Verifying the stroke-free phenotype by structured telephone interview

被引:120
作者
Meschia, JF
Brott, TG
Chukwudelunzu, FE
Hardy, J
Brown, RD
Meissner, I
Hall, LJ
Atkinson, EJ
O'Brien, PC
机构
[1] Mayo Clin Jacksonville, Dept Neurol, Jacksonville, FL 32224 USA
[2] Mayo Clin Jacksonville, Pharmacol Sect, Jacksonville, FL 32224 USA
[3] Mayo Clin Jacksonville, Clin Studies Unit, Jacksonville, FL 32224 USA
[4] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Biostat Sect, Rochester, MN 55905 USA
关键词
cerebral ischemia; transient; linkage (genetics); questionnaires; stroke; ischemic;
D O I
10.1161/01.STR.31.5.1076
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Case-control, cohort, and twin studies support a genetic contribution to ischemic stroke risk. Sibling pair linkage methods require identification of concordant or discordant siblings or both. We designed and tested a structured telephone interview to verify the stroke-free phenotype, Methods-A coordinator unaware of medical record data used an 8-item questionnaire to conduct a structured telephone interview of 70 outpatients aged >60 years. The questionnaire inquired about the sudden onset of deficits in strength, sensation, vision, and language. A subject was defined as stroke free by interview if responses to all items on the questionnaire were negative. Results of the telephone interview were compared with data obtained from a systematic medical record review (benchmark). Results-interview time was 5 minutes or less for all subjects. All subjects who began the interview completed it. Records were reviewed in all subjects. Medical record review detected ischemic stroke or transient ischemic attack (TIA), or both, in 5 patients (7%). There were no significant differences in sex distribution or risk factor rates in patients who were designated stroke free or not stroke free by interview. Having 1 or more positive items on the questionnaire was significantly associated with finding stroke (P<0.001), TIA (P<0.001), or either stroke or TIA (P<0.001), on medical record review. The telephone interview had a sensitivity of 1.0 (95% CI 0.48 to 1.0), specificity of 0.86 (95% CI 0.75 to 0.93), positive predictive value of 0.36 (95% CI 0.13 to 0.65), and negative predictive value of 1.0 (95% CT 0.94 to 1.0). Conclusions-Our instrument can identify the stroke-free individual with a high degree of confidence in a very efficient manner. It may be particularly suited for centralized verification of stroke discordancy in multicentered sib-pair genetic studies.
引用
收藏
页码:1076 / 1080
页数:5
相关论文
共 24 条
[1]   A STUDY OF TWINS AND STROKE [J].
BRASS, LM ;
ISAACSOHN, JL ;
MERIKANGAS, KR ;
ROBINETTE, CD .
STROKE, 1992, 23 (02) :221-223
[2]  
BRYAN RN, 1991, AM J NEURORADIOL, V12, P611
[3]   The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen [J].
Chataway, J ;
Feakes, R ;
Coraddu, F ;
Gray, J ;
Deans, J ;
Fraser, M ;
Robertson, N ;
Broadley, S ;
Jones, H ;
Clayton, D ;
Goodfellow, P ;
Sawcer, S ;
Compston, A .
BRAIN, 1998, 121 :1869-1887
[4]   A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J].
DAVIES, JL ;
KAWAGUCHI, Y ;
BENNETT, ST ;
COPEMAN, JB ;
CORDELL, HJ ;
PRITCHARD, LE ;
REED, PW ;
GOUGH, SCL ;
JENKINS, SC ;
PALMER, SM ;
BALFOUR, KM ;
ROWE, BR ;
FARRALL, M ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE, 1994, 371 (6493) :130-136
[5]  
FELLER W, 1950, EXPT DESIGNS, P2
[6]   A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families [J].
Gaffney, PM ;
Kearns, GM ;
Shark, KB ;
Ortmann, WA ;
Selby, SA ;
Malmgren, ML ;
Rohlf, KE ;
Ockenden, TC ;
Messner, RP ;
King, RA ;
Rich, SS ;
Behrens, TW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14875-14879
[7]   White matter changes with normal aging [J].
Guttmann, CRG ;
Jolesz, FA ;
Kikinis, R ;
Killiany, RJ ;
Moss, MB ;
Sandor, T ;
Albert, MS .
NEUROLOGY, 1998, 50 (04) :972-978
[8]   A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 [J].
Hanis, CL ;
Boerwinkle, E ;
Chakraborty, R ;
Ellsworth, DL ;
Concannon, P ;
Stirling, B ;
Morrison, VA ;
Wapelhorst, B ;
Spielman, RS ;
GogolinEwens, KJ ;
Shephard, JM ;
Williams, SR ;
Risch, N ;
Hinds, D ;
Iwasaki, N ;
Ogata, M ;
Omori, Y ;
Petzold, C ;
Rietzsch, H ;
Schroder, HE ;
Schulze, J ;
Cox, NJ ;
Menzel, S ;
Boriraj, VV ;
Chen, X ;
Lim, LR ;
Lindner, T ;
Mereu, LE ;
Wang, YQ ;
Xiang, K ;
Yamagata, K ;
Yang, Y ;
Bell, GI .
NATURE GENETICS, 1996, 13 (02) :161-166
[9]   Parental history of cardiovascular disease and risk of stroke - A prospective follow-up of 14,371 middle-aged men and women in Finland [J].
Jousilahti, P ;
Rastenyte, D ;
Tuomilehto, J ;
Sarti, C ;
Vartiainen, E .
STROKE, 1997, 28 (07) :1361-1366
[10]   Validation of the ACAS TIA/stroke algorithm [J].
Karanjia, PN ;
Nelson, JJ ;
Lefkowitz, DS ;
Dick, AR ;
Toole, JF ;
Chambless, LE ;
Hayes, R ;
Howard, VJ .
NEUROLOGY, 1997, 48 (02) :346-351