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Hi all,
I have a dataset for about 440 patients (identified by Patient) and each patient is randomly allocated to one of 2 different methods of surgery (Group). They are measured on a set of about 10 outcome variables (e.g. ROM) at 4 different time points (with no missing data): 1.) baseline (the two methods should not be significantly different) 2.) 6 weeks post-surgery (observations have the lowest values during the post-surgical recovery period, then generally improve from here on) 3.) 3 months 4.) 6 months One of 12 examiners measure a particular patient at a particular time point. It is not balanced, in that there is variation in the number of patients measured by each examiner, and most examiners only take measurements at 1 to 3 time points and a few of them were across the two different methods (but at different time points). A few examiners appear to consistently record higher observation values (and the biggest problem with this is at baseline), so I fitted examiner as a random effect using the MIXED procedure: MIXED ROM BY Time Group Examiner Patient /CRITERIA = CIN(95) MXITER(100) MXSTEP(5) SCORING(1) SINGULAR (0.000000000001) HCONVERGE(0, ABSOLUTE) LCONVERGE(0, ABSOLUTE) PCONVERGE (0.000001, ABSOLUTE) /FIXED = Time Group(Time) | SSTYPE(3) /METHOD = REML /EMMEANS = TABLES(OVERALL) /EMMEANS = TABLES(Time) /EMMEANS = TABLES(Time*Group) /RANDOM Examiner Patient | COVTYPE(VC) . The problem is the trend is still distorted (we expect an equal start for the two methods at baseline and a dip at 6 weeks). The marginal plots of Examiner*Time in GLM shows that some Examiners are contrary to the expected trend (e.g. higher measurements at 6 weeks post-surgery, some of which appear to be a problem with outliers). There are a few possible options I/we were thinking of: 1.) As two or three of the outcome variables are expected to be less affected by the surgery (and of less interest to the study), but still strongly affected by examiner effect, is there some way of obtaining the examiner effect from these variables to plug into the model for the other outcome variables? 2.) A method of time series analysis (I have never done this before, so I have no idea what it might do)? 3.) Need for a different variance structure that account for the heterogeneity of variance within examiner (those examiners that were contrary to expected trend appear to be less consistent)? I tried COV(UN) as suggested by someone in another forum (but without Patient as random effect as SPSS ran out of memory even when I "SET WORKSPACE=614800."). Thanks for your patience in getting this far and for any help/suggestions you can give :) ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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Nicola,
Instead of: /RANDOM Examiner Patient | COVTYPE(VC) Try using: /RANDOM INTERCEPT | SUBJECT(Patient) COVTYPE(VC) /RANDOM INTERCEPT | SUBJECT(Examiner) COVTYPE(VC) If I'm reading your note correctly, in both syntax specifications, you're requesting an estimate of the variance term for Patient and the variance term for Examiner, but in the first specification, it's producing a 452x452 (diagonal) covariance matrix and in the second it's producing two 1x1 matrices. Then, when you want to account for possible heterogeneity between examiners: /RANDOM INTERCEPT | SUBJECT(Patient) COVTYPE(VC) /RANDOM Examiner | COVTYPE(UN) And it will produce a 1x1 matrix with the variance term for Patient and a 12x12 covariance matrix for Examiner. That should, I think, solve your memory problems. Cheers, Alex -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Nicola Sent: Monday, February 23, 2009 8:42 PM To: [hidden email] Subject: Using MIXED to account for Examiner variability Hi all, I have a dataset for about 440 patients (identified by Patient) and each patient is randomly allocated to one of 2 different methods of surgery (Group). They are measured on a set of about 10 outcome variables (e.g. ROM) at 4 different time points (with no missing data): 1.) baseline (the two methods should not be significantly different) 2.) 6 weeks post-surgery (observations have the lowest values during the post-surgical recovery period, then generally improve from here on) 3.) 3 months 4.) 6 months One of 12 examiners measure a particular patient at a particular time point. It is not balanced, in that there is variation in the number of patients measured by each examiner, and most examiners only take measurements at 1 to 3 time points and a few of them were across the two different methods (but at different time points). A few examiners appear to consistently record higher observation values (and the biggest problem with this is at baseline), so I fitted examiner as a random effect using the MIXED procedure: MIXED ROM BY Time Group Examiner Patient /CRITERIA = CIN(95) MXITER(100) MXSTEP(5) SCORING(1) SINGULAR (0.000000000001) HCONVERGE(0, ABSOLUTE) LCONVERGE(0, ABSOLUTE) PCONVERGE (0.000001, ABSOLUTE) /FIXED = Time Group(Time) | SSTYPE(3) /METHOD = REML /EMMEANS = TABLES(OVERALL) /EMMEANS = TABLES(Time) /EMMEANS = TABLES(Time*Group) /RANDOM Examiner Patient | COVTYPE(VC) . The problem is the trend is still distorted (we expect an equal start for the two methods at baseline and a dip at 6 weeks). The marginal plots of Examiner*Time in GLM shows that some Examiners are contrary to the expected trend (e.g. higher measurements at 6 weeks post-surgery, some of which appear to be a problem with outliers). There are a few possible options I/we were thinking of: 1.) As two or three of the outcome variables are expected to be less affected by the surgery (and of less interest to the study), but still strongly affected by examiner effect, is there some way of obtaining the examiner effect from these variables to plug into the model for the other outcome variables? 2.) A method of time series analysis (I have never done this before, so I have no idea what it might do)? 3.) Need for a different variance structure that account for the heterogeneity of variance within examiner (those examiners that were contrary to expected trend appear to be less consistent)? I tried COV(UN) as suggested by someone in another forum (but without Patient as random effect as SPSS ran out of memory even when I "SET WORKSPACE=614800."). Thanks for your patience in getting this far and for any help/suggestions you can give :) ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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