Slade Laura, Blackman Maya, Mistry Hiten D, Bone Jeffrey N, Wilson Milly, Syeda Nuhaat, Poston Lucilla, von Dadelszen Peter, Magee Laura A
Robinson Research Institute, The University of Adelaide, Adelaide, Australia.
Department of Obstetrics and Gynaecology, Women's and Children's Hospital, Adelaide, Australia.
PLoS Med. 2025 Jan 22;22(1):e1004471. doi: 10.1371/journal.pmed.1004471. eCollection 2025 Jan.
In 2017, the American College of Cardiology and American Heart Association (ACC/AHA) lowered blood pressure (BP) thresholds to define hypertension in adults outside pregnancy. If used in pregnancy, these lower thresholds may identify women at increased risk of adverse outcomes, which would be particularly useful to risk-stratify nulliparous women. In this secondary analysis of the SCOPE cohort, we asked whether, among standard-risk nulliparous women, the ACC/AHA BP categories could identify women at increased risk for adverse outcomes.
Included were pregnancies in the international SCOPE cohort with birth at ≥20 weeks' gestation, 2004 to 2008. Women were mostly of white ethnicity, in their 20s, and of normal-to-overweight body mass index (BMI). Excluded were pregnancies ending in fetal loss at <20 weeks' gestation, and those terminated at any point in pregnancy. Women were categorized by highest BP during pregnancy, using ACC/AHA criteria: normal (BP <120/80 mmHg), "Elevated BP" (BP 120 to 129 mmHg/<80 mmHg), "Stage-1 hypertension" (systolic BP [sBP] 130 to 139 mmHg or diastolic BP [dBP] 80 to 89 mmHg), and "Stage-2 hypertension" that was non-severe (sBP 140 to 159 mmHg or dBP 90 to 109 mmHg) or severe (sBP ≥160 mmHg or dBP ≥110 mmHg). Primary outcomes were preterm birth (PTB), low birthweight, postpartum hemorrhage, and neonatal care admission. Adjusted relative risks (aRRs) and diagnostic test properties were calculated for each outcome, according to: each BP category (versus "normal"), and using the lower limit of each BP category as a cut-off. RRs were adjusted for maternal age, BMI, smoking, ethnicity, and alcohol use. Of 5,628 women in SCOPE, 5,597 were included in this analysis. When compared with normotension, severe "Stage 2 hypertension" was associated with PTB (24.0% versus 5.3%; aRR 4.88, 95% confidence interval, CI [3.46 to 6.88]), birthweight <10th centile (24.4% versus 8.8%; aRR 2.70 [2.00 to 3.65]), and neonatal unit admission (32.9% versus 8.9%; aRR 3.40 [2.59 to 4.46]). When compared with normotension, non-severe "Stage 2 hypertension" was associated with birthweight <10th centile (16.1% versus 8.8%; aRR 1.82 [1.45 to 2.29]) and neonatal unit admission (15.4% versus 8.9%; aRR 1.65 [1.31 to 2.07]), but no association with adverse outcomes was seen with BP categories below "Stage 2 hypertension." When each BP category was assessed as a threshold for diagnosis of abnormal BP (compared with BP values below), only severe "Stage 2 hypertension" had a useful (good) likelihood ratio (LR) of 5.09 (95% CI [3.84 to 6.75]) for PTB. No BP threshold could rule-out adverse outcomes (i.e., had a negative LR <0.2). Limitations of our analysis include lack of ethnic diversity and use of values from clinical notes for BP within 2 weeks before birth. This study was limited by: its retrospective nature, not all women having BP recorded at all visits, and the lack of detail about some outcomes.
In this study, we observed that 2017 ACC/AHA BP categories demonstrated a similar pattern of association and diagnostic test properties in nulliparous women, as seen in the general obstetric population. BP thresholds below the currently used "Stage 2 hypertension" were not associated with PTB, low birthweight, postpartum hemorrhage, or neonatal unit admission. This study does not support implementation of lower BP values as abnormal in nulliparous pregnant women.
2017年,美国心脏病学会和美国心脏协会(ACC/AHA)降低了血压(BP)阈值,以界定非孕期成人的高血压。若应用于孕期,这些较低的阈值可能会识别出不良结局风险增加的女性,这对于对未生育女性进行风险分层尤为有用。在对SCOPE队列的这项二次分析中,我们探讨了在标准风险的未生育女性中,ACC/AHA血压类别是否能够识别出不良结局风险增加的女性。
纳入了国际SCOPE队列中2004年至2008年妊娠≥20周分娩的孕妇。女性大多为白人,年龄在20多岁,体重指数(BMI)为正常至超重。排除妊娠<20周胎儿丢失以及孕期任何阶段终止妊娠的情况。根据ACC/AHA标准,将女性按孕期最高血压分类:正常(血压<120/80 mmHg)、“血压升高”(血压120至129 mmHg/<80 mmHg)、“1级高血压”(收缩压[sBP]130至139 mmHg或舒张压[dBP]80至89 mmHg)以及非重度(sBP 140至159 mmHg或dBP 90至109 mmHg)或重度(sBP≥160 mmHg或dBP≥110 mmHg)的“2级高血压”。主要结局为早产(PTB)、低出生体重、产后出血以及新生儿重症监护病房收治。针对每个结局,根据以下情况计算调整后的相对风险(aRRs)和诊断试验特性:每个血压类别(与“正常”相比),并将每个血压类别的下限作为临界值。RRs针对产妇年龄、BMI、吸烟、种族和饮酒情况进行了调整。SCOPE队列中的5628名女性中,5597名纳入了本分析。与血压正常相比,重度“2级高血压”与早产相关(24.0%对5.3%;aRR 4.88,95%置信区间,CI[3.46至6.88])、出生体重<第10百分位数(24.4%对8.8%;aRR 2.70[2.00至3.65])以及新生儿重症监护病房收治(32.9%对8.9%;aRR 3.40[2.59至4.46])。与血压正常相比,非重度“2级高血压”与出生体重<第10百分位数(16.1%对8.8%;aRR 1.82[1.45至2.29])以及新生儿重症监护病房收治(15.4%对8.9%;aRR 1.65[1.31至2.07])相关,但低于“2级高血压”的血压类别与不良结局无关联。当将每个血压类别作为诊断血压异常的临界值进行评估时(与低于该值的血压值相比),仅重度“2级高血压”对于早产具有有用(良好)的似然比(LR)为5.09(95%CI[3.84至6.75])。没有血压临界值能够排除不良结局(即阴性LR<0.2)。我们分析的局限性包括缺乏种族多样性以及使用出生前2周内临床记录中的血压值。本研究的局限性在于:其回顾性性质、并非所有女性每次就诊时都记录了血压,以及某些结局缺乏详细信息。
在本研究中,我们观察到2017年ACC/AHA血压类别在未生育女性中显示出与一般产科人群相似的关联模式和诊断试验特性。低于当前所用“2级高血压”的血压阈值与早产、低出生体重、产后出血或新生儿重症监护病房收治无关。本研究不支持将较低的血压值判定为未生育孕妇的异常血压。