hoarseness

声音嘶哑
  • 文章类型: Journal Article
    结节性筋膜炎(NF)是一种良性和自限性成纤维细胞增殖,起源于浅筋膜并延伸到皮下组织或肌肉。它通常表现在20至35岁的个体中,在60岁以上的患者中观察到罕见的情况。我们在此报告一例涉及一名75岁男性右声带NF。由于有1个月的声音嘶哑和呼吸困难的病史,该患者在我们医院的耳鼻喉科寻求医疗护理。通过术前病理检查无法确诊。入院后,完成了各种检查并进行了手术治疗,术后组织病理学发现右声带中存在NF。声带的NF是一种罕见的临床实体。鉴于其快速发展和明显渗透的倾向,它通常会带来诊断挑战,因为它可以模拟各种恶性软组织肿瘤。因此,在通过病理检查确认NF的诊断之前,必须彻底排除其他肿瘤性病变。局部手术切除仍然是主要的治疗方式。
    Nodular fasciitis (NF) is a benign and self-limiting fibroblastic proliferation that originates from the superficial fascia and extends into the subcutaneous tissue or muscle. It typically manifests in individuals aged 20 to 35 years, with rare occurrences observed in patients over the age of 60 years. We herein report a case involving a 75-year-old man with NF in the right vocal cord. The patient sought medical attention at the Department of Otolaryngology of our hospital because of a 1-month history of hoarseness and breathlessness. The diagnosis was unable to be confirmed through preoperative pathological examination. After admission to our hospital, various examinations were completed and surgical treatment was performed, and the postoperative histopathological findings revealed the presence of NF in the right vocal cord. NF of the vocal cord is a rare clinical entity. Given its rapid progression and propensity for marked infiltration, it often poses diagnostic challenges because it can mimic various malignant soft tissue tumors. Therefore, thorough exclusion of other neoplastic lesions is imperative prior to confirming the diagnosis of NF through pathological examination. Local surgical resection remains the primary treatment modality.
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  • 文章类型: Journal Article
    背景:不同方法超声引导喉上神经阻滞用于辅助清醒插管,但鲜为人知的是,哪种方法更优越。我们旨在比较成年患者清醒插管时超声引导下喉上神经阻滞的矢状和横向入路。
    方法:50例清醒经口气管插管患者随机接受矢状旁及横行超声引导喉上神经阻滞。主要结果是患者气管插管期间的气道麻醉质量等级。插管后的患者管耐受性评分,总手术时间,平均动脉压,心率,每个时间点的Ramsay镇静评分,拔管后1小时和24小时喉咙痛的发生率,插管前声音嘶哑,记录拔管后1小时和24小时。
    结果:矢状旁组患者的气道麻醉质量明显优于横行组(中位级别[IQR],0[0-1]vs.1[0-1],P=0.036)。矢状旁入路组患者的管耐受性评分较好(中位数评分[IQR],1[1-1]vs.1[1-1.5],P=0.042)和较短的总手术时间(中位时间[IQR],113s[98.5-125.5]vs.188s[149.5-260],P<0.001)比横向入路组的那些。矢状旁组拔管后24h咽喉痛的发生率较低(8%vs.36%,P=0.041)。在插管前,矢状旁组超过一半的患者出现声音嘶哑(72%vs.40%,P=0.023)。
    结论:与横向入路相比,超声引导下矢状旁入路在气道局部麻醉质量和喉上神经阻滞的总手术时间方面均有改善.
    背景:这种前瞻性,随机对照试验获得南京市第一医院伦理委员会批准(KY20220425-014),并在患者入组前在中国临床试验注册中心(2022年6月19日,ChiCTR2200061287)注册.从该试验的所有参与者获得书面知情同意书。
    BACKGROUND: Different approach ultrasound-guided superior laryngeal nerve block was used to aid awake intubation, but little is known which approach was superior. We aimed to compare the parasagittal and transverse approaches for ultrasound-guided superior laryngeal nerve block in adult patients undergoing awake intubation.
    METHODS: Fifty patients with awake orotracheal intubation were randomized to receive either a parasagittal or transverse ultrasound-guided superior laryngeal nerve block. The primary outcome was patient\'s quality of airway anesthesia grade during insertion of the tube into the trachea. The patients\' tube tolerance score after intubation, total procedure time, mean arterial pressure, heart rate, Ramsay sedation score at each time point, incidence of sore throat both 1 h and 24 h after extubation, and hoarseness before intubation, 1 h and 24 h after extubation were documented.
    RESULTS: Patients\' quality of airway anesthesia was significantly better in the parasagittal group than in the transverse group (median grade[IQR], 0 [0-1] vs. 1 [0-1], P = 0.036). Patients in the parasagittal approach group had better tube tolerance scores (median score [IQR],1[1-1] vs. 1 [1-1.5], P = 0.042) and shorter total procedure time (median time [IQR], 113 s [98.5-125.5] vs. 188 s [149.5-260], P < 0.001) than those in the transverse approach group. The incidence of sore throat 24 h after extubation was lower in the parasagittal group (8% vs. 36%, P = 0.041). Hoarseness occurred in more than half of the patients in parasagittal group before intubation (72% vs. 40%, P = 0.023).
    CONCLUSIONS: Compared to the transverse approach, the ultrasound-guided parasagittal approach showed improved efficacy in terms of the quality of airway topical anesthesia and shorter total procedure time for superior laryngeal nerve block.
    BACKGROUND: This prospective, randomized controlled trial was approved by the Ethics Committee of Nanjing First Hospital (KY20220425-014) and registered in the Chinese Clinical Trial Registry (19/6/2022, ChiCTR2200061287) prior to patient enrollment. Written informed consent was obtained from all participants in this trial.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    背景:这项随机对照试验旨在评估术前吸入布地奈德联合静脉注射地塞米松对甲状腺切除术患者全麻术后咽喉痛(POST)的疗效。
    方法:择期甲状腺切除术患者随机分为静脉注射地塞米松组(A组)和雾化吸入布地奈德联合静脉注射地塞米松组(B组)。所有患者均行全身麻醉。POST的发生率和严重程度,声音嘶哑,术后1、6、12和24小时咳嗽进行评价和比较。
    结果:A组和B组分别有48和49例患者,分别。B组术后6、12、24hPOST发生率明显低于A组(P<0.05)。此外,B组24小时咳嗽的发生率明显降低(P=0.047)。与A组相比,POST的严重程度在6时显著降低(P=.027),12(P=.004),休息24小时(P=0.005),在6(P=0.002),12(P=.038),B组吞咽过程中24小时(P=0.015)。两组之间在每个时间点的声音嘶哑的发生率和严重程度具有可比性(P>.05)。
    结论:术前吸入布地奈德联合静脉注射地塞米松可降低甲状腺切除术患者拔管后6、12和24小时POST的发生率和严重程度。此外,这种组合降低了术后24小时咳嗽的发生率.
    BACKGROUND: This randomized controlled trial aimed to evaluate the efficacy of preoperative inhaled budesonide combined with intravenous dexamethasone on postoperative sore throat (POST) after general anesthesia in patients who underwent thyroidectomy.
    METHODS: Patients who underwent elective thyroidectomy were randomly divided into the intravenous dexamethasone group (group A) and budesonide inhalation combined with intravenous dexamethasone group (group B). All patients underwent general anesthesia. The incidence and severity of POST, hoarseness, and cough at 1, 6, 12, and 24 hours after surgery were evaluated and compared between the 2 groups.
    RESULTS: There were 48 and 49 patients in groups A and B, respectively. The incidence of POST was significantly lower at 6, 12, and 24 hours in group B than that in group A (P < .05). In addition, group B had a significantly lower incidence of coughing at 24 hours (P = .047). Compared with group A, the severity of POST was significantly lower at 6 (P = .027), 12 (P = .004), and 24 (P = .005) hours at rest, and at 6 (P = .002), 12 (P = .038), and 24 (P = .015) hours during swallowing in group B. The incidence and severity of hoarseness were comparable at each time-point between the 2 groups (P > .05).
    CONCLUSIONS: Preoperative inhaled budesonide combined with intravenous dexamethasone reduced the incidence and severity of POST at 6, 12, and 24 hours after extubation compared with intravenous dexamethasone alone in patients who underwent thyroidectomy. Additionally, this combination decreased the incidence of postoperative coughing at 24 hours.
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  • 文章类型: Journal Article
    一名70多岁的男子因5厘米的颌下肿块被转诊,声音嘶哑,呼吸困难,没有咳嗽,痰中的血,或者吞咽困难.你的诊断是什么?
    A man in his 70s was referred for a 5-cm submandibular mass, hoarseness, and difficulty breathing with no cough, blood in sputum, or dysphagia. What is your diagnosis?
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  • 文章类型: Randomized Controlled Trial
    目的:本研究旨在比较气管插管前局部喉部利多卡因和静脉注射利多卡因对术后咽喉痛发生率和严重程度的影响。声音嘶哑,还有咳嗽.
    方法:这项前瞻性随机对照研究纳入了144例接受气管插管腹腔镜胆囊切除术的患者。将患者随机分为三组,并通过局部喉部喷雾剂(T组)接受2%利多卡因,静脉注射2%利多卡因(I组),插管前静脉给予等量生理盐水(C组)。喉咙痛的发生率和严重程度,声音嘶哑,收集拔管后0.5、1、6和24h的咳嗽反应。
    结果:T组咽喉痛的发生率明显低于I组和C组(6.4%vs.37.2%和86.7%,p<0.001),分别在拔管后0.5h,I组明显低于C组(37.2%vs.86.7%,p<0.001)。T组声音嘶哑和咳嗽的发生率均明显低于I组和C组(14.9%vs.97.7%和97.8%,p<0.001,19.1%与72.0%和93.3%,p<0.001),分别。喉咙痛的严重程度,T组的声音嘶哑和咳嗽明显低于I组和C组(p<0.05),I组明显低于C组(p<0.05)。
    结论:插管前局部喉部利多卡因和静脉注射利多卡因对预防咽痛均有积极作用。局部喉途径优于静脉途径。Chictr.org.cnID:ChiCTR2100042442。
    OBJECTIVE: The present study aimed to compare the effect of topical laryngeal lidocaine with intravenous lidocaine before endotracheal intubation on the incidence and severity of postoperative sore throat, hoarseness, and cough.
    METHODS: This prospective randomized controlled study enrolled 144 patients undergoing laparoscopic cholecystectomy with endotracheal intubation. The patients were randomized to three groups and received 2% lidocaine by topical laryngeal spray (group T), intravenous 2% lidocaine (group I), and the equivalent volume of intravenous saline (group C) before intubation. The incidence and severity of sore throat, hoarseness, and cough reaction at 0.5, 1, 6, and 24 h after extubation were collected.
    RESULTS: The incidence of sore throat was significantly lower in group T than in groups I and C (6.4% vs. 37.2% and 86.7%, p < 0.001), respectively at 0.5 h after extubation, and it was significantly lower in group I than that in group C (37.2% vs. 86.7%, p < 0.001). Both the incidence of hoarseness and cough were significantly lower in group T than in group I and in group C (14.9% vs. 97.7% and 97.8%, p < 0.001, and 19.1% vs. 72.0% and 93.3%, p < 0.001), respectively. The severity of sore throat, hoarseness and cough in group T was significantly lower than that in group I and that in group C (p < 0.05), and it was significantly lower in group I than in group C (p < 0.05).
    CONCLUSIONS: Both topical laryngeal lidocaine and intravenous lidocaine before intubation have positive effects on preventing sore throat. Topical laryngeal route was superior to intravenous route. Chictr.org.cn ID: ChiCTR2100042442.
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  • 文章类型: Randomized Controlled Trial
    背景:术后咽喉痛(POST)是一种令人不快的结果,可作为成人气管插管的结果。气管内导管(ETT)袖带的压力增加通常会导致局部粘膜损伤,导致喉咙痛。这项研究的目的是比较两种不同的ETT袖带压力监测系统与没有袖带压力监测成人POST的发生率和严重程度。
    方法:114名ASAI-III患者,18-65岁,和需要气管内插管的手术包括在这项研究中。患者被随机分为三组:对照组(C),袖带压力表(G),和自动袖带控制器(A)。C组术中不监测ETT袖带压力,但在G组和A组中使用袖带压力计和自动袖带控制器监测,分别。术后,在2、24和48小时评估患者POST的存在和严重程度,声音嘶哑和咳嗽.
    结果:111名患者完成了这项研究。术后48小时内G组40.5%的患者(n=37)(p=0.013)和A组23.7%的患者(n=38)(p<0.001)发生POST,C组为69.4%(n=36)。声音嘶哑没有显着差异,咳嗽,和吞咽困难。当比较A组和C组时,A组个体表现出较低的显著(≥2级)POST和声音嘶哑发生率(10.5%vs.41.7%,p=0.002;26.3%vs.58.3%,p=0.005)。手术后48小时内,患者组之间的严重咳嗽和吞咽困难的发生率没有显着差异。A组术后2、24h的POST评分均为0(0~0),2h时显著低于C组(1(0-2),p<0.001;24小时为1(0-1),p=0.001)。G组术后2h的POST评分为0(0-1.5),低于C组(P=0.024)。A组声音嘶哑程度0分(0~2分)优于C组(2分(0~2分),术后2小时p=0.006)。
    结论:结论:这项研究的结果表明,可以通过使用袖带压力表方法或自动袖带控制器方法来减少POST的发生。自动袖带控制器监测可以潜在地降低POST和声音嘶哑的严重性。
    背景:中国临床试验注册中心,标识符:ChiCTR2100054089,日期:08/12/2021.
    BACKGROUND: Postoperative sore throat (POST) is an unpleasant outcome that can occur as a result of tracheal intubation in adults. Increased pressure from the endotracheal tube (ETT) cuff often leads to local mucosal injury, resulting in sore throat. The purpose of this study was to compare the effect of two different ETT cuff pressure monitoring systems vs. no cuff pressure monitoring on the incidence and severity of POST in adults.
    METHODS: One hundred and fourteen ASA I-III patients of either gender, aged 18-65 years, and undergoing surgery requiring endotracheal intubation were included in this study. Patients were randomized into three groups: control (C), cuff pressure gauge (G), and automated cuff controller (A). The ETT cuff pressure was not monitored intraoperatively in group C but was monitored using a cuff pressure gauge and an automated cuff controller in groups G and A, respectively. Postoperatively, patients were assessed at 2, 24, and 48 h for the presence and severity of POST, hoarseness and cough.
    RESULTS: One hundred and eleven patients completed the study. POST occurred in 40.5% of the patients in group G (n = 37) (p = 0.013) and 23.7% of the patients in group A (n = 38) (p < 0.001) within 48 h after surgery, compared to 69.4% in group C (n = 36). There were no significant differences in hoarseness, coughing, and dysphagia across the groups at any time. When comparing groups A and C, individuals in group A exhibited a lower occurrence of significant (grade ≥ 2) POST and hoarseness (10.5% vs. 41.7%, p = 0.002; 26.3% vs. 58.3%, p = 0.005). The incidence of significant cough and dysphagia did not differ substantially across the patient groups within 48 h after surgery. POST scores in group A at 2, 24 h postoperatively were both 0 (0-0), which was significantly lower than those in group C (1 (0-2) at 2 h, p < 0.001 ; 1 (0-1) at 24 h, p = 0.001). POST in group G at 2 h postoperatively was graded as 0 (0-1.5) which was milder than group C (P = 0.024). The severity of hoarseness in group A with scores of 0 (0-2) was superior to that in group C (2 (0-2), p = 0.006) at 2 h postoperatively.
    CONCLUSIONS: In conclusion, the findings of this study indicated that the occurrence of POST can be reduced by using either the cuff pressure gauge approach or the automated cuff controller method. The automated cuff controller monitoring can potentially decrease the severity of POST and hoarseness.
    BACKGROUND: Chinese Clinical Trial Registry, identifier: ChiCTR2100054089, Date: 08/12/2021.
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  • 文章类型: Journal Article
    本研究旨在探讨原发性甲状腺鳞状细胞癌(PSCCT)和继发性SCCT(SSCCT)的临床超声特征,并评估细针穿刺(FNA)推荐SCCT的准确性与美国放射学学会甲状腺成像和报告数据系统(ACR-TIRADS)和中国TIRADS(C-TIRADS)。
    我们检索了26例SCCT患者(11例PSCCT,15SSCCT)来自我们医院的病理数据库(5,718例甲状腺恶性肿瘤患者),超过23年。回顾性分析26例27例SCCT患者的病历及超声资料,每个SCCT病灶根据两个TIRADS进行分类。
    对于26名患者(21名男性,5名女性),年龄范围为42-81岁,快速扩大的甲状腺/颈部结节(18/26,69.2%),吞咽困难(7/26,26.9%),声音嘶哑(6/26,23.1%),呼吸困难(5/26,19.6%),咳嗽(4/26,15.4%),颈部疼痛(2/26,7.7%),B症状(2/26,7.7%),和痰中的血液(1/26,3.8%)在诊断时出现。超声检查发现5例无症状患者(5/26,19.2%)。声音嘶哑在PSCCT中(5/11,45.5%)比SSCCT中(1/15,6.7%)更常见(P=0.032)。对于平均尺寸为3.7±1.3cm的27个SCCT,超声特征由固体(25/27,92.6%)或几乎完全固体组成(2/27,7.4%)组成,低回声(17/27,63%)和极低回声回声(10/27,37%),不规则/分叶状边缘伴甲状腺外延伸(27/27,100%),高的比宽的形状(13/27,48.1%),点状回声灶(6/27,22.2%),高血管(23/27,85.2%)和累及颈部淋巴(13/26,50.0%)。两个TIRADS共评估了27个SCCT为高恶性危险分层(≥TR4和4B),推荐的FNA为96.3-100%(26/27,27/27)。病理上,超过一半的PSCCT(7/12,58.3%)和四分之一的SSCCT(4/15,26.7%)分化差,而在5个PSCCT和11个SSCCT中观察到中度和高度分化的等级(P=0.007)。13例(50.0%)患者行根治性手术5例(5/13,38.5%)。
    SCCT是一种极其罕见且侵袭性的恶性肿瘤,以男性为主。PSCCT和SSCCT具有相似的临床和超声特征,除了肿瘤分化和声音嘶哑症状。SCCT在ACR-TIRADS和C-TIRADS中显示出高恶性危险分层,具有较高的FNA推荐率。
    UNASSIGNED: This study aimed to investigate the clinico-ultrasound features of primary squamous cell carcinoma of the thyroid (PSCCT) and secondary SCCT (SSCCT) and evaluate the accuracy of fine needle aspiration (FNA) recommendation for SCCT with American College of Radiology-Thyroid Imaging and Reporting Data System (ACR-TIRADS) and Chinese-TIRADS (C-TIRADS).
    UNASSIGNED: We retrieved 26 SCCT patients (11 PSCCT, 15 SSCCT) from our hospital\'s pathology database (5,718 patients with thyroid malignancy) over 23 years. Medical records and ultrasound data of the 26 patients with 27 SCCTs were analyzed retrospectively, and each SCCT focus was categorized based on the two TIRADSs.
    UNASSIGNED: For 26 patients (21 males, 5 females) with an age range of 42-81 years, rapidly enlarging thyroid/neck nodules (18/26, 69.2%), dysphagia (7/26, 26.9%), hoarseness (6/26, 23.1%), dyspnea (5/26, 19.6%), cough (4/26, 15.4%), neck pain (2/26, 7.7%), B symptoms (2/26, 7.7%), and blood in sputum (1/26, 3.8%) were presented at diagnosis. Five asymptomatic patients (5/26, 19.2%) were detected by ultrasound. Hoarseness was more common in PSCCT (5/11, 45.5%) than in SSCCT (1/15, 6.7%) (P=0.032). For 27 SCCTs with a mean size of 3.7 ± 1.3 cm, the ultrasound features consisted of solid (25/27, 92.6%) or almost completely solid composition (2/27, 7.4%), hypoechoic (17/27, 63%) and very hypoechoic echogenicity (10/27, 37%), irregular/lobulated margin with extra-thyroidal extension (27/27, 100%), taller-than-wide shape (13/27, 48.1%), punctate echogenic foci (6/27, 22.2%), hypervascularity (23/27, 85.2%) and involved neck lymph (13/26, 50.0%). A total of 27 SCCTs were evaluated as high malignancy risk stratification (≥TR4 and 4B) by the two TIRADSs and recommended FNA in 96.3-100% (26/27, 27/27). Pathologically, more than half of PSCCTs (7/12, 58.3%) and a quarter of SSCCTs (4/15, 26.7%) were poorly differentiated, while moderately and well-differentiated grades were observed in 5 PSCCTs and 11 SSCCTs (P=0.007). Thirteen patients (50.0%) underwent surgery with radical operation in 5 cases (5/13, 38.5%).
    UNASSIGNED: SCCT is an extremely rare and aggressive malignancy with a male predominance. PSCCT and SSCCT had similar clinical and ultrasound features except for tumor differentiation and the symptom of hoarseness. SCCT showed a high malignancy risk stratification in ACR-TIRADS and C-TIRADS, with a high rate of FNA recommendation.
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  • 文章类型: Randomized Controlled Trial
    背景:气管损伤,声带损伤,喉咙痛和声音嘶哑是双腔插管的常见并发症。
    目的:本研究旨在评估``视频双腔管``(VDLT)''对胸外科手术患者插管并发症的影响。
    方法:一项随机对照研究。
    方法:徐州市肿瘤医院,徐州,中国,从2023年1月到2023年6月。
    方法:一百八十二例接受单肺通气择期胸外科手术的患者随机分为两组:DLT组90例,VDLT组92例。
    方法:VDLT组选择VDLT进行插管,DLT组选择DLT进行插管。使用纤维支气管镜(FOB)记录气管和声带损伤。
    方法:主要结果是中重度气管损伤的发生率和声带损伤的发生率。次要结果包括术后24小时和48小时喉咙痛和声音嘶哑的发生率和严重程度。
    结果:DLT组中重度气管损伤的发生率为32/90(35.6%),VDLT组45/92(48.9%)(P=0.077;相对危险度1.38,95%CI,0.97~1.95)。DLT和VDLT组声带损伤发生率分别为31/90(34.4%)和34/92(37%),分别为(P=0.449)。VDLT组术后24h咽喉痛和声音嘶哑的发生率明显高于DLT组(咽喉痛:P=0.032,相对危险度1.63,95%CI,1.03~2.57;声音嘶哑:P=0.018,相对危险度1.48,95%CI,1.06~2.06)。
    结论:DLT和VDLT中重度气管损伤和声带损伤的发生率无统计学差异。在提高首次尝试成功率的同时,VDLT插管增加了术后24h咽喉痛和声音嘶哑的发生率。
    背景:中国临床试验注册中心:ChiCTR2300067348。
    BACKGROUND: Tracheal injuries, vocal cord injuries, sore throat and hoarseness are common complications of double-lumen tube (DLT) intubation.
    OBJECTIVE: This study aimed to evaluate the effects of \'video double-lumen tubes\' (VDLTs) on intubation complications in patients undergoing thoracic surgery.
    METHODS: A randomised controlled study.
    METHODS: Xuzhou Cancer Hospital, Xuzhou, China, from January 2023 to June 2023.
    METHODS: One hundred eighty-two patients undergoing elective thoracic surgery with one-lung ventilation were randomised into two groups: 90 in the DLT group and 92 in the VDLT group.
    METHODS: VDLT was selected for intubation in the VDLT group, and DLT was selected for intubation in the DLT group. A fibreoptic bronchoscope (FOB) was used to record tracheal and vocal cord injuries.
    METHODS: The primary outcomes were the incidence of moderate-to-severe tracheal injury and the incidence of vocal cord injury. The secondary outcomes included the incidence and severity of postoperative 24 and 48 h sore throat and hoarseness.
    RESULTS: The incidence of moderate-to-severe tracheal injury was 32/90 (35.6%) in the DLT group, and 45/92 (48.9%) in the VDLT group ( P  = 0.077; relative risk 1.38, 95% CI, 0.97 to 1.95). The incidence of vocal cord injury was 31/90 (34.4%) and 34/92 (37%) in the DLT and VDLT groups, respectively ( P  = 0.449). The incidence of postoperative 24 h sore throat and hoarseness was significantly higher in the VDLT group than in the DLT group (for sore throat: P  = 0.032, relative risk 1.63, 95% CI, 1.03 to 2.57; for hoarseness: P  = 0.018, relative risk 1.48, 95% CI, 1.06 to 2.06).
    CONCLUSIONS: There was no statistically significant difference in the incidence of moderate-to-severe tracheal injury and vocal cord injury between DLTs and VDLTs. While improving the first-attempt success rate, intubation with VDLT increased the incidence of postoperative 24 h sore throat and hoarseness.
    BACKGROUND: Chinese Clinical Trial Registry identifier: ChiCTR2300067348.
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