Connect
MJA
MJA

Traumatic spinal cord injury in Victoria, 2007–2016

Ben Beck, Peter A Cameron, Sandra Braaf, Andrew Nunn, Mark C Fitzgerald, Rodney T Judson, Warwick J Teague, Alyse Lennox, James W Middleton, James E Harrison and Belinda J Gabbe
Med J Aust 2019; 210 (8): . || doi: 10.5694/mja2.50143
Published online: 29 April 2019

Abstract

Objective: To investigate trends in the incidence and causes of traumatic spinal cord injury (TSCI) in Victoria over a 10‐year period.

Design, setting, participants: Retrospective cohort study: analysis of Victorian State Trauma Registry (VSTR) data for people who sustained TSCIs during 2007–2016.

Main outcomes and measures: Temporal trends in population‐based incidence rates of TSCI (injury to the spinal cord with an Abbreviated Injury Scale [AIS] score of 4 or more).

Results: There were 706 cases of TSCI, most the result of transport events (269 cases, 38%) or low falls (197 cases, 28%). The overall crude incidence of TSCI was 1.26 cases per 100 000 population (95% CI, 1.17–1.36 per 100 000 population), and did not change over the study period (incidence rate ratio [IRR], 1.01; 95% CI, 0.99–1.04). However, the incidence of TSCI resulting from low falls increased by 9% per year (95% CI, 4–15%). The proportion of TSCI cases classified as incomplete tetraplegia increased from 41% in 2007 to 55% in 2016 (P < 0.001). Overall in‐hospital mortality was 15% (104 deaths), and was highest among people aged 65 years or more (31%, 70 deaths).

Conclusions: Given the devastating consequences of TSCI, improved primary prevention strategies are needed, particularly as the incidence of TSCI did not decline over the study period. The epidemiologic profile of TSCI has shifted, with an increasing number of TSCI events in older adults. This change has implications for prevention, acute and post‐discharge care, and support.

Please login with your free MJA account to view this article in full


Please note: institutional and Research4Life access to the MJA is now provided through Wiley Online Library.


  • 1 Monash University, Melbourne, VIC
  • 2 The Alfred Hospital, Melbourne, VIC
  • 3 Victorian Spinal Cord Service, Austin Hospital, Melbourne, VIC
  • 4 National Trauma Research Institute, Melbourne, VIC
  • 5 Royal Melbourne Hospital, Melbourne, VIC
  • 6 University of Melbourne, Melbourne, VIC
  • 7 Royal Children's Hospital, Melbourne, VIC
  • 8 Murdoch Children's Research Institute, Melbourne, VIC
  • 9 Kolling Institute, University of Sydney, Sydney, NSW
  • 10 Agency for Clinical Innovation, Sydney, NSW
  • 11 Research Centre for Injury Studies, Flinders University, Adelaide, SA
  • 12 Health Data Research UK, Swansea University Medical School, Swansea University, Swansea, United Kingdom


Correspondence: ben.beck@monash.edu

Acknowledgements: 

We thank the Victorian State Trauma Outcome Registry and Monitoring (VSTORM) group for providing Victorian State Trauma Registry data. We also thank Sue McLellan for her assistance with providing the data. The VSTR is funded by the Department of Health and Human Services, Victoria and the Transport Accident Commission. Ben Beck was supported by an Australian Research Council Discovery Early Career Researcher Award Fellowship (DE180100825). Peter Cameron was supported by a National Health and Medical Research Council Practitioner Fellowship (545926). Warwick Teague's role as director of trauma services was supported by a grant from the Royal Children's Hospital Foundation. Belinda Gabbe was supported by an Australian Research Council Future Fellowship (FT170100048).

Competing interests:

No relevant disclosures.

  • 1. Bickenbach JR, Officer A, Shakespeare T, et al. International perspectives on spinal cord injury. Geneva: World Health Organization; International Spinal Cord Society, 2013. http://apps.who.int/iris/bitstream/10665/94190/1/9789241564663_eng.pdf?ua=1 (viewed May 2017).
  • 2. O'Connor PJ. Prevalence of spinal cord injury in Australia. Spinal Cord 2005; 43: 42–46.
  • 3. Access Economics, for the Victorian Neurotrauma Initiative. The economic cost of spinal cord injury and traumatic brain injury in Australia. June 2009. http://www.spinalcure.org.au/pdf/Economic-cost-of-SCI-and-TBI-in-Au-2009.pdf (viewed May 2017).
  • 4. Australian Institute of Health and Welfare. Spinal cord injury, Australia, 2014–15 (Cat. No. INJCAT 193; Injury Research and Statistics Series No. 113). Canberra: AIHW, 2018.
  • 5. Department of Health and Human Services (Victoria). Victorian State Trauma System. 2018. https://www2.health.vic.gov.au/hospitals-and-health-services/patient-care/acute-care/state-trauma-system (viewed Jan 2019).
  • 6. Cameron PA, Gabbe BJ, Cooper DJ, et al. A statewide system of trauma care in Victoria: effect on patient survival. Med J Aust 2008; 189: 546–550. https://www.mja.com.au/journal/2008/189/10/statewide-system-trauma-care-victoria-effect-patient-survival
  • 7. Australian Bureau of Statistics. The Australian statistical geography standard (ASGS) remoteness structure. Updated Mar 2018. http://www.abs.gov.au/websitedbs/d3310114.nsf/home/remoteness+structure (viewed Jan 2019).
  • 8. Australian Bureau of Statistics. 2033.0.55.001. Census of population and housing: Socio‐Economic Indexes for Areas (SEIFA), Australia, 2016: IRSAD. Mar 2018. http://www.abs.gov.au/ausstats/abs@.nsf/Lookup/by%20Subject/2033.0.55.001~2016~Main%20 (viewed Jan 2019).
  • 9. Charlson ME, Pompei P, Ales KL, et al. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis 1987; 40: 373–383.
  • 10. Australian Institute of Health and Welfare. Age‐standardised rate. METeOR Metadata Online Registry; Mar 2005. http://meteor.aihw.gov.au/content/index.phtml/itemId/327276 (viewed Sept 2016).
  • 11. Australian Bureau of Statistics. 3101.0. Australian demographic statistics, Mar 2013. Sept 2013. http://www.abs.gov.au/AUSSTATS/abs@.nsf/DetailsPage/3101.0Mar%202013?OpenDocument (viewed Aug 2016).
  • 12. Nijendijk JH, Post MW, Van Asbeck FW. Epidemiology of traumatic spinal cord injuries in The Netherlands in 2010. Spinal Cord 2014; 52: 258–263.
  • 13. Bjørnshave Noe B, Mikkelsen EM, Hansen R, et al. Incidence of traumatic spinal cord injury in Denmark, 1990–2012: a hospital‐based study. Spinal Cord 2015; 53: 436–440.
  • 14. Ahoniemi E, Alaranta H, Hokkinen E, et al. Incidence of traumatic spinal cord injuries in Finland over a 30‐year period. Spinal Cord 2008; 46: 781–784.
  • 15. Jain NB, Ayers GD, Peterson EN, et al. Traumatic spinal cord injury in the United States, 1993–2012. JAMA 2015; 313: 2236–2243.
  • 16. Lee B, Cripps R, Fitzharris M, et al. The global map for traumatic spinal cord injury epidemiology: update 2011, global incidence rate. Spinal Cord 2014; 52: 110–116.
  • 17. Chapman S, Alpers P, Jones M. Association between gun law reforms and intentional firearm deaths in Australia, 1979–2013. JAMA 2016; 316: 291–299.
  • 18. DeVivo MJ, Chen Y. Trends in new injuries, prevalent cases, and aging with spinal cord injury. Arch Phys Med Rehabil 2011; 92: 332–338.
  • 19. Bárbara‐Bataller E, Méndez‐Suárez JL, Alemán‐Sánchez C, et al. Change in the profile of traumatic spinal cord injury over 15 years in Spain. Scand J Trauma Resusc Emerg Med 2018; 26: 27.
  • 20. Kehoe A, Smith J, Edwards A, et al. The changing face of major trauma in the UK. Emerg Med J 2015; 32: 911–915.
  • 21. Australian Institute of Health and Welfare. Trends in hospitalised injury, Australia 1999–00 to 2014–15 (Cat. No. INJCAT 190; Injury Research and Statistics Series No. 110). Canberra: AIHW, 2018.
  • 22. Ambrose AF, Paul G, Hausdorff JM. Risk factors for falls among older adults: a review of the literature. Maturitas 2013; 75: 51–61.
  • 23. Gillespie LD, Robertson MC, Gillespie WJ, et al. Interventions for preventing falls in older people living in the community. Cochrane Database Syst Rev 2012; CD007146.
  • 24. Beck B, Cameron P, Lowthian J, et al. Major trauma in older persons. BJS Open 2018; 2: 310–318.
  • 25. Fehlings MG, Tetreault L, Nater A, et al. The aging of the global population: the changing epidemiology of disease and spinal disorders. Neurosurgery 2015; 77 (Suppl 1): S1–S5.
  • 26. Heffernan DS, Thakkar RK, Monaghan SF, et al. Normal presenting vital signs are unreliable in geriatric blunt trauma victims. J Trauma 2010; 69: 813–820.
  • 27. Kehoe A, Smith J, Bouamra O, et al. Older patients with traumatic brain injury present with a higher GCS score than younger patients for a given severity of injury. Emerg Med J 2016; 33: 381–385.
  • 28. Beck B, Cameron P, Fitzgerald MC, et al. Road safety: serious injuries remain a major unsolved problem. Med J Aust 2017; 207: 244–249. https://www.mja.com.au/journal/2017/207/6/road-safety-serious-injuries-remain-major-unsolved-problem
  • 29. Ackland HM, Pilcher DV, Roodenburg OS, et al. Danger at every rung: epidemiology and outcomes of ICU‐admitted ladder‐related trauma. Injury 2016; 47: 1109–1117.
  • 30. Cabilan C, Vallmuur K, Eley R, et al. Impact of ladder‐related falls on the emergency department and recommendations for ladder safety. Emerg Med Australas 2018; 30: 95–102.
  • 31. Gabbe BJ, Nunn A. Profile and costs of secondary conditions resulting in emergency department presentations and readmission to hospital following traumatic spinal cord injury. Injury 2016; 47: 1847–1855.
  • 32. Munce SE, Wodchis W, Guilcher SJ, et al. Direct costs of adult traumatic spinal cord injury in Ontario. Spinal Cord 2013; 51: 64–69.
  • 33. Braaf SC, Lennox A, Nunn A, et al. Experiences of hospital readmission and receiving formal carer services following spinal cord injury: a qualitative study to identify needs. Disabil Rehabil 2018; 40: 1893–1899.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Early success with room for improvement: influenza vaccination of young Australian children

Frank H Beard, Alexandra J Hendry and Kristine Macartney
Med J Aust 2019; 210 (11): . || doi: 10.5694/mja2.50141
Published online: 29 April 2019
Correction(s) for this article: Erratum | Published online: 14 December 2025

Immunisation providers should offer annual influenza vaccination for children aged 6 months to 5 years and report it to the Australian Immunisation Register


  • 1 National Centre for Immunisation Research and Surveillance, Children's Hospital at Westmead, Sydney, NSW
  • 2 University of Sydney, Sydney, NSW



Competing interests:

No relevant disclosures.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Qualified privilege legislation to support clinician quality assurance: balancing professional and public interests

Susannah Ahern, Ingrid Hopper and Erwin Loh
Med J Aust 2019; 210 (8): . || doi: 10.5694/mja2.50124
Published online: 22 April 2019

A review of the legislation may be warranted to assess the balance between professional and public interests

Patient health‐related datasets are protected by national and state‐based privacy laws which establish requirements for data security that safeguard identified patient information.1,2,3 Nevertheless, these data may potentially be accessed by third parties in accordance with the law — for example, in connection with freedom of information requests or legal proceedings — by statutory bodies such as the Australian Health Practitioner Regulatory Agency, or by jurisdictional health complaints commissions. Patient information from health service medical records is regularly used in medico‐legal proceedings, a recent significant example of which was the Bawa‐Garba case in the United Kingdom,4 discussed below.


  • Monash University, Melbourne, VIC


Correspondence: susannah.ahern@monash.edu

Competing interests:

No relevant disclosures.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Updated Australian consensus statement on management of inherited bleeding disorders in pregnancy

Scott Dunkley, Julie A Curtin, Anthony J Marren, Robert P Heavener, Simon McRae and Jennifer L Curnow
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50123
Published online: 15 April 2019

Abstract

Introduction: There have been significant advances in the understanding of the management of inherited bleeding disorders in pregnancy since the last Australian Haemophilia Centre Directors’ Organisation (AHCDO) consensus statement was published in 2009. This updated consensus statement provides practical information for clinicians managing pregnant women who have, or carry a gene for, inherited bleeding disorders, and their potentially affected infants. It represents the consensus opinion of all AHCDO members; where evidence was lacking, recommendations have been based on clinical experience and consensus opinion.

Main recommendations: During pregnancy and delivery, women with inherited bleeding disorders may be exposed to haemostatic challenges. Women with inherited bleeding disorders, and their potentially affected infants, need specialised care during pregnancy, delivery, and postpartum, and should be managed by a multidisciplinary team that includes at a minimum an obstetrician, anaesthetist, paediatrician or neonatologist, and haematologist. Recommendations on management of pregnancy, labour, delivery, obstetric anaesthesia and postpartum care, including reducing and treating postpartum haemorrhage, are included. The management of infants known to have or be at risk of an inherited bleeding disorder is also covered.

Changes in management as a result of this statement: Key changes in this update include the addition of a summary of the expected physiological changes in coagulation factors and phenotypic severity of bleeding disorders in pregnancy; a flow chart for the recommended clinical management during pregnancy and delivery; guidance for the use of regional anaesthetic; and prophylactic treatment recommendations including concomitant tranexamic acid.


  • 1 Institute of Haematology, Royal Prince Alfred Hospital, Sydney, NSW
  • 2 The Children's Hospital at Westmead, Sydney, NSW
  • 3 Australian Haemophilia Centres Directors’ Organisation, Melbourne, VIC
  • 4 Royal Prince Alfred Hospital, Sydney, NSW
  • 5 Royal Adelaide Hospital, Adelaide, SA
  • 6 Haemophilia Treatment Centre, Westmead Hospital, Sydney, NSW


Correspondence: scottmdunkley@gmail.com

Acknowledgements: 

We are grateful to Steph P'ng, John Rowell, Tim Brighton, Huyen Tran and Ian Douglas for their helpful feedback and comments. We acknowledge Ruth Hadfield for medical writing and editing assistance.

Competing interests:

No relevant disclosures.

  • 1. Nichols WL, Rick ME, Ortel TL, et al. Clinical and laboratory diagnosis of von Willebrand disease: a synopsis of the 2008 NHLBI/NIH guidelines. Am J Hematol 2009; 84: 366–370.
  • 2. Nichols WL, Hultin MB, James AH, et al. von Willebrand disease (VWD): evidence‐based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008; 14: 171–232.
  • 3. Gouw SC, van der Bom JG, Marijke van den Berg H. Treatment‐related risk factors of inhibitor development in previously untreated patients with hemophilia A: the CANAL cohort study. Blood 2007; 109: 4648–4654.
  • 4. White GC 2nd, Rosendaal F, Aledort LM, et al. Definitions in haemophilia: recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 2001; 85: 560.
  • 5. Plug I, Mauser‐Bunschoten EP, Brocker‐Vriends AH, et al. Bleeding in carriers of hemophilia. Blood 2006; 108: 52–56.
  • 6. Pavord SR, Rayment R, Madan B, et al. Management of inherited bleeding disorders in pregnancy. Green‐top Guideline No. 71 (joint with UKHCDO). BJOG 2017; 124: e193–e263.
  • 7. Dunkley SM, Russell SJ, Rowell JA, et al. A consensus statement on the management of pregnancy and delivery in women who are carriers of or have bleeding disorders. Med J Aust 2009; 191: 460–463. https://www.mja.com.au/journal/2009/191/8/consensus-statement-management-pregnancy-and-delivery-women-who-are-carriers-or
  • 8. Lee CA, Chi C, Pavord SR, et al. The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization. Haemophilia 2006; 12: 301–336.
  • 9. Canadian Hemophilia Society. Inherited bleeding disorders affecting women. http://www.hemophilia.ca/en/women/inherited-bleeding-disorders-affecting-women/ (viewed Aug 2018).
  • 10. Street AM, Ljung R, Lavery SA. Management of carriers and babies with haemophilia. Haemophilia 2008; 14 Suppl 3: 181–187.
  • 11. Gouw SC, van der Bom JG, Auerswald G, et al. Recombinant versus plasma‐derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study. Blood 2007; 109: 4693–4697.
  • 12. Chi C, Kadir RA. Management of women with inherited bleeding disorders in pregnancy. Obstet Gynaecol 2007; 9: 27–33.
  • 13. Stirling Y, Woolf L, North WR, et al. Haemostasis in normal pregnancy. Thromb Haemost 1984; 52: 176–182.
  • 14. Kadir RA, Lee CA. Obstetrics and gynecology: hemophilia. In: Lee CA, Berntorp EE, Hoots WK, editors. Textbook of haemophilia. 3rd ed. Oxford: Wiley, p. 337.
  • 15. Chi C, Lee CA, Shiltagh N, et al. Pregnancy in carriers of haemophilia. Haemophilia 2008; 14: 56–64.
  • 16. James AH, Konkle BA, Kouides P, et al. Postpartum von Willebrand factor levels in women with and without von Willebrand disease and implications for prophylaxis. Haemophilia 2015; 21: 81–87.
  • 17. Kadir RA, Lee CA, Sabin CA, et al. Pregnancy in women with von Willebrand's disease or factor XI deficiency. BJOG 1998; 105: 314–321.
  • 18. Bolton‐Maggs PH. The management of factor XI deficiency. Haemophilia 1998; 4: 683–688.
  • 19. Lavee O, Kidson‐Gerber G. Update on inherited disorders of haemostasis and pregnancy. Obstet Med 2016; 9: 64–72.
  • 20. Kadir RA, Economides DL, Braithwaite J, et al. The obstetric experience of carriers of haemophilia. BJOG 1997; 104: 803–810.
  • 21. Domschke C, Strowitzki T, Huth‐Kuehne A, et al. Successful in vitro fertilization and pregnancy in Glanzmann thrombasthenia. Haemophilia 2012; 18: e380–e381.
  • 22. Peavey M, Steward R, Paulyson‐Nunez K, James A. Successful prophylactic regimens for transvaginal oocyte retrieval in women with bleeding diatheses. Haemophilia 2013; 19: e189–e191.
  • 23. Kadir RA, Davies J, Winikoff R, et al. Pregnancy complications and obstetric care in women with inherited bleeding disorders. Haemophilia 2013; 19 Suppl 4: 1–10.
  • 24. Sanchez‐Luceros A, Meschengieser SS, Marchese C, et al. Factor VIII and von Willebrand factor changes during normal pregnancy and puerperium. Blood Coagul Fibrinolysis 2003; 14: 647–651.
  • 25. Srivastava A, Brewer AK, Mauser‐Bunschoten EP, et al. Guidelines for the management of hemophilia. Haemophilia 2013; 19: e1–e47.
  • 26. Kouides PA. Obstetric and gynaecological aspects of von Willebrand disease: best practice and research. Clin Haematol 2001; 14: 381–399.
  • 27. Federici AB, Mazurier C, Berntorp E, et al. Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study. Blood 2004; 103: 2032–2038.
  • 28. Mannucci PM. Use of desmopressin (DDAVP) during early pregnancy in factor VIII‐deficient women. Blood 2005; 105: 3382.
  • 29. Australian Government Therapeutic Goods Administration. Prescribing medicines in pregnancy database. https://www.tga.gov.au/prescribing-medicines-pregnancy-database (viewed Nov 2018).
  • 30. Karanth L, Barua A, Kanagasabai S, Nair S. Desmopressin acetate (DDAVP) for preventing and treating acute bleeds during pregnancy in women with congenital bleeding disorders. Cochrane Database Syst Rev 2015; (9): CD009824.
  • 31. Huq FY, Kadir RA. Management of pregnancy, labour and delivery in women with inherited bleeding disorders. Haemophilia 2011; 17 Suppl 1: 20–30.
  • 32. Nazir HF, Al Lawati T, Beshlawi I, et al. Mode of delivery and risk of intracranial haemorrhage in newborns with severe haemophilia A: a multicentre study in Gulf region. Haemophilia 2016; 22: e134–e138.
  • 33. Ljung R, Lindgren AC, Petrini P, Tengborn L. Normal vaginal delivery is to be recommended for haemophilia carrier gravidae. Acta Paediatr 1994; 83: 609–611.
  • 34. Van Der Linde R, Favaloro EJ. Tranexamic acid to prevent post‐partum haemorrhage. Blood Transfus 2018; 16: 321–323.
  • 35. WOMAN Trial Collaborators. Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post‐partum haemorrhage (WOMAN): an international, randomised, double‐blind, placebo‐controlled trial. Lancet 2017; 389: 2105–2116.
  • 36. Bolton‐Maggs PH, Chalmers EA, Collins PW, et al. A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol 2006; 135: 603–633.
  • 37. Haljamäe H. Thromboprophylaxis, coagulation disorders, and regional anaesthesia. Acta Anaesthesiol Scand 1996; 40(8 Pt 2): 1024–1040.
  • 38. Horlocker TT, Wedel DJ, Benzon H, et al. Regional anesthesia in the anticoagulated patient: defining the risks (the second ASRA Consensus Conference on Neuraxial Anesthesia and Anticoagulation). Reg Anesth Pain Med 2003; 28: 172–197.
  • 39. Stedeford JC, Pittman JA. Von Willebrand's disease and neuroaxial anaesthesia. Anaesthesia 2000; 55: 1228–1229.
  • 40. Curnow J, Pasalic L, Favaloro EJ. Treatment of von Willebrand Disease. Sem Thromb Hemost 2016; 42: 133–146.
  • 41. Rodeghiero F. Von Willebrand disease: pathogenesis and management. Thromb Res 2013; 131 Suppl 1: S47–S50.
  • 42. American Academy of Family Physicians. Advanced Life Support in Obstetrics (ALSO). http://www.aafp.org/cme/programs/also.html (viewed Mar 2019).
  • 43. Babarinsa IA, Hayman RG, Draycott TJ. Secondary post‐partum haemorrhage: challenges in evidence‐based causes and management. Eur J Obstet Gynecol Reprod Biol 2011; 159: 255–260.
  • 44. Hoveyda F, MacKenzie IZ. Secondary postpartum haemorrhage: incidence, morbidity and current management. BJOG 2001; 108: 927–930.
  • 45. Begley CM, Gyte GM, Devane D, et al. Active versus expectant management for women in the third stage of labour. Cochrane Database Syst Rev 2015; (3): CD007412.
  • 46. James DK, Steer P, Weiner C, Gonik B. High risk pregnancy: management options. 4th ed. St Louis, MO: Elsevier Saunders, 2011: p. 1504.
  • 47. Royal Australian and New Zealand College of Obstetricians and Gynaecologists. Management of postpartum haemorrhage (PPH). https://www.ranzcog.edu.au/RANZCOG_SITE/media/RANZCOG-MEDIA/Women%27s%20Health/Statement%20and%20guidelines/Clinical-Obstetrics/Management-of-Postpartum-Haemorrhage-(C-Obs-43)-Review-July-2017.pdf?ext=.pdf (viewed Nov 2018).
  • 48. Demers C, Derzko C, David M, Douglas J. Gynaecological and obstetric management of women with inherited bleeding disorders. Int J Gynaecol Obstet 2006; 95: 75–87.
  • 49. Andrew M, Paes B, Milner R, et al. Development of the human coagulation system in the healthy premature infant. Blood 1988; 72: 1651–1657.
  • 50. Kulkarni R, Lusher J. Perinatal management of newborns with haemophilia. Br J Haematol 2001; 112: 264–274.
  • 51. Kulkarni R, Lusher JM. Intracranial and extracranial hemorrhages in newborns with hemophilia: a review of the literature. J Pediatr Hematol Oncol 1999; 21: 289–295.
  • 52. Veldman A, Josef J, Fischer D, Volk WR. A prospective pilot study of prophylactic treatment of preterm neonates with recombinant activated factor VII during the first 72 hours of life. Pediatr Crit Care Med 2006; 7: 34–39.
  • 53. Australian Haemophilia Centre Directors’ Organisation. Guidelines for the treatment of inhibitors in haemophilia A and haemophilia B. Melbourne: AHCDO, 2010. http://www.ahcdo.org.au/documents/item/16 (viewed Nov 2018).
  • 54. Australian Haemophilia Centre Directors’ Organisation and National Blood Authority, Australia. Guidelines for the management of haemophilia in Australia. Melbourne: AHCDO, 2016. https://www.blood.gov.au/system/files/HaemophiliaGuidelines-interactive-updated-260317v2.pdf (viewed Nov 2018).

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Resilient health systems: preparing for climate disasters and other emergencies

Gerard J FitzGerald, Anthony Capon and Peter Aitken
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50115
Published online: 15 April 2019

A system that integrates all aspects of health care is essential for facing future challenges

After another Australian summer of record‐breaking temperatures, bushfires, floods and widespread drought, it is clear that our health systems should be strengthened to cope with the challenges of climate change. We must also reduce the carbon footprint of health care,1 and continue to advocate that Australia play its part in dealing with the fundamental causes of climate change. In May, the 21st biennial congress of the World Association for Disaster and Emergency Medicine (WADEM) will be hosted by Brisbane. The congress will bring together investigators and practitioners from around the world to discuss disaster health care, future risks, community vulnerabilities, and the strategies required by resilient health systems.


  • 1 Queensland University of Technology, Brisbane, QLD
  • 2 Sydney School of Public Health, University of Sydney, Sydney, NSW
  • 3 Health Disaster Management Unit, Queensland Health, Brisbane, QLD


Correspondence: gj.fitzgerald@qut.edu.au

Competing interests:

No relevant disclosures.

  • 1. Malik A, Lenzen M, McAlister S, McGain F. The carbon footprint of Australian health care. Lancet Planet Health 2018; 2: e27–e35.
  • 2. Hanna EG, McIver LJ. Climate change: a brief overview of the science and health impacts for Australia. Med J Aust 2018; 208: 311–315. https://www.mja.com.au/journal/2018/208/7/climate-change-brief-overview-science-and-health-impacts-australia
  • 3. Kishore N, Marqués D, Mahmud A, et al. Mortality in Puerto Rico after Hurricane Maria. N Engl J Med 2018; 379: 162–170.
  • 4. Burns P, Douglas K, Hu W. Primary care in disasters: opportunity to address a hidden burden of health care. Med J Aust 2019; 210: 297–299.
  • 5. Australian Institute of Health and Welfare. Emergency department care 2017–18: Australian hospital statistics (Cat. No. HSE 216; Health Services Series No. 89). Canberra: AIHW, 2018.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Primary care in disasters: opportunity to address a hidden burden of health care

Penelope L Burns, Kirsty A Douglas and Wendy Hu
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50067
Published online: 15 April 2019

General practitioners provide a flexible response to the changed needs of the disaster‐affected population

In Australia, “a land … of droughts and flooding rains,”1 disasters affect our lives annually, the majority of which are weather‐related.2 They are a part of the landscape, taking the form of cyclones, floods, bushfires, droughts and other phenomena. Cyclone Debbie, which hit northern Queensland in 2017, the Tathra bushfires, which affected the south coast of New South Wales in 2018, and the thunderstorm asthma event in Melbourne in 2016 are just a few recent examples. Such catastrophic events affect rural and urban communities and coastal and inland locations. No community in Australia is exempt, which is reflected in the recent shift in focus by national and international disaster management policy to prioritise improving local community capacity to respond and recover.3,4


  • 1 Australian National University, Canberra, ACT
  • 2 Western Sydney University, Sydney, NSW


Correspondence: Penelope.Burns@anu.edu.au

Acknowledgements: 

We thank the Royal Australian College of General Practitioners Foundation for their support on some early work in this field.

Competing interests:

No relevant disclosures.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

The importance of public health genomics for ensuring health security for Australia

Deborah A Williamson, Martyn D Kirk, Vitali Sintchenko and Benjamin P Howden
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50063
Published online: 15 April 2019

Coordination is required to future‐proof Australia's capacity and leadership in public health genomics

Infectious diseases are an ever‐present risk to society, particularly because of globalisation and the threat of antimicrobial‐resistant organisms. Recently, a World Health Organization (WHO) team conducted a joint external evaluation of Australia's core capacities under the International Health Regulations. The evaluation gave Australia a high scorecard in all areas relevant to protecting health from emerging infectious disease threats.1 However, an area that the evaluation team highlighted for critical improvement was the integration of whole genome sequencing‐based surveillance into existing communicable diseases control systems in the Australian setting.1 While Australia scored highly for laboratory testing of priority diseases, the team recommended “integration of laboratory testing data with epidemiological data particularly in the context of whole genome sequencing”.1


  • 1 University of Melbourne, Melbourne, VIC
  • 2 National Centre for Epidemiology and Population Health, Australian National University, Canberra, ACT
  • 3 University of Sydney, Sydney, NSW



Competing interests:

No relevant disclosures

  • 1. World Health Organization. Joint external evaluation of IHR core capacities of Australia: mission report, 24 November ‐ 1 December 2017. Geneva: WHO, 2018. http://apps.who.int/iris/handle/10665/272362 (viewed Feb 2019).
  • 2. Gardy JL, Loman NJ. Towards a genomics‐informed, real‐time, global pathogen surveillance system. Nat Rev Genet 2018; 19: 9–20.
  • 3. Australian Government Department of Health. National Framework for Communicable Disease Control Canberra: Commonwealth of Australia, 2014. http://www.health.gov.au/internet/main/publishing.nsf/Content/ohp-nat-frame-communic-disease-control.htm (viewed Feb 2019).
  • 4. Australian Government Department of Health. National Health Genomics Policy Framework 2018‐2021. http://www.health.gov.au/internet/main/publishing.nsf/Content/national-health-genomics-policy-framework-2018-2021 (viewed Feb 2018).
  • 5. Allard MW, Strain E, Melka D, et al. Practical value of food pathogen traceability through building a whole‐genome sequencing network and database. J Clin Microbiol 2016; 54: 1975–1983.
  • 6. Kwong JC, Stafford R, Strain E, et al. Sharing is caring: international sharing of data enhances genomic surveillance of Listeria monocytogenes. Clin Infect Dis 2016; 63: 846–848.
  • 7. Grant K, Jenkins C, Arnold C, et al. Implementing pathogen genomics: a case study. London: Public Health England, 2018. https://www.gov.uk/government/publications/implementing-pathogen-genomics-a-case-study (viewed Feb 2018).
  • 8. Dallman TJ, Byrne L, Ashton PM, et al. Whole‐genome sequencing for national surveillance of Shiga toxin‐producing Escherichia coli O157. Clin Infect Dis 2015; 61: 305–312.
  • 9. Baker KS, Dallman TJ, Field N, et al. Genomic epidemiology of Shigella in the United Kingdom shows transmission of pathogen sublineages and determinants of antimicrobial resistance. Sci Rep 2018; 8: 7389.
  • 10. Neuert S, Nair S, Day MR, et al. Prediction of phenotypic antimicrobial resistance profiles from whole genome sequences of non‐typhoidal Salmonella enterica. Front Microbiol 2018; 9: 592.
  • 11. Williamson D, Howden B, Stinear T. Mycobacterium chimaera spread from heating and cooling units in heart surgery. N Engl J Med 2017; 376: 600–602.
  • 12. Vasant BR, Stafford RJ, Jennison AV, et al. Mild Illness during outbreak of Shiga toxin‐producing Escherichia coli O157 infections associated with agricultural show, Australia. Emerg Infect Dis 2017; 23: 1686–1689.
  • 13. Gurjav U, Outhred AC, Jelfs P, et al. Whole genome sequencing demonstrates limited transmission within identified Mycobacterium tuberculosis clusters in New South Wales, Australia. PLOS One 2016; 11: e0163612.
  • 14. Kwong JC, Mercoulia K, Tomita T, et al. Prospective whole‐genome sequencing enhances national surveillance of Listeria monocytogenes. J Clin Microbiol 2016; 54: 333–342.
  • 15. Kwong JC, Lane CR, Romanes F, et al. Translating genomics into practice for real‐time surveillance and response to carbapenemase‐producing Enterobacteriaceae: evidence from a complex multi‐institutional KPC outbreak. PeerJ 2018; 6: e4210.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

The impact of rapid molecular diagnostic testing for respiratory viruses on outcomes for emergency department patients

Nasir Wabe, Ling Li, Robert Lindeman, Ruth Yimsung, Maria R Dahm, Kate Clezy, Susan McLennan, Johanna Westbrook and Andrew Georgiou
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50049
Published online: 8 April 2019

Abstract

Objective: To determine whether rapid polymerase chain reaction (PCR) testing for influenza and respiratory syncytial viruses (RSV) in emergency departments (EDs) is associated with better patient and laboratory outcomes than standard multiplex PCR testing.

Design, setting: A before‐and‐after study in four metropolitan EDs in New South Wales.

Participants: 1491 consecutive patients tested by standard multiplex PCR during July–December 2016, and 2250 tested by rapid PCR during July–December 2017.

Main outcome measures: Hospital admissions; ED length of stay (LOS); test turnaround time; patient receiving test result before leaving the ED; ordering of other laboratory tests.

Results: Compared with those tested by standard PCR, fewer patients tested by rapid PCR were admitted to hospital (73.3% v 77.7%; P < 0.001) and more received their test results before leaving the ED (67.4% v 1.3%; P < 0.001); the median test turnaround time was also shorter (2.4 h [IQR, 1.6–3.9 h] v 26.7 h [IQR, 21.2–37.8 h]). The proportion of patients admitted to hospital was also lower in the rapid PCR group for both children under 18 (50.6% v 66.6%; P < 0.001) and patients over 60 years of age (84.3% v 91.8%; P < 0.001). Significantly fewer blood culture, blood gas, sputum culture, and respiratory bacterial and viral serology tests were ordered for patients tested by rapid PCR. ED LOS was similar for the rapid (7.4 h; IQR, 5.0–12.9 h) and standard PCR groups (6.5 h; IQR, 4.2–11.9 h; P = 0.27).

Conclusion: Rapid PCR testing of ED patients for influenza virus and RSV was associated with better outcomes on a range of indicators, suggesting benefits for patients and the health care system. A formal cost–benefit analysis should be undertaken.

Please login with your free MJA account to view this article in full


Please note: institutional and Research4Life access to the MJA is now provided through Wiley Online Library.


  • 1 Centre for Health Systems and Safety Research, Australian Institute of Health Innovation, Macquarie University, Sydney, NSW
  • 2 NSW Health Pathology, Sydney, NSW
  • 3 Prince of Wales Hospital, Sydney, NSW
  • 4 Sydney Medical School, University of Sydney, Sydney, NSW


Correspondence: nasir.wabe@mq.edu.au

Acknowledgements: 

The project was part of a partnership project funded by a National Health and Medical Research Council of Australia Partnership Project Grant (APP1111925), in partnership with NSW Health Pathology and the Australian Commission on Safety and Quality in Healthcare.23

Competing interests:

No relevant disclosures.

  • 1. Chen Y, Kirk MD. Incidence of acute respiratory infections in Australia. Epidemiol Infect 2014; 142: 1355–1361.
  • 2. Shi T, McAllister DA, O'Brien KL, et al. Global, regional, and national disease burden estimates of acute lower respiratory infections due to respiratory syncytial virus in young children in 2015: a systematic review and modelling study. Lancet 2017; 390: 946–958.
  • 3. Varghese BM, Dent E, Chilver M, et al. Epidemiology of viral respiratory infections in Australian working‐age adults (20–64 years): 2010–2013. Epidemiol Infect 2018; 146: 619–626.
  • 4. Mahony JB. Detection of respiratory viruses by molecular methods. Clin Microbiol Rev 2008; 21: 716–747.
  • 5. Mahony J, Chong S, Merante F, et al. Development of a respiratory virus panel test for detection of twenty human respiratory viruses by use of multiplex PCR and a fluid microbead‐based assay. J Clin Microbiol 2007; 45: 2965–2970.
  • 6. Rogers BB, Shankar P, Jerris RC, et al. Impact of a rapid respiratory panel test on patient outcomes. Arch Pathol Lab Med 2015; 139: 636–641.
  • 7. Rappo U, Schuetz AN, Jenkins SG, et al. Impact of early detection of respiratory viruses by multiplex PCR assay on clinical outcomes in adult patients. J Clin Microbiol 2016; 54: 2096–2103.
  • 8. Bureau of Health Information. Healthcare observer: hospital data. http://www.bhi.nsw.gov.au/Healthcare_Observer (viewed June 2018).
  • 9. Li L, Georgiou A, Vecellio E, et al. The effect of laboratory testing on emergency department length of stay: a multihospital longitudinal study applying a cross‐classified random‐effect modeling approach. Acad Emerg Med 2015; 22: 38–46.
  • 10. Linehan E, Brennan M, O'Rourke S, et al. Impact of introduction of Xpert flu assay for influenza PCR testing on obstetric patients: a quality improvement project. J Matern Fetal Neonatal Med 2018; 31: 1016–1020.
  • 11. Li‐Kim‐Moy J, Dastouri F, Rashid H, et al. Utility of early influenza diagnosis through point‐of‐care testing in children presenting to an emergency department. J Paediatr Child Health 2016; 52: 422–429.
  • 12. Ko F, Drews SJ. The impact of commercial rapid respiratory virus diagnostic tests on patient outcomes and health system utilization. Expert Rev Mol Diagn 2017; 17: 917–931.
  • 13. Soto M, Sampietro‐Colom L, Vilella A, et al. Economic impact of a new rapid PCR assay for detecting influenza virus in an emergency department and hospitalized patients. PLoS One 2016; 11: e0146620.
  • 14. St John A, Price CP. Economic evidence and point‐of‐care testing. Clin Biochem Rev 2013; 34: 61–74.
  • 15. Mills JM, Harper J, Broomfield D, Templeton KE. Rapid testing for respiratory syncytial virus in a paediatric emergency department: benefits for infection control and bed management. J Hosp Infect 2011; 77: 248–251.
  • 16. Hawkins RC. Laboratory turnaround time. Clin Biochem Rev 2007; 28: 179–194.
  • 17. Jeong HW, Heo JY, Park JS, Kim WJ. Effect of the influenza virus rapid antigen test on a physician's decision to prescribe antibiotics and on patient length of stay in the emergency department. PLoS One 2014; 9: e110978.
  • 18. Doan Q, Enarson P, Kissoon N, et al. Rapid viral diagnosis for acute febrile respiratory illness in children in the Emergency Department. Cochrane Database Syst Rev 2014; CD006452.
  • 19. Poehling KA, Zhu Y, Tang YW, Edwards K. Accuracy and impact of a point‐of‐care rapid influenza test in young children with respiratory illnesses. Arch Pediatr Adolesc Med 2006; 160: 713–718.
  • 20. Blaschke AJ, Shapiro DJ, Pavia AT, et al. A national study of the impact of rapid influenza testing on clinical care in the emergency department. J Pediatric Infect Dis Soc 2014; 3: 112–118.
  • 21. Nitsch‐Osuch A, Stefanska I, Kuchar E, et al. Influence of rapid influenza test on clinical management of children younger than five with febrile respiratory tract infections. Adv Exp Med Biol 2013; 755: 237–241.
  • 22. Eccles M, Grimshaw J, Campbell M, Ramsay C. Research designs for studies evaluating the effectiveness of change and improvement strategies. Qual Saf Health Care 2003; 12: 47–52.
  • 23. Dahm MR, Georgiou A, Westbrook JI, et al. Delivering safe and effective test‐result communication, management and follow‐up: a mixed‐methods study protocol. BMJ Open 2018; 8: e020235.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Diagnosis of Mycobacterium ulcerans disease: be alert to the possibility of negative initial PCR results

Daniel P O'Brien, Maria Globan, Janet M Fyfe, Caroline J Lavender, Adrian Murrie, Damian Flanagan, Peter Meggyesy, Jonathan T Priestley and David Leslie
Med J Aust 2019; 210 (9): . || doi: 10.5694/mja2.50046
Published online: 8 April 2019

Mycobacterium ulcerans causes necrotising infections of the skin and soft tissue (Buruli ulcer), a disease that is endemic in the coastal regions of Victoria and northern Queensland. Most lesions (> 85%) are painless ulcers, but some are non‐ulcerative.1 As the incidence of Buruli ulcer rises in Victoria,2 Australian health practitioners are increasingly required to recognise this disease in people who reside in or have travelled to endemic areas, with early diagnosis vital for good outcomes.3

Please login with your free MJA account to view this article in full


Please note: institutional and Research4Life access to the MJA is now provided through Wiley Online Library.


  • 1 University Hospital Geelong, Geelong, VIC
  • 2 Mycobacterium Reference Laboratory, Victorian Infectious Diseases Reference Laboratory, Melbourne, VIC
  • 3 Sorrento Medical Centre, Sorrento, VIC
  • 4 South Coast Medical, Blairgowrie, VIC


Correspondence: DANIELO@BarwonHealth.org.au

Competing interests:

No relevant disclosures.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Family planning, antenatal and post partum care in multiple sclerosis: a review and update

Anneke Van Der Walt, Ai‐Lan Nguyen and Vilija Jokubaitis
Med J Aust 2019; 211 (5): . || doi: 10.5694/mja2.50113
Published online: 1 April 2019

Summary

 

  • Multiple sclerosis is more prevalent in women of childbearing age than in any other group. As a result, the impact of multiple sclerosis and its treatment on fertility, planned and unplanned pregnancies, post partum care and breastfeeding presents unique challenges that need to be addressed in everyday clinical practice.
  • Given the increasing number of disease‐modifying agents now available in Australia for the treatment of multiple sclerosis, there is a growing need for clinicians to provide their patients with appropriate counselling on family planning.
  • Providing better evidence regarding the relative risks and benefits of continuing therapy before, during and after pregnancy is an important research priority. International pregnancy registries are essential in developing better evidence‐based practice guidelines, and neurologists should be encouraged to contribute to these when possible.
  • The management of women with multiple sclerosis, especially when they are taking disease‐modifying agents, requires careful assessment of fertility and disease characteristics as well as a multidisciplinary approach to ensure positive outcomes in both mothers and their children.

 


  • 1 Monash University, Melbourne, VIC
  • 2 University of Melbourne, Melbourne, VIC
  • 3 Alfred Health, Melbourne, VIC
  • 4 Royal Melbourne Hospital, Melbourne, VIC



Competing interests:

Anneke Van der Walt has received travel support, speaking honoraria and served on advisory boards for Biogen Australia, Novartis, Merck, Sanofi, Roche and Teva. Ai‐Lan Nguyen has received grant support and travel support from Biogen Australia. Vilija Jokubaitis has received travel support and speaking honoraria from Biogen Australia.

  • 1. Niedziela N, Adamczyk‐Sowa M, Pierzchała K. Epidemiology and clinical record of multiple sclerosis in selected countries: a systematic review. Int J Neurosci 2014; 124: 322–330.
  • 2. Hauser S, Oksenberg J. The neurobiology of multiple sclerosis: genes, inflammation, and neurodegeneration. Neuron 2006; 52: 61–76.
  • 3. Australian Bureau of Statistics. Multiple sclerosis (Cat. No. 4429.0). Canberra: Commonwealth of Australia, 2012. http://www.abs.gov.au/ausstats/abs@.nsf/Lookup/4429.0main+features100182009 (viewed Dec 2017).
  • 4. Amato MP, Portaccio E. Fertility, pregnancy and childbirth in patients with multiple sclerosis: impact of disease‐modifying drugs. CNS Drugs 2015; 29: 207–220.
  • 5. Broadley SA, Barnett MH, Boggild M, et al. A new era in the treatment of multiple sclerosis. Med J Aust 2015; 203: 139–141. https://www.mja.com.au/journal/2015/203/3/new-era-treatment-multiple-sclerosis
  • 6. Confavreux C, Hutchinson M, Hours MM, et al. Rate of pregnancy‐related relapse in multiple sclerosis. N Engl J Med 1998; 339: 285–291.
  • 7. Vukusic S, Marignier R. Multiple sclerosis and pregnancy in the “treatment era”. Nat Rev Neurol 2015; 11: 280–289.
  • 8. Lu E, Wang BW, Alwan S, et al. A review of safety‐related pregnancy data surrounding the oral disease‐modifying drugs for multiple sclerosis. CNS Drugs 2014; 28: 89–94.
  • 9. Friend S, Richman S, Bloomgren G, et al. Evaluation of pregnancy outcomes from the Tysabri® (natalizumab) Pregnancy Exposure Registry: a global, observational, follow‐up study. BMC Neurol 2016; 16: 150.
  • 10. Therapeutics and Goods Administration. TGA eBusiness Services. Australian Government Department of Health and Ageing. https://www.tga.gov.au/prescribing-medicines-pregnancy-database (viewed Dec 2017).
  • 11. National Clinical Guideline Centre (UK). Multiple sclerosis: management of multiple sclerosis in primary and secondary care (NICE clinical guidelines no. 186). London: National Institute for Health and Care Excellence (UK), 2014. https://www.ncbi.nlm.nih.gov/books/NBK248064 (viewed Dec 2017).
  • 12. Cavalla P, Rovei V, Masera S, et al. Fertility in patients with multiple sclerosis: current knowledge and future perspectives. Neurol Sci 2006; 27: 231–239.
  • 13. Roux T, Courtillot C, Debs R, et al. Fecundity in women with multiple sclerosis: an observational mono‐centric study. J Neurol 2015; 262: 957–960.
  • 14. Borisow N, Döring A, Pfueller CF, et al. Expert recommendations to personalization of medical approaches in treatment of multiple sclerosis: an overview of family planning and pregnancy. EPMA J 2012; 3: 9.
  • 15. Cordeau D, Courtois F. Sexual disorders in women with MS: assessment and management. Ann Phys Rehabil Med 2014; 57: 337–347.
  • 16. Schairer LC, Foley FW, Zemon V, et al. The impact of sexual dysfunction on health‐related quality of life in people with multiple sclerosis. Mult Scler 2014; 20: 610–616.
  • 17. Multiple Sclerosis International Foundation. Intimacy and sexuality. MS in focus 2005; 6. https://www.msif.org/wp-content/uploads/2014/09/MS-in-focus-6-Intimacy-and-sexuality-English.pdf (viewed Dec 2017).
  • 18. Hellwig K, Correale J. Artificial reproductive techniques in multiple sclerosis. Clin Immunol 2013; 149: 219–224.
  • 19. Laplaud DA, Leray E, Barrière P, et al. Increase in multiple sclerosis relapse rate following in vitro fertilization. Neurology 2006; 66: 1280–1281.
  • 20. Hellwig K, Schimrigk S, Beste C, et al. Increase in relapse rate during assisted reproduction technique in patients with multiple sclerosis. Eur Neurol 2009; 61: 65–68.
  • 21. Hellwig K, Beste C, Brune N, et al. Increased MS relapse rate during assisted reproduction technique. J Neurol 2008; 255: 592–593.
  • 22. Michel L, Foucher Y, Vukusic S, et al. Increased risk of multiple sclerosis relapse after in vitro fertilisation. J Neurol Neurosurg Psychiatr 2012; 83: 796–802.
  • 23. Correale J, Farez MF, Ysrraelit MC. Increase in multiple sclerosis activity after assisted reproduction technology. Ann Neurol 2012; 72: 682–694.
  • 24. Hughes SE, Spelman T, Gray OM, et al. Predictors and dynamics of postpartum relapses in women with multiple sclerosis. Mult Scler 2014; 20: 739–746.
  • 25. Coyle PK. Switching therapies in multiple sclerosis. CNS Drugs 2013; 27: 239–247.
  • 26. Australian categorisation system for prescribing medicines in pregnancy. Therapeutic Goods Administration, 2011. www.tga.gov.au/australian-categorisation-system-prescribing-medicines-pregnancy (viewed Dec 2017).
  • 27. Gur C, Diav‐Citrin O, Shechtman S, et al. Pregnancy outcome after first trimester exposure to corticosteroids: a prospective controlled study. Reprod Toxicol 2004; 18: 93–101.
  • 28. Coyle PK. Multiple sclerosis and pregnancy prescriptions. Expert Opin Drug Saf 2014; 13: 1565–1568.
  • 29. Achiron A, Chambers C, Fox EJ, et al. Pregnancy outcomes in patients with active RRMS who received alemtuzumab in the clinical development program [abstract]. Mult Scler J 2015; 21: 581–582.
  • 30. Haghikia A, Langer‐Gould A, Rellensmann G, et al. Natalizumab use during the third trimester of pregnancy. JAMA Neurol 2014; 71: 891–895.
  • 31. Vukusic S, Kappos L, Wray S, et al. An update on pregnancy outcomes following ocrelizumab treatment in patients with multiple sclerosis and other autoimmune diseases [abstract]. Mult Scler J 2017; 23: 85–426.
  • 32. Glazaka A, Nolting A, Cook S, et al. Pregnancy outcomes during the clinical development programme of cladribine in multiple sclerosis (MS): an integrated analysis of safety for all exposed patients [abstract]. Mult Scler J 2017; 23: 976–1023.
  • 33. Kieseier BC, Benamor M. Pregnancy outcomes following maternal and paternal exposure to teriflunomide during treatment for relapsing‐remitting multiple sclerosis. Neurol Ther 2014; 3: 133–138.
  • 34. Finkelsztejn A, Brooks J, Paschoal FM, Fragoso YD. What can we really tell women with multiple sclerosis regarding pregnancy? A systematic review and meta‐analysis of the literature. BJOG 2011; 118: 790–797.
  • 35. Harirchian MH, Fatehi F, Sarraf P, et al. Worldwide prevalence of familial multiple sclerosis: a systematic review and meta‐analysis. Mult Scler Relat Disord 2018; 20: 43–47.
  • 36. Compston A, Coles A. Multiple sclerosis. Lancet 2008; 372: 1502–1517.
  • 37. Fragoso YD, Boggild M, Macias‐Islas MA, et al. The effects of long‐term exposure to disease‐modifying drugs during pregnancy in multiple sclerosis. Clin Neurol Neurosurg 2013; 115: 154–159.
  • 38. Houtchens MK, Kolb CM. Multiple sclerosis and pregnancy: therapeutic considerations. J Neurol 2013; 260: 1202–1214.
  • 39. Polifka JE, Friedman JM. Medical genetics: 1. Clinical teratology in the age of genomics. CMAJ 2002; 167: 265–273.
  • 40. Alwan S, Yee IM, Dybalski M, Guimond C, Dwosh E, Greenwood TM, et al. Reproductive decision making after the diagnosis of multiple sclerosis (MS). Mult Scler 2013; 19: 351–358.
  • 41. Ferrero S, Pretta S, Ragni N. Multiple sclerosis: management issues during pregnancy. Eur J Obstet Gynecol Reprod Biol 2004; 115: 3–9.
  • 42. Iorio R, Frisullo G, Nociti V, et al. T‐bet, pSTAT1 and pSTAT3 expression in peripheral blood mononuclear cells during pregnancy correlates with post‐partum activation of multiple sclerosis. Clin Immunol 2009; 131: 70–83.
  • 43. Broadley SA, Barnett MH, Boggild M, et al. Therapeutic approaches to disease modifying therapy for multiple sclerosis in adults: an Australian and New Zealand perspective: part 3, treatment practicalities and recommendations. J Clin Neurosci 2014; 21: 1857–1865.
  • 44. Daclizumab withdrawn from the market worldwide [erratum for Daclizumab for MS]. Drug Ther Bull 2018; 56: 38–21.
  • 45. Broadley SA, Barnett MH, Boggild M, et al. Therapeutic approaches to disease modifying therapy for multiple sclerosis in adults: an Australian and New Zealand perspective: part 1, historical and established therapies. J Clin Neurosci 2014; 21: 1835–1846.
  • 46. Hellwig K, Haghikia A, Gold R. Pregnancy and natalizumab: results of an observational study in 35 accidental pregnancies during natalizumab treatment. Mult Scler 2011; 17: 958–963.
  • 47. Glazer CH, Tøttenborg SS, Giwercman A, et al. Male factor infertility and risk of multiple sclerosis: a register‐based cohort study. Mult Scler 2017; 46: 1–8.
  • 48. Strijbos E, Coenradie S, Touw DJ, Aerden L. High‐dose methylprednisolone for multiple sclerosis during lactation: concentrations in breast milk. Mult Scler 2015; 21: 797–798.
  • 49. Hellwig K, Haghikia A, Gold R. Parenthood and immunomodulation in patients with multiple sclerosis. J Neurol 2010; 257: 580–583.
  • 50. Vukusic S, Durand‐Dubief F, Benoit A, et al. Natalizumab for the prevention of post‐partum relapses in women with multiple sclerosis. Mult Scler 2015; 21: 953–955.
  • 51. Hellwig K, Rockhoff M, Herbstritt S, et al. Exclusive breastfeeding and the effect on postpartum multiple sclerosis relapses. JAMA Neurol 2015; 72: 1132–1138.
  • 52. Conradi S, Malzahn U, Paul F, et al. Breastfeeding is associated with lower risk for multiple sclerosis. Mult Scler 2013; 19: 553–558.
  • 53. Pakpoor J, Disanto G, Lacey MV, et al. Breastfeeding and multiple sclerosis relapses: a meta‐analysis. J Neurol 2012; 259: 2246–2248.
  • 54. Anderson PO. Monoclonal antibodies. Breastfeed Med 2016; 11: 100–101.
  • 55. McConnell RA, Mahadevan U. Pregnancy and the patient with inflammatory bowel disease: fertility, treatment, delivery, and complications. Gastroenterol Clin North Am 2016; 45: 285–301.
  • 56. Levy RA, de Jesús GR, de Jesús NR, Klumb EM. Critical review of the current recommendations for the treatment of systemic inflammatory rheumatic diseases during pregnancy and lactation. Autoimmun Rev 2016; 15: 955–963.
  • 57. Baker TE, Cooper SD, Kessler L, Hale TW. Transfer of natalizumab into breast milk in a mother with multiple sclerosis. J Hum Lact 2015; 31: 233–236.

Author

remove_circle_outline Delete Author
add_circle_outline Add Author

Comment
Do you have any competing interests to declare? *

I/we agree to assign copyright to the Medical Journal of Australia and agree to the Conditions of publication *
I/we agree to the Terms of use of the Medical Journal of Australia *
Email me when people comment on this article

Online responses are no longer available. Please refer to our instructions for authors page for more information.

Pagination

Subscribe to