TY - JOUR
T1 - The CHIPS Randomized Controlled Trial (Control of Hypertension in Pregnancy Study)
T2 - Is Severe Hypertension Just an Elevated Blood Pressure?
AU - Magee, Laura A.
AU - von Dadelszen, Peter
AU - Singer, Joel
AU - Lee, Terry
AU - Rey, Evelyne
AU - Ross, Susan
AU - Asztalos, Elizabeth
AU - Murphy, Kellie E.
AU - Menzies, Jennifer
AU - Sanchez, Johanna
AU - Gafni, Amiram
AU - Helewa, Michael
AU - Hutton, Eileen
AU - Koren, Gideon
AU - Lee, Shoo K.
AU - Logan, Alexander G.
AU - Ganzevoort, Wessel
AU - Welch, Ross
AU - Thornton, Jim G.
AU - Moutquin, Jean-Marie
AU - CHIPS Study Group
PY - 2016/11
Y1 - 2016/11
N2 - To determine whether clinical outcomes differed by occurrence of severe hypertension in the international CHIPS trial (Control of Hypertension in Pregnancy Study), adjusting for the interventions of textquotedblleftless tighttextquotedblright (target diastolic blood pressure [dBP] 100 mm Hg) versus textquotedbllefttighttextquotedblright control (target dBP 85 mm Hg). In this post-hoc analysis of CHIPS data from 987 women with nonsevere nonproteinuric preexisting or gestational hypertension, mixed effects logistic regression was used to compare the following outcomes according to occurrence of severe hypertension, adjusting for allocated group and the influence of baseline factors: CHIPS primary (perinatal loss or high-level neonatal care for gt;48 hours) and secondary outcomes (serious maternal complications), birth weight lt;10th percentile, preeclampsia, delivery at lt;34 or lt;37 weeks, platelets lt;100texttimes109/L, elevated liver enzymes with symptoms, maternal length of stay >=10 days, and maternal readmission before 6 weeks postpartum. Three hundred and thirty-four (34.1 women in CHIPS developed severe hypertension that was associated with all outcomes examined except for maternal readmission (P=0.20): CHIPS primary outcome, birth weight lt;10th percentile, preeclampsia, preterm delivery, elevated liver enzymes (all Plt;0.001), platelets lt;100texttimes109/L (P=0.006), and prolonged hospital stay (P=0.03). The association between severe hypertension and serious maternal complications was seen only in less tight control (P=0.02). Adjustment for preeclampsia (464, 47.3 did not negate the relationship between severe hypertension and the CHIPS primary outcome (Plt;0.001), birth weight lt;10th percentile (P=0.005), delivery at lt;37 (Plt;0.001) or lt;34 weeks (Plt;0.001), or elevated liver enzymes with symptoms (P=0.02). Severe hypertension is a risk marker for adverse maternal and perinatal outcomes, independent of BP control or preeclampsia co-occurrence.Clinical Trial RegistrationtextemdashURL: http://pre-empt.cfri.ca/. Unique identifier: ISRCTN 71416914. URL: https://www.clinicaltrials.gov/. Unique identifier: NCT01192412.Novelty and Significance
AB - To determine whether clinical outcomes differed by occurrence of severe hypertension in the international CHIPS trial (Control of Hypertension in Pregnancy Study), adjusting for the interventions of textquotedblleftless tighttextquotedblright (target diastolic blood pressure [dBP] 100 mm Hg) versus textquotedbllefttighttextquotedblright control (target dBP 85 mm Hg). In this post-hoc analysis of CHIPS data from 987 women with nonsevere nonproteinuric preexisting or gestational hypertension, mixed effects logistic regression was used to compare the following outcomes according to occurrence of severe hypertension, adjusting for allocated group and the influence of baseline factors: CHIPS primary (perinatal loss or high-level neonatal care for gt;48 hours) and secondary outcomes (serious maternal complications), birth weight lt;10th percentile, preeclampsia, delivery at lt;34 or lt;37 weeks, platelets lt;100texttimes109/L, elevated liver enzymes with symptoms, maternal length of stay >=10 days, and maternal readmission before 6 weeks postpartum. Three hundred and thirty-four (34.1 women in CHIPS developed severe hypertension that was associated with all outcomes examined except for maternal readmission (P=0.20): CHIPS primary outcome, birth weight lt;10th percentile, preeclampsia, preterm delivery, elevated liver enzymes (all Plt;0.001), platelets lt;100texttimes109/L (P=0.006), and prolonged hospital stay (P=0.03). The association between severe hypertension and serious maternal complications was seen only in less tight control (P=0.02). Adjustment for preeclampsia (464, 47.3 did not negate the relationship between severe hypertension and the CHIPS primary outcome (Plt;0.001), birth weight lt;10th percentile (P=0.005), delivery at lt;37 (Plt;0.001) or lt;34 weeks (Plt;0.001), or elevated liver enzymes with symptoms (P=0.02). Severe hypertension is a risk marker for adverse maternal and perinatal outcomes, independent of BP control or preeclampsia co-occurrence.Clinical Trial RegistrationtextemdashURL: http://pre-empt.cfri.ca/. Unique identifier: ISRCTN 71416914. URL: https://www.clinicaltrials.gov/. Unique identifier: NCT01192412.Novelty and Significance
U2 - 10.1161/HYPERTENSIONAHA.116.07862
DO - 10.1161/HYPERTENSIONAHA.116.07862
M3 - Article
SN - 0194-911X
VL - 68
SP - 1153
EP - 1159
JO - Hypertension
JF - Hypertension
IS - 5
ER -