You are here

Hemodiyaliz ve Sürekli Ambulatuar Periton Diyalizi Hastalarının Kardiyovasküler Hastalık Risk Faktörleri Açısından Karşılaştırılması: 3 Yıllık İzlem

Comparison of Hemodialysis Patients With Continuous Ambulatory Peritoneal Dialysis Patients in Terms of Cardiovascular Disease Risk Factors: A Three-Year Follow-

Journal Name:

Publication Year:

Abstract (2. Language): 
End stage renal disease (ESRD) is known to be associated with well known risk factors of cardiovascular disease (CVD) like hypertension and dyslipidemia. The aim of this study is to compare 2 groups of ESRD patients, who are being followed by hemodialysis (HD) or continuous ambulatory peritoneal dialysis (CAPD) for at least 3 years, in terms of CVD risk factors, retrospectively. Totally 133 ESRD patients (Group I: 65 CAPD patients, Group II: 68 HD patients) who were followed for at least 3 years under the initial dialysis modality were included. The predialysis 3 months' laboratory (Total cho¬lesterol, LDL-cholesterol, HDL-cholesterol, triglyceride, LDL/HDL, albumin and C-reactive protein) and clinical findings (body weight, blood pressure, antihypertensive and antilipemic medication) of the patients were collected. The 1-12th and 25-36th months' laboratory and clinical findings were also recorded as the "first year" and "third year" follow-up results respectively. Groups were statistically comparable in terms of predialysis data. When the first year data of each group was compared according to the initial ones, total cholesterol significantly increased in Group I (p<0.01), albumin increased (p<0.0001), triglyceride increased (p<0.05) and HDL-cholesterol decreased (p<0.01) in Group II. Comparison of third year data of each group with initial ones revealed that HDL-cholesterol decreased in both groups (p<0.005, <0.0001 respectively) but also LDL-cholesterol decreased (p<0.01) in Group II. When the 1st year laboratory results of groups were compared, CAPD was found to be associated with relatively higher total cholesterol (p<0.01) and lower albumin (p<0.0001) levels. Blood pressure measurements were also higher in CAPD group (For both systolic and diastolic blood pressures p<0.001) in the 1st year. Third year data revealed that CAPD was associated with rela¬tively higher levels of LDL-cholesterol (p<0.05) and lower levels of albumin (p<0.01) but there was no other statistical difference between groups, in terms of other lipid parameters, CRP, blood pressure and medication rece¬ived. Conclusion: CAPD treatment is found to be associated with dyslipide-mia and hypertension when compared to HD, especially in the first year fol¬low-up period. This difference seems to continue in a lesser extend in the following years. CAPD patients are under persistent risk of hypoalbuminemia which may be secondary to hemodilution, peritoneal protein loss or protein malnutrition secondary to dextrose absorbtion from dialysis fluid.
Abstract (Original Language): 
sküler hastalık (KVH) risk faktörleri ile ilişkisi bilinen bir send-romdur. Çalışmamızda, diyaliz tedavisinin başlangıcından itibaren en az 3 yıldır hemodiyaliz (HD) ya da sürekli ambulatuar periton diyalizi (SAPD) yöntemlerinden biriyle takip edilmekte olan 2 grup SDBY hastası, KVH risk faktörleri açısından retrospektif olarak karşılaştırılmıştır. Toplam 133 SDBY hastası (Grup I: 65 SAPD hastası, Grup II: 68 HD hastası) çalışmaya dahil edilmiştir. Diyaliz öncesi son 3 aylık laboratuvar (Total kolesterol, LDL-koles-terol, HDL-kolesterol, trigliserid, LDL/HDL, albümin ve C-reaktif protein) ve klinik bulgular (vücut ağırlığı, kan basıncı, antihipertensif ve antihiperlipide-mik tedavi) ile 1-12 ve 25-36 ay arası laboratuvar ve klinik bulgular "birinci yıl" ve "üçüncü yıl" verileri adıyla retrospektif olarak kaydedilmiştir. Gruplar diyaliz öncesi veriler göz önüne alındığında istatistiksel açıdan benzer bulunmuştur. Her grubun birinci yıl verileri ile diyaliz öncesi verilerinin karşılaştırılması sonucunda Grup I'de total kolesterol düzeylerinde anlamlı artış (p<0,01), Grup II'de albümin (p<0,0001) ve trigliseridde (p<0,05) artış ile HDL-kolesterol düzeylerinde düşüş (p<0,01), diyaliz öncesi verilerle üçüncü yıl verilerinin karşılaştırılmasında ise Grup I'de HDL kolesterol düzeylerinde düşüş (p<0,005), Grup II'de HDL (p<0,0001) ve LDL kolesterol (p<0,01) düzeylerinde düşüş olduğu görülmüştür. Grupların birinci yıl verilerinin birbiriyle karşılaştırılması sonucunda SAPD göreli olarak daha yüksek total kolesterol (p<0,01) ve daha düşük albümin (p<0,0001) düzeyleri ile ilişkili bulunmuştur. Aynı yıl içinde SAPD hastalarının sistolik ve diastolik kan basınç ortalaman da HD hastalarına göre daha yüksek seyretmiştir (p<0,001). Üçün¬cü yıl izleminde ise SAPD tedavisinin görece yüksek LDL-kolesterol (p<0,05) ve düşük albümin (p<0,01) ile ilişkili olduğu görülmüş, ancak bunlar dışında diğer olası aterosklerotik risk faktörleri (lipid parametreleri, CRP, kan basınç izlemleri) anlamlı bir fark saptanmamıştır. Sonuç: SAPD tedavisinin HD yön¬temine göre hipertansiyon ve dislipidemi gibi aterogenik risk faktörleri ile daha kuvvetli ilişki içinde olduğu görülmüştür. Bu ilişki, izleyen yıllarda azal¬arak devam etse de, kendisini en kuvvetli olarak birinci yılda göstermekte¬dir. SAPD hastaları sürekli olarak hipoalbüminemi riski altındadırlar. Bu du¬rum hemodilüsyon, peritoneal protein kaybı ya da diyalizattaki dekstrozun emilmesiyle gelişen protein malnütrisyonuna bağlı olabilir.
FULL TEXT (PDF): 
5-13

REFERENCES

References: 

1. United States Renal Data System. USRDS 1998 Annual Data Report. US Department of Health and Human Services. The National Institute of Health, National Institute of Diabets and Digestive and Kidney Diseases, Bethesda MD. August 1998.
2. Venkatesan J, Henrich WL. Anemia, hypertension and myocardial dysfunction in end stage renal disease. Semin Nephrol 1997;17:257.
3. Collins AJ. Cardiovascular mortality in end-stage renal disease. Am J Med Sci. 2003 Apr; 325(4):163.
4. Churchill DN, Taylor DW, Cook RJ, et al. Canadian he-modialysis morbidity study. Am J Kidney Dis 1992;19:214.
5. Rocco MV, Flanigan MJ, Beaver S, et al. Report from the 1995 Core Indicators for Peritoneal Dialysis Study Group. Am J Kidney Dis 1997;30:165.
6. Rahman M, Dixit A, Donley V, et al. Factors associated with inadequate blood pressure control in hypertensive hemodialysis patients. Am J Kidney Dis 1999;33:498.
7. Appel G. Lipid abnormalities in renal disease. Kidney Int
1991;39(1):169.
8. Nascimento MM, Pecoits-Filho R, Lindholm B, et al. Inf¬lammation, malnutrition and atherosclerosis in end-stage renal disease: a global perspective. Blood Purif
2002;20(5):454.
9. Buckalew, VM Jr, Berg, RL, Wang, SR, et al. Prevalence of hypertension in 1,795 subjects with chronic renal dise¬ase: The Modification of Diet in Renal Disease Study ba¬seline cohort. Am J Kidney Dis 1996;28(6):811.
10. Amar J, Vernier I, Rossignol E, et al. Nocturnal blood pressure and 24-hour pulse pressure are potent indica¬tors of mortality in hemodialysis patients. Kidney Int
2000;57:2485.
11. Mazzuchi N, Carbonelli E, Fernandez-Cean J. Importance of blood pressure control in hemodialysis patient survi¬val. Kidney Int 2000;58:2147.
12. Salem MM. Hypertension in haemodialysis population: any relationship to 2-years survival? Nephrol Dial Transplant 1999;14:125.
13. Port FK, Hulbert Shearon TE, Wolfe RA, et al. Predialysis
blood pressure and mortality risk in a national sample of maintenance hemodialysis patients. Am J Kidney Dis
1999;33:507.
14. Senti M, Romero R, Pedro-Botet J, et al. Lipoprotein ab¬normalities in hyperlipidemic and normolipidemic men on hemodialysis with chronic renal failure. Kidney Int
1992;41:1394.
15. Attman PO, Samuelsson O, Alaupovic P, et al. Lipoprote-in metabolism and renal failure. Am J Kidney Dis
1993;21:573.
16. Armodottir M, Thysell H, Dallongeville J, et al. Evidence that reduced lipoprotein lipase activity is not a primary pathogenetic factor for hypertriglyceridemia in renal fa¬ilure. Kidney Int 1995;48:779.
17. Seres DS, Strain GW, hashim SA et al. Improvement of plasma lipoprotein profiles during high-flux dialysis. Am J Soc Nephrol 1993;3(7):1409.
18. Levine DM, Gordon BR. Lipoprotein (a) levels in patients recieving renal replacement therapy: Methodologic issu¬es and clinical implications. Am J Kidney Dis
1995;26(1):162.
19. Maggi E, Bellazzi R, Falaschi F, et al. Enhanced LDL oxi¬dation in uremic patients: an additional mechanism for accelerated atherosclerosis? Kidney Int 1994;45(3):876.
20. Özdemir FN, Güz G, Sezer S, et al. Atherosclerosis risk is higher in continuous ambulatory peritoneal dialysis pati¬ents than in hemodialysis patients. Artif Organs
2001;25(6):448.
21. Sezer S, Özdemir FN, Arat Z, et al. What happens after conversion of treatment to continuous ambulatory perito¬neal dialysis from hemodialysis? Advances in Perit Dial
2000;16:177.
22. Massy ZA, Ma JZ, Louis TA, et al. Lipid lowering therapy in patients with renal disease. Kidney Int 1995;48(1):188.
23. Maiorca R. Cardiovascular problems in the choice of di¬alysis therapy for the elderly. Contrib Nephrol
1994;106:74.
12
Türk Nefroloji Diyaliz ve Transplantasyon Dergisi /Official Journal of the Turkish Society of Nephrology
HD ve SAPD Hastalarının Kardiyovasküler Hastalık Risk Faktörleri Açısından Karşılaştırılması: 3 Yıllık İzlem 0
24.
Fest
a A, Hanley AJ, Tracy RP, D'Agostino R Jr, Haffner SM. Inflammation in the prediabetic state is related to increased insulin resistance rather than decreased insulin secretion. Circulation. 2003 Oct 14;108(15):1822.
25. Wang T, Heimburger O, Waniewski J, Bergstrom J, Lindholm B. Increased peritoneal permeability is associated with decre¬ased fluid and small-solute removal and higher mortality in CAPD patients. Nephrol Dial Transplant 1998 May;13 (5): 1242.
26. Kagan A, Bar-Khayim Y, Schafer Z, Fainaru M. Heteroge¬neity in peritoneal transport during continuous ambula¬tory peritoneal dialysis and its impact on ultrafiltration, loss of macromolecules and plasma level of proteins, li-
pids and lipoproteins. Nephron 1993;63:32.
27. Kawaguchi Y, Hasegawa T, Nakayama M, et al. Issues af¬fecting the longevity of the continuous peritoneal dialy¬sis therapy. Kidney Int Suppl 1997;62:S105.
28. Tzamaloukas AH, Saddler MC, Murata GH, et al. Sympto¬matic fluid retention in patients on continuous peritone¬al dialysis. J Am Soc Nephrol 1995;6(2):198.
29. Chung SH, Heimburger O, Stenvinkel P, Wang T, Lind-holm B. Influence of peritoneal transport rate, inflamma¬tion, and fluid removal on nutritional status and clinical outcome in prevalent peritoneal dialysis patients. Perit
Dial Int 2003 Mar-Apr;23 (2):174.

Thank you for copying data from http://www.arastirmax.com