Oral drug treatments in patients with erectile dysfunction and multiple comorbidities: a retrospective observational study.

OBJECTIVE: To investigate factors associated with demographic/clinical characteristics and drug selection in patients with erectile dysfunction (ED). The prevalence of ED is increasing worldwide. Studies have shown that ED is associated with age, lifestyle and comorbidities. However, the factors associated with patient characteristics as well as drug selection are incompletely understood.
SETTING: A tertiary medical centre in Kuala Lumpur, Malaysia. PARTICIPANTS: A total of 219 patients (range 23-80 years) who had received phosphodiesterase type-5 (PDE-5) inhibitors as ED treatment were evaluated. INCLUSION CRITERIA: Adult patients aged ≥18 years, diagnosed with ED, and prescribed with sildenafil, tadalafil or vardenafil. EXCLUSION CRITERIA: Patients diagnosed with ED but who did not receive any PDE-5 inhibitor, or those with missing data. PRIMARY AND SECONDARY OUTCOME MEASURES: Factors associated with demographic and clinical characteristics as well as drug selection were assessed.
RESULTS: Ischaemic heart disease (p=0.025), benign prostatic hyperplasia (p<0.001), obesity (p=0.005), lower urinary tract symptoms (LUTS) (p=0.006) and α-blockers (p<0.001) were significantly associated with elderly patients with ED. Additionally, LUTS (p=0.038) and α-blockers (p=0.008) were significantly associated with the selection of PDE-5 inhibitor.
CONCLUSIONS: These data showed that elderly patients with ED were significantly associated with comorbidities and α-blockers, whereas LUTS and α blockers were associated with drug selection. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

This article represents utilisation of drug treatment and factors associated with comorbidities and concomitant drugs in patients with erectile dysfunction (ED) with multiple comorbidities. The prevalence of ED is increasing worldwide and research papers from the perspective of pharmaceutical care are currently scarce and limited. This research could provide an insight to healthcare providers specifically and to patients generally. Findings of this study could serve as preliminary data to optimise a pharmaceutical care concept and to ensure quality-use of drug treatments in patients with ED. This could further ensure patients with ED obtain an optimum pharmaceutical care despite having significant numbers of comorbidities. So far, no papers discussing the association of drug treatment with clinical characteristics and comorbidities in patients with ED have been published. This paper could serve as a platform to enhance future studies in an attempt to deliver an optimum pharmaceutical care for patients with ED with multiple comorbidities and finally to promote their quality of life.

This was a retrospective study in which data availability was highly dependent on medical records. Important information such as erectile function and hormone levels could not be retrieved from such medical records. Also, individual physical factors on the selection of phosphodiesterase type-5 inhibitors were not considered. Nevertheless, a retrospective design is the most appropriate to assess patient characteristics and selection of drug treatment in patients with ED. Face-to-face interviews would limit a complete data retrieval of patients’ clinical comorbidities and drug treatment history.

Introduction

Erectile dysfunction (ED) can be defined as the inability to attain/maintain penile erection sufficiently to undertake sexual intercourse satisfactorily.1 ED can more precisely describe this problem than can ‘impotence’.2 The prevalence of ED increases with age, from 6.5% in men aged 20–29 years to 77.5% in men aged ≥75 years.3 In Malaysia, the prevalence of ED in men aged 40–79 years is 69.5%.4

ED can have vasculogenic, neurogenic, anatomical, hormonal, drug-induced or psychogenic aetiologies.5 Various therapies are available for ED: orally administered phosphodiesterase type-5 (PDE-5) inhibitors, intracavernosal injection of vasoactive agents and transurethral delivery of alprostadil, vacuum constriction devices and penile prostheses.6 Testosterone can be given to patients with ED with hypogonadism.7

ED is more prevalent in men with comorbidities such as cardiovascular disease (OR 1.45; 95% CI 1.16 to 1.81) and diabetes mellitus (DM; OR 3.13; 95% CI 2.35 to 4.16).8 A community health survey conducted in Boston (Massachusetts, USA) reported that the prevalence of patients with ED with heart disease, DM, hypertension and obesity was 52.3%, 49.3%, 35.4% and 23.5%, respectively.9 ED is also associated with lifestyle factors such as physical activity, smoking and alcohol consumption (p<0.01).9 A cross-sectional survey conducted in Malaysia found that a larger proportion of patients with ED had hypertension (58.7%), followed by DM (40.9%), hyperlipidaemia (35.5%), obesity (13.1%) and heart disease (8.3%).4

PDE-5 inhibitors such as sildenafil, vardenafil and tadalafil are first-line therapies for ED with proven safety and efficacy.10 Various studies showed that PDE-5 inhibitors improve the erectile function in men with comorbidities such as hypertension, DM and hyperlipidaemia.11 In 2011, the Food and Drug Administration (FDA) in the USA approved tadalafil as a treatment for the signs and symptoms of benign prostatic hyperplasia (BPH) and ED if both conditions occur simultaneously.12 However, there is a risk of hypotension if PDE-5 inhibitors are administered with α-blockers.10 Hence, factors such as comorbidities and concurrent medication can affect the selection of PDE-5 inhibitors.

Studies on the characteristics of patients with ED and the factors associated with the selection of drug treatment in Malaysia are lacking. We aimed to overcome this hiatus in the present study.

Patients and methods

Study design and setting

This was a cross-sectional retrospective study conducted at the University of Malaya Medical Center (UMMC; Malaysia), a teaching hospital with 1000 beds. Approval from the Medical Committee of UMMC (reference number: 956.33) was obtained before the study was carried out.

Study population and sampling frame

The study involved patients diagnosed with ED with any comorbidity who had received a PDE-5 inhibitor as a treatment option for ED. The sampling frame was from February 2012 to January 2013. The sampling size required was calculated using Epi Info Program ver7.0. The level of significance (α) was set as 0.05 and the desired power of the study (1−β) was 80%. Assuming that the expected proportion of patients with ED was 69.5%4 and the confidence limit 5%, the minimum sample size was calculated to be 139 patients.

Study procedures

A total of 309 Registration Number (R/N) patients prescribed with sildenafil, tadalafil or vardenafil from February 2012 to January 2013 were generated from the Pharmacy Information System (PIS). Sampling was conducted to include patients as the study sample. A total of 286 (92.6%) medication records and case notes were retrieved from the Patient Medical Record (PMR) office.

The inclusion criteria were adult patients aged ≥18 years, diagnosed with ED and prescribed with sildenafil, tadalafil or vardenafil. The exclusion criteria were patients diagnosed with ED but who did not receive any PDE-5 inhibitor, or those with missing data.

Data collection

Data included demographic information (eg, age, ethnicity, height, weight, body mass index (BMI)). Clinical characteristics (eg, duration of ED, smoking, alcohol consumption, comorbidities, medication regimen, laboratory results) were also recorded.

‘Comorbidities’ were defined as coexisting ailments that required long-term therapy.13

‘Elderly’ was defined as patients aged ≥65 years.14

‘Normal weight’ was defined as a BMI (in kg/m2) of 18.5–22.9, ‘overweight’ as 23–27.4 and ‘obesity’ as ≥27.5.15

‘Sudden onset’ was defined as the early detumescence of erection during sexual intercourse but maintenance of a normal nocturnal erection. ‘Gradual onset’ was defined as the slow progression of ED with weakening of erection rigidity.16

‘Pharmacological causes’ were defined as the use of medications such as antihypertensive agents that can cause ED.17

‘Psychological causes’ were defined as an ability to have an erection in some circumstances but not in others due to performance anxiety, stress or depression.17

‘Medical causes’ were defined as ED due to medical conditions such as DM or hypertension.17

‘Surgical causes’ were defined as ED due to surgery, irradiation or procedures that involved the prostate gland, bladder, colon, rectum, spinal cord or brain.17

‘Hormonal causes’ were defined as ED due to a decrease in serum testosterone levels.17

Statistical methods

All the data collected and extracted were analysed using SPSS ver21 (SPSS, Chicago, Illinois, USA). Normally distributed data were expressed as frequency and mean±SD. Non-normally distributed data were expressed as median and IQRs. Categorical data (eg, patient characteristics, comorbidities) were expressed as percentages. The association or correlation of patient characteristics with ED was examined using the Pearson χ2 with continuity correction and Fisher's exact test if adjustment was necessary. p<0.05 was considered significant. An overview of the study procedure is shown in figure 1.

Figure 1

Overview of study procedure.

Results

A total of 309 patients were identified from the study population through the PIS. Of these, 286 medical records (92.6%) were retrieved from the PMR office. The remainder of the medicals records could not be retrieved from the PMR office. Sixty-seven patients were excluded because they did not fulfil the inclusion criteria, so 219 patients were included.

Demographic and clinical characteristics

The age of patients did not show a normal distribution (Shapiro-Wilk test; p<0.001) (table 1). The age range was 23–80 years (median 58 years). The mean body weight was 74.5 (±12.8) kg (range 43.9–107.0 kg). Data on clinical characteristics were available for only 122 of 219 patients (55.7%) for the duration of ED. The median duration of ED was 3 years (range, 6 months to 25 years). Only nine patients (4.1%) had information on ED onset.

Table 1

Demographic and clinical characteristics of patients with erectile dysfunction

Variables/characteristics	Number of patients (%)	p Value
Nationality		<0.001†
Malaysian	216 (98.6)
Non-Malaysian	3 (0.4)
Ethnicity		<0.001†
Malay	69 (31.5)
Chinese	110 (50.2)
Indian	33 (15.1)
Others	7 (3.2)
Age category (years)		<0.001†
20–29	3 (1.4)
30–39	15 (6.9)
40–49	27 (12.3)
50–59	74 (33.8)
60–69	64 (29.2)
70–79	35 (16.0)
80 and above	1 (0.4)
Mean±SD	57.4±11.24
BMI (kg/m2)*		0.091
Normal body weight	25 (11.4)
Overweight	37 (16.9)
Obese	43 (19.6)
Unknown	114 (52.1)
Cigarettes		<0.001†
Current smoker	31 (14.1)
Ex-smoker	26 (11.9)
Non-smoker	76 (34.7)
Unknown	86 (39.3)
Alcohol consumption		<0.001†
Current drinker	37 (16.9)
Ex-drinker	3 (1.4)
Non-drinker	66 (30.1)
Unknown	113 (51.6)
ED duration (years) (n=122)		<0.001†
Below 1 year	7 (5.7)
1–4	79 (64.8)
5–9	26 (21.3)
10–14	6 (4.9)
15–19	1 (0.8)
20 and above	3 (2.5)
Onset (n=9)		0.02†
Sudden	1 (11.1)
Gradual	8 (88.9)
Presence of morning erection (n=69)		0.001†
Yes	22 (31.9)
No	36 (52.2)
Occasionally	11 (15.9)

*Normal body weight-BMI: 18.5–22.9 kg/m2; Overweight-BMI: 23–27.4 kg/m2; obese-BMI ≥27.5 kg/m2.

†χ², significance level at p<0.05.

BMI, body mass index.

Figure 2 shows the distribution of concomitant comorbidities in patients with ED. Hypertension, hyperlipidaemia and DM were the most common comorbidities in patients with ED. The other comorbidities were fatty liver disease (1.8%), spinal-cord injury (1.8%), tuberculosis (1.4%), atrial fibrillation (0.9%), heart failure (0.5%), hepatic dysfunction (0.5%), renal cell cancer (0.5%), colon cancer (0.5%), thyrotoxicosis (0.5%), chronic hepatitis B (0.5%), HIV (0.5%), Hashimoto disease (0.5%), hypothyroidism (0.5%) and systemic lupus erythematosus (0.5%).

Figure 2

Types of comorbidities in patients with erectile dysfunction (BPH, benign prostatic hyperplasia; IHD, ischaemic heart disease; LUTS, lower urinary tract symptom).

Concurrent medications

There was a significant difference between the number of patients with ED who were taking medications commonly used by patients with ED(eg, anti-DM, antihypertensive, lipid-lowering, antiplatelet, antidepressant) and those who were not (p<0.001; table 2). The number of patients with ED who were taking antihypertensive agents (57.1%) and lipid-lowering agents (55.7%) was significantly higher than those who were not on these treatments (p<0.001). The number of patients with ED who used anti-DM agents (45.2%), antiplatelet agents (18.3%), antidepressants (4.1%), bronchodilator agents (3.7%) or α-blockers (24.7%) was significantly less than those who did not take such agents (p<0.001).

Table 2

Distribution of the patients with ED according to concurrent medications

Medications	Number of patients (%)†	p Value*
Diabetic agents		<0.001
Oral agents	74 (33.8)
Insulin	6 (2.7)
Insulin and oral agents	19 (8.7)
No	120 (54.8)
Antihypertensive agents		<0.001
Yes	125 (57.1)
No	94 (42.9)
Lipid lowering agents		<0.001
Yes	122 (55.7)
No	97 (44.3)
Antiplatelet agents		<0.001
Yes	40 (18.3)
No	179 (81.7)
Antidepressants		<0.001
Yes	9 (4.1)
No	210 (95.9)
Bronchodilator agents		<0.001
Yes	8 (3.7)
No	211(96.3)
α-Blockers		<0.001
Yes	54 (24.7)
No	165 (75.3)

*χ2, significance level at p<0.05.

†Percentages are calculated based on total patients with ED (N=219).

Oral treatments

Sildenafil was the most commonly (65.3%) prescribed PDE-5 inhibitor, followed by tadalafil (16.9%) and vardenafil (17.8%).

Common comorbidities in patients taking PDE-5 inhibitors

Hypertension, hyperlipidaemia and DM were the most common comorbidities in patients using sildenafil and tadalafil. For those taking vardenafil, hypertension, hyperlipidaemia and BPH were the most common comorbidities (figure 3).

Figure 3

Common comorbidities in patients taking sildenafil (N=143), tadalafil (N=37), vardenafil (N=39) (BPH, benign prostatic hyperplasia; IHD, ischaemic heart disease; LUTS, lower urinary tract symptom).

Factors associated with patient characteristics

Association of age with comorbidities

Ischaemic heart disease (IHD; p=0.025), BPH (p<0.001), obesity (p=0.005) and lower urinary tract symptoms (LUTS; p=0.006) were associated with elderly patients with ED but other comorbidities were not (table 3).

Table 3

Association of age (elderly) with types of comorbidities and medications

Comorbidities/medication	Elderly		p Value*
	Yes	No
Hypertension			0.458†
Yes	34 (61.8%)	90 (54.9%)
No	21 (38.2%)	74 (45.1%)
Diabetes mellitus			0.173†
Yes	21 (38.2%)	82 (50.0%)
No	34 (61.8%)	82 (50.0%)
Hyperlipidaemia			0.613†
Yes	30 (54.5%)	81 (49.4%)
No	25 (45.5%)	83 (50.6%)
Depression			0.683‡
Yes	1 (1.8%)	6 (3.7%)
No	54 (98.2%)	158 (96.3%)
Ischaemic heart disease			0.025†
Yes	10 (18.2%)	11 (6.7%)
No	45 (81.8%)	153 (93.3%)
Benign prostatic hyperplasia			<0.001†
Yes	43 (50.9%)	33 (20.1%)
No	27 (49.1%)	131 (79.9%)
Obesity			0.005†
Yes	3 (13.0%)	40 (48.8%)
No	20 (87.0%)	42 (51.2%)
LUTS			0.006‡*
Yes	12 (21.8%)	12 (7.3%)
No	43 (78.2%)	152 (92.7%)
No. of comorbidities			0.650§
None	3 (5.5%)	23 (14.5%)
One	9 (16.4%)	24 (14.6%)
Two	10 (18.2%)	33 (20.1%)
Three	20 (36.4%)	49 (29.9%)
Four	12 (21.8%)	29 (17.7%)
Five	1 (1.8%)	5 (3.0%)
Six	0 (0.0%)	1 (0.6%)
Diabetic agents			0.054§
Oral agents	35 (63.6%)	85 (51.8%)
Insulin	18 (32.7%)	56 (34.1%
Insulin and oral agents	2 (3.6%)	4 (2.4%)
No	0 (0.0%)	19 (3.6%)
Antihypertensive agents			0.595†
Yes	33 (61.1%)	92 (52.8%)
No	21 (38.9%)	73 (44.2%)
Lipid lowering agents			0.502†
Yes	28 (50.9%)	94 (57.3%)
No	27 (49.1%)	70 (42.7%)
Antiplatelet agents			0.164†
Yes	41 (74.5)	138 (84.1%)
No	12 (21.8)	26 (15.9%)
Antidepressants			0.683‡
Yes	54 (98.2%)	157 (95.7%)
No	1 (1.8%)	7 (4.3%)
Bronchodilator agents			0.867†
Yes	0 (0.0%)	8 (4.9%)
No	55 (100.0%)	156 (95.1%)
α-Blockers			<0.001†*
Yes	28 (51.9)	26 (15.8)
No	26 (48.1)	139 (84.2)

LUTS, lower urinary tract symptom.

*χ2, significance level at p<0.05.

†Continuity correction.

‡Fisher's exact test.

§Pearson's χ2; statistically significant (p<0.05).

Association of age with medications

The use of α-blockers was significantly associated with elderly patients with ED (p<0.001) but other medications were not (Pearson's χ2 test or Fisher's exact test, table 3).

Factors associated with selection of PDE-5 inhibitors

Concurrent comorbidities

LUTS were associated with the selection of PDE-5 inhibitors (table 4).

Table 4

Association of PDE-5 inhibitors with comorbidities and concurrent medication

Comorbidities/medications	Sildenafil (N=143)	Number of patients (%)	Vardenafil (N=39)	p Value
		Tadalafil (N=37)
Hypertension				0.852†
Yes	79 (55.2)	22 (59.5)	23 (59.0)
No	64 (44.8)	15 (49.5)	16 (41.0)
Diabetes mellitus				0.073†
Yes	68 (47.6)	22 (59.5)	13 (33.3)
No	75 (52.4)	15 (40.5)	26 (66.7)
Hyperlipidaemia				0.607†
Yes	76 (53.1)	17 (45.9)	18 (46.2)
No	67 (46.9)	20 (54.1)	21 (53.8)
Obesity				0.795†
Yes	31 (39.7)	6 (50.0)	6 (40.0)
No	47 (60.3)	6 (50.0)	9 (60.0)
Depression				0.304‡
Yes	3 (2.1)	2 (5.4)	2 (5.1)
No	140 (97.9)	35 (94.6)	37 (94.9)
IHD				0.257‡
Yes	15 (10.5)	1(2.7)	5 (12.8)
No	128 (89.5)	36 (97.3)	34 (87.2)
BPH				0.449†
Yes	38 (26.6)	9 (24.3)	14 (35.9)
No	105 (73.4)	28 (75.7)	25 (64.1)
LUTS				0.038‡
Yes	11 (7.7)	4 (10.8)	9 (23.1)
No	132 (92.3)	33 (89.2)	30 (76.9)
Diabetic agents				0.084†
Oral agents	52 (36.4)	15 (40.5)	17 (17.9)
Insulin	3 (2.1)	0 (0.0)	3 (7.7)
Insulin and oral agents	11 (7.7)	5 (13.5)	3 (7.7)
No	77 (53.8)	17 (45.9)	26 (66.7)
Antihypertensive agents				0.417†
Yes	91 (63.6)	23 (62.2)	29 (74.4)
No	52 (36.4)	14 (37.8)	10 (25.6)
Lipid lowering agents				0.477†
Yes	78 (54.5)	19 (51.4)	25 (64.1)
No	65 (45.5)	18 (48.6)	14 (35.9)
Antiplatelet agents				0.413†
Yes	29 (20.3)	4 (10.8)	7 (17.9)
No	114 (79.7)	33 (89.2)	32 (82.1)
Antidepressants				0.120‡
Yes	3 (2.1)	2 (5.4)	3 (7.7)
No	140 (97.9)	35 (94.6)	36 (92.3)
Bronchodilator agents				0.120‡
Yes	3 (2.1)	2 (5.4)	3 (7.7)
No	140 (97.9)	35 (94.6)	36 (92.3)
α-Blockers				0.008†
Yes	31 (21.7)	17 (43.6)	6 (16.2)
No	112 (78.3)	22 (56.4)	31 (83.8)

*Statistically significant (p<0.05).

†Computed using Pearson's χ2.

‡Computed using Fisher's exact test.

BPH, benign prostatic hyperplasia; IHD, ischaemic heart disease; LUTS, lower urinary tract symptom.

Concurrent medications

α-Blockers showed a significant association with the selection of oral drugs (p=0.008, table 4).

Discussion

We noted a significant association between IHD and elderly patients with ED. In the USA in 2010, the prevalence of IHD in elderly patients was reported to be 19.8%.18 In Malaysia in 2006, IHD was the second leading cause of death (15.5% of individuals who died in government hospitals).19 The Men's Attitudes to Life Events and Sexuality (MALES) study (27 839 participants) found that men with IHD had a higher prevalence of ED.20 Endothelial dysfunction causes a reduction in the level of nitric oxide (NO), which is responsible for muscle relaxation in the penis, and might be the mechanism that links IHD and ED.21 The arterial size hypothesis is based on an association between ED and chronic heart disease.22 This hypothesis suggests that obstruction of the penile artery precedes obstruction of the coronary artery.22 If so, ED can be used to predict the risk of IHD (one retrospective study showed that ED appeared first in 71% of patients).23 Hence, elderly patients with IHD should be aware of the risk of ED.

There was a significant association between BPH and being an elderly patient with ED (p<0.001). In Malaysia, the prevalence of BPH is >50% in men aged ≥60 years.24 BPH is usually associated with a series of LUTS, including nocturia, increased urinary hesitancy, frequency and urgency, as well as a weak dribbling stream of urine and increased postvoiding residual volumes.25

Several studies have indicated that BPH with associated LUTS increased incidence of ED.20 26

Medications used in BPH treatment may affect normal erectile function.21 The contradictory facts of improving versus disrupting erectile function were not well understood; however, at least one study has shown that the use of α-blockers may cause ED.27 The use of 5α- reductase inhibitors has been associated with decreased erectile function due to low levels of NO and thus related to a decline in dihydrotestosterone levels.28 Other than drugs, surgery for treatment of ED may also affect erectile function. For instance, one of the long-term complications of transurethral resection of the prostate (TURP) in patients with BPH is ED. One study found that 12% of patients with ED underwent TURP for BPH.29 Thus, elderly patients with BPH should be aware of the risk of ED.

Being elderly and having ED was found to be associated with obesity (p=0.005). According to the Third National Health and Morbidity Survey, the prevalence of overweight and obesity in elderly patients in Malaysia is 29.2%.30 Another study conducted in the rural area of Selangor in Malaysia found that the prevalence of obesity in patients aged ≥60 years was 9.3%.31 In the Health Professionals Follow-up Study (22 086 participants in the USA), obesity was found to increase the risk of ED compared with an ideal BMI (relative risk 1.9; CI 1.6 to 2.2).32 Several mechanisms could link ED with obesity. First, visceral obesity induces an inflammatory response that can lead to endothelial dysfunction.33 Second, obesity and associated comorbidities such as the metabolic syndrome can cause a lower level of testosterone in plasma that can lead to hypogonadism.33 This hypothesis is supported by a study involving 2435 men with ED which found that obesity was associated with lower levels of testosterone in the body.34 Conversely, one study showed that physical activity and weight reduction improved erectile function in one-third of obese men with ED.35 Thus, obesity is a modifiable risk factor that can prevent or improve the outcome of ED.

LUTS were commonly present in elderly patients with ED. One study in a tertiary hospital in Malaysia found that the prevalence of moderate-to-severe LUTS was 42.7% in men aged ≥40 years.36 Several studies have established the relationship between ED and LUTS. For example, a local population-based survey found that men with moderate and severe LUTS had a 1.4-times increased risk of getting ED.37 A prospective study conducted in five Asian countries involving 916 patients reported ED in 80% of patients with LUTS.38 That study also found a reduction of International Index of Erectile Function (IIEF)-5 scores with increasing age.38 Also, a survey conducted in the USA and six European countries found that 90% of 12 815 patients had LUTS, and that 83% of patients were sexually active.39 Nevertheless, ED was present in almost half of the patients who had LUTS.39 A possible explanation for this association is a reduction in NO levels in the penis and prostate muscle.40 Hence, because of evidence showing an association between LUTS and ED, elderly patients should be assessed for sexual function during LUTS management.

Only α-blockers were significantly associated with elderly patients with ED. α-Blockers are used mainly for BPH treatment or as adjunct therapy if blood pressure is not well controlled.3 41 42 In Malaysia, the prevalence of BPH is >50% in men aged >60 years.24 α-Blockers such as tamsulosin used in BPH have been found to have a negative impact on erectile function27 but alfuzosin has been reported to have a positive impact on erectile function in experimental models.43 Thus, caution with the use of α-blockers in elderly patients with ED is needed.

There was a significant association between LUTS and drug selection. Evidence-based guidelines on the selection of PDE-5 inhibitors in patients with ED with different comorbidities are lacking. The distribution of LUTS was higher for vardenafil, followed by tadalafil and sildenafil. One study in animals investigating the efficacy of PDE-5 inhibitors for LUTS treatment found that, compared with tadalafil and sildenafil, vardenafil was the most potent drug for the relaxation of prostate and urethral tissue.44 Additionally, we previously found that vardenafil and tadalafil could inhibit proliferation of stromal cells in the prostate gland and hence prevent enlargement of the prostate gland.44 Tadalafil is the only drug approved by the FDA for treatment of the signs and symptoms of BPH (specifically known as LUTS).12 This could be the reason behind the greater usage of vardenafil and tadalafil in patients with LUTS: they can be used for the treatment for ED and LUTS. Patients who took 5 mg of tadalafil reported a significant improvement in symptoms of ED and BPH.45

There was a significant association between the α-blockers and the type of PDE-5 inhibitor. The combined treatment can promote an improvement in both psychometric parameters of voiding dysfunction (namely, International Prostate Symptom Score (IPSS) scores) and ED (namely, IIEF-EF), and a significant amelioration of the Qmax.46 47

The distribution was higher in tadalafil, followed by sildenafil and vardenafil. Tadalafil has been shown to elicit the least significant reduction in blood pressure when taken with a uroselective or non-uroselective α-blocker.48 In contrast, a greater reduction in blood pressure has been noted if sildenafil is given together with an α-blocker.49 The combination of vardenafil and an α-blocker resulted in an increased prevalence of hypotension compared with the placebo group in one study.50 This could be the reason behind the higher usage of tadalafil with the α-blocker in the present study.

Conclusion

ED was prevalent in men aged ≥50 years. Patients with ED often had comorbidities such as hypertension, DM and hyperlipidaemia. IHD, BPH, obesity and LUTS were associated with elderly patients with ED. Thus, elderly patients with these diseases should be aware of the risk of ED. The presence of LUTS and α-blockers was significantly associated with the selection of PDE-5 inhibitor. Hence, further studies on the combinations of α-blockers and PDE-5 inhibitors are required to develop more effective pharmacological management of LUTS and ED.