| Literature DB >> 15535454 |
Abhinandana Anantharaju1, David H Van Thiel.
Abstract
In many patients, long-term heavy drinking leads to chronic liver disease, liver failure, and even death. Orthotopic liver transplantation (OLT) is the only definitive treatment for end-stage liver disease, including alcoholic liver disease (ALD). Because of a shortage of donor organs, OLT for ALD patients remains controversial out of concerns that patients may resume drinking, thereby harming the transplanted organ. Therefore, transplant centers conduct careful screening procedures that assess patients' coexisting medical problems and psychosocial status to identify those patients who are medically most suited for the procedure and who are most likely to remain abstinent after OLT. Studies assessing the outcomes of ALD patients after OLT found that the survival rates of the transplanted organ and the patient were comparable to those of patients with nonalcoholic liver disease and that relapse rates among the ALD patients were low. Similarly, ALD patients and patients with other types of liver disease had comparable rates of compliance with complex medication regimens after OLT. Enhanced efforts to identify risk factors for relapse among OLT candidates with ALD and to target interventions specifically to those patients who are at high risk of relapse may further improve patient outcome and enhance the acceptance of OLT for alcoholic patients in the general population.Entities:
Mesh:
Year: 2003 PMID: 15535454 PMCID: PMC6668877
Source DB: PubMed Journal: Alcohol Res Health ISSN: 1535-7414
Studies Reporting Outcomes of Orthotopic Liver Transplantation (OLT) in Patients With Alcoholic Liver Disease
| Study | Period | No. of Patients | No. of Patients Lost to Followup | Months of Followup After OLT | Patients Employed (Part-Time/Full-Time) (%) | Used 6-Month Abstinence Criteria? | Survival (%) | Patients Who Relapsed (%) | Research Method Used | Patients Who Experienced Graft Dysfunction Because of Relapse (%) | Deaths Related to Relapse (%) | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
| ||||||||||||||
| Before OLT | After OLT | 1-yr | 2-yr | 3-yr | 4-yr | ||||||||||
| Starzl et al. | 1980–87 | 41 | 11 | 12–36 | N/A | N/A | No | 73 | - | - | - | 3 | Retrospective | 3 | 3 |
| Kumar et al. | 1982–88 | 73 | 21 | 25 | 0 | 54 | No | 74 | - | - | - | 11.5 | Phone interview | 2 | 2 |
| Bird et al. | 1980–89 | 24 | 6 | 4–84 | N/A | 94 | No | 66 | - | - | - | 22 | Retrospective | 17 | 0 |
| Stevens et al. | 1985–90 | 10 | - | 1–24 | N/A | N/A | No | - | - | - | - | 0 | Retrospective | 0 | 0 |
| Knechtle et al. | 1984–90 | 41 | 30 | N/A | 63 | 33 | No | 83 | - | - | 71 | 13 | Psychiatric interview | 0 | 0 |
| Goldstein et al. | 1985–91 | 41 | 4 | 6–66 | N/A | N/A | Yes | 86 | - | - | 72 | 13.5 | Retrospective | N/A | N/A |
| Gish et al. | 1988–91 | 29 | 0 | 12–41 | N/A | 80 | No | 93 | - | - | - | 21 | Prospective, combined | - | 0 |
| Osorio et al. | 1988–91 | 43 | 0 | 7–38 | 62 | 59 | Yes | 100 | - | - | - | 19 | Mailed questionnaire | N/A | 0 |
| 1982–93 | 58 | 14 | 33 | 48 | 89 | No | 71 | 66 | - | 63 | 31 | Clinic interview | 16 | 3.4 | |
| Howard et al. | 1987–92 | 20 | 20 | 12–72 | N/A | N/A | N/A | 79 | - | - | - | 95 | Extensive interviews | 10 | N/A |
| Raakow et al. | 1988–94 | 78 | 0 | 0.5–64 | N/A | 99 | No | 96 | 96 | - | 85 | 22 | Retrospective | - | 2.6 |
| Gerhardt et al. | 1985–91 | 67 | 26 | 36–96 | N/A | N/A | No | 90 | 84 | 82 | 76 | 49 | Phone interview | N/A | 4.5 |
| Tringali et al. | 1988–90 | 103 | 45 | 18–46 | 33 | 40 | No | - | - | - | - | 21 | Retrospective, combined | N/A | N/A |
| Zibari et al. | 1986–92 | 42 | 0 | N/A | 0 | 76 | No | 74 | 71 | 71 | - | 7 | Retrospective, combined | 0 | 0 |
| 1987–91 | 59 | 9 | 6–89 | N/A | N/A | No | 80 | - | - | 77 | 34 | Combined | N/A | 2 | |
| Foster et al. | 1986–94 | 84 | 21 | 28–70 | N/A | N/A | No | 79 | 75 | - | - | 21 | Combined | 17 | 5 |
| Anand et al. | 1987–94 | 39 | 0 | 7–63 | N/A | N/A | No | 79 | - | - | 79 | 13 | Clinic interview | 2.6 | 0 |
| Everson et al. | 1988–96 | 68 | 6 | < 90 | N/A | N/A | N/A | 91 | - | - | - | 30 | Phone interview | 9.7 | 6.5 |
| Stefanini et al. | 1986–96 | 18 | 7 | < 118 | 0 | 73 | Yes | 75 | 75 | - | 75 | 27 | Retrospective, combined | 27 | N/A |
| Fabrega et al. | N/A | 44 | 0 | 20–59 | N/A | N/A | Yes | - | - | - | - | 18 | Urine alcohol measurement | 7 | N/A |
| Tang et al. | 1987–96 | 71 | 15 | NA | 8 | 52 | No | 83 | 80 | - | - | 48 | Clinic interview | N/A | 1.4 |
| Pageaux et al. | 1989–94 | 53 | 0 | 42 | N/A | 30 | No | 75 | 69 | 67 | 62 | 32 | Clinic interview | 4 | 2 |
For full citations of these studies, see References.
Percentage of Liver Transplant Patients in Whom the Transplanted Organ Was Still Functional at 1, 3, and 5 Years After the Procedure, Listed According to the Underlying Causes of the Patient’s Liver Disease
| Underlying Cause of the Liver Disease | Number of Patients | Survival (%) | ||
|---|---|---|---|---|
|
| ||||
| 1-Year | 3-Year | 5-Year | ||
| Hepatitis C virus (HCV) infection | 9,525 | 77.3 | 67.5 | 61.0 |
| Alcoholic liver disease (ALD) | 6,527 | 77.1 | 68.9 | 60.8 |
| Acute hepatic necrosis | 3,546 | 66.9 | 59.4 | 54.2 |
| Other postnecrotic | 3,500 | 72.7 | 63.8 | 56.6 |
| Primary sclerosing cholangitis | 3,469 | 83.0 | 77.8 | 74.1 |
| Primary biliary cirrhosis | 3,345 | 80.3 | 75.5 | 71.3 |
| ALD + HCV infection | 2,402 | 79.8 | 67.9 | 61.7 |
| Metabolic disease | 1,958 | 77.3 | 71.6 | 67.3 |
| Autoimmune | 1,381 | 78.8 | 71.5 | 66.0 |
| Liver cancer (hepatocellular carcinoma) | 1,187 | 68.1 | 51.2 | 37.5 |
| All Causes | 46,940 | 74.5 | 67.4 | 62.7 |
Necrosis is tissue death occurring in groups of cells; cholangitis is an inflammation of the bile ducts; biliary cirrhosis is an inflammation of the liver resulting when bile flow through small ducts in the liver is obstructed; autoimmune diseases are those conditions in which the body’s immune system erroneously attacks the body’s own cells.
SOURCE: United Network for Organ Sharing (UNOS) registry, 1988–2001. Public data from UNOS/OPTN scientific registry (http://www.unos.org). Accessed December 2002.