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    "textoCompleto" => "NEFROLOGÍA. Vol. XX. Suplemento 3. 2000 Comparative survival in hemodialysis and peritoneal dialysis P. G. Blake Director Peritoneal Dialysis. Associate Professor Medicine. Optimal Dialysis Research Unit. London Health Sciences Centre. University of Western Ontario. London. Ontario. Canada. INTRODUCTION With the spread in popularity of PD, and particularly of CAPD, in the 1980's, it was inevitable that comparisons would be made between the success of the modality and that of conventional HD. Such comparisons can be done on the basis of quality of life, hospitalization, technique survival and cost effectiveness. But the most critical «hard» end point is, of course, patient survival. Initial studies addressing this issue from a variety of centres in North America and Western Europe were published between 1985 and 1995 and, in general, showed no consistent survival advantage for either modality-6. 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Some studies use «intention to treat» (ITT) methodology, some use «treatment received» (TR) and others use both. Neither method is inherently superior as each attempts to answer a different question. ITT studies are most useful clinically in that they determine whether the initial modality selection influences ultimate survival. TR studies, however, may be more likely to detect any real difference that may exist between the two modalities. 5. Almost all studies adjust for age, sex, and diabetic status. Ideally, they should also correct for the number and severity of baseline comorbid conditions as well as functional status. This is not always the case in practice because, as already noted, registry-based studies rarely have more than limited comorbidity data. This is particularly important because it is a common observation that patients who present late, or in a critically ill state with end stage renal disease, tend to be initially treated with HD. This may introduce a bias in favour of PD if correction for this baseline comorbidity is not adequate. To minimize this, 12 COMPARATIVE SURVIVAL IN HEMODIALYSIS AND PERITONEAL DIALYSIS data from the first 90 days on dialysis are typically omitted in these studies, but this may not be sufficient. 6. The statistical technique used to compare survival on the two modalities is typically the Cox Proportional Hazards model which presumes that the relative risks (or hazards) between the two modalities stay constant with the time. This is clearly not the case in practice. A number of studies have noted that the death rate in the first 1-2 years is relatively higher on HD than PD, but that the opposite tends to be the case in subsequent years 9, 12. This disproportionality is the fundamental cause underlying much of the confusion in the literature and explains why PD looks better in studies based on incident as compared to prevalent patients. 7. Modality switches from PD to HD are much commoner than those in the opposite direction. In a pure ITT analysis, this is not an issue, but, in TR analyses or in ITT analyses that are modified by censoring at the time of a modality switch, it is a potential problem and there is a concern that mortality occurring on the second modality may unfairly be attributed to the first modality. This is typically dealt with by using a «period of grace» of 60-90 days after a modality switch. During this time, any deaths are attributed to the previous modality. In practice, this tends to have less effect on the outcome of studies than might be expected. 8. Practices are continually changing in both PD and HD&#59; ideally, comparative studies should deal with a contemporary period, or else the results will be very out of date and may not be applicable to present day patients. 9. As already stated, correction for baseline comorbidity is important. Correction for ongoing comorbidity or for laboratory variables measured subsequent to initiation of dialysis is not appropriate, however, as these may be a consequence of the therapies being compared. For example, ongoing adjustment for residual renal function might correct away one of the advantages of PD while ongoing adjustment for serum albumin would be similarly unfair to HD. CONTEMPORARY STUDIES Against this background, some of the apparently contrasting outcomes in recent studies can be ex- plained. The Bloembergen study has some weaknesses. It was a point prevalent one and so omitted a lot of early time on dialysis 7. Because of the disproportionate hazards issue mentioned above, this makes HD look better relative to PD. It also did not correct for comorbidity and dealt with a period that is more than a decade ago. The Fenton study was methodologically superior in that it was based on incident patients and used both ITT and TR analyses which gave similar results 9, 13. It included correction for comorbid conditions, but this was inevitably limited and there is concern that PD patients in Canada may be significantly more healthy at baseline. Newer studies have clarified these issues somewhat. Vonesh y cols. have repeated the Bloembergen type analysis on more recent cohorts of US dialysis patients with a switch from a point prevalent to a period prevalent methodology in more recent years 14. The advantage of HD over PD has decreased in successive cohorts to the point of being statistically and clinically insignificant, although an excess mortality persists in older diabetics and in black patients. These results may be explained by the fact that a period prevalent analysis includes a greater proportion of data from the early years on PD and so gives correspondingly better results for PD. An additional explanation may be that there has been an actual improvement in relative outcomes on PD over the past decade. Collins y cols., using an ITT methodology with censoring after modality switches on over 100,000 incident US patients from the period 1994 to 1998, have shown that non diabetic patients have better survival on PD, while older female diabetics, in particular, do better on HD 15. This again, emphasizes how incident studies which are generally preferred, are associated with better results for PD, relative to HD. Recently, Murphy y cols. have presented detailed comorbidity data on a contemporary incident Canadian dialysis cohort 16. They have shown that there is no difference in outcome between PD and HD patients in Canada when correction for baseline comorbidity and functional status is very detailed. It thus appears that the methodology used has an enormous influence on the result of comparative mortality studies. It is desirable that incident patients be studied and when this is done, the advantage for HD seen in the US is no longer as marked as is the case in the Bloembergen study. Indeed, it may not be present at all as suggested by the recent data from Collins y cols. and Vonesh y cols. 13 P. G. BLAKE When correction for comorbidity is comprehensive, the advantage for PD in Canada that was noted in the Fenton study is no longer found. Thus, the differences between the two modalities in the two countries are not as marked as initially appeared to be the case. DATA OUTSIDE NORTH AMERICA All these data come from North American studies. Much less published information is, unfortunately, available from elsewhere. Australian data on incident patients using ITT show an advantage for HD, but a more contemporary study in prevalent patients, showed no difference 16-18. In the Lombardy Registry from Northern Italy, HD had a significant survival advantage, but there was a significant excess of baseline comorbidity in PD patients 8, 19. The opposite trend was seen in studies by Maiorca y cols. from an adjacent region of Northern Italy, and so it is difficult to draw comprehensive conclusions 3. European Registry data addressing comparative mortality has not been published in recent years, but new information becoming available suggests that mortality on PD was historically higher, but that the gap has closed steadily over the past 20 years. CONCLUSION In conclusion, these analyses are very complex and much influenced by the methodology used. PD, in general, appears to do well early on, but less so later, perhaps due to better retention of residual renal function in the early years and also perhaps due to less unmeasured baseline comorbidity. HD, in many studies, seems to do better in later years and may be relatively superior in older diabetics, while PD may have the advantage in younger diabetics. Results to date, do not reflect recent radical changes in PD prescription practices and these may impact on results that become available in the future. None of these data come from prospective randomized control studies and there is no justification for directing different sub groups to a particular modality. For now, modality selection should depend on individual patient issues and, most notably, patient preference. Patients who are doing poorly on a given modality, despite optimal practices, should be considered for early modality switch. However, the two modalities should be considered as complementary rather 14 than competitive and many patients may well require both during their time of dialysis. REFERENCES 1. Burton PR, Walls J: Selection-Adjusted Comparison of LifeExpectancy of Patients on Continuous Ambulatory Peritoneal Dialysis, Haemodialysis and Renal Transplantation. Lancet 1: 1115-1119, 1987. 2. Serkes KD, Blagg CR, Nolph KD, Vonesh EF, Shapiro F: Comparison of Patient and Technique Survival in Continuous Ambulatory Peritoneal Dialysis and Hemodialysis, a Multi-Center Study. Perit Dial Int 10: 15-19, 1990. 3. Maiorca R, Vonesh EF, Cavalli P, De Vecchi A, Giangrande A, La Greca G y cols.: A Multi-Center Selection-Adjusted Comparison of Patient and Technique Study Survivals on CAPD and Hemodialysis. Perit Dial Int 11: 118-127, 1991. 4. Posen GA, Jeffery JR, Fenton SSA, Arbus GS: Results from the Canadian Renal Failure Registry. Am J Kidney Dis 15: 397401, 1990. 5. Gentil MA, Carriazo A, Pavón MI, Rosado M, Castillo D, Ramos B y cols.: Comparison of Survival in Continuous Ambulatory Peritoneal Dialysis in Hospital, Haemodialysis: A Multi Centric Study. Nephrol Dial Transplant 6: 444-451, 1991. 6. Nelson CB, Port FK, Wolfe RA, Guire KE: Comparison of Continuous Ambulatory Peritoneal Dialysis in Hemodialysis Patient Survival with Evaluation of Trends During the 1980's. J Am Soc Nephrol 3: 1147-1155, 1992. 7. Bloembergen WE, Port FK, Mauger EA, Wolfe RA: Comparison in Mortality Between Patients Treated with Hemodialysis and Peritoneal Dialysis. J Am Soc Nephrol 6: 177-183, 1995. 8. Canada-USA (CANUSA) Peritoneal Dialysis Study Group: Adequacy of Dialysis and Nutrition in Continuous Peritoneal Dialysis&#59; Association with Clinical Outcome. J Am Soc Nephrol 7: 198-207, 1996. 9. Blake PG, Bloembergen WE, Fenton SSA. Changes in the Demographics in Prescription of Peritoneal Dialysis During the Last Decade 32: (Suppl 4) S44-S51, 1998. 10. Ward RA, Brier ME: Retrospective Analyses of Large Medical Data Bases: What Do They Tell Us? J Am Soc Nephrol 10: 429-432, 1999. 11. Port FK, Wolfe RA, Bloembergen WE, Held PJ, Young EW: The study of outcomes for CAPD versus hemodialysis patients. Perit Dial Int 16: 628-633, 1996. 12. Foley RN, Parfrey PS, Kent GM: Early and late mortality in ESRD: Hazards of the Cox model. J Am Soc Nephrol 8: 284A, 1997. 13. Schaubel DE, Morrison HI, Fenton SS: Comparing Mortality Rates in CAPD/CCPD and Hemodialysis. The Canadian Experience: Factor or Fiction? Perit Dial Int 18: 478-484, 1998. 14. Vonesh EF, Moran J: Mortality in ESRD: A Reassessment of Differences Between Patients Treated with Hemodialysis and Peritoneal Dialysis. J Am Soc Nephrol 10: 354-365, 1999. 15. Collins A, Ma J, Xia H, Ebben J: CAPD/CCPD in Incident Patients is Equal to or Better Than Hemodialysis, Except in Females Aged >=55 Years. J Am Soc Nephrol 9: 204A, 1998. 16. Murphy SE, Foley RN, Barrett BJ, Parfrey PS, Kent GM, Morgan J y cols.: Comparative Mortality of HD and PD in Canada. J Am Soc Nephrol 1998, 9: 1208A. COMPARATIVE SURVIVAL IN HEMODIALYSIS AND PERITONEAL DIALYSIS 17. D i s n e y A: Demography and survival of patients receiving t r e a t m e n t for chronic renal failure in Australia and New Z e a l a n d : Report on dialysis and renal transplantation treatment from the Australia and New Zealand Dialysis a n d Transplant Registry. Am J Kidney Dis 2 5 : 165-175, 1995. 18. Murphy BG, Carlin JB, Livingston B, Disney A, Becker G: An Analysis of Factors Predicting Mortality in Patients on Renal Replacement Therapy. J Am Soc Nephrol 7: 748A, 1996. 19. Locatelli F, Marcelli D, Conte F y cols.: 1983-1992: Report on Regular Dialysis and Transplantation in Lombardy. Am J Kidney Dis 25: 196-205, 1995. 15 "
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    "textoCompleto" => "NEFROLOGÍA. Vol. XX. Suplemento 3. 2000 Comparative survival in hemodialysis and peritoneal dialysis P. G. Blake Director Peritoneal Dialysis. Associate Professor Medicine. Optimal Dialysis Research Unit. London Health Sciences Centre. University of Western Ontario. London. Ontario. Canada. INTRODUCTION With the spread in popularity of PD, and particularly of CAPD, in the 1980's, it was inevitable that comparisons would be made between the success of the modality and that of conventional HD. Such comparisons can be done on the basis of quality of life, hospitalization, technique survival and cost effectiveness. But the most critical «hard» end point is, of course, patient survival. Initial studies addressing this issue from a variety of centres in North America and Western Europe were published between 1985 and 1995 and, in general, showed no consistent survival advantage for either modality-6. 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Blake Division of Nephrology London Health Sciences Centre 375 South Street London, Ontario, Canada 1. A large number of patients are required to show a significant survival difference between the two modalities and so such studies are typically based on national or regional registry data. However, even the best registries have limitations in terms of the completeness of data collection and the availability of information on baseline patient characteristics, such as comorbidity. 2. Such studies are, by their nature, retrospective and should not be interpreted as if they are prospective randomized control trials. 3. Most of the studies are based on incident patients, but some, including that by Bloembergen y cols., are prevalent based 7. In general, incident-based studies are preferable as they avoid the bias that may result from an excess of early events on one or other modality. 4. Some studies use «intention to treat» (ITT) methodology, some use «treatment received» (TR) and others use both. Neither method is inherently superior as each attempts to answer a different question. ITT studies are most useful clinically in that they determine whether the initial modality selection influences ultimate survival. TR studies, however, may be more likely to detect any real difference that may exist between the two modalities. 5. Almost all studies adjust for age, sex, and diabetic status. Ideally, they should also correct for the number and severity of baseline comorbid conditions as well as functional status. This is not always the case in practice because, as already noted, registry-based studies rarely have more than limited comorbidity data. This is particularly important because it is a common observation that patients who present late, or in a critically ill state with end stage renal disease, tend to be initially treated with HD. This may introduce a bias in favour of PD if correction for this baseline comorbidity is not adequate. To minimize this, 12 COMPARATIVE SURVIVAL IN HEMODIALYSIS AND PERITONEAL DIALYSIS data from the first 90 days on dialysis are typically omitted in these studies, but this may not be sufficient. 6. The statistical technique used to compare survival on the two modalities is typically the Cox Proportional Hazards model which presumes that the relative risks (or hazards) between the two modalities stay constant with the time. This is clearly not the case in practice. A number of studies have noted that the death rate in the first 1-2 years is relatively higher on HD than PD, but that the opposite tends to be the case in subsequent years 9, 12. This disproportionality is the fundamental cause underlying much of the confusion in the literature and explains why PD looks better in studies based on incident as compared to prevalent patients. 7. Modality switches from PD to HD are much commoner than those in the opposite direction. In a pure ITT analysis, this is not an issue, but, in TR analyses or in ITT analyses that are modified by censoring at the time of a modality switch, it is a potential problem and there is a concern that mortality occurring on the second modality may unfairly be attributed to the first modality. This is typically dealt with by using a «period of grace» of 60-90 days after a modality switch. During this time, any deaths are attributed to the previous modality. In practice, this tends to have less effect on the outcome of studies than might be expected. 8. Practices are continually changing in both PD and HD&#59; ideally, comparative studies should deal with a contemporary period, or else the results will be very out of date and may not be applicable to present day patients. 9. As already stated, correction for baseline comorbidity is important. Correction for ongoing comorbidity or for laboratory variables measured subsequent to initiation of dialysis is not appropriate, however, as these may be a consequence of the therapies being compared. For example, ongoing adjustment for residual renal function might correct away one of the advantages of PD while ongoing adjustment for serum albumin would be similarly unfair to HD. CONTEMPORARY STUDIES Against this background, some of the apparently contrasting outcomes in recent studies can be ex- plained. The Bloembergen study has some weaknesses. It was a point prevalent one and so omitted a lot of early time on dialysis 7. Because of the disproportionate hazards issue mentioned above, this makes HD look better relative to PD. It also did not correct for comorbidity and dealt with a period that is more than a decade ago. The Fenton study was methodologically superior in that it was based on incident patients and used both ITT and TR analyses which gave similar results 9, 13. It included correction for comorbid conditions, but this was inevitably limited and there is concern that PD patients in Canada may be significantly more healthy at baseline. Newer studies have clarified these issues somewhat. Vonesh y cols. have repeated the Bloembergen type analysis on more recent cohorts of US dialysis patients with a switch from a point prevalent to a period prevalent methodology in more recent years 14. The advantage of HD over PD has decreased in successive cohorts to the point of being statistically and clinically insignificant, although an excess mortality persists in older diabetics and in black patients. These results may be explained by the fact that a period prevalent analysis includes a greater proportion of data from the early years on PD and so gives correspondingly better results for PD. An additional explanation may be that there has been an actual improvement in relative outcomes on PD over the past decade. Collins y cols., using an ITT methodology with censoring after modality switches on over 100,000 incident US patients from the period 1994 to 1998, have shown that non diabetic patients have better survival on PD, while older female diabetics, in particular, do better on HD 15. This again, emphasizes how incident studies which are generally preferred, are associated with better results for PD, relative to HD. Recently, Murphy y cols. have presented detailed comorbidity data on a contemporary incident Canadian dialysis cohort 16. They have shown that there is no difference in outcome between PD and HD patients in Canada when correction for baseline comorbidity and functional status is very detailed. It thus appears that the methodology used has an enormous influence on the result of comparative mortality studies. It is desirable that incident patients be studied and when this is done, the advantage for HD seen in the US is no longer as marked as is the case in the Bloembergen study. Indeed, it may not be present at all as suggested by the recent data from Collins y cols. and Vonesh y cols. 13 P. G. BLAKE When correction for comorbidity is comprehensive, the advantage for PD in Canada that was noted in the Fenton study is no longer found. Thus, the differences between the two modalities in the two countries are not as marked as initially appeared to be the case. DATA OUTSIDE NORTH AMERICA All these data come from North American studies. Much less published information is, unfortunately, available from elsewhere. Australian data on incident patients using ITT show an advantage for HD, but a more contemporary study in prevalent patients, showed no difference 16-18. In the Lombardy Registry from Northern Italy, HD had a significant survival advantage, but there was a significant excess of baseline comorbidity in PD patients 8, 19. The opposite trend was seen in studies by Maiorca y cols. from an adjacent region of Northern Italy, and so it is difficult to draw comprehensive conclusions 3. European Registry data addressing comparative mortality has not been published in recent years, but new information becoming available suggests that mortality on PD was historically higher, but that the gap has closed steadily over the past 20 years. CONCLUSION In conclusion, these analyses are very complex and much influenced by the methodology used. PD, in general, appears to do well early on, but less so later, perhaps due to better retention of residual renal function in the early years and also perhaps due to less unmeasured baseline comorbidity. HD, in many studies, seems to do better in later years and may be relatively superior in older diabetics, while PD may have the advantage in younger diabetics. Results to date, do not reflect recent radical changes in PD prescription practices and these may impact on results that become available in the future. None of these data come from prospective randomized control studies and there is no justification for directing different sub groups to a particular modality. For now, modality selection should depend on individual patient issues and, most notably, patient preference. Patients who are doing poorly on a given modality, despite optimal practices, should be considered for early modality switch. However, the two modalities should be considered as complementary rather 14 than competitive and many patients may well require both during their time of dialysis. REFERENCES 1. Burton PR, Walls J: Selection-Adjusted Comparison of LifeExpectancy of Patients on Continuous Ambulatory Peritoneal Dialysis, Haemodialysis and Renal Transplantation. Lancet 1: 1115-1119, 1987. 2. Serkes KD, Blagg CR, Nolph KD, Vonesh EF, Shapiro F: Comparison of Patient and Technique Survival in Continuous Ambulatory Peritoneal Dialysis and Hemodialysis, a Multi-Center Study. Perit Dial Int 10: 15-19, 1990. 3. Maiorca R, Vonesh EF, Cavalli P, De Vecchi A, Giangrande A, La Greca G y cols.: A Multi-Center Selection-Adjusted Comparison of Patient and Technique Study Survivals on CAPD and Hemodialysis. Perit Dial Int 11: 118-127, 1991. 4. Posen GA, Jeffery JR, Fenton SSA, Arbus GS: Results from the Canadian Renal Failure Registry. Am J Kidney Dis 15: 397401, 1990. 5. Gentil MA, Carriazo A, Pavón MI, Rosado M, Castillo D, Ramos B y cols.: Comparison of Survival in Continuous Ambulatory Peritoneal Dialysis in Hospital, Haemodialysis: A Multi Centric Study. Nephrol Dial Transplant 6: 444-451, 1991. 6. Nelson CB, Port FK, Wolfe RA, Guire KE: Comparison of Continuous Ambulatory Peritoneal Dialysis in Hemodialysis Patient Survival with Evaluation of Trends During the 1980's. J Am Soc Nephrol 3: 1147-1155, 1992. 7. Bloembergen WE, Port FK, Mauger EA, Wolfe RA: Comparison in Mortality Between Patients Treated with Hemodialysis and Peritoneal Dialysis. J Am Soc Nephrol 6: 177-183, 1995. 8. Canada-USA (CANUSA) Peritoneal Dialysis Study Group: Adequacy of Dialysis and Nutrition in Continuous Peritoneal Dialysis&#59; Association with Clinical Outcome. J Am Soc Nephrol 7: 198-207, 1996. 9. Blake PG, Bloembergen WE, Fenton SSA. Changes in the Demographics in Prescription of Peritoneal Dialysis During the Last Decade 32: (Suppl 4) S44-S51, 1998. 10. Ward RA, Brier ME: Retrospective Analyses of Large Medical Data Bases: What Do They Tell Us? J Am Soc Nephrol 10: 429-432, 1999. 11. Port FK, Wolfe RA, Bloembergen WE, Held PJ, Young EW: The study of outcomes for CAPD versus hemodialysis patients. Perit Dial Int 16: 628-633, 1996. 12. Foley RN, Parfrey PS, Kent GM: Early and late mortality in ESRD: Hazards of the Cox model. J Am Soc Nephrol 8: 284A, 1997. 13. Schaubel DE, Morrison HI, Fenton SS: Comparing Mortality Rates in CAPD/CCPD and Hemodialysis. The Canadian Experience: Factor or Fiction? Perit Dial Int 18: 478-484, 1998. 14. Vonesh EF, Moran J: Mortality in ESRD: A Reassessment of Differences Between Patients Treated with Hemodialysis and Peritoneal Dialysis. J Am Soc Nephrol 10: 354-365, 1999. 15. Collins A, Ma J, Xia H, Ebben J: CAPD/CCPD in Incident Patients is Equal to or Better Than Hemodialysis, Except in Females Aged >=55 Years. J Am Soc Nephrol 9: 204A, 1998. 16. Murphy SE, Foley RN, Barrett BJ, Parfrey PS, Kent GM, Morgan J y cols.: Comparative Mortality of HD and PD in Canada. J Am Soc Nephrol 1998, 9: 1208A. COMPARATIVE SURVIVAL IN HEMODIALYSIS AND PERITONEAL DIALYSIS 17. D i s n e y A: Demography and survival of patients receiving t r e a t m e n t for chronic renal failure in Australia and New Z e a l a n d : Report on dialysis and renal transplantation treatment from the Australia and New Zealand Dialysis a n d Transplant Registry. Am J Kidney Dis 2 5 : 165-175, 1995. 18. Murphy BG, Carlin JB, Livingston B, Disney A, Becker G: An Analysis of Factors Predicting Mortality in Patients on Renal Replacement Therapy. J Am Soc Nephrol 7: 748A, 1996. 19. Locatelli F, Marcelli D, Conte F y cols.: 1983-1992: Report on Regular Dialysis and Transplantation in Lombardy. Am J Kidney Dis 25: 196-205, 1995. 15 "
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