“…The ability of the study participant and next-of-kin to provide these data is of critical importance; validating these variables against an external record is often not possible; and, although they have generally been shown to be reliable (Rogot and Reid, 1975;Kolonel et al, 1977;Herrmann, 1985;Horwitz and Yu, 1985;Lerchen and Samet, 1986;Rocca et al, 1986;Chong et al, 1989;Thorogood and Vessey, 1989;Kelly et al, 1990;Nelson et al, 1990Nelson et al, , 1994Velema et al, 1991;Boyle and Brann, 1992;Wang et al, 1992;Johnson et al, 1993;Poulter et al, 1996;Hamilton and Mack, 2000;Phipps et al, 2000;Nadalin et al, 2003;Villanueva and Garcia, 2006;Slanger et al, 2007) and relatively complete (Kolonel et al, 1977;Pickle et al, 1983;Lerchen and Samet, 1986;Rocca et al, 1986;Nadalin et al, 2003;Campbell et al, 2007), conclusions may differ by survey instrument, population, or disease under study (Blot and McLaughlin, 1985;Nelson et al, 1990). Moreover, with one exception (Johnson et al, 1993), most studies to date have either reported on the reliability of proxy respondents in providing responses at the same time and setting as the study participant or compared the participants' own responses on two occasions over a short timespan.…”