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      Observed change in peak oxygen consumption after aortic valve replacement and its predictors

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      , ,
      Open Heart
      BMJ Publishing Group

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          Abstract

          Objective

          To assess the change in peak oxygen consumption (pVO 2) and determine its outcome predictors after aortic valve replacement (AVR) for aortic stenosis (AS).

          Methods

          Patients with AS and preserved left ventricular ejection fraction who were referred for single AVR had cardiopulmonary exercise testing prior to and 9 months post-AVR. Predictors of outcome for pVO 2 were determined by multivariate linear and logistic regression analyses. A significant change in pVO 2 was defined as a relative change that was more than twice the coefficient of repeatability by test–retest (>10%).

          Results

          The pre-AVR characteristics of the 37 study patients included the following: median age (range) 72 (46–83) years, aortic valve area index (AVAI) 0.41 (SD 0.11) cm 2/m 2, mean gradient (MG) 49.1 (SD 15.3) mm Hg and New York Heart Association (NYHA)≥II 27 (73%). Pre-AVR and post-AVR mean pVO 2 was 18.5 and 18.4 mL/kg/m 2 (87% of the predicted), respectively, but the change from pre-AVR was heterogeneous. The relative change in pVO 2 was positively associated with the preoperative MG (β=0.50, p=0.001) and negatively associated with brain natriuretic peptide > upper level of normal according to age and gender (β=−0.40, p=0.009). A relative increase in pVO 2 exceeding 10% was found in 9 (24%), predicted by lower pre-AVR AVAI (OR 0.18; 95% CI 0.04 to 0.82, p=0.027) and lower peak O 2 pulse (OR 0.94; 95% CI 0.88 to 0.99, p=0.045). Decreases in pVO 2 exceeding 10% were found in 11 (30%) and predicted by lower MG (OR 0.93; 95% CI 0.86 to 0.99, p=0.033).

          Conclusions

          Change in pVO 2 was heterogeneous. Predictors of favourable and unfavourable outcomes for pVO 2 were identified.

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          Most cited references20

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          Comparative reproducibility and validity of systems for assessing cardiovascular functional class: advantages of a new specific activity scale.

          Reproducibility and validity are prerequisites for a useful clinical scale. We therefore prospectively tested the reproducibility and validity of the New York Heart Association criteria and the Canadian Cardiovascular Society criteria for the assessment of cardiac functional class and compared these criteria with a new Specific Activity Scale based on the metabolic costs of specific activities. The New York Heart Association estimates made by two physicians had a reproducibility of only 56%, and only 51% of the estimates agreed with treadmill exercise performance. Functional estimates based on the Canadian Cardiovascular Society criteria were significantly more reproducible (73%), but not significantly more valid. The Specific Activity Scale was as reproducible as the Canadian Cardiovascular Society criteria, and its 68% validity was significantly higher than the validities of the other systems. The easily administered Specific Activity Scale was equally reproducible and valid when used by a nonphysician. It was especially better than the other systems for the evaluation of true class II patients and was significantly less likely to underestimate treadmill performance. Although no set of questions can perfectly predict exercise tolerance, the Specific Activity Scale deserves wider prospective testing.
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            An evaluation of internal-mammary-artery ligation by a double-blind technic.

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              Reproducibility of 6-minute walking test in patients with COPD.

              The reproducibility of the 6-min walking test (6MWT) needs to be more solidly studied. This study aimed to investigate the reproducibility of two 6MWTs performed on subsequent days in a large and representative sample of patients with chronic obstructive pulmonary disease (COPD), and to quantify the learning effect between the two tests, as well as its determinants. In a retrospective observational study, 1,514 patients with COPD performed two 6MWTs on subsequent days. Other measurements included body composition (dual X-ray absorptiometry), dyspnoea (Medical Research Council scale) and comorbidity (Charlson index). Although the 6MWT was reproducible (intraclass correlation coefficient = 0.93), patients walked farther in the second test (391 m, 95% CI 155-585 m versus 418 m, 95% CI 185-605 m; p<0.0001). On average, the second 6MWT increased by 27 m (or 7%), and 82% of patients improved in the second test. Determinants of improvement ≥ 42 m in the second test (upper limit of the clinically important change) were as follows: first 6MWT <350 m, Charlson index <2 and body mass index <30 kg · m(-2) (OR 2.49, 0.76 and 0.60, respectively). The 6MWT was statistically reproducible in a representative sample of patients with COPD. However, the vast majority of patients improved significantly in the second test by an average learning effect of 27 m.
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                Author and article information

                Journal
                Open Heart
                Open Heart
                openhrt
                openheart
                Open Heart
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2053-3624
                2016
                26 May 2016
                : 3
                : 1
                : e000309
                Affiliations
                Department of Cardiology, Roskilde University Hospital , Roskilde, Denmark
                Author notes
                [Correspondence to ] Dr Lars Kjøller-Hansen; lak@ 123456regionsjaelland.dk
                Article
                openhrt-2015-000309
                10.1136/openhrt-2015-000309
                4885434
                27252876
                68d16307-e5b9-4ea8-9652-2aebc0fb4186
                Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

                History
                : 26 June 2015
                : 18 March 2016
                : 25 April 2016
                Categories
                Valvular Heart Disease
                1506
                Original research article

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