BibliographyChapter 1. An Introduction to Secondary Data AnalysisBlack, N. 2003. Secondary use of personal data for health and health services research: Why identifiable data are essential. Journal of Health Services Research & Policy 8(Suppl 1):36–40.
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Chapter 2. Health Services Utilization DataBartlett, D L, Ezzati-Rice, T M, Stokley, S, Zhao, Z. 2001. Comparison of NIS and NHIS/NIPRCS vaccination coverage estimates. American Journal of Preventive Medicine 20(4 Suppl):25–27.
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Gilchrist, V J, Stange, K C, Flocke, S A, McCord, G, Bourguet, C C. 2004. A comparison of the National Ambulatory Medical Care Survey (NAMCS) measurement approach with direct observation of outpatient visits. Medical Care 42(3):276–280.
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Luo, Y H, Zack, M. 2005. Computations of confidence intervals for estimates in the United States National Hospital Discharge Survey, 1979–2000. Preventing Chronic Disease 2(3):A06. Epub 2005 Jun 15.
Merrill, R M, Dearden, K A. 2004. How representative are the surveillance, epidemiology, and end results (SEER) program cancer data of the United States? Cancer Causes & Control 15(10):1027–1034.
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Chapter 3. Health Behaviors and Risk Factors DataAndresen, E M, Catlin, T K, Wyrwich, K W, Jackson-Thompson, J. 2003. Retest reliability of surveillance questions on health related quality of life. Journal of Epidemiology and Community Health 57(5):339–343.
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Chapter 4. Data on Multiple Health TopicsFronstin, P. 2000. Counting the uninsured: A comparison of national surveys. Employee Benefit Research Institute Issue Brief 225:1–19.
Himes, J H, Faricy, A. 2001. Validity and reliability of self-reported stature and weight of US adolescents. American Journal of Human Biology 13(2):255–260.
James, M K, Miller, M E, Anderson, R T, Worley, A S, Longino, C F Jr. 1997. Benefits of linkage to the National Death Index in the Longitudinal Study of Aging. Journal of Aging and Health 9(3):298–315.
Korenman, S, Goldman, N, Fu, H. 1997. Misclassification bias in estimates of bereavement effects. American Journal of Epidemiology 145(11):995–1002.
Kuczmarski, M F, Kuczmarski, R J, Najjar, M. 2001. Effects of age on validity of self-reported height, weight, and body mass index: Findings from the Third National Health and Nutrition Examination Survey, 1988–1994. Journal of the American Dietetic Association 101(1):28–34.
Vargas, C M, Burt, V L, Gillum, R F, Pamuk, E R. 1997. Validity of self-reported hypertension in the National Health and Nutrition Examination Survey III, 1988–1991. Preventive Medicine 26(5 Pt 1):678–685.
Yabroff, K R, Gordis, L. 2003. Assessment of a national health interview survey-based method of measuring community socioeconomic status. Annals of Epidemiology 13(10):721–726.
Chapter 5. Fertility and Mortality DataAdams, M. 2001. Validity of birth certificate data for the outcome of the previous pregnancy, Georgia, 1980–1995. American Journal of Epidemiology 154(10):883–888.
Baumeister, L, Marchi, K, Pearl, M, Williams, R, Braveman, P. 2000. The validity of information on “race” and “Hispanic ethnicity” in California birth certificate data. Health Services Research 35(4):869–883.
Campbell, A A, Mosher, W D. 2000. A history of the measurement of unintended pregnancies and births. Maternal and Child Health Journal 4(3):163–169.
Cowper, D C, Kubal, J D, Maynard, C, Hynes, D M. 2002. A primer and comparative review of major US mortality databases. Annals of Epidemiology 12(7):462–468.
DiGiuseppe, D L, Aron, D C, Ranbom, L, Harper, D L, Rosenthal, G E. 2002. Reliability of birth certificate data: A multi-hospital comparison to medical records information. Maternal and Child Health Journal 6(3):169–179.
Johansson, L A, Westerling, R, Rosenberg, H M. 2006. Methodology of studies evaluating death certificate accuracy were flawed. Journal of Clinical Epidemiology 59(2):125–131.
Kaufmann, R B, Morris, L, Spitz, A M. 1997. Comparison of two question sequences for assessing pregnancy intentions. American Journal of Epidemiology 145(9):810–816.
Klerman, L V. 2000. The intendedness of pregnancy: A concept in transition. Maternal and Child Health Journal 4(3):155–162.
Lydon-Rochelle, M T, Cardenas, V, Nelson, J L, Tomashek, K M, Mueller, B A, Easterling, T R. 2005. Validity of maternal and perinatal risk factors reported on fetal death certificates. American Journal of Public Health 95(11):1948–1951.
Lydon-Rochelle, M T, Holt, V L, Nelson, J C, Cardenas, V, Gardella, C, Easterling, T R, Callaghan, W M. 2005. Accuracy of reporting maternal in-hospital diagnoses and intrapartum procedures in Washington State linked birth records. Paediatric and Perinatal Epidemiology 19(6):460–471.
Martin, J A, Hoyert, D L. 2002. The national fetal death file. Seminars in Perinatology 26(1):3–11.
Mosher, W D. 1998. Design and operation of the 1995 National Survey of Family Growth. Family Planning Perspectives 30(1):43–46.
Northam, S, Knapp, T R. 2006. The reliability and validity of birth certificates. Journal of Obstetric, Gynecologic and Neonatal Nursing 35(1):3–12.
Rothwell, C J. 2004. Reengineering vital registration and statistics systems for the United States. Preventing Chronic Disease 1(4):A03. Epub 2004 Sep 15.
Shulman, H B, Gilbert, B C, Msphbrenda, C G, Lansky, A. 2006. The Pregnancy Risk Assessment Monitoring System (PRAMS): Current methods and evaluation of 2001 response rates. Public Health Reports 121(1):74–83.
Chapter 6. Medicare and Medicaid DataCooper, G S, Yuan, Z, Stange, K C, Amini, S B, Dennis, L K, Rimm, A A. 1999. The utility of Medicare claims data for measuring cancer stage. Medical Care 37(7):706–711.
Chattopadhyay, A, Bindman, A B. 2005. Accuracy of Medicaid payer coding in hospital patient discharge data: Implications for Medicaid policy evaluation. Medical Care 43(6):586–591.
Doctor, J N, Chan, L, MacLehose, R F, Patrick, D L. 2000. Weighted health status in the Medicare population: Development of the Weighted Health Index for the Medicare Current Beneficiary Survey (WHIMCBS). Journal of Outcome Measurement 4(4):721–739.
Fisher, E S, Baron, J A, Malenka, D J, Barrett, J, Bubolz, T A. 1990. Overcoming potential pitfalls in the use of Medicare data for epidemiologic research. American Journal of Public Health 80(12):1487–1490.
Gyllstrom, M E, Jensen, J L, Vaughan, J N, Castellano, S E, Oswald, J W. 2002. Linking birth certificates with Medicaid data to enhance population health assessment: Methodological issues addressed. Journal of Public Health Management and Practice 8(4):38–44.
Hoffman, E D, Klees, B S, Curtis, C A. 2002. Overview of the Medicare and Medicaid programs. Health Care Financing Review Statistical Supplement1–348.
Jones, N III, Jones, S L, Miller, N A. 2004. The Medicare Health Outcomes Survey program: Overview, context, and near-term prospects. Health and Quality of Life Outcomes 2:33. Available online at: http://www.hqlo.com/content/2/1/33. Accessed July 6, 2006.
Koroukian, S M, Cooper, G S, Alfred, Rimm A A. 2002. Ability of Medicaid claims data to identify incident cases of breast cancer in the Ohio Medicaid population. Health Services Research 38(3):947–960.
Morgan, R O, Wei, I I, Virnig, B A. 2004. Improving identification of Hispanic males in Medicare: Use of surname matching. Medical Care 42(8):810–816.
Saydah, S H, Geiss, L S, Tierney, E, Benjamin, S M, Engelgau, M, Brancati, F. 2004. Review of the performance of methods to identify diabetes cases among vital statistics, administrative, and survey data. Annals of Epidemiology 14(7):507–516.
Wang, P S, Walker, A, Tsuang, M, Orav, E J, Levin, R, Avorn, J. 2000. Strategies for improving comorbidity measures based on Medicare and Medicaid claims data. Journal of Clinical Epidemiology 53(6):571–578.
Weiner, M, Stump, T E, Callahan, C M, Lewis, J N, McDonald, C J. 2003. A practical method of linking data from Medicare claims and a comprehensive electronic medical records system. International Journal of Medical Informatics 71(1):57–69.
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Zhan, C, Miller, M R. 2003. Administrative data based patient safety research: A critical review. Quality and Safety in Health Care 12(Suppl 2):58–63.
Chapter 7. Other Sources of DataBarrett, R E. 1994. Using the 1990 U.S. Census for Research. Thousand Oaks, CA: Sage.
Best, A E. 1999. Secondary data bases and their use in outcomes research: A review of the Area Resource File and the Healthcare Cost and Utilization Project. Journal of Medical Systems 23(3):175–181.
Davis, J. 1991. The NORC General Social Survey: A user's guide. Thousand Oaks, CA: Sage.
A Guide to the Data Resources of the Henry A. Murray Research Center of Radcliffe College, A Center for the Study of Lives. 1996. Cambridge, MA: Radcliffe Institutes for Advanced Study.
Mays, V M, Ponce, N A, Washington, D L, Cochran, S D. 2003. Classification of race and ethnicity: Implications for public health. Annual Review of Public Health 24:83–110.
Heijden, P J M, Puijenbroek, E P, Buuren, S, Hofstede, J W. 2002. On the assessment of adverse drug reactions from spontaneous reporting systems: The influence of under-reporting on odds ratios. Statistics in Medicine 21:2027–2044.
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