Patients with cardiovascular disease are particularly susceptible to respiratory infections.
A link between common infectious illnesses and cardiovascular diseases has been known for some time. Increasing evidence supports that influenza infections can be a trigger for acute myocardial infarction (AMI) and stroke and that influenza vaccination reduces the risk for cardiovascular morbidity and mortality, particularly in individuals aged 65 and older with high medical risk conditions, including cardiovascular disease. Because of this, the American Heart Association (AHA) and American College of Cardiology (ACC) recommend that patients with cardiovascular disease receive influenza vaccination to prevent flu-related respiratory diseases and other complications, including cardiovascular events. For more information on the flu vaccine and how to prevent the flu visit the CDC webpage.
COVID-19
The novel coronavirus disease 2019 (COVID-19) is an infectious respiratory disease caused by a novel coronavirus first detected in China that has now spread internationally. The World Health Organisation has declared COVID-19 a pandemic. The virus responsible for the disease is named “SARS-CoV-2” and the disease it causes has been dubbed COVID-19.
This is a rapidly emerging situation. While most individuals infected with the virus are likely to experience mild symptoms and recover without intensive medical intervention, some persons will develop more severe symptoms and require intensive care support. Fatality rates are low (2.3% based on published reports) but this is likely to change as further information becomes available.
What we have learned from initial epidemiological reports of persons with COVID-19 pneumonia in Wuhan, China (Wang D et al, JAMA 2020;323(11):1061-1069) suggests that older persons with underlying chronic medical conditions may be at higher risk of contracting the disease and have a worse prognosis. In the recently published report of 138 hospitalized patients with confirmed COVID-19 infection, the median age was 56 (range 22 to 92) years and 54% were male. More than 46% had one or more comorbidities, with hypertension (31.2%), cardiovascular disease (14.5%), and diabetes (10.1%) being the most common coexisting conditions. Patients that required ICU care were older and more likely to have underlying cardiovascular and cerebrovascular conditions compared with those that did not require ICU support. Acute cardiac injury (7.2%) and arrhythmia (16.7%) were among the more common complications reported, especially in those requiring ICU care. Fatality rates are also higher for individuals with comorbid CV and diabetes conditions.
Based on available clinical information, the ACC issued a COVID-19 Cardiovascular Guidance for the Clinical Care Team to better care for patients, especially those with existing cardiovascular disease that may contract the virus.
COVID-19 clinical operations
Keeping your clinical trial on track in an evolving environment.
RAAS Antagonists and COVID-19
Angiotensin converting enzyme 2 (ACE2) receptors have been shown to be the entry point into human cells for SARS-CoV-2, the virus that causes COVID-19. In preclinical studies, angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs) have been shown to upregulate ACE2 expression in the heart leading to speculation of potential increased risk of COVID-19 infection in persons on these medications. The Heart Failure Society of America (HFSA), ACC, and American Heart Association (AHA) have just released a statement addressing this concern and emphasise there are no experimental or clinical data showing a benefit or adverse outcome with use of these drugs or among COVID-19 patients with cardiovascular disease. Combined, these organisations emphasize the continuation of ACE inhibitors/ARBs for patients currently prescribed them for indications in which they have shown benefit in accordance with clinical practice standards. The European Society of Cardiology (ESC) has issued a similar statement on this topic.
Additional COVID-19 resources for those with cardiovascular disease can be found on the American Heart Association website.
ICON is an experienced partner who can help you navigate the clinical development challenges in cardiovascular and metabolic diseases. To speak with one of our experts, please contact us.
Cardiovascular, Metabolic and Circulation insights
ICON's Cardiovascular team contributes regularly to industry publications and media coverage of cardiovascular clinical trials. Stay up to date with ICON's latest thought leadership on cardiovascular clinical trials.
In this section
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Digital Disruption
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Clinical strategies to optimise SaMD for treating mental health
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Digital Disruption: Surveying the industry's evolving landscape
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Clinical trial data anonymisation and data sharing
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Clinical Trial Tokenisation
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Closing the evidence gap: The value of digital health technologies in supporting drug reimbursement decisions
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Digital disruption in biopharma
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Disruptive Innovation
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Personalising Digital Health
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The triad of trust: Navigating real-world healthcare data integration
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Clinical strategies to optimise SaMD for treating mental health
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Patient Centricity
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Agile Clinical Monitoring
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Capturing the voice of the patient in clinical trials
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Charting the Managed Access Program Landscape
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Developing Nurse-Centric Medical Communications
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Exploring the patient perspective from different angles
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Patient safety and pharmacovigilance
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A guide to safety data migrations
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Taking safety reporting to the next level with automation
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Outsourced Pharmacovigilance Affiliate Solution
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The evolution of the Pharmacovigilance System Master File: Benefits, challenges, and opportunities
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Sponsor and CRO pharmacovigilance and safety alliances
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Understanding the Periodic Benefit-Risk Evaluation Report
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A guide to safety data migrations
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Patient voice survey
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Patient Voice Survey - Decentralised and Hybrid Trials
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Reimagining Patient-Centricity with the Internet of Medical Things (IoMT)
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Using longitudinal qualitative research to capture the patient voice
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Agile Clinical Monitoring
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Regulatory Intelligence
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An innovative approach to rare disease clinical development
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Using innovative tools and lean writing processes to accelerate regulatory document writing
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Current overview of data sharing within clinical trial transparency
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Global Agency Meetings: A collaborative approach to drug development
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Keeping the end in mind: key considerations for creating plain language summaries
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Navigating orphan drug development from early phase to marketing authorisation
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Procedural and regulatory know-how for China biotechs in the EU
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RACE for Children Act
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Early engagement and regulatory considerations for biotech
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Regulatory Intelligence Newsletter
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Requirements & strategy considerations within clinical trial transparency
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Leveraging historical data for use in rare disease trials
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Patient Centricity in Orphan Drug Development
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The key to remarkable rare disease registries
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Therapeutic spotlight: Precision medicine considerations in rare diseases
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Advanced therapies for rare diseases
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Decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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Decentralised and Hybrid clinical trials
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Practical considerations in transitioning to hybrid or decentralised clinical trials
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Navigating the regulatory labyrinth of technology in decentralised clinical trials
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Biopharma perspective: the promise of decentralised models and diversity in clinical trials
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eCOA implementation
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Implications of COVID-19 on statistical design and analyses of clinical studies
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Increasing Complexity and Declining ROI in Drug Development
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Evidence Synthesis: A solution to sparse evidence, heterogeneous studies, and disconnected networks
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Making Sense of the Biosimilars Market
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Navigating the Challenges and Opportunities of Value Based Healthcare
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Payer Reliance on ICER and Perceptions on Value Based Pricing
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Payers Perspectives on Digital Therapeutics
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RWE Generation Cross Sectional Studies and Medical Chart Review
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Survey results: How to engage healthcare decision-makers
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