Literature DB >> 12456552

Are annual blood tests in preschool cystic fibrosis patients worthwhile?

A Jaffé1, R Buchdahl, A Bush, I M Balfour-Lynn.   

Abstract

AIM: To investigate whether routine annual assessment blood tests in cystic fibrosis (CF) patients under 5 years influence management.
METHODS: Retrospective review of the results of the first annual assessment blood tests of patients with CF less than 5 years of age during a four year period (1995-99). Management changes were identified from a follow up letter to the general practitioner or local paediatrician.
RESULTS: A total of 169 patients (100 female), median age 2.2 years (range 0.3-4.9) were identified. Venepuncture was successful in 93% of patients. Of the 32 individual blood parameters measured, the overall success rate in obtaining a result was 81%. Eleven per cent of patients underwent subsequent management changes, including liver ultrasound, fasting glucose, and a short course of iron. Of particular importance, vitamin A and E concentrations were low in 9% of patients, which prompted an increase in prescribed dose.
CONCLUSIONS: These results support the recommendations for routine blood tests at annual review in preschool CF children. The results may help to rationalise which tests are performed and thus reduce laboratory costs.

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Year:  2002        PMID: 12456552      PMCID: PMC1755836          DOI: 10.1136/adc.87.6.518

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  9 in total

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2.  Prevalence of liver disease in cystic fibrosis.

Authors:  R Scott-Jupp; M Lama; M S Tanner
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Review 3.  Nutritional assessment and management in cystic fibrosis: a consensus report. The Consensus Committee.

Authors:  B W Ramsey; P M Farrell; P Pencharz
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4.  Annual review or continuous assessment?

Authors:  S B Carr; R Dinwiddie
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Authors:  A P Feranchak; M K Sontag; J S Wagener; K B Hammond; F J Accurso; R J Sokol
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6.  Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosis.

Authors:  M N Bronstein; R J Sokol; S H Abman; B A Chatfield; K B Hammond; K M Hambidge; C D Stall; F J Accurso
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7.  Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group.

Authors:  P M Farrell; M R Kosorok; M J Rock; A Laxova; L Zeng; H C Lai; G Hoffman; R H Laessig; M L Splaingard
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8.  Relative anemia and iron deficiency in cystic fibrosis.

Authors:  J L Ater; J J Herbst; S A Landaw; R T O'Brien
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9.  Functional iron deficiency in adults with cystic fibrosis.

Authors:  M N Pond; A M Morton; S P Conway
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  9 in total
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2.  Iron Deficiency in Cystic Fibrosis: A Cross-Sectional Single-Centre Study in a Referral Adult Centre.

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  2 in total

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