Minimally Invasive Video-Assisted Thyroidectomy Versus Conventional Thyroidectomy: A Single-Blinded, Randomized Controlled Clinical Trial
G El-Labban
Citation
G El-Labban. Minimally Invasive Video-Assisted Thyroidectomy Versus Conventional Thyroidectomy: A Single-Blinded, Randomized Controlled Clinical Trial. The Internet Journal of Surgery. 2009 Volume 22 Number 2.
Abstract
Introduction
Neck surgery is one of the newest and most interesting applications of minimally invasive surgery. Many reports on the use of this technique in thyroid surgery, particularly with regard to eliminating the unattractive scars sometimes caused by conventional surgery, are conducted.1-11
Minimal-access thyroid surgery was conceived primarily in Europe and Asia. A number of groups11-17 have made pioneering contributions to this field. While a variety of minimally invasive approaches have been endorsed, the technique most widely practiced in North America is the minimally invasive video-assisted thyroidectomy (MIVAT), as originally described by Miccoli et al.12 As with many new surgical techniques, adoption of MIVAT in the United States has been slow and somewhat deliberate. Increasingly, however, high-volume thyroid surgical centers have embraced this approach, and modest-sized case series have been published detailing their experiences.18-19
A more comprehensive reflection of the North American experience with MIVAT, consolidated data were compiled prospectively at 4 academic medical centers, paying specific attention to the safety and feasibility of this approach.20
Several surgeons reported their experiences with minimally invasive and video-assisted surgery of the neck.2,12,13,21-40
Although all these evidence-based data reporting short- and long-term outcome after endoscopic resections for different thyroid diseases showed clear advantages in comparison with traditional procedures, mini-invasive thyroid surgery has not been already accepted.13,19,41-46 One of the reasons for this initial refusal is partly due to technical difficulty of endoscopic resection requiring adequate training both in open and endoscopic procedures before safely performing gland resection.46
MIVAT has the potential to offer similar advantages over conventional thyroidectomy. However, almost a decade after the early descriptions of endoscopic thyroidectomy, MIVAT remains in an early phase of its evolution with a variety of techniques practiced in a relatively small number of specialist centers internationally.47
While the feasibility of MIVAT approaches has been well documented, few studies have observed these techniques in the setting of a randomized trial. The minimally invasive approaches have demonstrated some advantages in terms of cosmetic and pain outcomes.13,42 While this approach appears anecdotally to have benefits over conventional thyroidectomy, a randomized clinical trial is needed to avoid the selection bias which is inherent in retrospective studies and surgical case series. 48
The aim of this study was to compare the outcomes of MIVAT with conventional surgery in patients presenting with unilateral thyroid nodules or follicular lesions.
Patients And Methods
Study design
A single-blinded, randomized clinical trial comparing MIVAT with conventional hemithyroidectomy was undertaken within the Suez Canal University Hospital. The trial was approved by the Faculty of Medicine, Suez Canal University Research Ethics Committee, and written informed consent was obtained from all participants prior to entry into the trial.
The study population included those patients with unilateral, thyroid nodules or follicular lesions requiring hemithyroidectomy for further histological diagnosis. Patients with small solitary toxic thyroid nodules were also eligible for participation. Patients were considered for randomization if they had unilateral nodular disease with a maximum nodule diameter of less than or equal to 3.0cm and were able to give informed consent. Participants were considered ineligible if preoperative fine-needle cytology showed thyroid carcinoma, nodule diameter was greater than 3.0cm, active thyroiditis was evident, or there was a history of previous neck surgery or head and neck irradiation.
Operative technique
Patients were randomized to undergo diagnostic hemithyroidectomy by either MIVAT or conventional method. All patients were blinded to the allocated procedure preoperatively. The procedure was performed by the same surgeon, and the surgeon was aware of the procedure type at the time of randomization. All patients underwent preoperative fiberoptic laryngoscopy to assess vocal cord movement. Both procedures were performed by a standardized technique. All patients had local infiltration of subcutaneous tissues beneath the incision with 5ml of Marcaine 0.5% with adrenaline.
The technique for MIVAT has been described previously by Miccoli et al.13 The gasless video-assisted thyroid surgery was used. The patients were operated on under general endotracheal anesthesia. The patient was placed in the supine position and the neck was not hyperextended. Depending on the nodule size, a 2cm or 2.5cm horizontal skin incision was made 2cm above the clavicle. An upper flap was created by subplatysmal dissection and elevated to create a tent-like working space, which provided a comfortable space for simultaneous insertion of a 3.3-mm 0° laparoscope and instruments through the same skin incision. With endoscopic assistance, subplastysmal dissection was carefully performed to avoid bleeding. The cervical linea alba was divided longitudinally as far up as the thyroid cartilage. The overlying strap muscles were dissected off the thyroid. The strap muscles on the affected side were retracted using an Army-Navy retractor to expose the thyroid and hold open the dissection space. A Fr. 10 suction catheter was attached to the scope for continuous suction of warm air in the wound to prevent blurry scope optics. The middle thyroid vein or the small veins between jugular vein and thyroid were divided with harmonic scalpel. An Allis tissue forceps was applied to the upper portion of the thyroid, allowing a downward and lateral traction of the thyroid. The avascular space between the upper pole of the thyroid and the cricothyroid muscle was opened to identify the external branch of the superior laryngeal nerve. The superior thyroid vessels were selectively isolated and divided using harmonic scalpel. Following division of the superior thyroid vessels, the upper portion of the thyroid was gently extracted from the incision using an Allis forceps. Gentle traction over the thyroid enabled the gland to be extracted without rupture. Then the inferior thyroid artery was exposed, and the parathyroid glands and recurrent laryngeal nerve were identified clearly. The inferior thyroid artery was ligated and not divided on the thyroid capsule distal to its supply of the parathyroid glands. The thyroid was freed from the trachea by ligating the small vessels and dissecting the ligament of Berry. The isthmus was then dissected from the trachea and divided by the harmonic scalpel. The specimen excised was extracted from the wound and a small suction drain was left inside. The wound was closed with absorbable sutures.
Conventional hemithyroidectomy was performed utilizing a 5–6-cm Kocher incision and division of the ipsilateral strap muscles. After this exposure, the operative technique then mirrored that used in the MIVAT approach. A standard dressing was applied for both MIVAT and conventional cases, with adhesive surgical tape placed horizontally across the neck. The patients were observed in the 24-hour ward and discharge was planned for the morning of the following day.
Outcome measures
The primary endpoints of the study were measurement of postoperative pain after 24 and 48 hours from operation and self-rated patient satisfaction with cosmetic outcome 3 months postoperatively. Postoperative pain scores were measured using a 10-point visual analog scale (VAS) postoperatively. A higher numeric pain score represented more severe pain. Satisfaction with cosmetic outcome was measured at the follow-up using a 10-point VAS.
The secondary outcome measures were operative time, incidence of temporary and permanent recurrent laryngeal nerve injury, postoperative hematoma formation, length of incision, and duration of hospital stay.
The operative time was measured from initiation of the incision to conclusion of the skin closure to the nearest minute. Recurrent laryngeal nerve function was assessed with preoperative and postoperative fiberoptic laryngoscopy. Postoperative hematoma was considered significant if it required return to the operating room (OR) for evacuation. Incision length was measured at the final follow-up to the closest millimeter.
Results
Patient characteristics
The clinical characteristics of patients in the two groups were similar. There was a predominance of females in both groups, and the mean nodule size was equivalent between the groups without any significant difference. The clinical characteristics are summarized in table 1.
Figure 1
Surgical treatment
No patients in the MIVAT group required conversion to conventional surgery. The operative time as measured from initiation of the skin incision to conclusion of subcuticular closure was greater for the MIVAT cases compared to conventional (P<0.0001). On average, the MIVATS procedure had an operative time that was 16 minutes longer in duration than the conventional procedure. There were no significant differences in estimated intra-operative blood loss or length of hospital stay. There were 2 patients who developed temporary recurrent laryngeal nerve paralysis in the MIVAT group and 1 in the conventional group. There was only one patient with permanent recurrent laryngeal nerve injury in the MIVAT group. No patient required return to the operating room for evacuation of hematoma. The operative details and complication rates are summarized in table 2.
Figure 2
Outcome measures
Pain scores as measured on the ten point VAS were significantly lower in the MIVAT group after the first postoperative day when compared with the conventional group. The mean pain score after day 1 was 2.6 for the MIVAT group and 3.4 for the conventional group. There was no statistically significant difference in pain scores measured after 48 hours postoperatively (p>0.05). The mean doses of intramuscular diclofenac sodium given after operation were significantly lower in the MIVAT group (40mg) when compared with the conventional group (66mg) (p<0.0001). At 3 months postoperatively, participants in the MIVAT group reported a significantly greater satisfaction with the cosmetic outcome of their procedure compared to the conventional group. The mean satisfaction rating for the MIVAT group was 9.1 versus 4.9 for the conventional group on a scale of 1 to 10, with 10 representing the best possible outcome. In the MIVAT group, there was a significantly smaller incision length compared to the conventional group (3.2±0.9 versus 5.4±0.7 cm, respectively). The outcome data for pain scores and satisfaction with cosmetic appearance are summarized in table 3.
Figure 3
Discussion
This study shows that in patients with small thyroid nodules the minimally invasive approach to thyroidectomy has some advantages over conventional thyroidectomy. The benefits of the MIVAT technique were demonstrated by less pain in the early postoperative period and superior cosmetic results at 3-month follow-up. The MIVAT approach represents a refinement in operative technique for thyroidectomy which is applicable to small symptomatic nodules, toxic nodules, and follicular lesions, requiring further histological assessment.
The advantages of minimally invasive thyroidectomy have been demonstrated by other groups. As in this study, the major benefits center on reductions in pain and improvements in cosmetic results.13,15,45,49-52 The majority of these studies have evaluated the MIVAT technique.
The operative time for MIVAT remains greater than that of conventional surgery, a finding which is common to a number of studies of minimally invasive approaches to the thyroid.23,42,45 With greater experience, it is likely that operative times for MIVAT will decrease, particularly with the refinement of electrothermal vessel sealing devices which have now become the preferred method for vessel control and dissection in open and minimally invasive thyroidectomy. This technology, in addition to the fact that MIVAT minimizes the amount of unnecessary dissection required to expose the thyroid, will likely result in the decrease in operative times in the future. We hypothesize that the smaller skin incision and decreased area of dissection associated with MIVAT results in less disruption of the cutaneous nerve supply, thus translating to less postoperative pain. To avoid the potential problem of information bias influencing the reporting of pain and cosmetic scores, we blinded patients preoperatively. Postoperatively, there is the potential for bias in reporting of pain scores from the MIVAT group; however, the combined reduction after day 1 pain scores and analgesic requirement suggests that the improvement effect is real. Similar benefits in terms of pain reduction have been reported in other series. 45, 48, 53
In conclusion, MIVAT is a safe procedure that produces outcomes, in view of short-term adverse events, similar to those of open thyroidectomy, it needs a longer operative time to be accomplished and is superior in terms of immediate postoperative pain and cosmetic results.
