A nurse is evaluating a 4-year old child who has cystic fibrosis

The Cystic Fibrosis (CF) Service at Queensland Children’s Hospital (QCH) is the largest paediatric CF clinic in Australia. We provide comprehensive specialist care for all children diagnosed with CF across Queensland and Northern New South Wales. Presently we care for around 450 children and adolescents from birth until age 18 years. Every year around 20 newly diagnosed babies are referred to QCH CF clinic from Queensland, interstate and overseas. We have a dedicated multidisciplinary CF team who provide inpatient, outpatient and community liaison services. We also provide outreach services to regional hospitals to help deliver CF care closer to home and are actively involved in the education and training of health professionals who care for children with CF from around the state. We have an established research unit and we are involved in national and international clinical trials of new CF therapies.

The CF telephone service

Our CF nurses provide a telephone service for patients and carers during office hours (Monday to Friday, 8am-4pm).
t: 07 3068 2303

There is also a 24-hour physician on-call service for patients with CF operating out of QCH.
t: 07 3068 1111

Transition to adult CF services

The paediatric clinic at QCH has strong links with the adult CF services at The Prince Charles Hospital and the Mater Adult Hospital. As children grow and mature we assist with their transition to adult care by educating teenagers about their health, supporting and encouraging self-care and promoting positive health behaviours. We work closely with the adult CF centres to ensure that the transfer of our adolescent patients across to the adult CF services is timely and seamless.

Research

The CF clinic at QCH is actively engaged in cystic fibrosis research including national and international clinical trials of new CF treatments.

Clinics

Outreach CF services are available twice yearly throughout Queensland in the following locations:

  • Gold Coast
  • Cairns
  • Townsville
  • Rockhampton
  • Mackay
  • Bundaberg
  • Toowoomba
  • Hervey Bay

Contact your local hospital in these areas for more information.

Who can access this service?

All children with cystic fibrosis aged from birth to their 18th birthday can access this service.

Catchment area

The Cystic Fibrosis service is available to children living in Queensland and Northern New South Wales. CF services are also available to children with CF living in other areas in accordance with state and national agreements.

Do I need a referral?

You will need a formal referral to access this service.

How do I get a referral?

Referrals are accepted from:

  • general practitioners
  • paediatric specialists.

Other referral information

Infants newly diagnosed through newborn screening

Babies newly diagnosed with cystic fibrosis through newborn screening (the heel prick test) will automatically receive an appointment at the CF clinic. Parents/carers will be contacted by the CF clinic nurse to arrange their first appointment.

Please bring the following items to your child’s appointment:

  • Medicare card
  • Private health insurance details
  • Pension/healthcare/Department of Veteran Affairs cards

For enquiries regarding referrals or for more information contact us on 07 3068 2300.

Information for health professionals

The Cystic Fibrosis service at QCH provides specialist multidisciplinary care for all aspects of CF. The CF service provides:

  • inpatient and outpatient treatment services
  • CF telephone service (office hours) provided by CF nurses
  • new diagnosis education, management and support
  • school and home visits and community liaison
  • outreach clinics
  • transition services
  • clinical research and clinical trials
  • education and training of allied health, nursing and medical professionals in CF care.

Referral instructions

Newly diagnosed patients may be referred to the cystic fibrosis service by contacting the CF specialist nurse via the Queensland Children’s Hospital switchboard during office hours.
t: 07 3068 1111

The CF clinic receives notification of all newly diagnosed infants with CF through the state wide newborn screening program. Parents and carers of newly diagnosed infants are contacted by the CF nurse to arrange an appointment.

Referrals for children with CF who have recently relocated to Queensland are accepted, up to a child’s 16th birthday. After 16 years of age the patient may be referred to adult services where appropriate. The clinic requires a referral letter from the child’s previous CF specialist and an indefinite referral from their local general practitioner for continuing care.

Patients/carers should be advised to bring the following items to their child’s appointment:

  • Medicare card
  • List of current medications
  • Private health insurance details
  • Pension/healthcare/Department of Veteran Affairs cards
  • Relevant tests or imaging (as appropriate)

Cystic Fibrosis Standards of Care Australia 2008
Australian and New Zealand Nursing Standards of Care for Cystic Fibrosis 2015
Nutrition Guidelines for Cystic Fibrosis in Australia and New Zealand 2017
Physiotherapy for Cystic Fibrosis in Australia and New Zealand Clinical Practice Guideline 2016
Cystic Fibrosis Australia
Therapy resources for CF

Our team

Research and experience has shown that the best way to care for children with CF is through a multidisciplinary approach. We have a dedicated multidisciplinary CF team made up of specialist cystic fibrosis doctors and nurses, dietitians, physiotherapists, social workers, occupational therapists, and mental health professionals. We also have access to a wide range of paediatric medical and surgical specialists, along with diagnostic and pharmacy services to support our patients in all aspects of CF care.

We believe the best way to care for children with CF is through a strong, cooperative partnership between patients, their families and their CF team. We practice family centred care and aim to tailor CF treatment to suit the individual child and family wherever possible.

Director

Prof Alan Isles

Cystic Fibrosis Service Leads

Professor Alan Isles, Paediatric Respiratory Physician, Director Respiratory and Sleep Medicine
Professor Claire Wainwright, Paediatric Respiratory Physician, Lead Cystic Fibrosis Service
Dr Tonia Douglas, Paediatric Respiratory and Sleep Physician, Lead Cystic Fibrosis Service
Elizabeth Shevill, Nurse Practitioner, Nursing Lead Cystic Fibrosis Service

Senior Medical Officers

Dr Scott Burgess
Professor Anne Chang
Dr Jasneek Chawla
Dr Leanne Gauld
Dr Vikas Goyal
Dr Nitin Kapur
Dr David Kilner
Dr Sadasivam Suresh

Cystic fibrosis specialist nurses

Penny Mitchell, Clinical Nurse Consultant (CNC)
Peta Yarrow, Clinical Nurse Consultant (CNC)
Ruth Hollins, Clinical Nurse (CN)
Nicola Boyle, nurse

Dietitians

Megan Farquar
Sarah Kane

Physiotherapists

Ryan Black
Joanne Leavitt
Rachel Langton

Social workers

Kylie Swyer
Lara Davies

Occupational therapist

Bianca Richards

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1. Sawicki GS, Sellers DE, Robinson WM. High treatment burden in adults with cystic fibrosis: challenges to disease self-management. J. Cystic Fibrosis (2009) 8:91–6. 10.1016/j.jcf.2008.09.007 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

2. Hurley MN, McKeever TM, Prayle AP, Fogarty AW, Smyth AR. Rate of improvement of CF life expectancy exceeds that of general population–Observational death registration study. J Cystic Fibrosis (2014) 13:410–5. 10.1016/j.jcf.2013.12.002 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

3. Registry CFFP. Patient Registry Annual Data Report (2016). [Google Scholar]

4. Dodge JA, Lewis PA, Stanton M, Wilsher J. Cystic fibrosis mortality and survival in the UK: 1947–2003. Eur Respir J. (2007) 29:522–6. 10.1183/09031936.00099506 [PubMed] [CrossRef] [Google Scholar]

5. Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatric Gastroenterol Nutr. (2002) 35:246–59. 10.1097/00005176-200209000-00004 [PubMed] [CrossRef] [Google Scholar]

6. Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. Cystic fibrosis adult care: consensus conference report. Chest (2004) 125:1S−39S. 10.1378/chest.125.1_suppl.1S [PubMed] [CrossRef] [Google Scholar]

7. Alvarez JA, Ziegler TR, Millson EC, Stecenko AA. Body composition and lung function in cystic fibrosis: association with adiposity and normal weight obesity. Nutrition (2016) 32:447–52. 10.1016/j.nut.2015.10.012 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

8. Stallings V, Stark L, Robinson K, Feranchak A, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc. (2008) 108:832–9. 10.1016/j.jada.2008.02.020 [PubMed] [CrossRef] [Google Scholar]

9. Kalnins D, Wilschanski M. Maintenance of nutritional status in patients with cystic fibrosis: new and emerging therapies. Drug Design Dev Ther. (2012):2012–6. 10.2147/DDDT.S9258 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

10. O'Donohoe R, Fullen BM. Adherence of subjects with cystic fibrosis to their home program: a systematic review. Respirat Care (2014) 59:1731–46. 10.4187/respcare.02990 [PubMed] [CrossRef] [Google Scholar]

11. Stark LJ. Can nutrition counselling be more behavioural? Lessons learned from dietary management of cystic fibrosis. Proc Nutr Soc. (2003) 62:793–9. 10.1079/PNS2003294 [PubMed] [CrossRef] [Google Scholar]

12. Zemanick E, Harris J, Conway S, Konstan M, Marshall B, Quittner A, et al.. Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy. J Cystic Fibrosis (2010) 9:1–16. 10.1016/j.jcf.2009.09.003 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

13. Sullivan JS, Mascarenhas MR. Nutrition: prevention and management of nutritional failure in cystic fibrosis. J Cystic Fibrosis (2017) 16:S87–93. 10.1016/j.jcf.2017.07.010 [PubMed] [CrossRef] [Google Scholar]

14. Panagopoulou P, Fotoulaki M, Nikolaou A, Nousia-Arvanitakis S. Prevalence of malnutrition and obesity among cystic fibrosis patients. Pediatrics Int. (2013) 56:89–4. 10.1111/ped.12214 [PubMed] [CrossRef] [Google Scholar]

15. Lai HJ, Shoff SM. Classification of malnutrition in cystic fibrosis: implications for evaluating and benchmarking clinical practice performance. Am J Clin Nutr. (2008) 88:161–6. 10.1093/ajcn/88.1.161 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

16. van Gool K, Norman R, Delatycki MB, Hall J, Massie J. Understanding the cost of care for cystic fibrosis: an analysis by age and health state. Value Health (2013) 16:345–55. 10.1016/j.jval.2012.12.003 [PubMed] [CrossRef] [Google Scholar]

17. Gu Y, Garcia-Pérez S, Massie J, van Gool K. Cost of care for cystic fibrosis: an investigation of cost determinants using national registry data. Eur J Health Econom. (2015) 16:709–17. 10.1007/s10198-014-0621-5 [PubMed] [CrossRef] [Google Scholar]

18. Kettler L, Sawyer S, Winefield H, Greville H. Determinants of adherence in adults with cystic fibrosis. Thorax (2002) 57:459–64. 10.1136/thorax.57.5.459 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

19. Coleman-Jensen A, Nord M, Andrews M, Carlson S. Household Food Security in the United States in 2011. United States Department of Agriculture; (2012). [Google Scholar]

20. Coleman-Jensen A, Rabbitt M, Gregory C, Singh A. Household Food Security in the United States in 2014. United States Department of Agriculture; (2015). [Google Scholar]

21. Bank IF. Food Insecurity in Idaho (2015). [Google Scholar]

22. Charkhchi P, Fazeli Dehkordy S, Carlos RC. Housing and food insecurity, care access, and health status among the chronically ill: an analysis of the behavioral risk factor surveillance system. J Gen Int Med. (2018) 33:644–50. 10.1007/s11606-017-4255-z [PMC free article] [PubMed] [CrossRef] [Google Scholar]

23. McDonald C, Christensen N, Lingard C, Peet K, Walker S. Nutrition knowledge and confidence levels of parents of children with cystic fibrosis. ICAN (2009) 1:325–31. 10.1177/1941406409355192 [CrossRef] [Google Scholar]

24. Steinkamp G, Wiedemann B. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project. Thorax (2002) 57:596–601. 10.1136/thorax.57.7.596 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

25. Goodin B.(2005). Nutrition issues in cystic fibrosis. Pract Gastroenterol, 27:76–94. Available online at: https://www.practicalgastro.com/pdf/GoodinArticle_May05.pdf [Google Scholar]

26. Cruz I, Marciel KK, Quittner AL, Schechter MS. Anxiety and depression in cystic fibrosis. Semin Respir Crit Care Med. (2009) 30:569–78. 10.1055/s-0029-1238915 [PubMed] [CrossRef] [Google Scholar]

27. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)–a metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. (2009) 42:377–81. 10.1016/j.jbi.2008.08.010 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

28. Bickel G, Nord M, Price C, Hamilton W, Cook J. Measuring food security in the United states - guide to measuring household food security. In: Drive PC, Alexandria V, editors. Office of Analysis N, and Evaluation, Food and Nutrition Service USDA, Alexandria, VA: (2000). p. 305–2133. [Google Scholar]

29. Stanojevic S, Wade A, Stocks J, Hankinson J, Coates AL, Pan H, et al.. Reference ranges for spirometry across all ages: a new approach. Am J Res Crit Care Med. (2008) 177:253–60. 10.1164/rccm.200708-1248OC [PMC free article] [PubMed] [CrossRef] [Google Scholar]

30. Piccioni P, Borraccino A, Forneris M, Migliore E, Carena C, Bignamini E, et al.. Reference values for forced expiratory volumes and pulmonary flows in 3–6 year children: a cross-sectional study. Respir Res. (2007) 8:14. 10.1186/1465-9921-8-14 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

31. Centers for Disease Control and Prevention . Body Mass Index. (2015). [Google Scholar]

32. Kaisere ML, Cafer A. Understanding high incidence of severe obesity and very low food security in food pantry clients: implication for social work. Social Work Public Health (2018) 33:125–39. 10.1080/19371918.2017.1415181 [PubMed] [CrossRef] [Google Scholar]

33. Food Research and Action Center Understanding the Connections: Food Insecurity and Obesity (2015). [Google Scholar]

34. Berkowitz S, Basu S, Meigs J, Seligman H. Food insecurity and health care expenditures in the United States, 2011–2013. Health Serv Res. (2017) 53:1600–20. 10.1111/1475-6773.12730 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

35. Tarasuk V, Cheng J, de Oliveira C, Dachner N, Gunderson C, Kurdyak P. Association between household food insecurity and annual health care costs. Can Med Assoc J. (2015. 187:E429–36. 10.1503/cmaj.150234 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

36. Swindle TM, Whiteside-Mansell L, McKelvey L. Food insecurity: validation of the two-item screen using convergent risks. J Child Family Stud. (2013) 22:932–41. 10.1007/s10826-012-9652-7 [CrossRef] [Google Scholar]

37. Gundersen C, Engelhard EE, Crumbaugh AS, Seligman HK. Brief assessment of food insecurity identifies high-risk US adults. Public Health Nutr. (2017) 20:1367–71. 10.1017/S1368980017000180 [PubMed] [CrossRef] [Google Scholar]

38. Council on Community Pediatrics CoN. Promoting food security for all children. Pediatrics (2015) 136:1431–8. 10.1542/peds.2015-3301 [PubMed] [CrossRef] [Google Scholar]


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Demographics of study patients with cystic fibrosis.

Adult with CF (18-50+ years)Child with CF (< 1 to 17 years)Parent of a child with CF*
Number of participants444343
GENDER
Male21Not collected7
Female2336
EDUCATION
Some high school3Not collected2
High school128
Some college17NA16
College graduate8NA13
Some graduate school1NA1
Master's degree or higher3NA3
SUPPLEMENTAL FOOD PROGRAMS
Number of participants receiving food assistance122929
BODY MASS INDEX
Malnourished: < 10th percentileNA2NA
Underweight: < 50th percentileNA20
Normal/healthy weight: > 50th to < 95th percentileNA9NA
Overweight/obese: ≥ 95th percentileNA2NA
Underweight: < 18.5 kg/m24NANA
Normal/healthy weight: 18.5–24.9 kg/m231NANA
Overweight: 25–29.9 kg/m27NANA
Obese: > 30 kg/m22NANA
FORCED EXPIRATORY VOLUME IN ONE SECOND (FEV1)
Normal: FEV1 > 90610NA
Mild obstruction: FEV1 70–901010NA
Moderate obstruction: FEV1 40–70234NA
Severe obstruction: FEV1 < 4040NA
Testing not done (< 6 years old)NA19NA