Volv Global SA

Volv Global SA

Gesundheits- und Sozialwesen

Epalinges, Vaud 716 Follower:innen

Volv Global SA is a Digital Health & Life-Sciences Company based in Lausanne, Switzerland.

Info

Volv Global SA is a Digital Health & Life-Sciences Company based in Lausanne, Switzerland. We are a leader in applying AI to healthcare with a focus on rare or difficult-to-diagnose diseases. Volv’s leading AI methodology inTrigue uses machine learning to detect undiagnosed rare and orphan disease patients in population-scale data such as electronic health and claims records. Volv’s product inClude, enriches disease understanding with new insights, delivering increased value to healthcare providers, patients, and payers alike.

Website
http://www.volv.global
Branche
Gesundheits- und Sozialwesen
Größe
11–50 Beschäftigte
Hauptsitz
Epalinges, Vaud
Art
Privatunternehmen
Gegründet
2017
Spezialgebiete
Healthcare, Life Sciences, Predictive Analytics, Innovation, Technology, Data science, AI und InSights for Rare Diseases

Orte

  • Primär

    Route de la Corniche

    Digital Health Hub, Building SE-A,

    Epalinges, Vaud 1066, CH

    Wegbeschreibung

Beschäftigte von Volv Global SA

Updates

  • Volv Global SA hat dies direkt geteilt

    Profil von Leon van Wouwe anzeigen, Grafik

    Versatile leader in clinical development operations, building the bridges for wellbeing, between biotech, health tech, clinical researchers, clinicians and patients

    It’s been a pleasure to talk with Jessica Lynn from Patient Worthy about the challenges in rare disease diagnosing and how new technologies can help in this. With Volv Global SA #inTrigue #inClude #driveforchange #rarediseaseresearch #iainhealthare

    Profil von Jessica Lynn anzeigen, Grafik

    Creative Copywriter | Optimization Editor | Expert in Social Networking and SEO

    🦾 How can we use #AI to address challenges in rare disease? I’ve seen a lot of chatter online recently about AI and machine learning. Some people are (understandably) skeptical; others see its broad application as undeniably beneficial. In the rare disease space, I view AI as having huge potential. There are over 300 million people living with #RareDiseases worldwide. And there are over 10,000 known rare diseases, with new genetic conditions being discovered all the time. Since these diseases are often not well-understood or have small communities — I recently interviewed Gabby, who is the only known person with her rare disease in the US — rare diseases are hard to diagnosis. People often wait years, sometimes decades, for answers. AI can read patterns in data and identify where undiagnosed patients exist. What groups of symptoms or characteristics physicians should look out for. I recently spoke with Leon van Wouwe, the Chief Innovation Director at Volv Global SA. Volv Global is a world-class leader in applying AI to healthcare with a focus on rare or difficult-to-diagnose diseases. In our interview, we cover the growing onset of artificial intelligence in healthcare, the importance of remembering the human dimension, and how Volv’s inTrigue methodology has already been used to improve diagnostics in Fabry disease and Pompe disease in the UK. Read now 🔗: https://lnkd.in/etpJJMSz #RareDisease #ArtificialIntelligence #PompeDisease #FabryDisease #HealthTech

    Volv Harnesses AI for Rare DIsease Detection - Patient Worthy

    Volv Harnesses AI for Rare DIsease Detection - Patient Worthy

    patientworthy.com

  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    AATD Conclusions What can be learned from this Machine Learning approach to patient cohort finding? We found: 1/ The Asian, Black or African American, and Hispanic or Latino populations were underrepresented in the AATD-diagnosed patient pool when compared to actual US demographics. 2/ Although racial and ethnic biases were evident, the prediction model accurately identified patients with likely undiagnosed AATD earlier in their diagnostic journey in these subpopulations. 3/ Among patients diagnosed with AATD, there were fewer treated than tested individuals. 4/ Treatment rates were lower in non-White and Hispanic patients. 5 / Evaluating by race and ethnicity, a larger proportion of non-White and Hispanic or Latino patients with likely undiagnosed AATD had asthma. If you would like to see how this process can help your efforts to reduce health disparities in underserved communities, please message us directly.

  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    AATD Study Results - 2 of 3: The Treatment Disparity - by race and ethnicity among patients with AATD. Among patients diagnosed with AATD: Across all race and ethnicity groups, there were numerically fewer treated than tested individuals (Figures A and B). Treatment rates were lower among non-White patients (Black or African American = 24.53%, other non-White = 21.99%, Asian or Pacific Islander = 14.89%, Figure A) and Hispanic or Latino patients (16.69%, Figure B) compared with White patients (37.86%, Figure A) and non-Hispanic or Latino patients (34.24%, Figure B).

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  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    AATD Study Results 1 of 3: Cohort Evaluation ― Potential Diagnostic Disparity. Relative to the US population distribution, non-White and Hispanic patients with AATD (positive cohort), appear to be underrepresented. The machine-learning prediction model may more accurately reflect respective populations of underrecognized AATD. Implicit biases surreptitiously influence judgment and can, without intent, contribute to discriminatory behavior. [Source: Greenwald AG, Dasgupta N, Dovidio JF, Kang J, Moss-Racusin CA, Teachman BA. Implicit bias remedies: treating discriminatory bias as a public health problem. Psychol Sci Public Interest 2022;23:7-40.] Our work suggests that ML based diagnostic support tools may help negate some of these implicit biases. If you would like a copy of the full study in PDF format, please comment below, or message us direct.

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  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    Overcoming Racial and Ethnic Biases in the Diagnosis of Patients With Alpha-1 Antitrypsin Deficiency in the United States Using a Machine-Learning Model. The Objective: To develop a prediction model to identify symptomatic patients of different races and ethnicities with likely risk of AATD using claims data from a large US database. Implicit and explicit biases are among many factors that contribute to disparities in health and health care. (Tackling Implicit Bias in Health Care Published July 9, 2022 N Engl J Med 2022;387:105-107 DOI: 10.1056/NEJMp2201180 ) In partnership with Takeda, we took to designing a machine learning process to find likely candidates and overcome racial biases in the detection of this disease that may result in serious lung or liver disease. AATD is largely underdiagnosed, with an estimated prevalence of 100,000 individuals with AATD in the US; however, fewer than 10,000 individuals are diagnosed (Ashenhurst JR, et al. Chest. 2022;161(2):373-381.) Previously, AATD was thought to affect only White individuals of European descent. Recent studies have shown that people of different races and ethnicities have genotypes consistent with those with moderate-to-severe AATD-related lung disease. (Quinn M, et al. Ther Clin Risk Manag. 2020;16:1243-1255. de Serres FJ, Blanco I. Ther Adv Respir Dis. 2012;6(5):277-295.) The Process: Data from the Komodo Health US claims database (April 26, 2016 to January 31, 2023) were divided into “positive,” “negative,” and “target” cohorts. A machine-learning model for detecting AATD was trained on positive and negative cohorts without using codes revealing AATD diagnosis and treatment.The learned model was applied to the target cohort to flag patients with likely undiagnosed AATD. Results: This approach produced a highly performant prediction model capable of detecting undiagnosed people living with AATD, validated by expert clinicians. (For a deeper look at how this unique ML process could be applied to other indications, please message us directly.)

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  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    See you all there in Barcelona! Volv are really looking forward to this years event. #WODC2024 #Volv

    Unternehmensseite von World Orphan Drug Congress Europe anzeigen, Grafik

    2.123 Follower:innen

    We have over 40 sponsors confirmed for #WODC 2024! With 5 months still to go, this is just the start of the fantastic exhibitors we have attending. 📢EXCLUSIVE OFFER: We are offering 50% off for first-time exhibitors to join us at WODC! ⏰ There are only 6 spots available on a first come first serve basis so email Michael Hodge (Michael.hodge@terrapinn.com) to discuss the opportunity. Meet our sponsors: Alexion Pharmaceuticals, Inc. AstraZeneca Rare Disease, Chiesi Group, Clinigen, Pfizer, Volv Global SA, Sanofi, UCB, Initiate, Allucent, Takeda, Partners4Access, ICON plc, Charles River Associates, Marken, Mendelian, Premier Research, OMAKASE CONSULTING, Remap Consulting, World Wide Clinical Trials, Veristat, WEP Clinical, ERGOMED, Cascador Health, Alira Health, GeneScape , HomeNurse4U, QuickSTAT , Parexel, OPEN Health, PDC CRO, IDEA Regulatory, Pharma Business Partners, BAP Pharma, SKC Beratungsgesellschaft mbH, Prime , Illingworth Research Group (a Syneos Health Company), PCM TRIALS - Quality Mobile Research

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  • Volv Global SA hat dies direkt geteilt

    Profil von Leon van Wouwe anzeigen, Grafik

    Versatile leader in clinical development operations, building the bridges for wellbeing, between biotech, health tech, clinical researchers, clinicians and patients

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  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    Health Equity & AI: helping address the issue of bias in healthcare Overcoming Racial and Ethnic Biases in the Diagnosis of Patients With Alpha-1 Antitrypsin Deficiency in the United States Using a Machine-Learning Model • Previously, AATD was thought to affect only White individuals of European descent[2,3] • Recent studies have shown that people of different races and ethnicities have genotypes consistent with those with moderate-to-severe AATD-related lung disease[2,3] We here at Volv Global SA supported by Takeda developed a prediction model to identify symptomatic patients of different races and ethnicities with likely risk of AATD using claims data from a large US database. Our Conclusions The Asian, Black or African American, and Hispanic or Latino populations were underrepresented in the AATD-diagnosed patient pool when compared to actual US demographics. Although racial and ethnic biases were evident, the prediction model accurately identified patients with likely undiagnosed AATD earlier in their diagnostic journey in these subpopulations. Among patients diagnosed with AATD: • There were fewer treated than tested individuals • Treatment rates were lower in non-White and Hispanic patients Evaluating by race and ethnicity, a larger proportion of non-White and Hispanic or Latino patients with likely undiagnosed AATD had asthma. #healthequity #equity #rarediseases #volv #inTrigue #innovation

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  • Unternehmensseite von Volv Global SA anzeigen, Grafik

    716 Follower:innen

    Profil von 💭 Christopher Rudolf anzeigen, Grafik

    Founder and CEO at Volv Global SA

    World Orphan Drug Congress USA 𝗖𝗼𝘂𝗻𝘁𝗱𝗼𝘄𝗻! On 𝗔𝗽𝗿𝗶𝗹 𝟮𝟯-𝟮𝟱, 𝟮𝟬𝟮𝟰, I will be back at the Boston Convention and Exhibition Center, MA, for the World Orphan Drug Congress USA, together with 💭 Christopher Rudolf and Mike Musson, representing 𝘁𝗲𝗮𝗺 Volv Global SA! 💡 𝗡𝗲𝘄 𝘁𝗵𝗶𝘀 𝘆𝗲𝗮𝗿, 𝗶𝗻 𝗔𝗜 & 𝗗𝗶𝗴𝗶𝘁𝗮𝗹 𝗛𝗲𝗮𝗹𝘁𝗵: In our 𝗽𝗿𝗲-𝗰𝗼𝗻𝗳𝗲𝗿𝗲𝗻𝗰𝗲 𝘄𝗼𝗿𝗸𝘀𝗵𝗼𝗽, we will be building on #WODC2023 workshop outputs. And be showing you the 𝗻𝗲𝘄 𝗰𝗮𝗽𝗮𝗯𝗶𝗹𝗶𝘁𝗶𝗲𝘀 we developed from that, and explore the 𝗻𝗲𝘄 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗽𝗼𝘀𝘀𝗶𝗯𝗶𝗹𝗶𝘁𝗶𝗲𝘀 that these new capabilities open up with you, such as: 🔔 𝗘𝗮𝗿𝗹𝗶𝗲𝗿 𝗱𝗲𝘁𝗲𝗰𝘁𝗶𝗼𝗻 𝘁𝗼𝗼𝗹𝘀 ⏱ 𝗙𝗮𝘀𝘁 𝗽𝗿𝗼𝗴𝗿𝗲𝘀𝘀𝗶𝗼𝗻 𝗮𝗻𝗱 𝘀𝘂𝗯𝗽𝗼𝗽𝘂𝗹𝗮𝘁𝗶𝗼𝗻 𝗶𝗱𝗲𝗻𝘁𝗶𝗳𝗶𝗰𝗮𝘁𝗶𝗼𝗻 𝗳𝗼𝗿 𝗽𝗿𝗶𝗼𝗿𝗶𝘁𝘆 𝗻𝗲𝗲𝗱𝘀 𝗮𝘀𝘀𝗲𝘀𝘀𝗺𝗲𝗻𝘁 🏥 𝗜𝗺𝗽𝗮𝗰𝘁 𝗼𝗻 𝗵𝗲𝗮𝗹𝘁𝗵 𝘀𝘆𝘀𝘁𝗲𝗺𝘀 𝗰𝗮𝗽𝗮𝗰𝗶𝘁𝘆 𝗺𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁 Do sign up for the workshop and come see us at the Volv Global SA 𝗯𝗼𝗼𝘁𝗵 (#513) Looking forward to see many familiar faces, and welcoming new people #driveforchange #orphandrugdevelopment! #inTrigue #inAdvance #inFlow #inVolv #rarediseaseresearch #aiinhealthcare #aiinnovations #improvinghealthcare At the Terrapinn World Orphan Drug Congress USA O with Justin Franks, Giovanna Ronzetti, Rachel T. and many others.

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