treatment outcomes

治疗结果
  • 文章类型: Journal Article
    抗精神病药物(AP)治疗精神分裂症谱系障碍(SSD)通常是有效的,然而,相当比例的人反应不佳。儿童创伤(CT)亚型(身体,性,和情感虐待,身体和情感上的忽视)可能会影响治疗效果;然而,研究是稀缺的。AP反应的异质性可以通过区分CT亚型来解释。本研究基于卑尔根-斯塔万格-特隆赫姆-因斯布鲁克(BeStInTro)研究。CTQ-SF评估SSD中的CT亚型(n=98)。在使用APs治疗的一年中,检查了CT亚型与PANSS测量的精神病症状的关系。通过线性混合效应(LME)模型。结果对CT亚型有意义,在从基线到52周的整个治疗过程中,性虐待和身体忽视程度的增加与精神病症状的平均水平增加相关.因此,AP的有效性可能会受到SSD中CT亚型的影响。结果支持临床指南,建议将重点放在SSD创伤的评估和治疗上。
    Treatment with antipsychotics (APs) for schizophrenia spectrum disorders (SSDs) is generally effective, however, a significant proportion does not respond favorably. Childhood trauma (CT) subtypes (physical, sexual, and emotional abuse, physical and emotional neglect) could influence treatment effectiveness; however, research is scarce. Heterogeneity in AP response could be explained by differentiating by CT subtype. The present study was based on the Bergen-Stavanger-Trondheim-Innsbruck (BeSt InTro) study. CTQ-SF assessed CT subtypes in SSDs (n = 98). CT subtypes were examined in relation to psychosis symptoms measured by PANSS during one year of treatment with APs, by means of linear mixed effects (LME) models. Results were significant for CT subtypes, where increased levels of sexual abuse and physical neglect were associated with increased mean levels of psychosis symptoms throughout the course of treatment from baseline to 52 weeks. AP effectiveness may thus be influenced by CT subtype in SSDs. The results support clinical guidelines recommending a focus on assessment and treatment of trauma in SSDs.
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  • 文章类型: Journal Article
    背景:用于增加软组织的可注射填充剂是美容医学领域中最受欢迎的程序之一,特别是在解决皮肤老化的临床迹象。在软组织填充物中,几十年来,非永久性填料已安全地用于许多医疗应用。
    目的:本次上市后观察的目的,开放标签,不受控制,多中心,前瞻性研究(PMS)旨在评估可注射的基于聚L-乳酸的胶原刺激剂(Lanluma®,研究产品)。
    方法:该分析基于从研究人员和参与者在第一次注射(T0,2022年9月)到之后9个月(T3,2023年6月)之间收集的临床结果数据(安全性和有效性)。
    结果:总体而言,70名参与者进行了99次颈部治疗(31%),上臂(20%),手(17%),大腿(16%)和大腿(15%)。肿块(颈部,上臂,手)和结节(颈部,手,大腿)是研究者报告的最常见的不良事件(AE)。都是治疗相关的。没有人是认真的,严重的或致命的。治疗后未报告AE。研究人员和参与者都报告说,在九个月的随访期内,对五个身体部位的治疗有很高的满意度。
    结论:这些积极的临床结果可以归因于最佳实践和建议的正确实施。和研究产品的流变特性。在25个月随访时,应根据研究的最终分析目标重新考虑9个月的随访分析。
    BACKGROUND: Injectable fillers for soft tissue augmentation stand out as one of the most favored procedures in the field of aesthetic medicine, especially in addressing the clinical signs of skin aging. Among soft tissue fillers, non-permanent fillers have been safely used in numerous medical applications for several decades.
    OBJECTIVE: The aim of this post-market observational, open-label, uncontrolled, multicentered, prospective study (PMS) was to evaluate the effects of an injectable poly-L-lactic acid-based collagen stimulator (Lanluma®, the study product).
    METHODS: This analysis is based on the clinical outcomes data (safety and effectiveness) collected from investigators and participants between the first injection (T0, September 2022) and 9 months thereafter (T3, June 2023) in the treatment of five body-contouring areas.
    RESULTS: Overall, 70 participants had 99 treatment sessions of the neck (31%), upper arm (20%), hand (17%), thigh (16%) and décolleté (15%). Lumps (neck, upper arm, hand) and nodules (neck, hand, thigh) were the most frequent adverse events (AEs) reported by investigators. All were treatment related. None were serious, severe or fatal. No AEs were reported following treatment of the décolleté. Both investigators and participants reported high levels of satisfaction during the nine-month follow-up period with the treatments in five body areas.
    CONCLUSIONS: These positive clinical outcomes can be attributed to a proper implementation of best practices and recommendations, and the rheological properties of the study product. This 9-month follow-up analysis should be reconsidered in light of the study\'s objectives for the final analysis at the 25-month follow-up.
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  • 文章类型: Journal Article
    利福平耐药结核病(RR-TB)仍然是一个严重的全球公共卫生问题。我们评估了中国RR-TB患者的治疗结果和相关影响因素。
    本研究回顾性纳入了2018年5月至2020年4月在中国开始RR-TB治疗的1339例患者。数据是从电子病历中收集的。采用多变量logistic回归分析确定不良结局的影响因素。
    在1339例RR-TB患者中,78.8%(1055/1339)取得治疗成功(治愈或治疗完成),5.1%(68/1339)经历了治疗失败,1.1%(15/1339)在治疗期间死亡,10.1%(135/1339)失去随访,4.9%(66/1339)未进行评估。约67.7%(907/1339)的患者经历了至少一个不良事件(AE)。最常见的AE是肝功能减退(507/1339,37.9%),其次是高尿酸血症(429/1339,32.0%),贫血(368/1339,27.5%),电解质扰动(318/1339,23.7%),周围神经炎(245/1339,18.3%),胃肠道反应(203/1339,15.2%)。多因素分析显示年龄≥60岁[调整比值比(aOR):1.96,95%置信区间(CI):1.39-2.77],少数民族(AOR:2.36,95%CI:1.42-3.93),吸烟(AOR:1.50,95%CI:1.10-2.04),心脏病(AOR:2.90,95%CI:1.33-6.31),肿瘤(AOR:9.84,95%CI:2.27-42.67),免疫妥协(AOR:2.17,95%CI:1.21-3.91),再治疗的结核病(aOR:1.46,95%CI:1.08-1.97),和经历的胃肠道反应(aOR:2.27,95%CI:1.52-3.40)与不良结局相关.体重指数(BMI)≥18.5kg/m2,包含bedaquiline的方案和经历的不良事件(AE),如肝功能减退,白细胞减少症,周围神经炎,和视神经炎与良好的结局相关。
    在中国三级结核病医院,RR-TB患者的治疗成功率很高。年龄≥60岁,少数民族,吸烟状况,合并症,再治疗的结核病,和经历的胃肠道反应是不良治疗结局的独立预后因素.
    UNASSIGNED: Rifampin-resistant tuberculosis (RR-TB) remains a serious global public health concern. We assessed treatment outcomes and associated influencing factors among RR-TB patients in China.
    UNASSIGNED: This research enrolled 1339 patients who started RR-TB treatment between May 2018 and April 2020 in China retrospectively. Data were collected from the electronic medical records. Multivariable logistic regression analysis was used to identify the influencing factors related to unfavorable outcomes.
    UNASSIGNED: Of the 1339 RR-TB patients, 78.8% (1055/1339) achieved treatment success (cured or treatment completed), 5.1% (68/1339) experienced treatment failure, 1.1% (15/1339) died during treatment, 10.1% (135/1339) were lost to follow-up, and 4.9% (66/1339) were not evaluated. About 67.7% (907/1339) of patients experienced at least one adverse event (AE). The most common AE was hypohepatia (507/1339, 37.9%), followed by hyperuricemia (429/1339, 32.0%), anemia (368/1339, 27.5%), electrolyte disturbance (318/1339, 23.7%), peripheral neuritis (245/1339, 18.3%), and gastrointestinal reactions (203/1339, 15.2%). Multivariate analysis showed that age ≥60 years [adjusted odds ratio (aOR): 1.96, 95% confidence interval (CI): 1.39-2.77], national minority (aOR: 2.36, 95% CI: 1.42-3.93), smoking (aOR: 1.50, 95% CI: 1.10-2.04), cardiopathy (aOR: 2.90, 95% CI: 1.33-6.31), tumors (aOR: 9.84, 95% CI: 2.27-42.67), immunocompromise (aOR: 2.17, 95% CI: 1.21-3.91), re-treated TB (aOR: 1.46, 95% CI: 1.08-1.97), and experienced gastrointestinal reactions (aOR: 2.27, 95% CI: 1.52-3.40) were associated with unfavorable outcomes. Body mass index (BMI) ≥18.5 kg/m2, regimens containing bedaquiline and experienced adverse events (AEs) such as hypohepatia, leukopenia, peripheral neuritis, and optic neuritis were associated with favorable outcomes.
    UNASSIGNED: High rates of treatment success were achieved for RR-TB patients at tertiary tuberculosis hospitals in China. Age ≥60 years, national minority, smoking status, comorbidities, re-treated TB, and experienced gastrointestinal reactions were independent prognostic factors for unfavorable treatment outcomes.
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  • 文章类型: Journal Article
    PARAGON-HF研究(ARNI与ARB在射血分数保留的心力衰竭中的总体结果的前瞻性比较)研究了沙库巴曲缬沙坦在射血分数保留的心力衰竭(HF)中的作用。结果,使用常规统计方法进行分析,没有发现心血管死亡和HF总住院的主要复合终点显着降低。最近的临床试验使用胜率统计数据,可以将多个结果方面纳入主要终点,并可以用更少的患者检测出积极的结果。在这项研究中,我们通过分析PARAGON-HF研究中纳入患者的结果,评估沙库巴曲-缬沙坦对结局的影响.
    在PARAGON-HF研究中,4822例射血分数保留的HF患者被随机分为沙库巴曲-缬沙坦组或缬沙坦组。在本研究中,主要结局是心血管死亡时间的分层复合,HF住院总数,第一次因HF住院的时间,肾脏综合结局的时间,8个月时堪萨斯城心肌病问卷总症状评分的变化,使用胜率统计模型进行分析。
    使用这种方法,我们发现,与接受缬沙坦的患者相比,接受沙库巴曲-缬沙坦的患者有更多的临床获益(胜率,1.13[95%CI,1.04-1.23];P=0.005)。无论左心室射血分数高于或低于中位数,这种临床优势在患者中都很明显。也就是说,左心室射血分数为57%,并且与性别无关(左心室射血分数的P相互作用=0.76,性别为0.73)。
    采用创新的赢率方法,沙库巴曲-缬沙坦在射血分数保留的HF患者中显示出显著的临床获益。值得注意的是,无论左心室射血分数和性别如何,均可观察到这种获益.
    URL:https://www。clinicaltrials.gov;唯一标识符:NCT01920711。
    UNASSIGNED: The PARAGON-HF study (Prospective Comparison of ARNI With ARB Global Outcomes in Heart Failure With Preserved Ejection Fraction) investigated the effect of sacubitril-valsartan in heart failure (HF) with preserved ejection fraction. The results, which were analyzed using conventional statistical methods, did not find a significant reduction in the primary composite end point of cardiovascular death and total hospitalization for HF. Recent clinical trials used win ratio statistics that enable the incorporation of multiple outcome aspects into the primary end point and can detect positive outcomes with fewer patients. In this study, we assessed the effect of sacubitril-valsartan on outcomes using the win ratio to analyze results from patients included in the PARAGON-HF study.
    UNASSIGNED: In the PARAGON-HF study, 4822 patients with HF with preserved ejection fraction were randomized either to sacubitril-valsartan or valsartan groups. In the present study, the primary outcome was a hierarchical composite of time to cardiovascular death, total number of hospitalization for HF, time to first hospitalization for HF, time to renal composite outcome, and change in the Kansas City Cardiomyopathy Questionnaire total symptom score at 8 months analyzed using a win ratio statistical model.
    UNASSIGNED: Using this approach, we found that a greater number of patients who received sacubitril-valsartan experienced clinical benefits compared with those who received valsartan (win ratio, 1.13 [95% CI, 1.04-1.23]; P=0.005). This clinical advantage was evident in patients regardless of whether the left ventricular ejection fraction was above or below the median, that is, the left ventricular ejection fraction of 57%, and regardless of sex (Pinteraction=0.76 for the left ventricular ejection fraction and 0.73 for sex).
    UNASSIGNED: Employing the innovative win ratio approach, sacubitril-valsartan demonstrated significant clinical benefits among patients with HF with preserved ejection fraction. Notably, this benefit was observed irrespective of left ventricular ejection fraction and sex.
    UNASSIGNED: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01920711.
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  • 文章类型: Journal Article
    不良的治疗依从性导致结核病患者(PWTB)的治疗完成度降低和随访损失增加。药物监测显示一些改善依从性的证据。
    我们于2019年5月至2022年2月在南非的18个初级卫生诊所进行了一项集群随机试验。纳入药物敏感性结核病(DS-TB)患者(年龄≥2岁)。向所有参与者提供了在标准护理(SoC)臂中保持沉默的监视器。在干预部门,每周审查依从性报告,并酌情加强了参与者的支持(文本,电话,家访,动机咨询)。主要结果是坚持,其计算为打开盒子的天数(代替药物服用)/总预期治疗天数作为二元变量(<80%对≥80%)。分析考虑了集群设计。该试验在泛非试验登记处PACTR20190268115772注册。
    我们招募了2727名参与者(38%为女性,中位年龄36岁(IQR27-45岁),其中2584人具有可用的依从性数据.与SoC组相比,干预组的主要结局(≥80%的依从性)更高(81.0%对50.8%,调整后风险比(ARR)1.51(1.36-1.66)。同样,与SoC组相比,干预组的总体依从性百分比更高(88.5%对69.7%,调整后风险差异16.8%(13.3%-20.4%))。
    DS-TB患者干预组的治疗依从性提高。我们认为对依从性的影响很重要,并保证继续使用和评估这些技术。
    这项研究由比尔和梅林达·盖茨基金会资助,UintedStates,遏制结核病伙伴关系,瑞士,和南非医学研究理事会,南非。
    UNASSIGNED: Poor treatment adherence contributes to lower treatment completion and higher loss to follow-up among people with tuberculosis (PWTB). Medication monitors have shown some evidence of improved adherence.
    UNASSIGNED: We conducted a cluster randomised trial in 18 primary health clinics in South Africa between May 2019-February 2022. Persons (aged ≥ 2 years) with drug-sensitive tuberculosis (DS-TB) were enrolled. All participants were provided with monitors which were silent in the standard of care (SoC) arm. In the intevention arm, weekly adherence reports were reviewed and participants received intensified support as appropriate (text, phone call, home visit, motivational counselling). The primary outcome was adherence, which was calculated as days box was opened (proxy for drug taken)/total expected treatment days as a binary variable (<80% versus ≥80%). Analysis took into account clustered design. The trial was registered with the Pan African Trial Registry PACTR20190268115772.
    UNASSIGNED: We enrolled 2727 participants (38% women, median age 36 (IQR 27-45 years), of whom 2584 had available adherence data. The primary outcome (measured as ≥80% adherence) was higher in intervention versus SoC arm (81.0% versus 50.8%, adjusted risk ratio (ARR) 1.51 (1.36-1.66). Similarly, overall percentage adherence was higher in intervention versus SoC arm (88.5% versus 69.7%, adjusted risk difference 16.8% (13.3%-20.4%)).
    UNASSIGNED: People with DS-TB had improved treatment adherence in the intervention arm. We believe the effect on adherence is important and warrants continued use and evaluation of these technologies.
    UNASSIGNED: The study is funded by Bill & Melinda Gates Foundation, Uinted States, the Stop TB Partnership, Switzerland, and the South African Medical Research Council, South Africa.
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  • 文章类型: Journal Article
    背景关于印度患者的基底细胞癌(BCC)的数据很少。这项回顾性研究是为了探索流行病学,危险因素,临床和病理方面,以及北印度患者队列中BCC的长期治疗结果。方法收集2017年1月1日至2022年12月31日在皮肤科门诊登记的确诊为BCC的患者资料。结果83例患者中,56.6%为女性,中位年龄为62岁(6-85岁)。大多数患者(81.9%)有单个BCC病变,导致总共126个评估病变。BCC出现时的中位大小为1.90cm,结节性BCC是最常见的组织病理学亚型(39.7%)。在82.5%的患者中观察到头颈部受累,与马拉尔地区,鼻子,轨道周围区域是最常见的受影响的部位。在45.2%的病例中,色素沉着在临床上很明显。手术切除是主要的治疗方式(71.1%的患者)。中位随访时间为40个月(6~57个月)。5例患者复发,与接受药物或破坏性治疗的患者(43.6±3.482个月)相比,手术治疗组(55.58±0.98个月)的无病生存期更长(p=0.003)。结论这项基于医院的研究数据表明,北印度BCC患者对女性有轻微的偏爱,大多数病例发生在他们生命的第七个十年。这种情况通常发生在暴露于阳光的区域,如黄斑区域和鼻子,色素病变的比例很高。手术切除后复发罕见,总体治疗结果良好.
    Background There is scant data on basal cell carcinoma (BCC) in Indian patients. This retrospective study was conducted to explore epidemiology, risk factors, clinical and pathological aspects, and long-term treatment outcomes of BCC in a cohort of North Indian patients. Methods Data about patients registered in the dermatosurgery clinic between 01 January 2017 and 31 December 2022 with a confirmed diagnosis of BCC was collected. Results Among the 83 patients, 56.6% were females, and the median age was 62 years (6-85 years). Most patients (81.9%) had a single BCC lesion, resulting in a total of 126 assessed lesions. The median size of BCC at presentation was 1.90 cm, with nodular BCC being the most common histopathological subtype (39.7%). Head and neck region involvement was observed in 82.5% of patients, with the malar region, nose, and periorbital region being the most commonly affected sites. Pigmentation was clinically evident in 45.2% of cases. Surgical excision was the primary treatment modality (71.1% of patients). The median follow-up duration was 40 months (6-57 months). Recurrence occurred in five patients, with a longer disease-free survival period observed in the surgically treated group (55.58 ± 0.98 months) compared to patients treated with medical or destructive therapies (43.6 ± 3.482 months) (p = 0.003). Conclusion The data from this hospital-based study indicated a slight predilection for females among North Indian patients with BCC, with most cases occurring during their seventh decade of life. The condition commonly occurred on sun-exposed areas such as the malar region and nose, with a high percentage of pigmented lesions. Recurrence following surgical excision was rare, and overall treatment outcomes were favourable.
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  • 文章类型: Journal Article
    背景:可注射较短的耐多药结核病(MDR-TB)方案,据报道,与更长的治疗方案相比,耐多药结核病的治疗成本更低,更有效。根据世界卫生组织(WHO)2016年的正式建议,埃塞俄比亚于2018年4月推出了可注射的较短方案(SR)。虽然世卫组织的建议是基于来自一些亚洲和非洲国家广泛的方案研究的证据,在埃塞俄比亚背景下,关于患者结局的信息很少.因此,我们旨在评估耐多药结核病患者接受可注射SR的治疗结局,并确定与结局相关的因素.
    方法:在埃塞俄比亚对2018年4月至2020年3月期间接受治疗的245例耐多药结核病患者进行了一项基于多中心机构的回顾性队列研究。从患者的病历中收集数据,并使用SPSS版本25进行分析。描述性统计用于总结结果,而推理分析用于研究治疗结果和生存状态的预测因素。
    结果:共有245名患者被纳入研究,其中129人(52.7%)为女性。患者的中位年龄为27岁(IQR:21-33)。总体治疗成功率为87.8%,156例(63.7%)治愈,59例(24.1%)患者完成治疗。不良结局占12.2%,16(6.5%)治疗失败,8例(3.3%)死亡,6例(2.4%)失访。大多数不利的结果发生在治疗的早期阶段,事件发生的中位时间为1.8个月(95%CI:0.99-2.69)。使用Khat(一种绿叶灌木,因其兴奋剂作用而滥用)并被诊断为耐多药结核病,而不是仅对利福平具有抗性,被确定为与不良结局相关的独立因素。
    结论:在埃塞俄比亚的方案管理背景下,发现用于耐多药结核病的可注射SR具有积极的治疗结果。
    BACKGROUND: The injectable shorter multi-drug resistant tuberculosis (MDR-TB) regimen, has been reported to be less costly and more effective in the treatment of MDR-TB compared to the longer regimen. Ethiopia introduced the injectable shorter regimen (SR) in April 2018 following official recommendation by the World Health Organization (WHO) in 2016. While the WHO recommendation was based on evidence coming from extensive programmatic studies in some Asian and African countries, there is paucity of information on patient outcomes in the Ethiopian context. Thus, we aimed to assess the treatment outcomes and identify factors associated with the outcomes of MDR-TB patients on injectable SR.
    METHODS: A multi-center facility-based retrospective cohort study was conducted in Ethiopia on 245 MDR-TB patients who were treated between April 2018 and March 2020. Data were collected from patients\' medical records and analyzed using SPSS version 25. Descriptive statistics was used to summarize the results while inferential analysis was employed to investigate predictors of treatment outcomes and survival status.
    RESULTS: A total of 245 patients were included in the study, with 129 (52.7%) of them being female. Median age of the patients was 27 (IQR: 21-33). The overall treatment success rate was 87.8%, with 156 (63.7%) cured and 59 (24.1%) patients who completed treatment. The unfavorable outcomes accounted for 12.2%, with 16 (6.5%) treatment failure, 8 (3.3%) death and 6 (2.4%) lost to follow up. Majority of the unfavorable outcomes occurred during the early phase of therapy, with median time to event of 1.8 months (95% CI: 0.99-2.69). The use of khat (a green leafy shrub abused for its stimulant like effect) and being diagnosed with MDR-TB than rifampicin resistant only, were identified as independent factors associated with unfavorable outcomes.
    CONCLUSIONS: The injectable SR for MDR-TB was found to have positive treatment outcomes in the context of programmatic management in Ethiopia.
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  • 文章类型: Journal Article
    目的:这项真实世界的研究旨在描述患者和临床特征,在法国接受abemaciclib治疗的HR+/HER2-转移性乳腺癌患者的治疗模式和结果,意大利和西班牙。材料与方法:对接受abemaciclib常规护理的HR+/HER2-晚期/转移性乳腺癌成年女性进行了多中心图表审查。通过Kaplan-Meier曲线估计真实世界无进展生存期(rwPFS)。结果:这项研究包括来自法国的151、173和175名患者,意大利和西班牙,分别。Abemaciclib主要是在激素治疗的同时作为一线治疗。rwPFS中位数>20个月,1年rwPFS率>70%。结论:三个国家的有效性相似,与关键研究一致。
    在法国诊所使用Abemaciclib,意大利和西班牙这项研究描述了患者,他们接受的治疗以及对最常见的晚期乳腺癌患者的治疗结果。这些患者在法国的常规乳腺癌护理中服用abemaciclib加激素治疗,意大利和西班牙。用于进行这项研究的信息取自患者的医疗图表。在现实世界的研究中,abemaciclib主要用作晚期乳腺癌的初始治疗。三个国家的Abemaciclib有效性相似,证实了先前研究的结果。我们的研究支持对HR+/HER2-晚期乳腺癌患者使用abemaciclib。
    Aim: This real-world study aimed to describe patient and clinical characteristics, treatment patterns and outcomes for patients with HR+/HER2- metastatic breast cancer receiving abemaciclib in France, Italy and Spain. Materials & methods: A multicenter chart review was conducted for adult females with HR+/HER2- advanced/metastatic breast cancer who received abemaciclib in routine care. Real-world progression-free survival (rwPFS) was estimated via Kaplan-Meier curves. Results: This study included 151, 173 and 175 patients from France, Italy and Spain, respectively. Abemaciclib was mostly prescribed as first-line therapy concomitantly with hormone therapy. Median rwPFS was >20 months and the 1-year rwPFS rate was >70%. Conclusion: Effectiveness was similar across the three countries and aligns with pivotal studies.
    Abemaciclib use in the clinic in France, Italy & SpainThis study describes patients, the treatments they have received and the results of those treatments for patients with the most common type of advanced breast cancer. These patients were taking abemaciclib plus hormonal therapy in routine breast cancer care in France, Italy and Spain. The information used to conduct this study was taken from patients\' medical charts. In this real-world study, abemaciclib was mostly used as the initial treatment for advanced breast cancer. Abemaciclib effectiveness was similar across the three countries confirming findings from previous studies. Our study supports the use of abemaciclib for patients with HR+/HER2- advanced breast cancer.
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  • 文章类型: Journal Article
    背景:结核病流行病学与社会经济条件密切相关,控制和治疗具有挑战性。早期诊断和适当的治疗将有助于预防各种结核病相关的发病率。药物不良反应等因素,运输成本,家庭支持,距离治疗中心,个人习惯,同病态条件,和患者对其就业的多重义务,家庭和社会对治疗结果有影响。
    目的:了解初诊肺结核患者中影响肺结核治疗转归的因素。
    方法:采用普选抽样方法,纳入地区结核病中心NTEP登记的261例结核病患者。第一次随访在密集阶段结束时进行,即2个月结束。第二次随访是在治疗完成后进行的,即6月底
    结果:大多数59%的参与者在第2个月随访时被诊断为涂片阴性,45.21%和28.73%的参与者在第6个月随访时分别被诊断为治愈和治疗完成。73.95%的参与者有成功的结果。多因素logistic回归分析显示,结核病的治疗结果受房屋类型(puccahouse)的影响,咳嗽的存在,既往有结核病史,家庭支持,家人的监督和主管的支持。
    结论:总体治疗成功率为73.95%。结核病成功结局的因素是年龄,结核病过去的历史,房子的类型,咳嗽和发烧,体重增加,家庭支持,家人的监督和主管的支持。
    BACKGROUND: Tuberculosis disease epidemiology is closely related to social and economic conditions which make its prevention, control and cure challenging. Early diagnosis and adequate treatment will help to prevent various tuberculosis related morbidities. Factors such as adverse effects of drugs, transportation cost, family support, distance to the treatment center, personal habits, co morbid conditions, and patients\' multiple obligations concerning to their employment, family and society have an impact on the treatment outcomes.
    OBJECTIVE: To know the factors affecting tuberculosis treatment outcome among newly diagnosed tuberculosis patients.
    METHODS: A total of 261 Tuberculosis patients registered in NTEP under District tuberculosis centre were enrolled using universal sampling method. First follow up was done at the end of intensive phase i.e. End of 2 months. Second follow up was done after completion of treatment i.e., End of 6th month.
    RESULTS: Majority 59% participants were diagnosed as smear negative at 2nd month follow up and 45.21% and 28.73% participants were diagnosed as cured and treatment completed respectively at 6th month follow up. 73.95% participants had successful outcome. Multivariate logistic regression analysis showed that treatment outcomes of tuberculosis were affected by type of house (pucca house), presence of cough, past history of tuberculosis, family support, supervision by family and support of supervisor.
    CONCLUSIONS: Overall treatment success rate was 73.95%. The contributing factors for successful outcome of tuberculosis were age, past history of TB, type of house, presence of cough and fever, weight gain, family support, supervision by family and support of supervisor.
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  • 文章类型: Journal Article
    背景:硬脑膜穿刺后头痛(PDPH)是腰椎穿刺后的常见并发症,硬膜外镇痛,或者神经轴麻醉.头痛疾病的国际分类,第三版将PDPH归类为自限条件;然而,新出现的证据,包括我们的发现,表明PDPH可以有一个延长的病程,挑战这种传统观点。
    目的:为了阐明持续性PDPH(pPDPH)的诊断特征和治疗结果,提供对其人口概况和诊断特征的见解。
    方法:我们执行了一个匿名,基于网络的调查针对年龄≥18岁的诊断或怀疑患有pPDPH的个体。招聘是通过Facebook上的自助小组进行的。调查包括有关诊断程序的问题,治疗方案,结果,和医疗咨询。
    结果:该调查获得了179/347(51.6%)个人填写问卷的回复率。179例中有9例(5.0%)证实了脑脊液(CSF)泄漏。在70/179(39.1%)个体中观察到无CSF泄漏的颅内低血压迹象。所有参与者都接受了大脑和脊柱的磁共振成像扫描,113/179例(63.1%)进行了计算机断层扫描脊髓造影。药物,包括镇痛药,茶碱,加巴喷丁,提供最小的短期救济。硬膜外血贴片治疗在136/179(76.0%)中导致轻度至中度的短期改善,22/179(12.3%)显著改善,179人中有8人(4.5%)完全有效。对于长期结果,118/179(66.0%)个体报告轻度至中度改善.在42/179(23.5%)患者中进行了手术干预,20/42(47.6%)个体在术中发现假性脑膜膨出。手术后,21/42(50.0%)的参与者经历了轻度到中度的改善,12/42(28.6%)表现出更明显的改善,42人中有5人(11.9%)取得完全成效。
    结论:本研究强调了pPDPH管理的复杂性。诊断的延迟会影响治疗的有效性,包括硬膜外补血和手术干预,导致持续的症状。这强调了定制和适应性治疗策略的重要性。研究结果主张进行更多的研究,以加深对pPDPH的理解并改善长期患者的预后。
    Post-dural puncture headache (PDPH) is a frequent complication following lumbar puncture, epidural analgesia, or neuraxial anesthesia. The International Classification of Headache Disorders, third edition categorizes PDPH as a self-limiting condition; however, emerging evidence, including our findings, suggests that PDPH can have a prolonged course, challenging this traditional view.
    To elucidate the diagnostic characteristics and treatment outcomes of persistent PDPH (pPDPH), offering insights into its demographic profiles and diagnostic features.
    We executed an anonymous, web-based survey targeting individuals aged ≥18 years diagnosed with or suspected of having pPDPH. Recruitment occurred through self-help groups on Facebook. The survey comprised questions regarding diagnostic procedures, treatment regimens, outcomes, and healthcare consultation.
    The survey achieved a response rate of 179/347 (51.6%) individuals completing the questionnaire. Cerebrospinal fluid (CSF) leaks were confirmed in nine of 179 (5.0%) cases. Signs of intracranial hypotension without a CSF leak were observed in 70/179 (39.1%) individuals. All participants underwent magnetic resonance imaging scans of the brain and spine, with computed tomography myelography performed in 113/179 (63.1%) cases. Medications, including analgesics, theophylline, and gabapentin, provided minimal short-term relief. Epidural blood patch treatments resulted in slight-to-moderate short-term improvement in 136/179 (76.0%), significant improvement in 22/179 (12.3%), and complete effectiveness in eight of 179 (4.5%) individuals. For long-term outcomes, slight-to-moderate improvement was reported by 118/179 (66.0%) individuals. Surgical interventions were carried out in 42/179 (23.5%) patients, revealing pseudomeningoceles intraoperatively in 20/42 (47.6%) individuals. After surgery, 21/42 (50.0%) of the participants experienced slight-to-moderate improvement, 12/42 (28.6%) showed more pronounced improvement, and five of the 42 (11.9%) achieved complete effectiveness.
    This study underscores the complexities of managing pPDPH. The delay in diagnosis can impact the effectiveness of treatments, including epidural blood patch and surgical interventions, resulting in ongoing symptoms. This underscores the importance of tailored and adaptable treatment strategies. The findings advocate for additional research to deepen the understanding of pPDPH and improve long-term patient outcomes.
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