Severe

严重
  • 文章类型: Journal Article
    背景:严重烧伤,尽管在护理和预防方面取得了进步,会对长期发病率产生深远的影响,影响生活质量和社会经济地位。我们的目标是探索预测独立恢复的因素,严重烧伤患者的预期速度和时间,以及使用的进展衡量标准。
    方法:对四个数据库的系统搜索(MEDLINE,EMBASE,Cochrane,CINAHL)进行了一项研究,该研究报告了与成年(>15岁)队列中独立功能的身体能力有关的结果,这些队列在开发的专业烧伤服务中治疗后长达30年遭受严重烧伤(>20%TBSA)。提取的数据包括五个独立域中影响功能实现速率和时间的因素,以及使用的结果衡量标准。
    结果:纳入21项符合条件的研究,包括1298名重度烧伤幸存者,合并平均年龄为39.6岁,平均TBSA为25.8%。影响独立功能恢复的最重要的复发因素是年龄,女性性别,烧伤严重程度,延长ICU和住院时间,先前的精神健康状况,和急性后的心理问题。即使在受伤后的2年以上,基于运动的康复也为主要烧伤患者带来了好处。27%至97%的患者出院至独立生活,而报告的复工率从52%到80%不等。烧伤特定健康量表-简介,功能独立性度量,物理综合评分(SF-36)是最广泛使用的结果评分系统。
    结论:主要烧伤幸存者的恢复时间较长,有可能出现持续性慢性损伤,始终低于基线功能水平。年龄和性别等不可改变的因素,和疾病特征,如烧伤大小与相关的身体,生理和心理后遗症是促成的。需要进一步的研究来探索重大烧伤和多发性创伤重症监护患者的具体里程碑的成就,虽然早期有针对性的康复解决身体问题,心理,和职业需求有前途的潜在利益。
    Major burn injury, despite advancements in care and prevention, can have a profound impact on long-term morbidity, affecting quality of life and socioeconomic standing. We aim to explore factors predicting recovery of independence, the expected rate and time in majorly burned patients, and the measures of progress used.
    A systematic search of four databases (MEDLINE, EMBASE, COCHRANE, CINAHL) was conducted for studies reporting outcomes pertaining to physical ability indicative of independent function in adult (>15 y) cohorts who had suffered a major burn (>20% TBSA) up to 30 years after treatment in a developed specialised burn service. Data extracted included factors affecting rate of and time to achievement of function in five independence domains, as well as the outcome measures used.
    21 eligible studies were included comprising 1298 major burns survivors with a combined mean age of 39.6 y and a mean TBSA of 25.8%. The most significant recurring factors impacting recovery of independent function were older age, female gender, burn severity, prolonged ICU and hospital admission, preceding mental health conditions, and post-acute psychological issues. Exercise-based rehabilitation conferred benefits on major burn patients even over 2 years following injury. Discharge to independent living from hospital occurred in 27% to 97% of patients, while reported return to work rates varied from 52% to 80%. Burns Specific Health Scale-Brief, Functional Independence Measure, and Physical Composite Score (SF-36) were the most widely used outcome scoring systems.
    Major burn survivors have protracted recovery with potential for persistent chronic impairments, remaining consistently below baseline levels of function. Non-modifiable factors such as age and gender, and disease characteristics such as burn size with associated physical, physiological and psychosocial sequelae are contributory. Further research is required to explore achievement of specific milestones of major burn and polytrauma critical care patients, while early targeted rehabilitation addressing physical, psychological, and vocational needs has promising potential benefit.
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  • 文章类型: Journal Article
    特应性皮炎(AD)是儿童最常见的炎症性皮肤病。患有严重AD的儿童具有以皮肤病变为特征的多维疾病负担,瘙痒,频繁感染,睡眠剥夺,和高合并症。这些不仅影响儿童的心理健康和整体生活质量,也影响他们的父母和照顾者。对于患有严重AD的幼儿,很少有适合长期使用的有效治疗选择。由于它们的不利影响,实践指南认为系统性药物不适合这个年龄组,尽管它们在极端情况下仍在标签外使用。生物dupilumab最近已被批准用于6-11岁的重度(欧盟)和中度至重度(美国)AD儿童。为这些临床需求未得到满足的患者提供了希望。本综述的目的是描述dupilumab批准前6-11岁的AD患者的未满足需求,并总结支持dupilumab在这些儿童中的安全性和有效性的现有临床数据。
    Atopic dermatitis (AD) is the most common inflammatory skin disease in children. Children with severe AD have a multidimensional disease burden characterized by skin lesions, itching, frequent infections, sleep deprivation, and a high rate of comorbidities. These impact the mental health and overall quality of life of not only the children but also of their parents and caregivers. There are few effective available treatment options for young children with severe AD that are suitable for long-term use. Due to their adverse effects, practice guidelines consider systemic agents inappropriate for this age group, although they are still used off-label in extreme cases. The biologic dupilumab has recently been approved for children aged 6-11 years with severe (EU) and moderate-to-severe (USA) AD, offering hope to this population of patients with a high unmet clinical need. The purpose of this review is to describe the unmet needs of AD patients aged 6-11 years prior to dupilumab approval and to summarize existing clinical data supporting dupilumab\'s safety and efficacy in these children.
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  • 文章类型: Journal Article
    识别成人严重呼吸道合胞病毒(RSV)疾病的危险因素可以促进他们适当的疫苗推荐。我们进行了系统的文献综述(PubMed/Embase的最近10年),以确定高收入国家严重RSV感染结局的风险因素的定量估计。RSV感染的严重结局包括住院,超额死亡率,下呼吸道感染,或综合措施:严重RSV,其中包括这些结果和其他结果,如机械通气和延长住院时间。在筛选的1494篇文章中,26符合资格标准。我们发现强有力的证据表明,以下因素会增加严重结局的风险:年龄,先前存在的合并症(例如,心脏,肺,和免疫功能低下的疾病,以及糖尿病和肾脏疾病),和生活条件(社会经济地位和养老院居住)。在患有合并症的年轻成年人中,严重结局的频率通常与老年人相似。提示免疫衰老和慢性疾病都是导致风险升高的因素。
    PROSPERO(CRD42022315239)。
    Identification of risk factors for severe respiratory syncytial virus (RSV) disease in adults could facilitate their appropriate vaccine recommendations. We conducted a systematic literature review (last 10 years in PubMed/Embase) to identify quantitative estimates of risk factors for severe RSV infection outcomes in high-income countries. Severe outcomes from RSV infection included hospitalization, excess mortality, lower respiratory tract infection, or a composite measure: severe RSV, which included these outcomes and others, such as mechanical ventilation and extended hospital stay. Among 1494 articles screened, 26 met eligibility criteria. We found strong evidence that the following increased the risk of severe outcomes: age, preexisting comorbid conditions (eg, cardiac, pulmonary, and immunocompromising diseases, as well as diabetes and kidney disease), and living conditions (socioeconomic status and nursing home residence). The frequency of severe outcomes among younger adults with comorbidities was generally similar to that experienced by older adults, suggesting that immunosenescence and chronic conditions are both contributing factors for elevated risk.
    UNASSIGNED: PROSPERO (CRD42022315239).
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  • 文章类型: Meta-Analysis
    背景:用于重症急性胰腺炎(SAP)预测的评分系统应与测试前概率结合使用,以建立SAP的测试后概率,但是缺乏这种数据。
    目的:研究常用评分系统的预测价值及其在修改SAP预测前概率中的作用。
    方法:在PROSPERO注册后遵循PRISMA语句和MOOSE检查表,PubMed从成立之初一直搜索到2022年9月。回顾性,prospective,关于定义为修订的亚特兰大标准的急性胰腺炎患者的横断面研究或临床试验,SAP的报告率,并在急性胰腺炎严重程度床边指数(BISAP)中使用至少一个评分,急性生理学和慢性健康检查(APACHE)-II,兰森,包括系统性炎症反应综合征(SIRS)及其敏感性和特异性。进行随机效应模型荟萃分析。结合测试前概率和似然比(LR)来估计Fagan列线图上的测试后概率。合并严重性率用作SAP的测试前概率,合并敏感性和特异性以计算LR并产生测试后概率。建立了异质性的先验假设,并计划了敏感性分析。
    结果:43项研究纳入14,116例急性胰腺炎患者:42例BISAP,30与APACHE-II,27与兰森,8与SIRSSAP合并预测试概率为16.6%-25.3%。BISAP的SAP阳性/阴性评分的测试后概率为47%/6%,APACHE-II的43%/5%,兰森48%/5%,SIRS为40%/12%。在18项比较BISAP的研究中,APACHE-II,和Ranson在6740例合并预测SAP概率为18.7%的患者中,BISAP评分为阳性时的测试后概率为48%,46%为APACHE-II,兰森的50%。当分数为负数时,BISAP的测试后概率降至7%,兰森6%,5%为APACHE-Ⅱ。质量,设计,和研究的起源国不能解释观察到的高度异质性。
    结论:最常用的预测SAP的评分系统表现不佳,对决策没有帮助。
    Scoring systems for severe acute pancreatitis (SAP) prediction should be used in conjunction with pre-test probability to establish post-test probability of SAP, but data of this kind are lacking.
    To investigate the predictive value of commonly employed scoring systems and their usefulness in modifying the pre-test probability of SAP.
    Following PRISMA statement and MOOSE checklists after PROSPERO registration, PubMed was searched from inception until September 2022. Retrospective, prospective, cross-sectional studies or clinical trials on patients with acute pancreatitis defined as Revised Atlanta Criteria, reporting rate of SAP and using at least one score among Bedside Index for Severity in Acute Pancreatitis (BISAP), Acute Physiology and Chronic Health Examination (APACHE)-II, RANSON, and Systemic Inflammatory Response Syndrome (SIRS) with their sensitivity and specificity were included. Random effects model meta-analyses were performed. Pre-test probability and likelihood ratio (LR) were combined to estimate post-test probability on Fagan nomograms. Pooled severity rate was used as pre-test probability of SAP and pooled sensitivity and specificity to calculate LR and generate post-test probability. A priori hypotheses for heterogeneity were developed and sensitivity analyses planned.
    43 studies yielding 14,116 acute pancreatitis patients were included: 42 with BISAP, 30 with APACHE-II, 27 with Ranson, 8 with SIRS. Pooled pre-test probability of SAP ranged 16.6%-25.3%. The post-test probability of SAP with positive/negative score was 47%/6% for BISAP, 43%/5% for APACHE-II, 48%/5% for Ranson, 40%/12% for SIRS. In 18 studies comparing BISAP, APACHE-II, and Ranson in 6740 patients with pooled pre-test probability of SAP of 18.7%, post-test probability when scores were positive was 48% for BISAP, 46% for APACHE-II, 50% for Ranson. When scores were negative, post-test probability dropped to 7% for BISAP, 6% for Ranson, 5% for APACHE-II. Quality, design, and country of origin of the studies did not explain the observed high heterogeneity.
    The most commonly used scoring systems to predict SAP perform poorly and do not aid in decision-making.
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  • 文章类型: Journal Article
    背景:细胞因子如白细胞介素-5(IL-5)在疟疾发病机制中的作用尚不清楚。本系统综述试图综合严重和无并发症疟疾之间IL-5水平的变化。以及在疟疾和未患病的对照组之间。
    方法:该系统评价已在国际前瞻性系统评价注册(PROSPERO;CRD42022368773)上注册。在WebofScience中搜索报告疟疾患者(任何严重程度)和/或未感染个体中IL-5水平的研究,PubMed,EMBASE,Scopus,中部,和MEDLINE,10月1日至10日,2022年。使用加强流行病学观察研究报告(STROBE)指南报告观察性研究,将所有纳入研究的偏倚风险降至最低。疟疾和未感染对照之间IL-5水平的差异,并在严重和不复杂的疟疾之间进行了叙事合成。
    结果:在数据库中确定的1177篇文章中,23符合资格标准,并纳入本系统评价。定性综合显示不同严重程度的临床疟疾和未感染对照之间IL-5水平的异质性。大多数纳入的研究(12/15研究,80%)发现疟疾病例和未感染对照之间的IL-5水平没有变化。同样,大多数研究发现,严重(无论并发症)和单纯性疟疾之间的IL-5水平没有差异(4/8研究,50%)。定性综合显示,大多数研究发现严重和非严重疟疾之间的IL-5水平没有差异。
    结论:综合评价表明,不同临床严重程度的疟疾患者和未感染对照患者的IL-5水平没有变化。鉴于已发表的关于疟疾中IL-5水平的研究数量有限,有必要进行更多的研究,以确定这种细胞因子在疟疾发病机制中的功能。
    BACKGROUND: The role of cytokines such as interleukin-5 (IL-5) in the pathogenesis of malaria remains unclear. This systematic review sought to synthesize variations in IL-5 levels between severe and uncomplicated malaria, as well as between malaria and controls not afflicted with the disease.
    METHODS: This systematic review was registered at the International Prospective Register of Systematic Reviews (PROSPERO; CRD42022368773). Searches for studies that reported IL-5 levels in patients with malaria (any severity) and/or uninfected individuals were performed in Web of Science, PubMed, EMBASE, Scopus, CENTRAL, and MEDLINE, between 1st and 10th October, 2022. The risk of bias among all included studies was minimized using the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines for reporting observational studies. The differences in IL-5 levels between malaria and uninfected controls, and between severe and uncomplicated malaria were synthesized by narrative synthesis.
    RESULTS: Among 1177 articles identified in the databases, 23 matched the eligibility criteria and were included in this systematic review. Qualitative syntheses showed the heterogeneity of IL-5 levels between different severities of clinical malaria and uninfected controls. The majority of the included studies (12/15 studies, 80%) found no change in IL-5 levels between malaria cases and uninfected controls. Similarly, most studies found no difference in IL-5 levels between severe (regardless of complications) and uncomplicated malaria (4/8 studies, 50%). The qualitative syntheses revealed that most studies found no difference in IL-5 levels between severe and non-severe malaria.
    CONCLUSIONS: The comprehensive review suggests that IL-5 levels are unchanged in patients with different levels of clinical severity of malaria and uninfected controls. Given the limited number of published studies on IL-5 levels in malaria, there is a need for additional research to determine the function of this cytokine in the pathogenesis of malaria.
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  • 文章类型: Case Reports
    背景:鉴于其大小和位置,肝脏是腹部创伤的第三大损伤器官。由于最近的进步,人们一致认为,非手术治疗是目前治疗血流动力学稳定患者的主要手段.然而,那些血流动力学不稳定的患者,通常表现为与主要血管病变相关的严重肝损伤,需要手术治疗.此外,即使在血流动力学稳定的情况下,主胆管的相关损伤也必须进行手术,从而在三级转诊肝胆胰中心设置中带来治疗挑战。
    方法:我们介绍了一名38岁的男性患者,该患者患有美国创伤外科协会的V级肝损伤和相关的门静脉右支和胆总管撕脱伤,由于挤压多发伤。病人被转介到最近的急诊医院,因为失血性休克,通过结扎右门静脉分支和右肝动脉进行损伤控制手术,和止血包装。之后,患者立即转诊至我们的三级肝胆胰中心.我们进行了解包,右肝切除术和肝空肠Roux-en-Y吻合术。术后第9天,患者出现了高输出吻合口胆漏,需要重新做胆管空肠吻合术。术后时期的标志是手术切口不完全的内脏,非手术通过负压处理。随访是最佳的,55个月没有并发症。
    结论:结论:目前的情况清楚地支持,通过适当的治疗管理,在严重的肝外伤与相关的血管和胆道损伤中取得了良好的结果。在三级转诊肝胆胰腺中心进行,其中逐步和复杂的手术方法是强制性的。
    BACKGROUND: Given its size and location, the liver is the third most injured organ by abdominal trauma. Thanks to recent advances, it is unanimously accepted that the non-operative management is the current mainstay of treatment for hemodynamically stable patients. However, those patients with hemodynamic instability that generally present with severe liver trauma associated with major vascular lesions will require surgical management. Moreover, an associated injury of the main bile ducts makes surgery compulsory even in the case of hemodynamic stability, thereby imposing therapeutic challenges in the tertiary referral hepato-bilio-pancreatic centers\' setting.
    METHODS: We present the case of a 38-year-old male patient with The American Association for the Surgery of Trauma grade V liver injury and an associated right branch of portal vein and common bile duct avulsion, due to a crush polytrauma. The patient was referred to the nearest emergency hospital and because of the hemorrhagic shock, damage control surgery was performed by means of ligation of the right portal vein branch and right hepatic artery, and hemostatic packing. Afterwards, the patient was referred immediately to our tertiary hepato-bilio-pancreatic center. We performed depacking, a right hepatectomy and Roux-en-Y hepaticojejunostomy. On the 9th postoperative day, the patient developed a high output anastomotic bile leak that required a redo of the cholangiojejunostomy. The postoperative period was marked by a surgical incision site of incomplete evisceration that was managed non-operatively by negative wound pressure. The follow-up was optimal, with no complications at 55 mo.
    CONCLUSIONS: In conclusion, the current case clearly supports that a favorable outcome in severe liver trauma with associated vascular and biliary injuries is achieved thru proper therapeutic management, conducted in a tertiary referral hepato-bilio-pancreatic center, where a stepwise and complex surgical approach is mandatory.
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  • 文章类型: Meta-Analysis
    背景:超氧化物歧化酶(SOD)在疟疾发病机理中的证据不一致。本研究旨在综合疟疾患者血SOD水平的证据,并确定血SOD水平与疟疾严重程度的关系。
    方法:研究方案为PROSPERO注册(CRD42023393806)。相关文章的搜索是在MEDLINE进行的,Embase,Scopus,奥维德,PubMed,谷歌学者。进行了(i)有和没有疟疾的个体之间的SOD血液水平不同以及(ii)重度和非重度疟疾个体之间的SOD血液水平不同的合成。使用随机效应模型汇总效应估计值(Cohen'sd)和95%置信区间(CI)。
    结果:从数据库搜索中检索到1874篇文章,其中28项研究纳入了综述。与没有疟疾感染的人相比,疟疾患者的血液SOD水平较低(P<0.01,科恩d:-2.06,95%CI:-2.99-(-1.14),I2:98.96%,2181例疟疾病例/1186例未感染病例)。重度和非重度疟疾患者的血SOD水平无差异(P=0.09,Cohen\'sd:-1.57,95%CI:-3.39-0.26),I2:96.02%,69例严重疟疾病例/256例非严重疟疾病例)。
    结论:与没有疟疾感染的患者相比,疟疾患者的血液SOD水平较低。需要进一步的研究来确定SOD在怀孕期间预防疟原虫感染的程度。
    Aims: The evidence of superoxide dismutase (SOD) in the pathogenesis of malaria is inconsistent. This study aimed to synthesize the evidence of blood levels of SOD in patients with malaria and determine the association of blood levels of SOD with the severity of malaria. Results: A total of 1874 articles were retrieved from database searches and 28 studies were included in the review. The blood levels of SOD were lower in individuals with malaria compared with those without malaria infection (p < 0.01, Cohen\'s d: -2.06, 95% CI: -2.99 to -1.14), I2: 98.96%, 2181 malaria cases/1186 uninfected cases). There were no differences in blood levels of SOD between severe and nonsevere malaria patients (p = 0.09, Cohen\'s d: -1.57, 95% CI: -3.39 to 0.26), I2: 96.02%, 69 severe malaria cases/256 nonsevere malaria cases). Innovation and Conclusion: The blood levels of SOD were lower in malaria patients compared with those without malaria infection. Further studies will be required to determine the extent to which SOD might prevent Plasmodium infections during pregnancy. Antioxid. Redox Signal. 40, 222-235.
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  • 文章类型: Review
    COVID-19疾病有不同的临床表现,从无症状到轻度症状到严重的肺炎表现,急性呼吸窘迫综合征,感染性休克,弥散性血管内凝血,和/或多器官衰竭。实时逆转录-聚合酶链反应是检测严重急性呼吸综合征-冠状病毒-2的金标准。在本研究中,我们旨在预测各种血液和生化指标对早期识别并发症和评估疾病严重程度的意义.总共将病例分为两个研究组,即,根据临床表现,严重和非严重。在210例病例中,非重症186例(88.5%),重症24例(11.5%)。在研究的各种血液学和生化标志物中,血红蛋白,白细胞总数,中性粒细胞计数,淋巴细胞计数,中性粒细胞与淋巴细胞的比率,血小板与淋巴细胞比率,白蛋白,乳酸脱氢酶,C反应蛋白,铁蛋白,D-二聚体,发现和白细胞介素-6具有P<0.05,并且与疾病的严重程度显着相关。
    COVID-19 disease has variable clinical presentations, ranging from asymptomatic to mild symptoms to severe manifestation with pneumonia, acute respiratory distress syndrome, septic shock, disseminated intravascular coagulation, and/or multiple organ failure. The real-time reverse transcription-polymerase chain reaction is gold standard test for severe acute respiratory syndrome-coronavirus-2 detection. In the present study, we aimed to predict the significance of various hematological and biochemical markers for early identification of complications and assessing the severity of the disease. A total of cases were divided into two study groups, namely, severe and nonsevere based on clinical presentation. Out of 210 cases, 186 (88.5%) cases were nonsevere and 24 (11.5%) cases were severe. Among various hematological and biochemical markers studied, hemoglobin, total leukocyte count, neutrophil count, lymphocyte count, neutrophil-to-lymphocyte ratio, platelet-to-lymphocyte ratio, albumin, lactate dehydrogenase, C-reactive protein, ferritin, D-dimer, and interleukin-6 are found to have P < 0.05 and significantly correlated with the severity of disease.
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  • 文章类型: Journal Article
    未经批准:关于前后脊柱融合术(APSF)是否存在争议,而不是后路脊柱融合术(PSF),为治疗严重的胸部青少年特发性脊柱侧凸(AIS)提供益处。本系统评价和荟萃分析比较(1)Cobb角矫正,(2)并发症和再手术率,(3)肺功能,(4)熔接段数,和5)两组患者报告的结果测量(PROMs)。
    UNASSIGNED:搜索电子数据库以确定符合以下纳入标准的研究:比较研究(3级或以上),严重的胸曲线(≥70°),年龄≤16岁,AIS病因,≥95%患者群体的Lenke1-4曲线和随访≥1年。使用GRADE和MINORS标准对文献进行质量和偏倚分级。
    未经评估:纳入了8项研究,由等级定义为低或中等水平证据。三项研究显示APSF组的曲线校正效果更好;然而,meta分析显示,组间曲线校正无显著差异(95%CI-3.45~12.96,P=0.26).APSF组并发症较多,无统计学意义(95%CI0.53-3.39,P=0.54;I2=0%,P=0.78)。两组都没有重新操作。两项研究报告了肺功能;一项在APSF组中显示出更好的功能,PSF组中其他功能更好。一项研究表明,APSF组中融合的节段较少,然而,在meta分析中没有观察到显著性(95CI-1.65-0.31,P=0.18).三项研究报告了PROM,组间没有差异。
    UNASSIGNED:已发现APSF和PSF具有可比的结果。目前的证据不能支持关于对曲线校正的影响的未来实践指南的建议,并发症,重新运营,肺功能或PROMs。
    未经证实:III级,三级研究的系统评价。
    UNASSIGNED: Debate exists as to whether anterior-posterior spinal fusion (APSF), rather than posterior-only spinal fusion (PSF), provides benefit for treating severe thoracic adolescent idiopathic scoliosis (AIS). This systematic review and meta-analysis compare (1) Cobb angle correction, (2) complication and reoperation rate, (3) pulmonary function, (4) number of fused segments, and 5) patient-reported outcome measures (PROMs) in both groups.
    UNASSIGNED: Electronic databases were searched to identify studies that met the following inclusion criteria: comparative studies (level 3 or above), severe thoracic curves (≥ 70°), age ≤ 16, AIS aetiology, Lenke 1-4 curves and follow-up ≥ 1 year for ≥ 95% of patient population. Literature was graded for quality and bias using GRADE and MINORS criteria.
    UNASSIGNED: Eight studies were included, defined by GRADE as low or moderate level evidence. Three studies showed superior curve correction in the APSF group; however, the meta-analysis showed no significant difference in curve correction between groups (95% CI - 3.45-12.96, P = 0.26). There were more complications in the APSF group, without statistical significance (95% CI 0.53-3.39, P = 0.54; I 2 = 0%, P = 0.78). There were no re-operations in either group. Two studies reported pulmonary function; one showed better function in the APSF group, the other better function in the PSF group. One study showed fewer fused segments in the APSF group, however, no significance was observed in the meta-analysis (95%CI - 1.65-0.31, P = 0.18). Three studies reported PROMs with no differences reported between groups.
    UNASSIGNED: APSF and PSF have been found to have comparable results. The present evidence cannot support recommendations for guidelines on future practice with regards to effect on curve correction, complications, re-operations, pulmonary function or PROMs.
    UNASSIGNED: Level III, Systematic review of Level-III studies.
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  • 文章类型: Journal Article
    背景:冠状病毒病(COVID-19)患者表现出不同的肝功能损害模式,根据越来越多的证据。
    目的:在本研究中,我们试图对重度和非重度COVID-19患者的肝脏检查参数进行全面分析.
    方法:我们对已发表的肝脏表现进行了荟萃分析,并描述了COVID-19的肝脏损伤。我们搜索了PubMed,谷歌学者,Embase,科克伦图书馆,medRxiv,bioRxiv,和三个中国电子数据库,截至2020年4月18日,符合Meta分析的首选报告项目。我们使用固定或随机效应模型分析了按COVID-19严重程度分层的肝脏化学汇总数据。
    结果:对56项研究的荟萃分析,包括11052名患者,发现重症COVID-19病例的合并平均丙氨酸氨基转移酶(ALT)为35.9IU/L,而非重症COVID-19病例为27.3IU/L。严重病例的平均天冬氨酸氨基转移酶(AST)水平为44.3IU/L,而非严重病例为27.9IU/L。此外,无论疾病严重程度如何,AST水平通常高于ALT水平。严重病例倾向于具有比非严重病例更高的γ-谷氨酰转移酶水平但更低的白蛋白水平。
    结论:重度COVID-19更可能与肝脏检查结果异常有关。密切监测肝脏化学可以帮助早期发现疾病进展。
    BACKGROUND: Coronavirus disease (COVID-19) patients exhibit different patterns of liver impairment, according to growing evidence.
    OBJECTIVE: In this study, we sought to provide a comprehensive analysis of liver test parameters in patients with severe and non-severe COVID-19.
    METHODS: We performed a meta-analysis of published liver manifestations and described the liver damage in COVID-19. We searched PubMed, Google Scholar, Embase, Cochrane Library, medRxiv, bioRxiv, and three Chinese electronic databases through April 18, 2020, in accordance with the Preferred Reporting Items for Meta-Analyses. We analyzed pooled data on liver chemistries stratified by COVID-19 severity using a fixed or random-effects model.
    RESULTS: A meta-analysis of 56 studies, including 11052 patients, found that the pooled mean alanine aminotransferase (ALT) in severe COVID-19 cases was 35.9 IU/L whereas in non-severe COVID-19 cases was 27.3 IU/L. Average aspartate aminotransferase (AST) levels were 44.3 IU/L in severe cases compared to 27.9 IU/L in non-severe cases. In addition, AST levels are often higher than ALT levels regardless of disease severity. The severe cases tended to have a higher gamma-glutamyltransferase level but a lower albumin level than the non-severe cases.
    CONCLUSIONS: Severe COVID-19 was more likely to be associated with abnormal liver test results. Monitoring liver chemistry closely can help detect disease progression early.
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