Literature DB >> 20458644

The potential research impact of patient reported outcomes on osteogenesis imperfecta.

Catherine A Brownstein1, Paul Wicks.   

Abstract

BACKGROUND: Osteogenesis imperfecta (OI) is an inherited connective tissue disorder with many phenotypic presentations ranging from mild to severe. It is often called "brittle bone disease." Treatment consists of physical therapy, surgical interventions, medications and, in some cases, experimental therapies. Because treatment is not standardized and is often experimental, information on the success of different methods is usually not available or well documented. QUESTIONS/PURPOSES: We therefore asked if social networking can make OI patients' lives better. How would a bone disorder community work? Is it possible for patients to know how well they are doing in comparison to others like them, and if they are getting the most successful treatment for their disease?
METHODS: An evaluation of how PatientsLikeMe®, a personal research and social networking website and database for patients with life changing illnesses, can aid in improving patient outcomes through the anonymous sharing of medical information.
RESULTS: PatientsLikeMe® could help patients answer the question, "Given my condition, what is the best outcome I could hope to achieve, and how do I get there?" Participants could record their real-time day-to-day progress in achieving their treatment goals, such as preventing fractures, and share that with the community to help patients, caregivers, researchers and industry learn more about OI.
CONCLUSIONS: Social networking can change the lives of Osteogenesis Imperfecta patients for the better, and make them a part of the treatment discovery process. Here we present a possible OI online community and demonstrate its potential utility for patients and medical professionals alike.

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Year:  2010        PMID: 20458644      PMCID: PMC3049620          DOI: 10.1007/s11999-010-1373-x

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  7 in total

1.  Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication.

Authors:  Ronald C Kessler; Wai Tat Chiu; Olga Demler; Kathleen R Merikangas; Ellen E Walters
Journal:  Arch Gen Psychiatry       Date:  2005-06

2.  The power of social networking in medicine.

Authors:  Catherine A Brownstein; John S Brownstein; David S Williams; Paul Wicks; James A Heywood
Journal:  Nat Biotechnol       Date:  2009-10       Impact factor: 54.908

Review 3.  New uses of bisphosphonates: osteogenesis imperfecta.

Authors:  Jean-Pierre Devogelaer
Journal:  Curr Opin Pharmacol       Date:  2002-12       Impact factor: 5.547

4.  Hearing loss in Finnish adults with osteogenesis imperfecta: a nationwide survey.

Authors:  Kaija Kuurila; Ilkka Kaitila; Reijo Johansson; Reidar Grénman
Journal:  Ann Otol Rhinol Laryngol       Date:  2002-10       Impact factor: 1.547

5.  The epidemiology of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).

Authors: 
Journal:  Parkinsonism Relat Disord       Date:  2000-07-01       Impact factor: 4.891

Review 6.  Osteogenesis imperfecta: recent findings shed new light on this once well-understood condition.

Authors:  Donald Basel; Robert D Steiner
Journal:  Genet Med       Date:  2009-06       Impact factor: 8.822

7.  Social uses of personal health information within PatientsLikeMe, an online patient community: what can happen when patients have access to one another's data.

Authors:  Jeana H Frost; Michael P Massagli
Journal:  J Med Internet Res       Date:  2008-05-27       Impact factor: 5.428

  7 in total
  6 in total

Review 1.  Big Data in Science and Healthcare: A Review of Recent Literature and Perspectives. Contribution of the IMIA Social Media Working Group.

Authors:  M M Hansen; T Miron-Shatz; A Y S Lau; C Paton
Journal:  Yearb Med Inform       Date:  2014-08-15

Review 2.  Web-based patient-reported outcomes in drug safety and risk management: challenges and opportunities?

Authors:  Anjan K Banerjee; Simon Ingate
Journal:  Drug Saf       Date:  2012-06-01       Impact factor: 5.606

3.  Crowdsourced health research studies: an important emerging complement to clinical trials in the public health research ecosystem.

Authors:  Melanie Swan
Journal:  J Med Internet Res       Date:  2012-03-07       Impact factor: 5.428

4.  "Not all my friends need to know": a qualitative study of teenage patients, privacy, and social media.

Authors:  Maja van der Velden; Khaled El Emam
Journal:  J Am Med Inform Assoc       Date:  2012-07-06       Impact factor: 4.497

Review 5.  Patient-driven innovations reported in peer-reviewed journals: a scoping review.

Authors:  Maria Reinius; Pamela Mazzocato; Sara Riggare; Ami Bylund; Hanna Jansson; John Øvretveit; Carl Savage; Carolina Wannheden; Henna Hasson
Journal:  BMJ Open       Date:  2022-01-24       Impact factor: 2.692

6.  Alemtuzumab in Multiple Sclerosis: Lessons from Social Media in Enhancing Patient Care.

Authors:  Louise Rath; Nirosen Vijiaratnam; Olga Skibina
Journal:  Int J MS Care       Date:  2017 Nov-Dec
  6 in total

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