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Clin Exp Reprod Med > Epub ahead of print
Saber-Khalaf, Fathi, El-hamed, Mahmoud, ElShibany, and Mohamed: Hydrocelectomy versus conservative follow-up for symptomatic hydroceles in infertile men: A pilot study

Abstract

Objectives

To evaluate the advantages and disadvantages of hydrocele repair in infertile men. The outcome measures were changes in testicular size, semen analysis, and natural pregnancy rate postoperatively.

Methods

This pilot study was conducted between January 2021 and April 2024. Inclusion criteria were male patients with a 1-year history of infertility associated with symptomatic hydroceles >100 mL and abnormal semen parameters. Thirty-one men underwent hydrocele surgery, while 30 opted for conservative follow-up. Repeat semen analysis and testicular ultrasonography were performed 6 months after surgery.

Results

Primary infertility was reported in 65% of the patients, and two-thirds had unilateral hydroceles. Both groups were comparable in baseline semen parameters, testicular size, and demographic data. The natural pregnancy rate was documented 1 year after surgery. Pregnancy rates were higher in the surgery group than in the conservative group (7 [22.58%] and 5 [16.67%], respectively), although this difference was not statistically significant. No statistically significant differences were observed in semen analysis post-surgery or follow-up. A mild but statistically significant reduction in testicular size was noted after surgery (p<0.001). More than 80% of patients reported satisfaction with the surgery. The overall complication rate was 15%, with only two patients requiring further surgical intervention.

Conclusion

Hydrocelectomy can be offered safely to infertile men. It is associated with high patient satisfaction and minimal side effects. Larger randomized controlled trials are required to confirm its positive effects on natural pregnancy.

Introduction

Hydroceles are pathological collections of fluid in the tunica vaginalis. They may be communicating or non-communicating. In adults, hydroceles are the most common cause of benign scrotal swellings, with an estimated incidence of 1% in the adult population [1]. Adult hydroceles are most often idiopathic, but they may also develop as a result of infection, tumors, trauma, or iatrogenic lymphatic obstruction following varicocelectomy [2].
Hydroceles can usually be managed conservatively. However, surgery may be required in approximately 20% of men diagnosed with hydroceles [3]. Treatment options include open surgical procedures, such as the Jaboulay or Lord techniques, or minimally invasive approaches such as aspiration and sclerotherapy [4,5]. Expected complications after these surgeries include hematoma, infection, chronic pain, recurrence or persistent swelling, trauma to cord structures, or testicular atrophy, with estimated overall complication rates of 20% for open procedures and 5% for minimally invasive techniques [3,6]. Given these risks, some andrologists discourage surgery for hydroceles in young adults who have not yet completed their families.
Conversely, some studies have demonstrated detrimental effects of hydroceles on spermatogenesis, which may result from pressure effects or alterations in testicular temperature [7,8]. Other studies have reported reduced testicular volume in both children and adults with hydroceles [9].
Thus, whether hydroceles should be surgically treated in young men seeking fertility remains a matter of debate among andrologists. To our knowledge, no clinical studies have systematically examined the advantages and disadvantages of hydrocelectomy in infertile men. The present study aimed to evaluate the benefits and risks of hydrocele surgery in this population. The outcome measures were changes in testicular size, semen analysis, and natural pregnancy rate postoperatively.

Methods

This pilot study was conducted between January 2021 and April 2024. Eligibility criteria included male patients with a one-year history of infertility associated with symptomatic hydroceles >100 mL and abnormal semen parameters. Exclusion criteria were patients with azoospermia; severe oligospermia with sperm count <5 million/mL; other causes of male subfertility such as clinical varicoceles, hypogonadism, or low-normal testosterone (total testosterone <12 nmol/L); small-sized testes (testicular volume <10 mL); previous treatment for male infertility; exposure to gonadotoxins or anabolic drugs; prior genital surgery; history of smoking or alcohol consumption; abnormal female factor evaluation; or wife’s age over 35 years.
Patients were referred to our fertility unit for evaluation of potentially correctable causes of male infertility. Two abnormal semen analyses were already available at the time of referral. History-taking included type and duration of infertility, relevant medical and surgical history, history of smoking, alcohol, or drug use, and sexual history. Physical examination was performed in both supine and standing positions. Morning fasting levels of testosterone, follicle-stimulating hormone, and luteinizing hormone were measured in all patients as part of infertility evaluation. Scrotal ultrasonography was performed routinely to assess hydrocele volume, presence of varicoceles, and testicular size.
The procedure, including its risks and benefits, was discussed with all patients. Thirty-one patients elected to undergo hydrocelectomy (study group), while a control group of 30 patients chose conservative follow-up. Both groups were encouraged to adopt a healthy lifestyle, increase physical activity, and avoid excessive heat exposure and tight clothing. Both groups were also prescribed a male fertility supplement (L-carnitine, zinc, selenium, coenzyme Q10, vitamin C, and folic acid), administered as sachets twice daily for 4 months.
Surgery was performed under spinal anesthesia using a median raphe incision. The testes and epididymis were examined for any gross abnormalities. The color and volume of hydrocele fluid were recorded. The surgical technique involved eversion with or without excision of excess tunica, followed by plication of the edges. Patients were discharged 2 hours after surgery unless a drain was required. Postoperative follow-up was performed 6 weeks later to assess wound healing and complications.
Repeat semen analysis and testicular ultrasonography were performed 6 months after surgery. Patient satisfaction was assessed using the Surgical Satisfaction Questionnaire (SSQ-8) [10]. The natural pregnancy rate was documented 1 year after surgery. Patients who did not achieve natural pregnancy were referred for in vitro fertilization.
The study was approved by the Institutional Review Board of South Valley University (Code SVU/MED/URO016/1-21) and was conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants.

1. Statistical analysis

Data were analyzed using the SPSS ver. 27 (IBM Co.). Normality was assessed using the Kolmogorov-Smirnov and Shapiro-Wilk tests, and all continuous variables were found to be non-normally distributed. Continuous data were expressed as mean±standard deviation (SD) for parametric variables or as median and interquartile range for non-parametric variables.
Differences between the two groups were analyzed using the Mann-Whitney U test for non-parametric data. The Wilcoxon signed-rank test was used to compare baseline values with 6-month postoperative values, as the data were not normally distributed. Nominal data were expressed as percentages, and differences between groups were analyzed using the chi-square test. A two-tailed p<0.05 was considered statistically significant.

Results

A total of 61 patients were recruited for the study. The mean±SD age of men in the hydrocele surgery group (study group) and the follow-up group (control group) was 34.97±8.19 and 35.40±6.93 years, respectively. The mean±SD age of their wives was 24.84±4.04 and 26.07±4.53 years, respectively. The hydrocele volume ranged from 100 to 500 mL in both groups, with a mean±SD of 251.61±135.7 mL. Primary infertility was reported in more than 65% of patients, and two-thirds presented with unilateral hydroceles. No statistically significant differences were found between the two groups in demographic data, hydrocele volume, testicular size, or semen parameters (Table 1).
At 6 months postoperatively, there were no statistically significant differences between the two groups regarding testicular size and semen parameters. The natural pregnancy rate was higher in the hydrocelectomy group compared with the conservative group (7 [22.58%] vs. 5 [16.67%]), respectively, although the difference was not statistically significant (Table 2).
Within the hydrocelectomy group, no statistically significant changes were observed in semen parameters (semen volume; total sperm count/ejaculate; sperm count; percentage of total motility; percentage of progressive motility; and percentage of normal forms) 6 months after surgery. However, testicular size showed a statistically significant reduction from 14.52±4.04 mL preoperatively to 12.77±3.99 mL postoperatively (p<0.001). This reduction was mild and remained within the normal range (Table 3). By contrast, there were no statistically or clinically significant changes in semen parameters or testicular size in the conservative follow-up group (Table 4).
Subgroup analysis stratified patients according to hydrocele volume: <200 mL (n=11) and ≥200 mL (n=20). Testicular size decreased significantly in both subgroups, but there were no statistically significant changes in semen parameters (Table 5). At 6 months postoperatively, all patients (n=20) with hydrocele volume ≥200 mL were satisfied with surgery. Among patients with hydrocele volume <200 ml, three were dissatisfied, three were neutral, and five were satisfied.
Regarding complications, three patients (9%) experienced recurrence of hydrocele at 6 months, but these recurrences were small, painless, and managed conservatively. Hematoma occurred in two patients (6%); one of these required surgical drainage.

Discussion

We recruited patients with symptomatic hydroceles >100 mL in size. Although hydroceles <200 mL are often considered mild, young and active patients with hydroceles >100 mL were frequently found to be symptomatic. In another study, hydroceles >100 mL were also classified as large hydroceles [11]. Our study showed that more than 80% of patients were satisfied following hydrocelectomy, while 9% reported neutral satisfaction. Semen parameters were comparable to those of patients managed conservatively. Although testicular size decreased significantly after surgery, this reduction was not clinically significant. In contrast, the pregnancy rate was slightly higher in the surgery group.
It is well established that hydroceles can significantly alter testicular morphology by reducing the number of seminiferous tubules, primarily spermatids, and by disturbing the structure and arrangement of seminiferous tubules [12]. Histopathologic changes associated with hydroceles include interstitial fibrosis, basement membrane thickening, and disorganization of spermatogenic cells [7,13]. These alterations may result from the pressure exerted by the hydrocele on the testis, the detrimental effects of highly proteinaceous hydrocele fluid, or other mechanisms underlying hydrocele formation. Indeed, the hydrostatic pressure of hydroceles has been shown to exceed the pressure within scrotal blood vessels [14].
In this study, testicular volume decreased significantly after surgery. This finding is consistent with Mihmanli et al. [15], who reported that postoperative testicular volume was significantly lower than preoperative values. They attributed this to hydrocele-related compression obstructing testicular vessels, which in turn causes stasis of venous and lymphatic outflow. Such stasis results in swelling and increased testicular size preoperatively, while postoperative volume reduction reflects relief of pressure and regression of testicular swelling.
We employed the eversion and excision technique. The overall complication rate was 15%, with most events managed conservatively. Only one patient (3%) required surgical drainage of a postoperative hematoma (Clavien-Dindo grade III). This complication rate was notably lower than that reported in previous studies using the same technique, which ranged between 19% and 54% [4,6]. Most of our patients expressed satisfaction after surgery. This finding aligns with the results of Ahorlu et al. [16], who reported that hydroceles negatively impact comfort, work performance, sexual function, social interaction, and relationships, and that patients experience substantial improvements in these domains following hydrocelectomy.
To our knowledge, this is the first study to evaluate both the benefits and risks of hydrocelectomy in infertile men. Although the small sample size limited our ability to demonstrate a superior effect of hydrocelectomy on semen parameters and pregnancy rates, the study confirmed that surgery is not contraindicated in young infertile men. Moreover, surgery was associated with high satisfaction, primarily due to relief of pain and discomfort related to scrotal swelling. The main limitations of this study are the small sample size, short follow-up period, and non-randomized design.
In summary, hydrocele surgery in infertile men with large symptomatic hydroceles was associated with high patient satisfaction and minimal complications. Larger randomized controlled trials with extended follow-up are necessary to assess the effects of hydrocelectomy on spermatogenesis and natural pregnancy outcomes.

Conflict of interest

No potential conflict of interest relevant to this article was reported.

Author contributions

Conceptualization: MSK, AF, MAE, OM, AME, OM. Methodology: MSK, AF. Formal analysis: OM (Osama Mahmoud). Data curation: AF, OM (Omar Mohamed). Project administration: MSK. Visualization: MSK, AF, MAE, OM, AME, OM. Software: MSK, OM(Omar Mohamed). Validation: MSK, AF, MAE, OM, AME, OM. Investigation: MSK, AF, OM, OM. Supervision: MSK. Writing-original draft: MSK. Writing-review & editing: MSK. Approval of final manuscript: MSK, AF, MAE, OM, AME, OM.

Table 1.
Demographic data and clinical data at baseline
Variable Hydrocele follow-up (n=30) Hydrocele surgery (n=31) p-value
Age (yr)
 Min–Max 22–45 21–52
 Mean±SD 35.4±6.93 34.97±8.19
 Median (IQR) 35 (29–43) 34 (29–41) 0.706
Wife age (yr)
 Min–Max 18–35 18–34
 Mean±SD 26.07±4.53 24.84±4.04
 Median (IQR) 26 (23–30.25) 24 (23–27) 0.293
Infertility type
 1 yr 20 (66.67) 21 (67.74) 0.929
 2 yr 10 (33.33) 10 (32.26)
Laterality
 Unilateral 22 (73.33) 23 (74.19) 0.939
 Bilateral 8 (26.67) 8 (25.81)
Side of unilateral cases
 RT 12 (54.55) 14 (60.87) 0.668
 LT 10 (45.45) 9 (39.13)
Duration of hydrocele (mo)
 Min–Max 2–8 2–6
 Mean±SD 3.7±1.29 3.45±1.15
 Median (IQR) 3.5 (3–4) 3 (2–4) 0.560
Testicular size (mL)
 Min–Max 5–20 5–20
 Mean±SD 13.93±4.26 14.52±4.04
 Median (IQR) 15 (10.75–17.25) 15 (12–18) 0.628
Sperm count (million/mL)
 Min–Max 6–45 6–45
 Mean±SD 21.97±11.08 22.23±10.74
 Median (IQR) 22 (11.75–32) 22 (15–30) 0.977
Progressive motility (%)
 Min–Max 0–40 0–40
 Mean±SD 21.77±9.75 20.52±10.7
 Median (IQR) 23 (16.5–29.25) 23 (13–29) 0.728
Normal morphology (%)
 Min–Max 0–5 0–5
 Mean±SD 3.07±1.2 2.81±1.17
 Median (IQR) 3 (2–4) 3 (2–4) 0.329

Values are presented as number (%) unless otherwise indicated. Comparisons were made between the two study groups using the Mann-Whitney U test for continuous data. p>0.05 was considered not statistically significant, p<0.05 considered statistically significant, p<0.01 considered highly statistically significant.

SD, standard deviation; IQR, interquartile range; RT, right; LT, left.

Table 2.
Comparison between the two groups after surgery or follow-up
Variable Hydrocele follow-up (n=30) Hydrocele surgery (n=31) p-value
Testicular size
 Min–Max 5–20 4–20
 Mean±SD 13.93±4.26 12.77±3.99
 Median (IQR) 15 (10.75–17.25) 13 (10–16) 0.201
Sperm count (million/mL)
 Min–Max 3–59 3–59
 Mean±SD 23.9±11.78 24.19±12.55
 Median (IQR) 23 (15–30.25) 22 (15–30) 0.902
Progressive motility (%)
 Min–Max 0–35 0–35
 Mean±SD 22.27±9.4 21.55±9.6
 Median (IQR) 24 (19–28) 23 (13–29) 0.628
Normal morphology (%)
 Min–Max 0–5 0–5
 Mean±SD 2.97±1.16 2.71±1.27
 Median (IQR) 3 (2–4) 3 (2–4) 0.504
Pregnancy
 No 25 (83.33) 24 (77.42) 0.561
 Yes 5 (16.67) 7 (22.58)

Values are presented as number (%) unless otherwise indicated. Comparisons were made between the two study groups using the Mann-Whitney U test for continuous data and the chi-square test for categorical data. p>0.05 was considered not statistically significant, p<0.05 considered statistically significant, p<0.01 considered highly statistically significant.

SD, standard deviation; IQR, interquartile range.

Table 3.
Comparison between baseline and 6 months postoperative in hydrocele surgery group
Hydrocele surgery (n=31) p-value
Baseline 6-mo postoperative
Sperm count (million/mL)
 Min–Max 6–45 3–59
 Mean±SD 22.23±10.74 24.19±12.55
 Median (IQR) 22 (15–30) 22 (15–30) 0.397
Progressive motility (%)
 Min–Max 0–40 0–35
 Mean±SD 20.52±10.7 21.55±9.6
 Median (IQR) 23 (13–29) 23 (13–29) 0.342
Normal morphology (%)
 Min–Max 0–5 0–5
 Mean±SD 2.81±1.17 2.71±1.27
 Median (IQR) 3 (2–4) 3 (2–4) 0.935
Testicular size (mL)
 Min–Max 5–20 4–20
 Mean±SD 14.52±4.04 12.77±3.99
 Median (IQR) 15 (12–18) 13 (10–16) <0.001

Comparisons were made between baseline and 6-month postoperative using the Wilcoxon signed-rank test for continuous data. p>0.05 was considered not statistically significant, p<0.05 considered statistically significant, p<0.01 considered highly statistically significant.

SD, standard deviation; IQR, interquartile range.

Table 4.
Comparison between baseline and 6 months postoperative in hydrocele follow-up group
Hydrocele follow-up (n=30) p-value
Baseline 6-mo follow-up
Sperm count (million/mL)
 Min–Max 6–45 3–59
 Mean±SD 21.97±11.08 23.9±11.78
 Median (IQR) 22 (11.75–32) 23 (15–30.25) 0.321
Progressive motility (%)
 Min–Max 0–40 0–35
 Mean±SD 21.77±9.75 22.27±9.4
 Median (IQR) 23 (16.5–29.25) 24 (19–28) 0.310
Normal morphology (%)
 Min–Max 0–5 0–5
 Mean±SD 3.07±1.2 2.97±1.16
 Median (IQR) 3 (2–4) 3 (2–4) 0.942
Testicular size (mL)
 Min–Max 5–20 5–20
 Mean±SD 13.93±4.26 13.93±4.26
 Median (IQR) 15 (10.75–17.25) 15 (10.75–17.25) 0.999

Comparisons were made between baseline and 6-month follow-up using the Wilcoxon signed-rank test for continuous data. p>0.05 was considered not statistically significant, p<0.05 considered statistically significant, p<0.01 considered highly statistically significant.

SD, standard deviation; IQR, interquartile range.

Table 5.
Comparison between baseline and 6 months postoperative in hydrocele surgery group according to hydrocele volume levels
Hydrocele volume
<200 mL (n=11) p-value ≥200 mL (n=20) p-value
Baseline 6-mo postoperative Baseline 6-mo postoperative
Testicular size (mL)
 Min–Max 5–20 4–20 9–20 8–20
 Mean±SD 13.27±4.86 11.73±4.69 15.2±3.46 13.35±3.54
 Median (IQR) 15 (10–16) 12 (9–15) 0.010 15 (12.25–18.75) 13.5 (10–16) <0.001
Sperm count (million/mL)
 Min–Max 9–33 11–43 6–45 3–59
 Mean±SD 19.91±8.09 21.82±9.79 23.5±11.96 25.5±13.91
 Median (IQR) 20 (12–23) 21 (13–30) 0.472 22 (16–31.5) 22.5 (17.5–33.75) 0.585
Progressive motility (%)
 Min–Max 3–34 4–33 0–40 0–35
 Mean±SD 25.18±8.3 23.45±8.45 17.95±11.18 20.5±10.23
 Median (IQR) 25 (23–30) 25 (21–29) 0.245 21.5 (8.25–23) 21 (12.25–27.25) 0.052
Normal morphology (%)
 Min–Max 1–4 1–5 0–5 0–4
 Mean±SD 2.91±0.94 3.36±1.03 2.75±1.29 2.35±1.27
 Median (IQR) 3 (2–4) 3 (3–4) 0.059 3 (2–4) 3 (2–3) 0.222

SD, standard deviation; IQR, interquartile range.

References

1. Mihmanli I, Kantarci F. Sonography of scrotal abnormalities in adults: an update. Diagn Interv Radiol 2009;15:64-73.
pmid
2. Ding H, Tian J, Du W, Zhang L, Wang H, Wang Z. Open non-microsurgical, laparoscopic or open microsurgical varicocelectomy for male infertility: a meta-analysis of randomized controlled trials. BJU Int 2012;110:1536-42.
crossref pmid
3. Lundstrom KJ, Soderstrom L, Jernow H, Stattin P, Nordin P. Epidemiology of hydrocele and spermatocele; incidence, treatment and complications. Scand J Urol 2019;53:134-8.
crossref pmid
4. Ku JH, Kim ME, Lee NK, Park YH. The excisional, plication and internal drainage techniques: a comparison of the results for idiopathic hydrocele. BJU Int 2001;87:82-4.
crossref pmid pdf
5. Erdas E, Pisano G, Pomata M, Pinna G, Secci L, Licheri S, et al. Sclerotherapy and hydrocelectomy for the management of hydrocele in outpatient and day-surgery setting. Chir Ital 2006;58:619-25.
pmid
6. Kiddoo DA, Wollin TA, Mador DR. A population based assessment of complications following outpatient hydrocelectomy and spermatocelectomy. J Urol 2004;171(2 Pt 1):746-8.
crossref pmid
7. Dandapat MC, Padhi NC, Patra AP. Effect of hydrocele on testis and spermatogenesis. Br J Surg 1990;77:1293-4.
crossref pmid pdf
8. Gupta N, Gupta M, Chanchlani R. A study to evaluate the effect of hydrocoele on testis and spermatogenesis: a cross-sectional study from Bhopal, India. Int Surg J 2015;2:523-6.
crossref
9. Jedrzejewski G, Wozniak MM, Madej T, Kryza R, Zielonka-Lamparska E, Wieczorek AP. The differences in testicular volumes in boys 8-36 months old with undescended, retractile and hydrocele testis: usefulness of scrotal screening ultrasound. Early Hum Dev 2012;88:185-9.
crossref pmid
10. Haff RE, Stoltzfus J, Lucente VR, Murphy M. The Surgical Satisfaction Questionnaire (SSQ-8): a validated tool for assessment of patient satisfaction following surgery to correct prolapse and/or incontinence. J Minim Invasive Gynecol 2011;18(6 Suppl):S49-50.
crossref
11. Nassour AJ, Ashrafi D, Patel D. Techniques: mini-incision and plication (MIP) cure hydrocele: a minimally invasive surgical variation. Can Urol Assoc J 2022;16:E294-7.
crossref pmid pmc pdf
12. Bhatnagar BN, Dube B, Shukla AP. Testicular histology in tropical vaginal hydrocele. Int Surg 1970;53:167-70.
pmid
13. Rados N, Trnski D, Keros P, Rados J. The biomechanical aspect of testis hydrocele. Acta Med Croatica 1996;50:33-6.
pmid
14. Srinath C, Ananthakrishnan N, Lakshmanan S, Vikram K. Effect of tropical vaginal hydroceles on testicular morphology and histology. Indian J Urol 2004;20:109-12.
crossref
15. Mihmanli I, Kantarci F, Kulaksizoglu H, Gurses B, Ogut G, Unluer E, et al. Testicular size and vascular resistance before and after hydrocelectomy. AJR Am J Roentgenol 2004;183:1379-85.
crossref pmid
16. Ahorlu CK, Dunyo SK, Asamoah G, Simonsen PE. Consequences of hydrocele and the benefits of hydrocelectomy: a qualitative study in lymphatic filariasis endemic communities on the coast of Ghana. Acta Trop 2001;80:215-21.
crossref pmid
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