Effects of nutritional status and dietetic interventions on survival in Cystic Fibrosis patients before and after lung transplantation

被引:51
|
作者
Hollander, F. M. [1 ,2 ]
van Pierre, D. D. [3 ]
de Roos, N. M. [3 ]
van de Graaf, E. A. [2 ]
Iestra, J. A. [4 ]
机构
[1] Univ Med Ctr Utrecht, Dept Dietet, NL-3508 GA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Cyst Fibrosis & Lung Transplantat Ctr, NL-3508 GA Utrecht, Netherlands
[3] Wageningen Univ, Div Human Nutr, NL-6700 AP Wageningen, Netherlands
[4] Univ Med Ctr Utrecht, Dept Publ Hlth, Julius Ctr Hlth Sci & Primary Care, NL-3508 GA Utrecht, Netherlands
关键词
Cystic Fibrosis; Lung transplantation; Nutritional status; Nutritional intervention; Body Mass Index; Fat Free Mass; FAT-FREE MASS; PERCUTANEOUS ENDOSCOPIC GASTROSTOMY; BODY-COMPOSITION; WEIGHT-GAIN; ADULTS; INDEX; BIOIMPEDANCE; IMPEDANCE; DEPLETION; SUPPORT;
D O I
10.1016/j.jcf.2013.08.009
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: This study retrospectively investigated nutritional status, dietetic intervention and intake in Cystic Fibrosis (CF) patients before and after lung transplantation (LTX). Methods: Body Mass Index (BMI), Fat Free Mass Index (FFMI) and nutritional intake were retrieved from 75 out-patients aged 15-53 years. Patients were seen every 3-4 months during the waiting list time (range 0-81 months) and up to 116 months after LTX. Survival was measured in months. Results: The median BMI at baseline was 19.2 kg/m(2) (range: 15.3 to 28.4 kg/m(2)) with 29 patients (39%) below <= 18.5 kg/m(2). FFMI (measured in 65 patients) had a median of 15.2 kg/m(2) (range: 11.1 to 22.4 kg/m(2)) with 39 patients (60%) <= 16.7 kg/m(2) (men) or <= 14.6 kg/m(2) (women). Median energy intake was 2800 kcal, 239 kcal higher than the estimated energy requirement. However, 8 patients consumed >= 500 kcal less than recommended. Protein intake was 104 (range 60-187) g or 1.9 g/kg per day. Despite dietetic intervention with oral nutritional supplements (ONS) (36 patients), tube feeding (12 patients), or both (13 patients), HMI and FFMI hardly improved pre-LTX. LTX was performed in 51 patients (68%); 10 patients died during follow-up, median survival time was 41 months. A BMI 18.5 kg/m(2) was more prevalent in patients who died before LTX (6/9) or who died after LTX (4/10) than in patients who were still alive on the waiting list (5/15) or who survived LTX (14/41). Results for FFMI were comparable. From 6-12 months post-LTX, BMI and FFMI markedly improved, especially in underweight patients. Conclusion: A BMI <= 18.5 kg/m(2) and an FFMI <= 16.7 kg/m(2) (men) or <= 14.6 kg/m(2) (women) appears to impair survival in LTX candidates with CF. Patients maintained a low body weight before LTX. After LTX weight gain is achieved. CD (C) 2013 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:212 / 218
页数:7
相关论文
共 50 条
  • [41] Pre-transplant Panel Reactive Antibody and Survival in Adult Cystic Fibrosis Patients After Lung Transplantation
    Don Hayes
    Dmitry Tumin
    Joseph D. Tobias
    Lung, 2016, 194 : 429 - 435
  • [42] High incidence of gastric bezoars in cystic fibrosis patients after lung transplantation
    Dellon, ES
    Morgan, DR
    Mohanty, SP
    Davis, K
    Aris, RM
    TRANSPLANTATION, 2006, 81 (08) : 1141 - 1146
  • [43] Cholangiocarcinoma after lung transplantation in a patient with cystic fibrosis
    Naderi, Amir Said Alizadeh
    Farsian, Farnas N.
    Lee, William Martens
    EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2008, 20 (11) : 1115 - 1117
  • [44] LATE-BREAKING ABSTRACT: Lung transplantation in cystic fibrosis patients in Israel: The importance of ethnicity and nutritional status
    Levine, Hagit
    Prais, Dario
    Raviv, Yael
    Rusanov, Victorya
    Rosengarten, Dror
    Saute, Milton
    Hoshen, Moshe
    Mussaffi, Huda
    Blau, Hannah
    Kramer, Mordechai R.
    EUROPEAN RESPIRATORY JOURNAL, 2015, 46
  • [45] Sleep and Respiratory Parameters After Lung Transplantation in Adult Patients With Cystic Fibrosis
    Kalkanis, Alexandros
    Papadopoulos, Dimitrios
    Vos, Robin
    Dupont, Lieven
    Buyse, Bertien
    Testelmans, Dries
    CLINICAL TRANSPLANTATION, 2024, 38 (11)
  • [46] Zinc Nutritional Status in Patients with Cystic Fibrosis
    Escobedo Monge, Marlene Fabiola
    Barrado, Enrique
    Alonso Vicente, Carmen
    Paz Redondo del Rio, Maria
    Manuel Marugan de Miguelsanz, Jose
    NUTRIENTS, 2019, 11 (01)
  • [47] Nutritional status is an important predictor of diaphragm strength in young patients with cystic fibrosis
    Hart, N
    Tounian, P
    Clément, A
    Boulé, M
    Polkey, MI
    Lofaso, F
    Fauroux, B
    AMERICAN JOURNAL OF CLINICAL NUTRITION, 2004, 80 (05) : 1201 - 1206
  • [48] Lung transplantation in cystic fibrosis patients - Medical followup
    Quattrucci, S
    Cimino, G
    Bertasi, S
    Rendina, E
    Venuta, F
    Vizza, CD
    Della Rocca, G
    Tomaselli, M
    Antonelli, M
    RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1998, 24 (02): : 21 - 23
  • [49] Infections in patients with cystic fibrosis following lung transplantation
    Kanj, SS
    Tapson, V
    Davis, RD
    Madden, J
    Browning, I
    CHEST, 1997, 112 (04) : 924 - 930
  • [50] Lung transplantation in patients with cystic fibrosis: The Israeli experience
    Prais, Dario
    Raviv, Yael
    Shitrit, David
    Yellin, Alon
    Sahar, Gideon
    Bendayan, Danielle
    Yahav, Yaacov
    Efrati, Ori
    Reichart, Nira
    Blau, Hannah
    Bakal, Ilana
    Buchman, Gila
    Saute, Milton
    Vidne, Bernardo
    Kramer, Mordechai R.
    ISRAEL MEDICAL ASSOCIATION JOURNAL, 2006, 8 (06): : 396 - 399