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. 2012 Nov;18(11):1729–1737. doi: 10.3201/eid1811.120329

Table 3. Characteristics for persons with invasive pneumococcal disease before and after implementation of a PCV7 vaccination program, the Netherlands, June 2004–May 2010*.

Characteristic
No. (%) by infecting serotype and vaccination period†
All serotypes PCV7 serotypes Non–PCV7 serotypes
Before (n = 1,216)
After (n = 1,144)
p value

Before(n = 565)
After (n = 268)
p value

Before (n = 650)
After (n = 876)
p value
Comorbidity
Immunocompromising condition‡ 216 (18) 255 (22) 0.013 88 (16) 73 (27) 0.001 128 (20) 182 (21) NS
Any comobidity§ 817 (67) 788 (69) NS 376 (67) 190 (71) NS 441 (68) 598 (68) NS
Disease course/outcome
ICU admission 258 (21) 243 (21) NS 115 (20) 60 (22) NS 143 (22) 183 (21) NS
Length of hospital stay, median (IQR) 11.0 (7.0–18.0) 9.0 (5.0–16.0) <0.001 11.0 (7.0–18.0) 9.0 (5.0–15.0) <0.001 11.0 (7.0–19.0) 10.0 (5.0–16.0) <0.001
Died 194 (16) 135 (12) 0.003 92 (16) 44 (16) NS 102 (16) 91 (10) 0.002
Deaths/100,000 persons 2.4 1.6 0.001 1.1 0.5 0.000 1.3 1.1 NS

*Cases are number of patients included in a study covering ≈25% of the Dutch population. Boldface, significant difference (p<0.05) between pre- and post-implementation period as calculated by χ2 test (% of cases), Mann-Whitney U test (median days of hospitalization), or incidence rate ratio (mortality rate). PCV7, 7-valent pneumococcal conjugate vaccine; NS, not significant (p>0.05). †Data are no. (%) except as indicated in first column. Vaccination periods: before, pre-implementation period (June 2004–May 2006); after, late post-implementation period (June 2008–May 2010). ‡Immunocompromising condition: primary immunodeficiency, HIV/AIDS, lymphoma, leukemia, myeloma, solid organ or stem cell transplant, current immunosuppressive therapy for malignancy or autoimmune disease, asplenia/splenectomy, sickle cell disease, and renal insufficiency (dialysis required and nephrotic syndrome). §Any comorbidity: malignancies (within previous 5 y) not considered to be immunocompromising; chronic obstructive pulmonary disease; asthma; diabetes mellitus; myocardial infarction; coronary artery condition; stroke/transient ischemic attack; cardiomyopathy; heart failure; heart valve disease; presence of cerebral/abdominal/thoracic aneurysms; thyroid disease; liver disease; intravenous drug use; long-term alcohol abuse; cerebrospinal fluid leak; recent physical trauma/skull fracture; and, for children, premature birth (<37 weeks for children 0–1 y old and <32 weeks for children 0–4 y old).