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1 ca will have substantial indirect effects on invasive pneumococcal disease.
2 We assessed the effect of vaccination on invasive pneumococcal disease.
3 thesis genes promote growth and virulence in invasive pneumococcal disease.
4 Surveillance identified 35,192 cases of invasive pneumococcal disease.
5 at contributes to morbidity and mortality of invasive pneumococcal disease.
6 ferred protection against recolonization and invasive pneumococcal disease.
7 cedented success in controlling vaccine-type invasive pneumococcal disease.
8 and adults who had recovered from documented invasive pneumococcal disease.
9 ation with Streptococcus pneumoniae precedes invasive pneumococcal disease.
10 sease have a 600-fold increased incidence of invasive pneumococcal disease.
11 Adults infected with HIV have high rates of invasive pneumococcal disease.
12 such as malaria, HIV/AIDS, tuberculosis, and invasive pneumococcal disease.
13 ted subjects who had recently recovered from invasive pneumococcal disease.
14 o examine the association between asthma and invasive pneumococcal disease.
15 laboratory-based program of surveillance for invasive pneumococcal disease.
16 ates and demographic data from patients with invasive pneumococcal disease.
17 s, persons with AIDS remain at high risk for invasive pneumococcal disease.
18 n nine sites in seven European countries for invasive pneumococcal disease.
19 Asthma is an independent risk factor for invasive pneumococcal disease.
20 nst pneumococcal carriage, otitis media, and invasive pneumococcal disease.
21 could be at substantially increased risk of invasive pneumococcal disease.
22 these mutant genotypes were associated with invasive pneumococcal disease.
23 include those at highest risk for death from invasive pneumococcal disease.
24 all ages are disproportionately affected by invasive pneumococcal disease.
25 The primary endpoint was first event invasive pneumococcal disease.
26 coccus pneumoniae provide protection against invasive pneumococcal disease.
27 omen with (n = 21) or without (n = 33) prior invasive pneumococcal disease.
28 ic in these patients who are at high risk of invasive pneumococcal disease.
29 de and timing of indirect effects of PCVs on invasive pneumococcal disease.
30 y activity, thus affecting the resistance to invasive pneumococcal disease.
31 not rescue cigarette smoke-exposed mice from invasive pneumococcal disease.
32 s far unrecognized role in the resistance to invasive pneumococcal disease.
33 e PCV13 can expect substantial reductions in invasive pneumococcal disease.
34 patients, in whom we identified 320 cases of invasive pneumococcal disease.
35 to identify community-acquired pneumonia and invasive pneumococcal disease.
36 ed in hearts of mice that had recovered from invasive pneumococcal disease.
37 eumococcal community-acquired pneumonia, and invasive pneumococcal disease.
38 ealth England funds national surveillance of invasive pneumococcal disease.
39 e (SCD) have significantly increased risk of invasive pneumococcal disease.
40 l, active, laboratory-based surveillance for invasive pneumococcal disease.
41 hat contribute to cardiac dysfunction during invasive pneumococcal disease: (1) cell wall-mediated in
43 seline, there was a 56% overall reduction in invasive pneumococcal disease (15.63 vs 6.85 per 100,000
44 94.8) and against antibiotic non-susceptible invasive pneumococcal disease (65.6%, 44.9 to 78.7).
45 Persons with asthma had an increased risk of invasive pneumococcal disease (adjusted odds ratio, 2.4;
46 uded vaccine effectiveness against all-cause invasive pneumococcal disease, against antibiotic non-su
49 se is associated with the overall decline in invasive pneumococcal disease among Alaska Native childr
54 e was associated with an overall decrease in invasive pneumococcal disease among HIV-infected adults,
55 is the strongest independent risk factor for invasive pneumococcal disease among immunocompetent, non
60 52% (95% CI -12 to 79) against all-serotype invasive pneumococcal disease and 94% (44 to 100) for se
61 been associated with decreases in PCV7-type invasive pneumococcal disease and nasopharyngeal (NP) ca
62 r than age 2 years have the highest rates of invasive pneumococcal disease and play an important role
63 atients with proven (blood culture-positive) invasive pneumococcal disease and pneumonia of unknown e
64 nization of mice with GlpO protected against invasive pneumococcal disease and provided additive prot
66 antibodies to PotD confer protection against invasive pneumococcal disease and that this protein shou
67 disease, against antibiotic non-susceptible invasive pneumococcal disease, and among children with a
68 ncy virus (HIV) infection increases rates of invasive pneumococcal disease, and its effect on coloniz
69 mately half of otherwise healthy adults with invasive pneumococcal disease are cigarette smokers.
70 ents who were 18 to 64 years old and who had invasive pneumococcal disease (as defined by the isolati
71 , Vietnam and several African countries with invasive pneumococcal disease, bacteremia, malaria and t
73 tios (IRRs) for vaccine and non-vaccine type invasive pneumococcal disease between July, 2013, and Ju
75 ommunity-acquired pneumonia and vaccine-type invasive pneumococcal disease but not in preventing comm
76 Patients with AIDS have a high incidence of invasive pneumococcal disease, but no population-based d
77 Older adults are at high risk of developing invasive pneumococcal disease, but the optimal timing an
79 propose that cigarette smoke predisposes to invasive pneumococcal disease by suppressing inflammator
80 i) different assumptions about the number of invasive pneumococcal disease cases adjusted for the inc
81 set of electronically reported and serotyped invasive pneumococcal disease cases in England and Wales
86 ency virus (HIV), the estimated incidence of invasive pneumococcal disease caused by PCV7 serotypes d
88 ave millions of lives annually by preventing invasive pneumococcal disease caused by Streptococcus pn
89 ever, we noted no changes in either group in invasive pneumococcal disease caused by the additional 1
90 mate temporal indirect effects by pooling of invasive pneumococcal disease changes by serotype and se
91 erimental or observational studies reporting invasive pneumococcal disease changes following PCV intr
92 t the potential differences in prevention of invasive pneumococcal disease compared with nonbacteremi
96 for preventing vaccine-type specific CAP and Invasive Pneumococcal Disease declined from 65% to 40% f
97 lent pneumococcal conjugate vaccine, overall invasive pneumococcal disease decreased 67% in Alaska Na
98 ction of the PCV programme, the incidence of invasive pneumococcal disease decreased by 55% (95% CI 3
99 In the 2-4 years age group, the incidence of invasive pneumococcal disease decreased by 56% (95% CI 2
100 en 1998 and 2002, annual incidence rates for invasive pneumococcal disease decreased from 19.0 to 12.
103 e children have some of the highest rates of invasive pneumococcal disease documented in the world.
104 There is, however, evidence of increasing invasive pneumococcal disease due to non-PCV13 serotypes
108 PnCRM7 vaccine prevents vaccine serotype invasive pneumococcal disease even in a high risk popula
109 We calculated cumulative incidence rates for invasive pneumococcal disease for 1994-2002 using popula
110 ounger than 5 years with suspected or proven invasive pneumococcal disease from 18 hospitals or insti
111 olates obtained from pediatric patients with invasive pneumococcal disease from 1994 to 2014 and 48 i
113 r children in October 2000, the incidence of invasive pneumococcal disease has declined dramatically,
115 ervational study of adults hospitalized with invasive pneumococcal disease in 2 Spanish hospitals was
119 mbian PCV programme reduced the incidence of invasive pneumococcal disease in children aged 2-59 mont
122 veness of two or more doses of PCV13 against invasive pneumococcal disease in children with HIV infec
123 ducing high-valency PCVs on the incidence of invasive pneumococcal disease in children younger than 5
124 e pooled IRR was 0.53 (95% CI 0.43-0.65) for invasive pneumococcal disease in children younger than 5
127 13-valent pneumococcal conjugate vaccine on invasive pneumococcal disease in England and Wales 4 yea
128 nterview Survey (NHIS) to determine rates of invasive pneumococcal disease in healthy adults (> or =1
129 seline (1998 to 1999) and 2003, the ratio of invasive pneumococcal disease in HIV-infected adults to
130 redisease alpha-PLY titer is associated with invasive pneumococcal disease in HIV-seropositive inject
132 conducted population-based surveillance for invasive pneumococcal disease in individuals aged 2 mont
133 After licensure of a conjugate vaccine for invasive pneumococcal disease in infants, new conjugate
134 from active population-based surveillance of invasive pneumococcal disease in metropolitan Atlanta we
135 was a report of the decreased occurrence of invasive pneumococcal disease in patients being provided
137 atins may be of prophylactic benefit against invasive pneumococcal disease in patients with SCD and,
139 to conduct population-based surveillance for invasive pneumococcal disease in select regions of the A
142 We measured the effect of these vaccines on invasive pneumococcal disease in The Gambia where the 7-
143 the experience at children's hospitals with invasive pneumococcal disease in the years pre- and post
145 ly reduced the incidence of vaccine-serotype invasive pneumococcal disease in young children and in u
148 3, the model suggests a reduction in overall invasive pneumococcal disease incidence in all cases.
151 ugate vaccine use would cause an increase in invasive pneumococcal disease incidence, while replacing
155 Although blacks remain at higher risk of invasive pneumococcal disease, introduction of childhood
156 monitor post-PCV changes in the incidence of invasive pneumococcal disease (IPD) among children under
157 e impact of the 7-valent PCV on all-serotype invasive pneumococcal disease (IPD) among children was r
158 we assessed the serotype-specific burden of invasive pneumococcal disease (IPD) among immunocompromi
159 haracteristics, and serotype distribution of invasive pneumococcal disease (IPD) among Navajo childre
160 Certain chronic diseases increase risk for invasive pneumococcal disease (IPD) and are indications
161 e USA and resulted in dramatic reductions in invasive pneumococcal disease (IPD) and moderate increas
162 r roles during early stages of infection and invasive pneumococcal disease (IPD) are less well define
163 coccal serotype dynamics among children with invasive pneumococcal disease (IPD) as predicted by the
164 onjugate vaccine (PCV) in protecting against invasive pneumococcal disease (IPD) calls for alternate
167 ugate vaccine to the United States, rates of invasive pneumococcal disease (IPD) caused by serotype 6
170 ectively) are highly effective in preventing invasive pneumococcal disease (IPD) caused by vaccine se
175 e, but direct comparisons of impacts against invasive pneumococcal disease (IPD) in equivalent popula
177 the effectiveness of >/=2 PCV7 doses against invasive pneumococcal disease (IPD) in human immunodefic
179 ent pneumococcal conjugate vaccine (PCV7) on invasive pneumococcal disease (IPD) in infants aged <90
180 tion, outcome, and quality of life lost from invasive pneumococcal disease (IPD) in the context of th
181 e serotype 1 is one of the leading causes of invasive pneumococcal disease (IPD) in West Africa, with
183 mber 2006 has markedly reduced the burden of invasive pneumococcal disease (IPD) including meningitis
187 irulence proteins in pediatric patients with invasive pneumococcal disease (IPD) is a valuable approa
190 ococcal conjugate (PCV7) vaccine's impact on invasive pneumococcal disease (IPD) is well described, b
191 ng 594 Streptococcus pneumoniae serotype 19A invasive pneumococcal disease (IPD) isolates collected f
192 alent pneumococcal conjugate vaccine (PCV7), invasive pneumococcal disease (IPD) rates among blacks w
194 Winnipeg, Canada, experienced a doubling of invasive pneumococcal disease (IPD) rates, with a signif
195 rmines the propensity of an isolate to cause invasive pneumococcal disease (IPD) remains unknown.
196 to assess the value of molecular assays for invasive pneumococcal disease (IPD) surveillance in Sout
197 y syndrome (AIDS) have a higher incidence of invasive pneumococcal disease (IPD) than other adults, a
198 vice to all children within the program with invasive pneumococcal disease (IPD) to confirm an adequa
199 ect of these programs on the epidemiology of invasive pneumococcal disease (IPD) to determine if PCV-
200 ut pneumococcal population genomics in adult invasive pneumococcal disease (IPD) under vaccine pressu
201 tibody titers and resistance of mice against invasive pneumococcal disease (IPD) was determined.
203 es (PCVs) are highly effective in preventing invasive pneumococcal disease (IPD), but deaths due to I
204 This study aimed to estimate, following invasive pneumococcal disease (IPD), the proportion of c
205 considerably to the burden of pneumonia and invasive pneumococcal disease (IPD), with the effectiven
216 14, 18C, 19F, and 23F, dramatically reduced invasive pneumococcal disease (IPD); however, the effect
217 ia, nonbacteremic pneumonia and nonpneumonia invasive pneumococcal diseases (IPD) in the pre-PCV era.
219 e sought to determine whether seasonality of invasive pneumococcal disease is caused by increased nas
220 njugate vaccines in infants, among whom most invasive pneumococcal disease is vaccine-preventable.
221 e (PCV7) in 2000 reduced macrolide-resistant invasive pneumococcal disease (MR-IPD) due to PCV7 serot
222 th (July 1-June 30) for all-cause pneumonia, invasive pneumococcal disease, non-invasive pneumococcal
223 fficacy, 45.0%; 95.2% CI, 14.2 to 65.3), and invasive pneumococcal disease occurred in 7 persons in t
225 among younger adults (eg, the proportion of invasive pneumococcal disease occurring in adults < 65 y
227 overed by PCV13 in a cohort of patients with invasive pneumococcal disease of respiratory origin and
230 igarette smoking is a strong risk factor for invasive pneumococcal disease, the underlying mechanisms
231 We assessed vaccine effectiveness against invasive pneumococcal disease using the indirect cohort
232 Among at-risk children, rate ratios for invasive pneumococcal disease (vs children without at-ri
233 existing conditions, the annual incidence of invasive pneumococcal disease was 4.2 episodes per 10,00
235 r more doses of PCV13 against PCV13-serotype invasive pneumococcal disease was 85% (95% CI 37 to 96)
236 Vaccine effectiveness against PCV7-serotype invasive pneumococcal disease was 87% (95% CI 38 to 97)
238 Population-based prospective surveillance of invasive pneumococcal disease was done in Southern Calif
239 d mean times to attaining a 90% reduction in invasive pneumococcal disease were 8.9 years (95% credib
240 study period, 173 of 1207 episodes (14%) of invasive pneumococcal disease were identified as PM; 76
241 atric patients in Bamako, Mali, 106 cases of invasive pneumococcal disease were identified from June
242 cal disease, 10 age-matched controls without invasive pneumococcal disease were randomly selected fro
243 data from population-based surveillance for invasive pneumococcal disease with data from the 1990 US
244 Native children are experiencing replacement invasive pneumococcal disease with serotypes not covered
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