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Combined local flap placement and negative-pressure wound therapy for the management of critical peritracheostomal pharyngocutaneous fistula 联合局部皮瓣置入和负压伤口疗法治疗危重的气管周围咽瘘。
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-10-09 DOI: 10.1016/j.anl.2024.09.008
Hideki Kadota , Chikafumi Oryoji , Seita Fukushima , Ryo Shimamoto , Kenichi Kamizono , Sei Yoshida

Objective

Peritracheostomal pharyngocutaneous fistula (PCF), a direct connection between the PCF and tracheal stoma due to a skin defect, is among the most problematic complications after total laryngectomy or pharyngolaryngectomy. Peritracheostomal PCFs can cause lethal complications, including severe pneumonia or carotid blowout, secondary to salivary leakage directly into the tracheal stoma, and their management is challenging without early invasive surgical closure. We aimed to evaluate the utility of our novel and minimally invasive combined local skin flap placement and negative-pressure wound therapy (NPWT) method for the management and conservative closure of peritracheostomal PCFs.

Methods

We retrospectively enrolled patients who developed a peritracheostomal PCF from July 2015 to September 2021 at our institution and affiliated hospitals. Postoperative PCFs were all initially managed with appropriate wound bed preparation. Subsequently, a small local flap of healthy, lower neck skin was elevated and transferred anterior to the PCF to replace the peritracheostomal skin defect. The flap served to provide a sufficient surface for film dressing attachment and facilitated airtight sealing during NPWT. We initiated NPWT after confirming the local skin flap was firmly sutured to the tracheal mucosa. A flexible hydrocolloid dressing was applied to the peritracheostomal skin flap, and a film dressing was placed on the flexible hydrocolloid dressing and surrounding cervical skin. We inserted the NPWT foam shallowly into the fistula tract and applied negative pressure (73.5–125 mmHg). NPWT was continued until the PCF was closed or became so small that salivary leakage was minimal and could be managed by conventional compression dressings.

Results

We enrolled six patients [male, n = 6; mean age, 66.5 years (range, 57–80 years)]. NPWT was applied for an average of 18.2 days (range, 2–28 days). During NPWT, air leakage occurred once (2 cases), only a few times (2 cases), or not at all (2 cases). In all patients, complete fistula closure was achieved in an average of 28.2 days (range, 15–55 days) after the start of NPWT, and no patient required further surgical intervention. There were no lethal complications (e.g., severe pneumonia) during treatment.

Conclusion

Our method of combined local flap placement and NPWT enabled effective management of salivary aspiration and accelerated wound healing, which allowed conservative fistula closure in all patients. We believe combined local flap placement and NPWT should be considered a first-line treatment for intractable peritracheostomal PCF.
目的:气管造口周围咽瘘(PCF)是指由于皮肤缺损导致 PCF 与气管造口直接相连,是全喉或咽喉切除术后最棘手的并发症之一。气管造口周围 PCF 可因唾液直接渗入气管造口而引起致命的并发症,包括重症肺炎或颈动脉喷血。我们的目的是评估我们的新型微创局部皮瓣置入和负压伤口疗法(NPWT)联合方法在气管造口周围 PCFs 的管理和保守闭合中的实用性:我们回顾性地纳入了2015年7月至2021年9月在本院及附属医院发生气管口周围PCF的患者。所有术后 PCF 最初都进行了适当的伤口床准备。随后,局部隆起一小块健康的下颈部皮肤瓣,并转移至 PCF 前方,以替代气管口周皮肤缺损。皮瓣为薄膜敷料的粘贴提供了足够的表面,并有助于在 NPWT 过程中实现气密性密封。在确认局部皮瓣与气管粘膜缝合牢固后,我们开始了 NPWT。在气管口周围皮瓣上使用柔性水胶体敷料,并在柔性水胶体敷料和周围颈部皮肤上放置薄膜敷料。我们将 NPWT 泡沫浅插入瘘道,并施加负压(73.5-125 mmHg)。NPWT 一直持续到 PCF 闭合或变得很小,以至于唾液渗漏极少,可以用常规加压敷料来处理:我们共收治了六名患者[男性,n = 6;平均年龄 66.5 岁(57-80 岁)]。NPWT 平均使用 18.2 天(2-28 天不等)。在 NPWT 过程中,发生过一次漏气(2 例)、几次漏气(2 例)或完全没有漏气(2 例)。在所有患者中,瘘管在 NPWT 开始后平均 28.2 天(15-55 天)内完全闭合,没有患者需要进一步手术治疗。治疗期间没有出现致命的并发症(如重症肺炎):结论:我们所采用的局部皮瓣置入和 NPWT 联合疗法能有效控制唾液吸入,加速伤口愈合,从而使所有患者的瘘管都能保守闭合。我们认为,局部皮瓣置入和 NPWT 联合疗法应被视为顽固性气管口周围 PCF 的一线治疗方法。
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引用次数: 0
Diagnosis and treatment of patulous Eustachian tube 咽鼓管病变的诊断和治疗。
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-10-04 DOI: 10.1016/j.anl.2024.09.007
Ryoukichi Ikeda
Symptoms of patulous Eustachian Tube (PET) were first described by Jago in 1858 and reported by Schwartze in 1864, recognizing PET as a clinical entity. This review summarizes the causes, epidemiology, diagnosis, and treatment of PET, with a particular emphasis on diagnosis and treatment, detailing the diagnostic criteria and silicone plug (Kobayashi plug) surgery proposed or developed in Japan. PET is often linked to weight loss from chronic illnesses, dieting, anorexia nervosa, hemodialysis, and bariatric surgery. It is also associated with pregnancy, oral contraceptive use, nasopharyngeal and muscular atrophy or scarring, and neuromuscular diseases. Interestingly, many PET cases lack an identifiable cause. The prevalence of PET ranges from 0.3 % to 7.0 %, with a higher incidence in females and typically occurring in adolescents and adults. Diagnosis relies on a combination of clinical history, physical examination, ET function test, and imaging. The Japan Otological Society (JOS) proposed standardized diagnostic criteria, where a “definite PET” diagnosis requires all three criteria (aural symptoms, tubal obstruction procedures, and objective findings), while “possible PET” requires two. Treatment includes conservative and surgical interventions. For persistent and severe cases that do not improve with conservative treatments, surgical options are explored. These surgical procedures are classified by the type of intervention, which includes tympanic membrane manipulation (such as tympanostomy tube insertion and mass loading of the tympanic membrane), plug surgery, ET injection, shim surgery, tuboplasty, and ET closure. The Kobayashi plug, a 23 mm long silicone plug, is specifically designed for PET treatment. Indications for its use include “definite PET,” a PHI-10 score of 26 or higher, and lack of improvement after six months of conservative treatment. Preoperative evaluations include CT scans to assess ET patency and confirm the bony portion. Surgery, mostly performed under local anesthesia, involves inserting the plug into the ET via a myringotomy, ensuring the correct size and position with endoscopic guidance. In conclusion, PET is a challenging condition with diverse etiologies and symptoms. Effective management requires a comprehensive diagnostic approach and tailored treatment plans, with the Kobayashi plug offering a promising solution for refractory cases. Further research and advancements in diagnostic techniques and therapeutic interventions will continue to enhance the management of PET.
1858 年,Jago 首次描述了咽鼓管闭塞(PET)的症状,1864 年,Schwartze 报道了这一症状,并承认 PET 是一种临床症状。本综述总结了 PET 的病因、流行病学、诊断和治疗,特别强调了诊断和治疗,详细介绍了日本提出或发展的诊断标准和硅胶塞(小林塞)手术。PET 通常与慢性病、节食、神经性厌食症、血液透析和减肥手术导致的体重减轻有关。它还与妊娠、口服避孕药、鼻咽和肌肉萎缩或瘢痕以及神经肌肉疾病有关。有趣的是,许多 PET 病例缺乏可确定的病因。PET 的发病率从 0.3 % 到 7.0 % 不等,女性发病率较高,通常发生在青少年和成年人身上。诊断需要结合临床病史、体格检查、ET 功能测试和影像学检查。日本耳科学会(JOS)提出了标准化诊断标准,其中 "明确 PET "诊断需要所有三项标准(耳部症状、输卵管阻塞手术和客观检查结果),而 "可能 PET "诊断需要两项标准。治疗包括保守治疗和手术治疗。对于保守治疗无效的顽固性严重病例,可选择手术治疗。这些手术方法按干预类型分类,包括鼓膜操作(如鼓膜造口管插入和鼓膜肿块加载)、塞子手术、ET 注射、垫片手术、输卵管成形术和 ET 闭合术。小林塞是一种 23 毫米长的硅胶塞,专门用于 PET 治疗。其使用指征包括 "明确的 PET"、PHI-10 评分达到或超过 26 分,以及保守治疗 6 个月后仍无改善。术前评估包括 CT 扫描,以评估 ET 的通畅性并确认骨性部分。手术大多在局部麻醉下进行,包括通过耳轮切开术将塞子插入 ET,在内窥镜引导下确保塞子的正确尺寸和位置。总之,PET 是一种具有挑战性的疾病,其病因和症状多种多样。有效的治疗需要全面的诊断方法和量身定制的治疗方案,小林栓为难治性病例提供了一种很有前景的解决方案。诊断技术和治疗干预方面的进一步研究和进步将继续提高 PET 的治疗水平。
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引用次数: 0
Endoscopic surgical management of juvenile nasopharyngeal angiofibroma: Correlating tumour characteristics, risk of hemorrhage, and recurrence 幼年鼻咽血管纤维瘤的内窥镜手术治疗:肿瘤特征、出血风险和复发的相关性
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-27 DOI: 10.1016/j.anl.2024.09.004
Alfredo García-Fernández, María Fernández-Rueda, Esther García-González, Nieves Mata-Castro

Objectives

Juvenile nasopharyngeal angiofibroma is an uncommon tumour primarily seen in young males. It is characterized by its vascular nature and aggressive growth pattern, presenting a significant surgical challenge. Endoscopic sinonasal surgery has become the treatment of choice, reducing both morbidity and blood loss, as well as recurrence rates. This study aims to present the clinical characteristics and surgical outcomes of patients with juvenile nasopharyngeal angiofibroma treated exclusively with endoscopic surgery at our centre.

Methods

A retrospective cohort study was conducted on cases of juvenile nasopharyngeal angiofibroma treated with endoscopic surgery at a single centre between 2013 and 2023.

Results

A total of 21 patients were included in the study, with a mean age of 17.7 years. 57.14 % of the patients presented with an advanced stage (Stage ≥ IIc Radkowsky). The median volume was 79.2 cm3. Pre-surgical embolization was performed in all cases. 7 patients (33.3 %) required blood transfusion. The need for blood transfusion was associated with greater tumour volume (p = 0.0028), intracranial extension (p = 0.025), extension to the infratemporal fossa (p = 0.024), and orbital extension (p = 0.026). There were 2 cases (9.5 %) of tumour recurrence/persistence, both classified as stage IIIb. Tumour persistence/recurrence was more common in patients with intracranial extension (p = 0.045).

Conclusion

Exclusive endoscopic resection of these tumours, regardless of volume and extension, does not increase the risk of blood loss or recurrence. Advanced-stage tumours, especially those with intracranial extension, present a higher risk of bleeding and tumour persistence. In these cases, the low morbidity of the endoscopic approach becomes more evident.
目标青少年鼻咽血管纤维瘤是一种不常见的肿瘤,主要见于年轻男性。其特点是血管性和侵袭性生长模式,给手术带来了巨大挑战。内窥镜鼻窦手术已成为首选治疗方法,可降低发病率和失血量以及复发率。本研究旨在介绍本中心完全采用内窥镜手术治疗的幼年鼻咽血管纤维瘤患者的临床特征和手术效果。研究方法对2013年至2023年期间在一个中心采用内窥镜手术治疗的幼年鼻咽血管纤维瘤病例进行回顾性队列研究。57.14%的患者为晚期(≥ IIc Radkowsky期)。肿瘤体积中位数为 79.2 立方厘米。所有病例都进行了术前栓塞。7名患者(33.3%)需要输血。需要输血与肿瘤体积增大(p = 0.0028)、颅内扩展(p = 0.025)、向颞下窝扩展(p = 0.024)和眼眶扩展(p = 0.026)有关。肿瘤复发/持续存在的病例有 2 例(9.5%),均为 IIIb 期。结论无论肿瘤的体积和扩展程度如何,对这些肿瘤进行全内镜切除并不会增加失血或复发的风险。晚期肿瘤,尤其是颅内扩展的肿瘤,出血和肿瘤持续存在的风险较高。在这些病例中,内窥镜方法的低发病率变得更加明显。
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引用次数: 0
Detailed characterization of auditory neuropathy in Perrault syndrome with TWNK variants 带有 TWNK 变体的佩罗综合征听觉神经病的详细特征描述
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-27 DOI: 10.1016/j.anl.2024.09.005
Marie N Shimanuki , Makoto Hosoya , Takanori Nishiyama , Takeshi Wakabayashi , Masafumi Ueno , Hiroyuki Ozawa , Hideki Mutai , Kiyomitsu Nara , Tatsuo Matsunaga , Naoki Oishi
Perrault syndrome is an autosomal recessive condition characterized by hearing loss and ovarian failure. Hearing loss in Perrault syndrome has been reported as sensorineural; however, only two cases in a single report have comprehensively investigated hearing in Perrault syndrome with TWNK variant, and the association between this variant and auditory neuropathy has not been established. The proband presented with hearing difficulties and primary amenorrhea. Hearing tests revealed mild hearing loss. Maximum speech intelligibility score was 95 % with normal otoacoustic emission. However, no auditory brainstem responses were observed, leading to the diagnosis of auditory neuropathy. Genetic tests identified compound heterozygous variants of TWNK (p.Ile253Met and p.Arg391His), which lead to the genetic diagnosis of Perrault syndrome. Electrocochleography suggests a decreased cochlear nerve function. The patient's sister was also subsequently genetically diagnosed with Perrault syndrome upon identification of the same TWNK variant and had auditory neuropathy with low-tone hearing loss on pure-tone audiometry. These cases highlight the importance of detailed hearing tests, including auditory brainstem response and genetic tests in patients with Perrault syndrome, even in cases of mild hearing loss, for accurate diagnosis and appropriate management.
佩罗综合征是一种常染色体隐性遗传病,以听力损失和卵巢功能衰竭为特征。据报道,佩罗综合征的听力损失是感音神经性的;然而,只有一份报告中的两个病例全面调查了佩罗综合征 TWNK 变异的听力情况,而且该变异与听觉神经病之间的关联尚未确定。该病例表现为听力障碍和原发性闭经。听力测试显示其有轻度听力损失。最大语言清晰度为 95%,耳声发射正常。然而,没有观察到听觉脑干反应,因此诊断为听觉神经病。基因检测发现了 TWNK 的复合杂合变异体(p.Ile253Met 和 p.Arg391His),从而得出佩罗综合征的基因诊断。电测听术表明患者的耳蜗神经功能减退。随后,患者的姐姐也在鉴定出相同的 TWNK 变异后被遗传学诊断为佩罗综合征,并且在纯音测听中出现听神经病变和低音听力损失。这些病例凸显了对佩罗综合征患者进行详细听力检测(包括听性脑干反应和基因检测)的重要性,即使是轻度听力损失病例,也要进行准确诊断和适当治疗。
{"title":"Detailed characterization of auditory neuropathy in Perrault syndrome with TWNK variants","authors":"Marie N Shimanuki ,&nbsp;Makoto Hosoya ,&nbsp;Takanori Nishiyama ,&nbsp;Takeshi Wakabayashi ,&nbsp;Masafumi Ueno ,&nbsp;Hiroyuki Ozawa ,&nbsp;Hideki Mutai ,&nbsp;Kiyomitsu Nara ,&nbsp;Tatsuo Matsunaga ,&nbsp;Naoki Oishi","doi":"10.1016/j.anl.2024.09.005","DOIUrl":"10.1016/j.anl.2024.09.005","url":null,"abstract":"<div><div>Perrault syndrome is an autosomal recessive condition characterized by hearing loss and ovarian failure. Hearing loss in Perrault syndrome has been reported as sensorineural; however, only two cases in a single report have comprehensively investigated hearing in Perrault syndrome with <em>TWNK</em> variant, and the association between this variant and auditory neuropathy has not been established. The proband presented with hearing difficulties and primary amenorrhea. Hearing tests revealed mild hearing loss. Maximum speech intelligibility score was 95 % with normal otoacoustic emission. However, no auditory brainstem responses were observed, leading to the diagnosis of auditory neuropathy. Genetic tests identified compound heterozygous variants of <em>TWNK</em> (p.Ile253Met and p.Arg391His), which lead to the genetic diagnosis of Perrault syndrome. Electrocochleography suggests a decreased cochlear nerve function. The patient's sister was also subsequently genetically diagnosed with Perrault syndrome upon identification of the same <em>TWNK</em> variant and had auditory neuropathy with low-tone hearing loss on pure-tone audiometry. These cases highlight the importance of detailed hearing tests, including auditory brainstem response and genetic tests in patients with Perrault syndrome, even in cases of mild hearing loss, for accurate diagnosis and appropriate management.</div></div>","PeriodicalId":55627,"journal":{"name":"Auris Nasus Larynx","volume":"51 6","pages":"Pages 933-939"},"PeriodicalIF":1.6,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142322215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preoperative assessment of hyperactive delirium risk after head and neck surgery with free tissue transfer reconstruction 采用游离组织转移重建的头颈部手术后谵妄风险的术前评估
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-20 DOI: 10.1016/j.anl.2024.09.001
Takayuki Imai , Teiko Takasago , Ayako Nakanome , Shinkichi Morita , Yuya Miyakura , Kento Sasaki , Kazue Ito , Takahiro Goto , Yukinori Asada

Objective

Hyperactive delirium with agitation following head and neck surgeries with free tissue transfer reconstruction (HNS-FTTR) represents a critical and potentially life-threatening postoperative complication. Although preoperative risk assessment is important, no established risk screening tool has been developed to accurately predict its occurrence.

Methods

In this retrospective observational study, we examined 192 consecutive patients who underwent HNS-FTTR between August 2019 and January 2024. We assessed the effectiveness of the existing delirium risk screening system, the DELirium Team Approach program which includes factors such as age ≥ 70 years, presence of brain disorders, dementia, alcohol consumption habits, a history of delirium, and use of benzodiazepines. Additionally, we explored the association between each risk factor and the onset of delirium.

Results

Delirium occurred in 43 patients (22.4 %). The risk screening tool effectively predicted the occurrence of hyperactive delirium after HNS-FTTR (OR: 8.316; 95 % CI: 2.205–36.060; p = 0.004), with a sensitivity of 95.3 % and a specificity of 28.9 %. Multivariate analysis revealed age ≥ 70 years (OR: 2.179; 95 % CI: 1.058–4.662; p = 0.0383) and alcohol consumption habits (OR: 2.554; 95 % CI: 1.260–5.268; p = 0.0098) as significant independent risk factors.

Conclusion

Our findings suggest that the risk screening system evaluated in this study appears to be sensitive, simple, and effective for the preoperative prediction of hyperactive postoperative delirium following HNS-FTTR.

目的头颈部游离组织转移重建手术(HNS-FTTR)后出现的躁动性谵妄是一种严重的、可能危及生命的术后并发症。虽然术前风险评估很重要,但目前还没有成熟的风险筛查工具来准确预测其发生。方法在这项回顾性观察研究中,我们对 2019 年 8 月至 2024 年 1 月期间接受 HNS-FTTR 手术的 192 例连续患者进行了检查。我们评估了现有的谵妄风险筛查系统--DELirium团队方法计划的有效性,该计划包括年龄≥70岁、存在脑部疾病、痴呆、饮酒习惯、谵妄史和苯二氮卓类药物的使用等因素。此外,我们还探讨了每个风险因素与谵妄发生之间的关联。风险筛查工具可有效预测 HNS-FTTR 后谵妄的发生(OR:8.316;95 % CI:2.205-36.060;p = 0.004),灵敏度为 95.3%,特异性为 28.9%。多变量分析显示,年龄≥ 70 岁(OR:2.179;95 % CI:1.058-4.662;p = 0.0383)和饮酒习惯(OR:2.554;95 % CI:1.260-5.268;p = 0.0098)是重要的独立风险因素。
{"title":"Preoperative assessment of hyperactive delirium risk after head and neck surgery with free tissue transfer reconstruction","authors":"Takayuki Imai ,&nbsp;Teiko Takasago ,&nbsp;Ayako Nakanome ,&nbsp;Shinkichi Morita ,&nbsp;Yuya Miyakura ,&nbsp;Kento Sasaki ,&nbsp;Kazue Ito ,&nbsp;Takahiro Goto ,&nbsp;Yukinori Asada","doi":"10.1016/j.anl.2024.09.001","DOIUrl":"10.1016/j.anl.2024.09.001","url":null,"abstract":"<div><h3>Objective</h3><p>Hyperactive delirium with agitation following head and neck surgeries with free tissue transfer reconstruction (HNS-FTTR) represents a critical and potentially life-threatening postoperative complication. Although preoperative risk assessment is important, no established risk screening tool has been developed to accurately predict its occurrence.</p></div><div><h3>Methods</h3><p>In this retrospective observational study, we examined 192 consecutive patients who underwent HNS-FTTR between August 2019 and January 2024. We assessed the effectiveness of the existing delirium risk screening system, the DELirium Team Approach program which includes factors such as age ≥ 70 years, presence of brain disorders, dementia, alcohol consumption habits, a history of delirium, and use of benzodiazepines. Additionally, we explored the association between each risk factor and the onset of delirium.</p></div><div><h3>Results</h3><p>Delirium occurred in 43 patients (22.4 %). The risk screening tool effectively predicted the occurrence of hyperactive delirium after HNS-FTTR (OR: 8.316; 95 % CI: 2.205–36.060; <em>p</em> = 0.004), with a sensitivity of 95.3 % and a specificity of 28.9 %. Multivariate analysis revealed age ≥ 70 years (OR: 2.179; 95 % CI: 1.058–4.662; <em>p</em> = 0.0383) and alcohol consumption habits (OR: 2.554; 95 % CI: 1.260–5.268; <em>p</em> = 0.0098) as significant independent risk factors.</p></div><div><h3>Conclusion</h3><p>Our findings suggest that the risk screening system evaluated in this study appears to be sensitive, simple, and effective for the preoperative prediction of hyperactive postoperative delirium following HNS-FTTR.</p></div>","PeriodicalId":55627,"journal":{"name":"Auris Nasus Larynx","volume":"51 6","pages":"Pages 929-932"},"PeriodicalIF":1.6,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142274648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of machine learning models to predict papillary carcinoma in thyroid nodules: The role of immunological, radiologic, cytologic and radiomic features 开发预测甲状腺结节乳头状癌的机器学习模型:免疫学、放射学、细胞学和放射学特征的作用
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-20 DOI: 10.1016/j.anl.2024.09.002
Luca Canali , Francesca Gaino , Andrea Costantino , Mathilda Guizzardi , Giorgia Carnicelli , Federica Gullà , Elena Russo , Giuseppe Spriano , Caterina Giannitto , Giuseppe Mercante

Objective

Approximately 30 % of thyroid nodules yield an indeterminate diagnosis through conventional diagnostic strategies. The aim of this study was to develop machine learning (ML) models capable of identifying papillary thyroid carcinomas using preoperative variables.

Methods

Patients with thyroid nodules undergoing thyroid surgery were enrolled in a retrospective monocentric study. Six 2-class supervised ML models were developed to predict papillary thyroid carcinoma, by sequentially incorporating clinical-immunological, ultrasonographic, cytological, and radiomic variables.

Results

Out of 186 patients, 92 nodules (49.5 %) were papillary thyroid carcinomas in the histological report. The Area Under the Curve (AUC) ranged from 0.41 to 0.61 using only clinical-immunological variables. All ML models exhibited an increased performance when ultrasound variables were included (AUC: 0.95–0.97). The addition of cytological (AUC: 0.86–0.97) and radiomic (AUC: 0.88–0.97) variables did not further improve ML models’ performance.

Conclusion

ML algorithms demonstrated low accuracy when trained with clinical-immunological data. However, the inclusion of radiological data significantly improved the models' performance, while cytopathological and radiomics data did not further improve the accuracy.

Level of evidence

Level 4.

目标约有 30% 的甲状腺结节无法通过传统诊断策略进行确诊。本研究的目的是开发能够利用术前变量识别甲状腺乳头状癌的机器学习(ML)模型。方法在一项回顾性单中心研究中,纳入了接受甲状腺手术的甲状腺结节患者。结果在186名患者中,有92个结节(49.5%)在组织学报告中属于甲状腺乳头状癌。仅使用临床免疫学变量的曲线下面积(AUC)在 0.41 到 0.61 之间。加入超声变量后,所有ML模型的性能都有所提高(AUC:0.95-0.97)。加入细胞学变量(AUC:0.86-0.97)和放射学变量(AUC:0.88-0.97)并没有进一步提高 ML 模型的性能。然而,加入放射学数据可显著提高模型的性能,而细胞病理学和放射组学数据并不能进一步提高准确性。
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引用次数: 0
Assessing volume growth of paranasal sinuses and nasal cavity in children using three-dimensional imaging software 利用三维成像软件评估儿童副鼻窦和鼻腔的体积增长情况
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-13 DOI: 10.1016/j.anl.2024.08.007
Kaoru Yamakawa , Hironobu Nishijima , Megumi Koizumi , Kenji Kondo

Objective

To investigate the accurate volume changes in the paranasal sinus and nasal cavity with age development, using three-dimensional (3D) imaging software

Methods

Paranasal sinus and nasal cavity volumes from computed tomography (CT) images in patients aged 0–24 years were measured using a 3D model to examine age-related changes. Paranasal sinus and nasal cavity growth were compared between age groups. Additionally, the correlation between body height and paranasal sinus growth was examined.

Results

A total of 139 CT scans from 137 patients were analyzed. Volume growth of maxillary, ethmoidal, sphenoid, frontal sinuses, and nasal cavity was observed until 18, 16, 20, 20, and 22 years, respectively. Maxillary sinus rapidly grew at 2–8 and 9–12 years, ethmoid sinus 2–8 and 13–16 years, sphenoid sinus 5–8 years, frontal sinus 2–10 years, and nasal cavity 7–12 years. The median volume after growth completion for maxillary, ethmoidal, sphenoid, frontal sinuses, and nasal cavities was 21,937 mm³, 4868 mm³, 5870 mm³, 3172 mm³, and 15,555 mm³, respectively. The left-right difference in the nasal cavity volume increased with age. Sinus and nasal cavity growth completion was delayed by 2–4 years compared to general height growth.

Conclusion

Growth of the ethmoid, maxillary, sphenoid, frontal sinus, and nasal cavity was completed in approximately 20 years. Compared to the results shown in reports based primarily on 2D measurements, the ethmoid and sphenoid sinuses and nasal cavity were found to continue to grow until older age than previously thought.

方法使用三维(3D)成像软件测量 0-24 岁患者计算机断层扫描(CT)图像中的副鼻窦和鼻腔体积,以研究与年龄相关的变化。比较了不同年龄组的副鼻窦和鼻腔生长情况。此外,还研究了身高与副鼻窦生长之间的相关性。观察到上颌窦、乙状窦、蝶窦、额窦和鼻腔的体积分别增长到 18、16、20、20 和 22 岁。上颌窦在 2 至 8 岁和 9 至 12 岁时迅速增长,筛窦在 2 至 8 岁和 13 至 16 岁时迅速增长,蝶窦在 5 至 8 岁时迅速增长,额窦在 2 至 10 岁时迅速增长,鼻腔在 7 至 12 岁时迅速增长。上颌窦、筛窦、蝶窦、额窦和鼻腔发育完成后的体积中位数分别为 21937 毫米³、4868 毫米³、5870 毫米³、3172 毫米³和 15555 毫米³。鼻腔容积的左右差异随着年龄的增长而增大。结论:乙状窦、上颌窦、蝶窦、额窦和鼻腔的生长大约在 20 年内完成。与主要基于二维测量的报告所显示的结果相比,发现乙状窦、蝶窦和鼻腔会继续生长,直到比以前认为的年龄更大。
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引用次数: 0
National epidemiological survey on pharyngeal, laryngeal, and tracheal stenosis in Japan: A National survey on airway stenosis 日本全国咽、喉和气管狭窄流行病学调查:全国气道狭窄调查
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-11 DOI: 10.1016/j.anl.2024.08.008
Yo Kishimoto , Kayoko Mizuno , Yoshitaka Kawai , Keisuke Mizuno , Hideki Hirabayashi , Kinya Furukawa , Noriko Morimoto , Kosaku Maeda , Koichi Kaneko , Koichi Omori

Objective

Airway stenosis impairs the quality of life of patients. However, the epidemiology and pathophysiology of airway stenosis remain underexplored owing to its rarity. Airway stenosis may go undetected for a long period without accurate diagnosis or treatment owing to the lack of established treatment guidelines. Thus, clinical information must be accumulated and analyzed to generate evidence-based treatment strategies for this rare entity.

Methods

A retrospective nationwide epidemiological survey was conducted targeting patients with pharyngeal, laryngeal, or tracheal stenosis in Japan. The initial survey was conducted across 1393 facilities between 2013 and 2017 to evaluate the treatment of airway stenosis. The clinical information of the patients was collected via a secondary survey.

Results

The primary survey revealed that airway stenosis was treated at only 43 % of the facilities over the 5-year period. The secondary survey revealed that 284 cases were registered across 57 facilities. The number of patients with acquired stenosis exceeded that of those with congenital stenosis. The larynx or cervical trachea was the most common site of stenosis, and intubation or tracheostomy was the most common cause of stenosis. Approximately 76 % of patients underwent surgical treatment, and tracheostomy was the most common procedure. Stenosis persisted in > 70 % of patients at the last visit.

Conclusions

This study clarified the clinical background of patients with pharyngeal, laryngeal, and tracheal stenosis in Japan and the surgical treatment received. The findings of this study confirmed the rarity of airway stenosis and the difficulty in treating this entity.

目的气道狭窄影响患者的生活质量。然而,由于气道狭窄的罕见性,对其流行病学和病理生理学的研究仍然不足。由于缺乏既定的治疗指南,气道狭窄可能长期得不到准确的诊断和治疗。因此,必须积累和分析临床信息,为这种罕见疾病制定以证据为基础的治疗策略。方法在日本针对咽、喉或气管狭窄患者开展了一项全国性流行病学回顾调查。首次调查于 2013 年至 2017 年间在 1393 家医疗机构进行,旨在评估气道狭窄的治疗情况。结果初步调查显示,5 年间仅有 43% 的医疗机构对气道狭窄进行了治疗。二次调查显示,57 家医疗机构登记了 284 个病例。后天性气道狭窄患者的人数超过了先天性气道狭窄患者。喉部或颈部气管是最常见的狭窄部位,插管或气管造口术是最常见的狭窄原因。约 76% 的患者接受了手术治疗,气管造口术是最常见的手术。结论 本研究阐明了日本咽、喉和气管狭窄患者的临床背景以及接受手术治疗的情况。研究结果证实了气道狭窄的罕见性和治疗难度。
{"title":"National epidemiological survey on pharyngeal, laryngeal, and tracheal stenosis in Japan: A National survey on airway stenosis","authors":"Yo Kishimoto ,&nbsp;Kayoko Mizuno ,&nbsp;Yoshitaka Kawai ,&nbsp;Keisuke Mizuno ,&nbsp;Hideki Hirabayashi ,&nbsp;Kinya Furukawa ,&nbsp;Noriko Morimoto ,&nbsp;Kosaku Maeda ,&nbsp;Koichi Kaneko ,&nbsp;Koichi Omori","doi":"10.1016/j.anl.2024.08.008","DOIUrl":"10.1016/j.anl.2024.08.008","url":null,"abstract":"<div><h3>Objective</h3><p>Airway stenosis impairs the quality of life of patients. However, the epidemiology and pathophysiology of airway stenosis remain underexplored owing to its rarity. Airway stenosis may go undetected for a long period without accurate diagnosis or treatment owing to the lack of established treatment guidelines. Thus, clinical information must be accumulated and analyzed to generate evidence-based treatment strategies for this rare entity.</p></div><div><h3>Methods</h3><p>A retrospective nationwide epidemiological survey was conducted targeting patients with pharyngeal, laryngeal, or tracheal stenosis in Japan. The initial survey was conducted across 1393 facilities between 2013 and 2017 to evaluate the treatment of airway stenosis. The clinical information of the patients was collected via a secondary survey.</p></div><div><h3>Results</h3><p>The primary survey revealed that airway stenosis was treated at only 43 % of the facilities over the 5-year period. The secondary survey revealed that 284 cases were registered across 57 facilities. The number of patients with acquired stenosis exceeded that of those with congenital stenosis. The larynx or cervical trachea was the most common site of stenosis, and intubation or tracheostomy was the most common cause of stenosis. Approximately 76 % of patients underwent surgical treatment, and tracheostomy was the most common procedure. Stenosis persisted in &gt; 70 % of patients at the last visit.</p></div><div><h3>Conclusions</h3><p>This study clarified the clinical background of patients with pharyngeal, laryngeal, and tracheal stenosis in Japan and the surgical treatment received. The findings of this study confirmed the rarity of airway stenosis and the difficulty in treating this entity.</p></div>","PeriodicalId":55627,"journal":{"name":"Auris Nasus Larynx","volume":"51 6","pages":"Pages 911-916"},"PeriodicalIF":1.6,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142167457","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The clinical manifestation and treatment of Meniere's Disease from the viewpoint of the water homeostasis of the inner ear 从内耳水分平衡的角度看美尼尔氏病的临床表现和治疗方法
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-09-07 DOI: 10.1016/j.anl.2024.08.002
Taizo Takeda , Setsuko Takeda , Akinobu Kakigi

Endolymphatic hydrops, a pathological feature of Ménière's disease, has been experimentally and clinically confirmed to be influenced by the blood circulation of vasopressin (VP). VP is a well-known hormonal regulator of water homeostasis. In addition, VP is influenced by various environmental changes, dehydration, fluctuation of atmospheric pressure, pregnancy, and other factors. Furthermore, VP is a key regulator of the hypothalamic-pituitary-adrenal (HPA) axis. The HPA axis is a major neuroendocrine system that controls reactions to emotional and physical stresses, as well as the sleep/wake cycle (circadian rhythm). Therefore, VP is susceptible to change via the HPA axis.

This review considers possible mechanisms of the formation of endolymphatic hydrops from the perspective of the vasopressin-aquaporin 2 system.

内淋巴水肿是梅尼埃病的一种病理特征,实验和临床证实它受血管加压素(VP)血液循环的影响。血管加压素是一种众所周知的水稳态激素调节剂。此外,VP 还受各种环境变化、脱水、气压波动、妊娠等因素的影响。此外,VP 还是下丘脑-垂体-肾上腺(HPA)轴的关键调节因子。HPA 轴是一个主要的神经内分泌系统,控制着对情绪和身体压力的反应,以及睡眠/觉醒周期(昼夜节律)。本综述将从血管加压素-quaporin 2 系统的角度探讨内淋巴水肿形成的可能机制。
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引用次数: 0
Open-type cholesteatoma is the predictive factor for residual disease in congenital cholesteatoma treated with TEES 开放型胆脂瘤是 TEES 治疗先天性胆脂瘤残留疾病的预测因素
IF 1.6 4区 医学 Q2 OTORHINOLARYNGOLOGY Pub Date : 2024-08-31 DOI: 10.1016/j.anl.2024.08.004
Toshinori Kubota, Tsukasa Ito, Takatoshi Furukawa, Hirooki Matsui, Takanari Goto, Chikako Shinkawa, Seiji Kakehata

Objective

To determine the predictive factors for residual disease occurring after surgical removal of congenital cholesteatomas and whether these predictive factors differ between microscopic ear surgery (MES) using data from the literature and transcanal endoscopic ear surgery (TEES) using data from our own institution.

Methods

Twenty-three patients with a congenital cholesteatoma who underwent surgical treatment at Yamagata University Hospital between December 2011 and December 2017 were retrospectively investigated. We divide TEES into three different approaches: non-powered TEES, powered TEES and dual MES/TEES. Main outcome measures were Potsic stage, closed or open congenital cholesteatoma type, TEES surgical approach, appearance of residual disease, tympanoplasty type and hearing outcome.

Results

A logistic regression analysis was conducted on the Potsic stage, closed or open type, TEES surgical approach and age to obtain the odds ratio for residual disease. The chance of residual disease significantly increased in the presence of an open-type congenital cholesteatoma (odds ratio: 30.82; 95 % confidence interval: 1.456–652.3; p = 0.0277), but not for any of the other factors including Potsic stage. The timing of the confirmation of residual disease after ossicular chain reconstruction was analyzed using a Kaplan-Meier analysis. The residual disease rate was significantly higher with an open-type congenital cholesteatoma (log-rank test, p < 0.05). In addition, all residual disease occurred within three years after surgery.

Conclusions

Our results showed that an open-type congenital cholesteatoma is the strongest predictive factor for residual disease when removing a congenital cholesteatoma by TEES.

目的 确定先天性胆脂瘤手术切除后发生残留疾病的预测因素,以及这些预测因素在使用文献数据的显微耳科手术(MES)和使用本机构数据的经内窥镜耳科手术(TEES)之间是否存在差异。方法 回顾性调查了 2011 年 12 月至 2017 年 12 月期间在山形大学医院接受手术治疗的 23 例先天性胆脂瘤患者。我们将TEES分为三种不同的方法:无动力TEES、有动力TEES和双MES/TEES。主要结果指标为Potsic分期、闭合性或开放性先天性胆脂瘤类型、TEES手术方式、残留病变的出现、鼓室成形术类型和听力结果。结果对Potsic分期、闭合性或开放性类型、TEES手术方式和年龄进行了逻辑回归分析,得出了残留病变的几率比。如果存在开放型先天性胆脂瘤,残留疾病的几率会明显增加(几率比:30.82;95% 置信区间:1.456-652.3;P = 0.0277),但与其他因素(包括 Potsic 分期)无关。采用卡普兰-梅耶分析法对骨链重建后确认残留疾病的时间进行了分析。开放型先天性胆脂瘤的残留病变率明显更高(log-rank检验,p <0.05)。结论我们的研究结果表明,在通过 TEES 切除先天性胆脂瘤时,开放型先天性胆脂瘤是残留疾病的最强预测因素。
{"title":"Open-type cholesteatoma is the predictive factor for residual disease in congenital cholesteatoma treated with TEES","authors":"Toshinori Kubota,&nbsp;Tsukasa Ito,&nbsp;Takatoshi Furukawa,&nbsp;Hirooki Matsui,&nbsp;Takanari Goto,&nbsp;Chikako Shinkawa,&nbsp;Seiji Kakehata","doi":"10.1016/j.anl.2024.08.004","DOIUrl":"10.1016/j.anl.2024.08.004","url":null,"abstract":"<div><h3>Objective</h3><p>To determine the predictive factors for residual disease occurring after surgical removal of congenital cholesteatomas and whether these predictive factors differ between microscopic ear surgery (MES) using data from the literature and transcanal endoscopic ear surgery (TEES) using data from our own institution.</p></div><div><h3>Methods</h3><p>Twenty-three patients with a congenital cholesteatoma who underwent surgical treatment at Yamagata University Hospital between December 2011 and December 2017 were retrospectively investigated. We divide TEES into three different approaches: non-powered TEES, powered TEES and dual MES/TEES. Main outcome measures were Potsic stage, closed or open congenital cholesteatoma type, TEES surgical approach, appearance of residual disease, tympanoplasty type and hearing outcome.</p></div><div><h3>Results</h3><p>A logistic regression analysis was conducted on the Potsic stage, closed or open type, TEES surgical approach and age to obtain the odds ratio for residual disease. The chance of residual disease significantly increased in the presence of an open-type congenital cholesteatoma (odds ratio: 30.82; 95 % confidence interval: 1.456–652.3; <em>p</em> = 0.0277), but not for any of the other factors including Potsic stage. The timing of the confirmation of residual disease after ossicular chain reconstruction was analyzed using a Kaplan-Meier analysis. The residual disease rate was significantly higher with an open-type congenital cholesteatoma (log-rank test, <em>p</em> &lt; 0.05). In addition, all residual disease occurred within three years after surgery.</p></div><div><h3>Conclusions</h3><p>Our results showed that an open-type congenital cholesteatoma is the strongest predictive factor for residual disease when removing a congenital cholesteatoma by TEES.</p></div>","PeriodicalId":55627,"journal":{"name":"Auris Nasus Larynx","volume":"51 5","pages":"Pages 898-904"},"PeriodicalIF":1.6,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142097336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Auris Nasus Larynx
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