Materials and Methods: This retrospective study analyzed 604 circumcision patients operated on using the three-stage guillotine method with thermocautery while preserving the glans. These procedures were performed by a single surgeon in the first two years of his specialization at Siverek State Hospital between October 2022 and September 2024.
Results: The mean operative time was 12.5±2.8 minutes (range: 8–25 minutes). The mean age of the patients was 7.04±4.1 years (range: 0.33–15.7 years). Bleeding in the form of minor leakage was observed in 3 patients (0.52%). Complications such as infection, penile injury, meatal stenosis, or secondary phimosis were not encountered in any patient.
Conclusion: Thermocautery shortens the duration of the procedure, reducing the child's exposure to anesthesia and surgical stress, while also lowering the risk of bleeding. Circumcision performed with a thermocautery is practical and safe when conducted by trained doctors in an appropriate setting.
Nowadays, a number of methods are used for circumcision, such as the Shang Ring, PlastiBell, Gomco clamp, Mogen clamp, Smart clamp, Tara clamp, and thermocautery. The search for more practical, cost-effective, safe, and less complicated can be more suitable [5,6]. Healing period and the rate of complications can be affected by the surgical technique and energy source selected. Nonetheless, there are still disagreements on the best circumcision technique. Thermocautery has been more wellliked recently as an economical and useful technique. Thermocautery is a device that cuts tissue with a high-temperature metal tip while simultaneously providing coagulation. Unlike electrocautery, it uses a directly heated metal tip and does not transmit electric current directly to the tissue. The main advantages of this method include effective hemostasis during cutting, minimal bleeding, shorter procedure time compared to traditional surgery, and ease of use in field conditions due to its portability and low cost. However, thermocautery carries risks of thermal damage such as burns and delayed wound healing in surrounding tissues due to heat [7].
The aim of this study is to compare the modified three-stage circumcision technique performed with the aid of a thermocautery device (Electroteknik Medical, İzmir) (Figure 1) in response to the high demand for circumcision in our region, and to contribute to the circumcision literature.
Patients who met the following exclusion criteria were excluded from the study: those individuals with penile anatomical anomalies (e.g., chordee, hypospadias, buried penis), patients undergoing additional perioperative surgical procedures, cases where thermocautery was not used, those requiring secondary surgeries, patients experiencing anesthesia-related complications, and individuals aged over 18 years.
Preoperative evaluations for all patients included physical examination in the outpatient clinic, complete blood count, bleeding parameters, and assessment by the anesthesia department. On the morning of the surgery, intravenous access was established after hospital admission. Before being taken to the operating room, patients received 0.1 mg/kg IV midazolam (Dormicum®) and were brought to the operating room accompanied by a nurse. Following induction of general anesthesia, dorsal penile block was applied with bupivacaine HCl (Marcaine 0.5%; AstraZeneca, Istanbul, Turkey) and prilocaine HCl (Citanest 2%; AstraZeneca, Istanbul, Turkey).
Surgical Technique
The settings of the thermocautery device were determined according
to the age of the participant: 500°C was used for patients
under 2 years of age, 550-650°C for patients between 2 and 10
years of age, and 700-750°C for patients over 10 years of age.
After local field preparation, the surgical site was draped under sterile conditions. In the first stage, the prepuce was completely retracted and the adhesions between the glans penis and the preputium were completely released. The prepuce was held with two clamps at the 6 and 12 o'clock positions, creating slight tension to adjust the length of the mucosa and foreskin. Then, a third straight clamp was placed under the clamps at the 6 and 12 o'clock positions and this was removed over the third clamp in a guillotine fashion with thermocautery, protecting the glans (Figure 2). In the second stage, only the outer preputial skin was clamped at the 12 and 6 o'clock positions, with the ventral aspect angled 15-20° upwards. After the tension was achieved, the outer prepuce was removed over the clamp in a guillotine fashion with thermocautery, again protecting the glans (Figure 3). In the third stage, the mucosa (inner prepuce) was clamped only at the 12, 3, 6, and 9 o'clock positions and shortened using a thermocautery device (Figure 4). The frenulum was preserved, leaving an average of 0.5–1 cm of mucosa intact. Active bleeding points were controlled by touching with the thermocautery (Figure 5).
To complete the procedure, 4/0–5/0 polyglactin 910 (VICRYL rapide®) sutures were typically placed at the 6–12, 2–10, and 4–8 o'clock positions, yielding a total of six sutures. Additional sutures were placed when necessary. The operative time was recorded as the time from the initial local site preparation to the placement of the final suture. After surgery, a topical antibiotic cream containing nitrofurazone was applied and the patient was transferred to the ward. Patients were usually discharged approximately six hours after the procedure. Follow-up assessments for complications were performed after one week, one month, and six months. Parents were informed of possible complications at discharge. Patients were evaluated in terms of operative time, bleeding, infection, urethral and penile injuries, secondary phimosis, meatal stenosis, urinary retention, and buried penis.
Statistical Analysis
The data was analyzed using SPSS 25.0 statistical software
package. Number, percentage, mean ± standard deviation (minimum
maximum) were used for descriptive statistics.
Thermocautery has been found to be a safe method when performed by skilled practitioners [11]. However, relatively few studies have been conducted on the use of thermocautery in circumcision [12–14]. In general, the occurrence of complications is influenced by the surgeon's experience, the environment, and technical factors. These complications range from minor issues such as bleeding and simple infections to rare but serious outcomes such as glans amputation, thermal burns, poor wound healing, infection, meatal stenosis, necrosis, urethral fistula, or even death [10].
Previous literature has reported circumcision complication rates ranging from 0.1% to 35% [15]. In a study conducted in the United Kingdom involving 66,519 circumcisions, the complication rate was found to be 2%. Among the complications, bleeding occurred in 533 patients (0.8%), revision surgery was required in 303 patients (0.5%), and meatal stenosis was observed in 7 patients [16].
A meta-analysis examining thermocautery-assisted circumcisions in 32,000 patients from 17 countries reported a complication rate of 2.48%, with minor bleeding being the most common complication (2.2%). The most severe complications reported were entrapment of the penis due to secondary phimosis (0.078%) and meatal obstruction (0.018%) [17].
In a study by Akyüz et al., the incidence of trapped penis following thermocautery-assisted circumcision was reported as 0.38% [18]. Another study involving 2,973 thermocautery procedures reported a complication rate of 0.2%, with meatal stenosis and secondary phimosis each observed in 0.03% of cases [19]. Similarly, in a study of 1,011 children who underwent thermocautery circumcision, complications were observed in 4 patients (0.4%), including secondary phimosis in one child, meatal stenosis in another, bleeding in one, and infection in another [14]. The main approach to treating secondary phimosis is surgery; surgical revision may be required, especially in cases where scar tissue is evident. However, in some cases diagnosed early and with minimal scar tissue, topical corticosteroid therapy may be tried. According to the results of Yalçın's study, topical steroid treatment was largely ineffective in 54 cases of secondary phimosis that developed after circumcision with thermocautery, and all patients required surgical revision [20]. In our study, similar to the literature, minor bleeding was observed in 3 patients (0.52%), but no major complications were encountered. Bleeding, which is the most commonly reported complication in the literature (2–35%), is often caused by frenular or dorsal vessels [21]. In our patients, bleeding was controlled with postoperative compression dressings.
We believe that mucosal edema is a frequently encountered yet often overlooked complication in thermocautery-assisted circumcision. The literature reports varying rates of mucosal edema (20–30%), which are generally considered clinically insignificant [17]. In the study by Arslan et al., edema was observed in one-fifth of the patients and was deemed clinically irrelevant [12]. Ngcobo and colleagues reported that 20 to 30 percent of patients experienced penile swelling on the second day after surgery, although the surgical procedure was not clearly specified [22]. In our study, some children exhibited varying degrees of edema, but it had no adverse effect on the healing process. Concerns have been raised about thermocautery-related heat production causing damage to penile nerves, potentially reducing penile sensitivity and impacting tissue healing. Although few histopathological case studies exist, they have demonstrated that tissue damage caused by the high temperatures generated by the device is extremely limited [13,18,23].
Saracoğlu et al. reported that circumcisions performed with the thermocautery technique resulted in shorter operation times and less bleeding, contributing to reduced overall surgical duration [24]. Another study evaluating 2,973 children undergoing thermocautery-assisted circumcision reported an average procedure time of 6.5 minutes [19]. Meanwhile, another report indicated an average operation time of 17 ± 2.3 minutes (range 10–23 minutes) [18]. When we compare these times with other techniques, in the study of Tuncer et al., the classical surgical technique took 14.38 ± 2.91 minutes, the thermocautery technique 5.02 ± 1.32 minutes and the Alisklamp 4.05 ± 1.0 minutes, and all three techniques were found to be statistically different from each other in terms of surgery time [14]. In Yalçın's study of 5122 cases where the dorsal slit method was applied, the average procedure time was calculated as 11.74 ± 2.04 minutes [25]. In our study, the circumcision duration was recorded as 12.5 ± 2.8 minutes (range 8–25 minutes). Some centers use single- or two-stage guillotine techniques [14,17,19]. Although our circumcision duration was slightly longer due to the three-stage technique, our low complication rate, particularly the absence of major longterm complications such as meatal stenosis or secondary phimosis, can be attributed to the applied circumcision technique and the specialized training of the surgeon, who received extensive education in a high-volume circumcision clinic.
Our study has certain limitations. Ideally, surgical techniques are best compared in prospective randomized trials; however, this is a retrospective study. Some minor complications may not have been noticed by the relatives of the patients or reported to the healthcare institution; this may have led to an underestimation of complication rates. The lack of a comparative control group in the study limits the ability to directly evaluate the efficacy and safety differences of the thermocautery technique compared to other methods. Long-term follow-up data are not available in our study; therefore, late complications, scar development or patient satisfaction could not be evaluated. Additionally, all circumcisions in this study were performed by a single surgeon.
Ethics Committee Approval: Ethical approval for this study was obtained from Mardin Artuklu University Clinical Research Ethics Committee (Ethics committee approval date number: 28.11.2022/ M5.TUT.019.
Informed Consent: An informed consent was obtained from all the patients.
Publication: The results of the study were not published in full or in part in form of abstracts.
Peer-review: Externally and intarnally peer-reviewed.
Authorship Contributions: Any contribution was not made by any individual not listed as an author. Concept – M.K., A.B.; Design – A.Ş., A.B.; Supervision – A.B.; Resources – A.Ş., A.B.; Materials – A.Ş., M.K.; Data Collection and/or Processing – A.Ş., M.K., Ü.U.; Analysis and/or Interpretation – M.K., Ü.U.; Literature Search – M.K., Ü.U.; Writing Manuscript – A.Ş., Ü.U.; Critical Review – A.B.
Conflict of Interest: The authors declare that they have no conflicts of interest.
Financial Disclosure: The authors declare that this study received no financial support.
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