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. 2019 Apr 17;37(17):2331–2339. doi: 10.1016/j.vaccine.2019.03.039

Delayed vaccination and its predictors among children under 2 years in India: Insights from the national family health survey–4

Tarun Shankar Choudhary a,, N Samarasimha Reddy b, Aditi Apte c, Bireshwar Sinha a, Sudipto Roy c, Nayana P Nair b, Kulandaipalayam Natarajan Sindhu b, Rutuja Patil c, Ravi Prakash Upadhyay a, Ranadip Chowdhury a
PMCID: PMC6996155  PMID: 30914221

Abstract

Objective

Delayed vaccination increases the susceptibility window for vaccine preventable diseases. Our analysis estimates the proportion of children between 10 and 23 months of age with delayed vaccination in India and the associated socio-demographic, maternal and child related factors.

Methods

We used individual level data from the National Family and Health Survey 4, conducted in 2015–2016. The primary outcome of the study was delayed vaccination for BCG, DPT- 1st dose and Measles. Delayed vaccination for each vaccine was defined as administration of the vaccine dose after 28 days of the minimum recommended age, as per the national immunization schedule in India. We estimated the proportion of children with delayed vaccination for each vaccine and used multivariable logistic regression to explore associated factors.

Findings

In the current analysis, 23.1%, 29.3% and 34.8% of children aged 10 to 23 months had delayed vaccination for BCG, DPT-1st dose and Measles respectively. Children from Muslim families (aOR 1.36 for BCG; aOR 1.45 for DPT-1; aOR 1.26 for Measles); birth weight < 2000 g (aOR 2.33 for BCG; aOR 1.53 for DPT-1; aOR 1.36 for Measles) had higher odds of delayed vaccination. Lower maternal education and belonging to a family from lower wealth quintile had higher odds of delayed vaccination. Children of mothers who had tetanus toxoid immunization during pregnancy had lower odds of delayed vaccination (aOR 0.69 for BCG; aOR 0.76 for DPT-1; aOR 0.78 for Measles).

Conclusion

The proportion of children with delayed vaccination is high in India. Vaccine timeliness should be a core indicator of the immunization program with greater focus on groups with higher chances of delayed vaccination i.e. home birth, low birth weight new-borns, poorer households, children of mothers with lower education and children from Muslim families.

Keywords: Timeliness, Delayed Vaccination, Measles, DPT, Child health, Epidemiology

1. Introduction

Globally, around 29% of under-five deaths were due to vaccine preventable diseases (VPD) in 2017 [1]. Despite a substantial decline in the under-five mortality, India accounted for the highest number of under-five deaths globally in 2016 [2]. VPDs like diarrhoea, pneumonia and measles were among the leading causes of under-five deaths in India resulting in about one-fourth of all under-five deaths between 2000 and 2015 [3]. India has high burden of Pertussis, Diphtheria, Japanese Encephalitis and Measles despite a national immunization program in place since the last five-decades [3], [4], [5]. Complete and timely vaccination can potentially reduce childhood mortality [6].

The Expanded Programme of Immunization was introduced in India in 1978. It has been scaled up considerably in terms of population covered as well as the number of targeted pathogens [7]. The proportion of children fully immunized at one year of age (defined as receiving BCG, Measles, and 3 doses each of oral polio and Diphtheria, Pertussis, Tetanus toxoid) has increased from 44% in 2005–6 as per National Family Health Survey (NFHS)-3 to 62% in 2015–16 (NFHS-4) [8], [9]. The Government of India launched “Mission Indradhanush” in December 2014 to increase vaccination coverage for under-five children and pregnant women and has now launched Intensified Mission Indradhanush (IMI) to achieve full vaccination for > 90% of potential beneficiaries by December 2018 [10], [11]. New vaccines (pentavalent vaccine, oral rotavirus vaccine, injectable polio vaccine and pneumococcal vaccine) have been added to the Universal Immunisation Program (UIP) as detailed in Supplementary Table 1 [7]. However, vaccine timeliness, although an important indicator of the programme’s quality, has been a relatively neglected aspect of programme performance.

The recommended age for vaccination is based on two factors; the earliest age at which the immunity afforded by placental transfer of maternal antibodies at birth wanes, thereby making the infants susceptible to pathogens and the earliest age at which safety and efficacy of the vaccine has been demonstrated [12]. Delay in vaccination increases the susceptibility window for developing VPDs at individual level and reduces herd immunity at population level [6], [12], [13]. Evidence from previous studies have demonstrated that delayed vaccination may increase the risk of Pertussis, Measles and Haemophilus influenzae B infections up to 6 folds and lead to outbreaks [14], [15], [16], [17]. In case of certain vaccines with fixed upper age limit (e.g. rotavirus) delayed vaccination leads to reduced coverage for the vaccine [18].

The available literature on vaccine timeliness and its associated factors is limited in India [19], [20], [21]. The primary objective of the current analysis was to estimate the proportion of children aged 10 to 23 months with delayed vaccination for BCG, DPT-1st dose and Measles at national and subnational level in India using the recent NFHS-4 data. We also examined the association of delayed vaccination with socio-demographic, maternal and child related factors to identify population sub-groups at higher risk of delayed vaccination.

2. Methodology

2.1. Data source

This analysis was based on individual level data from the 4th round of the NFHS, a nationally representative cross-sectional survey. It provides reliable estimates on fertility, mortality, reproduction, child health and other demographic indicators at national, state and district level [8]. Around 628,900 households in 29 states and 7 union territories in India were interviewed for NFHS-4, with a response rate of 98%. A two-stage stratified sampling design with villages in rural areas and Census Enumeration Blocks (CEBs) in urban areas, forming the primary sampling units (PSU), was adopted during the first stage. Within each PSU, the households were selected using systematic random sampling in the second stage. Clinical, anthropometric and biochemical measurements for men, women and children were done. Detailed description of the sampling design and instruments used in the survey have been provided elsewhere [8].

We used the children recode file (IAKR73FL.dta), available from the Demography and Health Survey (DHS) program website, for this analysis [22]. Information related to the antenatal care and postnatal care for the respective pregnancy, immunization status of the child, along with data for maternal and household characteristics of the child was included in the recode file. Information on the child's vaccination status in NFHS-4 was based either on the Mother and Child Protection card (MCP)/Health card or mother's recall. In the current analysis, we have only included children for whom date of vaccination for a given vaccine dose was available on the MCP/Health card. Children for whom data for immunisation was based on maternal recall or the date of vaccination was not available on the health card were excluded from the analysis (details in Fig. 1). Ethical clearance was not needed as the analysis used secondary data available in the public domain. The guidelines for data use as required by the DHS program were strictly followed.

Fig. 1.

Fig. 1

The detail of the case records from the child recode file used for the current analysis with the reasons for exclusion (NFHS 4, 2015–16).

2.2. Definition of primary outcome

The primary outcome of the study was delayed vaccination for BCG, DPT- 1st dose and Measles. Delayed vaccination for each vaccine was defined as administration of the vaccine dose after 28 days of the minimum recommended age, as per the national immunization schedule in India (Supplementary Table 1). Date of birth and age at vaccination (for individual vaccine dose) was calculated in century day code format. Vaccination was categorised as delayed if given on day 29 or later for BCG, 71 days or later (after 10 completed weeks) for DPT-1st dose and 303 days or later (after 10 completed months) for Measles vaccine (Supplementary Box 1).

2.3. Statistical analysis

Proportion of children with delayed vaccination was estimated for BCG, DPT-1st dose, and Measles vaccination at national level and for individual states and union territories. Median age at vaccination for BCG, DPT-1st dose and Measles vaccine was calculated. Univariate analysis was done to examine the association between socio-demographic, maternal, antenatal and child characteristics and delayed vaccination. Socio-demographic variables included religion, caste, place of residence and wealth quintile. Maternal and antenatal variables included maternal education, age at birth of 1st child, maternal tetanus immunisation during pregnancy and financial assistance for delivery. Child level variables included gender, place of delivery, birth weight and birth order. Details of the variables and the sub-categories are available in Supplementary Table 2.

Multivariable logistic regression models were built to examine the association between delayed vaccination for BCG, DPT- 1st dose and Measles, individually. Variables with a p-value < 0.25 on univariate analysis and those of known clinical or contextual importance were included in the multivariable logistic regression analysis [23]. Stepwise backward elimination based on design-based Wald test was used to finalise the model. A p-value of < 0.05 was considered statistically significant. STATA version 15.1 (StataCorp LLC, College Station, TX, USA) was used for all analysis and adjustment for sampling weight, clustering and strata was done using svyset command.

3. Results

We analysed data of 32,514 children for BCG, 32,635 children for DPT-1st dose and 27,017 children for delayed Measles vaccination (Fig. 1). Details of the background characteristics are provided in Table 1.

Table 1.

Background characteristics for delayed BCG, delayed DPT-1st dose and delayed Measles vaccination among children 10 to 23 months of age in India (NFHS 4, 2015–16).

BCG
DPT-1
BCG
Variables No Delay Delay No Delay Delay No Delay Delay
N (%) N (%) N (%) N (%) N (%) N (%)
Socio-demographic characteristics
Religion (total)
Hindu 17,900 (79.82) 5677 (76.12) 16840 (80.46) 6911 (76.33) 12984 (80.32) 6712 (77.84)
Muslim 3495 (14.19) 1377 (19.35) 3068 (13.45) 1713 (19.22) 2287 (13.1) 1521 (17.31)
Others* 2858 (6) 1207 (4.53) 3042 (6.1) 1061 (4.45) 2396 (6.58) 1117 (4.86)



Caste (total)
Scheduled caste 4778 (23.25) 1499 (22.42) 4350 (22.93) 1974 (23.55) 3259 (22.18) 1916 (24.11)
Scheduled tribe 4186 (9.62) 1673 (10.35) 4200 (9.59) 1685 (10.2) 3208 (9.35) 1602 (9.33)
Other backward classes 9632 (45.61) 3163 (48.21) 8878 (45.76) 4018 (47.84) 6849 (45.36) 3714 (46.44)
Others** 4484 (21.52) 1507 (19.02) 4390 (21.73) 1575 (18.4) 3463 (23.11) 1677 (20.12)



Wealth index (total)
Highest 4495 (18.7) 878 (11.43) 4360 (19.53) 992 (10.24) 3514 (20.4) 1333 (14.82)
Fourth 4843 (21.35) 1371 (16.69) 4754 (22.35) 1476 (15.36) 3686 (22.32) 1680 (19.18)
Middle 5242 (21.52) 1809 (20.56) 4974 (21.37) 2081 (20.75) 3871 (21.46) 2019 (20.8)
Second 5105 (20.32) 2191 (25.07) 4800 (19.6) 2549 (26.07) 3613 (19.19) 2216 (23.1)
Lowest 4568 (18.1) 2012 (26.26) 4062 (17.15) 2587 (27.58) 2983 (16.63) 2102 (22.1)



Place of residence (total)
Urban 6483 (31.01) 1878 (23.93) 6222 (31.27) 2087 (23.45) 4769 (31.21) 2370 (29.29)
Rural 17770 (68.99) 6383 (76.07) 16728 (68.73) 7598 (76.55) 12898 (68.79) 6980 (70.71)



Maternal and antenatal characteristics
Maternal education (total)
Higher 3150 (13.98) 709 (8.73) 3175 (15.1) 679 (6.75) 2535 (15.71) 963 (11.14)
Secondary 12828 (53.75) 4082 (47.12) 12333 (53.77) 4618 (47.54) 9632 (54.66) 4723 (50.04)
Primary 3116 (12.68) 1286 (15.44) 2915 (12.55) 1522 (15.49) 2171 (12.19) 1385 (14.65)
None 5159 (19.59) 2184 (28.71) 4527 (18.57) 2866 (30.23) 3329 (17.43) 2279 (24.17)



Maternal age at first child birth (total)
Less than 19 4181 (19.11) 1714 (21.98) 3856 (18.28) 2060 (23.48) 2884 (17.81) 1838 (21.95)
19 – 30 19537 (79.14) 6362 (76.81) 18515 (79.83) 7477 (75.57) 14325 (80.17) 7322 (76.83)
31 and above 535 (1.75) 185 (1.21) 579 (1.89) 148 (0.95) 458 (2.02) 190 (1.22)



Antenatal visits to health facility (total)
No ANC visits 2242 (9.78) 1245 (16.19) 2098 (9.51) 1440 (16.02) 1524 (8.87) 1076 (12.41)
1–3 visits 7412 (28.73) 3049 (38.01) 6822 (27.86) 3700 (38.2) 5238 (27.88) 3174 (33.05)
4–8 visits 9636 (41.06) 2837 (34.76) 9414 (42.12) 3113 (33.55) 7306 (42.14) 3372 (38.03)
>8 visits 3759 (20.43) 690 (11.04) 3548 (20.51) 858 (12.24) 2777 (21.11) 1155 (16.51)



Financial assistance at the time of delivery (total)
Yes 10928 (45.6) 2519 (40.39) 9746 (43.68) 3785 (48.01) 7433 (43.13) 3827 (45.92)
No 9960 (54.4) 3050 (59.61) 9589 (56.32) 3381 (51.99) 7466 (56.87) 3554 (54.08)



Tetanus injections before birth (total)
No tetanus injections 1121 (5.11) 502 (6.7) 1052 (5.23) 550 (6.18) 766 (4.88) 455 (5.89)
At least one tetanus injection 22032 (94.89) 7351 (93.3) 20935 (94.77) 8594 (93.82) 16149 (95.12) 8365 (94.11)



Child characteristics
Gender of the child (total)
Male 12643 (51.98) 4301 (52.28) 11981 (51.98) 5007 (51.51) 9214 (51.6) 4832 (52.29)
Female 11610 (48.02) 3960 (47.72) 10969 (48.02) 4678 (48.49) 8453 (48.4) 4518 (47.71)



Place of delivery (total)
Home births (total) 2438 (8.83) 2402 (26.34) 2823 (10.27) 2104 (20.12) 2151 (10.5) 1538 (14.49)
Private health facility 5570 (28.55) 2006 (28.9) 5658 (30.39) 1947 (24.34) 4420 (31.17) 2142 (27.83)
Public health facility 16245 (62.62) 3853 (44.76) 14469 (59.33) 5634 (55.54) 11096 (58.34) 5670 (57.69)



Birth weight (total)
<2000 g 728 (3.17) 362 (7.23) 678 (3.31) 414 (5.68) 566 (3.56) 369 (4.69)
2000–2499 g 2760 (13.13) 700 (12.56) 2453 (12.82) 1017 (13.4) 1924 (13.06) 998 (12.91)
≥2500 g 18338 (83.7) 4980 (80.21) 17250 (83.87) 6104 (80.92) 13241 (83.38) 6483 (82.4)



Birth order (total)
1st 10107 (42.7) 2949 (36.48) 9667 (43.41) 3460 (36.16) 7699 (45.06) 3562 (38.5)
2nd 8069 (34.73) 2544 (32.08) 7610 (34.8) 2991 (31.78) 5803 (34.42) 3046 (34.21)
3rd 3478 (13.56) 1397 (15.93) 3228 (13.11) 1675 (16.91) 2384 (12.53) 1500 (15.11)
4 or more 2599 (9) 1371 (15.51) 2445 (8.69) 1559 (15.15) 1781 (7.99) 1242 (12.17)
*

Others (Christians, Sikh, Buddhist/neo-Buddhist, Jain, Jewish, Parsi/Zoroastrian, no religion, Other (not defined)).

**

Others (do not belong to Scheduled caste/Tribe and other backward castes).

3.1. Delayed vaccination

The median age for BCG, DPT–1st dose and Measles vaccination was four days, 57 days (8 weeks and 1 day) and 292 days (9 months and 18 days) respectively (Fig. 2). Nationally, 23.1%, 29.3% and 34.8% of children aged 10 to 23 months had delayed vaccination for BCG, DPT-1st dose and Measles respectively. The proportion of children with delayed vaccination across different states and union territories in India ranged from 1.4% to 76.3% for BCG, 6.14% to 44.2% for DPT-1st dose and 20.9% to 46.7% for Measles (Fig. 3).

Fig. 2.

Fig. 2

The median age at vaccination (in days) for BCG, DPT-1 and Measles at State and National level in India for children 10 to 23 months of age (NFHS 4, 2015–16).

Fig. 3.

Fig. 3

Figure showing the proportion of children aged 10 to 23 months of age with delayed vaccination for BCG, DPT-1 and Measles at state and national level in India (NFHS 4, 2015–16).

3.2. Factors associated with delayed vaccination

Table 2, Table 3, Table 4 shows the results from the multivariable logistic regression analysis for delayed BCG, delayed DPT-1st dose and delayed Measles vaccination respectively. Children from Muslim families had higher odds of delayed BCG (aOR 1.36, 95% CI 1.17, 1.57), delayed DPT-1st dose (aOR 1.45, 95% CI 1.27, 1.65) and delayed Measles (aOR 1.26, 95% CI 1.09, 1.45) vaccination. Those with a birth weight < 2000 g had higher odds of delayed BCG (aOR 2.33, 95% CI 1.89, 2.89), delayed DPT-1st dose (aOR 1.53, 95% CI 1.26, 1.86) and delayed Measles (aOR 1.36, 95% CI 1.11, 1.67) vaccination. A dose-response like relationship was seen between the wealth index of child family and educational status of child’s mother. Compared to children from highest wealth quintile those from lower wealth quintiles had higher chances of delayed vaccination for BCG, DPT-1st dose and Measles in the adjusted analysis. Children of mothers with higher education (≥12 years of schooling) had lower odds of delayed vaccination for BCG, DPT-1st dose and Measles as compared to children of mothers with lower education. Maternal tetanus immunisation during pregnancy was associated with lower odds of delayed BCG (aOR 0.69, 95% CI 0.56, 0.85), delayed DPT-1st dose (aOR 0.76, 95% CI 0.62, 0.94) and delayed Measles vaccination (aOR 0.78, 95% CI 0.63, 0.97). Maternal age of <19 years at first childbirth was associated with higher odds of delayed DPT-1st dose (aOR 1.19, 95% CI 1.07, 1.32) and delayed Measles vaccination (aOR 1.18, 95% CI 1.06, 1.32). Children from rural areas had higher odds of delayed Measles vaccination (aOR 0.87, 95% CI 0.77, 0.98) but not for BCG or DPT-1st dose. Home births and births in a private health facility were associated with higher odds of delayed BCG (aOR 2.67, 95% CI 2.25, 3.17 and aOR 1.77, 95% CI 1.57, 1.99) and delayed DPT-1st dose vaccination (aOR 1.41, 95% CI 1.20, 1.64 and aOR 1.18, 95% CI 1.06, 1.31), respectively. Higher birth order of the child was found to have higher odds of delayed Measles vaccination. Gender of the child didn’t have a significant association with delayed BCG, delayed DPT-1st dose and delayed Measles vaccination.

Table 2.

Logistic regression model showing predictors for delayed BCG vaccination among infants 10–23 months of age in India (NFHS 4, 2015–16).

Socio-demographic characteristics BCG
n = 26611 (weighted)
Unadjusted odds ratio (95%CI) Adjusted Odds ratio (95% CI) p value
Religion
Hindu Reference Reference
Muslim 1.43 (1.29, 1.59) 1.36 (1.17, 1.57) 0.000
Others* 0.79 (0.69, 0.94) 1.03 (0.79, 1.35) 0.810



Wealth index
Highest Reference Reference
Fourth 1.28 (1.1, 1.49) 1.28 (1.05, 1.56) 0.016
Middle 1.56 (1.35, 1.81) 1.54 (1.24, 1.91) 0.000
Second 2.02 (1.75, 2.33) 1.77 (1.41, 2.23) 0.000
Lowest 2.37 (2.06, 2.73) 1.95 (1.51, 2.51) 0.000



Place of residence
Urban Reference Reference
Rural 1.43 (1.3, 1.57) 1.08 (0.95, 1.22) 0.268



Maternal and antenatal characteristics
Maternal education
Higher Reference Reference
Secondary 1.4 (1.23, 1.61) 1.23 (1.05, 1.46) 0.013
Primary 1.95 (1.67, 2.28) 1.33 (1.08, 1.64) 0.008
None 2.35 (2.04, 2.71) 1.37 (1.09, 1.71) 0.007



Mother received at least one tetanus toxoid injection during pregnancy
No Reference
Yes 0.75 (0.64, 0.88) 0.69 (0.56, 0.85) 0.000



Child characteristics
Gender of the child
Male Reference Reference
Female 0.99 (0.92, 1.06) 0.96 (0.88, 1.06) 0.434



Place of delivery
Public health facility Reference Reference
Private health facility 1.42 (1.3, 1.55) 1.77 (1.57, 1.99) 0.000
Home births 4.17 (3.76, 4.63) 2.67 (2.25, 3.17) 0.000



Birth weight
<2000 g 2.38 (1.98, 2.87) 2.33 (1.89, 2.89) 0.000
2000–2499 g 1 (0.88, 1.14) 1.03 (0.90, 1.18) 0.669
≥ 2500 g Reference Reference
*

Others (Christians, Sikh, Buddhist/neo-Buddhist, Jain, Jewish, Parsi/Zoroastrian, no religion, Other (not defined)).

Table 3.

Logistic regression model showing predictors for delayed DPT1 vaccination among infants 10 to 23 months of age in India (NFHS 4, 2015–16).

DPT1
n = 26649 (weighted)
Unadjusted odds ratio (95%CI) Adjusted Odds ratio (95% CI) p value
Socio-demographic characteristics
Religion
Hindu Reference Reference
Muslim 1.51 (1.36, 1.67) 1.45 (1.27, 1.65) 0.000
Others* 0.77 (0.65, 0.9) 1.18 (0.94, 1.49) 0.152



Wealth index
Highest Reference Reference
Fourth 1.31 (1.14, 1.51) 1.17 (0.98, 1.39) 0.082
Middle 1.85 (1.62, 2.12) 1.55 (1.30, 1.85) 0.000
Second 2.54 (2.24, 2.88) 1.76 (1.46, 2.12) 0.000
Lowest 3.07 (2.7, 3.49) 1.77 (1.44, 2.17) 0.000



Place of residence
Urban Reference Reference
Rural 1.48 (1.35, 1.63) 0.98 (0.87, 1.10) 0.731



Maternal and antenatal characteristics
Maternal education
Higher Reference Reference
Secondary 1.98 (1.73, 2.26) 1.51 (1.29, 1.76) 0.000
Primary 2.76 (2.38, 3.21) 1.62 (1.31, 1.91) 0.000
None 3.64 (3.17, 4.19) 1.81 (1.50, 2.19) 0.000



Maternal age at first child birth
Less than 19 1.36 (1.24, 1.48) 1.19 (1.07, 1.32) 0.001
19–30 Reference Reference
Above 30 0.53 (0.4, 0.72) 0.68 (0.48, 0.95) 0.023



Mother received at least one tetanus toxoid injection during pregnancy
No Reference
Yes 0.84 (0.71, 0.99) 0.76 (0.62, 0.94) 0.010



Child characteristics
Gender of the child
Male Reference Reference
Female 1.02 (0.95, 1.09) 0.99 (0.91, 1.07) 0.745



Place of delivery
Public health facility Reference Reference
Private health facility 0.86 (0.79, 0.93) 1.18 (1.06, 1.31) 0.002
Home births 2.09 (1.91, 2.3) 1.41 (1.20, 1.64) 0.000



Birth weight
<2000 g 1.78 (1.49, 2.13) 1.53 (1.26, 1.86) 0.000
2000–2499 g 1.08 (0.97, 1.21) 1.07 (0.95, 1.20) 0.267
≥ 2500 g Reference Reference
*

Others (Christians, Sikh, Buddhist/neo-Buddhist, Jain, Jewish, Parsi/Zoroastrian, no religion, Other (not defined)).

Table 4.

Logistic regression model showing predictors for delayed measles vaccination among infants 10 to 23 months of age in India (NFHS 4, 2015–16).

Measles
n = 22,693 (weighted)
Unadjusted odds ratio (95%CI) Adjusted Odds ratio (95% CI) p value
Socio-demographic characteristics
Religion
Hindu Reference Reference
Muslim 1.36 (1.21, 1.53) 1.26 (1.09, 1.45) 0.002
Others* 0.76 (0.66, 0.88) 0.88 (0.73, 1.06) 0.186



Wealth index
Highest Reference Reference
Fourth 1.18 (1.02, 1.37) 1.14 (0.97, 1.34) 0.124
Middle 1.33 (1.17, 1.52) 1.22 (1.03, 1.44) 0.020
Second 1.66 (1.45, 1.89) 1.37 (1.14, 1.64) 0.001
Lowest 1.83 (1.61, 2.08) 1.30 (1.08, 1.58) 0.007



Place of residence
Urban Reference Reference
Rural 1.1 (1.00, 1.20) 0.87 (0.77, 0.98) 0.026



Maternal and antenatal characteristics
Maternal education
Higher Reference Reference
Secondary 1.29 (1.13, 1.47) 1.20 (1.04, 1.40) 0.016
Primary 1.7 (1.45, 1.98) 1.42 (1.18, 1.72) 0.000
None 1.96 (1.70, 2.25) 1.41 (1.70, 1.70) 0.000



Maternal age at first child birth
less than 19 1.29 (1.17, 1.42) 1.18 (1.06, 1.32) 0.003
19–30 Reference Reference
Above 30 0.63 (0.48, 0.82) 0.72 (0.55, 0.96) 0.023



Mother received at least on tetanus toxoid injection during pregnancy
No Reference
Yes 0.82 (0.68, 0.98) 0.78 (0.63, 0.97) 0.025



Child characteristics
Gender of the child
Male Reference Reference
Female 0.97 (0.91, 1.05) 0.96 (0.89, 1.04) 0.370



Birth weight
<2000 g 1.33 (1.1, 1.61) 1.36 (1.11, 1.67) 0.003
2000–2499 g 1 (0.89, 1.13) 0.98 (0.86,1.11) 0.706
≥ 2500 g Reference Reference



Birth order
1 Reference Reference
2 1.16 (1.06, 1.27) 1.14 (1.03, 1.26) 0.012
3 1.41 (1.26, 1.58) 1.17 (1.02, 1.33) 0.021
4 or more 1.78 (1.58, 2.01) 1.27 (1.09, 1.48) 0.002
*

Others (Christians, Sikh, Buddhist/neo-Buddhist, Jain, Jewish, Parsi/Zoroastrian, no religion, Other (not defined)).

4. Discussion

Findings from our analysis shows that delay in vaccination for BCG, DPT- 1st dose and Measles is high in India. Nonetheless, the median age of vaccination was within the cut-off for timely vaccination at national level as well as within all the states and union territories except for the states of Assam, Manipur and Tripura for BCG vaccination in our analysis. This suggests that the program has been moderately successful at achieving timely vaccination. There was a considerable variation in the proportion of children with delayed vaccination within states and union territories.

The proportion of children with delayed vaccination was lowest for BCG which was coherent with higher rates of institutional delivery post implementation of the National Rural Health Mission (NRHM) in 2005 [8], [9]. Compared to states with low proportion of delayed BCG vaccination the states with a high proportion of delay had lower rates of institutional delivery. DPT-1st dose, part of a multi dose schedule, is an important vaccine from the delayed vaccination perspective. Delay in the first two doses will lead to delay in the 3rd dose by default since a minimum gap of 4 weeks between 2 consecutive doses must be maintained. Similar findings have been reported earlier by studies in India and globally [19], [21], [24]. Compared to an 8-week gap between consecutive vaccine doses in high income countries like USA, the immunization schedule in India follows a 4-week gap during the first 6 months of life. This tight schedule may also lead to higher delay in vaccination for multi-dose vaccines.

Children from Muslim families had higher odds of delayed vaccination for all vaccines. Religious beliefs has an influence on the uptake of health services in general and immunization services are sensitive to these, as previous studies in India have also reported higher odds of delayed vaccination among children from Muslim families [25], [26]. Belonging to lower wealth quintiles indicates low socioeconomic status of the family and they are more likely to have lower awareness and utilisation of health services as physical, financial and social barriers to access exist, despite the provision of essential services like vaccination free of charge [19], [25], [27].

Contrary to previous studies our analysis didn’t find residing in rural area as a significant predictor for delayed vaccination for BCG, DPT-1 vaccines and for Measles vaccine, it was associated with decreased odds of delayed vaccination [19], [20], [25], [28], [29]. The primary health care system in India is better structured in rural areas post the implementation of the National Rural Health Mission and NFHS 4 is the first national level survey which captures the effect of this health system reform.

Early age at first childbirth and lower maternal education was associated with a higher odd of delayed vaccination similar to previous studies from India and other Low and middle-income countries (LMICs), as most of these women are married early and the awareness and receptiveness to health messages and uptake of health services including vaccination is lower among these women [30], [31], [32]. Maternal tetanus immunisation during pregnancy was associated with lower odds of delayed vaccination which is consistent with findings from previous NFHS data and from other studies [33], [34].

Home birth is associated with delay in seeking healthcare especially at birth and showed 2.7 times increased risk of delay in BCG as compared to births in public health facility. Several private facilities in India (especially in rural areas and small towns) provide only intra-natal care and services like vaccination may not be provided, accounting for higher odds of delayed vaccination [35], [36]

Low birth weight, especially those below 2000 g at birth and prematurity are known to be associated with vaccination delay, an important reason being parental concern about the safety and benefit of vaccination [37], [38], [39]. In our analysis children with weight <2000 g had higher odds of delayed vaccination for all vaccines, although the association was strongest for BCG, which is recommended on the first day of life.

Birth order of 4 or more was associated with delayed vaccination for Measles vaccine. This might be due to lack of time and resources for care-seeking of a non- sick child as vaccination is mainly preventive and usually accorded with a lower order of priority. This is in consensus with the earlier literature vaccination delay from India and other countries [30], [40], [41].

We didn’t find any association between female gender and delayed vaccination for BCG, DPT-1st dose and Measles in our analysis. Vaccination services are now being provided closer to home which may led greater equity in access as well as utilisation of these services. This contrasts with earlier studies which report lower utilisation of healthcare services for female child in India [24], [25], [42].

4.1. Strengths and limitation

The current analysis is based on the largest and most recent, nationally representative survey data available. Age calculated was done in days to ensure higher accuracy. We tried to address recall bias by restricting our analysis to children for whom date of birth and date of vaccination for a given vaccine dose were available from the MCP/Health card. Although, exclusion of children who died in this period and those without vaccination card can be a cause of potential bias and an under-estimation of delayed vaccination, a limitation of the current analysis. We couldn’t study the association of delayed vaccination with the supply side factors as the data for same isn’t captured in the NFHS-4. The cross-sectional nature of the data also precludes commenting on causal associations.

4.2. Recommendation/Conclusion

Vaccine timeliness is an under-recognised problem in India despite high proportion of Indian children having delayed vaccination. Timeliness of vaccination should be integral to the routine immunization programme as delayed vaccination increases the susceptibility window to vaccine preventable diseases. Targeted approach for groups with higher chances of delayed vaccination i.e. children delivered at home, low birth weight new-borns, poorer households, children of mothers with lower education, children from Muslim families may be used when designing routine immunization micro-plan in the primary care settings. Due list generated as a part of the routine immunization microplanning can be used to track the children with delay in vaccination.

Acknowledgments

Acknowledgements

The Young investigators acknowledge the core support provided by the Bill and Melinda Gates Foundation (Grant ID OPP1110191). We thank the technical advisory group of the PRERNA platform and faculties at Centre for Health Research and Development, Society for Applied Studies, Delhi; KEM Hospital Research Centre, Pune and Christian Medical College, Vellore for their support and guidance. We also acknowledge the support of Knowledge Integration and Translational Platform, an initiative of the Department of Biotechnology, Government of India and Gates Foundation, through the Biotechnology Industry Research Assistance Council.

Sources of Support/Funding

None.

Conflict of Interest

None of the authors have any conflict of interest to declare.

Author’s Contribution

TSC was involved in conceptualization and protocol development, data acquisition, data analysis, wrote the first draft and revised the manuscript. RC, AA, SSR, KNS were involved in conducting the analyses, manuscript writing, revision and finalization. BS, SR, RP, NPN, RPU were involved in data analysis, manuscript writing, revision and finalization. All authors reviewed and approved the final version.

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.vaccine.2019.03.039.

Appendix A. Supplementary material

The following are the Supplementary data to this article:

Supplementary data 1
mmc1.docx (18.9KB, docx)

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