{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,10]],"date-time":"2026-10-10T01:02:24Z","timestamp":1791594144560,"version":"4.3.4"},"reference-count":37,"publisher":"American Medical Association (AMA)","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi230703-4\"><jats:title>Importance<\/jats:title><jats:p>The COVID-19 pandemic accelerated the use of telemedicine. However, data on the integration of telemedicine in prenatal health care and health outcomes are sparse.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-5\"><jats:title>Objective<\/jats:title><jats:p>To evaluate a multimodal model of in-office and telemedicine prenatal health care implemented during the COVID-19 pandemic and its association with maternal and newborn health outcomes.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-6\"><jats:title>Design, Setting, and Participants<\/jats:title><jats:p>This cohort study of pregnant individuals using longitudinal electronic health record data was conducted at Kaiser Permanente Northern California, an integrated health care system serving a population of 4.5 million people. Individuals who delivered a live birth or stillbirth between July 1, 2018, and October 21, 2021, were included in the study. Data were analyzed from January 2022 to May 2023.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-7\"><jats:title>Exposure<\/jats:title><jats:p>Exposure levels to the multimodal prenatal health care model were separated into 3 intervals: unexposed (T1, birth delivery between July 1, 2018, and February 29, 2020), partially exposed (T2, birth delivery between March 1, 2020, and December 5, 2020), and fully exposed (T3, birth delivery between December 6, 2020, and October 31, 2021).<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-8\"><jats:title>Main Outcomes and Measures<\/jats:title><jats:p>Primary outcomes included rates of preeclampsia and eclampsia, severe maternal morbidity, cesarean delivery, preterm birth, and neonatal intensive care unit (NICU) admission. The distributions of demographic and clinical characteristics, care processes, and health outcomes for birth deliveries within each of the 3 intervals of interest were assessed with standardized mean differences calculated for between-interval contrasts. Interrupted time series analyses were used to examine changes in rates of perinatal outcomes and its association with the multimodal prenatal health care model. Secondary outcomes included gestational hypertension, gestational diabetes, depression, venous thromboembolism, newborn Apgar score, transient tachypnea, and birth weight.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-9\"><jats:title>Results<\/jats:title><jats:p>The cohort included 151\u202f464 individuals (mean [SD] age, 31.3 [5.3] years) who delivered a live birth or stillbirth. The mean (SD) number of total prenatal visits was similar in T1 (9.41 [4.75] visits), T2 (9.17 [4.50] visits), and T3 (9.15 [4.66] visits), whereas the proportion of telemedicine visits increased from 11.1% (79\u202f214 visits) in T1 to 20.9% (66\u202f726 visits) in T2 and 21.3% (79\u202f518 visits) in T3. NICU admission rates were 9.2% (7014 admissions) in T1, 8.3% (2905 admissions) in T2, and 8.6% (3615 admissions) in T3. Interrupted time series analysis showed no change in NICU admission risk during T1 (change per 4-week interval, \u22120.22%; 95% CI, \u20130.53% to 0.09%), a decrease in risk during T2 (change per 4-week interval, \u22120.91%; 95% CI, \u20131.77% to \u22120.03%), and an increase in risk during T3 (change per 4-week interval, 1.75%; 95% CI, 0.49% to 3.02%). There were no clinically relevant changes between T1, T2, and T3 in the rates of risk of preeclampsia and eclampsia (change per 4-week interval, 0.76% [95% CI, 0.39% to 1.14%] for T1; \u22120.19% [95% CI, \u20131.19% to 0.81%] for T2; and \u22120.80% [95% CI, \u20132.13% to 0.55%] for T3), severe maternal morbidity (change per 4-week interval , 0.12% [95% CI, 0.40% to 0.63%] for T1; \u22120.39% [95% CI, \u20131.00% to 1.80%] for T2; and 0.99% [95% CI, \u20130.88% to 2.90%] for T3), cesarean delivery (change per 4-week interval, 0.06% [95% CI, \u20130.11% to 0.23%] for T1; \u22120.03% [95% CI, \u20130.49% to 0.44%] for T2; and \u22120.05% [95% CI, \u20130.68% to 0.59%] for T3), preterm birth (change per 4-week interval, 0.23% [95% CI, \u20130.11% to 0.57%] for T1; \u22120.37% [95% CI, \u20131.29% to 0.55%] for T2; and \u22120.15% [95% CI, \u20131.41% to 1.13%] for T3), or secondary outcomes.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi230703-10\"><jats:title>Conclusions and Relevance<\/jats:title><jats:p>These findings suggest that a multimodal prenatal health care model combining in-office and telemedicine visits performed adequately compared with in-office only prenatal health care, supporting its continued use after the pandemic.<\/jats:p><\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2023.24011","type":"journal-article","created":{"date-parts":[[2023,7,18]],"date-time":"2023-07-18T15:18:58Z","timestamp":1689693538000},"page":"e2324011","source":"Crossref","is-referenced-by-count":21,"title":["Prenatal Health Care Outcomes Before and During the COVID-19 Pandemic Among Pregnant Individuals and Their Newborns in an Integrated US Health System"],"prefix":"10.1001","volume":"6","author":[{"given":"Assiamira","family":"Ferrara","sequence":"first","affiliation":[{"name":"Division of Research, Kaiser Permanente Northern California, Oakland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mara","family":"Greenberg","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynecology, Kaiser Permanente Northern California, Oakland"},{"name":"Regional Perinatal Service Center, Kaiser Permanente Northern California, Santa Clara"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yeyi","family":"Zhu","sequence":"additional","affiliation":[{"name":"Division of Research, Kaiser Permanente Northern California, Oakland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lyndsay A.","family":"Avalos","sequence":"additional","affiliation":[{"name":"Division of Research, Kaiser Permanente Northern California, Oakland"},{"name":"Department of Health Systems Science, Kaiser Permanente Bernard J. 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