Long-term follow-up of distal intestinal obstruction syndrome in cystic fibrosis

被引:20
|
作者
Lavie, Moran [1 ,2 ]
Manovitz, Tzipora [1 ,2 ]
Vilozni, Daphna [1 ,2 ]
Levy-Mendelovich, Sarina [1 ,2 ]
Sarouk, Ifat [1 ,2 ]
Weintraubv, Ilana [1 ,2 ]
Shoseyov, David [3 ,4 ]
Cohen-Cymberknoh, Malena [3 ,4 ]
Rivlin, Joseph [5 ]
Efrati, Ori [1 ,2 ]
机构
[1] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Pediat Pulm Unit, IL-52621 Tel Hashomer, Israel
[2] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Natl Ctr Cyst Fibrosis, IL-52621 Tel Hashomer, Israel
[3] Hadassah Hebrew Univ Med Ctr, Cyst Fibrosis Ctr, IL-91120 Jerusalem, Israel
[4] Hadassah Hebrew Univ Med Ctr, Pediat Pulm Unit, IL-91120 Jerusalem, Israel
[5] Carmel Hosp, Cyst Fibrosis Ctr, IL-34362 Haifa, Israel
关键词
Distal intestinal obstruction syndrome; Cystic fibrosis; Meconium ileus; Treatment; Recurrence; MECONIUM ILEUS EQUIVALENT; DIAGNOSIS; CHILDREN; ADULTS; GASTROGRAFIN; PERSPECTIVE; MULTICENTER; POPULATION; GUIDELINES; MUTATIONS;
D O I
10.3748/wjg.v21.i1.318
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the long-term follow-up of distal intestinal obstruction syndrome (DIOS) in Israeli cystic fibrosis (CF) patients. METHODS: This is a multi-center, comparative, retrospective study in which we reviewed the medical records of all CF patients from three major CF centers in Israel who were treated in the period from 1980 to 2012. Patients diagnosed with DIOS were defined as the study group. The patients were diagnosed with DIOS based on their clinical presentation and typical findings on either abdominal X-ray or computerized tomography scan. For the control group, CF patients with no DIOS were matched to the patients in the study group for age, sex, and cystic fibrosis transmembrane conductance regulator (CFTR) mutations. For both groups, the collected data included age, sex, CFTR genotype, weight, height, and body mass index. Clinical data included respiratory function tests in the last five years prior to the study, respiratory function test immediately before and after the DIOS event, number of hospitalizations, sputum culture results, and CF-related conditions diagnosed according to the CF clinical practice guidelines. In the study group, data on the DIOS treatment and tendency for DIOS recurrence were also analyzed. RESULTS: The medical charts for a total of 350 CF patients were reviewed. Of the 350 CF patients, 26 (7.4%) were diagnosed with DIOS. The control group included 31 CF patients with no DIOS diagnosis. The mean follow-up period was 21.6 +/- 8.2 years. The total of DIOS episodes in the follow-up period was 60. The distribution of DIOS episodes was as follows: 6/26 (23.1%) study patients had one episode of DIOS intheir lifetime, 7/26 (26.9%) had two episodes, 7/26 (26.9%) had three episodes, and 6/26 (23.1%) had four or more episodes. Compared to the control group, DIOS patients had a significantly higher incidence of meconium ileus in the past (65.4% vs 0%, respectively, P < 0.02), more Aspergillus spp. colonization (34.6% vs 3.2%, respectively, P < 0.02), and a higher number of hospitalizations due to respiratory exacerbations (8.6 vs 6.2 mean total hospitalizations per follow-up period, respectively, P < 0.02). No other significant differences were found between the control and study groups. The conservative treatment of DIOS, which mainly includes hydration and stool softeners, was successful in 82% of the episodes. The survival rate was similar for both groups. CONCLUSION: CF patients with DIOS suffer from recurrent hospitalizations and airway pathogen acquisition. Although recurrence of DIOS is common, conservative treatment is successful in most patients.
引用
收藏
页码:318 / 325
页数:8
相关论文
共 50 条
  • [21] DISTAL INTESTINAL OBSTRUCTION SYNDROME IN CYSTIC FIBROSIS - A 10 YEAR ANALYSIS
    Patel, G.
    Bishop, J.
    Keatley, L.
    Chien, J.
    Middleton, P.
    RESPIROLOGY, 2014, 19 : 197 - 197
  • [22] Emergency colonoscopy for distal intestinal obstruction syndrome in cystic fibrosis patients
    Shidrawi, RG
    Murugan, N
    Hodson, ME
    Westaby, D
    GUT, 1999, 44 : A23 - A23
  • [23] Abdominal pain in cystic fibrosis: it is not always distal intestinal obstruction syndrome!
    Lurz, E.
    Kluwe, W.
    Casaulta, C.
    Latzin, P.
    Regamey, N.
    SWISS MEDICAL WEEKLY, 2009, 139 (21-22) : 27S - 27S
  • [24] Distal tibial triplane fractures: Long-term follow-up
    Rapariz, JM
    Ocete, G
    GonzalezHerranz, P
    LopezMondejar, JA
    Domenech, J
    Burgos, J
    Amaya, S
    JOURNAL OF PEDIATRIC ORTHOPAEDICS, 1996, 16 (01) : 113 - 118
  • [25] LIVER-CIRRHOSIS IN CYSTIC-FIBROSIS - THERAPEUTIC IMPLICATIONS AND LONG-TERM FOLLOW-UP
    FEIGELSON, J
    ANAGNOSTOPOULOS, C
    POQUET, M
    PECAU, Y
    MUNCK, A
    NAVARRO, J
    ARCHIVES OF DISEASE IN CHILDHOOD, 1993, 68 (05) : 653 - 657
  • [26] LONG-TERM FOLLOW-UP OF THE MAGPI OPERATION FOR DISTAL HYPOSPADIAS
    HASTIE, KJ
    DESHPANDE, SS
    MOISEY, CU
    BRITISH JOURNAL OF UROLOGY, 1989, 63 (03): : 320 - 322
  • [27] Interventions for treating distal intestinal obstruction syndrome (DIOS) in cystic fibrosis
    Green, Jessica
    Carroll, Will
    Gilchrist, Francis J.
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2018, (08):
  • [28] Emergency colonoscopy for distal intestinal obstruction syndrome in cystic fibrosis patients
    Shidrawi, RG
    Murugan, N
    Westaby, D
    Gyi, K
    Hodson, ME
    GUT, 2002, 51 (02) : 285 - 286
  • [29] Interventions for treating distal intestinal obstruction syndrome (DIOS) in cystic fibrosis
    Gilchrist, F. J.
    Green, J.
    Carroll, W.
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2021, (12):
  • [30] Interventions for preventing distal intestinal obstruction syndrome (DIOS) in cystic fibrosis
    Green, Jessica
    Gilchrist, Francis J.
    Carroll, Will
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2018, (06):