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Grand Multiparity and Pregnancy Related Complications among Women
Gynecology & Obstetrics

Gynecology & Obstetrics
Open Access

ISSN: 2161-0932

Research Article - (2017) Volume 7, Issue 5

Grand Multiparity and Pregnancy Related Complications among Women Who Gave Birth at Jimma University Specialized Hospital, Jimma, Southwest Ethiopia

Yesuf Ahmed Aragaw*, Mintesnot Mahtemsilllasie and Habtamu Jarso
Department of Obstetrics and Gynecology, Jimma University, Ethiopia
*Corresponding Author: Yesuf Ahmed Aragaw, Assistant Professor, Department of Obstetrics and Gynecology, Jimma University obstetrics and gynecology Jimma, Ethiopia, Tel: +251911004736 Email:

Abstract

Introduction: The term ‘Grand-multiparity’ was introduced by Solomon (1934), who called it the “dangerous multipara” [1]. Since then grand multiparity has been considered as a risk factor for both mother and the fetus [1-4]. The International Federation of Gynecology and Obstetrics define grand multiparity as delivery of the fifth or more newborn and in this study grand multiparity is defined when a pregnant woman have five or more births above the gestational age of 28 weeks [2]. The objective of this study is to compare maternal and perinatal outcome in grand multiparity and low parity. In developing countries grand multiparity is very common while in developed countries rare.

Methods and materials: Prospective cross sectional comparative study was done in Jimma University specialized Hospital in 2015. Data was collected from119 grand multiparous (parity >= 5) and 238 low parity (parity2-4) women who gave birth in the hospital and data were analyzed by using statically package social science (spss) 20.3. p-value<0.05 considered significant.

Result: There were 357 parous women participated in the study, among then 125 were grand multiparous making the incidence 8%. Grand multiparty was associated with anemia (3.5; 1.5-8.4), nonreassuring fetal condition intraparum (3.2; 1.3-8.0) and perinatal mortality (5; 1.7-7.4).

Conclusion: Grand multiparty was associated both maternal and perinatal mortality and morbidity. Limiting parity might decrease both maternal and perinatal mortality and both at community and health facility family planning awareness should be made.

Keywords: Grand multiparty; Perinatal mortality; Jimma; Ethiopia

Introduction

Grand-multiparty was introduced by Solomon (1934), who called it the “dangerous multipara” [1]. Grandmultiparity has been considered a risk factor for mother and fetus [1,3,4]. The international federation of gynecology and obstetrics defined grandmulitpariy is delivery of more than five births after fetal viability and this study grand multiparty is defined five or more births after gestational age of 28 weeks or fetal weight 1000 gm and above [2,4].

The incidence is 2-4% in developed countries where as very common in developing countries as high as 18.5% [5]. There were several Studies undertaken to evaluate the impact of grandmultiparity on obstetric outcome in a low and resource setting revealed that grandmultiparity continues to be of grave concern with an adverse impact on obstetric and perinatal outcome [6-13].

Although the older literature tends to suggest that multiparty is a risk factor for negative birth and maternal outcomes but more recent reports are not supportive. Comparison across studies was further complicated by confounding factors like maternal age, socioeconomic status, and levels of prenatal care, as well as by variations in study designs and in the definition of parity itself [14,15]. The aim of this study was to compare the maternal and perinatal outcome of grand multiparous and low parity (parity 2-4) and the incidence in south west Ethiopia.

Methods and Materials

Prospective comparative correctional study was done in Jimma University specialized Hospital from May to September 2015.

The study population were all singleton low parity [2-4] and grandmultity parity in the study period. The exclusion criteria multiple gestations, pregnant women with currently medical problem, women who delivered in other health institution and who were not accepted consent not included in the study whereas gravid women with low parity and parity five and above included in the study.

Sample size

The sample size was computed using OpenEpi, Version 3. The researcher used a secondary outcome parameter from a previously published study in order to avoid having smaller sample size. The Minimum required sample size was 323 with 10% non-responding rate making sample size 357 where the estimated ratio of unexposed (a lower parity) -to-exposed (grand multiparas) group is 2:1. Based on the power of the study (1-β) of 80% (confidence interval (CI), 95%) with least extreme odds ratio of 2.00 (Table 1).

 
For: Two-sided confidence level(1-alpha) 95
  Power(% chance of detecting) 80
  Ratio of Controls to Cases 02:01
  Hypothetical proportion of controls with exposure 40
  Hypothetical proportion of cases with exposure: 57.14
  Least extreme Odds Ratio to be detected: 2
  Kelsey  Fleiss Fleiss with CC
Sample Size - Cases 100 99 108
Sample Size - Controls 199 198 215
Total sample size: 299 297 323

Table 1: Sample Size for Unmatched Case-Control Study using OpenEpi, Version 3.

Sampling technique

Beginning from the first date of data collection, all grand multiparous that full fill the inclusion and exclusion criteria were taken as a case and for each case the next two consecutive low parity mothers who full fill the inclusion criteria considered as control. Data were collected using questionnaire containing maternal sociodemographic characteristics, antenatal profile, intrapartum and postpartum condition of the mother and newborn by trained midwife and neonatal outcome checked by phone on the 7th day birth for those who were discharged before. The principal investigators and other supervisor resident checked quality of the data before discharging a patient.

Data were analyzed using statistical package for social science (SPSS) version 20.3 software. To calculate the mean difference in continuous outcome variables between the two groups, student’s independent t-test were used. In the test of association between the predictor- and outcome-variables, the effects of potential confounders were controlled using Generalized Linear Models with a linear regression. Furthermore, for the categorical outcome variables association for each predictor variables was calculated using chi-square. When association was found with chi square between predictor variables and categorical outcome variables, binary logistic regression was used to measure association using Odd ratios with 95% CI and potential confounders were controlled by running multivariable logistic regression. Mean differences and tests of association had 95% Confidence Intervals as an indicator of statistical significance and precision. Adjusted P -Values less than or equal to 0.05 was considered statistically significant.

An official letter obtained from Jimma university ethical review board committee and oral consent was asked before interviewing and extraction of data from patient card.

Results

Socio-demographic/economic characteristics

A total of 357 pregnant mothers (119 grand multiparas and 238 with low parity (control)) participated in this research during the study period. The mean age among grand multiparas was 31.7 ± 4.1 years whereas that of control (low parity) was 27 ± 4.1 years. Majority of grand multiparas 98 (82.4%) and low parity 154 (64.7%) are Oromo by ethnicity and almost all grand multiparas 116 (97.5%) and low parity 236 (99.2%) were married. 106 (89.1%) and 141 (59.1%) among grand multiparas and low parity were living rural area respectively. Most of grand multiparas 103 (86.6%) and majority of low parity 156 (65.5%) are Muslim by religion. Majority of grand multiparas 88 (73.9%) were not able to read and write; however, only 72(30%) of low parity groups cannot read and write. Regarding to occupational status, 58(48.7%) and 140(58.8%) grand multiparas and controls are house wife respectively. The mean monthly income of grand multiparas is 1295.8 ± 958.6 Ethiopian birr whereas 1974.5 ± 1355.4 Ethiopian birr for low parity. Table 1 shows sociodemographic characteristics of study subject.

There were 1572 deliveries in the study period in Jimma university specialized Hospitals. There were 125 grand multiparas out of this 6 were having twin deliveries and excluded. The hospital grand multiparous delivery prevalence was 8 % during the study period (Table 2).

Variable Grand multiparas Low parity
Age Category Frequency  % Frequency  %
<20 0 0 5 2.1
20-24 2 1.7 50 21.0
25-29 29 24.4 111 46.6
30-34 43 36.1 53 22.3
>34 45 37.8 19 8.0
Mean age ±SD 31.7±4.1   27 ± 4.1  
  Ethnicity Oromo 98 82.4 154 64.7
Amhara 5 4.2 47 19.7
Gurage 5 4.2 7 2.9
Dawuro 7 5.9 27 11.3
Tigre 1 0.8 1 0.4
Others 3 2.5 2 0.8
Marital status Married 116 97.5 236 99.2
Divorced 1 0.8 1 0.4
Widowed 2 1.7 0 0
Single 0 0 1 0.4
Residence urban 13 10.9 97 40.8
Rural 106 89.1 141 59.2
Religion Orthodox 10 8.4 65 27.3
Muslim 103 86.6 156 65.5
Protestant 6 5.0 16 6.7
Others 0 0 1 .4
Educational status Cannot read and write 88 73.9 72 30.3
Primary or can read and write 22 18.5 102 42.9
Secondary 6 5.0 52 21.8
Collage and above 3 2.5 12 5.0
Occupational status Farmer 49 41.2 40 16.8
House wife 58 48.7 140 58.8
Government employee 6 5.0 38 16.0
Student 1 0.8 2 0.8
Merchant 5 4.2 17 7.1
Daily laborer 0 0 1 0.4
Monthly income (mean ± SD) 1295.8 ±958.6     1974.5±1355.4  

Table 2: Socio-demographic characteristics of grandmultiparity and low parity groups at JUSTH, south west Ethiopia from May 2015 to September 2015.

Antepartum complications: From a total of 119 grandmultiparas women 64 (53.8%) had anemia as antepartum complication whereas 40 (16.8%) of low parity mothers had anemia. Antepartum hemorrhage was identified in 24 (20.2%) and 18 (7.6%) of grand multiparas and low parity respectively. Hypertensive disorders of pregnancy reported in 13 (10.9%) of grand multiparas where as16 (6.7%) in low parity group. Malpresentation was detected in 39 (32.8%) and 32 (13.4%) of grandmultiparas and low parity groups respectively. Regarding to IUFD, it is observed in 26 (21.8%) and 18 (7.6%) of grandmultiparas and low parity respectively. Identification of at least one of antepartum complication was recorded in 85 (71.4%) and 78 (32.8%) grandmultiparas and low parity respectively. Anemia was the commonest complication in grand multiparous women which three to four times that of low parity during antepartum but there is no deference in malpresention, hypertension disorders and antepartum hemorrhage between the groups (Table 3).

Variables Grandmultiparous    n=119
N (%)
Low parity n=238
N (%)
p COR (95% CI) p* AOR(95%CI)
Anemia 64 (53.8) 40 (16.8) <0.001 5.8(3.5-9.5) <0.001 3.5(1.5-8.4)**
APH 24 (20.2) 18 (7.60) <0.001 3.1(1.6-6.0) 0.89 1.0(0.3-2.7)
Hypertensive disorders of pregnancy 13 (10.9) 16 (6.7) 0.18 1.7(0.8-3.7)    
Malpresentation including intrapartum 39 (32.8) 32 (13.4) <0.001 3.1(1.8-5.4) 0.54 1.3 (0.5-3.1)
IUFD including intrapartum 26 (21.8) 18 (7.6) <0.001 3.4(1.8-6.5) 0.71 1.6 (0.1-17.5)
At least one antepartum complication 85 (71.4) 78 (32.8) <0.001 5.1(3.2-8.3) <0.001 3.2(1.8-5.6)*
**
* - after adjusting for socio-demographic factors, ANC profile and pre-existing
Problems.
** - statistically significant at p-value <0.05 after confounders including socio-demographic factors, ANC profile and pre-existing Problems APH and IUFD are controlled with  multivariable logistic regression.
***- statistically significant at p-value <0.05 after adjusting for socio-demographic factors, ANC profile and pre-existing Problems using chi square and multivariable logistic regression.

Table 3: Association of parity with antepartum complications of pregnancy at JUSTH, south west Ethiopia from May 2015 to September 2015.

Intrapartum complications: When we look at the intra partum complication identified in study groups, the reported mean duration of labor is 12.4 and 13 hours in grandmultiparas and low parity respectively. Labor abnormality is noticed in in majority of grandmultiparas 64 (56.6%) and 65 (29.4%) of low parity groups and meconium stained amniotic fluid observed in 37 (40.2%) of grandmultiparas and 42 (25.2%) of low parity mothers. Fetal heart beat abnormality was detected 25 (26.9%) of grandmultiparous mother during labor and 32 (14.5%) in low parity groups. Intra partal uterine rupture was found in 17 (14.3%) and 5 (2.1%) of grandmultiparas and control multiparas respectively. Majority of grandmultiparas 74 (62.2%) and 113 (47.5%) of low parity groups gave birth with major operations. Most of grandmultiparas 100 (84%) and majority 132 (55.5%) of mothers with low parity have at least one intrapartum complication. Grand multiparous women had been associated with 2.7(CI: 1.4-5.3) times intrapartum complication as to compared to low parity, specifically non reassuring fetal heart status (NRFHS) three times more common in grand multiparous laboring mother but when compare risk of uterine rupture, operative delivery and meconium stained amniotic fluid aren’t any difference (Table 4).

Variables Grandmultiparous=119
N (%)
Low parity n=238
N (%)
p COR(95% CI) p* AOR(95%,CI)
Duration of labor(mean) 12.4±6.2 13.0±5.7 0.37 0.68(-1.9-0.7)    
Labor abnormality 64(56.6) 65(29.4) <0.001 3.1(2.0-5.0) 0.81 1.0(0.4-1.9)
MSAF 37(40.2) 42(25.2) 0.02 1.9(1.1-3.3) 0.73 1.1(0.6-2.1)
NRFHRP (25)26.9 32(14.5) 0.01 2.2(1.2-4) 0.01 3.2(1.3-8.0)**
Uterine rupture 17(14.3) 5(2.1) <0.001 7.8(2.8-21.6) 0.99 1.1(0.2-4.7)
Vaginal delivery 45(37.8) 125(52.5) <0.001 0.5(0.3-0.7) 0.76 1.0(0.4-1.9)
Major operative delivery 74(62.2) 113(47.5) <0.001 2.1(1.3-2.30 0.84 1.0(0.4-2.2)
At least one intrapartumcomplications 100(84) 132(55.5) <0.001 4.2(2.4-7.3) 0.002 2.7(1.4-5.3)***
* -after adjusting for socio-demographic factors, ANC profile, preexisting problems identified and major specific antepartum complications.
** Statistically significant at p-value<0.05 after adjusting for socio-demographic factors, ANC profile, preexisting problems identified, labor abnormality, MSAF,gestational age using chi square and multivariable logistic regression.
*** Statistically significant at p-value<0.05 after adjusting for socio-demographic factors, ANC profile, preexisting problems identified using chi square and multivariable logistic regression.

Table 4: Association of parity with Intrapartum complications at JUSTH, south west Ethiopia from May 2015 to September 2015.

Postpartum complications: PPH was diagnosed in 26 (21.8%) of grandmultiparous and in 27 (11.3%) of low parity groups. Puerperal sepsis was seen in 28 (23.5%) of grandmultiparous and 20 (8.4%) of low parity groups. Blood was transfused for 19 (16%) and 11(4.6%) of grandmultiparous and control groups respectively. The mean duration of hospital stay for grand multiparous was 4.5 days whereas 2.9 days for low parity groups. Genital tract injury was encountered in 52 (21.8%) of low parity groups while 13(10.9%) of grandmultiparous. Having at least one postpartum complication observed in 80 (67.2%) and 87 (36.6%) of grandmultiparous and other multiparas controls respectively.

Grand multiparous women 60% less likely faced genital injuries compare to low parity women whereas grandmuliparous three times (CI, 1.5-6.3) more likely develop postpartum complications. In this paper the postpartum hemorrhage, puerperal sepsis and hospital stay are not associated with poor outcomes grandmultiparity (Table 5).

Variables Grandmultiparous n=119
N (%)
Low parity n=238
N (%)
p COR(95% CI) p* AOR(95%CI)
Postpartum hemorrhage 26(21.8) 27(11.3) 0.01 2.2(1.2-3.9) 0.84 1.0(0.2-3.3)
Puerperal sepsis 28(23.5) 20(8.4) <0.001 3.4(1.8-6.3) 0.8 1.1(0.3-4.0)
Genital tract injury 13(10.9) 52(21.8) 0.01 0.4(0.2-0.8) 0.046 0.4(0.2-0.9)**
Need for transfusion 19(16) 11(4.6) <0.001 3.9(1.8-8.5) 0.1 3.6(0.6-20.3)
hospital stay(mean) 4.5±3.3 2.9±3.1 <0.001 1.6(0.9-2.3)    
At least one postpartum complication 80(67.2) 87(36.6) <0.001 3.6(2.2-5.7) 0.001 3.1(1.5-6.3)***
*-adjusting for socio-demographic factors, ANC profile, preexisting problems, antenatal and intrapartal complications.
** Statistically significant at p-value<0.05 after adjusting for socio-demographic factors, ANC profile, labor abnormality, instrumental delivery using chi square and multiple logistic regression.
*** Statistically significant at p-value<0.05 after adjusting for socio-demographic factors, ANC profile, preexisting problems, using chi square and multiple logistic regression.

Table 5: Association of parity with postpartum maternal complications at JUSTH, south west Ethiopia from May 2015 to September 2015.

Neonatal complications: Regarding the neonatal outcome, low 5th minutes Apgar score recorded in 23 (24.7%) and 15 (6.8%) of grandmultiparous and low parity groups respectively. Perinatal mortality was 34 (28.6%) among grand multiparous while 22 (9.2%) in low parity mothers. Low birth weight measured in 14 (11.8%) newborns of grand multiparous and 12 (5%) of low parity babies. Macrosomic baby was 21 (17.6%) among grand multiparous and 16 (6.7%) among low parity groups. Preterm delivery has complicated 19 (19%) and 14 (6.1%) of grandmultiparous and low parity deliveries respectively. NICU admission was observed in 27 (29%) for grandmultiparous women babies and 25 (11.4%) for low parity new born. Macrosomia is three times common in grand multiparous than in low parity whereas 5th minute APGAR score, perinatal mortality (PMR), morbidity and low birth weight are the same outcomes. Perinatal outcomes in between the two parity groups are demonstrated in (Table 6) below and perinatal mortality, low 5th minutes APGAR, low birth weight, NICU admissions and preterm newborns are higher among grand multiparous compare to low parity, however, which are not significantly associated. Macrosomic babies three times more likely to be delivered from grand multiparous ladies compare to low parity groups which is significant (p=0.03, OR- 2.9) (95% CI 1.1-7.8).

Variables Grandmultiparous
n=119
N (%)
Low parity
n=238
N (%)
p COR(95% CI) p* AOR(95%CI)
Low 5th minutes APGAR score 23(24.7) 15(6.8) <0.001 4.5(2.2-9.1) 0.5 1.4(0.5-4)
Perinatal mortality 34(28.6) 22(9.2) <0.001 3.9(2.1-7.1) 0.56 1.4(0.5-4.2)
Low birth weight 14(11.8) 12(5) 0.03 2.5(1.1-5.6) 0.7 1.6(0.9-27.9)
Macrosomia 21(17.6) 16(6.7) <0.001 3.0(1.5-6.0) 0.03 2.9(1.1-7.8)**
Preterm 19(19) 14(6.1) <0.001 3.6(1.7-7.5) 0.96 1.0(0.2-3.2)
NICU
PMR
27(29)
34(28.6)
25(11.4)
22(9.2)
<0.001
<0.001
3.2(1.7-5.9)
7(1.6-11.2)
0.32
0.02
1.5(0.7-3.3)
5(1.7-7.3)

Table 6: association of perinatal outcomes between grandmultiy parity and low parity at JUSTH, south west Ethiopia from May 2015 to September 2015.

Perinatal outcomes in between the two parity groups are demonstrated in Table 5 below and perinatal mortality, low 5th minutes APGAR, low birth weight, NICU admissions and preterm newborns are higher among grandmultiparous compare to low parity, however, which are not significantly associated. Macrosomic babies three times more likely to be delivered from grandmultiparous ladies compare to low parity groups which is significant (p=0.03, OR-2.9) (95%CI 1.1- 7.8).

Discussion

The prevalence of grandmultiparity in our study population was 8%, which is lower compare to other similar hospital based study done in Ethiopia twenty-two years back in this hospital (16%) as well in Nigeria (18.5%) however, it is still higher than from South Africa retrospective case control hospital based study finding (5%). In most developed countries like USA (2-4% of all pregnancies) [16-26]. This decrement in the prevalence of grand multiparous from developed countries is due to the advancement of family planning. In our studies also we found lower contraceptive use before the index pregnancy among grandmultiparous compare to the control multiparous [27,28].

Regarding antepartum complication in grand multiparous women, anemia during pregnancy was three to four times more common in grand multiparous women than in low parity. This fact also supported by number of other studies [29-35]. On the contrary, there are finding that showed no difference between the two groups [2,9]. The finding that more grandmultiparous women had low hematocrit (<33%) antenatal in comparison with multiparous women might be because women having repeated pregnancies do not have time to replenish their iron stores before their next pregnancy [36-40].

Even if some study support increase antepartum complications like antepartum hemorrhage, hypertensive disorder of pregnancy, malprsention, premature rupture of membrane and antepartum fetal death, there was no significant difference in in these complication in grand multiparous and low parity.

In this study there was no significant maternal intrapartum complication unlike other study done in Sweden and Israel obstructed labor was significant. The logic behind is true even this paper, because of number of residence in involved in labor management that might not be progressed in to complication. But there was three times significant fetal intrapartum fetal heart beat abnormality compared to low parity group. This is explained by most grand multiparous women had anemia and this may contribute to fetal heart beat abnormally. There was no significant difference interms of labor abnormality, intrapartum infection, meconium stained liquors and mode of deliveries like other study done Saudi Arabia, Lebanese [41-43].

As to the mode of delivery there was no significant association between the two groups in our study, and this finding similar to studies conducted in Tanzania and India [1,2]. There was no in rate of operative delivery, and indication difference in our study unlike study done Saudi Arabia, Australia [10,13]. In the above cited studies majority of grandmulitiparous had previous scar.

Such fact also supported by our finding indirectly as the genital tract injury in grandmultiparas was significantly fewer compared to low parity groups which in consistent with other studies.

Risk of uterine rupture is higher among grandmultiparous but it is not statistical significant while it is found to be significant in other studies. This might be explained by the presence of good intrapartum monitoring in the study hospital.

Even though postpartum hemorrhage is found to be increased among grand multiparous in number of studies conducted in Asia, Africa and Ethiopia but in this study showed that there was no difference in immediate postpartum hemorrige which similar finding study done in Jordan by Abu-Heija et al. The reason might be the study area teaching Hospital with number of obstetric residence, medical intern and midwifery student who actively managed active third stage of labor and reduce postpartum hemorrh age caused by uterine atony. Being multiparous reduces genital laceration which is similar finding to other studies [6,8].

In this study there were two maternal deaths from all study population who full fill the inclusion criteria’s and both occurred among grand multiparous group. In other number of study as parity increased maternal mortality also increased which is supported by study in Nigeria, Ethiopia [6,9]. This mainly because of grand multiparous had old age, low educational status and poor antenatal care follow up and late arrival to labor and delivery unit so that those complication would occur and contribute for maternal mortality.

Even though , there were number of study concluded that grand multiparty was risk factor for low birth weight and the other hand number of studies including this paper and meta-analysis showed that grand multiparty was not risk factor for low birth weight if other antepartum maternal complication controlled. The other significant finding in this study was macrosomia three times more in grand multiparous than low parity which is similar to other study in developed countries in Israel, Belgium and USA.

Low 5th minutes APGAR score was comparable in both groups which goes to the finding by Nassar AH et al. Lebanon where as other studies found that neonates delivered from grand multiparas were more closely associated with a low Apgar score compared with lower-parity women [1,3]. Similarly NICU admission found to be high among grand multiparous; however, it was not statistical significant unlike other studies where they observed to be higher among grandmultiparous group compare to low parity mothers.

The finding in this paper regarding perinatal mortality showed that five-fold increased perinatal mortality in grand multiparas compare to the low parity, it was the same other study finding in Tanzania, Scandinavians, Belgium hospital based studies. This high number of mortality due to associated intrapartum fetal heart beat abnormality, macrosomia and other high number of neonate with low APGAR score and neonatal intensive care admission.

The limitation of this study is doesn’t control antepartum factors like nutrition and other postpartum maternal and new born condition after 7th day of delivery.

In conclusion, the incidence of grandmultiparity still common and grand multiparty increases both maternal and neonatal complications. Grand multiparty is associated with increased with anemia in antepartum, fetal heart abnormality and genital injury in postpartum. The perinatal mortality was very high as compared to low parity. Increasing awareness in community as well as in healthy institution about family planning and provision and quality of intrapartum and postpartum care might improve both maternal and new born outcome.

References

  1. Mgaya AH, Massawe SN, Kidanto HL, Mgaya HN (2013) Grand multiparity: is it still a risk in pregnancy? BMC Pregnancy Childbirth 13:241.
  2. Monjurul H, Ehsanul H, Suriya B Kader (2008) Pregnancy complications of grandmultiparity at a rural setting of South Africa. Iranian J of Reprod Med 6: 25-31.
  3. Munim S,Rahbar MH, Rizvi RM,Mushtaq N (2000) The Effect of Grandmultiparity on Pregnancy related complications: The Aga Khan University Experience. JPMA50:54-58.
  4. Roman H, RobillardPY, Verspyck E, Hulsey TC, Marpeau L, Barau G (2004) Obstetric and neonatal outcomes in grand multiparity. ObstetGynecol103:1294-1299 .
  5. A Performance, monitoring & accountability 2020 (PMA)ETHIOPIA :Addis Ababa University’school of Public Health at the College of Health Sciences (AAU/SPH/CHS), 2014.
  6. Ujah IAO, Aisien OA, Mutihir JT, Vanderjagt DJ, Glew RH, et al. (2005) Factors Contributing to Maternal Mortality in North-Central Nigeria: A Seventeen-year Review. Afr J Reprod Health9:27-40.
  7. Samueloff A, Mor-YosefS, Seidman DS, Rabinowitz R, Simon A, et al. (1989) Grand multiparity--a nationwide survey. Isr J Med Sci25:625.
  8. Chan BC, Lao TT (2008) Effect of parity and advanced maternal age on obstetric outcome. Int J GynaecolObstet102:237.
  9. Agrawal S, Agarwal A, Das V (2011) Impact of grandmultiparity on obstetric outcome in low resource setting. J ObstetGynaecol Res 37:1015.
  10. Geidam AD, Audu BM, Oummate Z (2011) Pregnancy outcome among grand multiparous women at the University of Maiduguri Teaching Hospital: a case control study. J ObstetGynaecol 31:404.
  11. Shahida SM, Islam MA, Begum S, Hossain MA, Azam MS (2011) Maternal outcome of grand multipara. Mymensingh Med J 20:381.
  12. Jacquemyn Y, Senten L, Vellinga S, Vermeulen K, and Martens G (2006) Does practice make perfect? An age-matched study on grand multiparity in Flanders Belgium. J Perinat Med 34:28.
  13. Bobrowski RA, Bottoms SF (1995) Underappreciated risks of the elderly multipara. Am J ObstetGynecol172:1764-1770.
  14. Ethiopia mini demographic and health survey(EMDHS): conducted under the aegis ofthe Ministry of Health and implemented by the Central Statistical Agency (CSA) (2014).
  15. Nassar AH, Fayyumy R, Saab W, Mehio G, Usta IMSO (2006) Grandmultiparas in modern obstetrics. Am J Perinatol23:345-350.
  16. Aliyu MH, Jolly PE, Ehiri JE, Salihu HM (2005) High parity and fetal morbidity outcomes. Birth 105:1045-1051.
  17. Aliyu MH, Jolly PE, Ehiri JE, SalihuHM (2005) High parity and adverse birth outcomes: exploring the maze. Birth 32:45-59.
  18. Simonsen SM, Lyon JL, Alder SC, Varner MW (2005) Effect of grand multiparity on intrapartum and newborn complications in young women. ObstetGynecol106:454-460.
  19. Yifru B and Asres B (2014) A Meta-Analysis of Selected Maternal and Fetal Factors for Perinatal Mortality. Ethiop J Health Sci 24: 55-68
  20. Fayed HM, Abid B. Stevens SF (1993) Risk factors in extreme grand multiparity. Elsevier Inc41: 17-22.
  21. DerejeNegussie, NebiyuMesfin (2006) review of maternal death in Jimma Universityspecialized hospital.
  22. Abu-Heija AT, Chalabi HE (1998) Great grand multiparity: is it a risk? J ObstetGynaecol 18:136-138.
  23. Martin JA, Hamilton BE, Ventura SJ, Osterman MJ, Mathews TJ (2013) Births: final data for 2011. Natl Vital Stat Rep 62:1-69.
  24. Tanbo TG, Bungum L (1987) The grand multipara- maternal and neonatal complications. ActaObstetGynecolScand66:53-56.
  25. Bugg GJ, Atwal GS, Maresh M (2002)Grandmultiparae in a modern setting. BJOG109:249-253.
  26. Toohey JS, Keegan KA Jr, Morgan MA, Francis J, Task S, et al. (1995) The "dangerous multipara": fact or fiction? Am J ObstetGynecol 172:683-686.
  27. Brunner J, Melander E, Krook-Brandt M, Thomassen PA (1992) Grand multiparity as an obstetric risk factor; a prospective case-control study. Eur J ObstetGynecolReprodBiol47:201-205.
  28. Solomon Mehari (1999) Grandmultiparity in Jimma hospital, from June 1992 to March 1993. Ethiop J HlthSci 9: 41-46.
  29. ZaheeraSaadia (2014) Grand-multiparity in Saudi Arabia- examining the obs tetric risk.Journal of Gynecology and Obstetrics 2: 16-19.
  30. Babinszki A, Kerenyi T, Torok O, Grazi V, Lapinski RH, et al. (1999) Perinatal outcome in grand and great-grand multiparity: effects of parity on obstetric risk factors. Am J ObstetGynecol181:669-674.
  31. Bai J, Wong FW, Bauman A, Mohsin M (2002) Parity and pregnancy outcomes. Am J ObstetGynecol186:274-278.
  32. Samson Gebremedhin (2014) Trend and socio-demographic differentials of Caesarean section rate in Addis Ababa, Ethiopia: analysis based on Ethiopia demographic and health surveys data. Gebremedhin Rep. Health, 11:14.
  33. Lyrenäs S (2002) Labor in the grand multipara. GynecolObstet Invest53:6-12.
  34. Humphrey MD (2003) Is grand multiparity an independent predictor of pregnancy risk? A retrospective observational study. Med J Aust 2003; 179:294-296.
  35. Seidman DS, Armon Y, Roll D, Stevenson DK, Gale R (1988) Grand multiparity: an obstetric or neonatal risk factor? Am J ObstetGynecol158:1034-1039.
  36. Fuchs K, Peretz BA, Marcovici R, Paldi E, Timor-Tritsh I (1985) The "grand multipara"--is it a problem? Int J GynaecolObstet 23:321-326.
  37. Al JF (2012) Grandmultiparity: a potential risk factor for adverse pregnancy outcomes. J Reprod Med 57:53-57.
  38. Shechter Y, Levy A, Wiznitzer A, Zlotnik A, Sheiner E (2010) Obstetric complications in grand and great grand multiparous women. J Maternal Fetal Neonatal Med 23:1211-1217.
  39. Shah PS (2010) Parity and low birth weight and preterm birth: a systematic review and meta-analyses. ActaObstetGynecolScand 89:862-875.
  40. Hilder L, Sairam S, Thilaganathan B (2007) Influence of parity on fetal mortality in prolonged pregnancy. Eur J ObstetGynecolReprodBiol132:167-170.
  41. Dyack C, Hughes PF, Simbakalia JB (1997) Vaginal delivery in the grand multipara following previous lower segment cesarian section. J ObstetGynaecolRes 23:219-222.
  42. Araneta MR, Barrett-Connor E (2010) Grand multiparity is associated with type 2 diabetes in Filipino American women, independent of visceral fat and adiponectin. Diabetes Care33:385-389.
  43. Ezechi O, Kalejaiye O (2000) Management of Anaemia in Pregnancy Clinical Sciences Division, Nigerian Institute of Medical Research, Yaba Lagos Nigeria.
Citation: Aragaw FA, Mahtemsilllasie M, Jarso H (2017) Grand Multiparity and Pregnancy Related Complications among Women Who Gave Birth at Jimma University Specialized Hospital, Jimma, Southwest Ethiopia. Gynecol Obstet (Sunnyvale) 7:438.

Copyright: © 2017 Aragaw FA, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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