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  6. Eradication of Haemophilus Influenzae in Children with Cystic Fibrosis, Paediatrics (701)
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Eradication of Haemophilus Influenzae in Children with Cystic Fibrosis, Paediatrics (701)

Warning

Objectives

This guideline aims to provide guidance for the RHC CF Team in the management of children with Cystic Fibrosis (CF) who attend the RHC CF Unit and who culture Haemophilus influenza in respiratory secretions.

Background

The role of Haemophilus influenzae in the progression of CF lung disease is not well elucidated with recent studies however it has long been recognised as a pathogen with guidelines including NICE recommending 2-4 weeks of treatment orally on first isolation:

 “The importance of this infection has been disputed, but most CF clinics would regard it as a significant pathogen. There is increasing evidence that non-typeable H.influenzae can form biofilms, lending weight to the argument that it is of pathogenic significance. The aim of treatment is to eradicate H.influenzae infection and prevent chronic infection.... Suggested antibiotics include co-amoxiclav, or doxycycline... Resistance to amoxicillin is common.1

Haemophilus influenzae 2

“For people with cystic fibrosis who develop a Haemophilus influenzae infection (diagnosed by a positive respiratory sample culture) but do not have clinical evidence of pulmonary infection, treat with an appropriate oral antibiotic.  For people with cystic fibrosis who develop a Haemophilus influenzae infection (diagnosed by a positive respiratory sample culture) and are unwell with clinical evidence of pulmonary infection, treat with an appropriate antibiotic, given orally or intravenously depending on the severity of the illness.”

In patients with CF, this organism is usually un-encapsulated (non-typeable) and therefore not covered by the H influenzae type b vaccine3

ERADICATION TREATMENT

Evaluation

  • ANNUAL AUDIT OF H. INFLUENZAE RATES
  • ANNUAL AUDIT OF H. INFLUENZAE ERADICATION
  • MONITORING OF H. INFLUENZAE RESISTANCE PATTERNS

Editorial Information

Last reviewed: 01/06/2022

Next review date: 01/05/2025

Author(s): Dr Jane Wilkinson; Dr Christine Peters; Dr Rosie Hague; Susan Kafka.

Version: 2

Approved By: Paediatric Drugs & Therapeutics Committee

Document Id: 701

References
  1. CF Trust Antibiotic Treatment  for Cystic Fibrosis  2009
  2. NICE : “ Cystic Fibrosis: Diagnosis and Management” 2017
  3. Lobo, J., Rojas-Balcazar, J. M., & Noone, P. G. (2012). Recent advances in cystic fibrosis. Clinics in chest medicine33(2), 307-328.
  4. Brompton Paediatric CF Guidelines 2017 https://www.rbht.nhs.uk/our-services/paediatrics/paediatric-cystic-fibrosis-clinics/care-children-cystic-fibrosis-2017
  5. Rayner RJ, Hiller EJ, Ispahani P, Baker M. Haemophilus infection in cystic fibrosis. Archives of Disease in Childhood. 1990;65(3):255-258.
  6. Scottish Paediatric Cystic Fibrosis Managed Clinical Network Prescribing Guidelines 2015
  7. The Leeds Method of Management. April, 2008.