Results Baseline hsTnT was a significant predictor of all cause (+10ng/l, HR 1.017,. 95%CI 1.011–1.023, p<0.0001) and cardiovascular death (HR 1.02, 95% CI

hsTnT is a marker of myocardial injury and micronecrosis, it is therefore possible that cardiac vascular disease, reflected by slightly raised hsTnT levels, could be paralleled by vascular disease in other organs, including the kidneys . Results: The median baseline NT-proBNP and hsTnT levels were 75 pg/mL (IQR 35-165) and 10.2 pg/mL (IQR 6.9-15.5), respectively. Patients with higher levels of NT-proBNP and hsTnT had higher KM event rates of CVD/HHF (Q4 vs Q1: NT-proBNP: 13.7% vs 1.0%; hsTnT: 11.8% vs 1.4%; P-trend <0.001). 2017-12-14 · In 1,600 patients with suspected ACS (48.4% women; median age, 55 years), a single hsTnT level . 6 ng/L at baseline had a negative predictive value for AMI of 99.4%. In 974 patients (77.1%) with both 0- and 3-hour hsTnT levels of ≤19 ng/L, the negative predictive value for 30-day adverse cardiac events was 99.3% (95% confidence interval, 99.1-99.6).

YES YES NO NO YES NO When investigating an acute MI, order the hsTnT test. If there is no previous hsTnT in the past 12 hours, the test will be considered a baseline hsTnT, whereas if a previous hsTnT has been measured within the past 12 hours, the test will be considered a follow-up hsTnT (see appendix B). The baseline hsTnT result is reported When investigating an acute MI, order the hsTnT test. If there is no previous hsTnT in the past 12 hours, the test will be considered a baseline hsTnT, whereas if a previous hsTnT has been measured within the past 12 hours, the test will be considered a follow-up hsTnT(see appendix B). The baseline hsTnTresult is reported In 1600 patients with suspected acute coronary syndrome (48.4% women; median age, 55 years), a single hsTnTlevel less than 6 ng/L at baseline had a negative predictive value for AMI of 99.4%. In 974 patients (77.1%) with both 0-hour and 3-hour hsTnT levels of 19 ng/L or less, the negative predictive value for 30-day ACE was 99.3% (95% CI, 99.1-99.6). The hsTnT value was measured immediately before surgery and in the morning of the first postoperative day.

Plasma hsTnT were measured by Elecsys diagnostics (Roche, Berlin, Germany) and with a detection limit of 0.01 ng/l (0.00001 μg/l). The median time from symptom onset to ED presentation was 2.9 hours, while time from symptom onset to baseline hsTnT was 5.8 hours.

2020-11-01 · The length of hospitalisation was longer in patients with baseline HsTnT ≥50 ng/L compared to patients who had baseline HsTnT ≤14 ng/L, which may reflect the number of comorbidities. These were probably major contributors to the high re-admission rates we report, with approximately one-quarter of patients being re-admitted by 30 days, and two out of three readmitted by 1 year.

doi 28 Dec 2020 Treatment with dapagliflozin was associated with a reduced relative risk of CV death/HHF for all baseline hsTnT and NT-proBNP levels. In multivariable linear regression analysis, there were significant correla- tions between hsTnT at baseline and age, male gender, creatinine, left ventricular mass generational troponin T assays. We hypothesize that similar to previous assays, concentrations of high-sensitivity troponin T. (hsTnT) on the 1st and 2nd 22 Mar 2021 Prognostic role of hsTnT. The baseline clinical characteristics of the population stratified by mortality status at follow up are reported in Table 1.

Results: The median baseline NT-proBNP and hsTnT levels were 75 pg/mL (IQR 35-165) and 10.2 pg/mL (IQR 6.9-15.5), respectively. Patients with higher levels of NT-proBNP and hsTnT had higher KM event rates of CVD/HHF (Q4 vs Q1: NT-proBNP: 13.7% vs 1.0%; hsTnT: 11.8% vs 1.4%; P-trend <0.001).

Linear regression analysis was used to identify predictors of baseline hsTnT lev-els and myocardial infarction. Results Elevated hsTnT was observed in 58 of the 204 patients (28.4%). The mean age was 68.3 years in the normal hsTnT group and 69.7 years in the elevated hsTnT group.

However, the relationship between hsTnT and renal outcomes remained strong (p < 0.001) even after adjusting for baseline eGFR. hsTnT is a marker of myocardial injury and micronecrosis, it is therefore possible that cardiac vascular disease, reflected by slightly raised hsTnT levels, could be paralleled by vascular disease in other organs, including the kidneys . Results: The median baseline NT-proBNP and hsTnT levels were 75 pg/mL (IQR 35-165) and 10.2 pg/mL (IQR 6.9-15.5), respectively. Patients with higher levels of NT-proBNP and hsTnT had higher KM event rates of CVD/HHF (Q4 vs Q1: NT-proBNP: 13.7% vs 1.0%; hsTnT: 11.8% vs 1.4%; P-trend <0.001). 2017-12-14 · In 1,600 patients with suspected ACS (48.4% women; median age, 55 years), a single hsTnT level . 6 ng/L at baseline had a negative predictive value for AMI of 99.4%.
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The median baseline NT-proBNP and hsTnT levels were 75 pg/mL (IQR 35-165) and 10.2 pg/mL (IQR 6.9-15.5), respectively. Elevated baseline baseline hsTnT was associated with NIHSS, creatinine, ST segment depression and inverted T waves, but not with stroke location or size.

We hypothesize that similar to previous assays, concentrations of high-sensitivity troponin T. (hsTnT) on the 1st and 2nd 22 Mar 2021 Prognostic role of hsTnT. The baseline clinical characteristics of the population stratified by mortality status at follow up are reported in Table 1. 22 Jan 2015 ABSTRACT High-sensitivity troponin T (hsTnT) helps in identifying pulmonary TABLE 1 Baseline characteristics, medical history, and initial Baseline hsTnT 13-51ng/L. OR. Delta hsTnT 3-4ng/L at 1 hr.
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ranging from a median of 62 in the lowest quartile to 94 in the highest quartile. Postoperative hsTnT elevation was present in 53.2% of the population. An association between MAP quartile and postoperative peak hsTnT was predomi-nantly observed in the lowest quartile (P<0.001): median hsTnT 17.6 (10.3e37.3), 14.9 (9.4e24.6), 13.8 (9.1e22.5

At baseline, samples for hsTnT measurement were taken in ethylenediamine tetraacetic acid tubes, centrifuged, and stored at −80 °C until analysis was performed for all samples at the same time point. Plasma hsTnT were measured by Elecsys diagnostics (Roche, Berlin, Germany) and with a detection limit of 0.01 ng/l (0.00001 μg/l). The median time from symptom onset to ED presentation was 2.9 hours, while time from symptom onset to baseline hsTnT was 5.8 hours. Clinicians should consider that the performance characteristics of hsTnT may not be duplicated at earlier times.

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Methods and Results: In the British Regional Heart Study, 3852 men aged 60 79 years without baseline HF (3165 without baseline chronic heart disease) were followed for a median of 12.6 years, during which 295 incident cases of HF occurred (7.7%). A 1-SD increase in log-transformed hsTnT was associated with

Table 1.