Abstract
Bad obstetric history (BOH) is reported worldwide and is associated with social and psychological impacts. Cytomegalovirus and herpes simplex virus play an important role in the induction of adverse outcomes of pregnancy. Highest CMV IgG prevalence rate was reported for India (91.05%), while the lowest rate was reported for Iran (14.28%). Unfortunately, six studies in Iraq reported a high prevalence of CMV IgM in non-married, pregnant and women with BOH. The range of recent CMV infection in pregnant women with BOH was from 1.4% in Jordan to 60.2% in Iraq. In women with BOH, the highest HSV 2 prevalence (16.8%) was noted in India, while the lowest rate (1.69%) was reported in India also. In Arab countries, among women with BOH, HSV 2 IgG and IgM seroprevalence higher rates were reported for Iraq. This literature review highlights the high bacterial and viral maternal infection rate in the developing world. Urgent, concerted action is required to reduce the burden of these infections. In addition to raising awareness about the severity of the problem of maternal infections in the developing world, data from this review will be beneficial in guiding public health policy, research interests and donor funding towards achieving improvement in health care delivery.
Key words: TORCH; Toxoplasma; Rubella; CMV; Cytomegalovirus; HSV
Cytomegalovirus:
Primary Cytomegalovirus (CMV) infection during pregnancy is a frequent and serious threat to the fetuses of pregnant women [222]. The rate of susceptibility to CMV during pregnancy is also well established in many global countries [223,224]. Eight European countries (France, Belgium, Spain, Italy, Germany, Austria, Portugal, and the Netherlands) routinely screen the majority of pregnant women serologically for CMV [225,226]. This routine serologic screening occurs without the recommendations or guidelines of any governmental agency, authority, or a professional medical society. In Iraq, such screening program is not followed routinely and pregnant women screening order depends on personal interest of the clinicians. Routine serologic screening for CMV of pregnant women in Europe has yielded very important advances in our understanding of CMV infections among pregnant women [227-230]. The major risk factor for maternal acquisition of CMV during pregnancy is frequent and prolonged contact with a child less than three years of age [231-235]. This occurs among women with a child in the home or among women employed in child care centers or schools [236-241]. Another group of high-risk women are those who are seronegative, young, and poor. Even for this group, contact with a young child is an independent predictor of delivering a CMV congenitally infected infant, as is a history of frequent sexual activity [235]. A recent study suggested that C MV is likely transmitted not only via the oral mucosal route, but also via the vaginal mucosal route [231].
Characteristics and results of studies reporting prevalence of maternal
CMV infection
Forty studies [1,3,36,86,89-93,95,96,167,170,171,182,204, 208,210,242-263] on maternal cytomegalovirus infection prevalence were identified (Tabl. V). The median prevalence of maternal IgG to CMV (calculated from 28 studies that reported this) was 92%, indicating a high proportion of mothers with previous exposure to CMV. Two hospital-based study in India (29.5%) [36] and Iran (28.58%) [262] identified a statistically significant higher prevalence of CMV IgM (indicating active or recent infection) in mothers with Bad Obstetric History (BOH), highlighting a role for maternal CMV infection in adverse pregnancy outcome in this setting. The highest prevalence of IgG in pregnant women was in Turkey [95] (98.9%, 1103 childbearing age women), while the lowest prevalence reported for Ireland [253] (30.4%, 1047 pregnant women). However, in women with BOH, the highest IgG prevalence rate was reported for India [3] (91.05%, 380 BOH), while the lowest rate was reported for Iran [262] (14.28%, 42 Aborted women). Active or recent infection high prevalence rate in pregnant women was reported for Poland [252] (13%, 1332 Pregnant women), while the lowest rate was reported for Turkey [204] (0%, 249 Pregnant women). In women with BOH the highest prevalence rate of IgM was reported for India [36] and the lowest one was reported for India [91]. In Arab countries, twenty- two studies [35,99-101,108,117- 119,129-131,139,147,216,221,264-269] on maternal CMV infection prevalence were identified (Tabl. VI). The median prevalence of maternal IgG to CMV was 77.8% indicating lower proportion of mothers with previous exposure to CMV as compared to global studies. Unfortunately, six studies in Iraq [100,101,117,129,264,266] reported a high prevalence of CMV IgM in non-married, pregnant and women with BOH. The range of active or recent CMV infection in pregnant women was from 2.3% in Jordan [269] to 57.2% in Iraq [129], while the range in women with BOH was from 1.4% in Jordan [269] to 60.2% in Iraq [100]. In pregnant women, maternal IgG to CMV prevalence higher rate was reported in Jordan [269] (88%, 260 pregnant women), while the lowest one was reported for Iraq [129] (77.8%, 180 pregnant women). In addition, in women with BOH, maternal IgG to CMV prevalence higher rate was reported for Jordan [269] (95%, 898 Aborted women), and the lowest one was reported in Iraq [99] (4.8%, 119 Aborted women).
Article |
Location, setting of study |
Type, duration of study |
Population |
Results |
Tabatabaee et al, [242] |
Iran, hospital |
Cross-sectional, 7 months |
1472 pregnant women |
97.68% seropositive,
prevalence of active
infection 4.35%. |
Das et al, 2007 [170] |
India, hospital |
Cross sectional study |
1115 BOH |
11% prevalence in BOH,
4% prevalence in normal
pregnant women |
Ocak et al, [171] |
Turkey, hospital |
Retrospective observational study,
2 years |
1652 pregnant women |
94.9%seropositivity for
anti-CMV IgG, 0.4%positive
for anti-CMV IgM |
Picone et al, [243] |
France, Hospital |
Cross sectional study prospective,
2 years |
4287 pregnant women |
46.8% IgG |
Tamer et al, [167] |
Turkey, antenatal Clinics |
Cross sectional study, |
1972 Pregnant women |
97.1% IgG, 2.6% IgM |
Surpam et al [86] |
India, Antenatal clinic |
Case control, |
150 BOH |
5.33% IgM |
Uyar Y et al [182] |
Turkey, Hospital |
Case control, 1 year |
600 Pregnant women |
97.3% IgG, 1% IgM |
Karabulut A et al [89] |
Turkey, Antenatal clinic |
Case control, 1 year |
1000 Pregnant women |
98.7% IgG, 1.2% IgM |
Kumari N et al [1] |
Nepal, Hospital |
Case control, 4 months |
12 BOH |
8.3% seropositive |
Nabi SN et al [90] |
Bangladesh, Hospital |
Case control, 10 months |
111 Pregnant women |
95.49% IgG, 0.9% IgM |
Baschale MD [244] |
Italy, Hospital |
Cross sectional, 2 years |
2385 Pregnant women |
92% IgG, 0.4% IgM |
Sadik MS et al [91] |
India, Hospital |
Case control, 2 years |
86 BOH |
23.25% IgG, 0% IgM |
Chopra S et al [36] |
India, Antenatal clinic |
Case control, 1 year |
200 BOH |
29.5% IgM |
Koksaldi-Motor et al [95] |
Turkey, Hospital |
Cross sectional, 1 year |
1103 women childbearing
age |
98.9% IgG |
Ozdemir M et al [204] |
Turkey, Hospital |
Cross sectional, 6 months |
249 Pregnant women |
98.7% IgG, 0% IgM |
Frischknecht F et al [92] |
Switzerland, Hospital |
Cross sectional, 1 yr |
723 Pregnant women in labor |
4.7% seropositive |
Vilibik-Cavlek T, et al
[96] |
Croatia, Hospital |
Cross sectional, 5 years |
Pregnant & non pregnant
women |
75.3% IgG, 0.09% IgM |
Sarawathy TS, et al [245] |
Malaysia, Antenatal clinic |
Cross sectional, 2 years |
125 Pregnant women |
84% IgG, 7.2% IgM |
Akinbami AA, et al [246] |
Nigeria, Hospital |
Cross sectional, 2 months |
179 Pregnant women |
97.2% IgG, |
Bagheri L, et al [247] |
Iran, Hospital |
Cross sectional, 3 months |
240 Pregnant women |
69.6% IgG, 2.5% IgM |
Arabpour M, et al [248] |
Iran, Hospital |
Cross sectional, 5 years |
844 childbearing age women |
93% IgG, 5.4% IgM |
Canon MJ, et al [249]
|
Global, Review
|
Review
|
|
45 – 100% seroprevalence
|
Ahmad RM, et al [250]
|
Nigeria, Hospital
|
Cross sectional,
|
90 Pregnant women
|
97.8% IgG
|
Seo S, et al [251]
|
Korea, Hospital
|
Cross sectional, 2 months
|
744 Pregnant women
|
98.1% IgG, 1.7% IgM
|
Gaj Z, et al , [252]
|
Poland, Hospital
|
Cross sectional, 11 years
|
1332 Pregnant women
|
76.7% IgG, 13% IgM
|
Knowles SJ, et al [253]
|
Ireland, Hospital
|
Cross sectional, 1 year
|
1047 Pregnant women
|
IgG 30.4% in Irish & 89.7%
in non- Irish women [Africa, Asia,
E. Europe]
|
Yamamoto AY, et al [254]
|
Brazil, Hospital
|
Cross sectional
|
985 Pregnant women
|
97% seroprevalence
|
Odland JO, et al [208]
|
Russia, Hospital
|
Case control, 4 months
|
182 Pregnant & 127 Aborted
women
|
78% versus 81.1%
seroprevalence
|
Chen MH, et al [255]
|
Taiwan, Hospital
|
Cross sectional, 10 months
|
483 Pregnant mother
|
91.1% IgG, 3.5% IgM
|
Gumber S et al [256]
|
India, Hospital
|
Cross sectional, 17 months
|
150 BOH
|
4.67% IgM
|
Dollard SC, et al [257]
|
USA, Hospital
|
Cross sectional,
|
6067 Women 12-49 yrs
|
58% IgG, 3% IgM
|
Enders G, et al [258]
|
Germany, Hospital
|
Retrospective, 15 years
|
40 324 Pregnant women
|
42.3% IgG
|
Correa CB, et al [259]
|
Cuba, Hospital
|
Cross sectional, 1 year
|
1131 Pregnant women
|
92.6% seropositive, 2.4%
active infection
|
Rajaii & Pourhasan [260]
|
Azerbaijan, University
Lab.
|
Cross sectional, 4 years
|
2049 Women 20-35 yrs [of
them 75 Pregnant]
|
88.53% IgG, 8.29% IgM, In
Pregnant 66.7%seropositive
|
Turbadkar D, et al [3]
|
India, Antenatal clinic
|
Case control, 1 year
|
380 BOH
|
91.05% IgG, 8.42% IgM
|
Ashrafunnessa et al [261]
|
Bangladesh, Hospital
|
Case control, 11 months
|
420 Pregnant women
|
68.6% IgG, 5% IgM
|
Inagaki ADM, et al [93]
|
Brazil, Antenatal clinic
|
Cross sectional, 1 year
|
9559 Pregnant women
|
76.6% IgG, 0.2% IgM
|
Falahi S, et al [262]
|
Iran, Hospital
|
Case control
|
42 BOH
|
14.28% IgG, 28.58% IgM
|
Ebadi p, et al [210]
|
Iran, Hospital
|
Case control, 3 years
|
120 BOH
|
78.33% seropositive
|
Oruc AS, et al [263]
|
Turkey, Hospital
|
Cross sectional,5 years
|
11 360 Pregnant women
|
98.5% IgG, 0.3% IgM
|
Table V. Characteristics and results of studies reporting prevalence of maternal CMV infection.
Article
|
Location, setting of study
|
Type, duration of study
|
Population
|
Results
|
Hammouda et al [108]
|
Egypt, Hospital
|
Case control
|
100 BOH
|
51% Seroprevalence
|
Abdulmohaymen N [99]
|
Iraq, Baghdad, Hospital
|
Case control, 9 months
|
119 Aborted women
|
17.7% IgM recurrent
spontaneous abortion
14.7% IgM non recurrent
spontaneous abortion.
4.8% IgG recurrent
spontaneous abortion
0% IgG non recurrent
spontaneous abortion
|
Jasim et al [100]
|
Iraq, Waset, Hospital
|
Case control, 1 year
|
162 Aborted women
|
55.5% IgG, 60.2% IgM
|
Al- Taie et al [101]
|
Iraq, Mosul, Private
laboratory
|
Case control, 1 year
|
100 BOH
|
24% IgM
|
Almishhadani & Aljanabi [119]
|
Iraq, Al- Anbar, Medical
Laboratory
|
Case control study, 3 years
|
230 Aborted women
|
90.4% IgG, 6.1% IgM
|
Majeed AK [117]
|
Iraq, Baghdad,
|
Case control, 3 years
|
135 Aborted women
|
20.7% IgG45.9% IgM
|
Alsaeed et al [118]
|
Iraq, Al-Hila, Hospital
|
Case control, 6 months
|
120 Aborted women
|
79.5% IgG, 18.8% IgM
|
Hadi NJ [130]
|
Iraq, Thi Qar, Hospital
|
Case control
|
190 Aborted women
|
16.84% IgG, 9.47% IgM
|
Salman YG [131]
|
Iraq, Kirkuk, Hospital
|
Case control, 11 months
|
84 BOH
|
8.02% Seropositive, 7.89%
IgM
|
Al- Azzawi RHM, [264]
|
Iraq, Baghdad, Hospital
|
Cross sectional, 8 months
|
161 Non married women
15-35 yrs
|
67.1% IgG, 41% IgM
|
Khalf MS, et al [265]
|
Iraq, Baghdad, Hospital
|
Case control, 17 months
|
108 BOH
|
15.7% IgM
|
Hannachi N, et al [221]
|
Tunisia, Hospital
|
Cross sectional,
|
404 Pregnant women
|
96.3% seroprevalence
|
Al- Hindi A, et al [139]
|
Palestine, IVF centre
|
Retrospective, 6 years
|
1954 Women with infertility
or abortion
|
6% IgM
|
Al- Shimmery MN [266]
|
Iraq, Diwanya, Hospital
|
Case control, 5 months
|
125 Aborted women
|
49.6% IgG, 22.4% IgM
|
Al-Khafaji & Al-Zabaidi [38]
|
Iraq, Thi Qar, Hospital
|
Case control, 10 months
|
60 aborted women
|
85% IgG, 65% IgM
|
Kafi SK, et al [267]
|
Sudan, Hospital
|
Cross sectional, 2 months
|
100 Pregnant women
|
95% IgG
|
Hamdan HZ, et al [216]
|
Sudan, Hospital
|
Cross sectional, 2 months
|
231 Pregnant women
|
72.2% IgG, 2.5% IgM
|
Ghazi HO, et al [147]
|
Saudi Arabia, Hospital
|
Cross sectional
|
926 Pregnant women
|
92.1% IgG
|
Al-Marzoqi AHM, et al [129]
|
Iraq, Babylon, Hospital
|
Cross sectional, 6 months
|
180 Pregnant women
|
77.8% IgG, 57.2% IgM
|
Abu- Madi MA, et al [35]
|
Qatar, Hospital
|
Cross sectional, 3 years
|
847 Women > 20 yr age
|
96.8% IgG, 2.7% IgM
|
Barah F [268]
|
Syria, University Laboratory
|
Cross sectional, 15 months
|
316 Female university
students
|
74.5% seropositive
|
Daboui & Al-Zaben [269]
|
Jordan, Medical centre
|
Case control, 2 months
|
260 Pregnant, 100 Unmarried
women, 898 Aborted women
|
IgM- 2.3% pregnant, 1%
unmarried, 1.4% Abortion.
IgG- 88% pregnant, 79%
unmarried, 95% abortion
|
Table VI. Characteristics and results of studies in Arab countries reporting prevalence of maternal CMV infection.
Herpes simplex virus
Herpes simplex virus (HSV) is an ubiquitous, enveloped, and double stranded DNA virus, belonging to the family of Herpesviridae transmitted across mucosal membranes and non-intact skin, that migrate to nerve tissues, where they persist in a latent state [270]. HSV-1 predominates in oro-facial lesions, and it is typically found in the trigeminal ganglia, whereas HSV- 2 is most commonly found in the lumbo-sacral ganglia [271]. Nevertheless these viruses can infect both oro-facial areas and the genital tract. In some developed countries type 1 has recently emerged as the prominent causative agent in genital lesions [272]. Changes in sexual behaviours of young adults may partly explain its higher incidence [273,274]. Herpes simplex virus (HSV) infections are caused by two strains, HSV-1 and HSV-2. Oro-labial infection is mainly caused by HSV-1, however, this strain is responsible for up to 53% of primary genital herpetic infection [270]. HSV-2 genital infection is much more likely to recur than genital HSV-1 infection, thus the presence of antibody to HSV-2 and a compatible clinical history would be strong presumptive evidence that the disease is recurrent genital herpes [275-277]. In addition to agent factor, genetic may play a role in susceptibility to HSV infection [278]. Primary genital HSV-1 or HSV-2 infection in pregnant women can result in abortion, premature labor and congenital and neonatal herpes [279-281]. HSV-2 infections in the newborn are particularly severe and frequently involve the CNS [282]. Recent changes in HSV-1 and HSV-2 infection epidemiology have been reported, with type incidence changes and sequential genital infections with HSV-1 and HSV-2 [272,283]. Little is known about the risk factors associated with HSV seropositivity in pregnant Iraqi women. Identification of the risk factors may help to improve the control measures of HSV infection. Although there is improve in the diagnosis and treatment of TORCH infections, it still represents a problem in developing countries. Clinical diagnosis of TORCH is difficult, since most of the maternal infections with adverse outcomes are initially asymptomatic. Routine TORCH complex screening during pregnancy is not recommended in Iraq and the extent to which it is performed is unknown. A first primary infection develops when a susceptible person (lacking of preexisting HSV-1 and HSV-2 antibodies) is exposed to HSV. Indeed, a first non-primary episode occurs when a person with preexisting HSV antibodies (against type 1 or 2) experiences a first episode with the opposite HSV type. Recurrent infection occurs in a person with preexisting antibodies against the same HSV type [271]. Infections during pregnancy may be transmitted to newborns: HSV-1 and HSV-2 may cause eye or skin lesions, meningo-encephalitis, disseminated infections, or foetal malformations. In recent years, genital herpes has become an increasing common sexually transmitted infection. From the late 1970s, HSV-2 seroprevalence has increased by 30%, resulting that one out of five adults is infected [284,285]. HSV seroprevalence in patients with STD varies from 17% to 40% (6% in the general population and 14% in pregnant women) [286,287]. Age and sex are important risk factors associated with the acquisition of genital HSV-2 infection. In fact, the prevalence of HSV infection rises with age, reaching the maximum around 40 years [284]. This infection appears related to the number of sexual partners, and regarding sex it is more frequent in women than in men [288,289]. In addition, ethnicity, poverty, cocaine abuse, earlier onset of sexual activity, sexual behavior, and bacterial vaginosis can facilitate a woman’s risk of infection before pregnancy [290,291]. Regarding pregnant population, there is a high prevalence of genital herpes, however, it is varies from country to others, depending on social and sexual behaviors and activity [289,292-294]. The risk of neonatal infection varies from 30% to 50% for HSV infections that onset in late pregnancy (last trimester), whereas early pregnancy infection carries a risk of about 1% [295-297]. Thirty-one studies [1,3,90,91,96,204,256,298-320] outlining the prevalence of maternal Herpes simplex virus 2 (HSV-2) were identified (Tabl. VII). These studies detected the presence of antibodies to HSV as a marker of maternal infection. Median prevalence of IgG HSV-2 was 18.2% which was reported for Belgium [315,357]. In pregnant women, higher seroprevalences were noted in Germany (82%), Turkey (63.1%), Zimbabwe (51.1%), and Iran (43.75%) [298,299,309,313]. However, the lowest seroprevalences were reported in two studies in Turkey [204,314], which reported a rates of 4.4% and 5%. In women with BOH, the highest prevalence (33.58%) was reported in India [3], while the lowest one (18.6%) was reported in India also [91]. Concerning IgM, the highest prevalence in pregnant women was reported in Turkey (13.8%, 130 pregnant women) [298], while the lowest rate was reported in Turkey (0%, 249 pregnant women) also [204]. In women with BOH, the highest prevalence (16.8%, 450 BOH) was noted in India [320], while the lowest rate (1.69%, 86 BOH) was reported in India also [91]. In Arab countries, nine studies [35,99-101,129,147,268,319,320] outlining the prevalence of maternal HSV-2 were identified (Table VIII). The median IgG seroprevalence was 27.1%, which was noted in Saudi Arabia [147]. A higher (27.1%, 926 pregnant women) IgG maternal seroprevalence in pregnant women was reported in Saudi Arabia [147], while the lower rate (6.5%, 459 pregnant women) was noted in Saudi Arabia also [319]. In women with BOH IgG seroprevalence was 60.6%, which was reported in Iraq [100]. Concerning IgM, the highest prevalence’s were reported in Iraq [100,129] for both pregnant women (28.9%, 180 pregnant women) and those with BOH (73.9%, 62 BOH).
Article |
Location, setting of study |
Type, duration of study |
Population |
Results |
Kurewa et al, [299] |
Zimbabwe, peri-urban clinics |
Cross sectional, 19 months |
691 Pregnant women
|
51.10% IgG
|
Yahya-Malima et al, [300] |
Tanzania,antenatal clinics (6) |
Cross sectional, |
1296 Pregnant women
|
20.7% prevalence of genital herpes
|
Chen et al, [301] |
China, antenatal clinic |
Cross sectional, 3 months |
502 pregnant women
|
10.8% seroprevalence
|
Haddow et al, [302] |
Australia, antenatal clinic |
Cross sectional, 2 years |
535 pregnant women
|
30% seroprevalence
|
Joesoef et al, [303] |
Indonesia, prenatal clinic |
Cross sectional, 15 months |
599 pregnant women
|
9.9% seroprevalence
|
Surpam et al [86] |
India, Antenatal clinic |
Case control, |
150 BOH
|
8.66% IgM
|
Kumari N et al [1] |
Nepal, Hospital |
Case control, 4 months |
12 BOH
|
33.3% Seropositive
|
Nabi SN et al [90] |
Bangladesh, Hospital |
Case control, 10 months |
111 Pregnant women
|
9.91% IgG, 1.8% IgM
|
Sadik MS et al [91] |
India, Hospital |
Case control, 2 years |
86 BOH
|
18.6% IgG, 1.69% IgM
|
Ozdemir M et al [204] |
Turkey, Hospital |
Cross sectional, 6 months |
249 Pregnant women
|
4.4% IgG, 0% IgM
|
Xu F et al [304] |
USA, Hospital |
Cross sectional, 4 years |
626 Pregnant women
|
22% seroprevalence
|
Kucera P et al [305] |
Switzerland, Hospital |
Cross sectional, |
1030 Pregnant women
|
21.2% seroprevalence
|
Patrick MD et al [306] |
Canada, antenatal clinic |
Cross sectional, 1 year |
1215 Pregnant women
|
17.3 % seroprevalence
|
Munjoma MW et al [307] |
Zimbabwe, Antenatal clinic |
Cross sectional, 6 months |
354 Pregnant women
|
49.1% seroprevalence
|
Diawara S et al [308] |
Senegal, Antenatal clinic |
Cross sectional, 6 months |
260 Pregnant women
|
22% seropositivity
|
Sauerbri A et al [309] |
Germany, Hospital |
Cross sectional, 8 years |
200 Pregnant women
|
82% IgG
|
Ades AE et al [310] |
UK, Hospital |
Cross sectional, 2 years |
3533 Pregnant women
|
10.4% IgG
|
Rathore S et al [311] |
Kashmir, Antenatal clinic |
Cross sectional, 2 year |
200 Pregnant women
|
7.5% IgG
|
Duran N [298] |
Turkey, Hospital |
Cross sectional, 21 months |
130 Pregnant women
|
63.1 % IgG, 13.8% IgM
|
Biswas D et al [312] |
India, Hospital |
Cross sectional, 2 years |
1640 Pregnant women
|
8.7% HSV-2 IgG
|
Shahraki AD et al [313] |
Iran, Hospital |
Cross sectional, |
96 Pregnant women
|
43.75% HSV-2 IgG
|
Dolar N et al [314] |
Turkey, Hospital |
Cross sectional, |
300 Pregnant women
|
5% HSV-2 IgG
|
Bodeus M, et al [315] |
Belgium, Hospital |
Cross sectional, |
1000 Pregnant women
|
18.2% HSV-2 IgG
|
Chen XS et al [301] |
China, Hospital |
Cross sectional, 3 months |
504 Pregnant women
|
10.8% seroprevalence
|
Sasadeusz JJ et al [316] |
Australia, Antenatal clinic |
Cross sectional, |
1371 Pregnant women
|
13.6% seroprevalence
|
Vilibik-Cavlek T, et al [96] |
Croatia, Hospital |
Cross sectional, 5 years |
Pregnant & non pregnant
women
|
6.8% IgG, 1.2% IgM
|
Straface G et al [317] |
Italy, Review |
Retrospective |
|
7.6 – 8.4% seroprevalence Italy
22% seroprevalence USA
|
Kim D et al [318] |
Korea, Hospital |
Retrospective, 19 months |
500 Pregnant women
|
17% HSV-2 seroprevalence
|
Gumber S et al [256] |
India, Hospital |
Cross sectional, 17 months |
150 BOH
|
3.33% IgM
|
Turbadkar D, et al [3] |
India, Antenatal clinic |
Case control, 1 year |
380 BOH
|
33.58% IgG, 3.6% IgM
|
Li et al [319] |
China, Hospital |
Cross sectional, |
1740 Pregnant women
|
23.56% seroprevalence
|
Haider M, et al [320] |
India, Hospital |
Case control |
450 BOH
|
16.8% IgM
|
Table VII. Characteristics and results of studies reporting prevalence of maternal HSV-2 infection.
Article
|
Location, setting of study
|
Type, duration of study
|
Population
|
Results
|
Abdulmohaymen N [99]
|
Iraq, Baghdad, Hospital
|
Case control, 9 months
|
119 Women with history of
abortion
|
8.1% IgM recurrent
spontaneous abortion
17.4% IgM non recurrent
spontaneous abortion.
|
Jasim et al [100]
|
Iraq, Waset, Hospital
|
Case control, 1 year
|
162 Women with
spontaneous abortion
|
60..6% IgG, 73.9% IgM
|
Al- Taie et al [101]
|
Iraq, Mosul, Private laboratory
|
Case control, 1 year
|
100 BOH
|
11% IgM
|
Alzahrani et al [319]
|
Saudi Arabia, Hospital
|
Cross sectional,
|
459 Pregnant women
|
6.5% IgG, 0.5% IgM
|
Obeid EO [320]
|
Saudi Arabia, Hospital
|
Cross sectional, 2 years
|
459 Pregnant women
|
6.8% IgG
|
Barah F [317]
|
Syria, University Laboratory
|
Cross sectional, 15 months
|
316 Female university
students
|
52% seropositive
|
Ghazi HO, et al [192]
|
Saudi Arabia, Hospital
|
Cross sectional
|
926 Pregnant women
|
27.1% IgG
|
Al-Marzoqi AHM, et al [174]
|
Iraq, Babylon, Hospital
|
Cross sectional, 6 months
|
180 Pregnant women
|
22.2% IgG, 28.9% IgM
|
Abu- Madi MA, et al [87]
|
Qatar, Hospital
|
Cross sectional, 3 years
|
847 Women > 20 yr age
|
26.3% IgG, 7.6% IgM
|
Table VIII. Characteristics and results of studies in Arab countries reporting prevalence of maternal HSV-2 infection
Gaps in existing knowledge
In the process of reviewing the subject, we identified several facility-based retrospective studies reporting causes of maternal mortality. Many of these studies attributed a proportion of deaths to infection or sepsis, but were unable to provide microbiological or serological evidence of the specific underlying mortality causes. Our review confirms the suspected high prevalence of parasitic and viral maternal infections in the developing world, as demonstrated by the median prevalence rates calculated for each pathogen studied. Of particular concern are the aetiology of infection. The literature review highlights a gap in existing knowledge on the epidemiology and impact of maternal infection, especially on the aetiology of infectious agents that lead to puerperal sepsis and subsequent mortality. Increased surveillance and diagnostic capabilities in healthcare facilities and in the community is needed to identify the aetiological agents responsible for puerperal sepsis and maternal mortality. The prevalence of maternal infection reported by the studies identified in this literature review may be an underestimate of actual rates of infection as not all pregnant women in developing countries may have access to or choose to access formalized antenatal care. This could be due to financial constraints, difficulties in accessing these facilities and personal or cultural beliefs. In addition, antenatal care services may not have the capacity to routinely screen for maternal infections, especially those that are asymptomatic and those that require serological tests such as PCR and ELISA to diagnose, due to limited resources or expertise. These infrastructural problems are essential contributors to the persistence of high maternal morbidity and mortality in developing countries and need to be overcome in order to accurately characterize the burden of maternal infections in these countries.
Conclusion
This literature review highlights the high bacterial and viral maternal infection rates in the developing world. Urgent, concerted action is required to reduce the burden of these infections. In addition to raising awareness about the severity of the problem of maternal infections in the developing world, data from this review will be beneficial in guiding public health policy, research interests and donor funding towards achieving improvement in health care delivery.
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