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  • 文章类型: Journal Article
    Alder黄(ALY)植原体(16SrV-C)与ALY有关,欧洲的几种Alnus(al木)和北美的A.rubra的一种疾病。在所有受影响的物种中,症状相似。然而,潜伏感染很常见。ALY植物质包括不同的菌株,这些菌株可能偶尔传播给葡萄树,从而导致一些葡萄树黄色疾病。在目前的研究中,视觉症状评估和基于PCR的方法,使用通用和群体特异性的植原体引物,以更新和扩展知识的发生,影响,在意大利南部的Basilicata和Campania地区,下降且无症状的a.glutinosa和A.cordata树的ALY植物血浆的遗传多样性。在所检查的80%的al木中检测到ALY植物质。在有症状的树上,没有观察到其他疾病原因。超过一半的测试植物支原体阳性的al木被证明是潜在感染的。在意大利南部新记录的ALY植物质菌株中,几乎在所检查的基因中都观察到了相当大的遗传变异。这些包括16SrRNA,16S/23SrDNA间隔区,核糖体蛋白rpsV(rpl22)和rpsC(rps3),地图,imp,和GroEL基因。在图谱基因序列水平上鉴定出11种新的基因型。然而,观察到的遗传差异与植物宿主物种无关,地理起源,和受感染的秃木表现出的症状。此外,这项研究表明,ALY植原体比以前认为的更广泛。
    Alder yellows (ALY) phytoplasma (16SrV-C) is associated with ALY, a disease of several Alnus (alder) species in Europe and A. rubra in North America. In all affected species, the symptoms are similar. However, latent infections are common. ALY phytoplasma includes different strains which may be occasionally transmitted to grapevines leading to some grapevine yellows diseases. In the current study, visual symptom assessment and PCR-based methods using universal and group-specific phytoplasma primers were used to update and extend knowledge on the occurrence, impact, and genetic diversity of ALY phytoplasma in declining and non-symptomatic A. glutinosa and A. cordata trees in the Basilicata and Campania regions of southern Italy. ALY phytoplasma was detected in 80% of alder trees examined. In symptomatic trees, no other cause of disease was observed. More than half of alder trees that tested phytoplasma-positive proved to be latently infected. A considerable genetic variability was observed among the newly recorded ALY phytoplasma strains in southern Italy in almost of the genes examined. These included 16S rRNA, 16S/23S rDNA spacer region, ribosomal protein rpsV (rpl22) and rpsC (rps3), map, imp, and groEL genes. Eleven new genotypes were identified at map gene sequence level. However, the genetic differences observed were not related to plant host species, geographical origin, and symptoms shown by infected alder trees. Also, this study indicates that ALY phytoplasma is more widespread than previously thought.
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    文章类型: Journal Article
    为减轻全球疟疾负担,特别是儿童和撒哈拉以南非洲的疟疾负担,已经做出了若干努力。该研究旨在评估疟疾控制活动对尼日利亚南部三级医院儿童疟疾趋势的影响。
    对所有疟疾诊断的病例记录进行回顾性审查,包括住院病例,门诊病人,急诊室,于2006年1月至2018年12月在哈考特港大学教学医院儿科就诊.
    在过去的12年中,诊断出了41,863例疟疾病例,每年的诊断和入院人数有所下降,从2006年到2018年。疟疾总入院人数为578,(44.5/年),严重疟疾发病率为1.26%,有164例疟疾死亡病例,年平均为12。疟疾寄生虫血症患儿的死亡原因为75例严重贫血(45.7%),14例低血糖(8.5%),17岁的脑型疟疾(10.4%),和其他共病的虚脱,22(13.4%)。36名儿童(22%)出现抽搐,入院后不久死亡,与误吸和呼吸衰竭的复合诊断。
    儿童疟疾疾病逐渐减少,入场,和死亡,尽管这是慢于预期的基于努力和战略的尼日利亚政府和各种组织。
    UNASSIGNED: Several efforts have been put in place to reduce the global burden of malaria especially in children and in sub-Saharan Africa. The study aimed to evaluate the impact of malaria control activities on the trend of childhood malarial diseases at a tertiary hospital in South-south Nigeria.
    UNASSIGNED: A retrospective review of the case records of all malaria diagnoses including in-patient, out-patient, and emergency room, seen in the Department of paediatrics at the University of Port Harcourt Teaching Hospital from January 2006 to December 2018 was conducted.
    UNASSIGNED: There were 41, 863 malaria cases diagnosed over the 12 years with a decline in yearly diagnosis and admissions, from the year 2006 through 2018. Total malaria admissions were 578, (44.5/ year), giving a severe malaria incidence of 1.26%, and there were 164 malaria death cases, with a yearly average of 12. The causes of death in the children with malarial parasitaemia were severe anaemia in 75 (45.7%), hypoglycaemia in 14 (8.5%), cerebral malaria in 17 (10.4%), and prostration with other co-morbidities, 22 (13.4%). Thirty-six children (22%) were convulsing and died soon after admission, with a compounding diagnosis of aspiration and respiratory failure.
    UNASSIGNED: There is a gradual reduction in childhood malaria disease, admission, and death, though this is slower than anticipated based on efforts and strategies put in place by the Nigerian government and various organizations.
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  • 文章类型: Journal Article
    目的:终末期肾脏疾病可能是一个缓慢的过程,并且对于足够的事件进行必要的随访可能具有挑战性。因此,替代肾脏终点,例如估计的肾小球滤过率(eGFR)斜率可能对评估心血管试验中的肾脏有吸引力,尤其是心力衰竭(HF)。
    结果:eGFR斜率可以在较短的随访期内产生有益的结果,降低了2型错误的风险,与其他替代肾脏终点(eGFR下降≥40%或肌酐加倍)相比,对eGFR变化的敏感性较低。然而,eGFR斜率有其急性效应的局限性,坡度计算/报告中的异质性,和线性的偏差。eGFR斜率是肾脏终点,可能非常适合HF试验。需要交叉合作的指南建议来优化eGFR斜率作为HF患者肾脏终点的使用。
    OBJECTIVE: End stage kidney disease can be a slow process and it may be challenging to achieve required follow-up for sufficient events. Therefore, a surrogate kidney endpoint, such as estimated glomerular filtration rate (eGFR) slope maybe attractive to assess the kidney in cardiovascular trials, especially heart failure (HF).
    RESULTS: eGFR slope can generate informative results in a shorter follow-up period, has decreased risk of type-2 error, and is less sensitive to eGFR shifts compared with other surrogate kidney endpoints (eGFR decline≥40% or doubling creatinine). However, eGFR slope has its limitations with acute effects, heterogeneity in slope calculation/reporting, and deviations from linearity. eGFR slope is a kidney endpoint which may be well-suited for HF trials. Cross-collaborated guideline recommendations are needed to optimize the use of eGFR slope as a kidney endpoint in patients with HF.
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  • 文章类型: Journal Article
    PhoenixdactyliferaL.是美国西南部经济和美学上重要的树木。在美国,大约有4900公顷的红枣被商业种植用于其可食用水果,包括约1600公顷的尤马地区和亚利桑那州的海德河谷(美国农业部,2023年)。2022年10月,在凤凰城都会区的三棵枣树上观察到了严重的腐烂。早期症状是棕色斑点,变成黑色的烧焦外观,沿着叶根和轴延伸,导致下部叶状体枯萎,干燥,和折叠。随着疾病的发展,末端芽坏死并最终塌陷。从马铃薯葡萄糖琼脂(PDA)上的坏死叶病变中分离出一种快速生长的真菌,该真菌最初是白色的,具有丰富的蓬松的气生菌丝体,在12小时光照下在22-25℃生长一周后逐渐变成深色橄榄质。在水琼脂中的松针上形成的分生孢子为黑色和球形。分生孢子细胞呈透明和圆柱形。分生孢子显示出厚壁,卵形至椭球形态,最初出现透明和无盐,过渡到1-纵隔,呈深棕色,条纹外观,测量19.6至23.0μmx10.3至12.2μm(n=20)。对于分子鉴定,从两个分离株的菌丝体中提取基因组DNA。使用引物ITS5/ITS4对rDNA和β-微管蛋白(TUB)基因的内部转录间隔区(ITS)区域的部分DNA序列进行扩增和测序(White等人。1990)和Bt2a/Bt2b(Glass和Donaldson1995)。将所得的ITS(PP346666)和TUB(PP372690)序列存入GenBank。对ITS和TUB序列的BLASTn搜索显示,与希腊引起棕榈腐烂的Neodeightoniaphoenicum菌株的序列(JX456475,KF766198和OK338070)具有99%至100%的相似性(Ligoxigakis等人。2013),中国侏儒枣树叶斑病(张和宋2022),和前CBS122528型文化。基于这些形态和分子数据,该真菌被鉴定为N.phoenicum。在温室中进行了两次致病性测试(每日温度:18〜30oC,相对湿度:45%〜95%)在4种健康的1岁枣树植物上。通过用针刺破叶片的表皮(每个叶柄约20个刺),并从4天大的PDA真菌培养物中接种琼脂圆盘,从而使每株植物的3个较老叶片的叶柄受伤。通过将普通PDA放置在叶柄的伤口上,对照由4株模拟接种的植物组成。接种五周后,所有接种的叶子都显示出黑色烧焦的症状,叶柄腐烂,和叶子坏死,与在原始患病树上观察到的症状相同,而对照组没有任何症状。将真菌重新分离并通过形态学确认为N.phoenicum。据报道,N.phoenicum会导致叶斑病,拍摄枯萎病,在世界各地的不同棕榈品种上,茎和根腐烂以及黑色烧焦。然而,根据我们的知识,这是在亚利桑那州首次报道的由N.phoenicum引起的黑色烧焦和腐烂病。黄牛的可能传播可能具有重大的经济影响,需要通过适当的疾病管理措施立即予以关注。
    Phoenix dactylifera L. is an economically and aesthetically important tree in the southwestern US. Approximately 4900 ha of dates are commercially grown for its edible fruit in the US, including about 1600 ha in the Yuma area and the Hyder Valley of Arizona (USDA, 2023). In October 2022, a severe rot was observed on three date palms in the Phoenix Metropolitan area. Early symptoms were brown spots that turned to a black scorch appearance extending along the leaf base and rachis, leading to the lower fronds\' wilting, drying, and folding. As the disease progressed upwards, the terminal bud became necrotic and eventually collapsed. Isolation from the necrotic leaf lesions on a potato dextrose agar (PDA) consistently yielded a fast-growing fungus that was initially white with abundant fluffy aerial mycelium, which gradually turned dark olivaceous after growing at 22-25oC under 12 h light for a week. Pycnidial conidiomata formed on pine needles in a water agar were black and globose. Conidiogenous cells were hyaline and cylindrical. The conidia exhibited a thick-walled, ovoid to ellipsoid morphology, initially appearing hyaline and aseptate and transitioned to 1-septate with a dark brown, striated appearance, measuring 19.6 to 23.0 μm x 10.3 to 12.2 µm (n = 20). For molecular identification, genomic DNA was extracted from the mycelia of two isolates. Partial DNA sequences of the internal transcribed spacer (ITS) region of rDNA and β-tubulin (TUB) gene were amplified and sequenced using primers ITS5/ITS4 (White et al. 1990) and Bt2a/Bt2b (Glass and Donaldson 1995). The resulting sequences of ITS (PP346666) and TUB (PP372690) were deposited in the GenBank. A BLASTn search of ITS and TUB sequences revealed a 99 to 100% similarity with the sequences (JX456475, KF766198, and OK338070) of Neodeightonia phoenicum strains causing palm rot in Greece (Ligoxigakis et al. 2013), leaf spot on pygmy date palm in China (Zhang and Song 2022), and an ex-type CBS 122528 culture. Based on these morphological and molecular data, the fungus was identified as N. phoenicum. A pathogenicity test was conducted twice in a greenhouse (daily temperatures:18 ~ 30 oC, relative humidity: 45% ~ 95%) on 4 healthy 1-year-old date palm plants. The petioles of 3 older leaves per plant were wounded by pricking the epidermis of the leaf with a needle (ca 20 pricks per petiole) and inoculated with agar discs from a 4-day-old PDA culture of the fungus. The control consisted of 4 mock-inoculated plants by placing plain PDA on the wounds of leaf petioles. Five weeks after inoculation, all the inoculated leaves showed symptoms of black scorch, petiole rot, and leaf necrosis, which were the same as those symptoms observed on the original diseased trees, while the controls did not show any symptoms. The fungus was re-isolated and confirmed as N. phoenicum by morphology. N. phoenicum has been reported to cause leaf spot, shoots blights, stalk and root rots as well as black scorch on different palm species all over the world. However, to our knowledge, this is the first report of N. phoenicum causing black scorch and rot disease in Arizona. The possible spread of N. phoenicum could have a significant economic impact and requires immediate attention through suitable disease management initiatives.
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  • 文章类型: Journal Article
    患有镰状细胞病(SCD)的儿童可能会遇到认知困难,包括处理速度减慢。因此,我们调查了处理速度是否随时间变化。从1992年至2001年,103名3-16岁的SCD参与者(n≤8.99=45;n≥9.00=58)完成了认知评估。MRI可用于54名参与者。在1992年至2002年期间,58名与会者同意进行一到两次进一步评估。使用线性混合效应建模的重复测量回归确定了处理速度指数(PSI)的纵向变化,检查年龄(连续变量)和时间点(即,评估1或3)和控制MRI梗塞状态(即,没有梗塞,无声梗塞,或中风)。首次评估时年龄≤8.99和≥9.00的患者出现PSI下降。处理速度编码子测试的下降最为突出,时间点和年龄之间有显著的相互作用,t(31)=2.64,p=0.01。这种下降可能反映了发育迟缓,可能是由于疾病进展,处理速度提高较慢。虽然SCD治疗有了显著的改善,主要在高收入国家,处理速度仍然是目标;因此,结合处理速度的临床监测可能有助于识别延迟并允许早期干预。
    Children with sickle cell disease (SCD) may experience cognitive difficulties, including slowed processing speed. Thus, we investigated if processing speed changes over time. From 1992-2001, 103 participants with SCD aged 3-16 years (n ≤ 8.99 = 45; n ≥ 9.00 = 58) completed cognitive assessments. MRI was available for 54 participants. Between 1992-2002, 58 participants consented to one or two further assessments. A repeated measures regression using linear mixed-effects modelling determined longitudinal changes in processing speed index (PSI), examining the interaction between age (continuous variable) and timepoint (i.e., assessment 1 or 3) and controlling for MRI infarct status (i.e., no infarct, silent infarct, or stroke). Those aged ≤8.99 and ≥9.00 at first assessment experienced PSI decline. Declines were most prominent for the processing speed coding subtest, with a significant interaction between timepoint and age, t(31) = 2.64, p = 0.01. This decline may reflect a developmental delay, likely due to disease progression, with slower improvements in processing speed. Although there have been significant improvements in SCD treatments, mostly in high-income countries, processing speed still remains a target; thus, incorporating clinical monitoring of processing speed may help identify delay and allow for early intervention.
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  • 文章类型: Journal Article
    儿童性别比例表示0至6岁年龄组中女孩与男孩的比例。它是任何人口的重要指标,最重要的是女童在社会中的地位。该研究试图以定性的方式研究儿童性别比下降背后的原因。
    我们在不同年龄段进行了5次焦点小组讨论和12次深度访谈的定性研究,孕妇,和其他股东。与参与者进行了半结构化的开放式访谈指南,内容涉及儿童性别比下降的原因以及使其正常化的措施。经过专题分析,主要主题和子主题是在协商一致后选择的。
    研究表明,男性儿童偏好是理论部分中确定的主要主题,女性脆弱性是次要主题,社会经济地位,识字,文化,种姓和宗教作为子主题。作为第二个孩子,女性孩子偏好的主题也出现了,小心,深情,和文化因素作为次主题。在建议/干预方面,教育,咨询,确定了政府政策和媒体以及有关性别确定和女性致死的建议。
    儿童性别比例的下降应被视为一个积极的社会问题,从而更多地关注女性的提升和对父权制性质问题的启发,减少文化/宗教信仰。
    UNASSIGNED: Child sex ratio signifies the proportion of girls compared with boys in 0 to 6 years of age group. It is an important indicator for any population and most significantly about the status of the girl child in the society. The study tried to approach in a qualitative manner to study the rationale behind the declining of child sex ratio.
    UNASSIGNED: We conducted a qualitative study using five focus group discussions and 12 in-depth interviews among various age groups, pregnant women, and other stake holders. The participants were approached with a semi-structured open-ended interview guide regarding the rationale of declined child sex ratio and measures to normalize it. After a thematic analysis, main themes and subthemes were selected after consensual agreement.
    UNASSIGNED: The study showed that male child preference is the main theme identified in the rationale part with subthemes of female vulnerability, socioeconomic status, literacy, cultural, and caste and religion as subthemes. The theme of female child preference also came up with as second child, care taking, affectionate, and cultural factors as subthemes. In the area of suggestions/interventions, education, counseling, government policies and media along with suggestions regarding sex determination and female feticide were identified.
    UNASSIGNED: The decline in child sex ratio should be taken as an active social issue thus focusing more into female upliftment and enlightening into the issues of patriarchal nature, with reduction of cultural/religious beliefs.
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  • 文章类型: Journal Article
    目的:新的证据表明,人的肺和肾之间有密切的关系。这项研究评估了肾功能下降是否与大规模社区队列中的肺功能加速下降有关。
    方法:共有10,028名前瞻性Ansung-Ansan队列受试者符合与肾功能下降相关的肺功能变化的纵向分析(肾小球滤过率<60ml/min/1.73m2)。采用Logistic回归分析评价基线肾功能下降的相关因素,和线性混合模型比较了倾向评分匹配(PSM)后有肾功能下降和无肾功能下降的参与者的肺功能变化.
    结果:在基线时,有和没有肾功能下降的受试者表现出明显的特征,与肾功能下降相关的因素是年龄,基线强制肺活量,高血压,和白细胞(WBC)计数。1:4PSM的年龄,性别,身体质量指数,吸烟状况表明,肾功能下降和正常的患者之间,高血压患者的比例和白细胞计数有所不同。在PSM人群中,肾功能下降的患者在第一秒用力呼气量(FEV1)的下降幅度大于无肾功能下降的患者(p=0.0402);然而,当高血压和白细胞计数进一步匹配时,发现这些差异并不明显(p=0.0807).
    结论:我们的研究结果表明,在以社区为基础的普通人群中,肾功能下降与肺功能迅速下降没有直接关系。
    OBJECTIVE: Emerging evidence suggests that there is a close relationship between the human lung and kidney. This study evaluated whether decreased renal function was associated with accelerated pulmonary function decline in a large-scale community-based cohort.
    METHODS: A total of 10,028 subjects of the prospective Ansung-Ansan cohort were eligible for the longitudinal analysis of changes in pulmonary function associated with decreased renal function (glomerular filtration rate <60 ml/min/1.73 m2). Logistic regression analysis was performed to evaluate factors associated with decreased baseline renal function, and a linear mixed model compared changes in pulmonary function in participants with and without decreased renal function after propensity score matching (PSM).
    RESULTS: At baseline, subjects with and without decreased renal function showed distinct characteristics, and the factors associated with decreased renal function were age, baseline forced vital capacity, hypertension, and white blood cell (WBC) count. A 1:4 PSM of age, sex, body mass index, and smoking status showed that the proportion of those with hypertension and the WBC count differed between the patients with decreased and normal renal function. In the PSM population, those with decreased renal function had a greater decline in forced expiratory volume in the first second (FEV1) than those without (p=0.0402); however, these differences were not found to be evident when hypertension and WBC count were further matched (p=0.0807).
    CONCLUSIONS: The results of our study demonstrated that decreased renal function was not directly associated with the rapid decline in pulmonary function in a community-based general population setting.
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  • 文章类型: Journal Article
    这项研究的主要目标是确定北马其顿共和国沙门氏菌病的发展趋势,并确定北马其顿共和国沙门氏菌病的动态指数和下降/上升速度。该研究涵盖了从01.01.2012到31.12.2022的时期。用于实施本研究的数据来自北马其顿共和国公共卫生研究所。该研究包括2012年至2022年患有沙门氏菌病的2711名受试者。使用以下统计工作方法:线性趋势,具有恒定基数的动态索引,具有可变基数的动态索引(链索引),下降率,和增长率。研究结果表明,在2012-2022年期间,沙门氏菌病的患者数量最高(n=373)和发病率最高(18/100000)在2018年登记,而在2020年最低(n=119,I=5.8/100000)。从线性趋势值,可以得出结论,北马其顿共和国的沙门氏菌病呈下降趋势。与2014年相比,2015年北马其顿共和国沙门氏菌病的增幅最大,为71%。与2019年相比,北马其顿共和国的沙门氏菌病下降幅度最大的是2020年的48%。从研究中,可以得出结论,食品经营者和制造商正在遵守HACCP食品安全控制系统的程序,导致沙门氏菌病可能减少。
    The main goals of this research are to determine the developmental tendency of salmonellosis in the Republic of North Macedonia and to determine the index of dynamics and the rate of decline/increase of salmonellosis in the Republic of North Macedonia. The research covers the period from 01.01.2012 until 31.12.2022. The data used to implement this study were obtained from the Institute of Public Health of the Republic of North Macedonia. The research included 2711 subjects who were sick with salmonellosis from 2012 to 2022. The following statistical methods of work are used: linear trend, dynamic index with a constant base, dynamic index with a variable base (chain index), rate of decline, and rate of increase. The results of the study suggest that in the period 2012-2022, the highest number of patients (n=373) and the highest incidence (18/100000) of salmonellosis were registered in 2018, and the lowest in 2020 (n=119, I=5.8/100000). From the linear trend values, it can be concluded that salmonellosis in the Republic of North Macedonia shows a decreasing tendency. The biggest increase in salmonellosis in the Republic of North Macedonia was in 2015 by 71% compared to 2014. The biggest decrease in salmonellosis in the Republic of North Macedonia was in 2020 by 48% compared to 2019. From the study, it can be concluded that food operators and manufacturers are observing the procedures of the HACCP control system for food safety, leading to a possible decrease in salmonellosis.
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  • 文章类型: Observational Study
    背景:粘多糖贮积症(MPS)II是一种罕见的,X连锁溶酶体贮积病。大约三分之二的患者有中枢神经系统受累,一些表现为进行性认知障碍(神经病性疾病)。MPSII患者的认知和适应功能的自然史尚不明确。这两年,prospective,观察性研究评估了年龄≥2岁和<18岁的MPSII男孩的神经发育轨迹。
    结果:总体而言,55例患者入组。在基线,平均(标准差[SD])年龄为5.60(3.32)岁;所有患者均接受静脉注射艾杜磺酶。使用差异能力量表评估认知和适应功能,第二版(DAS-II)一般概念能力(GCA)和Vineland自适应行为量表,第二版(VABS-II)自适应行为综合(ABC)评分,分别。基线平均(SD)DAS-IIGCA和VABS-IIABC评分分别为78.4(19.11)和83.7(14.22),分别,表明低认知功能和中度低适应行为。超过24个月,观察到DAS-IIGCA(-3.8[12.7])和VABS-IIABC(-2.0[8.07])的平均(SD)评分适度恶化.DAS-IIGCA分数的变化差异很大,和数据表明存在四个潜在的患者亚组:(1)具有明显的早期损害和随后的快速下降的患者,(2)患者有明显的早期损害,然后稳定,(3)患者轻度早期损害,然后稳定,和(4)患者无损伤谁保持稳定。亚组分析显示,在基线时年龄<7岁的患者中,DAS-IIGCA评分比基线降低的数值更大(与年龄≥7岁的患者)和基线时DAS-IIGCA评分≤70的患者(与评分>70);组间差异无统计学意义。对于VABS-IIABC评分的个体变化,未发现明确的亚组或模式。总的来说,49例患者(89.1%)报告≥1次不良事件(AE),9例患者(16.4%)报告严重AE。
    结论:一些MPSII患者的认知能力迅速下降,而其他人在最初下降后保持相对稳定。这些见解为更详细地分析不同的患者亚组提供了基础,这可能会增强对影响MPSII认知和适应功能的因素的定义和理解。
    背景:ClinicalTrials.gov,NCT01822184。回顾性注册:2013年4月2日。
    BACKGROUND: Mucopolysaccharidosis (MPS) II is a rare, X-linked lysosomal storage disease. Approximately two-thirds of patients have central nervous system involvement with some demonstrating progressive cognitive impairment (neuronopathic disease). The natural history of cognitive and adaptive function in patients with MPS II is not well-defined. This 2-year, prospective, observational study evaluated the neurodevelopmental trajectories of boys with MPS II aged ≥ 2 years and < 18 years.
    RESULTS: Overall, 55 patients were enrolled. At baseline, mean (standard deviation [SD]) age was 5.60 (3.32) years; all patients were receiving intravenous idursulfase. Cognitive and adaptive function were assessed using the Differential Ability Scales, Second Edition (DAS-II) General Conceptual Ability (GCA) and the Vineland Adaptive Behavior Scales, Second Edition (VABS-II) Adaptive Behavior Composite (ABC) scores, respectively. Baseline mean (SD) DAS-II GCA and VABS-II ABC scores were 78.4 (19.11) and 83.7 (14.22), respectively, indicating low cognitive function and moderately low adaptive behavior. Over 24 months, modest deteriorations in mean (SD) scores were observed for DAS-II GCA (-3.8 [12.7]) and VABS-II ABC (-2.0 [8.07]). Changes in DAS-II GCA scores varied considerably, and data suggested the existence of four potential patient subgroups: (1) patients with marked early impairment and rapid subsequent decline, (2) patients with marked early impairment then stabilization, (3) patients with mild early impairment then stabilization, and (4) patients without impairment who remained stable. Subgroup analyses revealed numerically greater DAS-II GCA score reductions from baseline in patients aged < 7 years at baseline (vs. those aged ≥ 7 years) and in patients with DAS-II GCA scores ≤ 70 at baseline (vs. those with scores > 70); between-group differences were nonsignificant. No clear subgroups or patterns were identified for individual changes in VABS-II ABC scores. In total, 49 patients (89.1%) reported ≥ 1 adverse event (AE) and nine patients (16.4%) reported serious AEs.
    CONCLUSIONS: Some patients with MPS II had rapid declines in cognitive ability, whereas others remained relatively stable after an initial decline. These insights provide a basis for more detailed analyses of different patient subgroups, which may enhance the definition and understanding of factors that influence cognitive and adaptive function in MPS II.
    BACKGROUND: ClinicalTrials.gov, NCT01822184. Registered retrospectively: April 2, 2013.
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  • 文章类型: Journal Article
    社会处方(SP)是全民个性化护理的一部分,英国国家卫生服务机构的每个人都可以使用。然而,新出现的证据表明,在社会处方方面存在准入差异。这项研究旨在调查使用初级保健记录访问和分析社会处方数据的可行性。我们的次要目的是比较被提供转诊的患者的特征,提及或拒绝推荐社会处方,以探索获得社会处方方面可能的不平等。
    患者记录(n=3086)是从英格兰西北部的11个GP实践中提取的,以供接受,提供并拒绝社会处方推荐。收集的患者人口统计数据包括性别,年龄,种族,精神和身体健康诊断。将社会处方转诊中的患者特征与总体实践人群进行了比较(来自英国公共卫生的实践信息)。按组比较转诊率和下降率(例如男性/女性下降率)。
    GP转诊数据显示,对更广泛的健康决定因素的记录不一致。患者年龄,持续记录性别和身心健康状况.其他变量(婚姻状况,口译员需要,教育,残疾,性取向,非英语语言,国籍)仅零星记录,无法用于分析。转诊模式的做法各不相同。我们的初步发现确定了年轻年龄组和亚洲人的转诊不足,在有身体健康诊断的个体中,转诊率下降的幅度更高。
    记录差异意味着许多患者因素不能用于识别社会处方推荐和下降的趋势并评估公平性。初级保健数据记录必须保持一致,以了解与更广泛的健康决定因素有关的SP转诊趋势和不平等。初步结果表明,一些患者群体在SP转诊中可能代表性不足,然而,这需要进一步调查。
    UNASSIGNED: Social prescribing (SP) is part of universal personalised care and available to everyone in the UK National Health Service. However, emerging evidence suggests access disparities in social prescribing. This study aimed to investigate the feasibility of using primary care records to access and analyse data on social prescribing. Our secondary aim was to compare characteristics of patients who are offered referral, referred to or decline referral for social prescribing to explore possible inequalities in access to social prescribing.
    UNASSIGNED: Patient records (n=3086) were extracted from 11 GP practices across Northwest England for accepted, offered and declined social prescribing referrals. Patient demographics collected included sex, age, ethnicity, mental and physical health diagnoses. Patient characteristics in social prescribing referrals were compared to the overall practice population (practice information from Public Health England). Referral and decline rates were compared by group (e.g. male/female decline rates).
    UNASSIGNED: GP referral data showed inconsistent recording of wider determinants of health. Patient age, sex and mental and physical health conditions were consistently recorded. Other variables (marital status, interpreter need, education, disability, sexual orientation, non-English language, nationality) were recorded only sporadically and could not be used for analysis. Practices varied in referral patterns. Our preliminary findings identified under-referring of younger age groups and Asians, and higher declined referrals among individuals with physical health diagnoses.
    UNASSIGNED: Recording discrepancies meant that many patient factors could not be used to identify trends in social prescribing referrals and declines and assess equity. Primary care data recording must be consistent to understand SP referral trends and inequalities relating to the wider determinants of health. Preliminary results suggest some patient groups may be underrepresented in SP referrals, however this requires further investigation.
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