| 1. |
|
|
| 2. |
|
|
| 3. |
|
|
| 4. |
|
|
| 5. |
|
|
| 6. |
- Heimark, Sondre, et al.
(författare)
-
Which Target Blood Pressure in Year 2018? Evidence from Recent Clinical Trials
- 2018
-
Ingår i: High Blood Pressure and Cardiovascular Prevention. - : Springer Science and Business Media LLC. - 1120-9879 .- 1179-1985. ; 25:2, s. 151-158
-
Forskningsöversikt (refereegranskat)abstract
- The Systolic Blood Pressure Intervention Trial (SPRINT) suggested a favourable effect of lowering blood pressure to < 120/80 mmHg in high-risk hypertensive patients; however, new American guidelines in 2017 have not followed SPRINT but lowered its recommended treatment target to < 130/80 mmHg. We aimed to review the latest research from large randomised controlled trials and observational analyses in order to investigate the evidence for new treatment targets. We assessed recent data from the Action to Control Cardiovascular Risk in Diabetes Blood Pressure (ACCORD) study, the International Verapamil-Trandolapril Study (INVEST), the Telmisartan, Ramipril or Both in Patients at High Risk for Vascular Events trial (ONTARGET)/the Telmisartan Randomised AssessmenNt Study in aCE iNtolerant participants with cardiovascular Disease (TRANSCEND) study and The Losartan Intervention For Endpoint Reduction in Hypertension (LIFE) study. These studies confirm a positive effect on cardiovascular protection with blood pressure lowering treatment to between 120–140 mmHg in patients with and without diabetes, but no additional effect of lowering blood pressure to < 120 mmHg; possibly too aggressive treatment may increase both cardiovascular morbidity and mortality. Thus, a target blood pressure < 130/80 mmHg appears appropriate in most high-risk hypertensive patients. Additionally, early and sustained BP control below this target is required for optimal cardiovascular protection.
|
|
| 7. |
|
|
| 8. |
|
|
| 9. |
|
|
| 10. |
|
|
| 11. |
|
|
| 12. |
|
|
| 13. |
|
|
| 14. |
|
|
| 15. |
|
|
| 16. |
|
|
| 17. |
|
|
| 18. |
|
|
| 19. |
- Brunström, Mattias, et al.
(författare)
-
Effect of antihypertensive treatment in isolated systolic hypertension (ISH) : systematic review and meta-analysis of randomised controlled trials
- 2023
-
Ingår i: Blood Pressure. - : Taylor & Francis Group. - 0803-7051 .- 1651-1999. ; 32:1
-
Tidskriftsartikel (refereegranskat)abstract
- BACKGROUND: Isolated systolic hypertension (ISH) in middle-aged and elderly is associated with high cardiovascular risk, but no randomised controlled trial has assessed the effect of antihypertensive treatment in ISH using today's definition, i.e. systolic blood pressure (SBP) ≥140 mmHg and diastolic blood pressure (DBP) <90 mmHg.METHODS: A systematic review and meta-analysis of randomised controlled trials was performed. Studies with ≥1000 patient-years of follow-up, comparing more intensive versus less intensive BP targets, or active drug versus placebo, were included if the mean baseline SBP was ≥140 mmHg and the mean baseline DBP was <90 mmHg. The primary outcome was major adverse cardiovascular events (MACE). Relative risks from each trial were pooled in random-effects meta-analyses, stratified by baseline and attained SBP level.RESULTS: Twenty-four trials, including 113,105 participants (mean age 67 years; mean blood pressure 149/83 mmHg) were included in the analysis. Overall, treatment reduced the risk of MACE by 9% (relative risk 0.91, 95% confidence interval 0.88-0.93). Treatment was more effective if baseline SBP was ≥160 mmHg (RR 0.77, 95% CIs 0.70-0.86) compared to 140-159 mmHg (RR 0.92, 95% CIs 0.89-0.95; p = 0.002 for interaction), but provided equal additional benefit across all attained SBP levels (RR 0.80, 95% CIs 0.70-0.92 for <130 mmHg, RR 0.92, 95% CIs 0.89-0.96 for 130-139 mmHg, and RR 0.87, 95% CIs 0.82-0.93 for ≥140 mmHg; p = 0.070 for interaction).CONCLUSIONS: These findings support antihypertensive treatment of isolated systolic hypertension, regardless of baseline SBP, to target SBP <140 mmHg and even <130 mmHg if well tolerated.
|
|
| 20. |
|
|
| 21. |
|
|
| 22. |
|
|
| 23. |
- Gerdts, Eva, et al.
(författare)
-
Ingrid Toft (June 2, 1959-April 26, 2014)
- 2014
-
Ingår i: Blood Pressure. - : Taylor & Francis. - 0803-7051 .- 1651-1999. ; 23:4, s. 255-255
-
Tidskriftsartikel (populärvet., debatt m.m.)
|
|
| 24. |
- Hasvold, Pal, et al.
(författare)
-
Association Between Paradoxical HDL Cholesterol Decrease and Risk of Major Adverse Cardiovascular Events in Patients Initiated on Statin Treatment in a Primary Care Setting
- 2016
-
Ingår i: Clinical drug investigation. - : Springer Science and Business Media LLC. - 1173-2563 .- 1179-1918. ; 36:3, s. 225-233
-
Tidskriftsartikel (refereegranskat)abstract
- Background and Objectives Statin-induced changes in high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C) are unrelated. Many patients initiated on statins experience a paradoxical decrease in HDL-C. The aim of this study was to evaluate the association between a decrease in HDL-C and risk of major adverse cardiovascular events (MACE). Methods Data from 15,357 primary care patients initiated on statins during 2004-2009 were linked with data from mandatory national hospital, drug-dispensing, and cause-of-death registers, and were grouped according to HDL-C change: decreased >= 0.1 mmol/L, unchanged +/- 0.1 or >= 0.1 mmol/L increased. To evaluate the association between decrease in HDL-C and risk of MACE, a sample of propensity score-matched patients from the decreased and unchanged groups was created, using the latter group as reference. MACE was defined as myocardial infarction, unstable angina pectoris, ischaemic stroke, or cardiovascular mortality. Cox proportional hazards models were used to estimate relative risks. Results HDL-C decreased in 20 %, was unchanged in 58%, and increased in 22 % of patients initiated on statin treatment (96 % treated with simvastatin). The propensity score-matched sample comprised 5950 patients with mean baseline HDL-C and LDL-C of 1.69 and 4.53 mmol/L, respectively. HDL-C decrease was associated with 56 % higher MACE risk (hazard ratio 1.56; 95 % confidence interval 1.12-2.16; p < 0.01) compared with the unchanged HDL-C group. Conclusions Paradoxical statin-induced reduction in HDL-C was relatively common and was associated with increased risk of MACE.
|
|
| 25. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Achieving better blood pressure control.
- 2008
-
Ingår i: Blood pressure. - Stockholm : Informa Healthcare. - 1651-1999 .- 0803-7051. ; 17 Suppl 1, s. 3-4
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 26. |
|
|
| 27. |
|
|
| 28. |
|
|
| 29. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Health economy of the metabolic syndrome pandemic.
- 2005
-
Ingår i: Blood pressure. - Stockholm : Taylor & Francis. - 0803-7051 .- 1651-1999. ; 14:3, s. 131-2
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 30. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Hypertension control - a global challenge.
- 2005
-
Ingår i: Blood pressure. - Stockholm : Taylor & Francis. - 1651-1999 .- 0803-7051. ; 14 Suppl 1, s. 4-5
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 31. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Hypertension research into the new millennium.
- 2010
-
Ingår i: Blood pressure. - Stockholm : Informa Healthcare. - 1651-1999 .- 0803-7051. ; 19:1, s. 1-2
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 32. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Management of older hypertensive patients.
- 2008
-
Ingår i: Blood pressure. - Stockholm : Informa Healthcare. - 1651-1999 .- 0803-7051. ; 17:4, s. 184-5
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 33. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Medical decision making in hypertension.
- 2006
-
Ingår i: Blood pressure. - Stockholm : Taylor & Francis. - 0803-7051 .- 1651-1999. ; 15:4, s. 196-7
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 34. |
|
|
| 35. |
|
|
| 36. |
- Hedner, Thomas, 1949, et al.
(författare)
-
RAAS inhibition--a practice of medical progress.
- 2006
-
Ingår i: Blood pressure. - Stockholm : Taylor & Francis. - 1651-1999 .- 0803-7051. ; 15 Suppl 1, s. 5-6
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 37. |
|
|
| 38. |
|
|
| 39. |
|
|
| 40. |
|
|
| 41. |
- Hedner, Thomas, 1949, et al.
(författare)
-
Valuable lessons from VALUE.
- 2004
-
Ingår i: Blood pressure. - Stockholm : Taylor & Francis. - 0803-7051. ; 13:4, s. 196-7
-
Annan publikation (övrigt vetenskapligt/konstnärligt)
|
|
| 42. |
|
|
| 43. |
|
|
| 44. |
|
|
| 45. |
|
|
| 46. |
|
|
| 47. |
- Kjeldsen, Sverre E, et al.
(författare)
-
Predictors of cardiovascular events in patients with hypertension and left ventricular hypertrophy : the losartan inventervention for endpoint reduction in hypertension study
- 2009
-
Ingår i: Blood Pressure. - 0803-7051 .- 1651-1999. ; 18:6, s. 348-361
-
Tidskriftsartikel (refereegranskat)abstract
- Objective. We assessed readily available patient characteristics, including albuminuria (not included in traditional cardiovascular risk scores), as predictors of cardiovascular events in hypertension with left ventricular hypertrophy (LVH) and developed risk algorithms/scores for outcomes. Methods. The Losartan Intervention For Endpoint reduction in hypertension (LIFE) study compared effects of losartan-based versus atenolol-based therapy on cardiovascular events in 9193 patients with hypertension and LVH. Univariate and multivariate analyses identified baseline variables with significant impact on development of the primary composite endpoint (cardiovascular death, stroke and myocardial infarction) and its components. Multivariate analysis used a Cox regression model with stepwise selection process. Risk scores were developed from coefficients of risk factors from the multivariate analysis, validated internally using naïve and jack-knife procedures, checked for discrimination and calibration, and compared with Framingham coronary heart disease and other risk scores. Results. LIFE risk scores showed increasing endpoint rates with increasing quintile (first to fifth quintile, composite endpoint 2.8–26.7%, cardiovascular death 0.5–14.4%, stroke 1.2–11.3%, myocardial infarction 1.4–8.1%) and were confirmed with a jack-knife approach that adjusts for potentially optimistic bias. The Framingham coronary heart disease and other risk scores overestimated risk in lower risk patients and underestimated risk in higher risk patients, except for myocardial infarction. Conclusion. A number of patient characteristics predicted cardiovascular events in patients with hypertension and LVH. Risk scores developed from these patient characteristics, including albuminuria, strongly predicted outcomes and may improve risk assessment of patients with hypertension and LVH and planning of clinical trials.
|
|
| 48. |
|
|
| 49. |
|
|
| 50. |
|
|
