Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care system
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Anup D. Patel | H. Goodkin | A. Berg | W. Gaillard | I. Helbig | Z. Grinspan | R. Shellhaas | S. Massey | N. Abend | J. Mbwana | Erika Axeen | J. Bolton | David F Clarke | J. Coryell | S. Koh | Alison Kukla | L. Morgan | N. Singhal | Margaret M Storey | E. Yozawitz | M. Fitzgerald | S. Fridinger | Marisa S. Prelack | J. Buchhalter | Erika T Axeen | Nilika Singhal
[1] S. Moshé,et al. Recurrent status epilepticus in children , 1992, Annals of neurology.
[2] E. Wirrell,et al. Long-term psychosocial outcome in typical absence epilepsy. Sometimes a wolf in sheeps' clothing. , 1997, Archives of pediatrics & adolescent medicine.
[3] Richard E. Boyatzis,et al. Transforming Qualitative Information: Thematic Analysis and Code Development , 1998 .
[4] J. Cramer,et al. Quantitative Assessment of Seizure Severity for Clinical Trials: A Review of Approaches to Seizure Components , 2001, Epilepsia.
[5] A. Amin,et al. Through the Patient's Eyes , 2002, Medical education.
[6] K. Prasad,et al. Anticonvulsant therapy for status epilepticus. , 2007, The Cochrane database of systematic reviews.
[7] C. Elger,et al. Epilepsy: accuracy of patient seizure counts. , 2007, Archives of neurology.
[8] A. Berg,et al. Risk of recurrence after a first unprovoked seizure , 2008, Epilepsia.
[9] D. Hirtz,et al. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. , 2010, The New England journal of medicine.
[10] M. Brodie. Adverse antiepileptic drug effects: toward a clinically and neurobiologically relevant taxonomy , 2010 .
[11] Dipak Kalra,et al. Socio-technical considerations in epilepsy electronic patient record implementation , 2010, Int. J. Medical Informatics.
[12] J. H. Cross,et al. Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009 , 2010, Epilepsia.
[13] Vimla L. Patel,et al. Assessing performance of an Electronic Health Record (EHR) using Cognitive Task Analysis , 2010, Int. J. Medical Informatics.
[14] J. Rausch,et al. Patterns of nonadherence to antiepileptic drug therapy in children with newly diagnosed epilepsy. , 2011, JAMA.
[15] N. Barbaro,et al. Common data elements in epilepsy research: Development and implementation of the NINDS epilepsy CDE project , 2011, Epilepsia.
[16] K. Rhodes,et al. Auditing access to specialty care for children with public insurance. , 2011, The New England journal of medicine.
[17] Jessica S. Ancker,et al. The Triangle Model for evaluating the effect of health information technology on healthcare quality and safety , 2012, J. Am. Medical Informatics Assoc..
[18] T. Glauser,et al. Development and validation of the Pediatric Epilepsy Side Effects Questionnaire , 2012, Neurology.
[19] M. Barry,et al. Shared decision making--pinnacle of patient-centered care. , 2012, The New England journal of medicine.
[20] A. Berg,et al. Age at onset of epilepsy, pharmacoresistance, and cognitive outcomes , 2012, Neurology.
[21] J. Grimson,et al. Assessing the quality of epilepsy care with an electronic patient record , 2013, Seizure.
[22] C. Derry,et al. Sleep and epilepsy , 2013, Epilepsy & Behavior.
[23] J. H. Cross,et al. ILAE Official Report: A practical clinical definition of epilepsy , 2014, Epilepsia.
[24] Shaun A. Hussain,et al. Treatment of infantile spasms with very high dose prednisolone before high dose adrenocorticotropic hormone , 2014, Epilepsia.
[25] A. Berg,et al. Complete remission of childhood-onset epilepsy: stability and prediction over two decades. , 2014, Brain : a journal of neurology.
[26] Christian E. Elger,et al. Counting seizures: The primary outcome measure in epileptology from the patients’ perspective , 2015, Seizure.
[27] Rainu Kaushal,et al. Predicting frequent ED use by people with epilepsy with health information exchange data , 2015, Neurology.
[28] L. E. Peterson,et al. Improvement in Interstage Survival in a National Pediatric Cardiology Learning Network. , 2015, Circulation. Cardiovascular quality and outcomes.
[29] J. Douketis,et al. Risk of recurrence after a first unprovoked venous thromboembolism: external validation of the Vienna Prediction Model with pooled individual patient data , 2015, Journal of thrombosis and haemostasis : JTH.
[30] Shane W. Goodwin,et al. Development and assessment of a shortened Quality of Life in Childhood Epilepsy Questionnaire (QOLCE‐55) , 2015, Epilepsia.
[31] E. Kossoff,et al. Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort , 2016, Epilepsia.
[32] M. S. Perry. Meaningful Results in a Jiffy – a PERC of Multicenter Collaborations , 2016, Epilepsy currents.
[33] S. Jack,et al. SUDEP: What do adult patients want to know? , 2016, Epilepsy & Behavior.
[34] S. Jack,et al. SUDEP: To discuss or not? Recommendations from bereaved relatives , 2016, Epilepsy & Behavior.
[35] Sucheta Joshi,et al. Response to treatment in a prospective national infantile spasms cohort , 2016, Annals of neurology.
[36] L. Schwamm,et al. Feasibility of the collection of patient-reported outcomes in an ambulatory neurology clinic , 2016, Neurology.
[37] T. Ganslandt,et al. Common data elements for secondary use of electronic health record data for clinical trial execution and serious adverse event reporting , 2016, BMC Medical Research Methodology.
[38] B. Hafeez,et al. Feasibility of Automatic Extraction of Electronic Health Data to Evaluate a Status Epilepticus Clinical Protocol , 2016, Journal of child neurology.
[39] Anup D. Patel,et al. Increasing Ketamine Use for Refractory Status Epilepticus in US Pediatric Hospitals , 2017, Journal of child neurology.
[40] M. Likeman,et al. Safety and effectiveness of hormonal treatment versus hormonal treatment with vigabatrin for infantile spasms (ICISS): a randomised, multicentre, open-label trial , 2017, The Lancet Neurology.
[41] Rongrui Tang,et al. Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome. , 2017, The New England journal of medicine.
[42] Philippe Ryvlin,et al. Practice Guideline Summary: Sudden Unexpected Death in Epilepsy Incidence Rates and Risk Factors: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the American Epilepsy Society , 2017, Epilepsy currents.
[43] Vimal Patel,et al. Structured clinical documentation in the electronic medical record to improve quality and to support practice‐based research in epilepsy , 2016, Epilepsia.
[44] P. Camfield,et al. Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues , 2017, Epilepsy & Behavior.
[45] J. H. Cross,et al. Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology , 2017, Epilepsia.
[46] E. Wirrell,et al. Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel. , 2017, Pediatric neurology.
[47] T. Bertsche,et al. Seizure disorders and developmental disorders: impact on life of affected families—a structured interview , 2017, European Journal of Pediatrics.
[48] Tobias Loddenkemper,et al. Early-Life Epilepsies and the Emerging Role of Genetic Testing , 2017, JAMA pediatrics.
[49] Edouard Hirsch,et al. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology , 2017, Epilepsia.
[50] K. Kapur,et al. Association of Time to Treatment With Short-term Outcomes for Pediatric Patients With Refractory Convulsive Status Epilepticus , 2018, JAMA neurology.
[51] Anup D. Patel,et al. Neuroimaging of Early Life Epilepsy , 2018, Pediatrics.
[52] Nicolette de Keizer,et al. Time Spent on Dedicated Patient Care and Documentation Tasks Before and After the Introduction of a Structured and Standardized Electronic Health Record , 2018, Applied Clinical Informatics.
[53] Anup D. Patel,et al. Quality improvement in neurology: Child neurology quality measure set Executive summary , 2018, Neurology.
[54] D. Friedman,et al. Correlates of epilepsy self-management in MEW Network participants From the Centers for Disease Control and Prevention Managing Epilepsy Well Network , 2018, Epilepsy & Behavior.
[55] A. Berg,et al. Getting serious about the early-life epilepsies , 2018, Neurology.
[56] Anup D. Patel,et al. Effect of Cannabidiol on Drop Seizures in the Lennox–Gastaut Syndrome , 2018, The New England journal of medicine.
[57] Shane W. Goodwin,et al. Development and assessment of the Quality of Life in Childhood Epilepsy Questionnaire (QOLCE‐16) , 2018, Epilepsia.
[58] Jonas Duun-Henriksen,et al. Common data elements for epilepsy mobile health systems , 2018, Epilepsia.
[59] Jayetta Z. Hecker,et al. Comorbidities of Rare Epilepsies: Results from the Rare Epilepsy Network , 2018, The Journal of pediatrics.
[60] Amanda S. Lindy,et al. Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders , 2018, Epilepsia.
[61] M. Likeman,et al. Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial. , 2018, The Lancet. Child & adolescent health.
[62] Ajay S. Gulati,et al. Improving Care in Pediatric Inflammatory Bowel Disease. , 2018, Gastroenterology clinics of North America.
[63] Annapurna Poduri,et al. The ClinGen Epilepsy Gene Curation Expert Panel—Bridging the divide between clinical domain knowledge and formal gene curation criteria , 2018, Human mutation.
[64] George Zaharias. What is narrative-based medicine? Narrative-based medicine 1. , 2018, Canadian family physician Medecin de famille canadien.
[65] I. Haq,et al. Neurology steering board effects change for a major electronic health record vendor. , 2019, Neurology. Clinical practice.
[66] Philip J. Kroth,et al. Physician stress and burnout: the impact of health information technology , 2018, J. Am. Medical Informatics Assoc..
[67] G. Cavalleri,et al. Development of a genomics module within an epilepsy‐specific electronic health record: Toward genomic medicine in epilepsy care , 2019, Epilepsia.
[68] Genna R. Cohen,et al. Variation in Physicians’ Electronic Health Record Documentation and Potential Patient Harm from That Variation , 2019, Journal of General Internal Medicine.
[69] H. Lüders,et al. Critique of the 2017 epileptic seizure and epilepsy classifications , 2019, Epilepsia.
[70] Madison Berl,et al. Using EHRs to advance epilepsy care , 2019, Neurology. Clinical practice.
[71] Anup D. Patel,et al. Quality Improvement in Neurology , 2021, Neurology.