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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2767_Библиотеки_им_академика_М_И_Перельмана
.pdf
Index
https://t.me/medicina_free
bivariate model (cont’d)
presenting findings 333, 334
sensitivity analysis
sparse data and atypical data sets
summary statistics
239–241, 266, 320–321
297–303
264–265, 289–291,
317–320,320
undertaking meta-analysis
blinding
176, 184
Boolean operators
112–113
Box-Cox transformations
broad questions
87–88
250
222
case-control studies
risk of bias and applicability assessment
177–178
study design
categorical data
2
Chi
statistic 223, 232
39, 39, 42
151
China National Knowledge Infrastructure
103
(CNKI)
CINAHL
103–104, 115
clinical decisions 25
clinical pathway
defining the clinical pathway
unclear and multiple clinical pathways
80–83, 81–82
83–84
clinical reference standard 45
clinical study reports (CSR) 133
Clopper–Pearson method 61
CNKI see China National Knowledge
Infrastructure
CoCites
106
comparative studies
drawing conclusions
evaluating medical tests
359–362, 368
28
measures of test accuracy 54, 68–71, 69
meta-analysis 206, 211, 216, 230–238,
272–301
presenting findings 330, 333–336, 334–335
risk of bias and applicability assessment 178–
181, 180–181, 188, 189
study design
45–47, 46–47
composite reference standard 44, 302
concealment of allocation 179
conclusions see drawing conclusions
conference abstracts 132
confidence intervals
data collection 143–144
drawing conclusions 355–356, 360, 361,
364,365
measures of test accuracy 60–61, 68
meta-analysis 208, 210, 211, 216, 218, 226,
237, 238, 287, 305, 311
plain language summary
presenting findings
392
334, 336, 337, 344–345,
346
risk of bias and applicability
conflicts of interest
14
171
confounders
drawing conclusions
meta-analysis
presenting findings
consecutive enrolment
362, 368
231
340
176–177
consensus
data collection
159
drawing conclusions 367
consumer involvement
13
continuous data
data collection
151
measures of test accuracy 54
review questions
91
controlled vocabulary 110–112
counts 54
coupled forest plots 208, 209, 267
covariates
data collection
151
meta-analysis 215, 222–229
cross-classification
measures of test accuracy
54, 56, 57
planning a systematic review of test
accuracy
11
study design 37
cross-referencing 133–134
cross-sectional studies
review questions
88
study design 37, 38–39
CSR see clinical study reports
c-statistic see area under the curve
data collection 131–167
2x2 contingency tables 134–135, 141–144,
142, 143, 145–146, 149–150, 161
checklist of data items 136, 136–137
concepts and definitions 132
correspondence with investigators 134–135
demographics 138
extracting and converting study
results 141–151
extracting covariates 151
extracting data from reports 157–160
flow and timing 140–141
400

Index
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global measures 144
index test
individual patient data
managing and sharing data and tools
missing data and partial verification bias
multiple index tests from same study
multiple reports and complex reviews
multiple thresholds and extracting data from
other information to collect 151–152
participant characteristics and
sources of data
studies versus reports as unit of
study methods 137–138
subgroups of patients
target condition and reference
test failures 147
tools for data collection 152–157, 153–154
what data to collect
data mining 120
decision analysis 24
deep learning 121
delayed verification
deviance information criterion (DIC) 223
diagnostic odds ratios (DOR)
data collection
drawing conclusions
measures of test accuracy 63, 64
meta-analysis 219, 223, 228, 269
presenting findings 330–332, 331
relative diagnostic odds ratio 228
risk of bias and applicability assessment 192
Diagnostic Test Accuracy Editorial Team 5
DIC see deviance information criterion
Discussion section 350, 365–366
dissertations databases 104
DOR see diagnostic odds ratios
dot plots 147–148, 148
drawing conclusions 349–376
applicability of findings to review
assessing the strength of the evidence
Authors’ conclusions 350, 369–374
139–140, 146, 148, 149–150
133, 150
160–163, 161–163
140, 148
148–150, 149–150
158–159, 160–163, 161–163
ROC curves or graphics
138–139
setting
132–135
133–134
interest
standard
question 369
352–362
140,145
44
144
147–148, 148
150
135–137
360
Discussion section
GRADE approach
heterogeneity
implications for practice
implications for research
incomplete body of evidence
precision of summary estimates
risk of bias and applicability assessment
359, 363–364, 367
strengths and weaknesses of included
studies
strengths and weaknesses of review
Summary of findings tables
353–358
ecological bias
eligibility/inclusion criteria
data collection
drawing conclusions 369
literature searches 120–121
meta-analysis
plain language summary 384
presenting findings 328
review questions 77, 76, 88–93
risk of bias and applicability assessment
193, 195
study design
Embase 102–103, 105, 110–111, 115
errata
data collection
literature searches 114
explanatory studies 48–49
false negatives/false positives
data collection 141–148
drawing conclusions 351
evaluating medical tests 23, 25
measures of test accuracy 57, 68, 70
meta-analysis 219, 297, 312, 315
plain language summary 381
presenting findings 330–332, 341
risk of bias and applicability assessment
187, 192
study design
field tags 111
fixed-effect meta-analysis 214, 302–303
flow and timing
data collection
presenting findings 340
risk of bias and applicability assessment
191–195, 194–195
350, 365–366
362–365
359–360, 364
370–373
373–374
361–362
360–361
351,
366–367
367–368
350–352,
340
133–134, 138
205, 239
178,
36, 39–40
132
43
140–141
401

Index
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flow diagrams 174–175, 175
forest plots
coupled forest plots
data collection
heterogeneity
meta-analysis
208, 209, 267
151
338
208, 209, 210, 267, 297–298,
302,338
reviews without meta-analysis
fraudulent studies
full-text reports
fully paired design
funding
14
114, 159–160
120–121
179
345
funnel plots 242
Gelman-Rubin statistic
global measures
264
144
gold standard 45, 187
Google Scholar 106–107
GRADE approach 352, 362–365
graphics/figures
data collection
147–148, 148
plain language summary 388–390, 389,
390,396
risk of bias and applicability assessment
196, 196
see also presenting findings
grey literature
100, 107
guidelines 105
heterogeneity
drawing conclusions 359–360, 364
meta-analysis
205, 214–215, 222–230, 225,
226–227, 229, 230, 299–302
plain language summary
391
presenting findings 333, 336–340, 338, 339, 344
review questions 77
hierarchical summary receiver operating
characteristic (HSROC) model 215–216,
219–220, 220, 221
analysis with small numbers of
studies 238–239
Bayesian estimation of the model 268–272,
270, 272, 294–296, 295, 311–315, 315
comparing index tests 234–235, 235
comparison of summary curves 291–296
estimation of a summary curve 266–272
fitting model using R 306–311, 310–311
fitting model using SAS 267, 268, 292
imperfect reference standard 317–320
investigating heterogeneity 222–230,
228–230, 227, 229, 230
monitoring convergence
multiple thresholds per study
270–271
221–222,
305–315, 310–311, 315
sensitivity analysis
sparse data and atypical data sets
specification of HSROC in rjags
summary statistics
undertaking meta-analysis
239–241, 272
299, 302
268–272
271, 295, 317–320, 320
249–250
HSROC see hierarchical summary receiver
operating characteristic model
2
I
statistic 214
incomplete reporting 108
inconclusive results 145–147
inconsistency see heterogeneity
indexing systems
99–100, 102, 108, 110–111
index test
data collection
drawing conclusions
139–140, 146, 148, 149–150
351–352, 362, 372–373
inconclusive index test results 55–56
literature searches 100–101
measures of test accuracy 53–56, 57
meta-analysis 230–238, 233, 233, 234,
237,238
plain language summary
380–383, 386–387,
391–392
presenting findings
review questions
330, 345
77, 82, 85, 90–91
risk of bias and applicability assessment
182–186, 185–186, 191
study design
individual participation data (IPD)
37–38, 48
133, 150
information specialists 100–101, 108
intermediate results 55
interpretation bias 184, 188
IPD see individual participation data
joint classification
68, 69
Jones multiple thresholds model 222, 305–315,
310–311
journal articles 132
keyword searching 112–113, 119
language bias 113, 361
latent class analysis (LCA)
meta-analysis 241, 316–321, 318, 320
study design 45
Latin American Caribbean Health Sciences
Literature (LILACS) database 103, 115
LCA see latent class analysis
402

Index
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letters 132
likelihood ratios
data collection
drawing conclusions
measures of test accuracy
meta-analysis
presenting findings
LILACS see Latin American Caribbean Health
Sciences Literature
linear mixed-effects modelling
linked summary receiver operating characteristic
plots
linking reports 134
literature searches 97–129
co-citation searching 105–106, 115
controlled vocabulary and text
words
designing search strategies 108–115
documenting and reporting the search
process
drawing conclusions
forward citation searching 105–106
fraudulent studies, retracted publications,
errata and comments
future developments 121
handsearching
information specialists 100–101, 108
keyword searching 112–113, 119
language, date and type of document
restrictions
minimizing risk-of-bias through search
methods
performance measures for search
strategies
review author roles 100–101
search filters 113
searching for studies 98–101
selecting relevant studies 119–121
sources to search 101–108
structuring the search strategy 109–110,
110,111
text word or keyword searching 112–113
working in partnership 100
logistic regression models 71
machine learning 120, 157
management studies 43
Markov chain Monte Carlo (MCMC)
simulation 223, 250, 263, 263, 270, 270,
295, 315, 317, 318
measures of test accuracy 53–72
143
352
61–63
216, 223, 229, 282
332, 332, 344
222
210
110–112
115–119, 118
367
114
105, 115
113
114–115
99
analysis of primary test accuracy study
comparative studies
concepts and definitions
confidence intervals
inconclusive index test results
interpretation
other measures
positivity thresholds
predictive values
pre-test and post-test probabilities
proportion with the target condition
receiver operating characteristic curves
66–68, 67
sensitivity and specificity
target condition 56
types of test data 54–55
medical test evaluation 21–33
biomarker discovery/development
clinical evaluations of test accuracy 28
early evaluations of test accuracy 27
how diagnostic tests affect patient
outcomes
purposes of medical testing 28–31, 28
test accuracy 23–24
test development 26–28
types of medical tests
MEDLINE 102–103, 105, 108, 112, 114, 121
meta-analysis 203–247, 249–325
aims for reviews of test accuracy 204
analysis with small numbers of
studies
Bayesian statistics 61, 221, 241, 250, 261–266,
270, 268–272, 270, 272, 287–291, 290–291,
294–296, 295, 311–320, 315, 318, 343
comparing index tests
237, 238
comparison of summary curves
comparison of summary points 272–291
data collection 150
drawing conclusions 352, 366, 368, 369
estimation of a summary curve 266–272
estimation of a summary point 251–266
facilitating convergence 297–301, 298
fitting hierarchical models 215–241
fixed-effect meta-analysis 214, 302–303
graphical and tabular presentation 208–211,
209–210
heterogeneity
226–227, 229, 230
imperfect reference standard 241, 316–321,
318,320
68–71, 69
53–54
60–61
55–56
59–60
61–64, 62, 64
64–65, 65
58
57–58, 64–65,67
24–26
22–23, 22
238–239
230–238, 233, 233,235,
205, 214–215, 222–230, 225,
56–64
59
58–59
26–27
291–296
403

Index
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meta-analysis (cont’d)
literature searches 105
methodological developments
monitoring convergence
270–271, 295, 317, 318
multiple thresholds per study
305–315, 310–311, 315
plain language summary
planning a systematic review of test
accuracy
planning the analysis
presenting findings
340–346,342
publication bias
regression analysis 223–224, 227–228
reviews of test accuracy versus reviews of
interventions
sensitivity analysis
320–321
simplifying hierarchical models
303, 305
sparse data and atypical data sets
297–298, 302, 303, 305
special topics
summary statistics 264–265, 271, 289–291,
295, 317–320, 320
verification bias
when not to use in a review 204–205
see also bivariate model; hierarchical
summary receiver operating
characteristic model
meta-epidemiology 172
misclassification 187, 192
missing data
data collection
drawing conclusions 361–362
risk of bias and applicability assessment 194
multiple-group studies 39–42, 40
multiple index tests
data collection 148–150, 149–150
risk of bias and applicability assessment 184
multiple thresholds model
data collection 147–148, 148
hierarchical summary receiver operating
characteristic model 221–222, 305–315,
310–311, 315
Jones method 222, 305–315, 310–311
Steinhauser method 222, 305–315, 310–311
narrative summary
drawing conclusions 366
15
207–208
329–336, 334–335,
242–243
205–206
239–241, 266, 272,
241–243
241–242
134–135, 140, 144, 148
241
263–264, 270,
221–222,
387
301–305, 302,
296–305,
presenting findings 346, 347
risk of bias and applicability assessment
writing a plain language summary
narrow questions
national databases
network meta-analysis
non-randomized comparative accuracy
studies
objectives
odds ratios see diagnostic odds ratios
online publications
ordinal data 54
overall accuracy
paired comparative accuracy studies
panel-based reference
partial verification bias 148, 192
participant selection see recruitment
patient outcomes
altering clinical decisions and actions
changes to time frames and
populations
direct test effects 25
disease progression/recurrence 31
drawing conclusions
evaluating medical tests 24–26
influencing patient and clinician
perceptions
study design
peer review
data collection
literature searches 107, 117
PICO format
pilot testing 156–157
PIT format 84–86
plain language summary 377–397
aims of review 382, 395
audience and writing style 378–379
case example
concepts and definitions 377–378
contents and structure 379–392
description of index test 382, 394
description of study benefits 381, 394–395
how up to date the evidence is 392, 397
included studies 383–384
key messages 380–381, 394
limitations of the evidence 391–392, 397
multiple index tests 386–387, 392
presenting findings 384–390, 389, 390,
395–397,396
87–88
103
236
47
86, 87
132
63
44–45, 46
25–26
372–373
26
36
132, 157
84
394–397, 396
377–397
46, 46
197
25
404

Index
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review methods 382, 395–397
title
380
planning a systematic review of test
accuracy
author team
Cochrane protocols
conduct and reporting expectations
data management and quality assurance
Diagnostic Test Accuracy Editorial Team
funding and conflicts of interest
keeping review up to date
proposing a new review
rationale 7
resources and support 13–15
software tools 15
specific features of Cochrane Reviews 5–6
title formats
training 14–15
point estimates
drawing conclusions
measures of test accuracy
meta-analysis 211, 225, 265, 284
presenting findings 332, 333, 344, 346
review questions 77
point-of-care tests 79
populations
data collection
evaluating medical tests 25–26
plain language summary 380
review questions
study design 39–42, 40
positivity thresholds
data collection
measures of test accuracy
meta-analysis 212, 219, 222, 305–315, 310,
311,315
risk of bias and applicability assessment
post-test odds/probabilities 59, 345
pragmatic studies 48–49
precision
drawing conclusions 360–361, 365
literature searches 99, 108
meta-analysis 270
plain language summary 392
risk of bias and applicability assessment 171
predictive tests 31
predictive value
data collection 141–143, 142, 143
drawing conclusions 352, 366
measures of test accuracy 58
meta-analysis 217
3–18
11–13
7–11
5–6
14
6
6–7, 8
7, 8
359–360, 364
68
138
77, 80–81, 84–85, 89
147–148
64, 65
6
5
183
positive/negative predictive value
141–143, 142, 143
presenting findings
predisposition tests
preprints
presenting findings
pre-test odds/probabilities
prevalence
prior distribution function 261, 269–270,
PRISMA-S/PRISMA-DTA 5, 116–119, 118
probability 59, 70–71, 345
prognostic tests 30
proof-of-concept studies
prospective studies 48
PsycINFO 103–104
publication bias
PubMed 102–103, 106, 111
132
comparisons of test accuracy
334–335
confidence intervals for differences in test
accuracy
description of included studies
individual and summary estimates of
testaccuracy
investigations of sources of heterogeneity
336–340, 338, 339
meta-analysis
311, 310–311, 317–320, 320, 338
methodological quality of included
studies
narrative summary 197
plain language summary 377–397
re-expressing summary estimates
numerically
results of the search 328
Summary of findings tables 211, 345,
350–352, 353–358
summary points
uncertainty and heterogeneity in summary
statistics
when meta-analysis cannot be
performed
see also forest plots; summary receiver
operating characteristic plots
341–344, 342
287, 294
evaluating medical tests
study design 41
drawing conclusions 361–362, 365
funnel plots 242
literature searches 98, 107
meta-analysis 242
334, 341–344, 342
29
327–348
336–337
329–333, 331, 331–332
208–211, 209–210, 265,308–
329
340–344, 342
211–214, 333–334, 334
332
344–346
59, 345
27
58,
333–336,
328–329
405

Index
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QUADAS-2/QUADAS-C see risk of bias and
applicability assessment
quality assurance
random-effects meta-analysis
randomization
comparative accuracy studies
enrolment
review questions
sampling
study design
RDOR see relative diagnostic odds ratio
receiver operating characteristic (ROC) plots
data collection
measures of test accuracy 54, 66–68, 67
risk of bias and applicability assessment
see also hierarchical summary receiver
operating characteristic model; summary
receiver operating characteristic plots
recruitment
data collection 133, 137–138
risk of bias and applicability assessment
176–182, 180–181
reference lists
reference management software
reference standard
clinical reference standard
composite reference standard 44
data collection
delayed verification 44
evaluating medical tests 23
gold standard 45, 187
latent class analysis
literature searches 99, 120
measures of test accuracy 54, 57
meta-analysis 241, 302, 316–321, 318,320
multiple reference standards 42–43, 43
panel-based reference 44–45
plain language summary 391
presenting findings 340, 345
review questions 81, 92–93
risk of bias and applicability assessment 182,
187–190, 189–190
study design 37–38, 42–45, 43
regional databases 103
regression analysis 223–224, 227–228
regulatory reviews 133
relative diagnostic odds ratio (RDOR) 228
relative risks 71
reliability 159
replacement tests 78
6
214, 226,303
46–47, 47
176–177
77
192
179
144, 147–148
100, 105, 115, 119
119
45
140–145, 145
45, 241, 316–321, 318, 320
183
reporting bias
drawing conclusions
literature searches
158–159
reports
representativeness
requests for information
retracted publications
retrospective studies
review bias
review questions
add-on tests
aims of systematic reviews of test
broad versus narrow questions 87–88
concepts and definitions 75–76
defining the clinical pathway
defining the review question 84–88
drawing conclusions 369
eligibility criteria 77, 80, 88–93
identifying the clinical problem
index test 77, 82, 85, 90–91
investigations of heterogeneity 77
objectives 86, 87
plain language summary
populations 77, 80–81, 84–85, 89
reference standard 81, 92–93
replacement tests 78
risk of bias and applicability
role of a new test 77–80
target condition 57–58, 84–86, 91–92
triage tests 78, 82
unclear and multiple clinical pathways
RevMan
data collection
meta-analysis 215–216, 221, 253, 265
planning a systematic review of test
risk of bias and applicability
bias and imprecision 171
biases in test accuracy studies: empirical
bias versus applicability 171–172
concepts and definitions 170
drawing conclusions 351, 359, 363, 367–368
literature searches 114–115
narrative summary of assessment 197
presenting findings 196, 196, 327–328, 345
QUADAS-2
391
accuracy
assessment
accuracy 15
assessment 169–201
evidence 172
applicability assessment 174
361
113
177
108
114
48
75–95
79
76–77
80–83, 81–82
77–84
380–381
169–172
142–143
83–84
406

Index
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background 173
flow and timing
flow diagrams
index test
participant selection
performing the QUADAS-2
assessment
reference standard
189–190
risk of bias assessment
using and tailoring QUADAS-2
QUADAS-C
background
flow and timing 193–195, 195
index test 182–186, 185–186
participant selection 178–181, 180–181
reference standard
study design 43
risk stratification 29
ROC see receiver operating characteristic
Rutter and Gatsonis HSROC model see
hierarchical summary receiver operating
characteristic model
sample size
sampling methods 137–138
scientific misconduct 159–160
screening tests 29
search filters
search recall 99, 108
sensitivity/specificity
data collection
drawing conclusions
evaluating medical tests 23, 27
literature searches 99, 115
measures of test accuracy
meta-analysis 205–241, 218, 218, 220, 221,
presenting findings 330–336, 331–332, 334,
risk of bias and applicability assessment
setting
data collection
plain language summary 391
review questions 80–81
software tools 15
sparse data sets
meta-analysis 296–305, 297–298, 302, 303, 305
plain language summary 387
141, 142, 143
238, 252, 261–273, 276, 282, 287,
297–311, 305, 310–311, 320–321
335, 337, 341–346, 342, 346
181, 192
191–195, 194–195
174–175, 175
182–186, 185–186
176–182, 194–195
175–176
182, 187–190,
173–174
174
173
188–189, 189–190
113
141–144, 142, 148
350–352, 360, 361,366
57–58, 64–65,67
138–139
SROC see summary receiver operating
characteristic
staging tests
stakeholder involvement
standard error
data collection
meta-analysis
Steinhauser multiple thresholds model
study design
basic design for test accuracy study
clinical reference standard
comparative studies 45–47, 46–47
composite reference standard 44
concepts and definitions 35
delayed verification 44
gold standard
latent class analysis 45
multiple groups of participants 39–42, 40
multiple reference standards 42–43, 43
panel-based reference
pragmatic versus explanatory studies 48–49
prospective versus retrospective studies 48
risk of bias and applicability assessment 178
study methods
subgroups of patients 150
subject headings 112
subject-specific databases 103–104
Summary of findings tables
drawing conclusions
meta-analysis 211
presenting findings 345
summary receiver operating characteristic
comparisons of test accuracy
drawing conclusions 351, 360
individual and summary estimates of test
meta-analysis 208–210, 210, 265, 276
planning a systematic review of test
reviews without meta-analysis 345, 346
see also hierarchical summary receiver
surveillance 31
systematic reviews of interventions 24
tables of findings see Summary of findings tables
target condition
data collection 140–145
29–30
12–13
144
224, 239
305–315, 310–311
35–51
38–39
45
45
44–45, 46
137–138
350–352, 353–358
(SROC) plots
334–336, 335
accuracy 330–332, 331
accuracy
operating characteristic model
15
222,
36–39,
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Index
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target condition (cont’d)
drawing conclusions 360
evaluating medical tests
literature searches
measures of test accuracy
plain language summary
planning a systematic review of test accuracy
6–7
presenting findings
review questions
risk of bias and applicability assessment
187–190
study design
test failures
test positives/test negatives
data collection
evaluating medical tests 23, 30
measures of test accuracy
meta-analysis 219
presenting findings 330–331
review questions 82–83, 91
risk of bias and applicability assessment
study design 42–43
text words 110–112
therapeutic monitoring 31
theses databases 104
time frames
timing see flow and timing
title
plain language summary
35–39, 42–43, 48
147
141–144
25–26
23, 27
100, 120
53–72
380–381, 391
340–346, 342
57–58, 84–86, 91–92
54, 56, 64–65,65
380
192
planning a systematic review of test accuracy
title searches
training
treatment efficacy
treatment selection
triage tests
trial registries
data collection
literature searches
two-group/two-gate studies
uncertainty
drawing conclusions
measures of test accuracy 60
plain language summary
presenting findings 332
unexpected findings 151
univariate tests 214
unverified participants 192
validity
variance–covariance matrix 255, 256, 260,261,
verification bias
see also partial verification bias
web searching
Wilson score interval
Youden’s index
119
14–15
31
30
78, 82
133
107–108, 115
40–41, 40
351, 363, 373
391
359
287, 292, 297, 301, 303, 303
241–242, 391
106–107
61
63–64, 308–311, 310–311
7, 8
408
Соседние файлы в папке Библиотека им академика М.И. Перельмана
