Dear all
These are the direct links to the YouTube videos as there is a problem with my original instructions
https://youtu.be/_6Qh4LXuWnU (anaerobic threshold)
https://youtu.be/SVV5nKtS_uc (exercise and CPET)
My regards
Paul Older
Dear all
These are the direct links to the YouTube videos as there is a problem with my original instructions
https://youtu.be/_6Qh4LXuWnU (anaerobic threshold)
https://youtu.be/SVV5nKtS_uc (exercise and CPET)
My regards
Paul Older
Dear all
If you open YouTube you will see a column on the left showing you the various possibilities available.
CLICK on ‘Playlists‘ and a new page will open. This page will have three or more large icons. The one on the left is set up by me and has videos pertaining to CPET.
CLICK on ‘View full playlist’ under that icon and you will see that there are two choice of videos available to you.
The one on ‘Anaerobic threshold’ is a presentation of Professor Agostoni and could be of interest to all of you.
The other is an introduction to ‘Exercise and CPET’ which gives an insight of what CPET is all about for anyone interested.
Hope you find something of interest.
My best regards
Paul Older
.
Santana, J; Stanford Cardiovascular Institute, Stanford University, Stanford, CA, USA.;
Kim, D; Christle, J, et al
European journal of preventive cardiology,2025 Feb 07
Natalia, G; Almazov National Medical Research Center, Saint-Petersburg, Russia.
Lapshin, K; Berezina, A, et al.
Annals of thoracic medicine,2025 Jan-Mar
Wong, M; Asthma, Allergy and Clinical Immunology Service, Alfred Health, Australia.
Gardner, L; Denton, E, et al.
Journal of science and medicine in sport,2025 Feb
Bokov, P; Hôpital Robert Debré, Service de Physiologie Pédiatrique, Paris, France
Dudoignon, B; Fikiri Bavurhe; R;Couque, N; et al
Pediatric research,2025 Jan
Khilzi, Pulmonology Department-Hospital del Mar Pulmonary Hypertension Unit Barcelona Spain.
Karys; Piccari, Lucilla; Franco, Gerard, et al.
Pulmonary circulation,2025 Feb 05Although current guidelines recommend standard cardiopulmonary exercise testing (CPET) to evaluate symptomatic patients after pulmonary embolism (PE), CPET with simultaneous echocardiography could provide relevant information to evaluate right ventricular-pulmonary arterial coupling.
AIMS
The aim of this study was to investigate exercise-induced changes in echocardiographic variables of RV function or RV- arterial coupling in patients with residual thrombotic defects at 3 months after PE.
METHODS
This retrospective study investigated patients with residual thromboembolic disease on V/Q scintigraphy with persistent symptoms despite adequate anticoagulation after 3 months of acute PE, and resting echocardiography with a low probability of PH. At rest and during exercise, CPET and doppler echocardiography were performed following a standard protocol. Forty-five patients were included, completing a follow-up period of at least 24 months. The mean (standard deviation) age was 63 (15) years, and 24 (53%) patients were male.
RESULTS
Four patients developed CTEPH after 2 years follow up. Correlation analyses showed that the peak TAPSE was significantly associated with peak workload ( r = 0.454, p = 0.003), peak VO 2 ( r = 0.558, p < 0.001), VE/VECO 2 (AT) ( r = -0.531, p < 0.001), and oxygen pulse ( r = 0.375, p = 0.02). TAPSE/PASP was only slightly associated with peak workload ( r = 0.300, p = 0.045). By contrast, the change on TAPSE (from rest to peak) was significantly correlate with peak oxygen uptake ( r = 0.491, p = 0.01). Also, reduced VO 2 at AT and TAPSE/PASP was seen in patients with CTEPH. CPET with synchronic echocardiography could be a useful tool in early assessment of symptomatic patients with perfusion defects on imaging after 3 months of correctly treated PE.
T. Atanasovska, Melbourne Australia
T. Farr, R. Smith, A. C. Petersen, A. Garnham, M. J. Andersen, et al.
J Physiol 2024 Vol. 602 Issue 24 Pages 6849-6869
We investigated acute effects of the Na(+),K(+)-ATPase (NKA) inhibitor, digoxin, on muscle NKA content and isoforms, arterial plasma [K(+)] ([K(+)](a)) and fatigue with intense exercise.
In a randomised, crossover, double-blind design, 10 healthy adults ingested 0.50 mg digoxin (DIG) or placebo (CON) 60 min before cycling for 1 min at 60% V̇O2peak then at 95% V̇O2peak until fatigue. Pre- and post-exercise muscle biopsies were analysed for [(3)H]-ouabain binding site content without (OB-F(ab)) and after incubation in digoxin antibody (OB+F(ab)) and NKA alpha(1-2) and beta(1-2) isoform proteins. In DIG, pre-exercise serum [digoxin] reached 3.36 (0.80) nM [mean (SD)] and muscle NKA-digoxin occupancy was 8.2%. Muscle OB-F(ab) did not differ between trials, whereas OB+F(ab) was higher in DIG than CON (8.1%, treatment main effect, P = 0.001), whilst muscle NKA alpha(1-2) and beta(1-2) abundances were unchanged by digoxin. Fatigue occurred earlier in DIG than CON [-7.7%, 2.90 (0.77) vs. 3.14 (0.86) min, respectively; P = 0.037]. [K(+)](a) increased during exercise until 1 min post-exercise (P = 0.001), and fell below baseline at 3-10 (P = 0.001) and 20 min post-exercise (P = 0.022, time main effect). In DIG, [K(+)](a) (P = 0.035, treatment effect) and [K(+)](a) rise pre-fatigue were greater [1.64 (0.73) vs. 1.55 (0.73), P = 0.016], with lesser post-exercise [K(+)](a) decline than CON [-2.55 (0.71) vs. -2.74 (0.62) mM, respectively, P = 0.003]. Preserved muscle OB-F(ab) with digoxin, yet increased OB+F(ab) with unchanged NKA isoforms, suggests a rapid regulatory assembly of existing NKA alpha and beta subunits exists to preserve muscle NKA capacity. Nonetheless, functional protection against digoxin was incomplete, with earlier fatigue and perturbed [K(+)](a) with exercise.
KEY POINTS: Intense exercise causes marked potassium (K(+)) shifts out of contracting muscle cells, which may contribute to muscle fatigue. Muscle and systemic K(+) perturbations with exercise are largely regulated by increased activity of Na(+),K(+)-ATPase in muscle, which can be specifically inhibited by the cardiac glycoside, digoxin. We found that acute oral digoxin in healthy adults reduced time to fatigue during intense exercise, elevated the rise in arterial plasma K(+) concentration during exercise and slowed K(+) concentration decline post-exercise. Muscle functional Na(+),K(+)-ATPase content was not reduced by acute digoxin, despite an 8.2% digoxin occupancy, and was unchanged at fatigue. Muscle Na(+),K(+)-ATPase isoform protein abundances were unchanged by digoxin or fatigue. These suggest possible rapid assembly of existing subunits into functional pumps. Thus, acute digoxin impaired performance and exacerbated plasma K(+) disturbances with intense, fatiguing exercise in healthy participants. These occurred despite the preservation of functional Na(+),K(+)-ATPase in muscle.
Daza JF; University of Toronto, Toronto, Ontario, Canada
Chesney TR; Morales JF; Xue Y; Lee S; Amado LA; Pivetta B;
Mbadjeu Hondjeu AR; Jolley R; Diep C; Alibhai SMH; Smith PM; Kennedy ED;
Racz E; Wilmshurst L; Wijeysundera DN
Annals of Internal Medicine. 178(1):75-87, 2025 Jan.
BACKGROUND: Functional capacity is critical to preoperative risk
assessment, yet guidance on its measurement in clinical practice remains
lacking.
PURPOSE: To identify functional capacity assessment tools studied before
surgery and characterize the extent of evidence regarding performance,
including in populations where assessment is confounded by
noncardiopulmonary reasons.
DATA SOURCES: MEDLINE, EMBASE, and EBM Reviews (until July 2024).
STUDY SELECTION: Studies evaluating performance of functional capacity
assessment tools administered before elective noncardiac surgery to
stratify risk for postoperative outcomes.
DATA EXTRACTION: Study details, measurement properties, pragmatic
qualities, and/or clinical utility metrics.
DATA SYNTHESIS: 6 categories of performance-based tests and 5 approaches
using patient-reported exercise tolerance were identified. Cardiopulmonary
exercise testing (CPET) was the most studied tool (132 studies, 32 662
patients) followed by field walking tests (58 studies, 9393 patients)
among performance-based tests. Among patient-reported assessments, the
Duke Activity Status Index (14 studies, 3303 patients) and unstructured
assessments (19 studies, 28 520 patients) were most researched. Most
evidence focused on predictive validity (92% of studies), specifically
accuracy in predicting cardiorespiratory complications. Several tools
lacked evidence on reliability (test consistency across similar
measurements), pragmatic qualities (feasibility of implementation), or
concurrent criterion validity (correlation to gold standard). Only CPET
had evidence on clinical utility (whether administration improved
postoperative outcomes). Older adults (>=65 years) were well represented
across studies, whereas there were minimal data in patients with obesity,
lower-limb arthritis, and disability.
LIMITATION: Synthesis focused on reported data without requesting missing
information.
CONCLUSION: Though several tools for preoperative functional capacity
assessment have been studied, research has overwhelmingly focused on CPET
and only 1 aspect of validity (predictive validity). Important evidence
gaps remain among vulnerable populations with obesity, arthritis, and
physical disability.
Fakhri S; Boston University Medical Center, Boston, Massachusetts, USA.
Campedelli L; Risbano MG
European Journal of Clinical Investigation. 55(2):e14343, 2025 Feb.
BACKGROUND: Preload insufficiency is an underrecognized cause of exercise
intolerance identified during invasive cardiopulmonary exercise testing,
and defined hemodynamically by decreased biatrial filling pressures,
cardiac output, and oxygen consumption (VO2) at peak effort. Patients with
preload insufficiency, however, typically present with symptoms of dyspnea
on exertion, and/or exercise intolerance at submaximal efforts,
particularly when performing activities of daily living. The
cardiopulmonary hemodynamics and physiology at submaximal work levels of
preload insufficiency have not been previously investigated. We
hypothesized that preload insufficiency hemodynamics exist along a
continuum, with submaximal exercise values reflecting peak exercise
cardiopulmonary hemodynamics.
METHODS: We compared submaximal cardiopulmonary hemodynamics, measured at
anaerobic threshold, between preload insufficiency patients and
age-matched controls referred for dyspnea but with normal exercise
responses.
RESULTS: Our study included 66 patients: 41 with preload insufficiency
and 25 controls. Preload insufficiency patients exhibit significantly
reduced VO2, watts, and METS at submaximal levels compared to controls,
alongside earlier anaerobic threshold achievement and similar heart rates
at anaerobic threshold.
CONCLUSIONS: These findings underscore the profound impact of preload
insufficiency on submaximal exercise capacity, emphasizing the importance
of its recognition and management. This insight sets the stage for further
investigations into interventions targeting preload insufficiency at
submaximal exercise levels to enhance both exercise performance and
quality of life.