PMID- 30066653 OWN - NLM STAT- MEDLINE DCOM- 20190627 LR - 20190627 IS - 1472-6947 (Electronic) IS - 1472-6947 (Linking) VI - 18 IP - Suppl 2 DP - 2018 Jul 23 TI - Discovering and identifying New York heart association classification from electronic health records. PG - 48 LID - 10.1186/s12911-018-0625-7 [doi] LID - 48 AB - BACKGROUND: Cardiac Resynchronization Therapy (CRT) is an established pacing therapy for heart failure patients. The New York Heart Association (NYHA) class is often used as a measure of a patient's response to CRT. Identifying NYHA class for heart failure (HF) patients in an electronic health record (EHR) consistently, over time, can provide better understanding of the progression of heart failure and assessment of CRT response and effectiveness. Though NYHA is rarely stored in EHR structured data, such information is often documented in unstructured clinical notes. METHODS: We accessed HF patients' data in a local EHR system and identified potential sources of NYHA, including local diagnosis codes, procedures, and clinical notes. We further investigated and compared the performances of rule-based versus machine learning-based natural language processing (NLP) methods to identify NYHA class from clinical notes. RESULTS: Of the 36,276 patients with a diagnosis of HF or a CRT implant, 19.2% had NYHA class mentioned at least once in their EHR. While NYHA class existed in descriptive fields association with diagnosis codes (31%) or procedure codes (2%), the richest source of NYHA class was clinical notes (95%). A total of 6174 clinical notes were matched with hospital-specific custom NYHA class diagnosis codes. Machine learning-based methods outperformed a rule-based method. The best machine-learning method was a random forest with n-gram features (F-measure: 93.78%). CONCLUSIONS: NYHA class is documented in different parts in EHR for HF patients and the documentation rate is lower than expected. NLP methods are a feasible way to extract NYHA class information from clinical notes. FAU - Zhang, Rui AU - Zhang R AD - Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA. zhan1386@umn.edu. AD - College of Pharmacy, University of Minnesota, Minneapolis, MN, USA. zhan1386@umn.edu. FAU - Ma, Sisi AU - Ma S AD - Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA. AD - Department of Medicine, University of Minnesota, Minneapolis, MN, USA. FAU - Shanahan, Liesa AU - Shanahan L AD - Medtronic, Inc., Minneapolis, MN, USA. FAU - Munroe, Jessica AU - Munroe J AD - Medtronic, Inc., Minneapolis, MN, USA. FAU - Horn, Sarah AU - Horn S AD - Medtronic, Inc., Minneapolis, MN, USA. FAU - Speedie, Stuart AU - Speedie S AD - Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20180723 PL - England TA - BMC Med Inform Decis Mak JT - BMC medical informatics and decision making JID - 101088682 SB - IM MH - Aged MH - Cardiac Resynchronization Therapy MH - Disease Progression MH - *Electronic Health Records MH - Female MH - Heart Failure/*classification MH - Humans MH - Machine Learning MH - Male MH - Middle Aged MH - *Natural Language Processing MH - New York MH - Treatment Outcome PMC - PMC6069768 OTO - NOTNLM OT - Clinical notes OT - Electronic health records OT - Natural language processing OT - New York heart association (NYHA) COIS- AUTHORS' INFORMATION: Described in the title page. ETHICS APPROVAL AND CONSENT TO PARTICIPATE: Ethics approval for this study was obtained from the University of Minnesota Institutional Review Board (IRB). All patients were included based on their consent forms. COMPETING INTERESTS: The authors declare that they have no competing interests. PUBLISHER'S NOTE: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. EDAT- 2018/08/02 06:00 MHDA- 2019/06/30 06:00 PMCR- 2018/07/23 CRDT- 2018/08/02 06:00 PHST- 2018/08/02 06:00 [entrez] PHST- 2018/08/02 06:00 [pubmed] PHST- 2019/06/30 06:00 [medline] PHST- 2018/07/23 00:00 [pmc-release] AID - 10.1186/s12911-018-0625-7 [pii] AID - 625 [pii] AID - 10.1186/s12911-018-0625-7 [doi] PST - epublish SO - BMC Med Inform Decis Mak. 2018 Jul 23;18(Suppl 2):48. doi: 10.1186/s12911-018-0625-7.