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1 i-structured interviews were transcribed and deidentified.
2 m a clinical archive were used and data were deidentified.
3 oss-sectional study used publicly available, deidentified 2019 to 2022 data from the US Consumer Prod
6 ort study included retrospective analysis of deidentified administrative claims and electronic health
7 NG, AND PARTICIPANTS: This cohort study used deidentified administrative claims data for privately in
8 IPANTS: This retrospective cohort study used deidentified administrative claims data for privately in
9 IPANTS: This retrospective cohort study used deidentified administrative claims data for US adults wi
10 AND PARTICIPANTS: This cohort study analyzed deidentified administrative claims data from OptumLabs D
11 his retrospective cross-sectional study used deidentified administrative claims data from OptumLabs D
12 In this retrospective cohort study using deidentified administrative claims for Medicare Advantag
16 hort study is a population-based analysis of deidentified, aggregated electronic health record data c
20 ected from January 2012 to January 2018 were deidentified and compiled into the publicly available v.
22 sets (0.6%; 95% CI, 0.0%-1.5%) were actually deidentified and publicly available as of April 10, 2020
24 wardship program personnel at each hospital, deidentified and submitted in aggregate for benchmarking
30 AND PARTICIPANTS: This cohort study assessed deidentified application and matriculation data from the
31 AND PARTICIPANTS: This prognostic study used deidentified, archived colorectal cancer cases from Janu
33 ily meetings were recorded, transcribed, and deidentified before being screened for discussion of dea
34 cause all study patients had been previously deidentified by the Cancer Genome Atlas (TCGA), a public
36 In this retrospective cohort study, we used deidentified chargemaster data from 297 hospitals across
38 IPANTS: This retrospective cohort study used deidentified claims data from Blue Cross Blue Shield ben
39 IPANTS: This retrospective cohort study used deidentified claims data from commercially insured Blue
40 trospective cohort study was conducted using deidentified claims data from the MarketScan database.
41 the Wakely Consulting Group ACA database, a deidentified claims database built on data voluntarily s
42 used the OptumLabs Data Warehouse to analyze deidentified claims from approximately 74 million adults
43 fied Clinformatics Data Mart, which contains deidentified claims from patients with private insurance
45 cohort study used claims data from the Optum deidentified Clinformatics Data Mart Database between De
46 pective analysis of health data from Optum's deidentified Clinformatics Data Mart Database from 2016
47 used administrative claims data from Optum's deidentified Clinformatics Data Mart Database from Janua
48 e-series study used claims data from Optum's deidentified Clinformatics Data Mart database to assess
49 was conducted using US claims data (Optum's deidentified Clinformatics Data Mart database) for Janua
50 nwide commercial insurance database (Optum's deidentified Clinformatics Data Mart Database) from Janu
51 to September 30, 2015, obtained from Optum's deidentified Clinformatics Data Mart Database, a commerc
52 ohort study used medical claims from Optum's deidentified Clinformatics Data Mart Database, a commerc
53 tionwide data from 2004 to 2019 from Optum's deidentified Clinformatics Data Mart Database, an insura
54 were identified from the 2016 to 2020 Optum deidentified Clinformatics Data Mart Database, which is
59 insurance claims databases-Medicaid, Optum's deidentified Clinformatics Data Mart, and Merative Marke
61 ening algorithms, test performance data, and deidentified clinical and laboratory information regardi
63 TS: This retrospective cohort study obtained deidentified clinical data for 5382 patients from a nati
70 defined biomarker subgroups used data from a deidentified clinicogenomic database and included patien
72 PANTS: A prespecified cohort study using the deidentified clinicogenomic Tempus database of patients
75 : This cross-sectional analysis of national, deidentified commercial health insurance claims of youth
76 the OptumLabs Data Warehouse, a longitudinal deidentified commercial insurance claims database, from
78 ETTING, AND PARTICIPANTS: This analysis used deidentified, cross-sectional data on patients with MS a
79 review board permission was obtained to use deidentified CT colonography data for this prospective r
80 The Dose Imaging Registry (DIR) collects deidentified CT data, including examination type and dos
81 ted detailed forms in which they could enter deidentified data and volume statistics pertaining to pa
82 modifications, level of difficulty obtaining deidentified data and waivers, experiences with multisit
88 trospective cohort study was conducted using deidentified data from a national commercial insurance d
89 NTS: This population-based cohort study used deidentified data from a nationwide electronic health re
91 NG, AND PARTICIPANTS: This cohort study used deidentified data from an electronic health record-deriv
92 ARTICIPANTS: This cross-sectional study used deidentified data from an online medical forum, in which
93 IPANTS: This retrospective cohort study used deidentified data from Optum Insight's Clinformatics Dat
94 set was curated from publicly available and deidentified data from patients with HNSCC treated at MD
95 October 1, 2011, and July 25, 2015, based on deidentified data from phase 3, multicenter, randomized
96 his retrospective cross-sectional study used deidentified data from the Association of American Medic
97 als and Methods This secondary analysis used deidentified data from the Association of American Medic
99 ls followed from birth to age 20 years using deidentified data from the Better Evidence Better Outcom
100 IPANTS: This retrospective cohort study used deidentified data from the Hawai'i Tumor Registry of 622
101 ARTICIPANTS: This cross-sectional study used deidentified data from the MarketScan Commercial Claims
102 TS: This retrospective cohort study examined deidentified data from the National Cancer Database betw
103 ARTICIPANTS: This cross-sectional study used deidentified data from the Optum Clinformatics Data Mart
104 retrospective longitudinal cohort study used deidentified data from the Optum electronic health recor
107 een January 1, 2016, and June 30, 2019, used deidentified data from the US Optum Clinformatics Data M
108 IPANTS: This retrospective cohort study used deidentified data from US Veterans Health Administration
109 d a retrospective, observational study using deidentified data obtained from all consecutive patients
110 S: Retrospective cross-sectional study using deidentified data of medical graduates who completed the
111 ic health record-derived database to extract deidentified data of patients receiving care from US phy
112 his retrospective cross-sectional study used deidentified data on 37 610 medical students who matricu
114 AND PARTICIPANTS: A cross-sectional study of deidentified data on outpatients throughout the US was c
116 ic Stroke (CERTAIN) collaboration comprising deidentified data on patients with ischemic stroke treat
117 p a web-based registry for the collection of deidentified data on the management and course of neonat
119 RTICIPANTS: The study created cohorts from a deidentified data set composed of commercial laboratory
121 sing multiple cross-sectional analyses and a deidentified data set, we analyzed data from infants wit
125 retrospective cross-sectional analysis with deidentified data using the International Statistical Cl
130 multicenter retrospective cohort study used deidentified data with 6-year follow-up from the Medicar
133 Data from the Optum electronic health record deidentified database (2007-2017) were linked to the Med
134 he Flatiron Health electronic record-derived deidentified database diagnosed between 2011 and 2021, m
135 study used administrative claims data from a deidentified database of commercially insured and Medica
136 d the Optum Labs Data Warehouse, a national, deidentified database of electronic health records, to i
138 ANTS: This cohort study used an EHR-derived, deidentified database that included patients with stage
140 tabase, an electronic health record-derived, deidentified database with data from community and acade
141 ationwide, electronic health record-derived, deidentified database with median duration of follow-up
142 nationwide electronic health record-derived deidentified database, which includes data for approxima
147 In this cohort study, data from 3 different deidentified databases containing electronic health reco
150 small area estimation models were applied to deidentified death records from the National Center for
152 ARTICIPANTS: This cross-sectional study used deidentified death records from the National Vital Stati
155 nth Revision code L40.1) identified in Optum deidentified EHR data between July 1, 2015, and June 30,
156 stitutional dataset containing statistically deidentified EHR data for over 21 million individuals (E
157 record (EHR) research network containing the deidentified EHR data of more than 103 million patients,
158 n Examination Surveys (NHANES) and the Optum deidentified electronic health record (EHR) data set of
159 was a retrospective cohort study aggregating deidentified electronic health record data from January
160 AND PARTICIPANTS: This prognostic study used deidentified electronic health record data from the Univ
161 rospective cohort study used data from Optum deidentified electronic health record data set (7.7 mill
162 used patient-level data from the nationwide deidentified electronic health record database Flatiron
163 n-based cohort study used Flatiron Health, a deidentified electronic health record database of patien
166 dy used patient-level data from a nationwide deidentified electronic health record-derived database,
167 to be able to conduct medical research with deidentified electronic health records (96.8% v 87.7%; P
168 udy was conducted using data obtained from a deidentified electronic health records data set from Jan
170 s cross-sectional study used public data and deidentified electronic health records to describe the b
171 rch Collaborative, a centralized database of deidentified electronic medical record data from a netwo
172 ICIPANTS: This retrospective cohort study of deidentified electronic medical record data from the Tri
173 ed data from TriNetX, a national database of deidentified electronic medical records from both inpati
175 TS: This retrospective cohort study used the deidentified Flatiron-Health electronic health record-de
176 m January 2013 to March 2015 using archived, deidentified, formalin-fixed, paraffin-embedded GCA-nega
177 Retrospective cross-sectional evaluation of deidentified fundus photographs matched to spectacle-cor
179 nions regarding acceptable secondary uses of deidentified health information and consent models for o
180 tion, was performed on a database containing deidentified health records of 1.28 million patients acr
189 ver performance study was performed by using deidentified images acquired between 2008 and 2011 with
191 approval because the 10 image data sets were deidentified in the Osteoarthritis Initiative database,
192 s with concomitant catheterization data, and deidentified individual and group results were shared at
194 ilable devices in the United States provided deidentified individual patient data for independent ana
198 0 participants or more were invited to share deidentified individual-level data on the above four var
199 NG, AND PARTICIPANTS: This cohort study used deidentified individual-level faculty data from 136 uniq
206 (EHR) linked to closed claims data (Optum's deidentified Integrated Claims-Clinical dataset, TriNetX
207 s an anonymous, self-reported, confidential, deidentified, internet-accessible medication error repor
208 radiologists independently interpreted twice deidentified mammograms obtained in 153 women (age range
209 re-matched, cross-sectional study used Optum deidentified Market Clarity Data (claims and electronic
210 RTICIPANTS: Retrospective cohort study using deidentified medical and pharmacy claims and enrollment
211 the OptumLabs Data Warehouse, which includes deidentified medical and pharmacy claims and enrollment
212 children 17 years of age or younger analyzed deidentified medical and pharmacy claims in OptumLabs Da
213 udy of 794 809 insured US men was drawn from deidentified medical claims between January 2011 and Dec
214 led measure of comfort with secondary use of deidentified medical information and evaluated its corre
216 tors to get a patient's permission each time deidentified medical record information is used for rese
217 IPANTS: This retrospective cohort study used deidentified medical record review of 18 243 female-iden
218 s that most patients wish to be asked before deidentified medical records are used for research.
220 eptions after deliberation related to use of deidentified medical-record data by insurance companies.
221 ts at least once whether researchers can use deidentified medical-records data for future research.
222 comparative effectiveness cohort study used deidentified Medicare claims data from August 1, 2014, t
223 CIPANTS: This cross-sectional study assesses deidentified medication abortion prescription fulfilment
225 NTS: This cross-sectional study analyzed the deidentified metadata of ambulatory care health systems
226 board-approved retrospective data set of 84 deidentified, multi-institutional breast MR examinations
227 ing first-line ICI were abstracted using the deidentified nationwide Clinico-Genomic Database (CGDB)
230 RTICIPANTS: Using 2003 to 2017 data from the deidentified Optum Clinformatics Data Mart database from
231 etrospective cohort study used data from the deidentified Optum Cliniformatics Data Mart Database on
232 TS: This retrospective cohort study used the deidentified Optum Labs Data Warehouse, a claims databas
234 TS: This retrospective cohort study obtained deidentified OptumLabs electronic health record claims d
237 January 1, 2023 METHODS: This study utilized deidentified patient data from the TriNetX database.
241 levels and lipids, we analyzed 4.06 million deidentified patient laboratory test results from Septem
242 cal Data Warehouse (STARR), which aggregates deidentified patient records from Stanford Health Care.
244 -10-CM code for post-COVID-19 condition used deidentified patient-level claims data aggregated by Hea
250 from the Flatiron Health database containing deidentified, patient-level, electronic health record-de
254 ughout the United States collected residual, deidentified positive blood culture samples for analysis
256 tability Act-compliant secondary analysis of deidentified prospectively acquired PET/CT test-retest d
257 tability Act-compliant secondary analysis of deidentified prospectively acquired PET/CT test-retest d
258 ospective cohort study was performed using a deidentified, random sample of 4 999 999 fee-for-service
259 CIPANTS: We performed a cohort study using a deidentified, random sample of 4 999 999 fee-for-service
262 lation-based cohort study included data from deidentified records of all invasive melanomas diagnosed
263 e on August 18, 2021, and included data from deidentified records of patients tested, using the Tempu
266 ross-sectional, retrospective study analyzed deidentified results from blood lead tests performed at
267 he Optum Labs Data Warehouse, which contains deidentified retrospective administrative claims data an
268 titution, tertiary academic referral center, deidentified, retrospectively collected, ultra-widefield
269 Child care center directors reported weekly deidentified self-reported COVID-19 cases from all CCPs
270 ARTICIPANTS: This cross-sectional study used deidentified, self-reported data from 2003 to 2019 from
272 f the assay was evaluated using 211 residual deidentified stool samples tested with a GDH-and-toxin E
276 DESIGN, SETTING, AND PARTICIPANTS: Using deidentified student-level data of allopathic US medical
278 IPANTS: This cross-sectional study evaluated deidentified surgical videos of phacoemulsification cata
279 MA Combo 2 tests was assessed using unlinked/deidentified surplus clinical specimens previously analy
282 ween May 2020, and December 2022, within the deidentified, Tempus multimodal database, consisting of
283 en February 2021 and October 2023 within the deidentified, Tempus multimodal database, consisting of
286 combined with Virena software for automatic deidentified tracking of influenza activity across the L
287 recorded until reaching thematic saturation, deidentified, transcribed and translated, and analyzed u
288 search assistants independently coded all 30 deidentified transcripts and resolved discrepancies (kap
291 ugust-2020 and June-2022 were analyzed using deidentified United Network for Organ Sharing database.
292 ugh December 31, 2018, and data from a large deidentified US commercial health care database (Optum C
293 th outpatient MA-RSV infections from 3 large deidentified US databases across 6 RSV seasons, approxim
296 rovement collaborative submitted an unedited deidentified video of a representative laparoscopic SG.
298 s in evaluating over 130000 images that were deidentified with respect to age, sex, and race/ethnicit
299 med across 2 independent wound centers using deidentified wound photographs collected for routine car