Table 2.
Author, year [Ref] | Number of study groups | Safety assessment | Statistically significant differences in baseline characteristics and safety outcomes between primary and revaccination dose of PPSV-23 |
---|---|---|---|
Prospective cohort studies (n = 10) | |||
Tobudic, 20121 [31] | 1 (longitudinal cohort) | 7 day diary (after revaccination dose) | Population characteristics: Participants 1 year older at 2nd dose |
Safety: no comparison group | |||
Dransfield, 20121 [23] | 2 (1st vs. 2nd dose) | not assessed | Population characteristics: 2nd dose recipients older, more often white, more severe COPD disease |
Safety: − | |||
Hammitt, 2011 [11] | 3 (1st vs. 2nd or 3rd dose) | 4 day diary and interview on day 30 | Population characteristics: 2nd/3rd dose recipients older, more likely Alaska Natives/American Indians, more often with underlying comorbidities compared to 1st dose recipients |
Safety: local AEs and systemic AEs more frequent in revaccination group | |||
Jackson, 1999 [13] | 2 (1st vs. 2nd dose) | 13 day diary and telephone interview | Population characteristics: 2nd dose recipients more often females and less often with underlying comorbidities |
Safety: local AEs more frequent in revaccination group at days 0–2, no differences after 6 days. No differences regarding systemic AEs. Multivariate analysis: revaccination independently associated with risk of sizable local reaction | |||
Jackson, 2013 [22] | 1 (longitudinal cohort) | 13 day diary | Population characteristics: Participants 3.4–5 years older at 2nd dose |
Safety: local AEs and systemic AEs more frequent in revaccination group | |||
Manoff, 20102 [25] | 2 (1st vs. 2nd dose) | not assessed | Population characteristics: 2nd dose recipients more likely ever smoked |
Safety: − | |||
Musher, 20103 [12] | 2 (1st vs. 2nd dose) | 14 day diary | Population characteristics: 2nd dose recipients more often with underlying comorbidities |
Safety: local AEs and systemic AEs more frequent in revaccination group | |||
Musher, 20113,4 [28] | 2 longitudinal cohorts (1st vs. 2nd; 2nd vs. 3rd) | 14 day diary | Population characteristics: Participants of both longitudinal cohorts were ten years older at 2nd/3rd dose |
Safety5: local AEs and systemic AEs more frequent in revaccination group | |||
Ohshima, 2014 [29] | 1 (longitudinal cohort) | 14 day diary | Population characteristics: Participants were 7.6 years older at 2nd dose |
Safety: local AEs and systemic AEs more frequent in revaccination group | |||
Törling, 2003 [24] | 1 (longitudinal cohort) | not assessed | Population characteristics: Participants were 5.3 years older at 2nd dose and 11% had a new episode of pneumonia |
Safety: no comparison group | |||
Retrospective database studies (n = 3) | |||
Jackson, 2006 [27] | 3 (1st vs. 2nd vs. 3rd dose) | ICD-9-Codes | Population characteristics: 3rd dose recipients were older and had more likely underlying comorbidities |
Safety: Presumptive medically attended injection site reaction more frequent in 2nd dose recipients than in 1st dose recipients. No statistically significant differences between 1st dose and 3rd dose recipients | |||
Shih, 2002 [30] | 2 (1st vs. ≥ 2nd dose) | ICD-9-Codes | Population characteristics: 2nd dose recipients were older, more often white and had higher hospitalizations rates and a higher comorbidity (Charlson) Index |
Safety: Mulitivariate analysis: Revaccination independently associated with emergency room visits and office visits if PPSV-23 was administered within 5 years. No association after >5 years. | |||
Walker, 2005 [32] | 2 (1st or 2nd vs. ≥ 3rd dose) | ICD-9-Codes and medical records | Population characteristics: ≥ 3rd dose recipients were older and had more likely underlying lung diseases |
Safety: No differences in risk of medically attended AEs in the different groups | |||
Cross-sectional study (n = 1; telephone interview) | |||
D’Heilly, 2002 [26] | 2 (1st vs. ≥ 2nd dose) | Interview 8 months (on average) after vaccination | Population characteristics: not reported |
Safety: Multivariate analysis: Revaccination independently associated with redness or swelling at injection site during week after vaccination |
1Published as randomized controlled trial but treated as cohort study here; 2Substudy of Musher et al. [12]; 3Musher [28] is extension study of Musher et al. [12]; 4 two longitudinal cohorts: cohort one received 1st dose in 1997 and 2nd in 2007; cohort two received 2nd dose in 1997 and 3rd in 2007; 52nd vs. 3rd dose (1st vs. 2nd dose reported in Musher [12])