Abstract
Introduction: Post-thyroidectomy hematoma is a serious, potentially life-threatening complication and it is the most frequent indication for reoperation. In this study, we aimed to identify the risk factors and prevalence of post-thyroidectomy hematoma and perform a literature review of the incidence of post-thyroidectomy hematoma at other centers in Saudi Arabia.
Methods: We retrospectively enrolled 372 consecutive patients who had undergone thyroidectomy between January 2015 and December 2020. Patients with bleeding disorders were excluded from the study. Data were analyzed using SPSS software, version 20.0 (IBM Corp., Armonk, NY).
Results: Three female (0.8%) patients developed a hematoma after thyroidectomy. Two patients developed a hematoma 24 hours after surgery and were treated conservatively. The third patient developed a hematoma within two hours of surgery and required surgical intervention. None of the patients required a tracheostomy, and there was no mortality. No significant association was found between age, sex, final pathology, the extent of thyroidectomy, and risk of hematoma.
Conclusion: A post-thyroidectomy hematoma is a rare but dangerous complication. Identifying the risk factors for hematoma formation is of great importance, particularly when considering outpatient thyroidectomy. A large prospective multicenter study is needed for further investigation.
Keywords: risk factor, outpatient thyroidectomy, hematoma, complications of thyroidectomy, ambulatory thyroidectomy
Introduction
The thyroid gland is a highly vascularized organ, and thyroidectomy is a common and relatively safe procedure. However, like other procedures, there is a risk of postoperative complications [1,2]. Hypoparathyroidism, recurrent laryngeal nerve paralysis, loss of high-pitched voice, hematoma, and seroma are well-known post-thyroidectomy complications. Among these, hypocalcemia is considered the most common cause of hospital readmission, and hematoma is the most frequent indication for reoperation [3].
Although uncommon, a post-thyroidectomy hematoma is a serious, potentially life-threatening complication [4] with an incidence of 0.7 to 4.7% [1,5], and can reportedly reach 6.5% [2]. This is extremely important when considering ambulatory thyroidectomy [6]. Post-thyroidectomy hematoma formation may be related to patient predisposition, surgical technique, and thyroid pathology [6].
Post-thyroidectomy hematoma can present as neck swelling, choking sensation, neck pressure, respiratory distress, wound drainage, dysphagia, or difficulty with phonation [7]. In severe cases, cerebral anoxia with major neurological complications and even death may occur [1,5].
Post-thyroidectomy hematoma commonly occurs within the first six hours after surgery; however, it can occur even up to 24 hours after surgery [6]. The risk factors for post-thyroidectomy hematoma include coexisting morbidities (diabetes mellitus {DM}, obesity, chronic kidney disease, chronic obstructive pulmonary disease, congestive heart failure, bleeding disorder, sleep apnea, and hypertension), male sex, older age, certain thyroid diseases (Graves’ disease, malignancy, and Hashimoto's thyroiditis), retrosternal goiter, the extent of thyroidectomy, resected thyroid volume, redo-surgeries, drain use, high postoperative blood pressure, smoking, medications (antithrombotic agent), and prior neck radiation [1,5,8].
This study aimed to identify the risk factors and prevalence of post-thyroidectomy hematoma in our setting. Such factors should be considered when selecting patients for ambulatory thyroidectomy and those at higher risk for hematoma formation. Additionally, we have performed a literature review of the incidence of post-thyroidectomy hematoma at other centers in Saudi Arabia.
Materials and methods
This retrospective study was approved by the ethics committee at King Salman Armed Forces Hospital (KSAFH) in North-Western Region, Tabuk, Saudi Arabia. (No: KSAFH-REC-2017166). Informed consent from patients was not required, as secondary data were used with no direct patient contact.
The study included all patients who underwent thyroidectomies between January 2015 and December 2020 at KSAFH, the largest referral hospital in the Tabuk region. Patients with bleeding disorders were excluded from the study. Data collected included demographic information, final histopathologic type, and extent of thyroidectomy. The latter refers to the following: (1) Hemithyroidectomy, which involves the removal of one thyroid lobe and the isthmus; (2) Completion thyroidectomy, which is the removal of the remaining part of the thyroid gland; (3) Subtotal thyroidectomy, which involves the removal of one lobe of the gland, isthmus, and the majority of the other lobe; and (4) Total thyroidectomy, which is the removal of the entire thyroid gland. A drain was routinely placed in most total thyroidectomy and neck dissection cases.
Statistical analysis
Data were analyzed using the Statistical Package for the Social Sciences (SPSS) software for Windows, version 20.0 (IBM Corp., Armonk, NY). The Mann-Whitney U test was used to compare the age between the hematoma groups, which was presented as the median and interquartile range (IQR). Frequencies and proportions were used to describe nominal data. Fisher’s exact test was used to compare the nominal variables between the hematoma groups because of the low cell count in the contingency tables. Differences were considered statistically significant at p < 0.05.
Results
In total, 372 thyroidectomies were performed during the study period. There were 311 (83.63%) female and 61 (16.4%) male patients. Their ages ranged from 13 to 95 years old. The final pathology was benign in 205 (55.11%) patients and malignant in 167 (44.89%). There were 222 total thyroidectomies (59.68%), 70 right hemithyroidectomies (18.81%), 52 left hemithyroidectomies (13.98%), 21 completion thyroidectomies (5.65%), and seven subtotal thyroidectomies (1.88%).
Three female patients developed hematomas (0.8%). Two patients developed hematomas after 24 hours of surgery and were treated conservatively. The third patient developed a significant hematoma within two hours of surgery, which necessitated surgical intervention. There was no mortality, and no patient required a tracheostomy.
Table 1 shows that there were no significant associations between age, sex, final pathology, surgery type, and hematoma risk. The characteristics of the patients with hematoma, various risk factors for hematoma formation post-thyroidectomy, hospital stay, and management are summarized in Table 2.
Table 1. Associations of patient demographics, final pathology, and extent of thyroidectomy with the risk of hematoma formation.
*Significant at p <0.05; IQR: interquartile range
Hematoma | |||||
No N=369 | Yes N=3 | P-value* | |||
Age | Median (IQR) | 39(15) | 38(21) | 0.94 | |
Gender | Female | 308 (83.47%) | 3 (100%) | 1.00 | |
Male | 61 (16.53%) | 0 (0.00%) | |||
Final Pathology | Benign | 203 (55.01%) | 2 (66.67%) | 1.00 | |
Malignant | 166 (44.99%) | 1 (33.33%) | |||
Extent Of thyroidectomy | Total thyroidectomy | 221 (59.89%) | 1 (33.33%) | 0.260 | |
Right hemithyroidectomy | 69 (18.70%) | 1 (33.33%) | |||
Left hemithyroidectomy | 52 (14.09%) | 0 (0.00%) | |||
Sub-total thyroidectomy | 7 (1.90%) | 0 (0.00%) | |||
Completion thyroidectomy | 20 (5.42%) | 1 (33.33%) |
Table 2. Features of patients with post-thyroidectomy hematoma.
MNG: multinodular goiter, PTC: papillary thyroid carcinoma
Variables | Patient 1 | Patient 2 | Patient 3 |
A- When was the hematoma developed? | Next day (Mild-moderate hematoma) | Next day (Mild-moderate hematoma) | within 2 hours post operatively |
B- Risk Factors | |||
Age | 31 | 38 | 52 |
Gender | Female | Female | Female |
Thyroid function status | Hypothyroidism | Euthyroid | Euthyroid |
Diabetes mellites | No | No | No |
Hypertension | No | No | No |
Chronic kidney disease | No | No | No |
Obesity (BMI) | 23.3 | 35 | 28.2 |
Large goiter (or retrosternal) | No | Large goiter | Large goiter |
Type of surgery | Completion thyroidectomy | Right Hemi-thyroidectomy | Total thyroidectomy |
Presence of adhesions during surgery | Yes | No | Yes |
Type of pathology | PTC and MNG | MNG | MNG |
Neck dissection | Left neck dissection | No | No |
Graves' Disease | No | No | No |
Anticoagulants | No | No | Yes |
Bleeding disorder | No | No | No |
Previous neck radiation | No | No | No |
Prior thyroid surgery | Yes, subtotal thyroidectomy | No | No |
Use of energy-based vessel sealing devices (harmonic scalpel or LigaSure or bipolar) | Yes | Yes | Yes |
Use of the hemostatic agent Surgicel | Yes | Yes | Yes |
Use of a drain | No | Yes | Yes |
C-Management of Hematoma | |||
Mortality | No | No | No |
Tracheostomy | No | No | No |
Surgical intervention of hematoma | No | No | Exploration, evacuation of hematoma and control the bleeding |
Blood transfusion | No | No | No |
Source of the post thyroidectomy bleeding | Treated conservatively | Treated conservatively | Middle thyroid vein |
D-Hospital Stay | 3 days | 3 days | 4 days |
E- Blood pressure pre-, intra- and post-operatively: | Pre: 91/60 | Pre:111/52 | Pre :104/56 |
Intra :120/90 | Intra :110/60 | Intra :120/70 | |
Post: 114/70 | Post: 100/60 | Post :108/89 |
Discussion
The risk of hematoma formation in our cohort was 0.8%, which is in line with previous studies [1,4,5,8]. Table 3 shows the incidence of post-thyroidectomy hematomas in different cities in Saudi Arabia [9-13].
Table 3. Prevalence of post-thyroidectomy hematoma among the different cities in Saudi Arabia.
* NR; not reported
Authors | Reference | Year | City | Number of total patients | Patients with Hematoma | Treatment | Mortality |
Bawa et al. | [9] | 2021 | Bisha | 339 | 3(1.4%) | Two were treated surgically & one conservatively | None |
Alshareef et al. | [10] | 2020 | Makkah | 140 | 1(5%) | NR | NR |
Al-Hakami et al. | [11] | 2019 | Jeddah | 456 | 3(0.65) | NR | NR |
Alharbi and Ahmed | [12] | 2018 | Jazan | 320 | 4(1.25%) | Three were treated surgically | 1 died due to large wound hematoma |
Alshahrani et al. | [13] | 2013 | Riyadh | 88 | 1(1.1) | Conservatively | None |
Present study | 2022 | Tabuk | 372 | 3 (0.8) | One was treated surgically & two conservatively | None |
Although hematoma is frequently seen within the first six hours after surgery, bleeding can still occur up to 24 hours after surgery [6]. Two of our patients developed hematomas 24 hours post-surgery, and the third patient developed a significant hematoma within two hours of surgery. Notably, in 55-90 % of cases, the source of bleeding has been identified [7]. The most common locations for significant postoperative bleeding are the superior thyroid artery, inferior thyroid artery, thyroid ima, arteries at the anterolateral junction of the trachea and cricoid cartilage, tiny arteries in the ligament of Berry, and medial cricothyroid vessels [7]. In our study, the source of bleeding in patient 3 was the middle thyroid vein.
Comorbidities (such as DM and hypertension), male sex, older age, Graves’ disease, thyroid cancer, Hashimoto's thyroiditis, retrosternal goiter, thyroidectomy extent, redo-surgeries, drain use, smoking, antithrombotic agents, and prior neck radiation are well-known risk factors for post-thyroidectomy hematoma formation [1,5,8]. Table 2 shows the various risk factors for post-thyroidectomy hematoma formation in our study.
Despite its rarity, a post-thyroidectomy hematoma is a potentially fatal complication. In recent years, the number of outpatient thyroidectomy procedures has increased, as they are cost-effective and reduce hospitalization. Furthermore, the mortality rate in patients with post-thyroidectomy hematoma is three times higher than that in patients without hematoma [6]. Therefore, the risk factors for post-thyroidectomy hematoma formation should be identified [4,6].
Chereau et al. proposed a neck hematoma scoring system for ambulatory thyroidectomy. Patients with a score of ≤ 1 were considered candidates for ambulatory surgery. Furthermore, they found that male patients taking vitamin K antagonists and/or patients with DM were not candidates for ambulatory thyroidectomy [5].
Some preventive measures that could lower the risk of post-thyroidectomy hematomas can be taken before, during, or after surgery. Preoperatively, hypertension and hyperthyroidism should be controlled. Intraoperatively, good hemostasis, performing the Valsalva maneuver, using an ultrasonic or radiofrequency scalpel, and loosening the strap muscle re-approximation can reduce the risk of hematoma formation. Keeping the strap muscle re-approximation loose allows for the earlier detection of hematomas in the subcutaneous tissue. Controlling postoperative high blood pressure, nausea, and vomiting as well as using deep anesthesia extubation to reduce coughing are recommended [2,5,7].
It is uncertain whether drain use increases the risk of hematoma formation. According to Smith and Coughlin, suction drainage increases the risk of bleeding [14]; however, another study found that drain use has no effect on the postoperative risk of hematoma and seroma formation [2]. In our study, a drain had been placed in two patients. The use of energy vessel sealant devices reportedly decreases the risk of post-thyroidectomy hematomas [8]. Notably, sealing devices were used in the three patients who had developed a hematoma.
If acute respiratory distress occurs, the wound should be opened immediately at the bedside. However, this is usually only required in 0-25% of cases. Surgical exploration in the operating room in the absence of respiratory distress is recommended [7]. In the absence of compressive symptoms with delayed hematoma formation, conservative management is recommended and hematoma usually resolves within 3-6 weeks [7]. Two of our patients had no compression symptoms, had stable vitals, and were treated conservatively. In contrast, the third patient developed a large hematoma within two hours of surgery and experienced respiratory distress, necessitating immediate surgical intervention (evacuation and control of the bleeding source).
Our study had several strengths. First, we compared the incidence of post-thyroidectomy hematomas among different centers in Saudi Arabia. Second, it sheds light on the different risk factors for hematoma formation in our patients and in previous studies; thus, they will be considered in the future for our institution's planned “Outpatient Thyroidectomy” program. On the other hand, it had limitations such as a retrospective nature and a single-center study. As a result, a large prospective study is required.
Conclusions
Despite the fact that we observed a low incidence of hematoma, the current study sheds light on a potentially fatal post-thyroidectomy complication. It also provides a review of the literature on various potential risk factors that should be considered when selecting patients for ambulatory thyroidectomy and those at higher risk for hematoma formation.
Acknowledgments
The authors would like to thank Ms. Nouf Alturaiki for her assistance in the data analysis.
The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.
The authors have declared that no competing interests exist.
Human Ethics
Consent was obtained or waived by all participants in this study. Ethics committee at King Salman Armed Forces Hospital (KSAFH) in North-Western Region, Tabuk, Saudi Arabia issued approval KSAFH-REC-2017166. The study was approved by the ethics committee at King Salman Armed Forces Hospital (KSAFH) in North-Western Region, Tabuk, Saudi Arabia. (No: KSAFH-REC-2017166)
Animal Ethics
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
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