Adjusting for time-varying confounding in the subdistribution analysis of a competing risk
Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. In...
Ausführliche Beschreibung
Autor*in: |
Bekaert, Maarten [verfasserIn] Vansteelandt, Stijn [verfasserIn] Mertens, Karl [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2009 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Lifetime data analysis - [S.l.] : Proquest, 1995, 16(2009), 1 vom: 10. Okt. |
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Übergeordnetes Werk: |
volume:16 ; year:2009 ; number:1 ; day:10 ; month:10 |
Links: |
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DOI / URN: |
10.1007/s10985-009-9130-8 |
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Katalog-ID: |
SPR015364747 |
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520 | |a Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). | ||
650 | 4 | |a Causal inference |7 (dpeaa)DE-He213 | |
650 | 4 | |a Competing risk |7 (dpeaa)DE-He213 | |
650 | 4 | |a ICU |7 (dpeaa)DE-He213 | |
650 | 4 | |a Inverse weighting |7 (dpeaa)DE-He213 | |
650 | 4 | |a Nosocomial infection |7 (dpeaa)DE-He213 | |
650 | 4 | |a Time-dependent confounding |7 (dpeaa)DE-He213 | |
700 | 1 | |a Vansteelandt, Stijn |e verfasserin |4 aut | |
700 | 1 | |a Mertens, Karl |e verfasserin |4 aut | |
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10.1007/s10985-009-9130-8 doi (DE-627)SPR015364747 (SPR)s10985-009-9130-8-e DE-627 ger DE-627 rakwb eng 510 004 ASE 31.73 bkl 44.32 bkl Bekaert, Maarten verfasserin aut Adjusting for time-varying confounding in the subdistribution analysis of a competing risk 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 Vansteelandt, Stijn verfasserin aut Mertens, Karl verfasserin aut Enthalten in Lifetime data analysis [S.l.] : Proquest, 1995 16(2009), 1 vom: 10. Okt. (DE-627)271348410 (DE-600)1479719-7 1572-9249 nnns volume:16 year:2009 number:1 day:10 month:10 https://dx.doi.org/10.1007/s10985-009-9130-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-MAT SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 31.73 ASE 44.32 ASE AR 16 2009 1 10 10 |
spelling |
10.1007/s10985-009-9130-8 doi (DE-627)SPR015364747 (SPR)s10985-009-9130-8-e DE-627 ger DE-627 rakwb eng 510 004 ASE 31.73 bkl 44.32 bkl Bekaert, Maarten verfasserin aut Adjusting for time-varying confounding in the subdistribution analysis of a competing risk 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 Vansteelandt, Stijn verfasserin aut Mertens, Karl verfasserin aut Enthalten in Lifetime data analysis [S.l.] : Proquest, 1995 16(2009), 1 vom: 10. Okt. (DE-627)271348410 (DE-600)1479719-7 1572-9249 nnns volume:16 year:2009 number:1 day:10 month:10 https://dx.doi.org/10.1007/s10985-009-9130-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-MAT SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 31.73 ASE 44.32 ASE AR 16 2009 1 10 10 |
allfields_unstemmed |
10.1007/s10985-009-9130-8 doi (DE-627)SPR015364747 (SPR)s10985-009-9130-8-e DE-627 ger DE-627 rakwb eng 510 004 ASE 31.73 bkl 44.32 bkl Bekaert, Maarten verfasserin aut Adjusting for time-varying confounding in the subdistribution analysis of a competing risk 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 Vansteelandt, Stijn verfasserin aut Mertens, Karl verfasserin aut Enthalten in Lifetime data analysis [S.l.] : Proquest, 1995 16(2009), 1 vom: 10. Okt. (DE-627)271348410 (DE-600)1479719-7 1572-9249 nnns volume:16 year:2009 number:1 day:10 month:10 https://dx.doi.org/10.1007/s10985-009-9130-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-MAT SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 31.73 ASE 44.32 ASE AR 16 2009 1 10 10 |
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10.1007/s10985-009-9130-8 doi (DE-627)SPR015364747 (SPR)s10985-009-9130-8-e DE-627 ger DE-627 rakwb eng 510 004 ASE 31.73 bkl 44.32 bkl Bekaert, Maarten verfasserin aut Adjusting for time-varying confounding in the subdistribution analysis of a competing risk 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 Vansteelandt, Stijn verfasserin aut Mertens, Karl verfasserin aut Enthalten in Lifetime data analysis [S.l.] : Proquest, 1995 16(2009), 1 vom: 10. Okt. (DE-627)271348410 (DE-600)1479719-7 1572-9249 nnns volume:16 year:2009 number:1 day:10 month:10 https://dx.doi.org/10.1007/s10985-009-9130-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-MAT SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 31.73 ASE 44.32 ASE AR 16 2009 1 10 10 |
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10.1007/s10985-009-9130-8 doi (DE-627)SPR015364747 (SPR)s10985-009-9130-8-e DE-627 ger DE-627 rakwb eng 510 004 ASE 31.73 bkl 44.32 bkl Bekaert, Maarten verfasserin aut Adjusting for time-varying confounding in the subdistribution analysis of a competing risk 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 Vansteelandt, Stijn verfasserin aut Mertens, Karl verfasserin aut Enthalten in Lifetime data analysis [S.l.] : Proquest, 1995 16(2009), 1 vom: 10. Okt. (DE-627)271348410 (DE-600)1479719-7 1572-9249 nnns volume:16 year:2009 number:1 day:10 month:10 https://dx.doi.org/10.1007/s10985-009-9130-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-MAT SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 31.73 ASE 44.32 ASE AR 16 2009 1 10 10 |
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Enthalten in Lifetime data analysis 16(2009), 1 vom: 10. Okt. volume:16 year:2009 number:1 day:10 month:10 |
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Enthalten in Lifetime data analysis 16(2009), 1 vom: 10. Okt. volume:16 year:2009 number:1 day:10 month:10 |
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Causal inference Competing risk ICU Inverse weighting Nosocomial infection Time-dependent confounding |
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Lifetime data analysis |
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Bekaert, Maarten @@aut@@ Vansteelandt, Stijn @@aut@@ Mertens, Karl @@aut@@ |
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2009-10-10T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR015364747</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519131737.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201006s2009 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10985-009-9130-8</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR015364747</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s10985-009-9130-8-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">510</subfield><subfield code="a">004</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">31.73</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">44.32</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Bekaert, Maarten</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Adjusting for time-varying confounding in the subdistribution analysis of a competing risk</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2009</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium).</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Causal inference</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Competing risk</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ICU</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Inverse weighting</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Nosocomial infection</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Time-dependent confounding</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Vansteelandt, Stijn</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mertens, Karl</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Lifetime data analysis</subfield><subfield code="d">[S.l.] : Proquest, 1995</subfield><subfield code="g">16(2009), 1 vom: 10. 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Bekaert, Maarten |
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Bekaert, Maarten ddc 510 bkl 31.73 bkl 44.32 misc Causal inference misc Competing risk misc ICU misc Inverse weighting misc Nosocomial infection misc Time-dependent confounding Adjusting for time-varying confounding in the subdistribution analysis of a competing risk |
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510 004 ASE 31.73 bkl 44.32 bkl Adjusting for time-varying confounding in the subdistribution analysis of a competing risk Causal inference (dpeaa)DE-He213 Competing risk (dpeaa)DE-He213 ICU (dpeaa)DE-He213 Inverse weighting (dpeaa)DE-He213 Nosocomial infection (dpeaa)DE-He213 Time-dependent confounding (dpeaa)DE-He213 |
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adjusting for time-varying confounding in the subdistribution analysis of a competing risk |
title_auth |
Adjusting for time-varying confounding in the subdistribution analysis of a competing risk |
abstract |
Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). |
abstractGer |
Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). |
abstract_unstemmed |
Abstract Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46–59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient’s health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of ‘ICU mortality’ over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU’s (Belgium). |
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container_issue |
1 |
title_short |
Adjusting for time-varying confounding in the subdistribution analysis of a competing risk |
url |
https://dx.doi.org/10.1007/s10985-009-9130-8 |
remote_bool |
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author2 |
Vansteelandt, Stijn Mertens, Karl |
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doi_str |
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up_date |
2024-07-03T15:45:09.782Z |
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|
score |
7.400057 |