Outcome of gastrointestinal complications after liver transplantation for familial amyloidotic polyneuropathy

被引:0
|
作者
Lång, K
Wikström, L
Danielsson, Å
Tashima, K
Suhr, OB [1 ]
机构
[1] Univ Umea Hosp, Dept Med, SE-90185 Umea, Sweden
[2] Pitea Hosp, Dept Med, Pitea, Sweden
[3] Skelleftea Hosp, Dept Med, Skelleftea, Sweden
关键词
amyloidosis; hereditary; inborn errors of metabolism; malabsorption; bile acids; fat; small-intestinal bacterial contamination; transplantation; liver;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Gastrointestinal disturbances are important prognostic factors for mortality and morbidity after liver transplantation for familial amyloidotic polyneuropathy (FAP). However, the impact of liver transplantation on malabsorption and bacterial small-bowel contamination has not been evaluated. Methods: Twenty-three FAP patients were available for the study. They were examined for gastrointestinal disturbances as a part of the evaluation for liver transplantation for FAP. Bile acid malabsorption was diagnosed with the [Se-75]-homocholic acid taurate (SeHCAT) test; fat malabsorption by measuring faecal fat excretion; and bacterial small-bowel contamination with the hydrogen breath test (HBT). Results: No significant improvement of malabsorption test results were noted from the pretransplant evaluation 8 months (range, 2-20 months) before transplantation to the post-transplant evaluation performed a median of 20 months (range, 9-62 months)after the procedure. The SeHCAT test result became abnormal in two patients and normal in one, and changes in the test correlated with the time the patients were waiting for transplantation. Faecal fat excretion after transplantation correlated with duration of the disease and with fat excretion before transplantation. A significantly increased fat excretion was noted at the post-transplant evaluation. A change in HBT result was noted in only one patient, in whom the test result became normal; pre-transplant Values correlated with those obtained after transplantation. Conclusion: For most FAP patients no improvement in gastrointestinal function was found after transplantation. The finding underlines the importance of an early transplantation before the patients have developed gastrointestinal dysfunction.
引用
收藏
页码:985 / 989
页数:5
相关论文
共 50 条
  • [41] RENAL-FAILURE AFTER LIVER-TRANSPLANTATION FOR FAMILIAL AMYLOIDOTIC POLYNEUROPATHY - A MAJOR COMPLICATION
    PATACA, I
    RIBEIRO, S
    BUINHO, F
    MORBEY, K
    FREIRE, A
    LOBOS, AV
    NOLASCO, F
    MONTEIRO, E
    COSTA, AM
    PENA, J
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1995, 6 (03): : 1110 - 1110
  • [42] Presence of variant transthyretin in aqueous humor of a patient with familial amyloidotic polyneuropathy after liver transplantation
    Haraoka, K
    Ando, Y
    Ando, E
    Sun, XG
    Nakamura, M
    Terazaki, H
    Misumi, S
    Tanoue, Y
    Tajiri, T
    Shoji, S
    Ishizaki, T
    Okabe, H
    Tanihara, H
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2002, 9 (04): : 247 - 251
  • [43] Marked cardiomegaly in a patient with familial amyloidotic polyneuropathy after orthotopic liver transplantation: a case study
    Sakashita, Naomi
    Kagawa, Seiko
    Date, Risako
    Ueno, Tatsuro
    Nakagawa, Takenobu
    Yamashita, Taro
    Obayashi, Konen
    Ohshima, Toshinori
    Ueda, Mitsuharu
    Horiguchi, Hidehisa
    Ando, Yukio
    Takeya, Motohiro
    PATHOLOGY INTERNATIONAL, 2013, 63 (05) : 260 - 265
  • [44] De novo amyloid synthesis in ocular tissue in familial amyloidotic polyneuropathy after liver transplantation
    Ando, Y
    Ando, E
    Tanaka, Y
    Yamashita, T
    Tashima, K
    Suga, M
    Uchino, M
    Negi, A
    Ando, M
    TRANSPLANTATION, 1996, 62 (07) : 1037 - 1038
  • [45] Accelerating restrictive cardiomyopathy after liver transplantation in a patient with familial amyloidotic polyneuropathy: A case report
    Robin J.
    Meyers S.
    Nahlawi M.
    Puthumana J.
    Lomasney J.
    Mehlman D.
    Rigolin V.
    Davidson C.
    Journal of Medical Case Reports, 2 (1)
  • [46] Outcome of exercise electrocardiography in familial amyloidotic polyneuropathy patients, Portuguese type, under evaluation for liver transplantation
    Juneblad, K
    Näslund, A
    Olofsson, BO
    Suhr, OB
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2004, 11 (03): : 208 - 213
  • [47] LIVER-TRANSPLANTATION AS A THERAPY FOR FAMILIAL AMYLOIDOTIC POLYNEUROPATHY (FAP), PORTUGUESE TYPE
    MONTEIRO, E
    MORBEY, A
    VELOSO, J
    FREIRE, A
    COSTA, PP
    LUIS, MLS
    HEPATOLOGY, 1994, 20 (04) : A120 - A120
  • [48] The Coimbra University Hospital experience in liver transplantation in patients with familial amyloidotic polyneuropathy
    Perdigoto, R
    Furtado, AL
    Furtado, E
    Oliveira, FJ
    Geraldes, B
    Mota, O
    Ferrao, J
    Tome, L
    Viana, J
    TRANSPLANTATION PROCEEDINGS, 2003, 35 (03) : 1125 - 1125
  • [49] Liver mitochondrial function in familial amyloidotic polyneuropathy
    Silva, O. Castro e
    Sankarankutty, A. K.
    Souza, M. E. J.
    Picinato, M. A. N. C.
    Fina, C. F.
    Jordani, M. C.
    Mente, E. D.
    Cagnolatti, D.
    Teixeira, A. C.
    Souza, F. F.
    Martinelli, A. L. C.
    Rondon, L. Z.
    TRANSPLANTATION PROCEEDINGS, 2008, 40 (03) : 771 - 773
  • [50] Early liver transplantation is essential for familial amyloidotic polyneuropathy patients' quality of life
    Jonsén, E
    Suhr, OB
    Tashima, K
    Athlin, E
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2001, 8 (01): : 52 - 57