Archives of Disease in Childhood 2006;91:771-773
ORIGINAL ARTICLE
Does splenectomy in cystic fibrosis related liver disease improve lung function and nutritional status? A case series
1 Department of Respiratory Medicine, Royal Childrens Hospital, Melbourne, Australia
2 Department of Gastroenterology, Royal Childrens Hospital, Melbourne, Australia
Correspondence to:
Dr B Linnane
Department of Respiratory Medicine, Royal Childrens Hospital, Flemington Road, Parkville, VIC 3052, Australia; barry.linnane{at}rch.org.au
Aims: To review the effect of total splenectomy on lung function and nutrition in children with cystic fibrosis related liver disease (CFLD) and associated portal hypertension. The stated indications for surgery and the short and long term risks of the procedure were also documented.
Method: Over a 25 year period from January 1980 to June 2005, approximately 650 patients with cystic fibrosis (CF) were treated at the Royal Childrens Hospital, Melbourne, Australia. Nine patients with CFLD who underwent a splenectomy during that time were identified and their medical records were reviewed.
Results: FEV1% predicted dropped by 16±11% in the two years pre-splenectomy. This contrasts with the increase in FEV1% predicted of 2±16% in the two years post-splenectomy (p = 0.05). The cumulative gain in WAZ score (
WAZ pre) over the two years prior to splenectomy of 0.045±0.69 was not significantly different from the cumulative gain in WAZ score (
WAZ post) for the two years after splenectomy of 0.15±0.36 (p = 0.65). The average age at splenectomy was 14.8 years (SD = 3 years). The average weight of an excised spleen was 983 g (SD = 414 g). There were no deaths associated with splenectomy. The median length of follow up post-splenectomy was 6.0 years (range 0.715.8). There were no episodes of bacterial peritonitis or overwhelming sepsis.
Conclusions: Splenectomy may have a beneficial effect on lung function although this may not manifest itself until the second year post-splenectomy. Splenectomy in patients with CFLD appears to be a safe procedure.
Abbreviations: CF, cystic fibrosis; CFLD, cystic fibrosis related liver disease; FEV1, forced expiratory volume in 1 second; HAZ, z-score for height-for-age; WAZ, z-score for weight-for-age
Keywords: cystic fibrosis; splenectomy; portal hypertension; nutrition; respiratory function tests
Relevant Article
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Arch. Dis. Child. 2006 91: e5.
This article has been cited by other articles:
-
Van Biervliet, S., Robberecht, E.
(2007). Splenectomy in cystic fibrosis. Arch. Dis. Child.
92: 277-278
[Full Text]
eLetters:
Read all eLetters
- Splenectomy in cystic fibrosis
- Stephanie Van Biervliet, et al.
- ADC Online, 26 Sep 2006 [Full text]
- Enteric origins to hepatic and pulmonary dysfunction in cystic fibrosis?
- Richard G Fiddian-Green
- ADC Online, 3 Oct 2006 [Full text]
- Re: spenectomy in cystic fibrosis
- Richard G Fiddian-Green
- ADC Online, 3 Oct 2006 [Full text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.



