Avalon Healthcare Solutions’ Post

🧬 THIS WEBINAR will open eyes and opportunities for health plans—to better manage the challenging complexity and costs of genetic testing claims. 😯 First, some REALLY surprising stats related to claims that involve genetic testing: • Today there are over 175,000 genetic test products — a 1650% rise in the last ten years. • While only 1% of all claims, genetic tests represent a staggering 15-20% of medical services reviewed manually (e.g. prior auths and claim reviews). • Around 1/3 of all genetic tests are ordered in error, leading to significant impacts on treatment outcomes and financial waste. Answers and help are here! Experts from Lyric and Concert Genetics will be presenting "Genetic Tests and Payment Accuracy: Charting the Course for Smarter Claims Management" on Tuesday, March 5th at Noon ET. Reserve your seat today. NO slides—it's an engaging panel conversation with live Q&As and an easy-to-read takeaway transcript for attendees. Register through the link below: https://lnkd.in/diveGv44 #GeneticTesting #ClaimsManagement #HealthcareInnovation #PrecisionMedicine #PaymentAccuracy

Currently, there are over 175,000 genetic tests available in the market, and the growth is expected to double by 2025. As a result, providers and health plans are facing challenges in evaluating the reliability and usefulness of these tests, while also dealing with an insufficient coding and management system. The AvalonSelect Genetic Network, a select group of preferred genetic labs coupled with robust consultative services, complements a health plan's existing routine lab network and allows health plans to continue to leverage their current lab relationships while outsourcing the management of genetic testing, pricing, compliance enforcement, test quality assessment, new test evaluation, and contracting to Avalon. Learn more: https://ow.ly/Hjvz50SMIZr #AvalonHCS #AvalonSelectGeneticNetwork #GeneticTesting #HealthPlans

Mantara is looking forward to driving knowledge around PGx and helping people learn just how important this is. #PGx #pharmacogenomics #mantara #personalisedmedicine

Founder Hacks: It is hard for many medic colleagues to get out of the rigid boxed mentality of where a concept, idea can go. Good clinical practice is reliant on a good differential diagnosis list, not just the diagnosis. Disease can evolve. Biology is dynamic. Your initial ideas and thoughts should reflect that as well. Hence, more important than the eureka moment is the execution of the not so eureka moment. #founderstories #foundersjourney #executivedevelopment #executionmatters #scienceandtechnology #biotechnology #medicaldevice #scienceinnovation #founderhacks

Happy New Year! 🎉 As we enter the new year, have you thought about improving patient care and boosting your practice through the benefits of genetics? 💚 Have you explored the benefits of personalized medicine? 🧬Set Targeted Health Goals: Personalized insights enable patients to define and achieve health objectives with accuracy. 🧬Enhance Patient Satisfaction: Delivering customized care fosters a stronger doctor-patient relationship, leading to increased satisfaction. 🧬Optimize Treatment Plans: Tailor interventions based on genetic data, ensuring more effective and personalized healthcare. Curious to integrate genetics into your practice and elevate patient outcomes in 2024? #newyearnewgoals #personalizedmedicine #genetictesting #wellnessjourney 🚀🧬

Learn more about 3x4 Genetic Testing and discover how it can benefit you.

Today, on #WorldRareDiseaseDay our geneticist Dr. Herminia Fleitas👩⚕️, invites us to support and give visibility to the importance of research and early diagnosis of these types of pathologies, so that these patients can receive the best medical and therapeutic assistance in order to improve their quality of life. 🧬 Rare diseases are pathologies or disorders that affect a small part of the population and usually have a genetic component. ✊🏼 At Veritas we work every day to contribute to a better diagnosis of these patients, developing specific tools with solvency and scientific rigor. #RareDisease

Accurately determining how many people are affected by rare conditions is challenging, but studies using large-scale genetic databases are turning the tide. These powerful analyses, as conducted by HealthLumen for conditions such as #FabryDisease, and other conditions with a genetic basis, provide the robust data needed at each stage of the drug development lifecycle, helping to accelerate the process, so that rare disease patients gain faster access to the therapies they need. To read the article, visit https://bit.ly/4biFToI

🌟 Breaking News 🌟 Exciting developments in the field of medical research! A potential cure for Beta Thalassemia, a genetic blood disorder affecting many in England, is now within reach. Check out this insightful article from Hackaday for details on how this breakthrough could impact the lives of patients and their families. Let's spread the word and support advancements in healthcare. #MedicalBreakthrough #BetaThalassemia #HealthcareInnovation https://ift.tt/YjpIFS6

Identifying the root cause is the cornerstone of Functional Medicine. It requires an understanding of each patient's genetic, biochemical, and lifestyle factors, and leverages that data into personalized treatment plans that lead to improved patient outcomes. 📞 (786) 638-6699 💻 https://lnkd.in/eZDD2MGS #EssenceForWellness #MiamiFl #FunctionalMedicine