Tunisia

突尼斯
  • 文章类型: Case Reports
    胎盘植入是一种罕见但严重的胎盘附着异常。本研究的目的是分析流行病学,临床,胎盘植入的临床和进化特征,调查治疗管理并评估孕产妇和新生儿的发病率和死亡率。我们做了一个回顾,苏塞FarhatHached大学医院妇产科经组织学证实的胎盘植入患者的描述性研究,从2015年1月1日至2019年12月31日的4年期间。流行病学,临床,临床旁,从患者的医疗记录和手术报告中收集治疗和进化数据.在我们的系列中,我们确定了46例胎盘植入。我们患者的平均年龄为35±4.61岁。我们的每个病人都有一个伤痕累累的子宫。我们所有患者的平均分娩期限为闭经34周,分娩方式为剖腹产。行一线子宫切除术40例,保守治疗6例。16例患者出现了母体并发症。没有观察到产妇死亡。胎盘植入是一种罕见的疾病,与显着的母体和胎儿发病率有关。
    Placenta accreta is a rare but serious placental attachment abnormality. The aim of this study is to analyze the epidemiological, clinical, para-clinical and evolutionary features of placenta accreta, to investigate the therapeutic management and to assess maternal and neonatal morbidity and mortality. We conducted a retrospective, descriptive study of patients with histologically confirmed placenta accreta in the obstetrics and gynaecology department of the Farhat Hached University Hospital in Sousse, over a 4-year period from 1st January 2015 to 31st December 2019. The epidemiological, clinical, paraclinical, therapeutic and evolutionary data were collected from patients´ medical records and operative reports. In our series, we identified 46 cases of placenta accreta. The average age of our patients was 35±4.61 years. Each of our patients had a scarred uterus. The average term of delivery was 34 weeks of amenorrhoea and the mode of delivery was caesarean section for all our patients. First-line hysterectomy was performed in 40 patients and conservative treatment in 6. Sixteen patients developed maternal complications. No maternal death was observed. Placenta accreta is a rare condition associated with significant maternal and foetal morbidity.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    在过去的几十年里,在反刍动物中发现了几种瘟病毒,猪,and,最近,在非有蹄类宿主中。因此,瘟病毒的命名和分类法已经更新。突尼斯绵羊样瘟病毒(TSV,瘟病毒N)是一种与经典猪瘟病毒(CSFV)遗传密切相关的附加绵羊瘟病毒。在这项研究中,在意大利北部伦巴第地区的绵羊农场的瘟病毒感染调查中,我们从一只绵羊中鉴定并分离出一株瘟病毒,根据其基因组核苷酸身份,该绵羊被发现属于瘟病毒N种。绵羊本身和它的羔羊被发现持续感染。我们对三个病毒基因组区域(5'-UTR的片段,部分Npro,和整个E2区域)。总之,这些结果证实了在西西里岛通知后在意大利北部流通的TSV,意大利,和法国。与意大利语相关,突尼斯人,法国菌株表明,检测可能是由于国家之间的活动物交易造成的,这支持了卫生控制措施的需要。
    Over the last few decades, several pestiviruses have been discovered in ruminants, pigs, and, more recently, in non-ungulate hosts. Consequently, the nomenclature and taxonomy of pestiviruses have been updated. The Tunisian sheep-like pestivirus (TSV, Pestivirus N) is an additional ovine pestivirus genetically closely related to classical swine fever virus (CSFV). In this study, during a survey of pestivirus infections in ovine farms in the Lombardy region of Northern Italy, we identified and isolated a pestivirus strain from a sheep that was found to belong to Pestivirus N species based on its genomic nucleotide identity. The sheep itself and its lamb were found to be persistently infected. We performed molecular characterization and phylogenetic analysis of three viral genomic regions (a fragment of 5\'-UTR, partial Npro, and the whole E2 region). In conclusion, these results confirmed circulating TSV in Northern Italy after notification in Sicily, Italy, and France. Correlation with Italian, Tunisian, and French strains showed that detection might have resulted from the trading of live animals between countries, which supports the need for health control measures.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    这项工作的目的是提供证据,证明来自Sfaxsalina(突尼斯东南部)的返流黄腿鸥颗粒(n=18)中存在微塑料(MP)。这个人工区域受到很高的人为压力,并拥有黄腿海鸥,它们位于营养链的顶端,可以用作监测环境中垃圾的前哨物种,包括塑料污染。样品中发现的MP总数为309,63.8%纤维(4.95±3.51MP/g)和36.2%片段(2.87±1.74MP/g)。Micro-FTIR分析表明,大部分纤维归因于人造纤维素(40.7%)。在碎片中发现了乙烯乙酸乙烯酯(EVA)和聚乙烯(PE)。
    The aim of this work was to provide evidence on the presence of microplastics (MPs) in regurgitated Yellow-legged Gull pellets (n = 18) from Sfax salina (south-eastern Tunisia). This artificial area is subject to high anthropogenic pressure and hosts Yellow-legged Gulls, which are at the top of the trophic chain and can be used as sentinel species to monitor litter in the environment, including plastic pollution. The total number of MPs found in the samples was 309, 63.8 % fibres (4.95 ± 3.51 MPs/g) and 36.2 % fragments (2.87 ± 1.74 MPs/g). Micro-FTIR analysis evidenced that a large proportion of the fibres was attributed to artificial cellulose (40.7 %). Ethylene vinyl acetate (EVA) and polyethylene (PE) were found in the fragments.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    家族性低磷酸盐血症由于其广泛的临床表现和遗传异质性而提出了复杂的诊断挑战。这项研究旨在阐明在ALPL基因中具有罕见的c.896T>C突变的突尼斯家族中家族性低磷酸盐症的分子基础,提供对基因型-表型相关性和潜在治疗途径的见解。这项研究采用了全面的方法,综合生化检查,遗传分析,结构建模,和功能性见解来解开这种罕见突变的影响。遗传调查显示,在受影响的家庭成员中,ALPL基因中存在p.Leu299Pro突变。该突变策略性地位于催化位点和金属结合结构域附近,暗示潜在的功能后果。同源性建模技术用于预测TNSALP的3D结构,提供对突变的结构背景的见解。我们的发现表明,突变可能会引起催化位点和金属结合域附近的构象变化,可能影响底物识别和催化效率。分子动力学模拟有助于阐明在p.Leu299Pro突变存在下组织非特异性碱性磷酸酶同工酶(TNSALP)的动态行为。模拟表明突变位点附近的结构灵活性发生了变化,对酶的整体稳定性和功能有潜在的影响。这些动态变化可能会影响TNSALP的催化效率,揭示了突尼斯家族中观察到的临床表现的分子基础。受影响个体的临床表现突出了显著的表型异质性,强调家族性低磷酸盐症复杂的基因型-表型相关性。发病年龄的变异性,症状的严重程度,并观察到射线照相特征,强调需要对与p.Leu299Pro突变相关的临床谱进行细致的理解。这项研究通过描述ALPL基因中p.Leu299Pro突变的分子后果,促进了我们对家族性低磷酸盐症的理解。通过整合遗传,结构,和临床分析,我们提供了对疾病发病机制的见解,并为针对特定基因谱的个性化治疗策略奠定了基础.我们的发现强调了全面的遗传和临床评估在指导家族性低磷酸盐症的精准医学方法中的重要性。
    Familial Hypophosphatasia presents a complex diagnostic challenge due to its wide-ranging clinical manifestations and genetic heterogeneity. This study aims to elucidate the molecular underpinnings of familial Hypophosphatasia within a Tunisian family harboring a rare c.896 T > C mutation in the ALPL gene, offering insights into genotype-phenotype correlations and potential therapeutic avenues. The study employs a comprehensive approach, integrating biochemical examination, genetic analysis, structural modeling, and functional insights to unravel the impact of this rare mutation. Genetic investigation revealed the presence of the p.Leu299Pro mutation within the ALPL gene in affected family members. This mutation is strategically positioned in proximity to both the catalytic site and the metal-binding domain, suggesting potential functional consequences. Homology modeling techniques were employed to predict the 3D structure of TNSALP, providing insights into the structural context of the mutation. Our findings suggest that the mutation may induce conformational changes in the vicinity of the catalytic site and metal-binding domain, potentially affecting substrate recognition and catalytic efficiency. Molecular dynamics simulations were instrumental in elucidating the dynamic behavior of the tissue-nonspecific alkaline phosphatase isozyme (TNSALP) in the presence of the p.Leu299Pro mutation. The simulations indicated alterations in structural flexibility near the mutation site, with potential ramifications for the enzyme\'s overall stability and function. These dynamic changes may influence the catalytic efficiency of TNSALP, shedding light on the molecular underpinnings of the observed clinical manifestations within the Tunisian family. The clinical presentation of affected individuals highlighted significant phenotypic heterogeneity, underscoring the complex genotype-phenotype correlations in familial Hypophosphatasia. Variability in age of onset, severity of symptoms, and radiographic features was observed, emphasizing the need for a nuanced understanding of the clinical spectrum associated with the p.Leu299Pro mutation. This study advances our understanding of familial Hypophosphatasia by delineating the molecular consequences of the p.Leu299Pro mutation in the ALPL gene. By integrating genetic, structural, and clinical analyses, we provide insights into disease pathogenesis and lay the groundwork for personalized therapeutic strategies tailored to specific genetic profiles. Our findings underscore the importance of comprehensive genetic and clinical evaluation in guiding precision medicine approaches for familial Hypophosphatasia.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    目的:本研究旨在分析突尼斯北部拘留期间的死亡模式以及死亡原因。
    方法:作者进行了一项横断面回顾性研究,包括2005年至2019年在主要教学医院法律医学部检查的所有在押人员死亡。该部门覆盖突尼斯北部11个省中的10个省和13所监狱。
    结果:总共有197人伤亡,只有两个是女性。平均年龄为45.39±14.43岁。已知病史报告占63.5%,主要是心血管疾病,精神健康障碍和糖尿病。一半的死亡发生在医院。共有53名受害者在去世前被拘留不到一年。大多数死亡是由于疾病相关原因(78.7%;n=155);其中,69名受害者死于心血管疾病。自杀占伤亡人数和凶杀案的3.6%。
    结论:关于拘留情况的细节以及在某些情况下缺乏毒理学和组织病理学分析结果的一些缺失数据,这可能会使研究结果产生偏差。
    结论:突尼斯北部拘留期间的死亡主要涉及30至50岁的男性,他们主要死于心血管或肺部疾病。这些结果强调了增强监狱卫生系统能力的重要性。
    结论:据作者所知,这项研究是关于阿拉伯国家的死者数量和监狱数量的最大研究之一,可以得出监狱中死亡的伤亡模式。
    OBJECTIVE: This study aims to analyze the pattern of deaths in detention in Northern Tunisia as well as the causes of death.
    METHODS: The authors conducted a cross-sectional retrospective study including all the casualties of death in detention examined in the legal medicine Department in the main teaching hospital from 2005 to 2019. The department covers 10 out of the 11 governorates of Northern Tunisia and 13 prisons.
    RESULTS: Of a total of 197 casualties, only 2 were females. The mean age was 45.39 ± 14.43 years. A known medical history was reported in 63.5%, mainly cardiovascular disease, mental health disorders and diabetes. Half of the deaths occurred at the hospital. A total of 53 victims spent less than one year in custody before their death. Most deaths occurred due to disease-related causes (78.7%; n = 155); among these, 69 victims died from cardiovascular disease. Suicide accounted for 3.6% of the casualties and homicides for four cases.
    CONCLUSIONS: Several missing data regarding the details of the detention circumstances as well as the absence in some cases of the toxicological and histopathology analysis results, which could bias the study findings.
    CONCLUSIONS: Death in detention in Northern Tunisia involved mainly males between their 30s and their 50s who died mainly from cardiovascular or pulmonary disease. These results underscore the importance of empowering the penitentiary health system.
    CONCLUSIONS: To the best of the authors\' knowledge, this study is one of largest studies with regard to the number of decedents and the number of prisons from the Arab countries allowing to draw a pattern of casualties of death in prison.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    条形码研究为属于Ligia属的物种之间的系统发育关系提供了重要见解(甲壳动物,Isopoda)。在此,首次研究了来自突尼斯的意大利海域SlaterLigiaitalica的多样性。样本来自突尼斯的18个地方,分析包括以前在GenBank上发表的来自意大利和希腊的序列。使用线粒体COI基因的片段进行贝叶斯和最大似然系统发育分析。使用软件中的“条形码间隙”方法对推定的隐秘物种进行了探索。使用程序“空间中的等位基因”进行了遗传景观形状分析。分析显示,分散在突尼斯的L.italica进化枝(进化枝A1和A2),希腊(B分支)和意大利(C1和C2分支)。进化枝之间的高度遗传差异表明,L.italica构成了一个神秘的物种复合体。不同L.italica谱系之间的差异(分支A,B和C)发生在7-4.5Ma左右。在进化枝之间检测到的高遗传距离不是由于非典型的线粒体DNA或Wolbachia细菌的细胞内感染所致。地中海的复杂历史似乎在塑造Ligiaitalica的系统地理格局中发挥了重要作用。需要进行其他形态学和分子研究,以确认地中海Ligiaitalica中存在隐秘物种。
    Barcoding studies have provided significant insights into phylogenetic relationships among species belonging to the genus Ligia (Crustacea, Isopoda). Herein the diversity of the Italian sea slater Ligia italica from Tunisia is studied for the first time. Samples were collected from 18 localities in Tunisia, and the analysis included previously published sequences from Italy and Greece available in GenBank. Bayesian and Maximum Likelihood phylogenetic analyses were carried out using a fragment of the mitochondrial COI gene. Putative cryptic species were explored using the \'barcode gap\' approach in the software ASAP. A genetic landscape shape analysis was carried out using the program Alleles in Space. The analyses revealed highly divergent and well-supported clades of L. italica dispersed across Tunisia (Clades A1 and A2), Greece (Clade B) and Italy (Clades C1 and C2). High genetic dissimilarity among clades suggested that L. italica constitute a cryptic species complex. Divergence among different L. italica lineages (Clades A, B and C) occurred around 7-4.5 Ma. The detected high genetic distances among clades did not result from atypical mitochondrial DNAs or intracellular infection by Wolbachia bacteria. The complex history of the Mediterranean Sea appears to have played a significant role in shaping the phylogeographic pattern of Ligia italica. Additional morphological and molecular studies are needed to confirm the existence of cryptic species in Ligia italica in Mediterranean.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    筋膜虫病是一种世界性的人畜共患蜗牛传播的感染,会影响反刍动物,它在牲畜中造成了巨大的经济损失。对Sejnane地区(比塞特地区,突尼斯西北部)评估他们的知识,对法西斯主义的态度和实践。所有受访的羊主人都知道这种寄生虫感染(100%,204/204),其中,81%(165/204)报告了其羊群的临床病例史。根据33.73%(113/335)的数据,绵羊主要通过在潮湿地区放牧而感染筋膜病,79.9%(163/204)的农民认为潮湿的气候最有利于感染。体重减轻(28.40%,121/426)和颌下水肿(20.42%,87/426)是接受采访的绵羊主人引用的筋膜病的主要临床体征,其中大多数(98.53%;201/204)证实筋膜病会造成重大的经济损失。尽管使用了抗寄生虫药物,但Sejnane地区的筋膜瘤感染仍然存在。这主要是由于动物在潮湿的草地上吃草(39.88%,132/331)。治疗动物(51.47%,193/375),禁止在潮湿的草地上放牧(15.20%,57/357),禁止在湿土上放牧(14.33%,53/357)并避免牧场(10.93%,41/357)是采访的绵羊主人引用的主要预防措施。只有18,14%(37/204)的响应者知道筋膜病是一种人畜共患疾病。动物健康决策者和野战兽医在实施控制计划时可以考虑这些结果,以增加育种者对筋膜病的了解。
    Fasciolosis is a worldwide zoonotic snail-borne infection that affects ruminants, it causes high economic losses among livestock. A participatory epidemiological survey was conducted on 204 sheep owners of Sejnane region (District of Bizerte, Northwest Tunisia) to assess their knowledge, attitude and practice regarding fasciolosis. All interviewed sheep owners are aware of this parasitic infection (100%, 204/204), among them, 81% (165/204) reported history of clinical cases in their sheep flocks. According to 33.73% (113/335) of them, sheep get infected by fasciolosis mainly by grazing in wet areas, 79.9% (163/204) of these farmers think that wet climate is the most favourable for the infection. Weight loss (28.40%, 121/426) and submandibular oedema (20.42%, 87/426) are the main clinical signs of fasciolosis cited by interviewed sheep owners and the majority of them (98.53%; 201/204) confirmed that fasciolosis causes significant economic losses. Fasciolosis infection persists in Sejnane region despite the use of antiparasitic drugs, this is due mainly to the fact that animals graze in moist grass (39.88%, 132/331). Treat animals (51.47%, 193/375), prohibit grazing on moist grass (15.20%, 57/357), prohibit grazing on wet soils (14.33%, 53/357) and avoid pastures (10.93%, 41/357) are the main prevention measures cited by interviewed sheep owners. Only 18,14% (37/204) of responders knew that fascioliasis is a zoonotic disease. These results could be considered by animal health decision makers and field veterinarians when implementing control programmes in order to increase breeders\' knowledge of fasciolosis.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    目的:为了确定母亲状态对(血浆和红细胞)叶酸的影响,维生素B12,同型半胱氨酸,还有维生素D,以及它们与MTHFR(C677T和A1298C)和MTRRA66G多态性的相互作用,关于母体血浆二十二碳六烯酸(DHA),二十碳五烯酸(EPA),和花生四烯酸(ARA)水平和神经管缺陷(NTDs)的风险。
    方法:ARA,EPA,使用毛细管气相色谱法评估DHA组成。
    结果:对照组的ARA和DHA水平高于低血浆叶酸水平的病例。对于低红细胞叶酸状态,对照组的DHA水平高于病例母亲。对于高同型半胱氨酸水平,对照组的ARA和DHA水平高于病例母亲。NTD母亲的EPA和DHA水平较低,维生素B12水平较低。NTD母亲的DHA水平较低,维生素D水平较低。对于低血浆叶酸状态,在案例母亲中,MTHFRC677T基因中的DHA水平以及MTHFRA1298C基因中的ARA和EPA水平在三种基因型之间有所不同。MTHFRC677T基因中的DHA水平在三种基因型中在低和高同型半胱氨酸水平的情况下都不同。对于低维生素B12水平,在病例母亲中,MTHFRC677T基因的三种基因型之间的ARA和DHA水平不同。在MTHFRC677T基因中,在母亲维生素D水平低的情况下,三种基因型之间的ARA和DHA水平不同。
    结论:需要更先进的研究来验证与孕妇基因型相关的合适的生化参数状态。
    OBJECTIVE: To determine the effect of maternal status in (plasma and red blood cell) folate, vitamin B12, homocysteine, and vitamin D, as well as their interaction with MTHFR (C677T and A1298C) and MTRR A66G polymorphisms, on maternal plasma docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), and arachidonic acid (ARA) levels and the risk of neural tube defects (NTDs).
    METHODS: ARA, EPA, and DHA composition was assessed using capillary gas chromatography.
    RESULTS: ARA and DHA levels were higher in controls than in case mothers for low plasma folate status. For low red blood cell folate status, DHA levels were higher in controls than in case mothers. For high homocysteine levels, ARA and DHA levels were higher in controls than in case mothers. NTD mothers had lower EPA and DHA levels for low vitamin B12 levels. NTD mothers had lower DHA levels for low vitamin D levels. For low plasma folate status, DHA levels in the MTHFR C677T gene and ARA and EPA levels in MTHFR A1298C gene were different among the three genotypes in case mothers. DHA levels in the MTHFR C677T gene were different among the three genotypes in case mothers for both low and high homocysteine levels. For low vitamin B12 levels, ARA and DHA levels were different among the three genotypes of the MTHFR C677T gene in case mothers. In the MTHFR C677T gene, ARA and DHA levels were different among the three genotypes in case mothers for low vitamin D levels.
    CONCLUSIONS: More advanced research is required to verify a suitable biochemical parameter status in relation to the genotypes in pregnant women.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    The emergence of pandemics with dramatic consequences for human health has obscured endemic diseases that continue to pose a problem for human and animal health in several regions of the world. Among these diseases, cystic echinococcosis, a zoonotic parasitic infection caused by a group of cestodes, Echinococcus granulosus sensu lato, remains a real human and animal health problem in several regions of the world, including the Mediterranean Basin. Despite the implementation of a number of governmental control programmes using several tools (dog treatment, meat inspection, etc.), this infection is still highly prevalent in North Africa. Here we present a review of the epidemiology of cystic echinococcosis in Tunisia, an analysis of the constraints limiting the effectiveness of the control programmes implemented, and finally argue for the use of the One Health framework to improve the effectiveness of future programmes.
    UNASSIGNED: L’échinococcose kystique (infection par Echinococcus granulosus sensu lato) en Tunisie, une perspective « Une seule santé » pour un futur programme de contrôle.
    UNASSIGNED: L’émergence de pandémies affectant de manière très importante la santé humaine a occulté les maladies endémiques qui continuent de représenter un problème de santé animale et humaine dans plusieurs régions du monde. Parmi ces maladies, l’échinococcose kystique, une parasitose zoonotique provoquée par un groupe de cestodes, Echinococcus granulosus sensu lato, reste un réel problème de santé humaine et animale dans plusieurs régions du monde, incluant le Bassin méditerranéen. Malgré la mise en place de nombreux programmes de lutte utilisant plusieurs outils (traitement des chiens, inspection des viandes, etc.), cette infection est encore hautement prévalente en Afrique du Nord. Nous présentons ici une revue de l’épidémiologie de l’échinococcose kystique en Tunisie, une analyse des contraintes limitant l’efficacité des programmes de lutte mis en place, et finalement nous argumentons l’utilisation du concept « Une seule santé » pour améliorer l’efficacité des programmes futurs.
    UNASSIGNED: مرض الكيس المائي (العدوى بالطفيليEchinococcus granulosus sensu lato ) في تونس، منظور صحي واحد لبرنامج مكافحة مستقبلي.
    UNASSIGNED: أدى ظهور الأوبئة التي تؤثر بشكل كبير على صحة الإنسان إلى حجب الأمراض المستوطنة التي لا تزال تمثل مشكلة لصحة الحيوان والإنسان في العديد من مناطق العالم. ومن بين هذه الأمراض، لا يزال مرض الكيس المائي، مرض طفيلي مشترك المتسبب فيه مجموعة من الديدان الشريطية، المشوكة الحبيبية بالمعنى الواسع Echinococcus granulosus sensu lato ، يمثل مشكلة حقيقية لصحة الانسان و الحيوان في العديد من مناطق العالم، بما في ذلك حوض البحر الأبيض المتوسط. وعلى الرغم من تنفيذ عدد من برامج المكافحة باستخدام عدة أدوات (علاج الكلاب، فحص اللحوم، وغيرها)، إلا أن هذه العدوى لا تزال منتشرة بشكل كبير في شمال أفريقيا. نقدم هنا استعراضا لوبائيات مرض الكيس المائي في تونس، وتحليلا للقيود التي تحد من فعالية برامج المكافحة المطبقة، وأخيرا نناقش استخدام مفهوم الصحة الواحدة لتحسين فعالية البرامج المستقبلية.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: English Abstract
    背景:电子烟是一种新一代吸烟产品,其使用机制可以,理论上,尽量减少对健康的不良影响。
    目的:确定突尼斯医生样本对电子烟的知识和看法。
    方法:我们对突尼斯医生样本进行了为期两个月的描述性横断面研究。我们使用了关于医生对电子烟的知识和看法的在线自我问卷。
    结果:数据来自216名医生。在参与者中,97.2%的人熟悉电子烟,56.5%的人报告知识水平低,83.4%的人表示有动机更多地了解电子烟。总的来说,83.8%的医生认为电子烟对使用者的健康有害。根据73.1%的参与者的说法,使用该产品会增加患癌症的风险,68.5%的参与者患心血管疾病的风险,79.2%的参与者患慢性肺病的风险。认为电子烟对使用者的健康有害与医生的医学专业有关(p=0.032)。电子烟作为戒烟工具的建议与口科培训呈负相关(p=0.027)。
    结论:医师对电子烟的了解是异质的,反映了目前缺乏信息和共识。
    BACKGROUND: The electronic cigarette is a new-generation smoking product whose mechanism of use could, in theory, minimize adverse health effects.
    OBJECTIVE: Determine the knowledge and perceptions of a sample of Tunisian doctors regarding electronic cigarettes.
    METHODS: We conducted a descriptive cross-sectional study over a two-month period with a sample of Tunisian doctors. We used an online self-questionnaire on physicians\' knowledge and perceptions of e-cigarettes.
    RESULTS: Data were obtained from 216 physicians. Of the participants, 97.2% were familiar with e-cigarettes, 56.5% reported low knowledge, and 83.4% expressed motivation to learn more about e-cigarettes. Overall, 83.8% of doctors felt that electronic cigarettes are harmful to the user\'s health. Use of this product would increase the risk of cancer according to 73.1% of participants, the risk of cardiovascular disease according to 68.5% of participants, and the risk of chronic lung disease according to 79.2% of participants. The perception of e-cigarettes as harmful to the user\'s health was associated with the physicians\' medical specialty (p=0.032). The recommendation of e-cigarettes as a smoking cessation tool was negatively correlated with addictology training (p=0.027).
    CONCLUSIONS: Physicians\' knowledge of electronic cigarettes is heterogeneous, reflecting the current lack of information and consensus.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号