Searched over 200M research papers for "cardiopulmonary disease"
10 papers analyzed
These studies suggest that systemic inflammation, endothelial cell metabolism, and individualized rehabilitation are central to understanding and managing cardiopulmonary diseases, while novel research approaches and holistic management are essential for effective treatment.
20 papers analyzed
Cardiopulmonary diseases such as coronary artery disease (CAD), chronic heart failure (CHF), and chronic obstructive pulmonary disease (COPD) often coexist and share systemic inflammatory reactions. Inflammation is central to the pathogenesis of these diseases, with biomarkers like C-reactive protein (CRP) and interleukin-6 (IL-6) playing significant roles. This interconnectedness is referred to as the "cardiopulmonary continuum," where common risk factors trigger systemic inflammation, leading to the progression of both atherosclerotic diseases and COPD.
Cardiovascular diseases (CVD), including acute myocardial infarction (AMI) and pulmonary hypertension (PH), involve endothelial dysfunction and abnormal blood vessel responses. Emerging evidence suggests that endothelial cell metabolism shifts towards higher glycolysis (the Warburg effect) in these conditions, which may be pivotal in understanding cardiovascular pathogenesis and identifying new therapeutic targets. This metabolic shift disrupts vascular homeostasis and contributes to the progression of both AMI and PH.
For adults with congenital heart diseases, cardiopulmonary exercise testing (CPET) is crucial for assessing cardiovascular function and identifying pathological mechanisms such as circulatory failure and pulmonary hypertension. Common findings include reduced peak oxygen consumption, early anaerobic threshold, and ventilatory inefficiency, which are indicative of compromised exercise capacity and other pathophysiological abnormalities. CPET results are essential for tailoring rehabilitation programs and making informed lifestyle and therapeutic decisions.
As mortality from acute cardiopulmonary diseases decreases and populations age, patients often live with multiple chronic conditions. This multimorbidity, particularly involving the cardiopulmonary-metabolic axis, necessitates a shift from single-disease management to patient-tailored multimorbidity medicine. New research approaches are required to develop diagnostic models and therapeutic prediction models that consider the presence of multiple diseases. This paradigm shift aims to improve clinical practice and patient outcomes.
Residual exertional dyspnea (RED) persists in patients with cardiopulmonary diseases despite optimal therapy. RED is linked to various mechanisms, including increased metabolic cost of work, inspiratory constraints, and diaphragm dysfunction. Recognizing RED highlights the limitations of current treatment approaches and underscores the need for a holistic management strategy. This approach should address the complex interplay of multiple mechanisms contributing to dyspnea.
Following COVID-19 infection, many patients experience persistent cardiopulmonary symptoms and abnormalities. Studies show that while some cardiopulmonary measures improve over time, others remain abnormal compared to controls. Interestingly, persistent symptoms at six months post-COVID-19 do not always correlate with objective measures of cardiopulmonary health, indicating a complex recovery process.
Cardiopulmonary rehabilitation (CR) improves physical function and quality of life in severe COPD and heart failure (HF). However, predictors of mortality, such as baseline steps per day, six-minute walk distance, and NT-proBNP levels, can help identify patients who may not benefit from CR. These predictors are crucial for making informed decisions about CR referrals and management.
Cardiopulmonary bypass often leads to pulmonary dysfunction and is a risk factor for acute respiratory distress syndrome (ARDS). The inflammatory response involves activation of complement, leukocytes, and endothelial cells, leading to tissue damage and potential organ failure. Understanding these mechanisms is vital for managing and mitigating the risks associated with cardiopulmonary bypass.
Cardiopulmonary manifestations significantly impact mortality in systemic sclerosis (SSc) patients. Cardiac involvement, interstitial pulmonary disease, and pulmonary hypertension are primary causes of death. Despite improvements in survival rates, these internal organ involvements remain critical predictors of mortality.
In elderly COPD patients, cardiopulmonary endurance is influenced by disease severity, dyspnea, and lower limb muscle endurance. These factors collectively explain a significant portion of the variance in endurance, highlighting the importance of comprehensive management strategies to improve patient outcomes.
Cardiopulmonary diseases are complex and multifaceted, involving systemic inflammation, metabolic alterations, and multimorbidity. Effective management requires a holistic approach that considers the interconnectedness of heart and lung diseases, the role of endothelial dysfunction, and the impact of persistent symptoms and rehabilitation. Ongoing research and tailored therapeutic strategies are essential for improving patient outcomes in this challenging field.
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