TETANUS IMMUNIZATION AMONG PREGNANT WOMEN: COVERAGE RATE AND RATE OF PROTECTION AT TIME OF DELIVERY
Zamzam Ali Hezam Saleh Aljedry1, Alia A. Shaib2, Hassan A H. Al-Shamahy1, Ahmed Y. Al-Jaufy1
1Medical Microbiology and Clinical Immunology, Faculty of Medicine and Health Sciences, Sana’a University, Republic of Yemen.
2Department of Obstetrics and gynecology, Faculty of Medicine and Health Sciences, Sana’a University, Republic of Yemen.
DOI: https://doi.org/10.22270/ujpr.v4i1.233
Even though attempts have been effectively applied to eradicate the neonatal tetanus through widespread childhood vaccination and improved conditions at delivery, it remains major cause of infant mortality and continues a problem of public health in developing countries including Yemen. The aims of this study were to determine the tetanus immunization status, the association between the risk factors and failure of protection in pregnant women at time of delivery. This cross-sectional study included 476 women seeking care for delivery at Al Thawra Modern General Hospital and Al Sabain Hospital, women age ranged from 16-49 years old. Immunization information and factors affecting it were obtained through a standard questionnaire. Serum samples were collected and level of IgG antibody against Clostridium tetani was measured by ELISA technique. Protected women were defined as those with serum antibody levels >or=0.6 IU/ml. The total vaccine covering rate of tetanus was 87%, and maternal vaccine rate was 33.6%, the protective rate at time of delivery was 68.5%. There were significant association between unvaccinated (OR=18.6), older ages (OR=1.7), rural residency (OR=34) and malaria infection during pregnancy (OR=2.9); with protection failure in pregnant women at time of delivery. It can be concluded that the total vaccine coverage rate and antenatal tetanus vaccine rate were insufficient. In addition, the protective rate at time of delivery was low and large numbers of neonate are susceptible to neonatal tetanus and death. Vaccinating every pregnant woman with at least one dose of TT would be an affordable and effective way to protect against neonatal tetanus, and would be a step toward eliminating the deaths that continue to occur due to this preventable disease in Yemen.
Keywords: Coverage rate, neonatal tetanus, pregnancy, protective rate, Sana'a city-Yemen, tetanus vaccine.
INTRODUCTION
Tetanus is an acute infection, non-communicable disease with a high case fatality rate, caused by Clostridium tetani (C. tetani)1. Tetanus is a disease resulting from a specific toxin produced at site of injury by the anaerobic, spore forming organism C. tetani which is finding in soil and feces. Tetanus has been a major cause of death worldwide, largely due to inadequate vaccination and poor wound prophylaxis2. During sporulation the vegetative form of the organism develops into a spore form, giving a characteristic drumsticks appearance in blood smear. The spores of this organism are very resistant to disinfectants. Also, the spore form can survive for many years in soil3,4. Tetanus can affect all age groups but umbilical card infection during delivery is the most common form affecting newborn babies and mothers, case mortality of tetanus can be 100% if untreated and can range between 10-60% even under hospitalized care. There is no natural immunity against tetanus5. A significant number of women die every year due to maternal tetanus, most of these deaths occur in Africa, East and southern Asia1. The global incidence of tetanus has been estimated at approximately one million cases annually6. The World Health Organization5 reported that globally 49.000 newborns died of this disease in 2013 alone. Tetanus kills one newborn every eleven minute, approximately 134 babies every day1. Eradication of tetanus is difficult due to the abundance of tetanus bacterial spores in the environment; the goal is to work towards elimination of tetanus through vaccination7. Neonatal tetanus is a significant health problem in Yemen. Newborns can be successfully protected against tetanus by vaccinating women with tetanus toxoid, the coverage rate of vaccination with this vaccine proved to be affected by knowledge, attitude and practice of women about antenatal tetanus toxoid vaccine8. The World Health Organization aimed to achieve worldwide neonatal tetanus elimination by 2005, which was defined as the reduction of neonatal tetanus cases to less than 1 case per 1,000 live births in every district of every country9,10. However, high prevalence remained present in 21 countries including Yemen10. There is no recent study in Yemen that determines the vaccine coverage rate and the antibody level of tetanus at time of delivery. So, this study aimed to determine; vaccine coverage rate and the immunological status of tetanus among pregnant women at the time of delivery and factors associated of protection failure against tetanus.
SUBJECTS AND METHODS
This cross-sectional study was carried out during a period of 12 months, starting in August 2017 and ending in August 2018. Included 476 women seeking care for delivery at Al Thawra Modern General Hospital and Al Sabain Hospital, Sana’a city-Yemen. The study included women at time of delivery, and excluded pregnant women before time of delivery and pregnant women who are not sure about history of taking the tetanus vaccine. Serum samples were collected and measured for the level of IgG antibody against Clostridium tetani toxoid by commercially available ELISA technique (Roche). Protected women were defined as those with serum antibody levels > or = 0.6 IU/ml. A full history was taken from each studied individual; and the findings were recorded in a predesigned questionnaire in which data collection was based on face to face interviews. The data collected included demographic data, number of deliveries, number of abortions, body weight, mother’s knowledge about tetanus, and history of mother's tetanus vaccine and factors that might effect on immune response of women at time of delivery.
Statistical Analysis
To relate possible risk factors of vaccine failure for tetanus, the data were examined in a case-control study format. For women with evidence of vaccine failure (serum antibody levels<0.6 IU/ml) were matched up with those who were Protected (serum antibody levels > or=0.6 IU/ml).
Ethical Consideration
Ethical clearance for the study was taken from the Faculty of Medicine and Health Sciences Research Review Committee. Informed Consent was taken from the volunteers before the collecting specimens.
RESULTS
Table 1 shows the IgG antibody levels and the rates of protection and non-protection against tetanus among studied pregnant women at time of delivery. The protective rate at time of delivery was 68.5%, while 31.5% were not protected. Table 2 shows the association between age groups and non-protection rate against tetanus among studied pregnant women. There were significant association between older age and failure of protection in which the rate of failure in the older age group 36-49 years was 41.3% with odds ratio (OR) equal to 1.9, 95% CI=1.1-3.2, χ2=6.4, p=0.01, while the rate of failure was lower in other younger age groups. Table 3 shows vaccine coverage rates and factors associated with protection failure against tetanus among pregnant women at time of delivery. The total vaccine covering rate of tetanus was 87%, and maternal vaccine rate (antenatal tetanus vaccine) was 33.6%, also the childhood vaccine coverage was very low (0.3%), and school-age coverage rate was 40.9%. When factors of non-protection were considered, there were significant association between history of un-vaccinated women and non-protection against neonatal tetanus (NT) with protection failure rate equal to 85% and OR equal to 18.6, 95% CI=8-39, χ2=93, <0.001, rural residency with failure rate equal to 59% and OR equal to 34, 95% CI=1.8-6.5, χ2=16.2, <0.001; and malaria infection during pregnancy with failure rate equal to 59% and OR equal to 34, 95% CI=1.8-6.5, χ2=16.2, <0.001.
DISCUSSION
Fetuses have acquired passive immunity against tetanus if their mothers are adequately immunized; two or more doses of tetanus toxoid vaccine to the mother have been shown to reduce NT mortality by 94%11,12. The WHO recommends a primary series of three doses of DTP vaccine in the first year of life and three booster doses of tetanus toxoid in later childhood, and adulthood to prevent tetanus in all ages. The target date for global maternal neonatal tetanus elimination (MNTE) was 2015. But in August 2015, elimination had not been achieved in 21 countries including Yemen10. This study indicated that the rate of overly protection with IgG antibody level (≥0.6 IU/ml) was 68.5% among the studied pregnant women at time of delivery in Sana’a city, Yemen. This result is similar to that reported in Turkey where the rate of protective pregnant women was 69.0% with serum antibody level (≥0.6 IU/ml)13. In contrast, the present result is in disagreement with previous studies where the protection rates were as follow: in Yemen (87.70%)14, in Iraq (90%)15 and in India (94%)16. This low rate in our study could be due to that most mothers received only 1 and/or 2 doses of tetanus vaccine which leaded to failure protection of mothers to produce an adequate immune response at time of delivery. Also booster doses of TT are not routinely given in Yemeni family medical practice except in cases of serious injury. In this study, there statistical significant association between the failure of protection and older age group (p>0.05). The same results were found in Iraq (p<0.05)15, in Combodia (p<0.001)11, and in Taiwan where the level of anti-tetanus antibodies were decline with age from 4.8IU/ml in those aged 16-19 and to 0.82-0.87 IU/ml in those aged >51years (p=0.001)11. However, this study was in disagreement with other studies conducted in Turkey (p>0.05)13 and in Indonesia (p>0.05)17 in which no effect of age in the rate of protection failure. The present study indicated statistical significant association between residence in rural areas and failure of protection among studied pregnant women (p<0.001), which disagreed with previous studies as follows: in Yemen (p=0.96)14, in Turkey (p>0.05)13, in Cambodia (p=0.88)11 and in Senegal (p=0.067)18 in which no difference in the rate of failure between rural and urban areas. This indicated that the vaccine program covered urban more than rural areas in Yemen. In the current study the total vaccine covering rate of tetanus was 87%, and maternal vaccine rate (antenatal tetanus vaccine) was 33.6%, only also the childhood vaccine coverage was very low (0.3%), and school-age coverage rate was 40.9%. which disagreed with previous studies in Turkey13, in Cambodia11 and in Senegal18 in which vaccine covering rate of tetanus, maternal vaccine rate, childhood vaccine coverage rate and school-age coverage rate were above 90%. Our low rates could be due to the lack of vaccine register data base and therefore the vaccination history obtained verbally from the women may be unreliable. Also, it could be due to of the incorrect idea about vaccine contraindication with pregnancy as some women believe that taking the vaccine during pregnancy could cause abortion.
The current study found a significant association between un-vaccination with failure of protection in which the protection failure rate was 85% with OR=18.6 (p<0.001). This result is similar to previous studies conducted in India (p<0.05)16 and in Vietnam (p<0.05)19. However, this result is in disagreement with a study conducted in Portugal where the difference in antibody concentration (for both pre and post-vaccination) between those two groups were not statistically significant20. This difference may be due to the global status of serological immunity against tetanus varies between countries as a result of different national vaccination policies and the criteria used for determination of serum levels of tetanus antitoxin. The present study, found signification association between lower rate of protection failure and taking the vaccine during pregnancy (p<0.001). This result is in agreement with a previous study which indicated that when women take the vaccine during pregnancy this would provide the highest concentration of maternal antibodies to be transferred to their fetuses21. In this study, a statistical significant association between taking the last dose of tetanus vaccine and low failure rate of protection was found (14.8%) p=0.041). This result agreed with previous studies in other countries where the failure protection rates were as follow: in Iraq (8%),15, and in Tanzania (5.1%)22. The current study found statistical significant association between the malaria infection and failure of protection (57%, p<0.001). This result is in agreement with studies reported in Gambia23, and in Kenya24. This result can be explained by the findings of Cumberland et al.25 in which mother infected with malaria had reduce level of antibodies in spite of vaccination also they found that placental malaria reduce transfer of antibody to fetus 25. This result reflects the negative effect of malaria in immune system particularly in humeral immunity.
CONCLUSION
In conclusion, the total vaccine covering rate and antenatal tetanus vaccine rate were insufficient. In addition, the protective rate at time of delivery was low and large numbers of neonate are susceptible to neonatal tetanus and death. Vaccinating every pregnant woman with at least one dose of TT would be an affordable and effective way to protect against neonatal tetanus, and would be a step toward eliminating the deaths that continue to occur due to this preventable disease in Yemen.
ACKNOWLEDGMENTS
The authors would like to acknowledge Sana’a University, and the Microbiology Department of the National Centre of Public Health Laboratories (NCPHL) Sana'a, Yemen which provided working space.
CONFLICT OF INTEREST
No conflict of interest associated with this work.
AUTHOR’S CONTRIBUTION
This research work is part of a MSc. thesis. The candidate is the first authorr (ZAHSA) who conducted the laboratory and field works; and wrote up the thesis. The corresponding author (HAA) and (AYA) supervised the laboratory and field works, revised and edited the thesis draft and the manuscript and AAS helped in conducted the clinical work.
REFERENCES
Table 1: The IgG antibody levels and the rates of protection and non-protection against tetanus among studied pregnant women at time of delivery in Sana’a city, 2018
IgG Antibody Levels in IU/ ml |
No. |
% |
P |
Interpretation |
< 0.6 IU/ml |
150 |
31.5 |
<0.05 |
Susceptible for neonatal tetanus |
≥ 0.6 IU/ml |
326 |
68.5 |
Protective for neonatal tetanus |
|
Total |
476 |
100 |
|
|
Table 2: The association between age groups and non-protection against tetanus among studied pregnant women in Sana’a city, 2018
Age groups/years
|
No protection n=150 No. % |
OR
|
CI
|
χ2
|
P
|
|
16-25 n=234 |
72 |
30.7 |
0.88 |
0.0-1.3 |
0.39 |
0.53 |
26-35 n=167 |
45 |
26.9 |
0.71 |
0.4 -1.08 |
2.4 |
0.11 |
36-49 n=75 |
33 |
44 |
1.9 |
1.1-3.2 |
6.4 |
0.011 |
Total=476 |
150 |
31.5 |
|
|
|
|
OR - Odds ratio >1 (at risk), CI- Confidence intervals 95%, χ2- Chi-square 03.9 (significant), p Probability value <0.05 (significant)
Table 3: Vaccine coverage and factors associated with protection failure against tetanus among pregnant women at time of delivery, in Sana’a city, 2018
Factors
|
Vaccine coverage |
No protection n=150 No. % |
OR
|
CI
|
χ2
|
P
|
|
Vaccination |
|||||||
Infancy (3DPT) n= 373 |
373/476 78.4% |
76 |
20.4 |
0.04 |
0.02-0.07 |
151 |
<0.001 |
Childhood 1 dose n=30 |
30/476 6.3% |
4 |
13.3 |
0.3 |
0.1-0.89 |
5.1 |
0.02 |
School age 1 dose N=195 |
195/476 40.9% |
35 |
17.9 |
0.2 |
0.19-0.46 |
30.8 |
<0.001 |
Vaccination during pregnancy |
|||||||
2 doses (27 and 36 gestation) n=160 |
160/476 33.6% |
19 |
11.9 |
0.18 |
0.1-0.3 |
45 |
<0.001 |
One dose n=27 |
27/476 5.7% |
4 |
14.8 |
0.3 |
0.1-1 |
3.9 |
0.047 |
*MALARIA n=14 |
14/14 100% |
8 |
57.1 |
2.9 |
1.0-8.5 |
4.1 |
0.041 |
Total vaccinated n=414 |
414/476 87% |
97 |
23.4 |
0.0 |
undefined |
126 |
<0.001 |
Total unvaccinated n=62 |
62/476 13% |
53 |
85 |
18.6 |
8.8-39 |
93 |
<0.001 |
Residency |
|||||||
Urban n=432 |
392/432 90.7% |
124 |
28.7 |
0.13 |
0.06-0.3 |
30 |
<0.001 |
Rural n=44 |
22/44 50% |
26 |
59 |
34 |
1.8-6.5 |
16.2 |
<0.001 |
*All vaccinated at 27 and 36 gestation dose
OR - Odds ratio >1 (at risk), CI - Confidence intervals 95%, χ2- Chi-square 03.9 (significant), p Probability value <0.05 (significant)