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Liposomal Amphotericin B Induced Acute Reactions 两性霉素B脂质体诱导急性反应
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-19 DOI: 10.32552/2021.actamedica.566
M. Bahap, Pinar Bakir Ekinci, Ş. Alp, S. G. Oz, K. Demirkan
Three formulations of amphotericin B are available: liposomal, lipid complex and conventional. The liposomal amphotericin B is more preferred agent than other formulations because of its tolerability, safety and potent antifungal activity. However, the liposomal amphotericin B can cause infusion-related reactions. In this case report, we aimed to report a patient who developed infusion-related reactions during the treatment with the liposomal amphotericin B but eventually tolerated the prolonged infusion. In this case report, we present a patient who developed an infusion-related reaction during The liposomal amphotericin B treatment. A 26-year-old male patient with acute promyelocytic leukemia was hospitalized for the third course of chemotherapy. Due to the invasive fungal infection history in previous hospitalizations, the liposomal amphotericin B 400 mg (IV, 5 mg/kg) once daily was initiated as secondary antifungal prophylaxis. Swelling in infusion site and chest pain were reported within 10 minutes of the liposomal amphotericin B administration, and the infusion rate was slowed down to 400 mg/6 hours from 400 mg/2 hours. All these reactions disappeared with prolonged infusion time. The patient received a total of 7 liposomal amphotericin B doses subsequently without any reaction during the chemotherapy cycle. In our experience, the liposomal amphotericin B-induced infusion-related reactions can be resolved by prolonging the infusion time.
两性霉素B有三种剂型:脂质体、脂质复合物和常规剂型。脂质体两性霉素B由于其耐受性、安全性和抗真菌活性较好,是较理想的制剂。然而,两性霉素B脂质体可引起输注相关反应。在本病例报告中,我们的目的是报告一名患者在使用两性霉素B脂质体治疗期间出现输注相关反应,但最终耐受了长时间的输注。在本病例报告中,我们报告了一位在两性霉素B脂质体治疗期间发生输注相关反应的患者。一位26岁的男性急性早幼粒细胞白血病患者住院接受第三疗程的化疗。由于既往住院有侵袭性真菌感染史,因此开始每日一次两性霉素脂质体400mg(静脉注射,5mg /kg)作为二级抗真菌预防。两性霉素B脂质体给药后10分钟内出现输注部位肿胀和胸痛,输注速度由400mg /2小时降至400mg /6小时。随着注射时间的延长,这些反应逐渐消失。随后,患者共接受7次两性霉素B脂质体治疗,在化疗周期内无任何反应。根据我们的经验,两性霉素b脂质体诱导的输注相关反应可以通过延长输注时间来解决。
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引用次数: 0
NK/T cell Lymphoma as a Rare Cause of an Oronasal Fistula NK/T细胞淋巴瘤是引起口鼻瘘的罕见原因
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-17 DOI: 10.32552/2021.actamedica.544
Ahmad Izani Mohd Safian, A. Mohamad, R. Ramli, I. Mohamad
NK/T cell lymphoma is one of the most unique and rare forms of extranodal non-Hodgkin’s lymphoma, mostly derived from natural killer cell lineages and occasionally cytotoxic T cell lines. Due to the non-specific presentation of NK/T cell lymphoma such as nasal obstruction, nasal discharge, and epistaxis, diagnosis is often an issue and can be misleading. Oronasal fistula following a non-healing ulcer on the soft palate, can be one of the clinical presentations of NK/T cell lymphoma. Here, we are reporting a rare case of NK/T cell lymphoma in a 32-year-old gentleman who presented with an oronasal fistula post tissue biopsy for a non-healing ulcer over the soft palate. The tissue biopsy of the soft palate mass was revealed as NK/T cell lymphoma and was staged as Stage1b after computed tomographic imaging revealed a local tumour invasion without sign of nodal involvement and no metastasis. The patient eventually started with the SMILE Protocol and responded well up to the date. The ulcer healed but the fistula persisted. Primary closure was planned by the oromaxillofacial surgery team after completion of chemotherapy.
NK/T细胞淋巴瘤是结外非霍奇金淋巴瘤最独特和罕见的形式之一,主要来源于自然杀伤细胞系,偶尔也有细胞毒性T细胞系。由于NK/T细胞淋巴瘤的非特异性表现,如鼻塞、鼻溢液和鼻出血,诊断往往是一个问题,可能会误导。软腭溃疡未愈合后出现口鼻瘘,可能是NK/T细胞淋巴瘤的临床表现之一。在这里,我们报告一个罕见的NK/T细胞淋巴瘤病例,32岁的男士,因软腭溃疡未愈合,在组织活检后出现口鼻瘘。软腭肿块的组织活检显示为NK/T细胞淋巴瘤,计算机断层成像显示局部肿瘤浸润,无淋巴结累及征象,无转移,分期为Stage1b。患者最终开始使用SMILE方案,到目前为止反应良好。溃疡愈合,但瘘管仍然存在。化疗完成后,口腔颌面外科小组计划进行初步闭合。
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引用次数: 0
Could We Use Vital Signs and Lactate Levels Together to Predict the Prognosis in Abdominal Pain? 生命体征和乳酸水平能否共同预测腹痛的预后?
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-17 DOI: 10.32552/2021.actamedica.634
Filiz Froohari Damarsoy, Nalan Metin Aksu, E. Öztürk, Meltem Akkaş
Objectives: Abdominal pain occupies most of the emergency department admissions. This entity leads to research various markers for the early detection of causes in patients presenting with abdominal pain. There is limited data about collaborations between lactate levels and vital signs at admission in abdominal pain. Materials and Methods: Patients aged 18 years and older, who had presented with abdominal pain to the Emergency Department, in total 102 patients, were included to the study. The patients’ demographics, vital signs, abdominal physical examination findings, diagnosis and outcomes of patients were recorded. The 1 ml venous blood samples were collected by blood gase injectors from the patients and lactate levels were analyzed. Results: Female patients’ percentile was 68,6% and mean age was 39 years old. The systolic blood pressure levels were normal in 45 patients, low in 26% patients and high in 29% patients. The seventy-six of the patients had normal pulse rate and 26 of them were tachycardic. Most common diagnosis was non-specific abdominal pain (37,25%) and the least common was ovarian torsion/intracystic hemorrhage (0,98%) and obstruction due to hernia (0,98%). There was no statistically significant relation between lactate level and pulse rate (p=0,637), systolic blood pressure (p=0,052), diastolic blood pressure (p=0,095), respiratory rate (p=0,527), body temperature (p=0,040) and oxygen saturation (p=0,905). Similarly, no significant association occurred between lactate levels and diagnosis and outcomes. Conclusion: Further studies including more patients groups have to be done in order to attain more reliable data about this topic.
目的:腹痛占急诊科住院病人的大部分。这个实体导致研究各种标志物的早期发现的原因,在病人呈现腹痛。关于腹痛患者入院时乳酸水平与生命体征之间的合作关系的数据有限。材料与方法:本研究纳入了102例年龄在18岁及以上的急诊科腹痛患者。记录患者的人口学特征、生命体征、腹部体格检查结果、诊断及转归。采用血气注射器采集患者1 ml静脉血,分析乳酸水平。结果:女性患者百分位数为68.6%,平均年龄39岁。45例患者收缩压正常,26%患者收缩压低,29%患者收缩压高。76例患者脉搏正常,26例心动过速。最常见的诊断是非特异性腹痛(37.25%),最不常见的诊断是卵巢扭转/囊内出血(0.98%)和疝气梗阻(0.98%)。乳酸水平与脉搏率(p=0,637)、收缩压(p=0,052)、舒张压(p=0,095)、呼吸率(p=0,527)、体温(p=0,040)、血氧饱和度(p=0,905)无统计学意义。同样,乳酸水平与诊断和预后之间没有显著关联。结论:为了获得关于该主题的更可靠的数据,必须进行包括更多患者组的进一步研究。
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引用次数: 1
An Evaluation of Information Sources Regarding Drug Use and/or Poisoning Cases of Community Pharmacists in Ankara, Turkey 土耳其安卡拉社区药剂师药物使用和/或中毒病例信息来源评价
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-16 DOI: 10.32552/2021.actamedica.630
A. Çeliker, Emre Kara, S. Karahan
Objective: Exploring and categorizing the drug and/or poisoning information resources available in community pharmacies in Ankara according to some variables, and revealing common opinions regarding the future of the profession and information resources. Materials and Methods: This study was conducted as an online questionnaire for community pharmacists in Ankara. It had four headings on the pharmacists’ demographics, their general information resources, specific resources in specific topics, and 4 suggestions regarding the future of pharmacy and drug information resources. Results: The number of participants was 134 as 17.9% of 746 e-mail addresses. Mean ages±standart deviation were 40.9±12.0 years. The top 3 information sources on poisonings were the internet, colleagues, and physicians with 74.6%, 43.3%, and 30.6%, respectively. Participants in the “colleagues” group in terms of poisoning preferences had a shorter period after graduation (p=0.001). In the drug information inquiries package inserts, internet and colleagues were preferred mostly, with 69.4%, 63.4%, and 35.8%, respectively. Age groups and graduation years were statistically different regarding the “package inserts” and “colleagues” groups (p=0.012 and p=0.001, and p=0.019 and p<0.001, respectively). The most “totally agreed” suggestion was accepting the pharmacies’ being important drug and/or poison information resources for consumers with 68.7%. Conclusion: The pharmacists have been fulfilling their duty of “being an information resource” through rather limited resources. To equip community pharmacists properly, authorities, professional institutions, and universities need to contribute to the process in different ways together with pharmacists being aware of their responsibilities.
目的:根据一些变量对安卡拉社区药房现有药物和(或)中毒信息资源进行探索和分类,揭示对该行业未来发展和信息资源的共同看法。材料与方法:本研究采用在线问卷方式对安卡拉社区药师进行调查。包括药师的人口学特征、一般信息资源、专题信息资源4个标题,以及对未来药学和药品信息资源的4条建议。结果:参与人数为134人,占746个电子邮件地址的17.9%。平均年龄±标准差为40.9±12.0岁。中毒信息来源排名前3位的是网络、同事和医生,分别占74.6%、43.3%和30.6%。在中毒偏好方面,“同事”组的参与者在毕业后的时间较短(p=0.001)。在药品信息查询说明书中,网上查询和同事查询的比例最高,分别为69.4%、63.4%和35.8%。“外包装”组和“同事”组的年龄和毕业年限有统计学差异(p=0.012, p=0.001; p=0.019, p<0.001)。最“完全同意”的建议是接受药店是消费者重要的药物和/或毒物信息资源(68.7%)。结论:药师通过有限的资源,履行了“信息资源”的职责。为了使社区药剂师具备适当的能力,当局、专业机构和大学需要以不同的方式为这一进程作出贡献,同时药剂师也要意识到自己的责任。
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引用次数: 0
Conventional Synthetic Dmards in Psoriatic Arthritis: Changing Practice in Biologic Era; Real-Life Results from HURBIO-PsA Registry 银屑病关节炎的常规合成制剂:生物制剂时代的变革实践来自HURBIO-PsA注册表的真实结果
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-16 DOI: 10.32552/2021.actamedica.623
E. Bilgin, U. Kalyoncu
Objectives: Psoriatic arthritis is a chronic musculoskeletal disorder which may affect skin, joints, bone and enthesis. Conventional synthetic disease modifying anti-rheumatic drugs are first-line treatment options and biologic disease modifying anti-rheumatic drugs are recommended in psoriatic arthritis patients who are intolerant/not controlled well with conventional synthetic disease modifying anti-rheumatic drugs. Although survival data of the conventional synthetic disease modifying anti-rheumatic drugs without concomitant biologic disease modifying anti-rheumatic drugs are available, the effect of biologic disease modifying anti-rheumatic drugs on the retention of conventional synthetic disease modifying anti-rheumatic drugs is still a question of interest. Materials and Methods: Psoriatic arthritis patients who received at least 1 dose of biologic disease modifying anti-rheumatic drugs, using at least 1 conventional synthetic disease modifying anti-rheumatic drugs (methotrexate, leflunomide, hydroxychloroquine and sulfasalazine) at the time of biologic disease modifying anti-rheumatic drugs starting visit and registered in the Hacettepe University BIOlogical Database-Psoriatic Arthritis were included in this retrospective longitudinal analysis. Demographic and disease-specific data at first and last follow-up visit were collected. Unadjusted retention rate of each conventional synthetic disease modifying anti-rheumatic drugs was assessed. Overall prescription of conventional synthetic disease modifying anti-rheumatic drugs at first and last follow-up visit were compared. Results: A total of 266 (191(71.8%) female) patients was included. Median follow-up duration under biologic treatment was 43.4 (19.4-80.1) months. Median retention duration of each conventional synthetic disease modifying anti-rheumatic drugs were similar. Between the first and last visit; there was a 29.3% decrease in methotrexate use (61.7% vs. 43.6%; p<0.001), 8.4% decrease in leflunomide use (31.2% vs. 28.6%; p=0.30), 30.0% decrease in sulfasalazine use (11.3% vs. 7.9%; p=0.05), 31.1% decrease in hydroxychloroquine use (16.9% vs. 11.7%; p=0.001), 12.5 % decrease in glucocorticoids use (51.1% vs. 44.7%; p=0.015). At last visit, 59 (22.2%) patients were conventional synthetic disease modifying anti-rheumatic drugs -free: 20 (7.5%) patients were using only glucocorticoids, 39 (14.7%) patients were conventional synthetic disease modifying anti-rheumatic drugs + glucocorticoid-free. Conclusion: Although conventional synthetic disease modifying anti-rheumatic drugs were significantly discontinued in an important percent of patients after the initiation of biologic disease modifying anti-rheumatic drugs, percentage of patients using glucocorticoids at last visit was still high. Studies aiming to demonstrate when, in whom and how to discontinue conventional synthetic disease modifying anti-rheumatic drugs are needed.
目的:银屑病关节炎是一种慢性肌肉骨骼疾病,可影响皮肤,关节,骨骼和髋部。常规合成抗病性抗风湿药物是一线治疗选择,对于常规合成抗病性抗风湿药物不耐受/控制不好的银屑病关节炎患者,推荐使用生物抗病性抗风湿药物。虽然目前已有常规合成疾病修饰抗风湿药物的生存数据,但生物疾病修饰抗风湿药物对常规合成疾病修饰抗风湿药物保留的影响仍然是一个值得关注的问题。材料和方法:银屑病关节炎患者在开始使用生物疾病修饰抗风湿药物时接受至少1剂生物疾病修饰抗风湿药物,使用至少1种传统合成疾病修饰抗风湿药物(甲氨蝶呤、来氟米特、羟氯喹和磺胺嘧啶),并在Hacettepe大学生物数据库-银屑病关节炎中登记,纳入本回顾性纵向分析。收集首次和最后一次随访时的人口统计学和疾病特异性数据。评估各种常规合成疾病修饰抗风湿药物的未调整保留率。比较常规综合抗风湿药首访和末访时的总体处方。结果:共纳入266例患者,其中女性191例,占71.8%。生物治疗组的中位随访时间为43.4(19.4-80.1)个月。两种常规合成抗风湿药物的中位保留时间相似。在第一次和最后一次访问之间;甲氨蝶呤使用率下降29.3% (61.7% vs 43.6%;P <0.001),来氟米特使用率下降8.4% (31.2% vs 28.6%;P =0.30),磺胺吡啶的使用减少30.0% (11.3% vs. 7.9%;P =0.05),羟氯喹使用减少31.1% (16.9% vs. 11.7%;P =0.001),糖皮质激素使用减少12.5% (51.1% vs. 44.7%;p = 0.015)。末次访时,59例(22.2%)患者不使用常规综合抗风湿药物,20例(7.5%)患者仅使用糖皮质激素,39例(14.7%)患者使用常规综合抗风湿药物+不使用糖皮质激素。结论:虽然有相当一部分患者在开始使用生物疾病修饰类抗风湿药物后明显停用了常规合成疾病修饰类抗风湿药物,但最后一次就诊时使用糖皮质激素的患者比例仍然很高。需要进行旨在证明何时、对谁以及如何停用常规合成疾病修饰抗风湿药的研究。
{"title":"Conventional Synthetic Dmards in Psoriatic Arthritis: Changing Practice in Biologic Era; Real-Life Results from HURBIO-PsA Registry","authors":"E. Bilgin, U. Kalyoncu","doi":"10.32552/2021.actamedica.623","DOIUrl":"https://doi.org/10.32552/2021.actamedica.623","url":null,"abstract":"Objectives: Psoriatic arthritis is a chronic musculoskeletal disorder which may affect skin, joints, bone and enthesis. Conventional synthetic disease modifying anti-rheumatic drugs are first-line treatment options and biologic disease modifying anti-rheumatic drugs are recommended in psoriatic arthritis patients who are intolerant/not controlled well with conventional synthetic disease modifying anti-rheumatic drugs. Although survival data of the conventional synthetic disease modifying anti-rheumatic drugs without concomitant biologic disease modifying anti-rheumatic drugs are available, the effect of biologic disease modifying anti-rheumatic drugs on the retention of conventional synthetic disease modifying anti-rheumatic drugs is still a question of interest. \u0000Materials and Methods: Psoriatic arthritis patients who received at least 1 dose of biologic disease modifying anti-rheumatic drugs, using at least 1 conventional synthetic disease modifying anti-rheumatic drugs (methotrexate, leflunomide, hydroxychloroquine and sulfasalazine) at the time of biologic disease modifying anti-rheumatic drugs starting visit and registered in the Hacettepe University BIOlogical Database-Psoriatic Arthritis were included in this retrospective longitudinal analysis. Demographic and disease-specific data at first and last follow-up visit were collected. Unadjusted retention rate of each conventional synthetic disease modifying anti-rheumatic drugs was assessed. Overall prescription of conventional synthetic disease modifying anti-rheumatic drugs at first and last follow-up visit were compared. \u0000Results: A total of 266 (191(71.8%) female) patients was included. Median follow-up duration under biologic treatment was 43.4 (19.4-80.1) months. Median retention duration of each conventional synthetic disease modifying anti-rheumatic drugs were similar. Between the first and last visit; there was a 29.3% decrease in methotrexate use (61.7% vs. 43.6%; p<0.001), 8.4% decrease in leflunomide use (31.2% vs. 28.6%; p=0.30), 30.0% decrease in sulfasalazine use (11.3% vs. 7.9%; p=0.05), 31.1% decrease in hydroxychloroquine use (16.9% vs. 11.7%; p=0.001), 12.5 % decrease in glucocorticoids use (51.1% vs. 44.7%; p=0.015). At last visit, 59 (22.2%) patients were conventional synthetic disease modifying anti-rheumatic drugs -free: 20 (7.5%) patients were using only glucocorticoids, 39 (14.7%) patients were conventional synthetic disease modifying anti-rheumatic drugs + glucocorticoid-free. \u0000Conclusion: Although conventional synthetic disease modifying anti-rheumatic drugs were significantly discontinued in an important percent of patients after the initiation of biologic disease modifying anti-rheumatic drugs, percentage of patients using glucocorticoids at last visit was still high. Studies aiming to demonstrate when, in whom and how to discontinue conventional synthetic disease modifying anti-rheumatic drugs are needed.","PeriodicalId":50891,"journal":{"name":"Acta Medica Mediterranea","volume":"69 1","pages":""},"PeriodicalIF":0.3,"publicationDate":"2021-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79562289","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 Prevalence of Hilar Lymphadenopathy and Related Factors in Pneumoconiosis Patients of a University Hospital Occupational Diseases Polyclinic 某大学医院职业病综合门诊尘肺患者肺门淋巴结病患病率及相关因素分析
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-05 DOI: 10.32552/2021.actamedica.595
Yusuf Samir Hasanlı, M. Türk
Objective: Pneumoconiosis is a fatal, irreversible interstitial lung disease caused by various inorganic dust and chemicals. The disease is radiologically characterized by micronodules, pleural plaques, emphysema, mediastinal and hilar lymphadenopathies (HL). There are hypotheses that fibrotic lymph nodes increase the dust load of the lungs in patients with pneumoconiosis. Our aim is to determine the frequency of HL and related factors in pneumoconiosis patients admitted to our unit in the light of current data. Material and Methods: 76 patients diagnosed with pneumoconiosis who applied to our unit between November, 2015 and October, 2020 were retrospectively screened. Sociodemographic characteristics, radiological, laboratory and clinical findings were evaluated. The frequency of HL and related factors were analyzed. Results: We found the rate of HL as 29,3%. The average age was 43,78 ± 7,54. There was no significant age difference between patients with and without HL (44,41±8,90 / 43,34±6,93 p=0,578). All of the patients were male. As the ILO (International Labor Organization) category rose, we saw an increase in the number of HL. 59,1% of the patients with HL had at least one active complaint (dyspnea, cough or sputum). The most common complaint was dyspnea (50%). We found a statistically significant increase in NLR (Neutrophil to Lymphocyte Ratio) and TLR (Thrombocyte to Lymphocyte Ratio) values in patients with HL compared to those without (2,38±0,70; 1,97±0,59 p=0,016 and 133,79±39,06; 109,03±29,00 p=0,005). Another important finding was that the albumin values of patients with HL were found to be statistically significantly lower (4.42 ± 0.41; 4.67 ± 0.29 p = 0.008). Conclusion: 29.3% of patients had HL. We found significant increase in NLR and TLR in pneumoconiosis patients with HL and decrease in serum albumin levels. We think that these markers may have prognostic value in pneumoconiosis patients with lymphadenopathy.
目的:尘肺病是由多种无机粉尘和化学物质引起的致死性、不可逆的间质性肺疾病。该疾病的放射学特征为微结节、胸膜斑块、肺气肿、纵隔和肺门淋巴结病(HL)。有假说认为纤维化淋巴结增加尘肺患者肺部的粉尘负荷。我们的目的是根据目前的数据确定我们单位收治的尘肺患者HL的频率和相关因素。材料与方法:回顾性筛选2015年11月至2020年10月在我科室就诊的确诊尘肺患者76例。评估了社会人口学特征、放射学、实验室和临床结果。分析HL的发生频率及相关因素。结果:HL发生率为29.3%。平均年龄43,78±7,54岁。HL患者与非HL患者的年龄差异无统计学意义(44,41±8,90 / 43,34±6,93 p= 0.578)。所有患者均为男性。随着ILO(国际劳工组织)类别的增加,我们看到HL的数量有所增加。59.1%的HL患者至少有一种主诉(呼吸困难、咳嗽或咳痰)。最常见的主诉是呼吸困难(50%)。我们发现,与非HL患者相比,HL患者NLR(中性粒细胞与淋巴细胞比值)和TLR(血小板与淋巴细胞比值)值有统计学意义的增加(2,38±0,70;1,97±0,59 p=0,016和133,79±39,06;109年,03±29日00 p = 0005)。另一个重要发现是HL患者的白蛋白值有统计学意义(4.42±0.41;4.67±0.29 p = 0.008)。结论:29.3%的患者有HL。我们发现合并HL的尘肺患者NLR和TLR显著升高,血清白蛋白水平降低。我们认为这些指标可能对尘肺伴淋巴结病患者有预后价值。
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引用次数: 0
Laparoscopic Treatment of Hydatid Liver and Pancreas Disease: Some Technical Aspects and Importance 腹腔镜治疗包虫病肝和胰腺:一些技术问题和重要性
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-03 DOI: 10.32552/2021.actamedica.581
Elbrus Zarbaliyev, Murat Sevmiş, D. Sarsenov, P. Hacısalihoğlu, M. Caglikulekci
Objective: Hydatid cyst disease is a widespread zoonotic disease infecting humans as an intermediate host. Since the first description of this pathology, many modalities have been introduced into modern treatment protocols. Minimally invasive surgical treatment is well-described and widely used, but has many points where rationalization and modification can be applied. In this case series, we describe small differences in surgical technique and the corresponding treatment results. Materials and Methods: Out of 44 patients, 16 were included in this study. Patients were retrospectively evaluated in two groups in accordance with the preferred cyst aspiration technique, i.e. via a standard laparoscopic aspirator or a large diameter venous catheter (the control and study groups, respectively). Demographic, clinical and surgical data like duration of surgery, hospital stay and complication rates were evaluated in both groups. Results: Equal numbers of males and females participated, with a median age of 40 years. Most patients had a type III hydatid cyst (n=11, 68.75%). Surgery duration and hospital stay were significantly shorter in the study group, without a significant difference in terms of complication rates. Conclusion: Laparoscopic procedures quickly became plausible for selected hydatid cysts located in liver. Success of such procedures shows to be depending on the success and duration of the laparoscopic intervention. The latter, according to our calculations, seems to be inversely proportional to the diameter of the aspirator tip and its piping.
目的:包虫囊肿病是一种以中间宿主感染人类的广泛人畜共患疾病。自从第一次描述这种病理,许多模式已被引入到现代治疗方案。微创手术治疗已经得到了很好的描述和广泛的应用,但有许多地方可以进行合理化和修改。在这个病例系列中,我们描述了手术技术和相应治疗结果的微小差异。材料与方法:44例患者中,16例纳入本研究。根据首选的囊肿抽吸技术,即通过标准腹腔镜抽吸器或大直径静脉导管(分别为对照组和研究组),对患者进行回顾性评估。对两组患者的人口学、临床和手术数据(如手术时间、住院时间和并发症发生率)进行评估。结果:男女参与人数相等,中位年龄为40岁。大多数患者为III型包虫囊肿(n=11, 68.75%)。研究组的手术时间和住院时间显著缩短,并发症发生率无显著差异。结论:腹腔镜手术迅速成为可行的选择包虫病位于肝脏。这种手术的成功取决于腹腔镜干预的成功和持续时间。根据我们的计算,后者似乎与吸气器尖端及其管道的直径成反比。
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引用次数: 0
Non-inferiority of The Cementless Total TKA Compared to The Cemented TKA, A m-Metanalysis 无水泥全TKA与水泥全TKA的非劣效性比较,m- meta分析
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-11-01 DOI: 10.32552/2021.actamedica.564
T. Bonanzinga, F. M. Gambaro, Riccardo Garibaldi, Federico Adravanti, G. Fusco, M. Marcacci
Objective: Cemented total knee arthroplasty still represents the reference standard in the field of prothesis knee replacement; but since cementless total knee arthroplasties were introduced there have been strong discussions over the years among cemented and non-cemented total knee arthroplasties to establish which gives the best benefits for the patient and for the surgeon. The purpose of this meta-analysis is to systematically analyze the use of cemented and cementless total knee arthroplasties by investigating clinical and radiological outcomes and rate of complications, in order to assess which techniques confers more benefits to the patient and the surgeon. Materials and Methods: The current systematic review has been written in accordance to the Cochrane handbook and the PRISMA statement for reporting of systematic reviews incorporating network. Results: Six randomized controlled trials were finally included in this systematic review. The statistical analysis revealed no significant differences in all clinical scores of interest (Knee Society Score, clinical and functional, Oxford Knee Score, Visual Analogue Score) and a similar revision rate. Conclusion: the results of the current metanalysis suggest the non-inferiority of cementless fixation with respect to cemented total knee arthroplasties in terms of clinical outcomes and survival rates of the implants.
目的:骨水泥全膝关节置换术仍是人工膝关节置换术的参考标准;但自从无骨水泥全膝关节置换术被引入以来,多年来在骨水泥和非骨水泥全膝关节置换术之间一直有激烈的讨论,以确定哪一种对患者和外科医生都有最大的好处。本荟萃分析的目的是通过调查临床和影像学结果以及并发症的发生率,系统地分析骨水泥和无骨水泥全膝关节置换术的使用情况,以评估哪种技术对患者和外科医生更有利。材料和方法:本系统综述按照Cochrane手册和PRISMA网络系统综述报告声明撰写。结果:6个随机对照试验最终纳入本系统评价。统计分析显示,所有感兴趣的临床评分(膝关节社会评分、临床和功能评分、牛津膝关节评分、视觉模拟评分)和相似的修改率均无显著差异。结论:当前荟萃分析的结果表明,在临床结果和植入物存活率方面,无骨水泥固定相对于骨水泥全膝关节置换术具有非劣效性。
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引用次数: 0
Pediatric Liver Transplantation as Enzyme Replacement Therapy for Rare Metabolic Diseases with No Structural Liver Damage 儿童肝移植作为酶替代治疗罕见代谢性疾病无结构性肝损害
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-09-28 DOI: 10.32552/2021.actamedica.672
N. Çelik, R. Emiroğlu
Objective: Very rare monogenic metabolic diseases without structural liver damage can be cured by liver transplantation. This process is a surgical enzyme replacement therapy, and defective enzymes may or may not be confined to the liver. The aims of this single center study of children with metabolic diseases showing structurally normal liver parenchyma were to analyze the indications and post-operative outcomes of liver transplantation, identification of developmental and metabolic benefits of the procedure with recognition of peri-operative difficulties to improve the success rate. Materials and Methods: Patients under the age of 19-year-old who underwent liver transplantation for metabolic disorders with no structural liver injury between January 2015 and June 2021 analyzed retrospectively. Patient and graft survivals, indications for transplantation, presence of extra-hepatic enzyme deficiency causing other organ damage, inclusion of simultaneous or sequential kidney transplantation, immunosuppressive protocols, post-transplant complications, and metabolic outcomes were identified. Results: Eight children with primary hyperoxaluria type 1 (n = 4), Maple syrup urine disease (n = 1), Crigler-Najjar syndrome type 1 (n=1), familial hypercholesterolemia (n=1) and propionic acidemia (n = 1) received left lobe (n=6) and left lateral segment (2) allografts from living donors. The median age of 4 girls and 4 boys at time of transplantation was 6.8 years (range 2.2-12.7 years). The median follow-up time was 3.3 years (range 1.5-5.7 years). The most common post-transplant complications were biliary system complications and infections and, two patients died because of sepsis. Six patients are alive with normal functioning allografts and metabolically stable on unrestricted diet. Conclusion: Liver transplantation is a lifesaving treatment and improves patient’s and parent’s life quality for metabolic disorders with no parenchymal injury despite strict dietary restrictions and medical therapies. Especially, living donor liver transplantation is very important for populations with very low organ donation rates.
目的:肝移植可治愈极少数无结构性肝损害的单基因代谢性疾病。这个过程是一种外科酶替代疗法,有缺陷的酶可能局限于肝脏,也可能不局限于肝脏。本单中心研究的目的是分析肝脏实质结构正常的代谢性疾病患儿的适应证和术后结果,确定该手术对发育和代谢的益处,并认识到围手术期的困难,以提高成功率。材料与方法:回顾性分析2015年1月至2021年6月期间因代谢性疾病行肝移植且无结构性肝损伤的19岁以下患者。确定了患者和移植物的存活率,移植的适应症,肝外酶缺乏导致其他器官损伤的存在,包括同时或顺序肾移植,免疫抑制方案,移植后并发症和代谢结果。结果:8例原发性高草酸尿1型(n= 4)、枫糖尿病(n=1)、Crigler-Najjar综合征1型(n=1)、家族性高胆固醇血症(n=1)和丙酸血症(n=1)患儿接受了活体供体左肺叶(n=6)和左外侧段(2)同种异体移植。移植时4名女孩和4名男孩的中位年龄为6.8岁(范围2.2-12.7岁)。中位随访时间为3.3年(1.5-5.7年)。移植后最常见的并发症是胆道系统并发症和感染,2例患者死于败血症。6例患者存活,异体移植物功能正常,饮食不受限制,代谢稳定。结论:无实质损伤的代谢性疾病患者在严格的饮食限制和药物治疗下,肝移植是一种挽救生命的治疗方法,可提高患者和家长的生活质量。特别是,活体肝移植对于器官捐献率非常低的人群非常重要。
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引用次数: 0
The Comparison of ISUP Grades Between Prostate Biopsy and Radical Prostatectomy: The Incoherence and Related Factors 前列腺活检与根治性前列腺切除术ISUP分级的差异及相关因素
IF 0.3 4区 医学 Q4 Medicine Pub Date : 2021-09-27 DOI: 10.32552/2021.actamedica.580
E. Ceyhan, Burak Yılmaz, B. Öztürk
Objective: To assess the incoherence rates between prostate biopsies and radical prostatectomy specimens with the use of the International Society of Urological Pathology grading system and to identify the related factors. Materials and Methods: 89 radical prostatectomy patients were analyzed retrospectively. Patients with Gleason score≥6 were included to the study. Patients’ prostate spesific antigen levels, digital rectal examination, prostate biopsy parameters, prostate cancer risk groups and final prostatectomy pathologies were examined. Gleason scores and International Society of Urological Pathology grades of prostate biopsy and prostatectomy specimens were compared. The coherence, upgrading and downgrading rates of pathologies assessed and related factors were identified. Results: Patients’ mean age was 63.1±6.0 years. Prostate spesific antigen levels ranged from 2.8 to 114.0ng/mL(mean:14.8±16.7). The mean number of cores biopsied was 10.9±3.1. Number of patients in low, intermediate and high risk group were 27(30.3%), 34(38.2%) and 28(31.5%) respectively. The coherence, upgrading and downgrading rates according to International Society of Urological Pathology grading were 49.4%, 33.7% and 16.9% respectively. The low risk prostate cancer group showed the most coherent pathologies with the rate of 70.4%(p<0.05, both for International Society of Urological Pathology grading and Gleason scoring). There was no significant relation between prostate spesific antigen level, number of cores biopsied, percentage of cancer involvement, presence of perineural invasion coherence, upgrading and downgrading. Also no significant difference found between coherent, upgrading and downgrading pathologies with respect to the time to radical prostatectomy. Conclusion: The incoherence between prostate biopsy and radical prostatectomy is challenging. Risk of upgrading and downgrading should be considered in decision making. Low risk prostate cancer shows the most coherent pathology between prostate biopsy and radical prostatectomy.
目的:应用国际泌尿外科病理分级系统评估前列腺活检与根治性前列腺切除术标本的不一致性,并探讨相关因素。材料与方法:回顾性分析89例根治性前列腺切除术患者的临床资料。Gleason评分≥6的患者被纳入研究。检查患者前列腺特异性抗原水平、直肠指检、前列腺活检参数、前列腺癌危险人群及最终前列腺切除术病理。比较前列腺活检和前列腺切除术标本的Gleason评分和国际泌尿病理学会分级。确定了评估病理的一致性、升级率和降级率以及相关因素。结果:患者平均年龄63.1±6.0岁。前列腺特异性抗原水平范围为2.8 ~ 114.0ng/mL(平均值:14.8±16.7)。平均活检核数为10.9±3.1个。低危组27例(30.3%),中危组34例(38.2%),高危组28例(31.5%)。国际泌尿外科病理学会分级一致性为49.4%,升级率为33.7%,降级率为16.9%。低危前列腺癌组病理最一致,发生率为70.4%(国际泌尿病理学会分级和Gleason评分均p<0.05)。前列腺特异性抗原水平、活检核数、肿瘤受累百分比、神经周围浸润一致性、升级和降级之间无显著关系。在根治性前列腺切除术的时间方面,一致性、升级性和降级性病理之间也没有发现显著差异。结论:前列腺活检和根治性前列腺切除术之间的不一致性是具有挑战性的。在决策时应考虑升级和降级的风险。低危前列腺癌在前列腺活检和根治性前列腺切除术之间表现出最一致的病理。
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引用次数: 0
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Acta Medica Mediterranea
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