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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 杜裕康 | zh_TW |
dc.contributor.advisor | Yu-Kang Tu | en |
dc.contributor.author | 蔡上傑 | zh_TW |
dc.contributor.author | Shang-Jie Tsai | en |
dc.date.accessioned | 2021-06-17T04:52:07Z | - |
dc.date.available | 2023-11-10 | - |
dc.date.copyright | 2018-10-03 | - |
dc.date.issued | 2018 | - |
dc.date.submitted | 2002-01-01 | - |
dc.identifier.citation | AFSHARI, A., WETTERSLEV, J., BROK, J. & Mbmj, 335, 1248-1251.
ARMITAGE, P., MCPHERSON, C. & ROWE, B. 1969. Repeated significance tests on accumulating data. Journal of the Royal Statistical Society. Series A (General), 235-244. BAIN, L. J. & ENGELHARDT, M. 1987. Introduction to probability and mathematical statistics, Brooks/Cole. BERKEY, C. S., MOSTELLER, F., LAU, J. & ANTMAN, E. M. 1996. Uncertainty of the time of first significance in random effects cumulative meta-analysis. Controlled clinical trials, 17, 357-371. BHUTDA, G. & DEO, V. 2013. Five years clinical results following treatment of human intra-bony defects with an enamel matrix derivative: a randomized controlled trial. Acta Odontologica Scandinavica, 71, 764-770. BIGGERSTAFF, B. & TWEEDIE, R. 1997. Incorporating variability in estimates of heterogeneity in the random effects model in meta-analysis. Statistics in medicine, 16, 753-768. BIONDI-ZOCCAI, G. 2014. Network meta-analysis: evidence synthesis with mixed treatment comparison, Nova Science Publishers, Incorporated. BLUMENTHAL, N. & STEINBERG, J. 1990. The use of collagen membrane barriers in conjunction with combined demineralized bone-collagen gel implants in human infrabony defects. Journal of Periodontology, 61, 319-327. BOKAN, I., BILL, J. S. & SCHLAGENHAUF, U. 2006. Primary flap closure combined with Emdogain® alone or Emdogain® and Cerasorb® in the treatment of intra‐bony defects. Journal of clinical periodontology, 33, 885-893. BORENSTEIN, M., HEDGES, L. V., HIGGINS, J. & ROTHSTEIN, H. R. 2009. Cumulative Meta‐Analysis. Introduction to meta-analysis, 371-376. BORENSTEIN, M., HEDGES, L. V., HIGGINS, J. P. & ROTHSTEIN, H. R. 2011. Introduction to meta-analysis, John Wiley & Sons. BROK, J., THORLUND, K., WETTERSLEV, J. & GLUUD, C. 2008. Apparently conclusive meta-analyses may be inconclusive—trial sequential analysis adjustment of random error risk due to repetitive testing of accumulating data in apparently conclusive neonatal meta-analyses. International journal of epidemiology, 38, 287-298. BUCHER, H. C., GUYATT, G. H., GRIFFITH, L. E. & WALTER, S. D. 1997. The results of direct and indirect treatment comparisons in meta-analysis of randomized controlled trials. Journal of clinical epidemiology, 50, 683-691. CASPER, T. C. & PEREZ, O. A. 2006. An R Package for Group Sequential Boundaries Using Alpha Spending Functions. CHAMBRONE, D., PASIN, I. M., CHAMBRONE, L., PANNUTI, C. M., CONDE, M. C. & LIMA, L. A. 2010. Treatment of infrabony defects with or without enamel matrix proteins: A 24-month follow-up randomized pilot study. Quintessence International, 41. CHOW, S.-C. & LIU, J.-P. 2014. Design and analysis of clinical trials: concepts and methodologies, John Wiley & Sons (3th ed.).. CHUNG, K. M., SALKIN, L. M., STEIN, M. D. & FREEDMAN, A. L. 1990. Clinical evaluation of a biodegradable collagen membrane in guided tissue regeneration. Journal of periodontology, 61, 732-736. CLARKE, M. 2004. Doing new research? Don't forget the old. PLoS medicine, 1, e35. COCHRAN, W. G. 1954. Some methods for strengthening the common χ 2 tests. Biometrics, 10, 417-451. COOPER, N. J., SUTTON, A. J., MORRIS, D., ADES, A. & WELTON, N. J. 2009. Addressing between‐study heterogeneity and inconsistency in mixed treatment comparisons: application to stroke prevention treatments in individuals with non‐rheumatic atrial fibrillation. Statistics in medicine, 28, 1861-1881. CORTELLINI, P., CARNEVALE, G., SANZ, M. & TONETTI, M. S. 1998. Treatment of deep and shallow intrabony defects A multicenter randomized controlled clinical trial. Journal of clinical periodontology, 25, 981-987. CORTELLINI, P., PRATO, G. P. & TONETTI, M. S. 1995. Periodontal regeneration of human intrabony defects with titanium reinforced membranes. A controlled clinical trial. Journal of periodontology, 66, 797-803. CORTELLINI, P., PRATO, G. P. & TONETTI, M. S. 1996. Periodontal regeneration of human intrabony defects with bioresorbable membranes. A controlled clinical trial. Journal of periodontology, 67, 217-223. CORTELLINI, P. & TONETTI, M. S. 2011. Clinical and radiographic outcomes of the modified minimally invasive surgical technique with and without regenerative materials: a randomized‐controlled trial in intra‐bony defects. Journal of clinical periodontology, 38, 365-373. CORTELLINI, P., TONETTI, M. S., LANG, N. P., SUVAN, J. E., ZUCCHELLI, G., VANGSTED, T., SILVESTRI, M., ROSSI, R., MCCLAIN, P. & FONZAR, A. 2001. The simplified papilla preservation flap in the regenerative treatment of deep intrabony defects: clinical outcomes and postoperative morbidity. Journal of Periodontology, 72, 1702-1712. CREA, A., DASSATTI, L., HOFFMANN, O., ZAFIROPOULOS, G. G. & DELI, G. 2008. Treatment of Intrabony Defects Using Guided Tissue Regeneration or Enamel Matrix Derivative: A 3‐Year Prospective Randomized Clinical Study. Journal of periodontology, 79, 2281-2289. DE LEONARDIS, D. & PAOLANTONIO, M. 2013. Enamel Matrix Derivative, Alone or Associated With a Synthetic Bone Substitute, in the Treatment of 1‐to 2‐Wall Periodontal Defects. Journal of periodontology, 84, 444-455. DEEKS, J. J., ALTMAN, D. G. & BRADBURN, M. J. 2008. Statistical methods for examining heterogeneity and combining results from several studies in meta‐analysis. Systematic Reviews in Health Care: Meta-Analysis in Context, Second Edition, 285-312. DEMETS, D. L. 2006. Futility approaches to interim monitoring by data monitoring committees. Clinical Trials, 3, 522-529. DERSIMONIAN, R. & LAIRD, N. 1986. Meta-analysis in clinical trials. Controlled clinical trials, 7, 177-188. DERSIMONIAN, R. & LAIRD, N. 2015. Meta-analysis in clinical trials revisited. Contemporary clinical trials, 45, 139-145. DIAS, S., WELTON, N., CALDWELL, D. & ADES, A. 2010. Checking consistency in mixed treatment comparison meta‐analysis. Statistics in medicine, 29, 932-944. DIBATTISTA, P., BISSADA, N. F. & RICCHETTI, P. A. 1995. Comparative effectiveness of various regenerative modalities for the treatment of localized juvenile periodontitis. Journal of periodontology, 66, 673-678. DOGO, S. H., CLARK, A. & KULINSKAYA, E. 2017. Sequential change detection and monitoring of temporal trends in random‐effects meta‐analysis. Research synthesis methods, 8, 220-235. FICKL, S., THALMAIR, T., KEBSCHULL, M., BJournal of clinical periodontology, 36, 784-790. FRANCETTI, L., DEL FABBRO, M., BASSO, M., TESTORI, T. & WEINSTEIN, R. 2004. Enamel matrix proteins in the treatment of intra‐bony defects. Journal of clinical periodontology, 31, 52-59. FRANCETTI, L., TROMBELLI, L., LOMBARDO, G., GUIDA, L., CAFIERO, C., ROCCUZZO, M., CARUSI, G. & DEL FABBRO, M. 2005. Evaluation of efficacy of enamel matrix derivative in the treatment of intrabony defects: a 24-month multicenter study. International Journal of Periodontics & Restorative Dentistry, 25. FROUM, S. J., WEINBERG, M. A., ROSENBERG, E. & TARNOW, D. 2001. A comparative study utilizing open flap debridement with and without enamel matrix derivative in the treatment of periodontal intrabony defects: a 12-month re-entry study. Journal of Periodontology, 72, 25-34. GHEZZI, C., FERRANTINO, L., BERNARDINI, L., LENCIONI, M. & MASIERO, S. 2016. Minimally Invasive Surgical Technique in Periodontal Regeneration: A Randomized Controlled Clinical Trial Pilot Study. International Journal of Periodontics & Restorative Dentistry, 36. GLASS, G. V. 1976. Primary, secondary, and meta-analysis of research. Educational researcher, 5, 3-8. GOULD, G. M. 1898. The work of an association of medical librarians. Medical libraries, 1, 15. GRUSOVIN, M. G. & ESPOSITO, M. 2009. The efficacy of enamel matrix derivative (Emdogain) for the treatment of deep infrabony periodontal defects: a placebo-controlled randomised clinical trial. European journal of oral implantology, 2. GUIDA, L., ANNUNZIATA, M., BELARDO, S., FARINA, R., SCABBIA, A. & TROMBELLI, L. 2007. Effect of autogenous cortical bone particulate in conjunction with enamel matrix derivative in the treatment of periodontal intraosseous defects. Journal of periodontology, 78, 231-238. GUREVITCH, J., KORICHEVA, J., NAKAGAWA, S. & STEWART, G. 2018. Meta-analysis and the science of research synthesis. Nature, 555, 175. HAYBITTLE, J. 1971. Repeated assessment of results in clinical trials of cancer treatment. The British journal of radiology, 44, 793-797. HEDGES, L. & COOPER, H. 2009. Research synthesis as a scientific process. The handbook of research synthesis and meta-analysis, 1. HEIJL, L., HEDEN, G., SVôRDSTRJ Clin Periodontol, 24, 705-714. HIGGINS, J. & THOMPSON, S. G. 2002. Quantifying heterogeneity in a meta‐analysis. Statistics in medicine, 21, 1539-1558. HIGGINS, J., WHITEHEAD, A. & SIMMONDS, M. 2011. Sequential methods for random‐effects meta‐analysis. Statistics in medicine, 30, 903-921. HIGGINS, J. P. 2011. Green S. Cochrane handbook for systematic reviews of interventions version 5.1. 0. The cochrane collaboration, 5. HWANG, I. K., SHIH, W. J. & DE CANI, J. S. 1990. Group sequential designs using a family of type I error probability spending functions. Statistics in medicine, 9, 1439-1445. INSTITUTE INC, S. 2008. SAS/STAT® 9.2 user’s guide. SAS Institute Inc Cary, NC. IOANNIDIS, J. P. & TRIKALINOS, T. A. 2005. Early extreme contradictory estimates may appear in published research: the Proteus phenomenon in molecular genetics research and randomized trials. Journal of clinical epidemiology, 58, 543-549. JANSEN, J. P., FLEURENCE, R., DEVINE, B., ITZLER, R., BARRETT, A., HAWKINS, N., LEE, K., BOERSMA, C., ANNEMANS, L. & CAPPELLERI, J. C. 2011. Interpreting indirect treatment comparisons and network meta-analysis for health-care decision making: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 1. Value in Health, 14, 417-428. JENNISON, C. & TURNBULL, B. W. 1989. Interim analyses: the repeated confidence interval approach. Journal of the Royal Statistical Society. Series B (Methodological), 305-361. JENNISON, C. & TURNBULL, B. W. 1999. Group sequential methods with applications to clinical trials, CRC Press. KIM, K. & DEMETS, D. L. 1987. Design and analysis of group sequential tests based on the type I error spending rate function. Biometrika, 74, 149-154. KULINSKAYA, E. & WOOD, J. 2014. Trial sequential methods for meta‐analysis. Research synthesis methods, 5, 212-220. LACHIN, J. M. 2005. A review of methods for futility stopping based on conditional power. Statistics in medicine, 24, 2747-2764. LACHIN, J. M. 2009. Futility interim monitoring with control of type I and II error probabilities using the interim Z-value or confidence limit. Clinical Trials, 6, 565-573. LAN, K. G., HU, M. & CAPPELLERI, J. C. 2003. Applying the law of iterated logarithm to cumulative meta-analysis of a continuous endpoint. Statistica Sinica, 1135-1145. LAN, K. G. & WITTES, J. 1988. The B-value: a tool for monitoring data. Biometrics, 579-585. LAN, K. G. & DEMETS, D. L. 1983. Discrete sequential boundaries for clinical trials. Biometrika, 70, 659-663 LAU, J., ANTMAN, E. M., JIMENEZ-SILVA, J., KUPELNICK, B., MOSTELLER, F. & CHALMERS, T. C. 1992. Cumulative meta-analysis of therapeutic trials for myocardial infarction. New England Journal of Medicine, 327, 248-254. LEIMU, R. & KORICHEVA, J. 2004. Cumulative meta–analysis: a new tool for detection of temporal trends and publication bias in ecology. Proceedings of the Royal Society of London B: Biological Sciences, 271, 1961-1966. LESAFFRE, E., PHILSTROM, B., NEEDLEMAN, I. & WORTHINGTON, H. 2009. The design and analysis of split‐mouth studies: What statisticians and clinicians should know. Statistics in medicine, 28, 3470-3482. LOOS, B., LOUWERSE, P., VAN WINKELHOFF, A., BURGER, W., GILIJAMSE, M., HART, A. & VAN DER VELDEN, U. 2002. Use of barrier membranes and systemic antibiotics in the treatment of intraosseous defects. Journal of clinical periodontology, 29, 910-921. LU, G. & ADES, A. 2004. Combination of direct and indirect evidence in mixed treatment comparisons. Statistics in medicine, 23, 3105-3124. LU, G. & ADES, A. 2006. Assessing evidence inconsistency in mixed treatment comparisons. Journal of the American Statistical Association, 101, 447-459. LU, G., WELTON, N. J., HIGGINS, J., WHITE, I. R. & ADES, A. E. 2011. Linear inference for mixed treatment comparison meta‐analysis: a two‐stage approach. Research Synthesis Methods, 2, 43-60. LUMLEY, T. 2002. Network meta‐analysis for indirect treatment comparisons. Statistics in medicine, 21, 2313-2324. MANTEL, N. & HAENSZEL, W. 1959. Statistical aspects of the analysis of data from retrospective studies of disease. Journal of the national cancer institute, 22, 719-748. MAYFIELD, L., SJournal of clinical periodontology, 25, 585-595. MELAS, V. B., MIGNANI, S., MONARI, P. & SALMASO, L. 2016. Topics in Statistical Simulation, Springer. MELLADO, J. R., SALKIN, L. M., FREEDMAN, A. L. & STEIN, M. D. 1995. A comparative study of ePTFE periodontal membranes with and without decalcified freeze-dried bone allografts for the regeneration of interproximal intraosseous defects. Journal of periodontology, 66, 751-755. MEYLE, J., HOFFMANN, T., TOPOLL, H., HEINZ, B., AL‐MACHOT, E., JERVJournal of clinical periodontology, 38, 652-660. MINABE, M., KODAMA, T., KOGOU, T., TAKEUCHI, K., FUSHIMI, H., SUGIYAMA, T. & MITARAI, E. 2002. A comparative study of combined treatment with a collagen membrane and enamel matrix proteins for the regeneration of intraosseous defects. International Journal of Periodontics & Restorative Dentistry, 22. MORA, F., ETIENNE, D. & OUHAYOUN, J. 1996. Treatment of interproximal angular defects by guided tissue regeneration: 1 year follow‐up. Journal of oral rehabilitation, 23, 599-606. NACI, H. & O'CONNOR, A. B. 2013. Assessing comparative effectiveness of new drugs before approval using prospective network meta-analyses. Journal of clinical epidemiology, 66, 812. NIKOLAKOPOULOU, A., MAVRIDIS, D., EGGER, M. & SALANTI, G. 2018a. Continuously updated network meta-analysis and statistical monitoring for timely decision-making. Statistical methods in medical research, 27, 1312-1330. NIKOLAKOPOULOU, A., MAVRIDIS, D., FURUKAWA, T. A., CIPRIANI, A., TRICCO, A. C., STRAUS, S. E., SIONTIS, G. C., EGGER, M. & SALANTI, G. 2018b. Living network meta-analysis compared with pairwise meta-analysis in comparative effectiveness research: empirical study. bmj, 360, k585. NIKOLAKOPOULOU, A., MAVRIDIS, D. & SALANTI, G. 2014. Using conditional power of network meta‐analysis (NMA) to inform the design of future clinical trials. Biometrical Journal, 56, 973-990. NOMA, H., TANAKA, S., MATSUI, S., CIPRIANI, A. & FURUKAWA, T. A. 2017. Quantifying indirect evidence in network meta‐analysis. Statistics in medicine, 36, 917-927. O'BRIEN, P. C. & FLEMING, T. R. 1979. A multiple testing procedure for clinical trials. Biometrics, 549-556. O’CONNOR, A. B. 2010. Building comparative efficacy and tolerability into the FDA approval process. Jama, 303, 979-980. OGIHARA, S. & TARNOW, D. P. 2014. Efficacy of Enamel Matrix Derivative With Freeze‐Dried Bone Allograft or Demineralized Freeze‐Dried Bone Allograft in Intrabony Defects: A Randomized Trial. Journal of periodontology, 85, 1351-1360. OKUDA, K., MOMOSE, M., MIYAZAKI, A., MURATA, M., YOKOYAMA, S., YONEZAWA, Y., WOLFF, L. F. & YOSHIE, H. 2000. Enamel matrix derivative in the treatment of human intrabony osseous defects. Journal of periodontology, 71, 1821-1828. PAOLANTONIO, M., PERINETTI, G., DOLCI, M., PERFETTI, G., TETø, S., SAMMARTINO, G., FEMMINELLA, B. & GRAZIANI, F. 2008. Surgical treatment of periodontal intrabony defects with calcium sulfate implant and barrier versus collagen barrier or open flap debridement alone: a 12-month randomized controlled clinical trial. Journal of periodontology, 79, 1886-1893. PETITTI, D. B. 2000. Meta-analysis, decision analysis, and cost-effectiveness analysis: methods for quantitative synthesis in medicine, OUP USA. PETO, R., PIKE, M., ARMITAGE, P., BRESLOW, N., COX, D., HOWARD, S. V., MANTEL, N., MCPHERSON, K., PETO, J. & SMITH, P. 1976. Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design. British journal of cancer, 34, 585-612. PIETRUSKA, M., PIETRUSKI, J., NAGY, K., BRECX, M., ARWEILER, N. B. & SCULEAN, A. 2012. Four-year results following treatment of intrabony periodontal defects with an enamel matrix derivative alone or combined with a biphasic calcium phosphate. Clinical oral investigations, 16, 1191-1197. POCOCK, S. J. 1977. Group sequential methods in the design and analysis of clinical trials. Biometrika, 64, 191-199. PONTORIERO, R., WENNSTRJournal of Clinical Periodontology, 26, 833-840. PRITLOVE-CARSON, S., PALMER, R. & FLOYD, P. 1995. Evaluation of guided tissue regeneration in the treatment of paired periodontal defects. British Dental Journal, 179, 388. RATKA‐KRJournal of clinical periodontology, 27, 120-127. SALANTI, G., HIGGINS, J. P., ADES, A. & IOANNIDIS, J. P. 2008a. Evaluation of networks of randomized trials. Statistical methods in medical research, 17, 279-301. SALANTI, G., KAVVOURA, F. K. & IOANNIDIS, J. P. 2008b. Exploring the geometry of treatment networks. Annals of internal medicine, 148, 544-553. SANZ, M., TONETTI, M. S., ZABALEGUI, I., SICILIA, A., BLANCO, J., REBELO, H., RASPERINI, G., MERLI, M., CORTELLINI, P. & SUVAN, J. E. 2004. Treatment of intrabony defects with enamel matrix proteins or barrier membranes: results from a multicenter practice-based clinical trial. Journal of periodontology, 75, 726-733. SCHWARZER, G., CARPENTER, J. R. & RMeta-analysis with R, Springer. SCULEAN, A., BERAKDAR, M., CHIANTELLA, G. C., DONOS, N., ARWEILER, N. B. & BRECX, M. 2003. Healing of intrabony defects following treatment with a bovine‐derived xenograft and collagen membrane. Journal of clinical periodontology, 30, 73-80. SCULEAN, A., CHIANTELLA, G. C., WINDISCH, P., ARWEILER, N. B., BRECX, M. & GERA, I. 2005a. Healing of intra‐bony defects following treatment with a composite bovine‐derived xenograft (Bio‐Oss Collagen) in combination with a collagen membrane (Bio‐Gide PERIO). Journal of clinical periodontology, 32, 720-724. SCULEAN, A., PIETRUSKA, M., SCHWARZ, F., WILLERSHAUSEN, B., ARWEILER, N. B. & AUSCHILL, T. M. 2005b. Healing of human intrabony defects following regenerative periodontal therapy with an enamel matrix protein derivative alone or combined with a bioactive glass. Journal of clinical periodontology, 32, 111-117. SCULEAN, A., WINDISCH, P., CHIANTELLA, G. C., DONOS, N., BRECX, M. & REICH, E. 2001. Treatment of intrabony defects with enamel matrix proteins and guided tissue regeneration. Journal of Clinical Periodontology, 28, 397-403. SHADISH, W. R. & HADDOCK, C. K. 1994. Combining estimates of effect size. SHIH, W. J. & AISNER, J. 2015. Statistical design and analysis of clinical trials: principles and methods, CRC Press. SICILIANO, V. I., ANDREUCCETTI, G., SICILIANO, A. I., BLASI, A., SCULEAN, A. & SALVI, G. E. 2011. Clinical Outcomes After Treatment of Non‐Contained Intrabony Defects With Enamel Matrix Derivative or Guided Tissue Regeneration: A 12‐Month Randomized Controlled Clinical Trial. Journal of periodontology, 82, 62-71. SIDIK, K. & JONKMAN, J. N. 2005. Simple heterogeneity variance estimation for meta‐analysis. Journal of the Royal Statistical Society: Series C (Applied Statistics), 54, 367-384. SIDIK, K. & JONKMAN, J. N. 2007. A comparison of heterogeneity variance estimators in combining results of studies. Statistics in medicine, 26, 1964-1981. SILVESTRI, M., RICCI, G., RASPERINI, G., SARTORI, S. & CATTANEO, V. 2000. Comparison of treatments of infrabony defects with enamel matrix derivative, guided tissue regeneration with a nonresorbable membrane and Widman modified flap. Journal of clinical periodontology, 27, 603-610. SILVESTRI, M., SARTORI, S., RASPERINI, G., RICCI, G., ROTA, C. & CATTANEO, V. 2003. Comparison of infrabony defects treated with enamel matrix derivative versus guided tissue regeneration with a nonresorbable membrane. Journal of clinical periodontology, 30, 386-393. SIMPSON, R. & PEARSON, K. 1904. Report on certain enteric fever inoculation statistics. The British Medical Journal, 1243-1246. SIPOS, P., LOOS, B., ABBAS, F., TIMMERMAN, M. & VAN DER VELDEN, U. 2005. The combined use of enamel matrix proteins and a tetracycline‐coated expanded polytetrafluoroethylene barrier membrane in the treatment of intra‐osseous defects. Journal of clinical periodontology, 32, 765-772. SñNCHEZ-MECA, J. & MARýN-MARTýNEZ, F. 2008. Confidence intervals for the overall effect size in random-effects meta-analysis. Psychological Methods, 13, 31. SONG, F., ALTMAN, D. G., GLENNY, A.-M. & DEEKS, J. J. 2003. Validity of indirect comparison for estimating efficacy of competing interventions: empirical evidence from published meta-analyses. Bmj, 326, 472. SPIEGELHALTER, D. J., ABRAMS, K. R. & MYLES, J. P. 2004. Bayesian approaches to clinical trials and health-care evaluation, John Wiley & Sons. STALLARD, N. & FACEY, K. M. 1996. Comparison of the spending function method and the Christmas tree correction for group sequential trials. Journal of Biopharmaceutical Statistics, 6, 361-373. STAVROPOULOS, A., KARRING, E. S., KOSTOPOULOS, L. & KARRING, T. 2003. Deproteinized bovine bone and gentamicin as an adjunct to GTR in the treatment of intrabony defects: a randomized controlled clinical study. Journal of clinical periodontology, 30, 486-495. SU, Y. X. & TU, Y. K. 2018. Statistical Approaches to Adjusting Weights for Dependent Arms in Network Meta‐analysis. Research synthesis methods. SUTTON, A. J., ABRAMS, K. R., JONES, D. R., JONES, D. R., SHELDON, T. A. & SONG, F. 2000. Methods for meta-analysis in medical research. THORLUND, K., ENGSTRCopenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen, Denmark, 1, 1-115. TONETTI, M. S., CORTELLINI, P., LANG, N. P., SUVAN, J. E., ADRIAENS, P., DUBRAVEC, D., FONZAR, A., FOURMOUSIS, I., RASPERINI, G. & ROSSI, R. 2004. Clinical outcomes following treatment of human intrabony defects with GTR/bone replacement material or access flap alone. Journal of clinical periodontology, 31, 770-776. TONETTI, M. S., CORTELLINI, P., SUVAN, J. E., ADRIAENS, P., BALDI, C., DUBRAVEC, D., FONZAR, A., FOURMOUSIS, I., MAGNANI, C. & MULLER-CAMPANILE, V. 1998. Generalizability of the added benefits of guided tissue regeneration in the treatment of deep intrabony defects. Evaluation in a multi-center randomized controlled clinical trial. Journal of Periodontology, 69, 1183-1192. TONETTI, M. S., LANG, N. P., CORTELLINI, P., SUVAN, J. E., ADRIAENS, P., DUBRAVEC, D., FONZAR, A., FOURMOUSIS, I., MAYFIELD, L. & ROSSI, R. 2002. Enamel matrix proteins in the regenerative therapy of deep intrabony defects. Journal of clinical periodontology, 29, 317-325. TREJO, P., WELTMAN, R. & CAFFESSE, R. 2000. Treatment of intraosseous defects with bioabsorbable barriers alone or in combination with decalcified freeze-dried bone allograft: a randomized clinical trial. Journal of periodontology, 71, 1852-1861. TU, Y.-K. 2016. Node-splitting generalized linear mixed models for evaluation of inconsistency in network meta-analysis. Value in Health, 19, 957-963. TU, Y.-K. 2015. Using generalized linear mixed models to evaluate inconsistency within a network meta-analysis. Value in Health, 18, 1120-1125. TU, Y. K., NEEDLEMAN, I., CHAMBRONE, L., LU, H. K. & FAGGION, C. M. 2012. A bayesian network meta‐analysis on comparisons of enamel matrix derivatives, guided tissue regeneration and their combination therapies. Journal of clinical periodontology, 39, 303-314. WETTERSLEV, J., JAKOBSEN, J. C. & GLUUD, C. 2017. Trial Sequential Analysis in systematic reviews with meta-analysis. BMC medical research methodology, 17, 39. WETTERSLEV, J., THORLUND, K., BROK, J. & GLUUD, C. 2009. Estimating required information size by quantifying diversity in random-effects model meta-analyses. BMC medical research methodology, 9, 86. WHITE, I. R., BARRETT, J. K., JACKSON, D. & HIGGINS, J. 2012. Consistency and inconsistency in network meta‐analysis: model estimation using multivariate meta‐regression. Research synthesis methods, 3, 111-125. WHITEHEAD, A. 2002. Meta-analysis of controlled clinical trials, John Wiley & Sons. WHITEHEAD, J. 1997. The design and analysis of sequential clinical trials, John Wiley & Sons. WHITEHEAD, J. & BRUNIER, H. 1990. The double triangular test: a sequential test for the two-sided alternative with early stopping under the null hypothesis. Sequential Analysis, 9, 117-136. WHITEHEAD, J. & STRATTON, I. 1983. Group sequential clinical trials with triangular continuation regions. Biometrics, 227-236. WHITEHEAD, J. & TODD, S. 2004. The double triangular test in practice. Pharmaceutical Statistics, 3, 39-49. WOLF, F. M. 1986. Meta-analysis: Quantitative methods for research synthesis, Sage. YILMAZ, S., CAKAR, G., YILDIRIM, B. & SCULEAN, A. 2010. Healing of two and three wall intrabony periodontal defects following treatment with an enamel matrix derivative combined with autogenous bone. Journal of clinical periodontology, 37, 544-550. YUSUF, S., PETO, R., LEWIS, J., COLLINS, R. & SLEIGHT, P. 1985. Beta blockade during and after myocardial infarction: an overview of the randomized trials. Progress in cardiovascular diseases, 27, 335-371. ZUCCHELLI, G., AMORE, C., MONTEBUGNOLI, L. & DE SANCTIS, M. 2003. Enamel Matrix Protines Bovine Porous Bone Mineral in the Treatment of Intrabony Defects: Comparative Controlled Clinical Trial. Journal of periodontology, 74, 1725-1735. ZUCCHELLI, G., BERNARDI, F., MONTEBUGNOLI, L. & SANCTIS, M. D. 2002. Enamel Matrix Proteins and Guided Tissue Regeneration With Titanium-Reinforced Expanded PolytetrafluoroethyleneMembranes in the Treatment of Infrabony Defects: A Comparative Controlled Clinical Trial. Journal of periodontology, 73, 3-12. | - |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/71083 | - |
dc.description.abstract | 背景 統合分析(meta analysis)在近四十年被普遍使用在統合隨機分派臨床試驗(randomize controlled trial [RCT])的證據。而為了確認是否有必要針對某一項特定主題重複不斷地做研究,有學者提出了累積統合分析,藉由一系列依照時序進行的統合分析,加上森林圖的呈現,讓研究者可能在某一個時間點,看到兩種干預效果有明顯的差異。但這樣一系列的檢定,可能讓整體型一錯誤發生的機率上升,而檢定力也可能無法達到我們研究開始前所設定的標準。因此有學者將臨床試驗中常使用的期中分析(interim analysis)的想法引入統合分析,提出了試驗序貫分析方法(trial sequential analysis)以及近一步將間接證據考慮進去的序貫網絡統合分析(sequential network meta analysis),來校正統合分析中整體可容忍的型一錯誤。
目標 本研究利用序貫網絡統合分析,分析牙釉基質衍生物(enamel matrix derivatives)及引導組織再生術(guided tissue regeneration)的相關治療對於牙周病的改善是否有顯著差異,並且和一般的網絡統合分析結果進行比較。 材料及方法 本研究先對於統合分析、網絡統合分析及累積統合分析做介紹,再回顧期中分析中所使用的分組序貫方法(group sequential methods),例如α花費函數(α-spending function)及三角測試(triangular test),最後則介紹試驗序貫分析及序貫網絡統合分析。此外,本研究也針對序貫網絡統合分析所使用的R套件(sequentialnma)進行些微的修改,並用探討模擬資料使用序貫網絡統合分析的表現。而資料分析部分,我們使用Tu等人2012年在Journal of Clinical Periodontology所發表之研究的資料(Tu et al., 2012),並搜尋2011年1月到2017年12月的相關文獻進行資料的更新。將更新後的資料使用序貫網絡統合分析,分析不同的治療在改善牙周囊袋深度(probing pocket depth [PPD])及臨床附著水平(clinical attachment level [CAL])上,是否有顯著差異。 結果 我們總共納入了58篇研究進行分析。而序貫網絡統合分析和一般網絡統合分析的結果差異不大。在改善PPD及CAL上,我們得到除了和使用牙釉基質衍生物加上骨移植體並使用富血小板血漿治療(enamel matrix derivatives with platelet rich plasma and bone graft;EMD+PRP+BG)沒有顯著差異之外,其他六種治療都明顯優於翻瓣手術(flap operation)治療(雖然使用EMD+PRP+BG治療比翻瓣手術能多減少0.95公厘的牙周囊袋深度,但其信賴區間及重複信賴區間分別為[-0.88, 2.78]及[-2.31, 4.21],顯示兩組治療沒有顯著差異)。然而在其他的兩兩成對比較,都沒有任何治療顯著的優於另一治療。不過,在效應值為PPD改變量時,用牙釉基質衍生物(EMD)治療和使用引導組織再生術(GTR)治療的比較上,使用序貫網絡統合分析會得到和一般網絡統合分析下不同的結論:如果在一般網絡統合分析下,最後會得到GTR 治療優於EMD 治療的結論(其信賴區間為[0.06, 0.86]),但在序貫網絡統合分析之下,這兩種治療就沒有顯著差異了(其重複信賴區間為[-0.02, 0.94]).,並且需要進行後續的研究。至於在資訊的累積上,有統計上顯著差異的治療比較,相對於不顯著的治療比較都累積較高的資訊量(從0.77到2.52這個範圍中)。 結論 序貫網絡統合分析和一般網絡統合分析的結果雖然差異不大,但使用序貫網絡統合分析能讓我們在分析時控制整體研究的型一錯誤,使我們不會過早下錯誤的結論。並且透過證據的累積,我們能知道目前我們所有的資訊量,以及後續是否需要再進行相關研究,以節省研究的資源。 | zh_TW |
dc.description.abstract | Background: Meta-analyses and network meta-analyses (NMA) have become popular for scholars to evidence synthesis to attain a robust conclusion. To understand the trend in the results, cumulative meta-analysis has been proposed. However, cumulative meta-analysis undertakes a series of statistical tests. While the type I error rate is usually set at 5%, multiple testing gives rise to inflated type I error rate.
Objective: This thesis aims to compare the effects of different periodontal regenerative therapies on the treatment of teeth with periodontal diseases by using sequential network meta-analysis (SNMA), and also compares the SNMA results with the general network meta-analysis’s. Materials & Methods: To deal with the inflation of type I error rate, the group sequential methods (e.g. the α-spending function, the Whitehead triangular test), which were used in the interim analysis in the clinical trials, have been introduced into meta-analyses. Trial sequential analysis (TSA) proposed by Wetterslev and his colleagues, and sequential network meta-analysis proposed by Nikolakopoulou and her colleagues, are two useful methods to resolve this problem. SNMA also takes indirect evidence into account. In the thesis, we modified the “sequentialnma” package in R which was then used to analyze updated data from a network meta-analysis on the effects of different periodontal regenerative therapies in 2012 (Tu et al., 2012), by searching new studies from January, 2011 to December, 2017. And then we use SNMA, TSA and triangular test to compare guided tissue regeneration (GTR), enamel matrix derivatives (EMD) and their combination therapies regarding the probing pocket depth (PPD) reduction and clinical attachment level (CAL) gain. Results: A total of 58 studies were included in this thesis, and SNMA and NMA yield similar results. In terms of PPD reduction and CAL gain, the flap operation (FO) was significantly less effective than other treatments except for the EMD with platelet-rich plasma and bone graft therapy. Although the EMD with platelet-rich plasma and bone graft therapy had on average attained 0.95 mm greater PPD reduction than FO, but the confidence interval [-0.88, 2.78] and the repeated confidence interval [-2.31, 4.21] showed no statistical significance in their difference. No significant difference was found in other pairwise comparison. SNMA showed that the difference in PPD reduction between EMD and GTR was not statistically significant (the repeated confidence interval was [-0.02, 0.94]), while NMA showed that GTR attained greater PPD reduction than EMD (the confidence interval was [0.06, 0.86]). As for the accumulation of information in the analysis, the statistically significant comparisons usually had a greater proportion of the accumulated information (ranging from 0.77 to 2.52) than the nonsignificant one. Conclusion: Although SNMA and NMA achieved similar results, using SNMA could help control the type I error rate thereby reducing the risk of false-positive findings. SNMA also summarizes information accrued from the beginning up to a particular time, and decision can then be made with regards to whether or not evidence is sufficient to conclude the superiority of one treatment over another or the equivalence of two treatments. Resources can therefore be directed to where it is most needed in the future. | en |
dc.description.provenance | Made available in DSpace on 2021-06-17T04:52:07Z (GMT). No. of bitstreams: 1 ntu-107-R05849014-1.pdf: 10616527 bytes, checksum: 446ddadec0d88bf348711f2c81a01243 (MD5) Previous issue date: 2018 | en |
dc.description.tableofcontents | 口試委員會審定書 i
誌謝 ii 中文摘要 iii ABSTRACT vi 目 錄 ix 表目錄 xv 第一章 緒論 1 第二章 文獻回顧 6 2.1 傳統統合分析和網絡統合分析 6 2.1.1 變異數倒數方法 8 2.1.2 DerSimonian-Laird方法 9 2.1.3 Sidik-Jonkman方法 10 2.1.4 Biggerstaff-Tweedie方法 11 2.1.5 序貫網絡統合分析下的估計方式 11 2.2 累積統合分析 15 2.3 期中分析 15 2.3.1 Haybittle和Peto et al.界限 16 2.3.2 Pocock界限 17 2.3.3 O’Brien-Fleming界限 18 2.3.4 α花費函數 19 2.3.5 重複信賴區間 21 2.3.6 無益評估 22 2.3.7 三角測試 24 2.4 試驗序貫分析和序貫網絡統合分析 28 2.4.1 檢定統計量所形成的樣本路徑 30 2.4.2 需要的資訊量 30 2.4.3 有效界限 33 2.4.4 無益界限 34 第三章 研究方法在模擬資料的表現 36 3.1 「sequentialnma」套件 36 3.2 模擬資料在sequentialnma套件的表現 39 3.3 模擬資料在sequentialnma套件修改後的表現 47 第四章 牙周病治療的例子在序貫網絡統合分析的結果 53 4.1 未調整實驗設計下的分析結果 56 4.2 調整實驗設計下的分析結果 74 4.3 小結 75 第五章 討論 77 5.1 限制與未來展望 79 5.2 結論 81 參考文獻 83 附錄一、O’Brien-Fleming界限及近似其界限的α花費函數 95 附錄二、整體資訊量的計算 100 附錄三、I^2 與D^2 102 附錄四、第三章的模擬資料及其步驟和部分結果 103 附錄五、sequentialnma套件的修改 114 附錄六、第四章納入分析的研究之篩選過程及資料詳細資訊 122 附錄七、第四章資料分析所使用的程式語法 147 附錄八、第四章其餘分析結果 153 | - |
dc.language.iso | zh_TW | - |
dc.title | 使用序貫網絡統合分析比較牙周再生手術的成效 | zh_TW |
dc.title | Using Sequential Network Meta-Analysis to Compare the Effectiveness of Periodontal Regenerative Therapies | en |
dc.type | Thesis | - |
dc.date.schoolyear | 106-2 | - |
dc.description.degree | 碩士 | - |
dc.contributor.oralexamcommittee | 劉仁沛;簡國龍 | zh_TW |
dc.contributor.oralexamcommittee | Jen-Pei Liu;Kuo-Liong Chien | en |
dc.subject.keyword | 統合分析,網絡統合分析,累積統合分析,序貫網絡統合分析,試驗序貫分析,期中分析, | zh_TW |
dc.subject.keyword | meta analysis,network meta analysis,cumulative meta analysis,sequential network meta analysis,trial sequential analysis,interim analysis, | en |
dc.relation.page | 171 | - |
dc.identifier.doi | 10.6342/NTU201802013 | - |
dc.rights.note | 未授權 | - |
dc.date.accepted | 2018-07-31 | - |
dc.contributor.author-college | 公共衛生學院 | - |
dc.contributor.author-dept | 流行病學與預防醫學研究所 | - |
顯示於系所單位: | 流行病學與預防醫學研究所 |
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