| Literature DB >> 24935278 |
Aldo Ferreira-Hermosillo1, Edith Valdez-Martínez, Miguel Bedolla.
Abstract
BACKGROUND: In Mexico, diabetes mellitus is the main cause of end - stage kidney disease, and some patients may be transplant candidates. Organ supply is limited because of cultural issues. And, there is a lack of standardized clinical guidelines regarding organ donation. These issues highlight the tension surrounding the fact that living donors are being selected despite being prediabetic. This article presents, examines and discusses using the principles of non-maleficience, autonomy, justice and the constitutionally guaranteed right to health, the ethical considerations that arise from considering a prediabetic person as a potential kidney donor. DISCUSSION: Diabetes is an absolute contraindication for donating a kidney. However, the transplant protocols most frequently used in Mexico do not consider prediabetes as exclusion criteria. In prediabetic persons there are well known metabolic alterations that may compromise the long - term outcomes of the transplant if such donors are accepted. Even so, many of them are finally included because there are not enough donor candidates. Both, families and hospitals face the need to rapidly accept prediabetic donors before the clinical conditions of the recipient and the evolution of the disease exclude him/her as a transplant candidate; however, when using a kidney potentially damaged by prediabetes, neither the donor's nor the recipient's long term health is usually considered.Considering the ethical implication as well as the clinical and epidemiological evidence, we conclude that prediabetic persons are not suitable candidates for kidney donation. This recommendation should be taken into consideration by Mexican health institutions who should rewrite their transplant protocols.Entities:
Mesh:
Year: 2014 PMID: 24935278 PMCID: PMC4065609 DOI: 10.1186/1472-6939-15-45
Source DB: PubMed Journal: BMC Med Ethics ISSN: 1472-6939 Impact factor: 2.652
Studies linking glucose level with the development of kidney damage
| Fehrman-Ekholm et al. 2001 [ | Cohort study with a follow − up of 12 years (April 1964 − December 1995) | Sweden | Normal initial OGTT | Six developed T2DM |
| 348 relative living donors (93.5% inbreeding) | ||||
| Aroda et al. 2008 [ | Review study. Information from the National Centre for Chronic Disease Prevention and Health Promotion (2008) | USA | Fasting plasma glucose levels and OGTT | Risk to develop T2DM: |
| National Study | 0.7% normoglicemic, and | |||
| 5 − 10% IFG and IGT | ||||
| Nichols et al. 2007 [ | Cohort studies with a follow time of nine years (January 1994 − December 2003) | USA | Fasting plasma glucose levels between | From people with glucose levels between 100–109 mg/dL, 8.1% developed T2DM. |
| 5,452 members from the Kaiser Permanente Northwest | ||||
| From people with glucose levels between 110–125 mg/dl, 24.3% developed T2DM | ||||
| 100–109 mg/dl and 110–125 mg/dl | ||||
| Fox et al. | Cohort studies. | USA | Fasting plasma glucose levels and OGTT | Risk of 65% to develop CKF on people with IFG and IGT in comparison with control group |
| Framingham (Follow − up) | Initial time: 1991–1995 | 2,398 persons | ||
| 2005 [ | ||||
| Azar et al. 2007 [ | Cohort study with a follow − up of three years | Iran | Clinical and biochemical record | 55% presented hypertension. |
| Tabriz Medical Sciences University | ||||
| 7% Increased creatinine concentrations | ||||
| 86 living donors, no related | 10% presented severe depression |
CKF = Chronic Kidney Failure.