143 views

Uploaded by Vishal Kumar

kjbj

- Composition differences between organic and conventional meat: a systematic literature review and meta-analysis
- Hanson 2009-02 Risk Assessment Canadian Psychology
- Statistical Data Science (Gnv64)
- Dean Radin et al- Assessing the Evidence for Mind-Matter Interaction Effects
- Pharmacovigilantism and Avandia
- CAP PCT CURB 65.pdfdg
- PSA velocity article - JNCI
- Receiving Operating Caracterisitcs
- Systematic review
- Summer 2006 Promoting Academic Success Program: Influence on WASL Retake Scores—Revised
- A Meta-Analysis of Psychodynamic Psychotherapy Outcomes
- RDW prognosis PICU.pdf
- jurnal kdm
- Clozapine v. First and Second Generation Antipsychotics in Treatment-refractory Schizophrenia Systematic Review and Meta-Analysis
- JGR.pdf
- 372455 Interactive Datamining
- Risk Score
- AAC_Chap_1_20100304
- Tips on Critical Appraisal of Evidence
- Lembar Jawaban Ebm Evlin Kohar

You are on page 1of 24

1

1.1

midas command

Description

midas is a comprehensive program of statistical and graphical routines for undertaking meta-analysis of diagnostic test performance in Stata. The index and reference tests (gold standard) are dichotomous. Primary data synthesis is performed within the bivariate mixed-eects regression framework focused on making inferences about average sensitivity and specicity. The bivariate approach was originally developed for treatment trial meta-analysis (Houwelingen et al. 1993; van Houwelingen et al. 2002) and modied for synthesis of diagnostic test data using an approximate normal withinstudy model (Reitsma et al. 2005; Riley et al. 2007a,b, 2008; Arends et al. 2008). An exact binomial rendition (Chu and Cole 2006; Riley et al. 2007b; Arends et al. 2008) of the bivariate model assumes independent binomial distributions for the true positives and true negatives conditional on the sensitivity and specicity in each study. Likelihood-based estimation of the exact binomial approach may be performed by adaptive gaussian quadrature using Stata-native xtmelogit command (Stata release 10) or gllamm (Rabe-Hesketh et al. 2004, 2002), user-written command, both with readily available post-estimation procedures for model diagnostics and empirical Bayes predictions. Additionally, midas facilitates exploratory analysis of heterogeneity (unobserved, threshold-related and covariate etc.), publication and other precision-related biases. Bayes nomograms, likelihood-ratio matrices, and probability modifying plots may be derived and used to guide patient-based diagnostic decision making.

1.2

Syntax

if in , options

The required varlist is the data from the contingency tables of index and reference test results. The user provides the data in a rectangular array containing variables for the 2x2 elements a, b, c and d. Each data row contains the 2x2 data for one observation(i.e. study). The varlist MUST contain variables for a, b, c and d in that order:

1.3

Options

nip(integer) species the number of integration points used for maximum likelihood estimation based on adaptive gaussian quadrature. Default is set at 1 for midas even though the default in xtmelogit is 7. Higher values improve accuracy at the expense of execution times. Using xtmelogit with nip(1), model will be estimated by Laplacian approximation. This decreases substantially computational time and yet provides reasonably valid xed eects estimates. It may, however, produce biased estimates of the variance components. ebpred(for|roc) generates a forest plot or roc curve of empirical Bayes versus observed estimates of sensitivity and specicity. modchk(gof|bvn|inf|out|all) provides graphical model checking capabilities: modchk(gof) displays quantile plot of residual-based goodness-of t; modchk(bvn) displays Chi-squared probability plot of squared Mahalanobis distances for assessment of the bivariate normality assumption; modchk(inf) spikeplot for checking for particularly inuential observations using Cooks distance; modchk(out) displays a scatter plot for checking for outliers using standardized predicted random eects (standardized level-2 residuals); and modchk(all) provides a composite graphic of all four plots. Quality Assessment Options qtab(varlist ) creates a table showing frequency of methodological quality items. qbar(varlist ) calculates study-specic quality scores and plots a bargraph of methodological quality. qlab may be combined with qtab(varlist ) or qbar(varlist ) to use variable labels for table and bargraph of methodological items. Exploratory Graphics bivbox implements a bivariate generalization of the box plot for univariate data similar to the bivariate box plot(Rousseeuw et al. 1999). It is used to assess location, spread, correlation, skewness and tails of the data and for identifying possible outliers. chiplot creates a chiplot(Fisher and Switzer 2001) for judging whether or nor the paired performance indices are independent by augmenting the scatter plot with an auxiliary display. In the case of independence, the points will be concentrated in the central region, in the horizontal band indicated on the plot.

results(all) provide summary statistics for all performance indices, group-specic betweenstudy variances, likelihood ratio test statistics and other global homogeneity tests. results(het) provide group-specic between-study variances, likelihood ratio test statistics and other global homogeneity tests. results(sum) provides summary statistics for all performance indices i.e. sensitivity/specicity, positive/negative likelihood ratios and diagnostic score/odds ratios. table(dss|dlor|dlr) will create a table of study specic performance estimates with measure-specic summary estimates and results of homogeneity (chi-square) and inconsistency(I squared)tests. dss, dlr or dlor represent the paired performance measures sensitivity/specicity, positive/negative likelihood ratios and diagnostic score/odds ratios. Forest Plots Options id(varlist ) provides a label for studies allowing up to 4 variables. bforest(dss|dlr|dlor) creates summary graphs with study-specic(box) and overall(diamond) point estimates and condence intervals for each performance index pair using graph combine see [G] graph: graph combine. uforest(dss|dlr|dlor) creates univariate summary graphs with study-specic(box) and overall(diamond) point estimates and condence intervals allowed to extend between 0 and 1000 beyond which they are truncated and marked by a leading arrow. fordata adds study-specic performance estimates and 95% CIs to right y-axis. forstats adds heterogeneity statistics below summary point estimate. ROC Curve Options rocplane plots observed data in receiver operating characteristic space (ROC Plane) for visual assessment of threshold eect, a source of heterogeneity unique to diagnostic meta-analysis. The higher the cut-o value, the higher will be the specicity and the lower the sensitivity. This interdependence between sensitivity and specicity based

on threshold variability may be tested a priori using a rank correlation test such as Spearmans rho. In midas, the proportion of variation due to threshold eects is calculated as the squared correlation coecient estimated from the between-study covariance parameter. sroc(none|pred|conf|both) plots observed data points, summary operating sensitivityspecicity, and SROC curve without or with either or both of condence and prediction regions at default or specied condence level. sroc(nnoc|pnoc|cnoc|bnoc) plots observed data points, summary operating sensitivityspecicity without or with either or both of condence and prediction contours at default or specied condence level. No SROC curve is plotted with these choices. Heterogeneity Options galb(tpr|tnr|dlor|lrp|lrn) option produces Galbraith(radial) plots of standardized logit transformed proportion (tpr, tnr ) or log-transformed ratio(lrp, lrn and dlor) against the inverse of the its precision(x-axis). A regression line that goes through the origin is calculated, together with 95% boundaries (starting at +2 and -2 on the y-axis). Studies outside these 95% boundaries may be considered as outliers. regvars(varlist ) permits univariable meta-regression analysis of one or multiple dichotomous or continuous covariables, reporting results in table and forest plot Publication Bias Options pubbias When this option is invoked, midas performs linear regression of log odds ratios on inverse root of eective sample sizes as a test for funnel plot asymmetry in diagnostic meta-analysis. A non-zero slope coecient is suggestive of signicant small study bias (p value < 0.10). The regression line is superimposed on a funnel plot (see gure 8). Clinical Utility Options fagan(0-0.99) creates a plot showing the relationship between the prior probability specied by user, the likelihood ratio(combination of sensitivity and specicity), and posterior test probability. pddam(lbp ubp) produces a line graph of post-test probabilities versus prior probabilities between 0 and 1 using summary likelihood ratios. Summary unconditional

predictive values based on sensitivity analysis using uniformly distributed prior probabilities between lbp and ubp are estimated and displayed on graph. lrmatrix creates a scatter plot of positive and negative likelihood ratios with combined summary point. Plot is divided into quadrants based on strength-of-evidence thresholds to determine informativeness of measured test. Miscellaneous Options level(# ) species the signicance level for statistical tests, condence regions, prediction regions and condence intervals. mscale(# ) aects size of markers for point estimates on forest plots. scheme(string ) permits choice of scheme for graphs. The default is s2color. textscale(# ) allows choice of text size for graphs especially regarding labels for forest plots. zcf(# ) denes a xed continuity correction in the case where a study contains a zero cell during logit or log transformations only to calculate study-specic likelihood ratios and odds ratios. By default, midas adds 0.5 to each cell of a study where a zero is encountered. However, the zcf(# ) option allows the use of other constants between 0 and 1.

K Technical note

Although midas has pre-programmed graphical options, with Graph Editor (Stata Release 10 or later), you can change almost anything on your graph. You can add text, lines, arrows, and markers wherever you would like. You can right-click on any object to see a list of operations specic to the object and tool you are working with. This feature is most useful with the Pointer tool. However, there is no record of what you have done with the graph editor, so if you need to recreate the graph for some reason, you will have to redo everything that you have done with the graph editor. See [G] graph editor. K

1.4

Saved results

midas saves results as scalars in r() such as: r(mtpr) Mean sensitivity r(mtprse) standard error of mean sensitivity r(mtnr) Mean specicity r(mtnrse) Standard error of mean specicity r(mlrp) Mean likelihood ratio of a positive test result r(mlrpse) Standard error of mean likelihood ratio of a positive test result r(mlrn) Mean likelihood ratio of a negative test result r(mlrnse) Standard error of mean likelihood ratio of a negative test result r(mdor) Mean diagnostic odds ratio r(mdorse) Standard error of mean diagnostic odds ratio r(AUC) Area under summary ROC curve r(AUClo) Lower bound of area under summary ROC curve r(AUChi) Upper bound of area under summary ROC curve r(rho) Correlation between logits of sensitivity and specicity r(res1) Variance of logit of sensitivity r(res1se) Standard error of variance of logit of sensitivity r(res2) Variance of logit of specicity r(res2se) Standard error of variance of logit of specicity r(Islrt) Global inconsistency index from likelihood ratio test r(Islrtlo) Lower bound global inconsistency index r(Islrthi) Upper bound global inconsistency index

Example Dataset

This dataset was obtained as part of a systematic review and meta-analysis of the published literature on the staging performance of axillary positron emission tomography (FDG-PET) in breast cancer toward identication of the number, quality and scope of primary studies; quantication of overall classication performance (sensitivity and specicity), discriminatory power (diagnostic odds ratios) and informational value (diagnostic likelihood ratios); assessment of the impact of technical characteristics of test, methodological quality of primary studies and publication selection bias on estimates of diagnostic accuracy; and highlighting of any potential issues that require further research. We performed a comprehensive computer search of the English Language medical literature using primarily the PUBMED (MEDLINE) search engine and crosscitation with other databases to identify original peer-reviewed full-length human subject articles published between January 1, 1990 and January 31, 2008. Search was conducted using database-specic Boolean search strategies based on: (breast neoplasm OR breast cancer OR breast malignancy) AND (Positron emission tomography OR FDG-PET) AND (axillary staging OR axillary metastases OR axillary node metastases OR axillary node staging). Search strategies were augmented with a manual search of reference lists from identied articles and recent subject-area journals for additional articles. Details of the data set and 2 by 2 data for the rst 20 studies

as shown below were generated respectively with the describe and list commands of Stata:

. describe Contains data from f:\breastpet.dta obs: 39 vars: 33 size: 2,652 (99.9% of memory free) storage type str13 int int byte float float byte byte byte byte byte byte byte byte byte byte byte int byte byte byte byte int byte byte byte byte byte byte float str7 byte byte display format %-15s %8.0g %8.0g %8.0g %9.0g %9.0g %8.0g %10.0g %7.0g %8.0g %9.0g %9.0g %9.0g %7.0g %7.0g %10.0g %7.0g %8.0g %9.0g %8.0g %8.0g %8.0g %8.0g %8.0g %8.0g %8.0g %8.0g %9.0g %8.0g %9.2g %9s %10.0g %8.0g value label

variable name author year tp fp fn tn period prodesign ssize30 fulverif testdescr refdescr clindescr report consel brdspect blindref sampsize qscore age fast res dose upttime acquitime testcrit multiobs attcor axonly pmet Analysis patient blindtest

variable label first author Year of Publication True Positive False Positive False Negative True Negative Period of publication(before or after 1998) Prospective design Study size greater than 30 Full Verification of test results Satisfactory description of index test Statisfactory description of ref test Clinical Information Available Satisfactory reporting of results Consecutive selection of subjects Broad spectrum of disease blinded reference test interpretation Number Data Units Per Study Quality score Mean Age Prior Fasting of at leasst 4-6 hours Resolution of PET Camera Appropriate dose used Uptake Period specified Duration of image acqusition Test criteria described Multiple Observers Attenuation correction of PET images Dedicated axillary imaging Study-specfic Prevalence of axillary Metastases Unit of Data Analysis(Patient versus Nodes) Mode of analysis blinded index test interpretation

. list author year pmet sampsize tp fp fn tn in 1/20, sep(1) ab(32) abs noo author Tse Adler1 Hoh Crowe Avril Bassa Scheidhauer Utech Adler2 Palmedo Noh Smith Rostom Yutani1 Hubner Ohta Yutani2 Greco Schirrmeister Yang year 1992 1993 1993 1994 1996 1996 1996 1996 1997 1997 1998 1998 1999 1999 2000 2000 2000 2001 2001 2001 pmet .7 .47 .64 .5 .47 .81 .5 .35 .38 .3 .54 .42 .65 .38 .27 .59 .42 .43 .3 .33 sampsize 10 18 14 20 51 16 18 124 50 20 24 50 74 26 22 32 38 167 113 18 tp 4 8 6 9 19 10 9 44 19 5 12 19 42 8 6 14 8 68 27 3 fp 0 0 0 0 1 0 1 20 11 0 0 1 0 0 0 0 0 13 6 0 fn 3 1 3 1 5 3 0 0 0 1 1 2 6 2 0 5 8 4 7 3 tn 3 10 5 10 26 3 8 60 20 14 11 28 26 16 16 13 22 82 73 12

3

3.1

Model prediction and diagnostics

Post-estimation predictions may be obtained from the estimated model, parameter estimates and empirical Bayes estimates of the random eects with standard errors computed with the delta method. The predicted logits may then be transformed to obtain predictions of sensitivity and specicity. midas generates a forest plot or roc curve

10

of empirical Bayes versus observed estimates of sensitivity and specicity using the ebpred(for|roc) options. Figure 1 was obtained using the syntax below:

. midas tp fp fn tn, eb(for)

Model diagnostics are rarely performed because many non-statisticians and applied researchers consider meta-analysis as a data-processing procedure rather than a modeltting exercise (Sutton and Higgins 2008). However, with the application of complex likelihood-based meta-analytic models, it is important to evaluate possible model misspecication, goodness of t, and to identify outlying and possibly inuential data points. midas provides graphical model checking capabilities: quantile plot of residualbased goodness-of t; Chi-squared probability plot of squared Mahalanobis distances for assessment of the bivariate normality assumption; spikeplot for checking for particularly inuential observations using Cooks distance; a scatter plot for checking for outliers using standardized predicted random eects (standardized level-2 residuals); and composite graphic of all four plots such as gure 2 which was obtained using the syntax below:

. midas tp fp fn tn, modchk(all)

3.2

Quality Assessment

Methodologic quality of a study is the extent to which all aspects of a studys design and conduct can be shown to protect against systematic bias, nonsystematic bias that may arise in poorly performed studies, and inferential error. The recently developed quality assessment tool for diagnostic accuracy studies (QUADAS) (Whiting et al. 2005, 2004, 2003, 2006), is a rigorously constructed and validated tool that can be used by investigators undertaking new systematic reviews. The QUADAS tool consists of 14 items that cover patient spectrum, reference standard, disease progression bias, verication and review bias, clinical review bias, incorporation bias, test execution, study withdrawals, and intermediate results. Possible methods to address quality dierences are sensitivity analysis, subgroup analysis, or meta-regression analysis. Quality assessment may be summarized by stacked bars for each QUADAS item in a bar graph. midas provides the ability to represent the results of quality assessment by means of a bar graph. For example, gure 3 was obtained with the command syntax:

. midas tp fp fn tn, qbar(prodesign fulverif testdescr refdescr clindescr report > spectrum blindref blindtest) qlab

11

study

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39

0.00 0.25

Sensitivity

Specificity

0.50

0.75

1.00

0.00

0.25

0.50

0.75

1.00

MLE of mean sensitivity and specificity (solid vertical lines) Empirical Bayes (solid lines and markers) Observed data (dashed lines and markers)

Figure 1: Paired forest plot depiction of empirical Bayes predicted versus observed sensitivity and specicity

12

(a) GoodnessOfFit

0.75 0.50 0.25 0.00 0.00 0.25 0.50 0.75 Normal Quantile 1.00 Mahalanobis Dsquared 1.00 Deviance Residual 1.00 0.75 0.50 0.25 0.00 0.00

1.00

2.00 Cooks Distance

8

Standardized Residual(Diseased)

3.0

8

1.50

9

2.0 1.0

9 18 7 15 12 11 4 2 33 13 35 26 5 37 10 14 6 16 32 29 8 9 28 34 21 27 18 31 13 39 23 35 25 7 14 10 20 38 12 24 17 11 22 33 36 15 2 4 30 1 19 16 26 37 6 3 5 3 30 38 1 20 17 24 22 36 39 31 23 27 28

29

1.00

29

19 21 32 25

32

34

40

3.0

Figure 2: Graphical depiction of residual-based goodness-of-t, bivariate normality, inuence and outlier detection analyses

Statisfactory description of ref test Satisfactory reporting of results Satisfactory description of index test Representative Spectrum Prospective design Full Verification of test results Clinical Information Available Blinded reference test interpretation Blinded index test interpretation 0 20 40 60 percent Yes 80 100 No

Figure 3: Bar graph of quality assessment displaying stacked bars for each quality item including modied QUADAS criteria

Bivariate Boxplot

8

13

4

9

7 18 15 12

LOGIT_SENS

2

19 6 21 3 32 1 37 26

11 4 2 13 33 5 16 29 10 35

14

30 25 20 22 24 36 39 31

38 17

34 23 27 28

2 0 1 2 LOGIT_SPEC 3 4

Figure 4: Bivariate box plot with most studies clustering within the median distribution with seven outliers suggesting indirectly a lower degree of heterogeneity

3.3

Bivariate Association

midas uses a bivariate random eects modeling of sensitivity and specicity, therefore, it is expected that this pair of performance measures will be interdependent (see Figure 3). The bivariate box plot describes the degree of interdependence including the central location and identication of any outliers. The inner oval represents the median distribution of the data points. The outer oval represents the 95% condence bound. We obtained gure 4 with the syntax:

. midas tp fp fn tn, bivbox

It demonstrates a skewedness of the test performance measures toward a higher specicity with lower sensitivity, providing indirect evidence of some threshold variability.

3.4

Summary estimates of sensitivity and specicity and their 95% condence intervals can be calculated after anti-logit transformation of of the mean logit sensitivity and logit specicity and respective standard errors. These intervals take into account the heterogeneity beyond chance between studies (random eects model).

. midas tp fp fn tn, res(sum) nip(1)

14

SUMMARY PERFORMANCE ESTIMATES Parameter Sensitivity Specificity Positive Likelihood Ratio Negative Likelihood Ratio Diagnostic Odds Ratio Estimate 0.73 [ 0.96 [ 16.2 [ 0.29 [ 57 [ 95% CI 0.63, 0.92, 9.7, 0.21, 30, 0.80] 0.97] 27.3] 0.39] 107]

3.5

Heterogeneity Statistics

StudyId Veronesi/2006 Chung/2006 Stadnik/2006 Kumar/2006 GilRendo/2006 Weir/2005 Zornoza/2004 Wahl/2004 Lovrics/2004 Inoue/2004 Fehr/2004 Barranger/2003 Van_Hoeven/2002 Rieber/2002 Nakamoto2/2002 Nakamoto1/2002 Kelemen/2002 Guller/2002 Danforth/2002 Yang/2001 Schirrmeister/2001 Greco/2001 Yutani2/2000 Ohta/2000 Hubner/2000 Yutani1/1999 Rostom/1999 Smith/1998 Noh/1998 Palmedo/1997 Adler2/1997 Utech/1996 Scheidhauer/1996 Bassa/1996 Avril/1996 Crowe/1994 Hoh/1993 Adler1/1993 Tse/1992 COMBINED

SENSITIVITY (95% CI) 0.37 [0.28 0.47] 0.60 [0.43 0.74] 0.80 [0.28 0.99] 0.44 [0.28 0.62] 0.85 [0.77 0.90] 0.28 [0.10 0.53] 0.84 [0.76 0.90] 0.61 [0.51 0.70] 0.36 [0.18 0.57] 0.60 [0.42 0.76] 0.67 [0.09 0.99] 0.21 [0.05 0.51] 0.25 [0.11 0.43] 0.80 [0.56 0.94] 0.53 [0.27 0.79] 0.47 [0.21 0.73] 0.20 [0.01 0.72] 0.43 [0.18 0.71] 0.68 [0.43 0.87] 0.50 [0.12 0.88] 0.79 [0.62 0.91] 0.94 [0.86 0.98] 0.50 [0.25 0.75] 0.74 [0.49 0.91] 1.00 [0.54 1.00] 0.80 [0.44 0.97] 0.88 [0.75 0.95] 0.90 [0.70 0.99] 0.92 [0.64 1.00] 0.83 [0.36 1.00] 1.00 [0.82 1.00] 1.00 [0.92 1.00] 1.00 [0.66 1.00] 0.77 [0.46 0.95] 0.79 [0.58 0.93] 0.90 [0.55 1.00] 0.67 [0.30 0.93] 0.89 [0.52 1.00] 0.57 [0.18 0.90] 0.73[0.63 0.80] Q =273.36, df = 38.00, p = 0.00 I2 = 86.10 [82.45 89.75] 0.0

SENSITIVITY

StudyId Veronesi/2006 Chung/2006 Stadnik/2006 Kumar/2006 GilRendo/2006 Weir/2005 Zornoza/2004 Wahl/2004 Lovrics/2004 Inoue/2004 Fehr/2004 Barranger/2003 Van_Hoeven/2002 Rieber/2002 Nakamoto2/2002 Nakamoto1/2002 Kelemen/2002 Guller/2002 Danforth/2002 Yang/2001 Schirrmeister/2001 Greco/2001 Yutani2/2000 Ohta/2000 Hubner/2000 Yutani1/1999 Rostom/1999 Smith/1998 Noh/1998 Palmedo/1997 Adler2/1997 Utech/1996 Scheidhauer/1996 Bassa/1996 Avril/1996 Crowe/1994 Hoh/1993 Adler1/1993 Tse/1992 COMBINED

SPECIFICITY (95% CI) 0.96 [0.91 0.99] 1.00 [0.81 1.00] 1.00 [0.48 1.00] 0.95 [0.84 0.99] 0.98 [0.95 1.00] 0.86 [0.65 0.97] 0.98 [0.92 1.00] 0.80 [0.74 0.85] 0.97 [0.89 1.00] 0.96 [0.85 0.99] 0.62 [0.38 0.82] 1.00 [0.81 1.00] 0.97 [0.86 1.00] 0.95 [0.75 1.00] 0.86 [0.64 0.97] 0.95 [0.76 1.00] 1.00 [0.69 1.00] 0.94 [0.71 1.00] 0.67 [0.30 0.93] 1.00 [0.74 1.00] 0.92 [0.84 0.97] 0.86 [0.78 0.93] 1.00 [0.85 1.00] 1.00 [0.75 1.00] 1.00 [0.79 1.00] 1.00 [0.79 1.00] 1.00 [0.87 1.00] 0.97 [0.82 1.00] 1.00 [0.72 1.00] 1.00 [0.77 1.00] 0.65 [0.45 0.81] 0.75 [0.64 0.84] 0.89 [0.52 1.00] 1.00 [0.29 1.00] 0.96 [0.81 1.00] 1.00 [0.69 1.00] 1.00 [0.48 1.00] 1.00 [0.69 1.00] 1.00 [0.29 1.00] 0.96[0.92 0.97] Q =217.71, df = 38.00, p = 0.00 I2 = 82.55 [77.65 87.44] 0.3

SPECIFICITY

1.0

1.0

Figure 5: Forest plot showing study-specic (right-axis) and mean sensitivity and specicity with corresponding heterogeneity statistics

The impact of unobserved heterogeneity is traditionally assessed statistically using the quantity I 2 . It describes the percentage of total variation across studies that is attributable to the heterogeneity rather than chance(Higgins and Thompson 2002).

15

I 2 can be calculated from heterogeneity statistic and the degrees of freedom (Higgins and Thompson 2002). Alternatively, for mixed models, it is the intraclass correlation coecient expressed as a percentage with similar interpretation and is implemented in midas separately for sensitivity and specicity. I 2 lies between 0% and 100%. A value of 0% indicates no observed heterogeneity, and values greater than 50% may be considered substantial heterogeneity. The main advantage of I 2 is that it does not inherently depend on the number of studies in the meta-analysis (Higgins and Thompson 2002). The midas output of heterogeneity statistics is shown below and was generated from the syntax:

. midas tp fp fn tn, res(het) nip(1) HETEROGENEITY STATISTICS Heterogeneity (Chi-square): LRT_Q = 146.822, df =2.00, LRT_p =0.000 Inconsistency (I-square): LRT_I2 = 99, 95% CI = [ 98- 99] Proportion of heterogeneity likely due to threshold effect = 0.11 Interstudy Interstudy Interstudy Interstudy variation variation variation variation in in in in Sensitivity: Sensitivity: Specificity: Specificity: ICC_SEN MED_SEN ICC_SPE MED_SPE = = = = 0.31, 0.76, 0.29, 0.75, 95% 95% 95% 95% CI CI CI CI = = = = [ [ [ [ 0.180.700.120.680.45] 0.83] 0.45] 0.84]

3.6

Within midas, forest plots can be created for each test performance parameter individually or may be displayed as paired plots, for example, sensitivity paired with specicity. The user has the option of displaying heterogeneity statistics within the forest plots using the option forstats. Figure 5 was obtained using the command syntax:

. midas tp fp fn tn, texts(0.60) bfor(dss) id(author year) ford fors

3.7

Based on parameters estimated by the bivariate model, several summary ROC linear regression lines based on either the regression of logit sensitivity on specicity, the regression of logit specicity on sensitivity, or an orthogonal regression line by minimizing the perpendicular distances may be derived. These lines can be transformed back to the original ROC scale to obtain a summary ROC curve. In midas, derived logit estimates of sensitivity, specicity and respective variances are used to construct a hierarchical summary ROC curve. midas has several options for the display of the ROC curve. For example, gure 6 was obtained by using the syntax below:

. midas tp fp fn tn, sroc(both)

16

1.0

15

7 18

11 4 12 2 13 35 10 33 14 37 6 16 21 3 29 526 19

Sensitivity

38 1

30

32

25

0.5

17 20 24 36 22 39 31

Observed Data

34 27 28 23

Summary Operating Point SENS = 0.73 [0.63 0.80] SPEC = 0.96 [0.92 0.97] SROC Curve AUC = 0.95 [0.92 0.96] 95% Confidence Contour 95% Prediction Contour

0.0 1.0

0.5 Specificity

0.0

Figure 6: Summary ROC curve with condence and prediction regions around mean operating sensitivity and specicity point

17

The summary ROC curve is displayed along with the observed study data. The dashed line around the summary point estimate, represents the 95% condence region. The area under the curve (AUROC), serves as a global measure of test performance. The AUROC is the average TPR over the entire range of FPR values. The following guidelines have been suggested for interpretation of intermediate AUROC values: low (0.5>= AUC <= 0.7), moderate (0.7 >= AUC <= 0.9), or high (0.9 >= AUC <= 1) accuracy (Swets 1988).

3.8

Meta-regression

Meta-regression, the use of regression methods to incorporate the eect of covarying factors on summary measures of performance, has been used to explore between-study heterogeneity in therapeutic studies. In diagnostic studies, likewise, heterogeneity in sensitivity and specicity can result from many causes related to denitions of the test and reference standards, operating characteristics of the test, methods of data collection, and patient characteristics. Covariates may be introduced into a regression with any test performance measure as the dependent variable. As with any meta-regression, however, the sample size will correspond to the number of studies in the analysis with small number of studies limiting the power of regression to detect signicant eects. The syntax below produces both tabular and graphical output (Figure 7):

. midas tp fp fn tn, reg(prodesign age qscore sampsize fulverif testdescr refd > escr clindescr report spectrum blindref blindtest) (output omitted ) Parameter prodesign age qscore sampsize fulverif testdescr refdescr clindescr report spectrum blindref blindtest category Yes No LRTChi2 2.73 . 7.18 4.84 0.83 0.03 . 1.79 . 0.61 . 6.75 . 2.75 . 1.15 . 8.35 . 25.80 . Pvalue 0.26 . 0.03 0.09 0.66 0.99 . 0.41 . 0.74 . 0.03 . 0.25 . 0.56 . 0.02 . 0.00 . I2 27 . 72 59 0 0 . 0 . 0 . 70 . 27 . 0 . 76 . 92 . I2lo 0 . 38 7 0 0 . 0 . 0 . 34 . 0 . 0 . 48 . 85 . I2hi 100 . 100 100 100 100 . 100 . 100 . 100 . 100 . 100 . 100 . 99 .

18

prodesign Yes No age qscore sampsize fulverif Yes No testdescr Yes No refdescr Yes No **clindescr Yes No report Yes No spectrum Yes No **blindref Yes No **blindtest Yes No 0.37 1.00 Sensitivity(95% CI)

*p<0.05, **p<0.01, ***p<0.001

**prodesign Yes No age qscore sampsize **fulverif Yes No testdescr Yes No refdescr Yes No clindescr Yes No ***report Yes No *spectrum Yes No **blindref Yes No **blindtest Yes No 0.85 1.00 Specificity(95% CI)

*p<0.05, **p<0.01, ***p<0.001

19

3.9

The funnel plot is generally considered a good exploratory tool for investigating publication bias (Light and Pillemer 1984), plotting a measure of eect size against a measure of study precision, appearing symmetric if no bias is present. However, assessment of such a plot is very subjective. Thus, non-parametric and parametric linear regression methods have been developed to formally test for such funnel plot asymmetry (Begg and Mazumdar 1994; Egger and Smith 1998; Harbord et al. 2006; Macaskill et al. 2001; Peters et al. 2006; Rucker et al. 2008; Schwarzer et al. 2007, 2002). Using these methods for assessing publication bias in diagnostic test studies may produce misleading results (Song et al. 2002; Deeks et al. 2005). Formal testing for publication bias may be conducted by a regression of diagnostic log odds ratio against 1/sqrt(eective sample size), weighting by eective sample size (Deeks et al. 2005), with P < .10 for the slope coecient indicating signicant asymmetry.

. midas tp fp fn tn, pubbias

yb Bias Intercept

t -0.74 7.85

.05

32 39 33 18 8 35

.1

36 31 30

19

27

13

38 9

12

1/root(ESS)

.15

34 25 28 22 14 11 4 2 7 10 20 15 24 16 17 26

.2

21

.25

23

6 37

.3

29 1

10

100

1000

Using the syntax above yields funnel plot with superimposed regression line as shown in gure 8. The statistically non-signicant p-value (0.89) for the slope coecient suggests symmetry in the data and a low likelihood of publication bias. However, the test is known to have low power (Deeks et al. 2005).

20

3.10

The clinical or patient-relevant utility of a diagnostic test is evaluated using the likelihood ratios to calculate post-test probability(PTP) based on Bayes theorem as follows: Pretest Probability=Prevalence of target condition PTP= LR pretest probability/[(1pretest probability) (1-LR)] This concept is depicted visually with Fagans nomograms (Fagan 1975). When Bayes theorem is expressed in terms of log-odds, the posterior logodds are linear functions of the prior log-odds and the log likelihood ratios. A Fagan plot (see gure 9) consists of a vertical axis on the left with the prior log-odds, an axis in the middle representing the log-likelihood ratio and an vertical axis on the right representing the posterior log-odds. Lines are then drawn from the prior probability on the left through the likelihood ratios in the center and extended to the posterior probabilities on the right. Figure 9 demonstrates that FDG-PET is very informative raising probability of axil0.1 0.2 0.3 0.5 0.7 1 2 3 5 7 10 20 30 40 50 60 70 80 90 93 95 97 98 99 99.3 99.5 99.7 99.8 99.9

Prior Prob (%) = 25 LR_Positive = 16 Post_Prob_Pos (%) = 84 LR_Negative = 0.29 Post_Prob_Neg (%) = 9

99.9 99.8 99.7 99.5 99.3 99 Likelihood Ratio 1000 500 200 100 50 20 10 5 2 1 0.5 0.2 0.1 0.05 0.02 0.01 0.005 0.002 0.001 98 97 95 93 90 80 70 60 50 40 30 20 10 7 5 3 2 1 0.7 0.5 0.3 0.2 0.1

Figure 9: Fagan plot lary breast metastases over 3-fold when positive from 25% and lowering the probability of disease to as low as 9% when negative. It was generated with the syntax:

. midas tp fp fn tn, fagan(0.25)

21

3.11

Informativeness may also be represented graphically by a likelihood ratio scattergram or matrix (Stengel et al. 2003). It denes quadrants of informativeness based on established evidence-based thresholds: 1. Left Upper Quadrant, Likelihood Ratio Positive > 10, Likelihood Ratio Negative <0.1: Exclusion & Conrmation 2. Right Upper Quadrant, Likelihood Ratio Positive >10, Likelihood Ratio Negative >0.1: Conrmation Only 3. Left Lower Quadrant, Likelihood Ratio Positive <10, Likelihood Ratio Negative <0.1: Exclusion Only 4. Right Lower Quadrant, Likelihood Ratio Positive <10, Likelihood Ratio Negative >0.1: No Exclusion or Conrmation The likelihood ratio scattergram (gure 10) shows summary point of likelihood ratios obtained as functions of mean sensitivity and specicity (Leeang et al. 2008) in the right upper quadrant suggesting that FDG-PET is useful for conrmation of presence of axillary metastatic disease (when positive) and not for its exclusion (when negative). This gure was generated with the midas syntax:

. midas tp fp fn tn, lrmat

3.12

The conditional probability of disease given a positive OR negative test, the so-called positive (negative) predictive values are critically important to clinical application of a diagnostic procedure. They depend not only on sensitivity and specicity, but also on disease prevalence (p ). The probability modifying plot is a graphical sensitivity analysis of predictive value across a prevalence continuum dening low to high-risk populations. It depicts separate curves for positive and negative tests. The user draws a vertical line from the selected pre-test probability to the appropriate likelihood ratio line and then reads the post-test probability o the vertical scale. General summary statistics have also been introduced (Li et al. 2007) for when it may be of interest to evaluate the eect of p on predictive values: unconditional positive and negative predictive values, which permit prevalence heterogeneity. These measures are obtained by integrating their corresponding conditional (on p) versions with respect to a prior distribution for p. The prior posits assumptions about the risk level in a hypothetical population of interest, e.g. low, high, moderate risk, as well as the heterogeneity in the population.

22

100

35 13 33 15

12 11 4 2

14 10 5

38 16

17

LUQ: Exclusion & Confirmation LRP>10, LRN<0.1 RUQ: Confirmation Only LRP>10, LRN>0.1 LLQ: Exclusion Only LRP<10, LRN<0.1 RLQ: No Exclusion or Confirmation LRP<10, LRN>0.1 Summary LRP & LRN for Index Test With 95 % Confidence Intervals

26 30 20 31

10

18 7

19 37 3 6

24 39 27 36 28 22

23 1 8 32 9 25

21 29

34

1 0.1

Negative Likelihood Ratio

1.0

Positive Test Result LR+ =16.24 [9.66 27.31] Negative Test Result LR =0.29 [0.21 0.39]

0.8

Posterior Probability

0.6

0.4

0.2

0.0 0.0

0.2

0.4

0.6

0.8

1.0

Prior Probability

Prevalence Heterogeneity Uniform Prior Distribution = [0.25 0.75] Unconditional NPV =0.76 [0.74 0.78] Unconditional PPV =0.93 [0.91 0.96]

Using the syntax above generates gure 11, which plots the relationship between preand post-test probability based on the likelihood of a positive (above diagonal line) or negative (below diagonal line) test result over the 0-1 range of pre-test probababilities.

23

Tests with more informative positive results have curves tending toward the (0,1) location while tests with more informative negative results produce curves toward the (1,0) location.

References

Arends, L. R., T. H. Hamza, J. C. Houwelingen, M. H. HeijenbrokKal, M. G. M. Hunink, and T. Stijnen. 2008. Bivariate Random Effects Meta-Analysis of ROC Curves. Med Decis Making 28: 621628. http://dx.doi.org/10.1177/0272989X08319957. Begg, C. B., and M. Mazumdar. 1994. Operating characteristics of a rank correlation test for publication bias. Biometrics 50: 10881101. Chu, H., and S. R. Cole. 2006. Bivariate meta-analysis of sensitivity and specicity with sparse data: a generalized linear mixed model approach. J Clin Epidemiol 59(12): 13312; author reply 13323. http://dx.doi.org/10.1016/j.jclinepi.2006.06.011. Deeks, J. J., P. Macaskill, and L. Irwig. 2005. The performance of tests of publication bias and other sample size eects in systematic reviews of diagnostic test accuracy was assessed. J Clin Epidemiol 58(9): 882893. http://dx.doi.org/10.1016/j.jclinepi.2005.01.016. Egger, M., and G. D. Smith. 1998. Bias in location and selection of studies. BMJ 316(7124): 6166. Fagan, T. J. 1975. Letter: Nomogram for Bayes theorem. N Engl J Med 293(5): 257. Fisher, N., and P. Switzer. 2001. Graphical assessment of dependence: Is a picture worth a 100 tests? American Statistician 55: 233239. Harbord, R. M., M. Egger, and J. A. C. Sterne. 2006. A modied test for small-study eects in meta-analyses of controlled trials with binary endpoints. Stat Med 25(20): 34433457. http://dx.doi.org/10.1002/sim.2380. Higgins, J. P. T., and S. G. Thompson. 2002. Quantifying heterogeneity in a metaanalysis. Stat Med 21(11): 15391558. http://dx.doi.org/10.1002/sim.1186. van Houwelingen, H. C., L. R. Arends, and T. Stijnen. 2002. Advanced methods in meta-analysis: multivariate approach and meta-regression. Stat Med 21(4): 589624. Houwelingen, H. C. V., K. H. Zwinderman, and T. Stijnen. 1993. A bivariate approach to meta-analysis. Stat Med 12(24): 22732284. Leeang, M., J. Deeks, C. Gatsonis, and P. Bossuyt. 2008. Systematic Reviews of Diagnostic Test Accuracy. Ann Intern Med 149: 889897. Li, J., J. Fine, and N. Safdar. 2007. Prevalence-dependent diagnostic accuracy measures. Statistics in Medicine 26: 32583273.

24

Light, L., and D. Pillemer. 1984. Summing Up: The science of reviewing reaearch. Cambridge, MA: Harvard University Press. Macaskill, P., S. D. Walter, and L. Irwig. 2001. A comparison of methods to detect publication bias in meta-analysis. Stat Med 20(4): 641654. http://dx.doi.org/10.1002/sim.698. Peters, J. L., A. J. Sutton, D. R. Jones, K. R. Abrams, and L. Rushton. 2006. Comparison of two methods to detect publication bias in meta-analysis. JAMA 295(6): 676680. http://dx.doi.org/10.1001/jama.295.6.676. Rabe-Hesketh, S., A. Skrondal, and A. Pickles. 2002. Reliable estimation of generalized linear mixed models using adaptive quadrature. Stata Journal 2: 121. . 2004. GLLAMM Manual. University of CaliforniaBerkeley, Division of Biostatistics, Working Paper Series. Paper No. 160. http://www.bepress.com/ucbbiostat/paper160/. Reitsma, J. B., A. S. Glas, A. W. S. Rutjes, R. J. P. M. Scholten, P. M. Bossuyt, and A. H. Zwinderman. 2005. Bivariate analysis of sensitivity and specicity produces informative summary measures in diagnostic reviews. J Clin Epidemiol 58(10): 982 990. http://dx.doi.org/10.1016/j.jclinepi.2005.02.022. Riley, R. D., K. R. Abrams, P. C. Lambert, A. J. Sutton, and J. R. Thompson. 2007a. An evaluation of bivariate random-eects meta-analysis for the joint synthesis of two correlated outcomes. Stat Med 26(1): 7897. http://dx.doi.org/10.1002/sim.2524. Riley, R. D., K. R. Abrams, A. J. Sutton, P. C. Lambert, and J. R. Thompson. 2007b. Bivariate random-eects meta-analysis and the estimation of between-study correlation. BMC Med Res Methodol 7: 3. http://dx.doi.org/10.1186/1471-2288-7-3. Riley, R. D., J. R. Thompson, and K. R. Abrams. 2008. An alternative model for bivariate random-eects meta-analysis when the within-study correlations are unknown. Biostatistics 9(1): 172186. http://dx.doi.org/10.1093/biostatistics/kxm023. Rousseeuw, P., I. Ruts, and J. W. Tukey. 1999. The bagplot, a bivariate boxplot. American Statistician 53: 382387. Rucker, G., G. Schwarzer, and J. Carpenter. 2008. Arcsine test for publication bias in meta-analyses with binary outcomes. Stat Med 27(5): 746763. http://dx.doi.org/10.1002/sim.2971. Schwarzer, G., G. Antes, and M. Schumacher. 2002. Ination of type I error rate in two statistical tests for the detection of publication bias in meta-analyses with binary outcomes. Stat Med 21(17): 24652477. http://dx.doi.org/10.1002/sim.1224. . 2007. A test for publication bias in meta-analysis with sparse binary data. Stat Med 26(4): 721733. http://dx.doi.org/10.1002/sim.2588.

25

Song, F., K. S. Khan, J. Dinnes, and A. J. Sutton. 2002. Asymmetric funnel plots and publication bias in meta-analyses of diagnostic accuracy. Int J Epidemiol 31(1): 8895. Stengel, D., K. Bauwens, J. Sehouli, A. Ekkernkamp, and F. Porzsolt. 2003. A likelihood ratio approach to meta-analysis of diagnostic studies. J Med Screen 10(1): 4751. Sutton, A. J., and J. P. T. Higgins. 2008. Recent Developments in Meta-Analysis. Stat Med 27: 625650. Swets, J. A. 1988. Measuring the accuracy of diagnostic systems. Science 240: 1285 1293. Whiting, P., R. Harbord, and J. Kleijnen. 2005. No role for quality scores in systematic reviews of diagnostic accuracy studies. BMC Med Res Methodol 5: 19. http://dx.doi.org/10.1186/1471-2288-5-19. Whiting, P., A. W. S. Rutjes, J. Dinnes, J. Reitsma, P. M. M. Bossuyt, and J. Kleijnen. 2004. Development and validation of methods for assessing the quality of diagnostic accuracy studies. Health Technol Assess 8(25): iii, 1iii234. Whiting, P., A. W. S. Rutjes, J. B. Reitsma, P. M. M. Bossuyt, and J. Kleijnen. 2003. The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews. BMC Med Res Methodol 3: 25. http://dx.doi.org/10.1186/1471-2288-3-25. Whiting, P. F., M. E. Weswood, A. W. S. Rutjes, J. B. Reitsma, P. N. M. Bossuyt, and J. Kleijnen. 2006. Evaluation of QUADAS, a tool for the quality assessment of diagnostic accuracy studies. BMC Med Res Methodol 6: 9. http://dx.doi.org/8-6-9.

- Composition differences between organic and conventional meat: a systematic literature review and meta-analysisUploaded byOscar Espinoza
- Hanson 2009-02 Risk Assessment Canadian PsychologyUploaded byalessiozoppi
- Statistical Data Science (Gnv64)Uploaded byChappal Chor
- Dean Radin et al- Assessing the Evidence for Mind-Matter Interaction EffectsUploaded byHtemae
- Pharmacovigilantism and AvandiaUploaded byNathan Schachtman
- CAP PCT CURB 65.pdfdgUploaded byAndi Bintang
- PSA velocity article - JNCIUploaded byDan Stein
- Receiving Operating CaracterisitcsUploaded bystriider
- Summer 2006 Promoting Academic Success Program: Influence on WASL Retake Scores—RevisedUploaded byWashington State Institute for Public Policy
- Systematic reviewUploaded byVivien Iacob
- A Meta-Analysis of Psychodynamic Psychotherapy OutcomesUploaded byNatalia Mchedlishvili
- RDW prognosis PICU.pdfUploaded byJonathan Welch
- jurnal kdmUploaded byAngga Ghail
- Clozapine v. First and Second Generation Antipsychotics in Treatment-refractory Schizophrenia Systematic Review and Meta-AnalysisUploaded byElianAmadea
- JGR.pdfUploaded bydr. M.F. Romdhoni
- 372455 Interactive DataminingUploaded byluli_kbrera
- Risk ScoreUploaded bySeptiandry Ade Putra
- AAC_Chap_1_20100304Uploaded bynitinpp7225
- Tips on Critical Appraisal of EvidenceUploaded byxanderalelim
- Lembar Jawaban Ebm Evlin KoharUploaded bybetapduunsri14
- A REVIEW ON EVALUATION METRICS FOR DATA CLASSIFICATION EVALUATIONSUploaded byLewis Torres
- 3Uploaded byMuhammad Rehan Anis
- Mass Volume CurveUploaded byDeepakGujraniya
- 2005 frgc05Uploaded byluongxuandan
- Effects of Different Dietary Interventions on Blood PressureUploaded byFathanah Yanti Mph
- 18076048Uploaded byLavanya Priya Sathyan
- 18076048.pdfUploaded byLavanya Priya Sathyan
- nmi-suppl.1-2015-023Uploaded byIrvin Marcel
- 8.pdfUploaded byVajira Rohan
- Bio StatisticsUploaded byShashank Patil

- John C. Maxwell - Sometimes You Learn- Life Greatest Lessons Are Gained From Our Losses.pdfUploaded byMorenaMora
- [John C. Maxwell] There's No Such Thing as BusinesUploaded byGreBaptistChristianPre-School
- Electronics Ch13Uploaded byRobin Anderson
- Communication Electronics by Louis E. FrenzelUploaded byVishal Kumar
- Et Gate2013 Int CutoffUploaded byAkshay Mishra
- Solution 06Uploaded byKim Gerald Tejada
- Lect12-photodiode detectors.pdfUploaded bysatyabasha
- Fundamentals of RF and Microwave Noise Figure Measurements AN57_1Uploaded byjuancecconi
- Ques(3)Uploaded byVishal Kumar
- 455430920Website Work_2asda014Uploaded byVishal Kumar
- 229095378GATE 2015_Poster_FinalUploaded byVishal Kumar
- Interview Schedule for Engineering Service Examination 2013Uploaded byVishal Kumar
- Advt.No.08_2013_engUploaded bybabubhai23
- 274131404793Uploaded byVishal Kumar
- QUES(5)Uploaded byVishal Kumar
- EXP(5)Uploaded byVishal Kumar
- EXP(4)Uploaded byVishal Kumar
- EXP(3)Uploaded byVishal Kumar
- EXP(2)Uploaded byVishal Kumar
- EXP(1)Uploaded byVishal Kumar
- 14173_ch3Uploaded byvijay219
- Ques(4)Uploaded byVishal Kumar
- Ques(2)Uploaded byVishal Kumar
- Exp 1Uploaded byVishal Kumar
- GATE ECE-1992Uploaded byutpalwxyz
- 37613139wrd-recruitment-2013Uploaded byVishal Kumar
- made easyUploaded byVishal Kumar

- Positron Emission Tomography PaperUploaded byKurt Van Delinder
- Nursing ProcessUploaded byɹǝʍdןnos
- Chelation of Gadolinium Oxford 2009Uploaded bygasfgd
- Writing a better research article.docxUploaded byWaElinChawi
- Diet Diverticulite.pdfUploaded byAnonymous JIHJTWw4Th
- Pelvic PainUploaded byNitasha Maqsood
- Matary Surgical Instruments 2012 AllTebFamily.comUploaded byRaouf Ra'fat Soliman
- HBV ProphylaxisUploaded byAlex Cheung
- 2015 Toronto Consensus AGAUploaded byArturo Javier Fuentes
- Rhythms of LifeUploaded byjsenterprises
- BronchiectasisUploaded byien
- Pathogenesis of Micro and Macrovascular Complications of DiabetesUploaded byFrancesca Li
- Causes of Lactic AcidosisUploaded byerlinarachmawati
- Triads+in+Surgery+listUploaded byTalha Anwar
- Medscape EpisUploaded byifahInayah
- CSI Physical ExamUploaded bySympascho
- Improving Treatment and Liver FibrosisUploaded byKurnia Anhar
- CEC GuidelinesUploaded byHappy
- Effects of Conventional and Microwave Treatments on Inhibitory Activity and Structural Conformation of Trypsin Inhibitor ProteinUploaded byHoadaiKute
- WS5 IGRT 3D-4DUploaded bySoc. Portuguesa de Radioterapia Oncologia
- Asbestos FlyerUploaded byAlanCarolan
- Hypo Gonad IsmUploaded byemilyek
- HEALTH 1Uploaded byJoselito Requirme Agua
- mikedanziUploaded bypodx
- prostate careUploaded byRichie Florano Gruy
- The Interleukin 1ß Pathway in the Pathogenesis of OsteoarthritisUploaded bymskhatri3
- 1.Medical Imaging ProcessUploaded bySyakira Lurve Hana
- Cancer Aid Society (Internship)Uploaded byTanushka Gupta
- H pyeloriUploaded byMuhammad Asad
- Corby v. Unum Life Ins. Co.Uploaded byNorthern District of California Blog