, neurological impairment, and endocrine dysfunction (19). However, there are no specific criteria to confirm or exclude PE. The main purpose of the physical examination is to distinguish PE from ED or to rule out any underlying diseases or conditions that may cause PE.
Patient-reported outcome (PRO) questionnaires
Since it is difficult to determine whether a man has PE based on the patient history and physical examination, there is an apparent need for a valid and reliable screening instrument for PE. Rowland et al. (20) first utilized 2-question diagnostic utility based on the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) definition of PE for diagnosis in 2004. However, the decision of whether a particular question should be asked in each clinical session relies mainly on the physician. This situation may lead to varied sets of questions applied to the same patient and, consequently, result in inconsistent diagnoses by different physicians. Therefore, standardized questionnaires and surveys are proposed with the aim to evaluate subjective symptoms and perform comprehensive data collection. Currently, the index of premature ejaculation (IPE), the premature ejaculation diagnostic tool (PEDT), and the premature ejaculation profile (PEP) are the questionnaires that are applied most frequently in a clinical setting and that meet most of the criteria for test development and validation (21). They provide reliable, interpretable, and standardized assessment measures for the diagnosis and differentiation diagnosis of PE. Other self-reported questionnaires, including the Chinese Index of Premature Ejaculation (CIPE) (22) and the Arabic Index of Premature Ejaculation (AIPE) (23), are not recommended for clinical use due to the lack of adequate clinical data or not meeting the DSM-IV-TR criteria (9,21). The features, advantages, and limitations of these questionnaires are shown in Table 2.
Full table
IPE
The IPE questionnaire was developed and validated by Althof et al. in 2006 (8). It consists of 10 items in 3 domains for the assessment of PE-related issues, including control over ejaculation, satisfaction with sex life, and level of distress in men with this condition. The IPE questionnaire has been shown to correlate well with the IELT and have good known-groups’ validity and test-retest reliability. Compared to other valid questionnaires, the most apparent feature of the IPE is that it covers detailed core features of the overall experience of PE, thus providing a more comprehensive assessment. It is also relatively brief and easy to administer. Based on these advantages, IPE has been used to assess the outcome of PE treatment in clinical trials (24). However, lacking grading norms and diagnostic cut-off values can make the reassessment results used to evaluate improvement versus deterioration of the PE condition rather ambiguous, hence more difficult to determine treatment. Additionally, as DSM-5 has updated the definition of PE and limited the IELT to approximately 1 min, the DSM-IV-TR based IPE may need further modification and validation to adapt to the new definition.
PEDT
In determining the presence or absence of PE, Symonds et al. developed the PEDT questionnaire in 2007 and made this task valid and straightforward (9). This questionnaire consists of 5 items that meet the DSM-IV-TR criteria and assesses ejaculatory problems, such as aspects of ejaculatory control, frequency of sexual intercourse, minimal sexual stimulation, distress, and interpersonal difficulty. Each question is rated on a scale ranging from 0 to 4, and an index score is derived from the sum of the responses to the 5 questions. Since there are only a few questions that patients need to answer, clinicians can quickly identify whether a “probable PE” exists in a patient. By employing a 3-tiered cut-off score, the PEDT classifies cases as PE (≤8), possible PE (9 or 10), and absence of PE (≥11).
Moreover, the score is indicative of the need for further treatment in each case. For possible PE, clinicians need further investigation to determine the existence of dysfunction. However, it should be noted that PEDT is not suitable for evaluating the PE treatment efficacy or indicating a designed intervention, because this scoring system is not purposely designed with this objective. Meanwhile, similar to the IPE, the PEDT may also require a re-validation to adapt to the DSM-5 criteria.
PEP
The PEP is a 4-item PE assessment tool, developed and validated by Patrick et al. in 2009, that measures all domains of ejaculatory function as defined by the DSM-IV-TR: control over ejaculation, satisfaction with sexual intercourse, interpersonal difficulties, and distress related to ejaculation (10). Each question is rated with a scale ranging from 0 to 4, and higher scores indicate better function. An index score is calculated by averaging the sum score of the four specific PEP questions. This questionnaire is concise, easy to administer, and has good test-retest reliability and known-groups’ validity. The PEP has been used to evaluate the efficacy of Dapoxetine (25) and PSD-502 (24) in treating men with PE in clinical trials, as well as to characterize PE in observational studies (26). However, its simplicity is also its weakness, and its reliability is a concern. For example, the result of 1 domain of PE is determined solely with a single question (27). Theoretically, it is difficult to cover all men’s issues concerning PE with four questions, regardless of how well the four questions were designed. Another concern regarding the PEP is that there are no studies to further verify its validity and reliability based on the new DSM-5 diagnostic criteria for PE proposed by the ISSM, which resembles the IPE and the PEDT. Additionally, the lack of validated cut-off scores makes the PEP more suitable for clinical research rather than clinical practice.
Taken together, these validated PRO questionnaires serve as useful tools to assess PE for family practice physicians and sexual medicine experts. However, the discontinuity among these tools may restrict their applicability in clinical practice, since the data collected by each tool is non-unified and unconvertible. Further, the lack of cut-off scores on some questionnaires (IPE and PEP) makes it difficult for physicians to judge whether a patient has PE when solely relying on these measures. In a study conducted in Korea, the researchers found that the rate of application of these diagnostic tools is merely 42% in clinical practice, and clinicians are more inclined to make the PE diagnosis based on their patients’ subjective descriptions (28). In this regard, the combination of 2 to 3 validated questionnaires, such as the PEDT combined with the IPE or PEP, may be a feasible solution to improve PE assessing accuracy.
Moreover, it is important to realize that these measures cannot replace a detailed sexual history obtained by a professional clinician and can only serve as useful adjuncts (7). Recently, a new unpublished patient-reported outcome tool, the Patient Outcome for Premature Ejaculation (POPE), has been completed by the Ampio Pharmaceuticals and accepted by the FDA for the evaluation of PE therapy in the United States [Available at: https://adisinsight.springer.com/trials/700219252 (Date of access 7/10/2018) (2013)]. It is a revision of the PEP, in which the wording of the distress question is modified, and the three remaining questions are unaltered (27).
Ejaculation latency time
Establishment of the IELT
Despite assessment of the domains of control over ejaculation, sex satisfaction, and negative personal impact are recommended in the diagnosis of PE, currently PE diagnosis is highly relying on the IELT calculation. IELT is the time latency for ejaculation to occur, starting from the first penile-vaginal penetration (11). The first introduction of IELT was conducted by Waldinger et al. while studying paroxetine’s effects on PE treatment (11).
In the previous DSM criteria, no cut-off point for the ejaculatory latency was defined (29). Waldinger et al. assessed the ejaculatory latency in men with lifelong PE using a stopwatch and identified that the latency within 1 minute is manifested in 85% patients (30). Using the same methods, subsequent studies confirmed that 3 minutes is an optimal cut-off value for the diagnosis of acquired PE (31,32). These works clarified previous ambiguity in PE definition and revolutionized it by redefining the PE classification (33). Meanwhile, Waldinger and Serefoglu respectively identified the “variable” and “subjective” as the new PE categories to classify patients whose IELT is either undefinable or longer than the other two types of PE (34). Later, in the DSM-5, ISSM further updated the definition of the ejaculatory latency value as “approximately 1 minute following vaginal penetration” by adding “before the person wishes” (4). Definitive IELT values optimized the uniformity in clinical application and treatment research (35). Identifying the PE category was facilitated by the IELT, which is assessed by a stopwatch or is based on the patient’s estimation, since it provides a more plausible and definitive index to fulfill the preliminary screening (36). It has become a more prevalent index in PE research.
Limitations in intravaginal ejaculation latency time
Patrick et al. analyzed 408 PE versus 2,294 non-PE individuals by pooling them into tertile subgroups according to their IELT. The result revealed that the IELT tertile subgroups ideally manifested patients’ reported global impression and change in their ejaculatory problem. However, in their survey, the 1 min IELT criterion limited the inclusion of PE subjects (10). Also, data from other investigations revealed a vast overlap in IELT distribution between PE and non-PE subjects. This overlap is non-neglectable, although IELT was significantly shorter in PE (37).
Besides, the reliability of reported IELT was questioned. In Pryor’s research, the estimated and calculated IELT in males with or without PE was compared, and they concluded that while IELT was objectively correlated with PE severity, these patients were more inclined to overestimate their IELT to a greater extent (38). Their research revealed the tendency of overestimating IELT. Besides, the perceptive disparity between patients and their partners also should be noted (39). Patrick et al. pointed out that due to personal distress and psychological burdens, PE patients are more likely to resolve their problem by reporting an “estimated normal IELT” instead of seeking medical help. The estimated normal IELTs were 7 to 13 minutes, which is significantly longer than their partners (39). Their result was contradicted with Cal’s research; however, it is confirmed by the research performed by Rosen et al. (40,41), which suggests that combining patients reported outcome measurement might improve IELT validity in PE assessment and outcome (40).
Furthermore, IELT defines the penile intromission solely as intravaginal. It is non-neglectable that disparities in the penile thrust tracks and vaginal stress tone influenced on ejaculations (42). In Bhat’s investigation, the ejaculatory latency time was 240±38.6 seconds to 700±79.1 seconds, depending on different sexual stimulation (43). This result suggests that intensity and total amount of penile stimulation before ejaculation is variable. Nonetheless, IELT is inadequate in evaluating ejaculatory latency other than penovaginal contact. In noticing this limitation, Waldinger proposed the MELT, OELT, and AELT to assess ejaculatory latency regarding the aspects of masturbation, oral sex, and anal sex (44).
Additionally, IELT should be based on a calculation that starts at the first penovaginal intromission, whereas intercourse includes activities such as foreplay and change of coitus position. The demand for the first intromission is rather challenging to fulfill, not to mention that the use of a stopwatch is intrusive. Indeed, it may aggravate the PE problem due to a negative personal impact by disrupting sexual spontaneity and intercourse fluency (45).
These results suggest that by basing PE assessment on ejaculation latency, males were deemed as the sole culprit. However, it is advisable to consider and appraise the influence from both sexual partners, as well as consider the need for additional measures to characterize PE (39).
Penile sensory evaluation
Penile hypersensitivity was believed to be a significant factor in PE (46). Biothesiometry, or vibrometers, are devices that are capable of producing vibrations with different amplitudes. It was initially designed to assess abnormal afferent somatic pathways and peripheral neuropathies and subsequently was introduced in penile sensitivity evaluation (46). Technically, to assess penile sensitivity, a vibratory stimulator is required to sweep over the penis, including at the sites of the glans penis and the penile shaft. Also, this sensory threshold should be rectified with a synchronized hand vibrator on a peripheral site, mostly at the index finger (47). Thus, it is believed that the vibrometers would be able to provide objective penile sensory information, thereby facilitating PE diagnosis.
Controversies in penile biothesiometry research
Initial investigation on penile sensitivity with vibrating devices dates back to the 1970s (12). However, to date, these findings add more confusion to the interpretation of PE etiology. In revealing PE etiology, early research has both validated and disproved the existence of penile hypersensitivity (48,49). Furthermore, the correlation between IELT and penile sensory threshold was investigated by several studies with contradictory results (50,51). Interestingly, some research further revealed that the penile sensory thresholds were even higher in patients with PE, which contradicts the notion that penile hypersensitivity induces PE (51,52). These facts revealed a significant disparity in the field of penile biothesiometry research.
In the research studies conducted by Xin and Paick, the penile sensory threshold was compared between PE patients and potential PE patients (48,53), whereas in Guo and Vanden Broucke’s research, the selected subjects were labeled as either non-PE or PE for each assessment (50,54). In the latter research, the results only elucidate the features of penile sensitivity in “normal” and “abnormal” subjects. Although these authors attempted to decipher the penile sensory threshold in individuals with different ejaculatory thresholds, it is unclear whether these results are applicable in interpreting PE etiology.
The concomitance of ED and PE is prevalent. In some research, the potential effect of ED and neuropathology was excluded, and the PE criteria were defined as ejaculation latency less than 1min. Nevertheless, Rowland included subjects with primary PE, secondary PE, ED concomitant, ED patients, and patients without impotence in their investigation (51). It is clear that these researchers attempted to elucidate sexual dysfunction but, given that the etiology of both dysfunctions remains unclear, involving ED increases the complexity in comprehending the results of the study. Furthermore, it is noteworthy that the time when this research was conducted predates the introduction of the latest PE classification criteria. Thus, the yet-to-be optimized selection may potentially compromise the results.
Additionally, while both research studies performed by Xin and Paick investigated penile sensitivity in PE subjects, Xin enrolled 120 subjects, whereas Paick enrolled 33 subjects. The mean age gaps were inconsistent between the groups in their investigations (48,53). This indicated that inconsistent subjects’ selection criteria and limited sample size cannot rule out the potential selection bias and may undermine research validity. Also, Paick mentioned performing an intra-cavernous injection (53) in their research, while such operation was not mentioned in other research. This revealed an absence of standard operating procedure in guiding biothesiometry research. These facts may partially explain the disparities observed between these 2 studies.
Disparity in the investigation protocol
In the researches mentioned above, the settings of each vibrometer ensured that control of vibration intensity is subjective and facilitated. In these studies, even though all tests were performed by the same technician, the operational consistency in each test is subject to manual operations. Although the vibrating scales are within the range of micrometers in equipment, a manual operation seems difficult to perform in each test (52). This fact reveals a vague correlation between “vibration intensity” and penile sensitivity, and that the technique in studying penile sensitivity is probably inadequate.
First, future research should focus on the penile erectile property. In research studies performed by Xin and Rowland, penile sensory thresholds were evaluated with the flaccid penis (48,51,55). Meanwhile, Vanden Broucke et al. tested vibrating stimulations on the stretched and flaccid penis (50), whereas, Paick et al. evaluated penile sensitivity on the flaccid and erected penis (53). Though the difference was insignificant, the penile sensitivity tends to be higher when the penis was erected, especially in premature subjects. This result was further confirmed by Hill et al., who specifically investigated the correlation between penile erectile property and its sensitivity (56). Additionally, the maneuvers were either “performed by the same operator” or “attached the penis with the equipment on its own weight”. These states suggest that inconsistent requirements of erectile properties, combined with operation differences potentially underlies the heterogeneity in studies.
Still, the practical constraints of applied biothesiometers, especially the probe shape, were different between studies. Despite the range of vibration scales and the fact that the intensity produced in each device is similar and comparable, the disparity of penis-probe contacts in each investigation resulting from equipment design is non-neglectable (52,56), which has been described as “contacting with probe” or “resting of the device on its own weight” in each study. Notably, in the research performed by Vardi, the device was designed and referred from an investigation on a study evaluating the sensitivity of female genitalia (57), making probe-penis contact impossible. To solve this problem, they had to “attach an additional probe” to isolate the vibration away from the weight of the integrated equipment. Consequently, these facts imply that although the investigator can at least ensure operational consistency in their own study, the parameter and the result may not be translatable in different studies.
A similar operational difference is also manifested in the protocols in each type of research. In aiming to decipher the correlation between vibration intensity and penile hypersensitivity, Guo et al. applied a fixed frequency with various vibrating amplitudes in their protocol. Though a similar technique was applied in the research of Chen and Vanden Broucke, the vibrating frequencies of their stimulation were different, ranging from 80 to 120 Hz (49,50). This fact makes the vibrating frequency a new variant. Again, in Salonia’s investigation, they included the thermal stimulus in their investigation (52). While their findings revealed that the penile sensitivity in PE patients was variable in detecting “cold” stimulations, their results only highlight that it is not a “de-sensitivity” but “hyper-sensitivity” status in PE subjects (52).
In addition, as an examiner of peripheral sensory neuropathy, the stimulus of biothesiometry should be rectified with reference peripheral portion, typically at the index finger or finger pulp (46). Other referential sites, such as wrist, ankle, or right-hand palm, were applied in other investigations as well (49,51). It is suggested that the vibration perception threshold (VPT) provides important and meaningful information about nerve fiber dysfunction, and the proposed testing site is at the index finger or the first hallux (46). Thus, there is no evidence that testing other peripheral parts are equally valid as a reference point for the index finger.
Limitations in the penile biothesiometry test
There are limitations to stimulation innervated by vibrometers. First, it focuses solely on specific surface areas on the penis, while the coital stimulating pattern on the penis is yet to be determined. It is reasonable to believe that coital penile stimulation is more complicated and comprehensive than the single or multiple probes that require a piece of equipment. Meanwhile, Paick et al. argued that there was evidence that a programed vibrating pattern is adequate to induce ejaculation (53). Nevertheless, there are specific limitations in simulating coital stimulation with a vibrometer on the penis. Further efforts are needed to assess penile somatosensory innervation and to determine penile sensitivity by current vibrating innervation. Also, it was reported that anxiety affects patient’s ejaculation, as well as their perception sensitivity (58,59). It is reasonable to assume that patients’ sensory threshold is possibly affected by their consciousness and attentiveness during the sensory test.
In all, it has been decades since biothesiometry was first introduced to test penile sensation and diagnose PE. Currently, available results may seem controversial, but it is still one of the few approaches that provide subjective information about penile peripheral neurotransmission features. Meanwhile, penile hypersensitivity is still believed to be the main cause of some types of PE (60). Biothesiometry is still a promising method since it identifies the correlation between penile sensitivity and PE; however, certain amendments in operational technique and testing protocol should be performed to guarantee a plausible and interpretable result. The examination protocols, characteristics, and results of the aforementioned penile biothesiometry studies are shown in Table 3.
Full table
Penile electrophysiological test
Based on the notion that penile hypersensitivity is one of the leading causes of PE, the penile electrophysiological test was introduced in order to decipher the link between the neurological factor in penile hyperexcitation and primary PE (13).
The main electrophysiological tests introduced in PE diagnosis were the somatosensory evoked potentials (SEPs) and the bulbocavernosus reflex potentials (BCPs). To measure a penile somatosensory-related SEP, a stimulus electrode was placed on the penile shaft and glans penis and a recording electrode placed on the midline scalp and the electroencephalographic recording sites (60,61). The objective of this method is to give a cortical representation of the sensory stimuli arising from the genital area to the primary or secondary somatosensory cortex (S1 and S2) in the cerebral cortex (61).
Mechanism of SEP and BCP
Numerous types of SEP tests were used since their initial application. Currently, the main types of SEPs include somatosensory evoked potential of pudendal nerve (PNSEP), somatosensory evoked potential of dorsal nerve (DNSEP), and somatosensory evoked potential of the glans penis (GPSEP) (62). PNSEP is designed to evaluate the complete peripheral and central pudendal nerve afferent pathway of the perineal region, whereas the DNSEP and GPSEP were the optimized methods aimed at specifically assessing the neurophysiological properties of penis innervation (61). Although it is recommended that the stimuli should be applied at the penile shaft and glans penis when measuring these SEPs (63), Xin et al. pointed out that the accurate SEPs could not be recorded by stimulating the glans penis (64). Hence, he suggests that a proper modification should be made during the experiment to ensure a plausible result. Accordingly, lacking the standard of criteria and operational procedure is potentially introducing variability in SPE measurement in different research studies.
The bulbocavernosus reflex (BCR) and bulbocavernosus motor evoked potentials (BC-MEP) are designed to evaluate the afferent and efferent conduct through the pudendal nerve at the S2–S4 spinal segment (65). During the ejaculation process, an involuntary contraction over the genital-anal region is indicating the commencement of seminal expulsion. This response is easily recorded by BCR monitoring; hence, it is suggested that the BCR potential provides innate information on the primary penile conducting properties and its response to the innervating stimulations (66). To measure the BCR potential, two electrodes were placed on the distal shaft of the penis and the bulbocavernosus muscles (64).
Penile electrophysiological findings in PE
SPEs mainly provide a record of cortical and local response to sensory stimulations. In investigating PE patients, Fanciullacci et al. discovered that their SEP amplitude was statistically higher than the control group (67). This result revealed that penile hypersensitivity is a precursor to PE (67). Other research investigating PE patients further confirmed this conclusion with similar results (64,68). Moreover, experiments on both humans and animals revealed that local penile anesthesia reduces SEP amplitude stimulation at the glans penis and prolongs its latency (69,70). However, these results were contradicted with the results obtained by Perretti et al. (71). Similarly, in the investigation of SEPs in patients characterized with delayed ejaculation, a situation considered opposite to PE, Xia et al. discovered that these patients were characterized by penile hyperexcitability (72). These findings make the penile SEP test more perplexing.
Regarding the BCP, Zhou and Jiang discovered that the BCR threshold was significantly lower in PE patients compared with the control group (66,73). However, their result was contradicted with Perretti’s research (71). Hence, it is evident that disparities still exist in penile neurophysiology examination due to certain limitations.
Limitations in penile electrophysiological test
Recently, Gao et al. discovered positive structural abnormalities in the neural conduction pathways in PE patients (74). This finding confirmed the altered conductivity in the electrophysiological exams. However, the correlation between penile hypersensitivity and PE due to the hyperexcitable penile glans is merely partially confirmed, and accelerated peripheral conduction has only been proven by some research studies (60). It is presumed that several factors, such as age, height, gender, body temperature, site of stimulation, type of nerve fiber, degree of myelinization, and nerve pathway, may predispose to SPEs (64). Therefore, a more effective screening mechanism of the subjective and standardized operating process with a unified index is required in performing electrophysiological tests. The examining protocols, characteristics, and results of aforementioned penile electrophysiological investigations are shown in Table 4.
Full table
Currently, available PE research using penile electrophysiological is less frequent, and the studies investigating PE using this technique focus mainly on patients with primary ejaculatory dysfunctions. This may be because electrophysiological techniques are mainly suitable for monitoring the primary cortex and peripheral neural pathways at lower levels, while it is easier to rule out correlated and unidentified etiological conditions in patients with primary ejaculation dysfunctions (64). In the investigation carried out by Yilmaz, it was revealed that patients’ penile sensory threshold and SEPs remained unchanged, although fluoxetine alleviates the patients’ premature disorder by prolonging their IELT (65). In this case, it is suggested that the electrophysiological test only partially illustrates the penile sensory properties and is influenced by a variety of factors. Due to these limitations and controversies, the SPE and BCP are both applicable in providing neurophysiological data of subjects; however, their validity in determining penile hypersensitivity and in clarifying PE etiology is yet to be verified.
Discussion
Accurate PE evaluations have relied on previous ambiguous definitions and unvalidated examination techniques. Clinical diagnosis and research are mainly based on patient history, patient-reported outcome scores, and diagnosis tools. Undoubtedly, these diagnostic methods provided valuable information regarding the PE condition and the related negative personal consequences; however, there is a lack of feasible and plausible means of objective measurement to evaluate the ejaculatory latency and control over ejaculation.
In the meantime, calculating ejaculatory latency time, especially IELT, is becoming increasingly critical in evaluating and describing ejaculatory disorders. This index emphasizes calculation of the temporal dimension during penile thrusting before ejaculation, but it is noteworthy that this indicator tends to interpret and measure PE as an absolute objective and quantifiable behavior, which it is not. Namely, “intravaginal” thrust is one of the main patterns of penile stimulation to induce ejaculation. It is possibly not the only means that is involved in the actual coital process (75), even though the duration calculation is potentially biased due to compromised standard operating procedures. Hence, ejaculatory latent time provides a sophisticated but comprehensive indication for interpretation of the ejaculatory condition, not just as an outcome.
In simulating penile stimulation, the penile biothesiometry and electric pulses seem plausible. However, the current stimulating pattern was restricted in location and vibration or electrical pattern. This is because this technique continues to focus on measuring penile sensory level and deciphering penile hypersensitivity. It is unknown whether this notion is indicative of PE etiology, but vibrating stimulation does not simulate or resemble actual coitus sensation. In other words, the “vibration” does not resemble “thrusting.” Even though the vibrating strengths and frequency are readily presented and adjustable in each test, the “sensory threshold” is ideally presented as a vibrating or electrical stimulation value.
Penile stimulation substantially underlies the ejaculatory process. Multiple levels of motor-sensory reflexes are involved in the ejaculatory process, including penile erection, emission, chamber pressure formation, and sperm expulsion (76,77). As been described by Herbert, the maintenance of erectile status and ejaculation latency is dominantly innervated and modulated by stimulating the penis through thrusts (78). Also, he further demonstrated that in the pudendal nerve tampered rhesus monkeys, more intensive and prolonged penile thrusting is required to achieve ejaculation (78). He believed that because the neural pathways had been partially intersected, more penile stimulation was required to achieve a “sufficient” signal to trigger the expulsion phase of ejaculation. So, the increased amount and intensity of penile thrusts are the requirement for “sufficient stimulation” to induce ejaculation.
Although attempts at calculating penis thrust before ejaculation dates back to the 1970s (79), this criterion seemed to never enter into the mainstream since its reliability and accessibility were questioned, and it was subsequently substituted by the introduction of IELT (80). A conspicuous defect was that the focus was solely on the thrusting numbers, but omitted the parameters of thrust frequency, depth, and pausing intermission during thrusts-the typical scenes in real coitus. These co-factors are also significantly contributing to the penile stimulations. Other factors are affecting the ejaculation process. For example, 1 PE patient can withhold a single thrust during intravaginal intercourse and can wait for the second thrust after the ejaculation impulse has ceased in order to increase his pre-ejaculation thrust numbers and, consequently, the latency time.
Diagnosing PE is as complicated a task as finding an accurate definition for this condition. Considerable progress has been achieved in amending PE diagnostic guidelines and improving the PRO questionnaire. IELT provides a subjective index in PE description, but its accuracy and definiteness are yet to be validated. Based on the penile biothesiometry, PE assessments and parameters should be designed by referring to the natural course of penile thrust to justify ejaculator disorders. However, instead of calculating latency time or thrust number, the ejaculatory threshold should be appraised. In this case, determining the threshold requires calculating the stimulatory duration and scaling its magnitude along with its changing pattern. These data could be combined with data on the stimulatory intensity and frequency that the penis has endured before ejaculation, thus allowing for the evaluation and quantification of the total stimulus required to accomplish ejaculation.
Conclusions
Currently, available data on psychogenic or neurogenic etiology of PE are controversial and inconclusive. Present methods in PE assessment revolutionized PE research and allowed for a greater understanding of this condition. However, a single parameter is not enough to describe and quantify PE. Comprehensive penile stimulation simulates real sexual intercourse, and the intensity and duration parameters recorded before the ejaculatory threshold are more objective relative to a single chronological observation when describing and diagnosing PE.
Acknowledgments
Funding: This paper was supported by the Natural Science Foundation of China (No. 81671453, 81270691, and 81170565). Sichuan Science and Technology Program No. 19RKX0475 and Thousand Talent Plan of Sichuan Province.
Footnote
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau.2019.12.08). FQ and JY have a patent INTELLIGENT MONITOR OF ERECTILE FUNCTION issued. The other authors have no conflicts of interest to declare
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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