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Category Archives: clinical summaries
My first portal experience
Yes, after all these years of writing about EMRs, EHRs, PHRs, patient portals and the like, I have had my first real personal experience with a patient portal, courtesy of my internist. He still has a small practice, with four … Continue reading
Posted in Blue Button, clinical summaries, consumerism, EMR/EHR, health information exchange, health it, Healthcare IT, Meaningful Use, personal notes, PHR, practice management, primary care
Tagged Blue Button, care transitions, consumer health information, discharge notes, EMR, Health Information Exchange, HIMSS11, medication lists, patient portals, PHRs, Sage Software Healthcare, secure messaging, Vitera Healthcare Solutions
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Sampling of opinions on meaningful use Stage 2
I’ve been an absentee blogger yet again the last few weeks. Here’s something to chew on while I get caught up, a sampling of all the statements I received regarding the Stage 2 final rules for meaningful use, in the … Continue reading
Posted in ARRA, certification, clinical summaries, consumerism, EMR/EHR, health it, health reform, Healthcare IT, HHS, interoperability, Meaningful Use, medical informatics, ONC, PHR, regulations
Tagged AHIMA, CHIME, CMS, Health IT Now Coalition, HIMSS, Meaningful Use, MGMA, National Partnership for Women and Families, ONC, Society for Participatory Medicine
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Podcast: Carrie Handley on patient empowerment with an iPad
Did you happen to catch my story in MobiHealthNews on Thursday about Carrie Handley, the IT consultant-turned-cancer patient? She got frustrated with first a misdiagnosis and then the hassle of lugging around a binder full of paper records that she … Continue reading
Posted in clinical summaries, consumerism, mobile, patient safety, PHR, podcast, quality
Tagged Canada, Carrie Handley, consumer health information, continuity of care, iPad, Mark Versel, mobile, patient safety, PHRs
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Yes, you do have a right to your health records
Lest anyone forget — including the American Hospital Association, which wants to take 30 days post-discharge to supply copies of medical records to patients — HIPAA explicitly gives patients the right to access their own records. This is not new. … Continue reading
Posted in clinical summaries, consumerism, health reform, HHS, HIPAA, hospitals, Meaningful Use, patient safety, PHR, physicians, politics, privacy, quality
Tagged AHA, AHRQ, Carolyn Clancy, consumer health information, Meaningful Use, Office for Civil Rights
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