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1 IPD cases in PCV-eligible children aged <5 years (born s
2 IPD consists of five core databases, with the IMGT/HLA D
3 IPD due to non-PCV13 serotypes increased by 30% compared
4 IPD incidence was 12-fold higher (95% confidence interva
5 IPD incidence was highest in HIV-infected infants, rangi
6 IPD subjects were distinguished from APS with 94% specif
7 IPD was defined as a positive pneumococcal culture, poly
8 IPD were combined into 1 data set and an IPD meta-analys
9 IPD were pooled from six high-risk screening trials incl
10 IPD were provided from 25 trials, including 1 unpublishe
11 IPD were sought from investigators with eligible trials.
12 aggregated data: OR, 0.5; 95%% CI, 0.3-1.01; IPD, unstratified: OR, 0.7; 95% CI, 0.5-0.97; IPD, strat
13 nce was applied to postmortem sections of 10 IPD patients and 10 controls to quantify the abundance o
16 e the first release of the database in 2003, IPD-MHC has grown and currently hosts a number of specif
19 During the 8-year period, there were 3146 IPD cases and 150 IPD-related deaths (case fatality rate
27 ides was measured in plasma before and after IPD in HIV-infected individuals and compared to HIV-infe
28 onjugate vaccine (PCV) both before and after IPD, the proportion with IgG concentrations >/=0.35 micr
29 Vaccination with PCV before and/or after IPD was associated with lower IgG concentrations against
33 timely 3-dose PCV coverage of >92%, all-age IPD in Australia almost halved (IRR, 0.53; 95% confidenc
37 d 180 degrees ) can be discriminated from an IPD of 0 degrees , with higher thresholds indicating bet
40 e of IPD overall also declined by 12-32% and IPD caused by PCV13 minus PCV7 type IPD declined by 58-7
41 % (95% interval estimate [95% IE] 59-68) and IPD caused by PCV13 minus PCV7 serotypes declined by 93%
42 The pre-PCV7 proportion of VT carriage and IPD are the main determinants for the impact of PCV7 on
43 of vaccine serotype (VT) among carriers and IPD cases in the pre-PCV period, assuming that VT are el
44 uctions in vaccine-serotype colonization and IPD due to vaccine serotypes among children and women af
45 ple of controls but was found in all PAF and IPD patients, although with different skin innervation.
47 euritic p-syn inclusions differed in PAF and IPD, suggesting a different underlying pathogenesis; (3)
48 syn was a reliable in vivo marker of PAF and IPD; (2) neuritic p-syn inclusions differed in PAF and I
49 erotype-specific colonization prevalence and IPD incidence prior to and following childhood PCV immun
50 adjusted association between vaccination and IPD was protective (odds ratio [OR], 0.58; 95% confidenc
52 en years after pediatric PCV7 authorization, IPD due to PCV7 serotypes had decreased by 90% (95% CI,
53 used active population and laboratory-based IPD surveillance data from the Centers for Disease Contr
54 Retrospective analysis of population-based IPD surveillance data of the general population residing
55 te the observed negative association between IPD and the serotype 11A (ST11A) capsule O-acetyltransfe
56 9, and PhtE-pep40 were broadly recognized by IPD patient sera with prevalences of 96.4%, 92.9%, and 7
58 30 patients, including 16 well-characterized IPD patients and 14 patients fulfilling PAF diagnostic c
59 rminants for the impact of PCV7 on childhood IPD and can be combined in a simple model to provide pre
60 nst the reported impact of PCV7 on childhood IPD in high-income countries from a recent meta-analysis
61 l predicted the reported impact on childhood IPD of mature PCV programmes; the ratio of predicted and
65 eta-analyses of individual participant data (IPD) aim to collect, check, and reanalyze individual-lev
66 The aim of this individual participant data (IPD) meta-analysis (MA) was to assess the effects of ant
67 We conducted an individual participant data (IPD) meta-analysis of studies from sub-Saharan Africa to
69 1- and 2-stage individual participant data (IPD) meta-analysis, and a negative-control (paternal BMI
71 f aggregate and individual participant data (IPD), the latter of which was obtained by requesting ind
72 -effects model) and individual patient data (IPD) (logistic regression adjusted for confounders) were
80 s suggest that, while the risk of developing IPD may actually be decreased in patients with acute ast
81 t which a fixed interaural phase difference (IPD) of varphi (varied here between 30 degrees and 180 d
83 erentiation of idiopathic Parkinson disease (IPD) from multiple system atrophy (MSA) and progressive
84 denervation in idiopathic Parkinson disease (IPD) using (11)C-hydroxyephedrine ((11)C-HED) PET and de
85 all-serotype invasive pneumococcal disease (IPD) among children was reported to vary between high-in
91 onsusceptible invasive pneumococcal disease (IPD) decreased substantially after the US introduction o
93 rveillance of invasive pneumococcal disease (IPD) from 2002 for baseline and appropriate later compar
94 level data on invasive pneumococcal disease (IPD) from an active population-based surveillance system
95 pacts against invasive pneumococcal disease (IPD) in equivalent populations have not been performed.
98 ing causes of invasive pneumococcal disease (IPD) in West Africa, with ST618 being the dominant cause
100 patients with invasive pneumococcal disease (IPD) is a valuable approach to define novel vaccine cand
103 e's impact on invasive pneumococcal disease (IPD) is well described, but few reports exist on the add
104 ccine (PCV7), invasive pneumococcal disease (IPD) rates among blacks were twice the rates in whites.
105 ar assays for invasive pneumococcal disease (IPD) surveillance in South Africa from 2010 through 2012
106 idemiology of invasive pneumococcal disease (IPD) to determine if PCV-associated indirect protection
109 te, following invasive pneumococcal disease (IPD), the proportion of children with protective immunog
110 pneumonia and invasive pneumococcal disease (IPD), with the effectiveness of the 23-valent pneumococc
111 t in reducing invasive pneumococcal disease (IPD)-related morbidity and mortality, and whether seroty
127 ed through laboratory-based surveillance for IPD from 2005 through 2014 in South Africa was reviewed.
128 5 to 2012, population-based surveillance for IPD was conducted in Metropolitan Toronto and Peel Regio
129 .17-.22) were about 2-fold greater than for IPD due to extra serotypes in PCV13 (13v-non7v) in a sim
131 at increased risk of IPD and mortality from IPD compared with HUU children, especially as young infa
132 mass was unchanged in single SN neurons from IPD patients, we observed a significant reduction in the
133 nt reports suggest that mortality rates from IPD are unaffected in patients with asthma and that chro
136 idate genes and causal variants therein, how IPDs have been historically diagnosed, and how this is c
137 ve years after PPV23 program implementation, IPD incidence had declined significantly in immunocompro
138 timated a 28% reduction (95% CI, 18%-37%) in IPD-related 30-day mortality, from 3.4 deaths (95% CI, 3
139 solute differences and percentage changes in IPD incidence before and after the introduction of PCV13
140 We compared the model-predicted changes in IPD incidence with observed changes in IPD incidence, ac
141 es in IPD incidence with observed changes in IPD incidence, according to HIV status, in children aged
143 PCV (PCV13) were associated with declines in IPD rates in both sexes, rates of IPD after PCV13 were s
144 of mtDNA in respiratory chain deficiency in IPD, SN neurons, isolated with laser-capture microdissec
145 pe IPD in both races, overall disparities in IPD rates persisted because non-PCV7-type IPD rates are
146 ntroduction may reduce racial disparities in IPD, higher valency conjugate vaccines and strategies to
148 e in cardiac sympathetic neural integrity in IPD patients occurs at a modest rate over 2 y on (11)C-H
152 a better understanding of immune response in IPD and are worth evaluation in additional studies as po
155 response to many retinal insults, including IPDs, but the role of this increase in PR death is unkno
156 MBL2 polymorphisms did not predict increased IPD susceptibility in children born in Northern Europe.
158 uring the decade of PCV7 use (2000-2009), MR-IPD decreased rapidly until 2002 and subsequently stabil
159 -resistant invasive pneumococcal disease (MR-IPD) due to PCV7 serotypes (6B, 9V, 14, 19F, and 23F).
162 il the introduction of PCV13 in 2010 when MR-IPD incidence decreased further from 3.71 to 2.45/100000
164 PD cases responded to more proteins than non-IPD controls (8.6 +/- 8.4 vs 4.2 +/- 7.6 proteins; P = .
165 ; CI, .28-.44) differed from other 13v-non7v IPD (IRR, 0.73; CI, .35-1.48 for those aged <2 years and
166 observed cases of antibiotic-nonsusceptible IPD and cases that would have occurred if PCV13 had not
167 small increases in antibiotic-nonsusceptible IPD caused by non-PCV13 serotypes, no non-PCV13 serotype
168 to 2013, rates of antibiotic-nonsusceptible IPD caused by serotypes included in PCV13 but not in PCV
169 and 1327 cases of antibiotic-nonsusceptible IPD caused by serotypes included in PCV13 but not PCV7 w
175 ngs to other settings would depend on age of IPD onset, serotype profile, and timeliness of vaccinati
178 cant result in the only feasible analysis of IPD (unstratified model) (OR, 0.1; 95% CI, 0.0-0.4).
184 prospectively identified pediatric cases of IPD requiring hospitalization between 2005 and 2011 in 2
185 onvaccine serotype that is the main cause of IPD in many countries, including Nepal, Bangladesh, and
195 5 years and, particularly, the incidence of IPD caused by serotype 19A decreased dramatically follow
199 duction (P < .001), whereas the incidence of IPD due to the additional 6 serotypes in PCV13 and to no
200 ed and population-based data on incidence of IPD from the Active Bacterial Core surveillance (part of
203 PCV7 alone had been continued, incidence of IPD overall declined by 64% (95% interval estimate [95%
204 pproach to compare the reported incidence of IPD to that which would have been expected if PCV13 had
206 n, clinical characteristics, and outcomes of IPD in children with PCV13 and PCV7 vaccine failure.
207 e individual scan data, the probabilities of IPD, MSA, and PSP were computed and used to classify eac
208 ression models to estimate the proportion of IPD cases among adults aged >40 years that were caused b
210 overall IPD and estimated the proportion of IPD caused by serotypes included in the 13-valent pneumo
211 eclines in IPD rates in both sexes, rates of IPD after PCV13 were still significantly higher in male
216 We examined sex differences in rates of IPD, and trends after the introduction of pneumococcal c
224 e is increasing recognition that a number of IPDs are associated with severe pathologies, including a
228 e IPD rates on racial disparities in overall IPD and estimated the proportion of IPD caused by seroty
230 ith V-LRI seasonality, whereas non-pneumonia IPD peaked in autumn before V-LRI increase, suggesting d
231 t-Data Meta-analysis in Working Populations (IPD-Work) Consortium and open-access data archives.
232 s PPSV23 vaccine effectiveness in preventing IPD and the most resource-intensive type of community-ac
235 Compared with standard PRISMA, the PRISMA-IPD checklist includes 3 new items that address (1) meth
244 PCV13 introduction, dual macrolide-resistant IPD decreased 74.1% (incidence 0.32/100000 in 2013).
245 ses against all-serotype multidrug-resistant IPD was 96% (95% CI, 62%-100%) among HIV-uninfected chil
248 cessory genes identified among dual-serotype IPD isolates, four were common between isolate pairs.
250 assess factors associated with dual-serotype IPD, patient information obtained through laboratory-bas
251 was effective in preventing vaccine-serotype IPD in HIV-uninfected and HIV-exposed, uninfected childr
252 ial declines in overall and vaccine-serotype IPD in vaccinated children and in unvaccinated persons.
253 model-predicted changes in vaccine-serotype IPD incidence rates were similar to the observed changes
254 eness of >/=3 doses against vaccine-serotype IPD was 90% (95% CI, 14%-99%) among HIV-uninfected and 5
265 2006 preluded substantial alterations in the IPD population structure caused by serotype replacement.
266 (1) methods of checking the integrity of the IPD (such as pattern of randomization, data consistency,
284 cts of trends in PCV7-type and non-PCV7-type IPD rates on racial disparities in overall IPD and estim
285 eceived PPV23, and development of PPV23-type IPD was not associated with prior PPV23 vaccination (adj
292 is aim, we evaluated sera from children with IPD and age-matched controls against 141 20-mer syntheti
298 sectional study of infants aged <1 year with IPD enrolled in a national, laboratory-based surveillanc
299 included 468 cases younger than 5 years with IPD reported through routine surveillance to the NYC Dep
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