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Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC · 2026

Current State of Blood Pressure Measurement in Pregnant People in Canada: A National Interdisciplinary Survey.

СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Dubrofsky Lisa, Pasricha Sachin V, Snelgrove John W, Gundy Serena, Tran Karen C, Okun Nanette, Tobe Sheldon W, McLaughlin Kelsey

Аннотация

OBJECTIVES: Hypertension affects 26 900 pregnancies in Canada per year. Accurate blood pressure (BP) measurement is recognized as crucial to hypertension care outside pregnancy but has gained less attention in pregnancy. Canadian guidelines recommend measuring maternal BP with a manual auscultatory device, or an automated device validated in pregnancy. National adherence to this recommendation is unknown.

METHODS: We developed a 15-question survey to understand how health care professionals (HCPs) measure BP in pregnancy. We distributed it through Hypertension Canada's mailing list and the snowball sampling method.

RESULTS: Eighty-six HCPs from 7 provinces and various specialties (including 63% from internal medicine and 21% from obstetrics) responded. For clinic BP in pregnant people, respondents frequently use an appropriate cuff size (n = 82, 95%), take multiple readings (n = 77, 90%), and have patients sit with arm/back support (n = 72, 84%). HCPs often use automated clinic devices for pregnant people but are uncertain of their validation in pregnancy (n = 53, 62%). Respondents frequently recommend home BP measurement (n = 81, 94%) and asked patients to bring their home devices to the clinic to compare against clinic devices (n = 61, 71%) but most did not recommend a specific home device or specify one that is validated in pregnancy.

CONCLUSIONS: We identified 4 strengths of BP measurement in pregnancy: appropriate cuff size, taking multiple readings, recommending home measurement, and attempting calibration of home devices. The most concerning finding was the failure to use (in clinic) and recommend (at home) devices validated for pregnant people, due at least in part, to the limited number of devices validated for this population.