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Do Tunisian children with unilateral cleft lip and palate differ from normal individuals in dental maturity? A pilot study. 突尼斯单侧唇腭裂儿童在牙齿成熟度上与正常人有区别吗?一项试点研究。
Q3 Medicine Pub Date : 2024-10-05 DOI: 10.62438/tunismed.v102i10.4907
Manel Chalbi, Mehdi Khemiss, Miniar Rhaiem, Nadia Elabed, Mohamed Ali Chemli

Introduction: Cleft lip and palate (CLP) is the most common congenital malformation of the head and neck. Children with CLP often exhibit dental anomalies.

Aim: To evaluate the dental age (DA) of unilateral CLP in Tunisian children.

Methods: This was a cross-sectional study carried out in the department of pediatric dentistry at the University Hospital La Rabta, Tunis. Patients aged between 5 and 14 years, with no other congenital anomalies or syndromes in the craniofacial region other than CLP, were included. The patients' chronological ages were first calculated in years and months. DA was assessed in panoramic radiographs using Demirjian's method. The score of each stage is allocated, and the sum of the scores provides an evaluation of the subject's dental maturity.

Results: Fifty-three patients were included in the present study. No difference was observed between the two groups regarding the dental age. A strong and positive correlation between the DA and the chronological age in the two groups was observed (r=0.826). Estimated regression showed that chronological age alone explained 57,4% (r2=0.574) of the dental age variation in the study group and 64.5% (r2=0.645) in the control group.

Conclusion: For dental management, CLP children should have the same approach in orthodontics and pediatric dentistry as individuals without clefts, with a focus on the individualization of diagnosis and treatment planning.

简介唇腭裂(CLP)是头颈部最常见的先天性畸形。目的:评估突尼斯儿童单侧唇腭裂的牙龄(DA):这是突尼斯拉布塔大学医院儿童牙科开展的一项横断面研究。研究对象包括年龄在 5 至 14 岁之间、除 CLP 外没有其他颅面区域先天性畸形或综合征的患者。首先以年和月为单位计算患者的实际年龄。采用 Demirjian 方法对全景照片中的畸形进行评估。每个阶段的分数被分配,分数的总和可用于评估受试者的牙齿成熟度:本研究共纳入 53 名患者。两组患者的牙齿年龄没有差异。在两组患者中,牙合成熟度与实际年龄之间存在很强的正相关性(r=0.826)。估计回归结果表明,在研究组中,仅计时年龄就能解释57.4%的牙龄变化(r2=0.574),而在对照组中,仅计时年龄就能解释64.5%的牙龄变化(r2=0.645):结论:在牙科治疗方面,CLP 儿童应采用与无裂纹儿童相同的正畸和儿童牙科治疗方法,重点是诊断和治疗计划的个性化。
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引用次数: 0
Predictive factors of major low anterior resection syndrome after surgery for rectal tumors. 直肠肿瘤术后主要低位前切除综合征的预测因素。
Q3 Medicine Pub Date : 2024-10-05 DOI: 10.62438/tunismed.v102i10.5177
Mehdi Trabelsi, Imen Samaali, Neirouz Kammoun, Amine Ben Safta, Annouar Oueslati, Wejih Dougaz, Mehdi Khalfallah, Hichem Jerraya, Ibtissem Bouasker, Ramzi Nouira, Chadli Dziri

Aim: To describe the epidemiological and clinical data of impaired functional outcome secondary to anterior resection of the rectum and to identify the predictive factors of major low anterior resection syndrome (LARS) Methods: This retrospective study considered patients operated on for rectal tumors in surgical department in our hospital, between January 1st,2009 and December 31st, 2021. The primary outcome measure was the development of a major LARS immediately or after stoma closure. In order to identify independent predictors of major LARS, patients were divided into two groups: the "Major LARS" group and the "No Major LARS" group, and then we carried out a descriptive study, followed by an analytical study with logistic regression.

Results: We enrolled 42 patients operated for rectal tumor and had an anterior resection. Half of our patients developed LARS of which 14 developed major LARS. The median time to onset of LARS symptoms was 9 [2 -24] months. At the end of this study, 2 factors were retained: age (OR=2.48; CI95% [1.2- 5.10], p=0.012) and pT3T4 stage (OR=5.95; CI95% [1.07- 33.33], p=0.041) as independent predictive factors of a major LARS. Neoadjuvant therapy was also a risk factor for major LARS in our study with a statistically significant difference (p=0.025) between the two groups "Major LARS" and "No major LARS".

Conclusion: LARS should be appropriately considered in the management of rectal cancer. Based on our results and data from the literature, age and mesorectal invasion were found to be independent predictors of major LARS.

目的:描述直肠前切除术后功能受损的流行病学和临床数据,并确定主要低位前切除综合征(LARS)的预测因素 方法:这项回顾性研究考虑了 2009 年 1 月 1 日至 2021 年 12 月 31 日期间在我院外科接受直肠肿瘤手术的患者:这项回顾性研究的对象是2009年1月1日至2021年12月31日期间在我院外科接受直肠肿瘤手术的患者。主要结果指标是在造口关闭时或关闭后出现严重的 LARS。为了确定重度LARS的独立预测因素,我们将患者分为两组:"重度LARS "组和 "无重度LARS "组,然后进行了描述性研究,接着进行了逻辑回归分析研究:我们共收治了42名直肠肿瘤手术患者,他们都接受了前方切除术。半数患者发展为 LARS,其中 14 例发展为严重 LARS。出现 LARS 症状的中位时间为 9 [2 -24] 个月。本研究最后保留了两个因素:年龄(OR=2.48;CI95% [1.2-5.10],p=0.012)和pT3T4分期(OR=5.95;CI95% [1.07-33.33],p=0.041),作为严重LARS的独立预测因素。在我们的研究中,新辅助治疗也是导致重大 LARS 的风险因素,"重大 LARS "和 "无重大 LARS "两组之间的差异有统计学意义(p=0.025):结论:在治疗直肠癌时,应适当考虑 LARS。根据我们的研究结果和文献数据,我们发现年龄和直肠系膜侵犯是主要 LARS 的独立预测因素。
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引用次数: 0
Risk factors for uterine dehiscence and rupture in case of vaginal birth after cesarean section. 剖宫产术后阴道分娩子宫开裂和破裂的风险因素。
Q3 Medicine Pub Date : 2024-10-05 DOI: 10.62438/tunismed.v102i10.5015
Hana Hakim, Mohamed Derbel, Hajer Mtibaa, Basma Akrout, Khaled Trigui, Fatma Chaker, Fatma Khanfir, Kais Chaabane

Introduction: Vaginal delivery after caesarean section (VBAC) is recommended, but the rising rate of uterine rupture calls into question the safety of this practice.

Aim: To identify risk factors for uterine dehiscence and rupture.

Methods: This was a prospective, analytical and descriptive observational study, carried out in a tertiary care maternity. We included all parturients with one previous caesarean section undergoing trial of labor. We assessed the quality of the uterine scar which was evaluated after delivery.

Results: We included 300 patients with one previous caesarean section undergoing trial of labor. The trial of labor was successful (vaginal delivery) in 50.7% of cases. The uterine scar, assessed after delivery, was of good quality in 79% of cases. We noted 7 cases of uterine rupture, i.e. 2.3% of cases, and dehiscence in 56 patients, i.e. 18.6% of cases. Parity, conditions of previous caesarean section (programmed or emergency) and interpregnancy interval were significantly related to the labor outcome (p=0.004, p=0.001 and p=0.135 respectively). The occurrence of rupture or dehiscence was not significantly related to macrosomia, defined as a neonatal weight greater than 4000g (p=0.135).

Conclusion: Knowing the risk factors for uterine dehiscence and rupture would enable the obstetrician to properly assess the situation in order to make the correct decision and avoid neonatal and maternal complications.

导言:目的:确定子宫开裂和破裂的风险因素:这是一项前瞻性、分析性和描述性观察研究,在一家三级护理产科医院进行。我们纳入了所有曾进行过一次剖腹产手术并正在进行试产的产妇。我们对子宫疤痕的质量进行了评估,并在产后进行了评价:我们纳入了 300 名曾接受过一次剖腹产手术并进行试产的产妇。50.7%的病例试产成功(阴道分娩)。经产后评估,79%的病例子宫瘢痕质量良好。我们发现有 7 例子宫破裂(占 2.3%),56 例开裂(占 18.6%)。胎次、前次剖腹产的情况(计划或紧急)和孕间期与分娩结果有显著关系(分别为P=0.004、P=0.001和P=0.135)。子宫破裂或开裂的发生与巨大儿(新生儿体重超过4000克)无明显关系(P=0.135):了解子宫开裂和破裂的风险因素可使产科医生正确评估情况,从而做出正确的决定,避免新生儿和产妇并发症的发生。
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引用次数: 0
Atypical Multifocal Granular Cell Tumor with FLT3 Y842C Somatic Mutation: A case report and a review of the literature. 伴有FLT3 Y842C体细胞突变的非典型多灶性颗粒细胞瘤:病例报告和文献综述。
Q3 Medicine Pub Date : 2024-10-05 DOI: 10.62438/tunismed.v102i10.5172
Alexandra Zara Rozalen, Ruth Garcia, Samir Husami, Gustavo Marino, Victor E Nava

Introduction: Granular cell tumors (GCT) are predominantly benign neoplasms composed by cells with abundant eosinophilic granular cytoplasm. Although the majority of GCTs exhibit a benign clinical course, a minority display cytological atypia and may exhibit aggressive, cancer-like behavior. Definitive evidence of malignancy in GCTs is reliably established only through the presence of metastasis. Addi- tionally, a subset of GCTs demonstrates a high rate of recurrence, underscoring the need for better prog- nostic markers. Therefore, it is crucial to identify molecular markers associated with aggressive behavior in GCTs. Molecular analysis may be particularly beneficial in cases exhibiting cytological atypia to in- form clinical outcome prognostication and guide therapeutic strategies.

Observation: In this case report, a 45-year-old female with multiple gastrointestinal GCTs is pre- sented. The patient did not have any genetic syndromes commonly associated with GCT, such as neu- rofibromatosis type 1, Noonan syndrome or LEOPARD syndrome. The tumors not only demonstrated nuclear atypia, but also harbored a unique FLT3 Y842C somatic alteration identified by next-genera- tion sequencing. The patient remains asymptomatic and under endoscopic surveillance two years after diagnosis and complete resection of the neoplasms.

Conclusion: We presented an exceedingly rare case of multifocal atypical GCT in an adult without any previously known genetic syndrome. A tumoral FLT3 Y842C point mutation not previously reported in GCT was discovered. Although the precise significance of this finding is uncertain, FLT3 Y842C has been cataloged as likely pathogenic in ClinVar. This report underscores the potential predictive utility of next-generation sequencing in the characterization and management of rare neoplasms.

简介颗粒细胞瘤(GCT)主要是由具有大量嗜酸性颗粒胞质的细胞组成的良性肿瘤。虽然大多数 GCT 的临床表现为良性,但也有少数 GCT 会出现细胞学不典型性,并可能表现出侵袭性的癌症样行为。GCT恶性的确凿证据只有通过出现转移才能可靠地确定。此外,一部分 GCTs 具有很高的复发率,这突出表明需要更好的预后标志物。因此,确定与 GCT 侵袭行为相关的分子标记至关重要。分子分析对细胞学非典型性病例尤其有益,可用于临床结果预后和指导治疗策略:在本病例报告中,预发了一名患有多发性胃肠道 GCT 的 45 岁女性。患者没有任何与 GCT 常见的遗传综合征,如 1 型神经纤维瘤病、努南综合征或 LEOPARD 综合征。肿瘤不仅表现为核不典型性,而且通过新一代测序发现了独特的FLT3 Y842C体细胞改变。患者在确诊并完全切除肿瘤两年后仍无症状,并接受内镜监测:我们介绍了一例极为罕见的成人多灶性非典型 GCT 病例,该病例之前没有任何已知的遗传综合征。我们发现了一种肿瘤FLT3 Y842C点突变,此前在GCT中从未报道过。尽管这一发现的确切意义尚不确定,但FLT3 Y842C已被ClinVar列为可能的致病基因。该报告强调了新一代测序技术在罕见肿瘤的特征描述和管理中的潜在预测作用。
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引用次数: 0
Iatrogenic risk in elderly patients. 老年患者的先天性风险。
Q3 Medicine Pub Date : 2024-10-05 DOI: 10.62438/tunismed.v102i10.4970
Zohra Chadli, Kmar Kasraoui, Ibtissem Hannachi, Amel Chaabane, Rim Klii, Haifa Ben Romdhane, Naceur A Boughattas, Nadia Ben Fredj, Karim Aouam

Introduction-Aim: The iatrogenic risk in the elderly is a real public health problem due to its frequency and seriousness. Our study aimed to analyze the epidemiological, clinical and chronological aspects of adverse drug reactions occurring in elderly subjects and to identify the incriminated drugs.

Methods: We carried out a retrospective study of all the observations of adverse drug reactions in elderly subjects, notified to the Clinical Pharmacology department of Monastir over a period of 17 years (2004 - 2020). Drug skin tests were performed according to ENDA recommendations and imputability was analyzed using the French method of Bégaud et al. The drugs have been grouped according to the ATC classification.

Results: Among 545 events occurring in elderly subjects, drug responsibility was retained in 209 patients. They were 106 men and 103 women (gender-ratio=1.03). The average age of the patients was 72.3±6 years. Drug hypersensitivity reactions accounted for 75% of all adverse effects. The majority of these reactions were type IV (delayed). The incriminated drugs were: anti-infectives (47%), drugs for the musculoskeletal system (20%), drugs for the cardiovascular system (17%) and drugs for the central nervous system (5%).

Conclusion: Through this study, we noted a predominance of delayed drug hypersensitivity reactions as well as an increased involvement of anti-infectives and allopurinol in the occurrence of adverse effects in the elderly population.

导言--目的:老年人的先天性风险因其频发性和严重性而成为一个真正的公共卫生问题。我们的研究旨在分析发生在老年人身上的药物不良反应的流行病学、临床和年代学方面的情况,并确定引起不良反应的药物:我们对莫纳斯提尔临床药理学部门在 17 年内(2004-2020 年)收到的所有老年患者药物不良反应观察结果进行了回顾性研究。根据ENDA建议进行了药物皮试,并采用法国贝高(Bégaud)等人的方法分析了可归因性:结果:在老年受试者发生的 545 起事件中,有 209 名患者保留了药物责任。其中男性 106 人,女性 103 人(性别比=1.03)。患者的平均年龄为(72.3±6)岁。药物过敏反应占所有不良反应的 75%。这些反应大多为 IV 型(延迟型)。引起不良反应的药物包括:抗感染药物(47%)、肌肉骨骼系统药物(20%)、心血管系统药物(17%)和中枢神经系统药物(5%):通过这项研究,我们注意到延迟性药物超敏反应占主导地位,而且抗感染药物和别嘌呤醇在老年人群不良反应中的参与度更高。
{"title":"Iatrogenic risk in elderly patients.","authors":"Zohra Chadli, Kmar Kasraoui, Ibtissem Hannachi, Amel Chaabane, Rim Klii, Haifa Ben Romdhane, Naceur A Boughattas, Nadia Ben Fredj, Karim Aouam","doi":"10.62438/tunismed.v102i10.4970","DOIUrl":"10.62438/tunismed.v102i10.4970","url":null,"abstract":"<p><p>Introduction-Aim: The iatrogenic risk in the elderly is a real public health problem due to its frequency and seriousness. Our study aimed to analyze the epidemiological, clinical and chronological aspects of adverse drug reactions occurring in elderly subjects and to identify the incriminated drugs.</p><p><strong>Methods: </strong>We carried out a retrospective study of all the observations of adverse drug reactions in elderly subjects, notified to the Clinical Pharmacology department of Monastir over a period of 17 years (2004 - 2020). Drug skin tests were performed according to ENDA recommendations and imputability was analyzed using the French method of Bégaud et al. The drugs have been grouped according to the ATC classification.</p><p><strong>Results: </strong>Among 545 events occurring in elderly subjects, drug responsibility was retained in 209 patients. They were 106 men and 103 women (gender-ratio=1.03). The average age of the patients was 72.3±6 years. Drug hypersensitivity reactions accounted for 75% of all adverse effects. The majority of these reactions were type IV (delayed). The incriminated drugs were: anti-infectives (47%), drugs for the musculoskeletal system (20%), drugs for the cardiovascular system (17%) and drugs for the central nervous system (5%).</p><p><strong>Conclusion: </strong>Through this study, we noted a predominance of delayed drug hypersensitivity reactions as well as an increased involvement of anti-infectives and allopurinol in the occurrence of adverse effects in the elderly population.</p>","PeriodicalId":38818,"journal":{"name":"Tunisie Medicale","volume":"102 10","pages":"682-689"},"PeriodicalIF":0.0,"publicationDate":"2024-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11574366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142509770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Insights into the genetic theory of infectious diseases. 对传染病基因理论的见解。
Q3 Medicine Pub Date : 2024-09-05 DOI: 10.62438/tunismed.v102i9.4872
Abderrahmane Moundir, Leila Jeddane, Ahmed Aziz Bousfiha

Over the past century, classical approaches from microbiology and immunology have produced spectacular results in the control of infectious diseases. However, the recent SARS-COV-2 pandemic has highlighted our continued failure to control some infections. Other microorganisms still pose a threat to humanity such as HIV, Ebola, and influenza viruses. It seems that conventional approaches are not able to solve all the current problems caused by infectious diseases. Human genetics has shown that infections have a strong genetic determinism that can lead to a predisposition or resistance to infections. This explains much of the clinical variability observed in individuals infected with the same pathogen. The identification of the genetic etiology allows a better understanding of the pathogenesis of infectious diseases and, consequently, the consideration of appropriate preventive and therapeutic strategies. This review provides insights into the genetic theory and the concrete evidence to support it. We highlight the role of primary immunodeficiencies in the discovery of Mendelian and monogenic susceptibility to infections, then we show how genetic and phenotypic heterogeneity, redundancy, and resistance to infection manifest in the context of this genetic determinism. To effectively combat the constant threat of microbes, it is essential to integrate human genetics with microbiology to examine the interactions between pathogens and our immune system.

在过去的一个世纪里,微生物学和免疫学的经典方法在控制传染病方面取得了令人瞩目的成果。然而,最近的 SARS-COV-2 大流行凸显了我们仍然无法控制某些传染病。其他微生物仍然对人类构成威胁,如艾滋病毒、埃博拉病毒和流感病毒。传统方法似乎无法解决当前传染病造成的所有问题。人类遗传学表明,传染病具有很强的遗传决定性,可导致对传染病的易感性或抵抗力。这在很大程度上解释了在感染同一病原体的个体中观察到的临床变异性。查明遗传病因可以更好地了解传染病的发病机理,从而考虑采取适当的预防和治疗策略。本综述深入探讨了遗传理论和支持该理论的具体证据。我们强调了原发性免疫缺陷症在发现孟德尔和单基因易感性中的作用,然后说明了遗传和表型的异质性、冗余性和抗感染性是如何在这种遗传决定论的背景下表现出来的。为了有效应对微生物的持续威胁,必须将人类遗传学与微生物学结合起来,研究病原体与我们的免疫系统之间的相互作用。
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引用次数: 0
Enhancing Student Success: Implementing Mentoring Programs in Academic Settings: Focus on the Faculty of Medicine of Tunis. 提高学生成功率:在学术环境中实施指导计划:聚焦突尼斯医学院。
Q3 Medicine Pub Date : 2024-09-05 DOI: 10.62438/tunismed.v102i9.5316
Nadia Ben Amor, Lilia Kraoua, Rahma Damak, Soumeya Halayem, Lilia Zakhama, Iheb Labbene, Mohamed Jouini

In order to improve the learning outcomes, skills, sense of belonging and well-being of their students, faculties around the world have chosen to implement mentoring programs for their learners. Given the complexity of implementing this approach, our objectives in this review are, on the one hand, to discuss and support the principles and recommendations of a mentoring project in an academic setting and, on the other hand, to present the vision of the Faculty of Medicine of Tunis regarding this mentoring approach.

为了提高学生的学习成绩、技能、归属感和幸福感,世界各地的学院都选择为学生实施辅导计划。鉴于实施这种方法的复杂性,我们在本综述中的目标一方面是讨论和支持学术环境中导师项目的原则和建议,另一方面是介绍突尼斯医学院对这种导师方法的愿景。
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引用次数: 0
Hydatid cyst of the gluteal muscle: a case report and literature review. 臀肌水瘤囊肿:病例报告和文献综述。
Q3 Medicine Pub Date : 2024-09-05 DOI: 10.62438/tunismed.v102i9.5130
Soukaina Adadi, Rabi Isaka Amidou, Zina Lebbar, Hayat Ben Saghroune, Hamza Lakdim, Abdelmajid Elmrini, Zineb Tlamçani

Introduction: Echinococcosis is a relatively widespread anthropozoonosis in endemic regions, preferentially affecting the liver and lungs. Although rare, it can sometimes be localized in the muscles. The clinical symptoms are insidious and not very indicative, often leading to a delayed diagnosis. We reported a case of a hydatid cyst located in the gluteal muscle.

Observation: This was a 52-year-old female patient admitted for the appearance of a swelling in the left buttock region, progressively increasing in size. The radiological exam, revealed a large simple cyst originating from the gluteal muscle with purely liquid content. A surgical excision was performed, and the parasitological examination of the hydatid fluid confirmed the diagnosis.

Conclusion: Hydatid cysts in soft tissues are rare, slow-developing tumors with local extension. This diagnosis should be considered, especially in individuals from endemic countries. The treatment is primarily surgical, but the best way to combat hydatid disease, regardless of its location, remains prevention.

导言:棘球蚴病是一种在地方病流行地区较为普遍的人类包虫病,主要侵犯肝脏和肺部。虽然罕见,但有时也会出现在肌肉局部。该病的临床症状隐匿,不具有很强的指示性,往往导致诊断延误。我们报告了一例位于臀肌的包虫囊肿:这是一名 52 岁的女性患者,因左臀部出现肿胀并逐渐增大而入院。影像学检查显示,患者臀部肌肉内有一个巨大的单纯性囊肿,囊肿内为液体。手术切除后,对包虫液进行了寄生虫学检查,确诊为包虫囊肿:结论:软组织包虫囊肿是一种罕见的、发展缓慢的肿瘤,具有局部扩展性。结论:软组织包虫囊肿是一种罕见的、发展缓慢且有局部扩展的肿瘤,应考虑到这一诊断,尤其是来自地方病流行国家的患者。治疗方法主要是外科手术,但无论包虫病发生在哪个部位,防治包虫病的最佳方法仍然是预防。
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引用次数: 0
Evolution of treatment for unspecific back pain: From past to future. 非特异性背痛治疗的演变:从过去到未来
Q3 Medicine Pub Date : 2024-09-05 DOI: 10.62438/tunismed.v102i9.5162
Daniela Herrera, Christian Hartard, Helmi Ben Saad, Leonardo Montanari Mota, Viviane Alves Dos Santos, Chetna Sinha, Rahma Jedidi, Diana Hartard, Sara Khaled, Stefan Hartard, Manfred Hartard

Unspecific back pain (UBP) has long puzzled medical professionals. Historically, back pain (BP) was often attributed to mystical causes, treated with incantations or herbal concoctions. The Middle Ages shifted towards empirical practices, though still intertwined with superstition, using methods like leeches and bloodletting. The Renaissance introduced systematic healthcare approaches, laying the foundation for modern medicine. The 20th century saw significant advancements with diagnostic imaging, pharmacotherapy, physical therapy, and surgical interventions, though UBP remained elusive. Recent decades have seen a paradigm shift towards multidisciplinary approaches, addressing BP's multifactorial nature through holistic methods considering biomechanical, psychosocial, and lifestyle factors. This shift integrates quantitative research with hermeneutic interpretation, emphasizing evidence-based guidelines. Non-pharmacological interventions such as exercise therapy, electrotherapy, cognitive behavioral therapy, and mindfulness-based stress reduction have gained prominence, empowering individuals in their recovery. Technological innovations like virtual reality and artificial intelligence offer personalized treatment plans, optimizing outcomes. The future of BP treatment holds promise with advancements in regenerative medicine, neuromodulation, telemedicine, and remote monitoring platforms, enhancing accessibility and continuity of care, especially in underserved communities. However, challenges such as the opioid epidemic and healthcare disparities remain, necessitating judicious prescribing practices and equitable resource distribution. The evolving treatment landscape for UBP reflects the dynamic interplay between scientific progress, clinical innovation, and societal needs, aiming to alleviate the burden of back pain and improve quality of life.

长期以来,非特异性背痛(UBP)一直困扰着医学专家。在历史上,背痛(BP)通常被归结为神秘的原因,用咒语或草药治疗。中世纪开始转向经验疗法,但仍与迷信交织在一起,使用水蛭和放血等方法。文艺复兴时期引入了系统的医疗保健方法,为现代医学奠定了基础。20 世纪,影像诊断、药物治疗、物理治疗和外科干预取得了重大进展,但超导粒子仍难以实现。近几十年来,研究范式向多学科方法转变,通过考虑生物力学、社会心理和生活方式等因素的整体方法来解决血压的多因素性质。这种转变将定量研究与诠释学解释相结合,强调循证指南。运动疗法、电疗法、认知行为疗法和正念减压法等非药物干预措施日益突出,增强了个人的康复能力。虚拟现实和人工智能等技术创新提供了个性化的治疗方案,优化了治疗效果。随着再生医学、神经调控、远程医疗和远程监控平台的发展,未来的血压治疗前景广阔,特别是在服务不足的社区,医疗服务的可及性和连续性将得到加强。然而,阿片类药物流行和医疗保健差异等挑战依然存在,这就需要明智的处方实践和公平的资源分配。不断发展的UTBP治疗方法反映了科学进步、临床创新和社会需求之间的动态相互作用,旨在减轻背痛的负担并提高生活质量。
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引用次数: 0
A Unique Tongue Presentation Revealing a Bronchobiliary Fistula. 显示支气管胆管瘘的独特舌象
Q3 Medicine Pub Date : 2024-09-05 DOI: 10.62438/tunismed.v102i9.5127
Adil Zegmout, Youssef Zemmez, Hanane Asri, Hicham Souhi, Hanane El Ouazzani, Ismail Abderrahmane Rhorfi
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引用次数: 0
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