Target enrichment is an essential process for multiple types of DNA or genetic sequencing techniques, and depending on which technique is in question, the actual process will vary quite a bit in both degree and process. Let’s get into the discussion with a general definition of what target enrichment is.
What is Target Enrichment?
Target enrichment may involve different methods, depending on the particular type of sequencing, the exact sample, as well as the expected results (reason). It can still be defined in a more general sense as they all work towards selectively isolating the precise, genomic sections necessary for the sequencing.
Target enrichment is a preparatory step which amplifies both the speed and accuracy of the results derived from DNA sequencing. For finding and identifying nucleic acids and the variations between them with speed and supreme sensitivity, target enrichment is a time-tested and highly efficient step. It should be a standard procedure before the sequencing procedure can begin.
In instances of Targeted Next Generation Sequencing (TNGS), target enrichment has been found to be of crucial importance for reducing the time which would be necessary for previous generation of targeted sequencing to be completed. Next, we will focus more on TNGS and how target enrichment works towards making the modern sequencing process more accurate, cost effective and quicker.
More than a year after scientists identified the first cases of COVID-19, infection rates continue to rise in regions across the United States.
The virus has been particularly devastating for those who can afford it least: the elderly, underserved communities, low-income families, and people of all ages with chronic conditions.
COVID-19 infection, hospitalization, and death rates for these groups are dramatically higher than for other populations.
According to the CDC, eight out of ten reported COVID-19 deaths in the US are among individuals 65 or older. And data from the COVID Tracking Project reveals that Black or African American individuals are up to 1.5 times more likely to die from COVID-19 than white patients.
Patients with multiple chronic diseases are also at elevated risk. The CDC cites chronic kidney disease, COPD, obesity, and heart conditions as known contributors to poor outcomes from COVID-19, while Medicare statistics show extremely high rates of hypertension and hyperlipidemia, diabetes, and chronic kidney disease among hospitalized beneficiaries.
All these groups have another major risk factor in common. They are the populations that most often struggle to cope with the social determinants of health (SDOH), such as food security, social isolation, and access to healthcare, living wage employment, and transportation.
In the current economic environment, many of these individuals are even facing the hard choice of prioritizing food and shelter over the expenses of necessary healthcare and medications, despite the knowledge that avoiding care may increase their vulnerability to their preexisting conditions – and subsequently raise their chances of experiencing a worse outcome if they contract COVID-19.
Even with the prospect of mass vaccination on the horizon, it’s more important than ever for healthcare providers and health plans to understand and address the social determinants of health, starting with ensuring pharmacy access and medication adherence.
The role of medication adherence in population health management
Population health management focuses on staying one step ahead of the clinical and non-clinical factors that may lead to poor outcomes in targeted patient groups. For the six in ten Americans with at least one chronic disease, medication adherence is a critical component of maintaining good health.
Suboptimal medication adherence has significant impacts on chronic disease management and overall wellbeing. Incorrect use of medications contributes to tens of thousands of preventable deaths and half a trillion dollars in healthcare waste every year.
The reasons behind medication adherence issues are varied and challenging. Some patients experience undesirable side effects and change their doses without consulting their physicians, while others struggle to understand the importance of their prescriptions or fit their medications into their daily routines.
For patients with socioeconomic difficulties, the problem gets even more complex. Out-of-pocket drug costs are skyrocketing, leading large percentages of patients to abandon their medications unwillingly.
By Devin Partida, technology writer and the editor-in-chief, ReHack.com.
Medical billing records may help create a fuller picture of how the COVID-19 virus has impacted the country.
Researchers have started taking to repositories of claim and billing code data to learn more about patients — who they are, what challenges they faced and how they had to navigate the health care system during a pandemic.
Combined with other data on the financial impact of COVID, this research offers a much clearer view of how the pandemic has impacted patients and strained the American medical system.
1. Chronic Kidney Disease May Be the Most Common COVID-19 Comorbidity
In July, FAIR Health, a provider of health care solutions, released a report on how billing records could reveal more about COVID patients’ stories. Most prior case studies found that type 2 diabetes and hypertension were the most common comorbidities. Respiratory conditions, like asthma, COPD and sleep apnea, along with heart conditions, typically made up the rest of the top 10.
The billing data was mostly in line with these previous findings — but had one key difference. The No. 1 comorbidity was chronic kidney disease and failure, rather than hypertension or diabetes.
The FAIR Health report also diverged from other case studies in finding that anxiety was one of the top 10 comorbidities, coming in at ninth place.
An increasing number of entrepreneurs and innovators are tackling challenges in healthcare, but many of these solutions will never make it to market. It is critical to lay the right foundation by applying the principles of discovery and validation early in the process of innovation in healthcare technology.
Understanding the Basics of Discovery and Validation
Innovation thought leaders like Steve Blank have lauded the importance of discovery and validation. During the discovery phase, innovators gather data to substantiate market needs by talking to potential customers and other stakeholders. This data forms the first iteration of a business model.
Despite being informed by data, the business model also contains numerous assumptions. During validation, experiments are designed to test assumptions and reduce uncertainty. Often, experiments yield new insights and inform business model pivots while requiring innovators to conduct additional discovery. Innovators must collect enough data to feel confident about their assumptions without getting caught in an endless loop of testing.
This constant churn of trying to make sense of data helps get early stage healthcare innovations off the ground. For those in the healthcare field, the experience can be taxing. So-called “innovation fatigue” can set in fast, particularly for team members who don’t realize they’re embarking on a marathon instead of a sprint.
The pressures on healthcare organizations and employees make them even more susceptible to fatigue. Is it any wonder so many of them skip validation altogether? It might be tempting to make definitive decisions after an involved discovery excursion, but that won’t help stakeholders in the long run. Not testing after gathering insights can lead teams down an expensive road by building a solution and going to market prematurely.
Still, plenty of well-meaning healthcare innovators believe validation is not essential. Sometimes, it’s because they believe in the mythos of overnight success; they underestimate the time and resources required to explore and de-risk early stage opportunities, ultimately failing to anticipate the iterative nature of discovery and validation. Other times, they become overly confident in what they’ve seen and achieved during discovery and think no further iteration or learning is necessary.
To be sure, discovery gives healthcare innovation teams the knowledge to extract and shape a preliminary idea and begin to identify underlying risk quickly. Nevertheless, discovery alone means very little in practice. Validation is required if healthcare technology innovators really want to design experiments that will help resolve uncertainties, reduce risks, and pinpoint whether a hypothesized solution should persist, pivot, or perish.
Ultimately, organizations that lack a clear bridge from discovery to validation will see high-potential opportunities linger in their innovation pipelines. They never move because no one’s sure what to do with them. Eventually, these opportunities may fade away — meaning the healthcare system (and the people it serves) suffers.
We’re living in a world where consumers demand more from every transaction. Exceptional service is no longer a nice-to-have — it has become the status quo. Whether it’s a traveler paying for an Uber through an app or a patient receiving emergency department service, people want and have come to expect great service.
The healthcare industry is working to quickly adapt and meet these expectations as they come, often leading to a disheartening or unpleasant experience for patients. Why? There are complex infrastructure challenges in healthcare.
For example, consider the patient billing process: It may have stumbling blocks that can lead to friction, such as surprise at the final price when the medical bill arrives, limited bill payment options, insurance denials, or reduced coverages. These problems tend to come after patients receive clinical care, adding more stress on top of an already stressful situation. Essentially, people receive the care and treatment they deserve but could feel blindsided later because of a lack of price transparency.
That said, providers may not be in a position to have patient-focused financial conversations at every point of the journey from pre-registration through post-discharge. Often, providers are just as in the dark about what a procedure may ultimately cost patients out of pocket because data often is siloed within different systems. And even when those systems try to communicate, they don’t necessarily speak the same “language.”
Is the task of reinventing American healthcare billing a major undertaking? Sure. But improving the patient experience is still doable. It just requires every entity involved — from third-party payers to insurance companies to physicians’ offices — to treat patients while considering their perspectives and needs.
How to Overcome Barriers in Healthcare
Tackling this challenge now is key for a few reasons. First, providers will be able to more clearly empower patients to make the best decisions for themselves and their families. When healthcare providers operate with patient needs in mind, consumers feel less confused, more curious, and better equipped to make crucial health decisions.
Providers that offer simple billing and upfront costs analyses may also reduce patient noncompliance and nonpayment. When patients understand their financial obligations before receiving services, they can make better choices and plan ahead. The result? Healthcare providers will be able to stay in business and thrive.
With the advantages of taking a more patient-centered approach in mind, healthcare providers can take steps to make that approach a reality.
By Jamison Utter, director of product evangelism, Medigate.
Last year (2020) was a year of chaos, and one that demonstrated why robust cybersecurity is an essential priority for all healthcare organizations. From COVID-19 disruptions to rapidly increasing networks of managed and unmanaged devices, it’s never been more important to secure the critical infrastructure that forms the basis of clinical care.
This is easier said than done- after all, the growing reliance on digital platforms has opened opportunities for increased attacks and raised questions about data collection and privacy. Threats like Ryuk and other high-profile breaches made a notable impact on the industry’s understanding of cybersecurity, not only for their monetary implications, but the significant operational disruptions that these incidents caused. On a national level, we’re seeing care networks expanding alongside access to telehealth services and the implementation of remote patient monitoring tools– with significant amounts of PHI being broadcast and analyzed each day.
When looking at these trends, there are two immediate realizations that all healthcare leaders should understand: 1) the rate of attacks is only going to increase as healthcare operations become smarter and more connected and 2) we need a better solution that works alongside clinical practitioners, biomed departments and organizational leaders even as it protects them from malicious attackers. For many of these concerns, the answer is Zero Trust, or more specifically, Clinical Zero Trust (CZT), that is uniquely attuned to the needs of the healthcare industry.
What Is Clinical Zero Trust?
Zero Trust represents the concept of “trust nothing, verify everything” in terms of cybersecurity. It has since grown to represent a networking approach that centers the design and application of IT networks around the identity and access rights of users and their data. Clinical Zero Trust applies this same idea but to the cyber and physical environment of healthcare organizations.
Think of CZT as a strategy and not a technology; it is an end goal rather than a feature or ability. Cyber protections like firewalls and end-point security solutions make up some of the offerings that help create a CZT environment. A typical healthcare organization has a security system that prioritizes protecting devices and data– CZT shifts the focus to protect physical workflows, which are made up of the people and processes involved in delivering care.
This means the protected surface extends to the physical world, including everything associated with administering a procedure or delivering care. At first glance, it seems like an impossible task to protect physical things with cyber technologies, but in reality, when you look at the clinical setting holistically it makes it easier to identify interdependencies and develop strategies that will effectively protect the physical, business and digital processes to drive optimal patient outcomes.
The start of the global pandemic put incredible stress on the numerous healthcare heroes as well as their facilities, and the industry at large. Medical professionals, already faced with inordinate pressure under normal circumstances, have been working nonstop to perform heroic work day in and day out since the onset of the COVID-19 pandemic.
One thing this crisis has clearly illustrated is the need for medical professionals to have access to the latest tools that provide the greatest degree of flexibility, efficiency, and mobility. These tools certainly include the IT backbone underpinning healthcare facilities big and small, from the networks and software to the new wave of smaller, mobile devices.
Two areas of IT have seen tremendous uptake in the healthcare industry as it has adapted to the crisis, the first being through the accelerated shift to telemedicine. Telemedicine allows patients to get almost instant medical attention without the concerns of traveling to a doctor’s office or hospital during the coronavirus outbreak. Indeed, the telemedicine market is expected to swell to $155.1 billion by 2027 in large part due to the pandemic.
Overall, telemedicine is an efficient way for providers to see the highest possible number of patients at a lower cost with shorter waiting times. Doctors can schedule more appointments than they would during normal rounds while still maintaining a quality practice that offers individualized attention to each case.
Additionally, telehealth visits can be recorded, allowing clinicians to document progress and share information with relevant specialists on the go. Telemedicine fosters collaboration by combining high-speed internet and high-definition video for communication between colleagues who are sometimes seeing hundreds of people a day because of the coronavirus.
The healthcare industry has seen one of the most significant growth spurts in the last two centuries. Now more than ever, we fall back on the medical sector in our times of crisis. We saw how vital the industry is for us during the pandemic and what role medical health officials play in keeping the general population safe and healthy.
As important as they are, the non-medical community’s unsung heroes also need to be given attention sometimes. Without non-clinical officers’ expertise, the industry would not have grown and thrived the way it currently is. Management and administration are areas of the healthcare sector that we might not even consider. Doctors and nurses act as the industry’s faces. These officials streamline the general public’s process to seek medical treatment. Let’s not forget the non-clinical roles of staff in securing the administration of medical facilities.
This article will focus on healthcare opportunities in the sector and how to prepare yourself for non-clinical roles.
Community health worker
One of the most up and coming career choice for non-clinical healthcare officials is that of a community healthcare worker. These individuals look at specific at-risk populations and work with them in the community. One of the most common responsibilities which society bestows on these individuals is to educate the community.
If you are looking to enter the medical field, this would be the time to gain an education in the related discipline of your choosing. With technology at our disposal today, one can take advantage of online learning like never before. Sit at home and pursue your online general studies bachelor degree. With such a degree, several avenues open up to you, and you have a choice as to which career path you want to pursue in the future.