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Fibrinolysis and clinical outcomes in acute pulmonary embolism. Madras medical college pulmonary embolism (M-PER) registry from India 急性肺栓塞的纤维蛋白溶解和临床结果。印度马德拉斯医学院肺栓塞(M-PER)登记。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.008

Background

Acute pulmonary embolism (APE) is the third most common cause of vascular death. Data on APE from India and other low-and middle-income countries is sparse.

Objectives

Study the clinical characteristics, prognostic factors, in-hospital mortality (IMH) and 12 months mortality of patients with APE in India.

Methods

We prospectively enrolled 186 consecutive patients diagnosed with APE between November 2016 and November 2021 in Madras Medical College Pulmonary Embolism Registry (M-PER). All patients had electrocardiography and echocardiography. High risk patients and selected intermediate risk patients underwent fibrinolysis.

Results

75 % of our patients were below 50 years of age. 35 % were women. The mean time to presentation from symptom onset was 6.04 ± 10.01 days. 92 % had CT pulmonary angiography. Intermediate risk category (61.3 %) was the more common presentation followed by high risk (26.9 %). Electrocardiography showed S1Q3T3 pattern in 56 %. 76 % had right ventricular dysfunction and 12.4 % had right heart thrombi(RHT) by echocardiography. 50.5 % received fibrinolysis. Patients with RHT received fibrinolysis more frequently (78.3 % vs 46.6 %; p = 0.007). In-hospital mortality (IHM) was 15.6 %. Systemic arterial desaturation and need for mechanical ventilation independently predicted IHM. Ten patients (5.3 %) were lost to follow up. One year mortality was 26.7 % (47/176). One year mortality of patients discharged alive was similar among high, intermediate and low risk groups(14.8 % vs 1.9 % vs 10.5 %; p = 0.891).

Conclusions

Patients with PE are often young and present late in India. The in-hospital and 12 months mortality were high. Low and intermediate risk groups had a high post discharge mortality similar to high risk patients.

背景:急性肺栓塞(APE)是血管性死亡的第三大常见原因。印度和其他中低收入国家关于急性肺栓塞的数据很少:研究印度 APE 患者的临床特征、预后因素、院内死亡率(IMH)和 12 个月死亡率:我们在马德拉斯医学院肺栓塞登记处(M-PER)前瞻性地登记了 2016 年 11 月至 2021 年 11 月期间确诊为 APE 的 186 例连续患者。所有患者均进行了心电图和超声心动图检查。高危患者和部分中危患者接受了纤维蛋白溶解术:75%的患者年龄在50岁以下。女性占 35%。从症状出现到就诊的平均时间为 6.04 ± 10.01 天。92% 的患者接受了 CT 肺血管造影检查。中危(61.3%)是最常见的表现,其次是高危(26.9%)。56%的患者心电图显示为S1Q3T3型。超声心动图显示,76%的患者存在右心室功能障碍,12.4%的患者存在右心血栓(RHT)。50.5%的患者接受了纤维蛋白溶解治疗。RHT患者接受纤维蛋白溶解的比例更高(78.3% vs 46.6%;P = 0.007)。院内死亡率 (IHM) 为 15.6%。全身动脉饱和度降低和需要机械通气可独立预测院内死亡率。10名患者(5.3%)失去了随访机会。一年死亡率为 26.7%(47/176)。高危、中危和低危组患者出院后一年的死亡率相似(14.8% vs 1.9% vs 10.5%;P = 0.891):印度的 PE 患者通常比较年轻,发病时间较晚。结论:印度的 PE 患者多为年轻人,发病时间较晚,院内死亡率和 12 个月死亡率较高。低危和中危组出院后的死亡率与高危患者相似。
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引用次数: 0
Prevalence of atrial fibrillation on a 24-hour Holter in adult Indians 印度成年人 24 小时心电图中心房颤动的患病率。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.012

Objective

To evaluate paroxysmal atrial fibrillation (AF) prevalence in Indian adults who completed 24-Hour Holter monitoring.

Methods

A total of 23,847 patients (36.9 % women) were analyzed for AF duration using a software algorithm.

Results

AF was diagnosed in 4153 (17.4 %) patients with a median AF duration of 13 min and 55 s.

Conclusion

AF prevalence was high and largely untreated. The short duration of AF episodes indicates a low likelihood of detection during clinical visits, highlighting its potential underestimation in Indian healthcare.

目的评估完成 24 小时 Holter 监测的印度成年人中阵发性心房颤动(房颤)的发生率:使用软件算法对 23,847 名患者(36.9% 为女性)的房颤持续时间进行分析:结果:4153 名患者(17.4%)被诊断为房颤,中位房颤持续时间为 13 分 55 秒:结论:心房颤动发病率很高,且大多未得到治疗。心房颤动发作持续时间短,表明在临床就诊时被发现的可能性较低,这凸显了印度医疗机构可能低估了心房颤动的发病率。
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引用次数: 0
Heart failure, the global pandemic: A call to action consensus statement from the global presidential conclave at the platinum jubilee conference of cardiological society of India 2023 心力衰竭,全球流行病:2023 年印度心脏病学会白金庆典大会全球主席会议共识声明。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.04.004

Heart failure (HF) is emerging as a major public health problem both in high- and low - income countries. The mortality and morbidity due to HF is substantially higher in low-middle income countries (LMICs). Accessibility, availability and affordability issues affect the guideline directed therapy implementation in HF care in those countries. This call to action urges all those concerned to initiate preventive strategies as early as possible, so that we can reduce HF-related morbidity and mortality. The most important step is to have better prevention and treatment strategies for diseases such as hypertension, ischemic heart disease (IHD), type-2 diabetes, and rheumatic heart disease (RHD) which predispose to the development of HF. Setting up dedicated HF-clinics manned by HF Nurses, can help in streamlining HF care. Subsidized in-patient care, financial assistance for device therapy, use of generic medicines (including polypill strategy) will be helpful, along with the use of digital technologies.

心力衰竭(HF)正在成为高收入和低收入国家的一个主要公共卫生问题。在中低收入国家,心力衰竭导致的死亡率和发病率要高得多。在这些国家,可及性、可用性和可负担性问题影响着高血压治疗指南的实施。这一行动呼吁敦促所有相关人员尽早启动预防策略,从而降低与心房颤动相关的发病率和死亡率。最重要的一步是针对高血压、缺血性心脏病(IHD)、2 型糖尿病和风湿性心脏病(RHD)等容易诱发心房颤动的疾病制定更好的预防和治疗策略。设立专门的心房颤动诊所,由心房颤动护士负责,有助于简化心房颤动护理。住院治疗补贴、器械治疗资助、非专利药品的使用(包括多药策略)以及数字技术的使用都将有所帮助。
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引用次数: 0
Impact of capacity building and tele ECG based decision support on change in thrombolysis rate and inhospital and one year mortality in patients with STEMI, using hub and spoke model; multi-phasic intervention trial 能力建设和基于远程心电图的决策支持对 STEMI 患者溶栓率、住院和一年死亡率变化的影响,采用中心辐射模式;多相干预试验。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.005

Background

We report the impact of capacity building and teleconsultation on change in the thrombolysis rates and one-year mortality in patients with STEMI using a hub and the spoke model of STEMI care.

Methods

Twenty secondary care public hospitals were linked with a teaching hospital as a hub centre and the impact of the intervention on change in ischemic time, thrombolysis rates and all-cause in-hospital and one-year mortality was compared.

Results

29 patients with STEMI were treated during pre-intervention from April 2020 to June 2020 and 255 patients during the post-intervention period from July 2020 to Oct 2021 in spoke centres. 245 patients were reported to a hub centre during the study period. The thrombolysis rate was significantly higher in the spoke centres after intervention (65.5%vs. 27.5 % p < 0.001) and was also significantly higher than in patients treated in a hub centre (65.5 % vs. 45.7 % p < 0.01). The in-hospital mortality was significantly lower in patients treated at spoke centres compared to those treated at the hub centre (7.8 % vs. 15.5 % < 0.003). The significant difference in mortality rate continued at one year (11.0 % vs.18.4 % p < 0.01). The median time from symptoms to thrombolytic therapy was significantly lower in STEMI patients treated in spoke centres compared to a hub centre (230 min vs. 356 min p < 0.001).

Conclusion

The hub and spoke model of STEMI care is effective in increasing thrombolysis rate, and decreasing in-hospital and one-year mortality rate.

背景我们报告了能力建设和远程会诊对 STEMI 患者溶栓率和一年死亡率变化的影响,采用的是 STEMI 护理的 "中心-轮辐 "模式。结果干预前(2020 年 4 月至 2020 年 6 月)有 29 名 STEMI 患者在辐式中心接受治疗,干预后(2020 年 7 月至 2021 年 10 月)有 255 名患者在辐式中心接受治疗。在研究期间,有 245 名患者向中心报告。干预后,轮辐中心的溶栓率明显较高(65.5% vs. 27.5 % p < 0.001),也明显高于在枢纽中心接受治疗的患者(65.5% vs. 45.7 % p < 0.01)。在辐射中心接受治疗的患者的院内死亡率明显低于在中心接受治疗的患者(7.8% vs. 15.5% <0.003)。一年后,死亡率仍有明显差异(11.0% 对 18.4% p <0.01)。与枢纽中心相比,在辐条中心接受治疗的 STEMI 患者从出现症状到接受溶栓治疗的中位时间明显缩短(230 分钟 vs. 356 分钟 p < 0.001)。
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引用次数: 0
Comparison of the efficacy, safety, and tolerability of the FDC of telmisartan + bisoprolol with telmisartan + metoprolol succinate ER combination therapy for stage 1 and stage 2 hypertension: A double-blind, multicentric, phase-III clinical study 新型 FDC 替米沙坦+比索洛尔与对比替米沙坦+琥珀酸美托洛尔 ER 联合疗法治疗 1 期和 2 期高血压的疗效、安全性和耐受性比较:双盲、多中心、III 期临床研究。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.002

Aim

The present study compared the safety, efficacy, and tolerability of the new fixed-dose combination (FDC) of telmisartan 40 mg + bisoprolol 5 mg (TBP) tablets with the existing comparator FDC telmisartan 40 mg + metoprolol succinate ER 50 mg (TMS) tablets in patients with stage 1 and stage 2 hypertension.

Methodology

The multicentric, double-blind, parallel-group, comparative, prospective, phase-III clinical study involved 264 subjects with stage 1 and stage 2 hypertension from 10 centres across India. The selected subjects were randomized into two groups: group A received the TMS and group B received the new FDC TBP. The primary endpoint was the mean change in seated systolic blood pressure (SeSBP) and seated diastolic blood pressure (SeDBP) from baseline to week 12 in both the control and study arms. The secondary endpoint was achieving the target of SeSBP <140 mmHg and SeDBP <90 mmHg from baseline to week 12 in both groups. Safety and tolerability parameters were evaluated in both groups based on adverse effects (AEs) reported by the patients and the physician.

Results

Both treatment groups exhibited a reduction in BP after 2 weeks of treatment, which was sustained until 12 weeks. The mean change in SeSBP and SeDBP at weeks 2, 6, and 12 compared to the previous visit showed statistical significance (p < 0.001) in all cases for both groups A and B. The mean changes in SeSBP and SeDBP from baseline to study end were numerically higher in group B than in group A. The mean difference in SeSBP from baseline to study end was significantly higher in group B compared to group A (p = 0.029). By week 12, 88.28 % and 89.84 % of subjects in group B achieved SeSBP <140 mmHg and SeDBP <90 mmHg respectively, while 86.71 % and 91.40 % of subjects in group A achieved the same targets. Reported AEs were mostly mild to moderate in both treatment groups, and no serious AEs or deaths were reported. Tolerability was rated as ‘excellent’ by 93.75 % of subjects in group B and 91.40 % of subjects in group A.

Conclusion

Both the new FDC TBP and the existing comparator TMS combination therapy have comparable efficacy, tolerability, and safety for the management of stage 1 and stage 2 hypertension.

Trial registry name

Clinical Trials Registry of India (CTRI)

Trial registration no

CTRI/2021/11/037,926

Protocol no

MLBTL/05/2021

Protocol url

https://ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=62069&EncHid=&userName=bisoprolol

目的:本研究比较了新型固定剂量复方制剂(FDC)替米沙坦40毫克+比索洛尔5毫克(TBP)片剂与现有的比较药固定剂量复方制剂替米沙坦40毫克+琥珀酸美托洛尔ER50毫克(TMS)片剂在1期和2期高血压患者中的安全性、有效性和耐受性:这项多中心、双盲、平行组、比较性、前瞻性的 III 期临床研究涉及印度 10 个中心的 264 名 1 期和 2 期高血压患者。选定的受试者被随机分为两组:A 组接受 TMS,B 组接受新型 FDC TBP。主要终点是对照组和研究组的坐位收缩压(SeSBP)和坐位舒张压(SeDBP)从基线到第 12 周的平均变化。次要终点是达到 SeSBP 结果的目标:治疗 2 周后,两组患者的血压均有所下降,并持续到 12 周。第 2、6 和 12 周的 SeSBP 和 SeDBP 平均值变化与前次访视相比具有统计学意义(P 结论:第 2、6 和 12 周的 SeSBP 和 SeDBP 平均值变化与前次访视相比具有统计学意义(P 结论):新的 FDC TBP 和现有的参照物 TMS 联合疗法在治疗 1 期和 2 期高血压方面具有相似的疗效、耐受性和安全性。试验登记处名称:印度临床试验登记处(CTRI),试验登记号:CTRI/2021/11/037926 PROTOCOL NO:MLBTL/05/2021 PROTOCOL URL:https://ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=62069&EncHid=&userName=bisoprolol。
{"title":"Comparison of the efficacy, safety, and tolerability of the FDC of telmisartan + bisoprolol with telmisartan + metoprolol succinate ER combination therapy for stage 1 and stage 2 hypertension: A double-blind, multicentric, phase-III clinical study","authors":"","doi":"10.1016/j.ihj.2024.06.002","DOIUrl":"10.1016/j.ihj.2024.06.002","url":null,"abstract":"<div><h3>Aim</h3><p>The present study compared the safety, efficacy, and tolerability of the new fixed-dose combination (FDC) of telmisartan 40 mg + bisoprolol 5 mg (TBP) tablets with the existing comparator FDC telmisartan 40 mg + metoprolol succinate ER 50 mg (TMS) tablets in patients with stage 1 and stage 2 hypertension.</p></div><div><h3>Methodology</h3><p>The multicentric, double-blind, parallel-group, comparative, prospective, phase-III clinical study involved 264 subjects with stage 1 and stage 2 hypertension from 10 centres across India. The selected subjects were randomized into two groups: group A received the TMS and group B received the new FDC TBP. The primary endpoint was the mean change in seated systolic blood pressure (SeSBP) and seated diastolic blood pressure (SeDBP) from baseline to week 12 in both the control and study arms. The secondary endpoint was achieving the target of SeSBP &lt;140 mmHg and SeDBP &lt;90 mmHg from baseline to week 12 in both groups. Safety and tolerability parameters were evaluated in both groups based on adverse effects (AEs) reported by the patients and the physician.</p></div><div><h3>Results</h3><p>Both treatment groups exhibited a reduction in BP after 2 weeks of treatment, which was sustained until 12 weeks. The mean change in SeSBP and SeDBP at weeks 2, 6, and 12 compared to the previous visit showed statistical significance (<em>p</em> &lt; 0.001) in all cases for both groups A and B. The mean changes in SeSBP and SeDBP from baseline to study end were numerically higher in group B than in group A. The mean difference in SeSBP from baseline to study end was significantly higher in group B compared to group A (<em>p</em> = 0.029). By week 12, 88.28 % and 89.84 % of subjects in group B achieved SeSBP &lt;140 mmHg and SeDBP &lt;90 mmHg respectively, while 86.71 % and 91.40 % of subjects in group A achieved the same targets. Reported AEs were mostly mild to moderate in both treatment groups, and no serious AEs or deaths were reported. Tolerability was rated as ‘excellent’ by 93.75 % of subjects in group B and 91.40 % of subjects in group A.</p></div><div><h3>Conclusion</h3><p>Both the new FDC TBP and the existing comparator TMS combination therapy have comparable efficacy, tolerability, and safety for the management of stage 1 and stage 2 hypertension.</p></div><div><h3>Trial registry name</h3><p>Clinical Trials Registry of India (CTRI)</p></div><div><h3>Trial registration no</h3><p>CTRI/2021/11/037,926</p></div><div><h3>Protocol no</h3><p>MLBTL/05/2021</p></div><div><h3>Protocol url</h3><p><span><span>https://ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=62069&amp;EncHid=&amp;userName=bisoprolol</span><svg><path></path></svg></span></p></div>","PeriodicalId":13384,"journal":{"name":"Indian heart journal","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0019483224000750/pdfft?md5=ec2c77a9c028415128a47dbccdef593b&pid=1-s2.0-S0019483224000750-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141317056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessment of three-dimensional (3-D) left ventricular ejection fraction and speckled tracking echocardiographic strain parameters in non-ischemic left bundle branch block (LBBB) patients and their association with cardiovascular events – A prospective observational study 评估非缺血性左束支传导阻滞(LBBB)患者的三维(3-D)左室射血分数和斑点追踪超声心动图应变参数及其与心血管事件的关系--一项前瞻性观察研究。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.011

Objective

To investigate the association between three-dimensional (3-D) left ventricular ejection fraction (LVEF) and various speckle tracking echocardiographic (STE) strain parameters in non-ischemic left bundle branch block (LBBB) patients with major adverse cardiovascular events (MACE) during a one-year follow-up phase.

Method

A total of 50 patients with non-ischemic LBBB were assessed using various parameters of 3-D echocardiography. They were compared with their same-age and sex control group and then followed up with repeat 3-D echocardiography for MACE for one year.

Results

Composite outcomes were seen in (n = 11 [22 %], including cardiovascular mortality (n = 2 [4.0 %]) and hospitalization for heart failure (n = 9 [18.0 %]). Mean values of the left ventricle (LV) global longitudinal (GLS), circumferential (GCS), and radial (GRS) strains were −14.4 ± 5.6, −14.3 ± 5.8, and 15.3 ± 5.9 respectively in the study cases. Initial GLS values were significantly impaired among those who had clinical events (−9.2 vs −15.9). Also, significant worsening of GLS (p value < 0.001) was seen in patients with composite outcomes on follow-up. Cut-off values in receiver operating characteristic analyses for composite outcomes were: GLS more than −13.5, GCS more than −12.5, and GRS less than 14.5. Intra-class correlations for both intra-observer and inter-observer variability were found to be good.

Conclusion

Impaired LV GLS and low 3-D LVEF are significantly associated with the occurrence of MACE in patients with non-ischemic LBBB. This strong association of LV GLS with outcomes can aid in risk stratification, prognostication, and clinical decision-making in non-ischemic LBBB.

目的研究随访一年的非缺血性左束支传导阻滞(LBBB)患者的三维(3-D)左室射血分数(LVEF)与各种斑点追踪超声心动图(STE)应变参数之间的关系:使用三维超声心动图的各种参数对50名非缺血性左束支传导阻滞患者进行评估。将他们与同年龄、同性别的对照组进行比较,然后通过重复三维超声心动图检查随访一年,以了解 MACE:结果:11 例患者出现了综合结果,包括心血管死亡(2 例[4.0%])和心力衰竭住院(9 例[18.0%])。研究病例的左心室整体纵向应变(GLS)、周向应变(GCS)和径向应变(GRS)的平均值分别为-14.4 ± 5.6、-14.3 ± 5.8和15.3 ± 5.9。在发生临床事件的病例中,初始 GLS 值明显受损(-9.2 vs -15.9)。此外,在随访期间出现综合结果的患者中,GLS 也明显恶化(P 值小于 0.001)。在接收器操作特征分析中,综合结果的临界值为GLS大于-13.5,GCS大于-12.5,GRS小于14.5。观察者内和观察者间变异性的类内相关性良好:结论:左心室GLS受损和低3-D LVEF与非缺血性LBBB患者MACE的发生密切相关。LV GLS与预后的密切关系有助于非缺血性LBBB患者的风险分层、预后和临床决策。
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引用次数: 0
Overweight/obesity, pre-diabetes, diabetes and its association with hypertension and other factors among rural adults (≥18 years) in India 印度农村成年人(≥18 岁)的超重/肥胖、糖尿病前期、糖尿病及其与高血压和其他因素的关系。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.010

Background

Non-communicable diseases are important causes of morbidity and mortality throughout the world.

Methods

A community-based cross-sectional study conducted in 10 Indian states using multi-stage random sampling procedures. Information was collected on socio-economic and demographic particulars, anthropometric measurements such as height, weight and waist circumference, fasting blood glucose and blood pressure was measured. One day 24-h dietary recall was done for foods and nutrient intakes. Bivariate and multivariate step-wise logistic regression analyses was done.

Results

The prevalence of overweight/obesity among rural adults was 23.4 % (95 % CI: 22.9–23.9), while age adjusted prevalence of pre-diabetes was 8.4 % (95 % CI: 8.1–8.7) and diabetes was 6.8, (95 % CI 6.7–7.1), respectively. The prevalence of diabetes was lowest in Uttar Pradesh, West Bengal and Odisha (3–4%) and higher in Kerala and Tamil Nadu (12–15 %). The odds of diabetes was 5.5 times more among elderly, 1.3 times higher among Christians and among high income groups, and 2 times among overweight (CI: 1.50–2.50), obese (CI: 1.61–2.76) and abdominal obesity (OR; 1.57; CI: 1.29–1.91) and 1.6 times more among hypertensives. The odds of diabetes were high among those consuming the lower tertiles of carbohydrates, pulses, milk and milk products and folic acid.

Conclusion

the age-adjusted prevalence of diabetes and pre-diabetes was 6.8 % and 8.4 % respectively and the odds of diabetes was high among elderly, among high socio-economic groups, overweight/obese subjects and among hypertensives. Also, knowledge about symptoms of diabetes was low. There is a need to improve awareness for early diagnosis and treatment for control of diabetes and hypertension.

背景:非传染性疾病是全世界发病和死亡的重要原因 方法:采用多阶段随机抽样程序,在印度 10 个邦开展了一项基于社区的横断面研究。研究收集了有关社会经济和人口统计方面的信息,并对身高、体重和腰围等人体测量数据、空腹血糖和血压进行了测量。对食物和营养素摄入量进行了一天 24 小时膳食回顾。进行了二元和多元逐步逻辑回归分析:农村成年人的超重/肥胖患病率为 23.4%(95% CI:22.9-23.9),经年龄调整后的糖尿病前期患病率为 8.4%(95% CI:8.1-8.7),糖尿病患病率为 6.8(95% CI:6.7-7.1)。北方邦、西孟加拉邦和奥迪沙邦的糖尿病发病率最低(3%-4%),喀拉拉邦和泰米尔纳德邦的发病率较高(12%-15%)。老年人患糖尿病的几率是普通人的 5.5 倍,基督教徒和高收入人群的几率是普通人的 1.3 倍,超重(CI:1.50-2.50)、肥胖(CI:1.61-2.76)和腹部肥胖(OR;1.57;CI:1.29-1.91)的几率是普通人的 2 倍,高血压患者的几率是普通人的 1.6 倍。结论:经年龄调整后,糖尿病和糖尿病前期的发病率分别为 6.8%和 8.4%,老年人、社会经济地位高的群体、超重/肥胖者和高血压患者的糖尿病发病率较高。此外,对糖尿病症状的了解程度也很低。有必要提高对糖尿病和高血压早期诊断和治疗的认识,以控制病情。
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引用次数: 0
Prognostic value of residual SYNTAX score in patients with coronary artery disease undergoing percutaneous coronary intervention-cohort study 接受经皮冠状动脉介入治疗的冠心病患者残余 SYNTAX 评分的预后价值--队列研究。
IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2024-05-01 DOI: 10.1016/j.ihj.2024.06.006

Residual Syntax Score (RSS) is derived from Syntax Score to quantify the burden of residual coronary artery disease after percutaneous coronary intervention (PCI). As data is limited, we report predictive utility of Residual SYNTAX Score in relation to in hospital and 1 year mortality of the patients undergoing percutaneous coronary intervention (PCI).

残余语法评分(RSS)源自语法评分,用于量化经皮冠状动脉介入治疗(PCI)后残余冠状动脉疾病的负担。由于数据有限,我们报告了残余SYNTAX评分对接受经皮冠状动脉介入治疗(PCI)患者的住院死亡率和1年死亡率的预测作用。
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引用次数: 0
Apolipoprotein B - An ideal biomarker for atherosclerosis? 载脂蛋白 B--动脉粥样硬化的理想生物标志物?
IF 1.5 Q3 Medicine Pub Date : 2024-03-01 DOI: 10.1016/j.ihj.2023.12.001
Kavita Singh , Dorairaj Prabhakaran

This review article describes the pathophysiological mechanisms linking Apolipoprotein B (Apo-B) and atherosclerosis, summarizes the existing evidence on Apo B as a predictor of atherosclerotic cardiovascular disease and recommendations of (inter)national treatment guidelines regarding Apo B in dyslipidemia management. A single Apo B molecule is present in every particle of very low-density lipoprotein, intermediate density lipoprotein, low density lipoprotein, and lipoprotein(a). This unique single Apo B per particle ratio makes plasma Apo B concentration a direct measure of the number of circulating atherogenic lipoproteins. This review of global evidence on Apo B as a biomarker for atherosclerosis confirms that Apo B is a single atherogenic lipid marker present in all lipids sub-fractions except HDL-C, and thus, Apo B integrates and extends the information from triglycerides and cholesterol, which could simplify and improve care for atherosclerotic cardiovascular disease.

这篇综述文章描述了载脂蛋白 B(Apo-B)与动脉粥样硬化之间的病理生理机制,总结了载脂蛋白 B 作为动脉粥样硬化性心血管疾病预测因子的现有证据,以及各国(间)治疗指南对血脂异常管理中载脂蛋白 B 的建议。极低密度脂蛋白、中密度脂蛋白、低密度脂蛋白和脂蛋白(a)的每一个颗粒中都有一个载脂蛋白 B 分子。这种独特的每颗粒单一载脂蛋白 B 比率使血浆载脂蛋白 B 浓度成为循环中致动脉粥样硬化脂蛋白数量的直接测量指标。这份关于载脂蛋白 B 作为动脉粥样硬化生物标志物的全球证据综述证实,载脂蛋白 B 是一种单一的致动脉粥样硬化脂质标志物,存在于除高密度脂蛋白胆固醇以外的所有脂质亚组分中,因此,载脂蛋白 B 整合并扩展了甘油三酯和胆固醇的信息,可简化并改善动脉粥样硬化性心血管疾病的治疗。
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引用次数: 0
Dyslipidemia and peripheral arterial disease 血脂异常与外周动脉疾病。
IF 1.5 Q3 Medicine Pub Date : 2024-03-01 DOI: 10.1016/j.ihj.2024.01.010
Ajay Yadav , Vivek Sawant , Varinder Singh Bedi , Kanupriya Yadav

Peripheral arterial disease (PAD) affects 12 % of adult population and is increasing globally and in India. Peripheral arterial disease when associated with atherosclerosis in two or more other arterial beds such as coronary artery disease (CAD), mesenteric/renal artery and cerebrovascular disease (CVD), is known as polyvascular disease. The Reduction of Atherothrombosis for Continued Health (REACH) registry reported that 1 out of 6 patients had multi-vascular bed involvement. Progression of PAD to critical limb ischaemia (CLI) is seen in 1 % of affected patients per year, but patients who progress to CLI may have a 10- to 15-fold increased risk of cardiovascular death.

The 2019 ECS/EAS guidelines for the management of dyslipidaemias have suggested that for primary or secondary prevention in very high risk, patients should follow a therapeutic regimen that achieves >50 % LDL-C reduction from baseline and an LDL-C goal of <55 mg/dl. High Intensity Statin is mainstay of treatment but optimal management is inadequate. Statin treatment reduces all-cause mortality by 39 %, CV death by 41 %, CV outcomes by 34 %, ischaemic stroke by 28 %, acute limb ischaemia by 30 % and amputations by 35 %. Ezetimibe when added to statins in IMPROVE-IT trial, showed significant reduction of MACE. PCSK9 inhibitor (FOURIER TRIAL) showed reduction in primary end point in PAD vs Non PAD patients (3.5 % vs 1.6 %).

There is a critical need for an Indian multi-disciplinary task force for research on the direct impact of lipid-lowering agents on limb salvage rates and major limb-related events in PAD patients.

外周动脉疾病(PAD)影响着 12% 的成年人,在全球和印度都呈上升趋势。外周动脉疾病如果与冠状动脉疾病(CAD)、肠系膜/肾动脉和脑血管疾病(CVD)等其他两个或两个以上动脉床的动脉粥样硬化相关联,则被称为多血管疾病。减少动脉粥样硬化血栓形成,促进持续健康(REACH)登记报告显示,每 6 名患者中就有 1 人患有多血管病变。每年有1%的受影响患者会从PAD发展为严重肢体缺血(CLI),但发展为CLI的患者心血管死亡风险可能会增加10至15倍。2019年ECS/EAS血脂异常管理指南建议,对于极高风险的一级或二级预防,患者应采用一种治疗方案,使低密度脂蛋白胆固醇(LDL-C)比基线降低>50%,并使低密度脂蛋白胆固醇(LDL-C)达到以下目标
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Indian heart journal
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