Research Article - Biomedical Research (2017) Volume 28, Issue 3
Risk factors and adverse outcomes of preeclampsia: a tertiary care centrebased study in China
Yuan-yuan Su, Jin-zhi Zhang and Fang Wang*Department of Gynaecology, Affiliated Hospital of Hebei University, Hebei, China
- *Corresponding Author:
- Fang Wang
Department of Gynaecology
Affiliated Hospital of Hebei University, P.R. China
Accepted date: August 3, 2016
Abstract
Purpose: To determine the adverse outcomes of preeclampsia in a tertiary care centre in China and to evaluate the associated risk factors.
Design: Case control study.
Patients and Methods: Amid the reporting period from September 2014 to August 2015, 1312 women delivered in the referral center, out of which 192 (6.83%) women had preeclampsia.
Results: The frequency of preeclampsia was observed to be 6.83%. Compared to women in control group (n=192), preeclampsia group women are older in age (p=0.133), had more parities (p=0.323), lesser education level (p<0.001), higher spontaneous abortion history (p=0.433) and were living in urban areas. Significantly higher gestational age at delivery, caesarean delivery, and neonatal care unit admission, (all p<0.001) was noted in women with preeclampsia. With respect to adverse outcomes, significantly higher number of preterm deliveries, still births, low birth weight (all p<0.001), neonatal deaths (p=0.023) and maternal deaths (p=0.032) were noted in preeclampsia group. Significant association of parity and low education level with preeclampsia was noted. The preeclampsia risk was inversely associated with number of visits for prenatal care.
Conclusion: Our study demonstrated significantly higher gestational age at delivery, preterm delivery, caesarean delivery, neonatal care unit admission, still births, neonatal deaths and maternal deaths in cases.
Keywords
Maternal mortality, Perinatal, Preeclampsia, Pregnancy.
Introduction
Preeclampsia is distinguished by hypertension as well as proteinuria during pregnancy and is usually diagnosed in nearly 3 to 4% of pregnancies altogether. It is a main source of maternal as well as perinatal morbidity. The most serious manifestation (eclampsia) is linked with maternal morbidity globally [1-3]. Preeclampsia is a disorder with obscure etiology that might occur via various pathways, as demonstrated by fluctuating phenotypes which are delegated early or late based on gestational age of onset and by preeclampsia severity [4,5].
Women with preeclampsia history have an increased risk of developing preeclampsia in consequent pregnancies [6-11], yet the probability/recurrence is defined inadequately; past studies have either incorporated a greater part of women delivered around 37 gestation weeks in whom the recurrence risk is low [12] or have depended on information which was taken from routinely gathered clinical data where the diagnosis might be imprecise [13]. Women with past preeclampsia who required delivery around 34 gestation weeks are of specific concern since it is perceived that they are at more serious risk of recurrence and severe foetal outcomes. The danger of the preeclampsia development in these ladies is additionally questionable on the grounds that past reports have been of atypical populaces and/or negligible numbers of women [11,14].
Recurrent preeclampsia has likewise been associated with advanced rates of Small for Gestational Age (SGA) infant delivery, preterm delivery, and perinatal death in comparison with in a first pregnancy preeclampsia [7,14]. Although a greater rate of related neonatal complications may be foreseen, this has not been researched formally. Preeclampsia remains a major cause of maternal as well as perinatal mortality and morbidity, and causes complications in 2-8% of overall pregnancies. In China, the preeclampsia prevalence is approximately 5%. Globally the preeclampsia incidence seems to be rising, probably due to the greater prevalence of obesity and medical comorbidities, advancing maternal age and the usage of assisted reproductive techniques [15,16].
Successful discovery and treatment of preeclampsia and eclampsia inside of any nation or health region ought to at any rate be impacted by knowledge of clinician on the prevalence of the disease within their practice area. Research into preeclampsia and/or eclampsia may help clinicians and caregivers in decision making.
As per our knowledge none of the studies focused on determination of the risk factors and adverse outcomes of preeclampsia in China. The present study objectives were to determine the adverse outcomes of preeclampsia in China and to evaluate the associated risk factors.
Methods
This case control study was performed in a Tertiary Hospital, China over a time of one year from September 2014 to August 2015.
The study target population included women with preeclampsia as cases and women with normal pregnancies (no preeclampsia) as controls. The study got the approval from the Ethics Committee and patient confidentiality was strictly maintained. We collected the data from medical records department. The clinical and demographics variables obtained were noted below: age, education, medical history, obstetric history, parity, prenatal care, Body Mass Index (BMI; calculated as weight in kilograms divided by the square of height in meters), number of prenatal visits, and residence. Data on adverse maternal as well as perinatal outcomes (preterm delivery, perinatal death (neonatal death or still birth), maternal death, low birth weight etc.) was also collected. Preeclampsia was considered as two readings of blood pressure of minimum 140 mmHg systolic or minimum 90 mmHg diastolic, or rises of 30 mmHg systolic or 15 mmHg diastolic from that of the baseline on minimum of two occasions at ≥ 6 hours apart) post 20th week of pregnancy and proteinuria in prior normotensive women.
Maternal death was considered as intra hospital death of woman that observed on or before eighth day postnatal. Perinatal death was outlined as early neonatal death (intra hospital infant death that took place on or before seventh day post-delivery) or stillbirth (fresh/macerated). Preterm birth was considered as live-birth at less than 37 gestational weeks. Birth weight of less than 2500 grams of a live born baby irrespective of gestational age was considered as low birth weight.
Statistical analysis
Values were expressed as numbers and percentage as well as mean with Standard Deviation (SD). The associations of risk factors were evaluated by logistic regression analysis. Student t-tests or Chi square tests were used for comparison of maternal as well as perinatal characteristics of cases and controls. Analysis of all data collected was done using SPSS version 16.0 (SPSS Inc., Chicago, IL, USA). P value ≤ 0.05 was regarded as significant statistically.
Results
Altogether, 1312 women delivered in this study amid the reporting period, out of which 192 (6.83%) women had preeclampsia. The mean age of women with preeclampsia (cases) was 29.8 (5.2 (SD)) years whereas 28.4 (6.4) years in case of controls.
The clinical/demographic characteristics and adverse outcomes in Chinese women with preeclampsia including age, Body Mass Index (BMI), education level, medical history, obstetric history, parity, prenatal care, maternal as well as perinatal outcomes, haemoglobin and residence etc. are presented in Table 1.
Compared to women in control group, preeclampsia group women are older in age (p=0.133), had more parities (p=0.323), lesser education level (p<0.001), and higher spontaneous abortion history (p=0.433). More women in preeclampsia group were living in urban areas (54.7%). Largest group of the women were with primigravida (48.9%). Significantly higher gestational age at delivery, caesarean delivery, and neonatal care unit admissions, (all p<0.001) was noted in women with preeclampsia. With respect to adverse outcomes, significantly higher number of preterm deliveries, still births, low birth weight (all p<0.001), neonatal deaths (p=0.023) and maternal deaths (p=0.032) were noted in preeclampsia group. There were 8 (4.2%) maternal deaths in the preeclampsia group, compared to no maternal death in the control group.
There was no significant association noted for age, BMI (calculated as weight in kilograms divided by the square of height in meters), residence and haemoglobin. Parity as well as low education level was found to be significantly associated with preeclampsia as shown in Table 1. The preeclampsia risk was found to be inversely associated with the number of visits for prenatal care as shown in Table 1.
Characteristics | Cases (n=192) | Controls (n=192) | P value | Logistic regression analyses | |
---|---|---|---|---|---|
OR (95% CI) | P value | ||||
Age in years | 29.8 (5.2) | 28.4 (6.4) | 0.133 | 0.9 (0.7-1.0) | 0.182 |
BMI in kg/m2 | 24.8 (2.3) | 24.6 (2.2) | 0.524 | 0.8 (0.7-1.0) | 0.546 |
Education level | |||||
≥ Secondary or higher | 21/192 (10.9%) | 45/192 (23.4%) | <0.001 | 1 | |
≤ Primary or less | 171/192 (89.1%) | 147/192 (76.6%) | <0.001 | 2.2 (1.7-6.1) | 0.022 |
Spontaneous abortion history | |||||
No | 136/192 (70.8%) | 141/192 (73.4%) | 0.724 | 1 | |
Yes | 56/192 (29.2%) | 51/192 (26.6%) | 0.433 | 1.3 (0.7-2.1) | 0.304 |
Residence | |||||
Urban | 105/192 (54.7%) | 105/192 (54.7%) | 0.924 | 1 | |
Rural | 87/192 (45.3%) | 87/192 (45.3%) | 0.933 | 0.7 (0.4-1.4) | 0.122 |
Parity | |||||
Primigravida | 94/192 (48.9%) | 49/192 (25.5%) | <0.001 | 2.7 (1.4-5.4) | <0.001 |
Parous | 61/192 (31.8%) | 109/192 (56.8%) | <0.001 | 1 | |
Multiparous | 37/192 (19.3%) | 34/192 (17.7%) | 0.323 | 5.9 (3.4-10.4) | <0.001 |
Prenatal care | |||||
No | 104/192 (54.2%) | 57/192 (29.7%) | <0.001 | 13.9 (6.4-24.2) | <0.001 |
1 or 2 visits | 76/192 (39.6%) | 68/192 (35.4%) | 0.275 | 7.1 (3.4-15.4) | <0.001 |
>2 visits | 12/192 (6.3%) | 67/192 (34.9%) | <0.001 | 1 | |
Haemoglobin, g/L | 96 (15) | 96 (14) | 0.932 | 0.8 (0.7-1.0) | 0.332 |
Male neonate | 98/192 (51%) | 96/192 (50%) | 0.856 | 1.2 (0.8-2.1) | 0.527 |
Gestational age at delivery, wk | 36.4 (2.5) | 38.2 (1.3) | <0.001 | - | - |
Preterm delivery | 61/192 (31.8%) | 7/192 (3.6%) | <0.001 | - | - |
Caesarean delivery | 148/192 (77.1%) | 14/192 (7.3%) | <0.001 | - | - |
Neonatal care unit admission | 98/192 (51%) | 14/192 (7.3%) | <0.001 | - | - |
Neonatal death | 11/192 (5.7%) | 0 | 0.023 | - | - |
Still birth | 27/192 (14.1%) | 2/192 (1.0%) | <0.001 | - | - |
Birth weight (g) | 1612.9 (582) | 3024.5 (325) | <0.001 | - | - |
Maternal death | 8/192 (4.2%) | 0 | 0.032 | - | - |
BMI: Body Mass Index; CI: Confidence Interval; OR: Odds Ratio. Values are expressed as numbers and percentage/mean with standard deviation. |
Table 1. Clinical/demographic characteristics and adverse outcomes in Chinese women with preeclampsia.
Discussion
The frequency of preeclampsia observed in the present study was 6.83%. These frequencies were found to be higher than those reported in Sudan, where 3.5% preeclampsia prevalence was noted [17] and 5 out of 1000 were affected by eclampsia [18] and lower than those reported in Yemen, where 7.6% prevalence of preeclampsia was noted [19]. Also, in a multicenter study conducted recently [20], the prevalence of preeclampsia was noted to be 3.9%. In a study conducted by Surapaneni et al. reported rates of recurrent preeclampsia have large differences: women without a history of preeclampsia had preeclampsia pregnancy rates of 0.7% to 1.8%, while the women with history of preeclampsia during pregnancy had preeclampsia incidence of up to 26.8% ~ 28.0% [21]. In Hernandez-Diaz et al. study [5], a large sample data suggested 3.0% preeclampsia prevalence in pregnant women. The variability in frequencies of preeclampsia is probably not just denotes the variability of maternal risk factors distribution, however likewise be ascribed to contrasts in the facility as well as country characteristics, like diagnostic capacities or service accessibility etc.
Significantly higher gestational age at delivery, caesarean delivery, and neonatal care unit admissions was noted in women with preeclampsia. With regards to adverse outcomes, significantly higher number of preterm deliveries, still births, low birth weight, neonatal deaths and maternal deaths were noted in preeclampsia group. There was no significant association noted for age, BMI, residence and haemoglobin. Parity as well as low education level was found to be significantly associated with preeclampsia. The preeclampsia risk was found to be inversely associated with the number of visits for prenatal care. A study by Bilano et al. [20] demonstrated similar findings where primiparity as well as lack of prenatal care was shown to be the major predictors for preeclampsia. Also, high parity, lack of education, primiparity, and prenatal care were considered as the major predictors for preeclampsia in studies conducted in Sudan and Yemen [17,19]. Significant association of maternal mortality with preeclampsia was demonstrated in studies conducted by Adam GK et al. and Bilano et al. [18,20]. High frequency of caesarean deliveries and the birth weight deviations and association with preeclampsia history were reported in a study by de Oliviera et al. [22]. Preeclampsia history is an independent risk factor for preeclampsia recurrence, while it is influenced by many other factors.
Certain inherent limitations need to be considered during interpretation of the results of current study. This single-centre study has a restricted number of patients hence the generalization of results should be made with care. We were unable to evaluate all variables and were restricted by the treating physicians with respect to completeness of or proper documentation. Limited information was captured on the preeclampsia severity and the patient management.
Conclusion
Our data demonstrated significantly higher gestational age at delivery, preterm delivery, caesarean delivery, neonatal care unit admission, still births, neonatal deaths and maternal deaths in women with preeclampsia. Parity as well as low education level was found to be significantly associated with preeclampsia whereas the number of visits for prenatal care was inversely associated with preeclampsia risk. Future robust studies are needed in this area for research. Health education ought to be underlined to urge women to have children at younger age relatively. Special measures ought to be taken for proper risk factor identification (close monitoring), mobile midwives who can visit non-attenders, and enhancement of the living conditions as well as prenatal care in the small towns and countryside.
References
- Hogberg U. The World Health Report 2005: make every mother and child count-including Africans. Scand J Public Health 2005; 33: 409-411.
- Roberts CL, Ford JB, Algert CS, Antonsen S, Chalmers J, Cnattingius S, Gokhale M, Kotelchuck M, Melve KK, Langridge A, Morris C, Morris JM, Nassar N, Norman JE, Norrie J, Sørensen HT, Walker R, Weir CJ. Population-based trends in pregnancy hypertension and pre-eclampsia: an international comparative study. BMJ Open 2011; 1: e000101.
- Steegers EA, von Dadelszen P, Duvekot JJ, Pijnenborg R. Pre-eclampsia. Lancet 2010; 376: 631-644.
- Sibai B, Dekker G, Kupferminc M. Pre-eclampsia. Lancet 2005; 365: 785-799.
- Hernandez-Diaz S, Toh S, Cnattingius S. Risk of pre-eclampsia in first and subsequent pregnancies: prospective cohort study. BMJ 2009; 338: b2255.
- Makkonen N, Heinonen S, Kirkinen P. Obstetric prognosis in second pregnancy after preeclampsia in first pregnancy. Hypertens Pregn 2000; 19: 173-181.
- Hnat MD, Sibai BM, Caritis S, Hauth J, Lindheimer MD, MacPherson C, VanDorsten JP, Landon M, Miodovnik M, Paul R, Meis P, Thurnau G, Dombrowski M. National Institute of Child Health and Human Development Network of Maternal-Foetal Medicine-Units. Perinatal outcome in women with recurrent preeclampsia compared with women who develop preeclampsia as nulliparas. Am J Obstet Gynecol 2002; 186: 422-426.
- Trogstad L, Skrondal A, Stoltenberg C, Magnus P, Nesheim BI. Recurrence risk of preeclampsia in twin and singleton pregnancies. Am J Med Genet A 2004; 126A: 41-45.
- Hjartardottir S, Leifsson BG, Geirsson RT, Steinthorsdottir V. Recurrence of hypertensive disorder in second pregnancy. Am J Obstet Gynecol 2006; 194: 916-920.
- Brown MA, Mackenzie C, Dunsmuir W, Roberts L, Ikin K. Can we predict recurrence of pre-eclampsia or gestational hypertension? BJOG 2007; 114: 984-993.
- van Rijn BB, Hoeks LB, Bots ML, Franx A, Bruinse HW. Outcomes of subsequent pregnancy after first pregnancy with early-onset preeclampsia. Am J Obstet Gynecol 2006; 195: 723-728.
- Dukler D, Porath A, Bashiri A, Erez O, Mazor M. Remote prognosis of primiparous women with preeclampsia. Eur J Obstet Gynecol Reprod Biol 2001; 96: 69-74.
- Chappell L, Poulton L, Halligan A, Shennan AH. Lack of consistency in research papers over the definition of pre-eclampsia. Br J Obstet Gynaecol 1999; 106: 983-985.
- Sibai BM, Mercer B, Sarinoglu C. Severe preeclampsia in the second trimester: recurrence risk and long-term prognosis. Am J Obstet Gynecol 1991; 165: 1408-1412.
- MacKay AP, Berg CJ, Atrash HK. Pregnancy-related mortality from preeclampsia and eclampsia. Obstet Gynecol 2001; 97: 533-538.
- Steegers EA, von Dadelszen P, Duvekot JJ, Pijnenborg R. Pre-eclampsia. Lancet 2010; 376: 631-644.
- Adam I, Haggaz AD, Mirghani OA, Elhassan EM. Placenta previa and pre-eclampsia: analyses of 1645 cases at Medani maternity hospital, Sudan. Front Physiol 2013; 4: 32.
- Adam GK, Bakheit KH, Adam I. Maternal and perinatal outcomes of eclampsia in Gadarif Hospital, Sudan. J Obstet Gynaecol 2009; 29: 619-620.
- Al-Rukeimi AA, Al-Haddad A, Adam I. Risk factors for pre-eclampsia, eclampsia, and associated adverse outcomes in Hajjah, Yemen. Int J Gynaecol Obstet 2014; 127: 91-92.
- Bilano VL, Ota E, Ganchimeg T, Mori R, Souza JP. Risk factors of pre-eclampsia/ eclampsia and its adverse outcomes in low- and middle-income countries: a WHO secondary analysis. PLoS One 2014; 9: 91198.
- Surapaneni T, Bada VP, Nirmalan CP. Risk for Recurrence of Pre-eclampsia in the Subsequent Pregnancy. J Clin Diagn Res 2013; 7: 2889-2891.
- de Oliveira AC, Santos AA, Bezerra AR, de Barros AM, Tavares MC. Maternal Factors and Adverse Perinatal Outcomes in Women with Preeclampsia in Maceio, Alagoas. Arq Bras Cardiol 2016; 106: 113-120.