Tertiary Healthcare

三级医疗保健
  • 文章类型: Journal Article
    本研究旨在评估病因,儿童惊厥性癫痫持续状态(CSE)的治疗和结局,并强调在这种情况下影响患者结局的因素。
    在一项跨越2020-2023年的回顾性研究中,苏丹卡布斯大学医院急诊科(ED)治疗的93名CSE儿童,分析了高依赖性病房(HDU)和重症监护病房(ICU)。出院时的改良Rankin量表用于确定CSE结果。
    在研究的93名儿童(平均年龄4.84±3.64岁)中,主要是阿曼(92.47%),发现了14种病因。其中,急性症状(37.7%)和发热状态(31.2%)是CSE的主要原因。地西泮一线治疗58例(67.44%),中位癫痫发作持续时间为45分钟。在60分钟内成功控制了71例(76.34%)的癫痫发作。在55.9%的病例中观察到恢复到基线,而死亡率和残疾分别为5.38%和38.7%,分别。对于17个案例,病因和持续时间显着影响患者的结果(P<0.05)。
    急性症状状态是CSE最常见的病因。CSE持续时间较长与较高的死亡率和神经系统残疾有关。及时和适当的CSE管理至关重要。此外,识别和治疗CSE的根本原因是减少其持续时间和改善患者预后的关键步骤。
    UNASSIGNED: This study aimed to evaluate the aetiology, management and outcomes of convulsive status epilepticus (CSE) in children and highlight the factors influencing patient outcomes in such cases.
    UNASSIGNED: In a retrospective study spanning the 2020-2023 period, 93 children with CSE treated at Sultan Qaboos University Hospital\'s emergency department (ED), high dependency unit (HDU) and intensive care unit (ICU) were analysed. The Modified Rankin Scale at discharge was used to determine CSE outcomes.
    UNASSIGNED: Among the 93 children studied (mean age 4.84 ± 3.64 years), predominantly Omani (92.47%), 14 aetiologies were noted. Of them, acute symptomatic (37.7%) and febrile status (31.2%) were the primary causes of CSE. Diazepam was administered as the first-line treatment in 58 (67.44%) cases, with a median seizure duration of 45 minutes. Successful seizure control was achieved in 71 (76.34%) cases within 60 minutes. A return to baseline was observed in 55.9% of cases, while mortality and disability were noted in 5.38% and 38.7% of cases, respectively. For 17 cases, aetiology and duration significantly impacted patient outcomes (P <0.05).
    UNASSIGNED: Acute symptomatic status is the most common aetiology of CSE. A longer duration of CSE is associated with higher mortality and neurological disability. Prompt and appropriate management of CSE is essential. Furthermore, identifying and treating the underlying cause of CSE is a crucial step in reducing its duration and improving patient outcomes.
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  • 文章类型: Journal Article
    背景:贫血是一个全球性的公共卫生问题,影响发达国家和发展中国家所有年龄段的人。贫血在糖尿病患者中很常见;然而,它往往是未经诊断和治疗。这项研究的主要目的是评估进入国家医院康提医疗单位的2型糖尿病患者贫血的患病率和相关因素。
    方法:描述性,本研究对入住康提国家医院(NHK)内科病房的2型糖尿病(T2DM)患者进行了横断面研究.他们进行了预先测试,面试官管理,采用连续抽样的结构化问卷。使用SPSS26输入和分析数据。
    结果:共252名糖尿病患者被纳入。T2DM患者贫血患病率为31.3%。男性和女性的相应值分别为34.2%和65.8%。糖尿病患者贫血的独立预测因素是年龄较大,女性性别,血糖控制不佳,糖尿病病程>5年,糖尿病肾病,视网膜病变,神经病,慢性肾脏病(CKD)≥3期,缺血性心脏病(IHD),外周血管疾病(PVD),糖尿病足溃疡(DFU)和阿司匹林的使用。这些与2型糖尿病患者的贫血患病率显着相关。多因素logistic回归分析显示,女性性别,年龄≥65岁,糖尿病病程>5年,血糖控制不佳,阶段≥3CKD,糖尿病肾病和视网膜病变与贫血的发生几率较大相关.
    结论:我们发现NHK内科病房中31.3%的T2DM患者以前未被诊断为贫血。糖尿病诊断期间的贫血筛查,保持血糖控制和提高患者的意识可以降低贫血的患病率,改善患者生活质量,并有可能减少微血管并发症。
    BACKGROUND: Anaemia is a global public health issue that impacts individuals of all ages in both developed and developing countries. Anaemia is common in patients with diabetes mellitus; however, it is often undiagnosed and untreated. The main aim of this study was to assess the prevalence and associated factors of anaemia in patients with type 2 diabetes mellitus admitting to a medical unit at National Hospital Kandy.
    METHODS: A descriptive, cross-sectional study was conducted in type 2 diabetes mellitus (T2DM) patients admitted to a medical ward at National Hospital Kandy (NHK). They were assessed with a pre-tested, interviewer-administered, structured questionnaire using consecutive sampling method. The data was entered and analyzed using SPSS 26.
    RESULTS: Total 252 patients with diabetes were included. The prevalence of anaemia in patients with T2DM was 31.3%. The corresponding values for males and females were 34.2% and 65.8% respectively. Independent predictors for anaemia among diabetic patients were older age, female gender, poor glycemic control, diabetes duration > 5 years, diabetic nephropathy, retinopathy, neuropathy, stage ≥ 3 chronic kidney disease (CKD), ischaemic heart disease (IHD), peripheral vascular disease (PVD), diabetic foot ulcers (DFU) and usage of aspirin. These were significantly associated with the prevalence anemia among patients with type 2 diabetes mellitus. Multivariate logistic regression analysis revealed that female gender, age ≥ 65 years, diabetic duration > 5 years, poor glycaemic control, stage ≥ 3 CKD, diabetic nephropathy and retinopathy were associated with greater odds for the presence of anaemia.
    CONCLUSIONS: We found that 31.3% T2DM patients in a medical ward at NHK had previously undiagnosed anaemia. Anaemia screening during diabetes diagnosis, maintaining glycaemic control and raising patient awareness can reduce anaemia prevalence, improve patient quality of life and potentially reduce microvascular complications.
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  • 文章类型: Journal Article
    建议将XpertMTB/RIF用于儿童结核病(TB)的诊断。我们确定了XpertMTB/RIF在儿童肺结核诊断中的表现。探讨影响XpertMTB/RIF阳性的儿童特征。从2013年至2019年,前瞻性招募了患有肺结核症状的15岁以下儿童。收集两份痰液/清晨胃吸出物标本进行涂片检查(荧光显微镜检查),XpertMTB/RIF,和培养[分枝杆菌生长指示管(MGIT)/Lowenstein-Jensen(LJ)培养基]。使用LJ和/或MGIT培养阳性作为参考标准来评估XpertMTB/RIF的诊断性能。灵敏度,用95%置信区间(CI)计算特异性.进行分层分析;P<0.05被认为具有统计学意义。在总共1727名入学儿童中,分析1674(97%),至少一个痰/胃吸出物样品的完整结果。XpertMTB/RIF在痰中的敏感性为68.5%,在胃抽吸物中的敏感性为53.6%,而两者的特异性均为99%。与涂片相比,灵敏度为68.5%。33.7%(P<.001)和53.6%14.5%;(P<.001)在痰和胃吸出物中,分别。XpertMTB/RIF的灵敏度为23.9%,决定作为参考标准。XpertMTB/RIF阳性受性别影响显著,年龄,营养状况,胸部X线异常,结核感染状况,和暗示结核病的症状。与涂片相比,XpertMTB/RIF作为一项前期测试可改善儿童肺结核的诊断,但敏感性欠佳。有必要在儿童中使用具有改进灵敏度的新型结核病诊断工具。
    我们评估了XpertMTB/RIF在儿童肺结核诊断中的表现,并探讨了影响XpertMTB/RIF阳性的特征。从年龄<15岁的儿童收集痰和或清晨胃吸出物标本,症状提示肺结核。这是通过涂片检查(荧光显微镜),XpertMTB/RIF,和培养(分枝杆菌生长指示管(MGIT)/Lowenstein-Jensen(LJ)培养基)。使用LJ和/或MGIT培养阳性作为参考标准来评估XpertMTB/RIF的诊断性能。在总共1727名入学儿童中,分析1674(97%),至少一个痰/胃吸出物样品的完整结果。XpertMTB/RIF在痰中的敏感性为68.5%,在胃抽吸物中的敏感性为53.6%,高于涂片,特异性为99%。XpertMTB/RIF的敏感性为23.9%,决定以TB作为参考标准。XpertMTB/RIF阳性受性别影响,年龄,营养状况,胸部X线异常,结核感染状况,和暗示结核病的症状。与涂片相比,XpertMTB/RIF作为一种前期测试可改善儿童肺结核的诊断,但敏感性欠佳。有必要在儿童中使用具有改进灵敏度的新型结核病诊断工具。
    Xpert MTB/RIF is recommended for the diagnosis of tuberculosis (TB) in children. We determined the performance of Xpert MTB/RIF in the diagnosis of pulmonary TB in children. The characteristics of children influencing Xpert MTB/RIF positivity were explored. Children aged <15 years with symptoms suggestive of pulmonary TB were prospectively enrolled from 2013 to 2019. Two sputum/early morning gastric aspirate specimens were collected for examination by smear (fluorescence microscopy), Xpert MTB/RIF, and culture [Mycobacteria growth indicator tube (MGIT)/Lowenstein-Jensen (LJ) medium]. Diagnostic performance of Xpert MTB/RIF was evaluated using LJ and or MGIT culture positivity as the reference standard. Sensitivity, specificity with 95% confidence interval (CI) were calculated. Stratified analysis was done; P < .05 was considered statistically significant. Of the total 1727 enrolled children, 1674 (97%) with complete results for at least one sputum/gastric aspirate sample were analyzed. The sensitivity of Xpert MTB/RIF was 68.5% in sputum and 53.6% in gastric aspirate while the specificity was 99% for both. The sensitivity compared to smear was 68.5% vs. 33.7% (P < .001) and 53.6% vs. 14.5%; (P < .001) in sputum and gastric aspirate, respectively. The sensitivity of Xpert MTB/RIF was 23.9% with decision to treat as reference standard. Xpert MTB/RIF positivity was significantly influenced by sex, age, nutritional status, chest X-ray abnormality, TB infection status, and symptoms suggestive of TB. Xpert MTB/RIF as an upfront test compared to smear improves diagnosis of pulmonary TB in children yet the sensitivity is suboptimal. Newer TB diagnostic tools with improved sensitivity is warranted in children.
    We evaluated the performance of Xpert MTB/RIF in the diagnosis of pulmonary TB in children and explored the characteristics influencing Xpert MTB/RIF positivity. Sputum and or early morning gastric aspirate specimen was collected from children aged <15 years with symptoms suggestive of pulmonary TB. This was examined by smear (fluorescence microscopy), Xpert MTB/RIF, and culture (Mycobacteria growth indicator tube (MGIT)/Lowenstein–Jensen (LJ) medium). Diagnostic performance of Xpert MTB/RIF was evaluated using LJ and or MGIT culture positivity as the reference standard. Of the total 1727 enrolled children, 1674 (97%) with complete results for at least one sputum/gastric aspirate sample were analyzed. The sensitivity of Xpert MTB/RIF was 68.5% in sputum and 53.6% in gastric aspirate which was higher than smear and the specificity was 99%. The sensitivity of Xpert MTB/RIF was 23.9% with decision to treat for TB as reference standard. The Xpert MTB/RIF positivity was influenced by sex, age, nutritional status, chest X-ray abnormality, TB infection status, and symptoms suggestive of TB. Xpert MTB/RIF as an upfront test compared to smear improves the diagnosis of pulmonary TB in children yet the sensitivity is suboptimal. Newer TB diagnostic tools with improved sensitivity is warranted in children.
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  • 文章类型: Journal Article
    目标:尽管以前的研究已经描述了现象学诊断,他们缺乏对就诊运动障碍(MD)服务的患者的病因谱的描述。在这里,我们对MD现象学进行了分类,并描述了每种现象学在接受三级护理运动障碍服务的患者中的病因学分布。
    方法:收集的信息包括人口统计学特征(发病年龄,介绍时的年龄,性别,陈述前的疾病持续时间),主要的MD现象学[如帕金森病,肌张力障碍,共济失调,震颤,舞蹈病,弹道,肌阵鸣,Tics,刻板印象,不宁腿综合征(RLS)及其他],诊断评估和发现病因。
    结果:这项观察性研究包括1140例MD患者,历时5年。发病年龄中位数(IQR)为49(35-60)岁,就诊年龄为54(40-65)岁,中位病程为36(18-72)个月。近三分之二的患者是男性(M:F=731:409)。帕金森病(n=494,43.3%)是最常见的MD现象学观察,其次是肌张力障碍(n=219,19.2%),共济失调(n=125,11%),震颤(n=118,10.4%),肌阵鸣(n=73,6.4%),舞蹈病(n=40,3.5%),痉挛(n=22,1.9%),Tics(n=8,0.7%),和RLS(n=8,0.7%)。将33例(2.9%)患者分组在其他MD下。总的来说,神经退行性疾病(57.4%)是MDs的最常见原因.帕金森病,遗传性肌张力障碍,特发性震颤,遗传性共济失调,面肌痉挛,亨廷顿病是帕金森病最常见的病因,肌张力障碍,震颤,共济失调,肌阵鸣,和舞蹈症,分别。
    结论:帕金森病是在MD患者中观察到的最常见的现象学,接着是肌张力障碍,共济失调和震颤。神经退行性疾病是最常见的病因。
    OBJECTIVE: Although previous studies have described phenomenological diagnoses, they lacked description of aetiological spectrum in patients visiting movement disorders (MD) service. Herein, we classify the MD phenomenology and describe aetiology wise distribution of each phenomenology in patients visiting a tertiary care movement disorders service.
    METHODS: Collected information included demographic profile (age of onset, age at presentation, gender, duration of illness before presentation), predominant MD phenomenology [such as parkinsonism, dystonia, ataxia, tremor, chorea, ballism, myoclonus, tics, stereotypy, restless legs syndrome (RLS) and others], diagnostic evaluations and detected aetiology.
    RESULTS: This observational study included 1140 MD patients over a span of 5 years. The median (IQR) age of onset was 49 (35-60) years and age at presentation was 54 (40-65) years, with median duration of illness being 36 (18-72) months. Nearly two-third of patients were males (M:F=731:409). Parkinsonism (n=494, 43.3 %) was the most common MD phenomenology observed, followed by dystonia (n=219, 19.2 %), ataxia (n=125, 11 %), tremor (n=118, 10.4 %), myoclonus (n=73, 6.4 %), chorea (n=40, 3.5 %), spasticity (n=22, 1.9 %), tics (n=8, 0.7 %), and RLS (n=8, 0.7 %). Thirty-three (2.9 %) patients were grouped under miscellaneous MDs. Overall, neurodegenerative disorders (57.4 %) were the most common cause of MDs. Parkinson\'s disease, genetic dystonia, essential tremor, genetic ataxias, hemifacial spasm, and Huntington\'s disease were the most common aetiologies for parkinsonism, dystonia, tremor, ataxia, myoclonus, and chorea, respectively.
    CONCLUSIONS: Parkinsonism was the most common phenomenology observed in MD patients, and was followed by dystonia, ataxia and tremor. Neurodegenerative disorders were the most common aetiology detected.
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  • 文章类型: Journal Article
    本研究的目的是发现维生素D受体(VDR)多态性(Fokl,Taql和Apal)与印度南部糖尿病足溃疡(DFU)患者的维生素D水平。在这项病例对照研究中,将70例(DFU患者)的血浆维生素D水平和VDR基因型频率与来自印度南部的70例糖尿病(糖尿病[DM][非DFU])患者和70例明显健康的对照(HC)进行了比较。使用ELISA技术测量血浆维生素D水平,并使用实时聚合酶链反应对VDR多态性进行基因分型。使用逻辑回归来发现DFU与HC以及DFU与DM性状之间的关联。基于添加剂进行关联分析,以年龄和性别为协变量的显性和隐性模型。45.7%的DFU患者有足够的维生素D水平比48.6%和40%的DM患者和HC,分别。DFU与HC和DFU与DM性状的连锁不平衡分析表明,DFU患者的单核苷酸多态性(SNP)Taq1(rs731236)和Apal(rs7975232)处于强连锁不平衡状态。所有三组的等位基因和基因型频率相似。虽然加法模型没有显示出统计学意义,年龄和性别与三个SNP相关(Fokl,Taql和Apal)。在印度南部的DFU患者中,未发现VDR基因多态性与维生素D水平之间存在关联。另一方面,年龄和性别与三个SNP相关。
    Objective of the study was to find the association of vitamin D receptor (VDR) polymorphisms (Fokl, Taql and Apal) with vitamin D levels in diabetic foot ulcer (DFU) patients in South India. In this case-control study, plasma vitamin D levels and VDR genotype frequencies of 70 cases (DFU patients) were compared with 70 diabetic (diabetes mellitus [DM] [non-DFU]) patients and 70 apparently healthy controls (HC) from South India. Plasma vitamin D levels were measured using the ELISA technique, and genotyping of VDR polymorphisms was carried out using real-time polymerase chain reaction. Logistic regression was used to find the association between DFU versus HC and DFU versus DM traits. Association analysis was performed based on additive, dominant and recessive models with age and gender as covariates. A 45.7% of DFU patients have sufficient vitamin D levels than 48.6% and 40% of DM patients and HC, respectively. Linkage disequilibrium analysis for DFU versus HC and DFU versus DM traits shows that single nucleotide polymorphisms (SNPs) Taq1 (rs731236) and Apal (rs7975232) are in strong linkage disequilibrium in DFU patients. The alleles and genotype frequencies were similar in all three groups. Although the additive model does not show statistical significance, age and sex correlate with the three SNPs (Fokl, Taql and Apal). No association was found between VDR gene polymorphisms and vitamin D levels in DFU patients in Southern India. On the other hand, age and sex correlate with the three SNPs.
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  • 文章类型: Journal Article
    全球每年约有1000万至1200万新的梅毒感染。包括孕妇。这项研究确定了巴拉那州三级产科病房收治的孕妇中与梅毒相关的因素,巴西。这是一个两面派,2020年9月至2021年10月进行的配对病例对照研究(1:2比例)。怀孕患者(n=93)入住产科病房,通过性病研究实验室(VDRL)和快速试剂测试进行测试,与186个对照进行比较,年龄和住院时间相匹配。社会人口统计学,行为,产前,和产妇保健信息是通过访谈收集的。使用二元逻辑回归分析数据。结果表明,除白色以外的种族/肤色(OR:2.12;95CI:1.19-3.80;p<0.001),有一个以上的性伴侣(OR:3.69;95CI:1.70-8.00;p=0.001),作为前吸烟者(OR:2.07;95CI:1.07-4.01;p=0.030)和当前吸烟者(OR:4.31;95CI:1.55-11.98;p=0.005),以及有性传播感染史(OR:10.87;95CI:4.04-29.27;p<0.0.01)是妊娠梅毒的危险因素.总之,研究表明,社会人口统计学,行为,医疗保健相关变量与妊娠梅毒相关.因此,结合这些因素,为妊娠梅毒提供循证治疗,从业人员可从中获益.
    Approximately 10-12 million new syphilis infections occur annually worldwide, including in pregnant women. This study identified the factors associated with syphilis in pregnant women admitted to a tertiary maternity ward in the State of Paraná, Brazil. This is an ambispective, paired case-control study (1:2 ratio) conducted from September 2020 to October 2021. Pregnant patients (n = 93) admitted to the maternity ward, who were tested with the Venereal Disease Research Laboratory (VDRL) and rapid reagent test, were compared with 186 controls, matched by age and period of hospital admission. Sociodemographic, behavioral, prenatal, and maternity healthcare information was collected through interviews. The data were analyzed using binary logistic regression. Results showed that race/skin color other than white (OR: 2.12; 95%CI: 1.19-3.80; p < 0.001), having more than one sexual partner (OR: 3.69; 95%CI: 1.70-8.00; p = 0.001), being a former smoker (OR: 2.07; 95%CI: 1.07-4.01; p = 0.030) and a current smoker (OR: 4.31; 95%CI: 1.55-11.98; p = 0.005), as well as having a history of sexually transmitted infections (OR: 10.87; 95%CI: 4.04-29.27; p < 0.0.01) were risk factors for gestational syphilis. In summary, the study indicated that sociodemographic, behavioral, and healthcare-related variables were associated with gestational syphilis. Therefore, practitioners could benefit from incorporating these factors to deliver evidence-based treatment for gestational syphilis.
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  • 文章类型: Journal Article
    背景:在1型神经纤维瘤病(NF1)的较大队列中,听力损失作为合并症尚未被彻底研究。
    方法:我们回顾了在三级儿科医院就诊的NF1患者的现有听力测量数据,以评估听力损失的患病率和危险因素。
    结果:在2010年至2022年期间观察到的1172例NF1患者中,有90例具有可用的听力测量数据,90例患者中有48例(53%)具有一个或多个听力图显示听力损失。那些没有提到听力学的人被认为有正常的听力,导致NF1儿童和年轻人的保守听力损失估计为4%。在90名听力图的患者中,29(32%)有导电损耗(CHL),15人(17%)有感音神经性丧失(SNHL),和3(3%)有混合性听力损失。一名患者的听力损失类型未确定。对于患有CHL的儿童,六人永久性CHL继发于丛状神经纤维瘤,19CHL是由于活动性中耳功能障碍而短暂的,4例CHL病因不明。对于三个患有SNHL或混合性听力损失的儿童,病因包括耳毒性化疗史和/或SNHL家族史。在16名SNHL或混合性听力损失患者中,随着时间的推移,听力图超过一个,16人中有8人出现进行性听力下降,178人中有26人出现了听力阈值(15%).
    结论:我们的研究结果表明,考虑到与一般人群相比,NF1患者的听力损失率高于预期,应考虑对至少一部分NF1儿童进行听力测量评估。
    BACKGROUND: Hearing loss has not been thoroughly investigated as a comorbidity in larger cohorts with neurofibromatosis type 1 (NF1).
    METHODS: Available audiometric data were reviewed from patients with NF1 seen at a tertiary pediatric hospital to assess prevalence and risk factors for hearing loss.
    RESULTS: Of 1172 patients with NF1 seen between 2010 and 2022, 90 had available audiometric data and 48 of 90 patients (53%) had one or more audiogram revealing hearing loss. Those not referred to audiology were presumed to have normal hearing, resulting in a conservative hearing loss estimate of 4% for children and young adults with NF1. Of 90 patients with audiograms, 29 (32%) had conductive loss (CHL), 15 (17%) had sensorineural loss (SNHL), and 3 (3%) had mixed hearing loss. Hearing loss type was undetermined for one patient. For children with CHL, six had permanent CHL secondary to plexiform neurofibroma, 19 CHL were transient due to active middle ear dysfunction, and four CHL cases were indeterminate in etiology. For three children with SNHL or mixed hearing loss, etiology included history of ototoxic chemotherapy and/or family history of SNHL. In the 16 patients with SNHL or mixed hearing loss with more than one audiogram over time, progressive hearing decline was noted in eight of 16, and 26 of 178 hearing thresholds (15%) progressed.
    CONCLUSIONS: Our findings suggest that audiometric evaluations should be considered for at least a subset of children with NF1, given the higher-than-expected rate of hearing loss in patients with NF1 compared with the general population.
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  • 文章类型: Journal Article
    目的:COVID-19Omicron亚变体通常比以前的菌株引起更温和的疾病,然而,许多患者仍被送往医院接受急性护理。我们审核了入院原因和细节,以确定减少住院的机会。
    方法:我们回顾了2022年12月1日至2023年1月30日所有SARS-CoV-2检测呈阳性的住院患者。
    结果:在600例COVID-19聚合酶链反应阳性的患者中,222(37%)被认为是偶然诊断。有症状的COVID-19入院原因(375例患者,63%)包括恶化症状(226,60%),合并症恶化(89,24%),在家管理困难(38,10%)。几乎一半被归类为轻度感染(175,47%)。在231名70岁以上的患者中,只有55(24%)以前有过抗病毒治疗,和90(39%)有4+疫苗剂量。说英语以外的语言和具有澳大利亚以外的出生国的患者与较低的疫苗接种率显着相关,并且在入院前没有抗病毒药物。
    结论:三分之一的COVID-19住院患者是偶然的,一半是轻度疾病。许多患者没有在社区接受适当的疫苗接种或抗病毒药物。
    结论:提高疫苗接种和抗病毒药物的摄取,增加社区支持,关注来自不同文化和语言背景的人,可以减轻COVID-19对医院的负担。
    OBJECTIVE: COVID-19 Omicron subvariants typically cause milder disease than previous strains, yet many patients were still admitted to hospital for acute care. We audited reasons for and details of admissions to identify opportunities to reduce hospitalisations.
    METHODS: We reviewed all admitted patients who tested positive for SARS-CoV-2 from 1st December 2022 to 30th January 2023.
    RESULTS: Of 600 patients with a positive COVID-19 polymerase chain reaction, 222(37%) were considered incidental diagnoses. Reasons for admission for symptomatic COVID-19 (375 patients, 63%) included worsening symptoms (226, 60%), exacerbation of comorbidities (89, 24%), and difficulty managing at home (38, 10%). Almost half were classified as a mild infection (175, 47%). Of the 231 patients aged over 70 years, only 55 (24%) had prior antiviral therapy, and 90 (39%) had 4+ vaccine doses. Patients speaking language other than English and having country of birth other than Australia were significantly associated with lower vaccination rates and not having antivirals prior to admission.
    CONCLUSIONS: One-third of COVID-19 hospital admissions were incidental, and half were for mild disease. Many patients had not received appropriate vaccination or antivirals in the community.
    CONCLUSIONS: Improving uptake of vaccinations and antivirals, and increasing community support, with a focus on people from culturally and linguistically diverse backgrounds, may reduce the burden of COVID-19 on hospitals.
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  • 文章类型: Journal Article
    BACKGROUND: \"Who will educate us\" lamented a School Principal after she took part in our study and education session. There is palpable low breast cancer (BC) literacy with rising incidence and disproportionate mortality rates.
    METHODS: Breast Cancer Awareness Measure (BCAM) developed by Cancer Research UK was administered to 944 women. BCAM measures knowledge, age-related risk, and reported frequency of breast checking and other components. A woman is BC aware if she identified five or more nonlump symptoms, age-related risk, and reported breast checking once a week/month. At the end, each participant was given \"Be Breast Aware\" education; what/how to look for demonstrated on a model.
    RESULTS: 2.8% health professionals. 3.1% BC survivors. 78.8% had lump knowledge and 55.3% had non-lump knowledge of BC, 10% had age-related risk knowledge. 24.3% check breasts once a week/month. 41.9% aware BC is common after 50 years. 14/944 (1.5%) had BC awareness. 59.9% had breast symptoms, but never consulted a doctor, 31.1% were embarrassed, and 29.4% were scared to consult. Nearly 43% heard of breast screening, 28.4% had mammography, 26.3% had ultrasound. About 44.1% knew family history risk. Those practicing breast checking looked for a size change (24.5%), nipple position (17.4%), discharge (22.1%), pain (32.5%), and lump (24.7%) in standing (17.8%), supine (8.5%) using finger pads (15.8%) fingertips (21.6%), using circular movements (16.4%), and pinching breast tissue (19.6%).
    CONCLUSIONS: Health-care workers and BC survivors lack breast awareness which is alarming and indicates the need for BC awareness and post-BC treatment follow-up care education in these two groups and the general population. Some practice the wrong method (e.g., pinching tissue) of breast checking, which may lead to anxiety and unnecessary investigative costs. \"Be Breast Aware\" education based on the National Health Service 5-point plan given to 944 participants.
    Résumé Introduction:‘Qui nous éduquera ?’ s’est lamentée une directrice d’école après avoir participé à notre séance d’étude et d’éducation. Il existe un faible niveau de connaissances sur le cancer du sein, avec une incidence croissante et des taux de mortalité disproportionnés.Méthodologie:La mesure de sensibilisation au cancer du sein (B-CAM) développée par Cancer Research UK a été administrée à 944 femmes. B-CAM mesure les connaissances, le risque lié à l’âge et la fréquence signalée de l’auto-examen des seins, ainsi que d’autres composants. Une femme est consciente du cancer du sein si elle a identifié au moins 5 symptômes non nodulaires, un risque lié à l’âge et si elle a signalé un auto-examen des seins une fois par semaine/mois. À la fin, chaque participante a reçu une éducation ‘Be Breast Aware’; comment auto-examiner les seins a été démontré sur un modèle.Résultats:2,8% de professionnels de santé. 3,1 % de survivantes du cancer du sein. 78,8 % avaient une connaissance des symptômes nodulaires et 55,3 % avaient une connaissance non nodulaire du cancer du sein, et 10 % avaient une connaissance des risques liés à l’âge. 24,3 % vérifient leurs seins une fois par semaine/mois. 41,9 % savent que le cancer du sein est courant après 50 ans. 14/944 (1,5 %) étaient sensibilisées au cancer du sein. 59,9% avaient des symptômes mammaires mais n’avaient jamais consulté de médecin, 31,1% étaient gênées, 29,4% avaient peur de consulter. 43 % ont entendu parler du dépistage du cancer du sein, 28,4 % de la mammographie, 26,3 % de l’échographie. 44,1 % connaissaient le risque lié aux antécédents familiaux. Ceux qui pratiquent l’auto-examen des seins ont examiné le changement de taille des seins (24,5 %), la position du mamelon (17,4 %), l’écoulement (22,1 %), la douleur (32,5 %) et la grosseur (24,7 %) en position debout (17,8 %) en décubitus dorsal (8,5 %) en utilisant le bout des doigts (15,8 %) le bout des doigts (21,6 %), en utilisant des mouvements circulaires (16,4 %) et en pinçant le tissu mammaire (19,6 %)Conclusion:les travailleurs de la santé et les survivantes du cancer du sein manquent de sensibilisation aux seins, ce qui est alarmant et indique la nécessité pour la sensibilisation au cancer du sein et l’éducation aux soins de suivi post-traitement dans ces deux groupes et la population générale. Certaines pratiquent une mauvaise méthode d’auto-examen des seins, ce qui peut entraîner de l’anxiété et des coûts d’investigation inutiles. Éducation ‘Be Breast Aware’ basée sur le plan en 5 points du NHS dispensé à 944 participantes.
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