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[Department of Error] Department of Error

Van den Bent MJ, Baumert B, Erridge SC, et al. Interim results from the CATNON trial (EORTC study 26053-22054) of treatment with concurrent and adjuvant temozolomide for 1p/19q non-co-deleted anaplastic glioma: a phase 3, randomised, open-label intergroup study. Lancet 2017; 390: 1645–53—In the list of affiliations for this Article (published online first on Aug 8, 2017), “Prof R Stuff MD” should have read “Prof R Stupp MD”. This correction has been made to the online version as of Oct 5, 2017, and the printed Article is correct.

[Comment] Benefit with adjuvant chemotherapy in anaplastic astrocytoma

The role of chemotherapy for newly diagnosed anaplastic gliomas, particularly when combined with radiotherapy, has long been unresolved. Over the past few decades, despite no conclusive data, study findings have suggested that the addition of nitrosourea-based chemotherapy to radiotherapy could be beneficial. The NOA-04 trial1 revealed that initial treatment with chemotherapy (either temozolomide or procarbazine, lomustine, and vincristine [PCV]) or radiotherapy alone yielded similar results. Survival of patients with anaplastic glioma has been recognised as being strongly dependent on the presence or absence of the favourable 1p/19q co-deletion.

[Comment] A positive randomised trial in cutaneous T-cell lymphoma

The discovery that CD30 (Ki-1, TNFRSF8), a membrane protein belonging to the tumour necrosis factor receptor superfamily, is uniformly expressed in anaplastic large-cell lymphoma was instrumental in defining CD30-positive T-cell lymphoproliferative disorders.1 Less homogeneous expression of CD30 was also reported in cutaneous T-cell lymphoma, particularly in tumour-stage mycosis fungoides with large-cell transformation.2 Attempts to therapeutically target CD30 with SGN-30 (cAC10), a so-called naked chimeric anti-CD30 monoclonal antibody, were disappointing,3 with the exception of a small study4 in cutaneous T-cell lymphoma, which showed 16 (70%) of 23 patients achieving an overall response, with some durable complete responses.

[Series] Human reproduction and health: an evolutionary perspective

According to life history theory, increased investment in reproductive function (physiology and behaviour) at different times throughout the life course affects the risk of many diseases and, ultimately, longevity. Although genetic factors contribute to interindividual and interpopulation variation in reproductive traits, the dominant source of variability is phenotypic plasticity during development and adult life. Reproductive traits in both sexes evolved sensitivity to ecological conditions, as reflected in contemporary associations of hormone concentrations with geographical setting, nutritional status, and physical activity level.

[Comment] J-ALEX: alectinib versus crizotinib in ALK-positive lung cancer

Notable insights into the genetic landscape of non-small-cell lung cancer have helped drive improvements in the management of advanced disease. Although traditional treatments tend to be anchored solely in cytotoxic chemotherapy, more recent strategies incorporate targeted therapies for some patients. Anaplastic lymphoma kinase (ALK) rearrangements are one of the earliest validated molecular targets in non-small-cell lung cancer. Standard first-line therapy for advanced, ALK-positive non-small-cell lung cancer is the multitargeted ALK/ROS1/MET inhibitor, crizotinib,1,2 followed by more potent second-generation ALK inhibitors, like ceritinib or alectinib, upon progression.

Paradigm shift in monitoring and improving brain health

The world’s most prestigious gathering of medical practitioners in functional medicine and integrative care hosted a symposium in Los Angeles recently, featuring today’s greatest revolutionaries in changing how we view and treat brain health.

The Annual International Conference of the Institute for Functional Medicine chose scientifically-disruptive and broadly-acclaimed neuroscientist Dr Michael Merzenich to address its plenary session.

Dr Merzenich unveiled a revolutionary approach to monitoring, maintaining and improving brain health. The system uses apps and digital therapies.

Dr Merzenich is the Chief Scientific Officer of Posit Science, maker of BrainHQ brain exercises and assessments.

He joined Alzheimer’s experts Dr Dale Bredesen (of UCLA and the Buck institute) and Dr Rudolph Tanzi (of Harvard and Massachusetts General Hospital) for a discussion of the application of neuroplasticity to dementia.

The theme of the conference was The Dynamic Brain: Revealing the Potential of Neuroplasticity to reverse Neurodegeneration

Dr Merzenich discussed research supporting the idea that we can systematically harness brain plasticity and drive positive changes in brain systems through plasticity-based training.

“Breakthroughs in technology and science will permit people to monitor their brain health on a daily basis and take appropriate action to maintain their brain health using a device they already carry in their pockets,” he said.

“A phone with apps to assess current condition, to suggest holistic interventions, and to deliver the right brain exercises. This technology already exists, and all the pieces are coming together.”

Dr Merzenich believes we are in the midst of a paradigm shift regarding how we view and treat most aspects of brain health.

“We don’t have a magic pill to prevent or cure heart disease, and instead look to behavioural changes to reduce risk and early interventions to address symptoms,” he said.

“There is a rapidly growing consensus among thought leaders that we need a similar approach to cognitive disorders and improvement. This approach will include nutrition, physical exercise and environmental factors – but the single most important elements will be lifelong monitoring of brain health and appropriate plasticity-based brain exercises.”

Dr Merzenich is professor emeritus at University of California San Francisco, where he maintained a research lab for three decades. He ran the seminal experiments that led to the discovery of lifelong plasticity – the ability of the brain to change chemically, structurally and functionally based on sensory and other inputs. He pioneered harnessing the power of plasticity in the co-invention of the cochlear implant, which has restored hearing to 100,000s of people living with deafness. 

Dr Merzenich also pioneered the application of plasticity in the development of plasticity-based computerised brain exercises, which have helped millions of people.

Chris Johnson

[Correspondence] Body-mass index and all-cause mortality – Authors’ reply

Associations of measured body-mass index (BMI) with mortality within just a few years of the BMI measurement can be strongly distorted by reverse causality (ie, by life-threatening neoplastic, respiratory, vascular, or other diseases having caused weight loss before the BMI was measured). By contrast, associations of measured BMI with mortality several years after the BMI measurement should be little affected by reverse causality, although they can still be strongly affected by confounding, especially in populations in which low BMI is correlated with smoking.

Indigenous and non-Indigenous Australian children hospitalised for burn injuries: a population data linkage study

The known Rates of burn injuries are higher for Indigenous children than for non-Indigenous Australian children. 

The new Among Indigenous children admitted to hospital for burns, the proportion presenting with burns affecting more than 10% TBSA was greater than for non-Indigenous children, and their mean stay in hospital was longer. A smaller proportion of Indigenous children with burns were treated in a hospital with a paediatric tertiary burn unit. 

The implications Indigenous children with burns may require more intensive and specialised treatment and longer rehabilitation periods than non-Indigenous children because they more frequently present with burns affecting larger proportions of TBSA. 

Burns are a major cause of injury for children in Australia.1 Indigenous Australian children are disproportionally affected: they are more than twice as likely to be hospitalised for a burn injury as non-Indigenous children, and mortality is five times as high.24 Despite this high burden, little is known about the characteristics of burn injuries to Indigenous children or whether they differ from those to non-Indigenous children.5

A study in Western Australia4 found that a larger proportion of Indigenous than of non-Indigenous children admitted to hospital for burns presented with flame burns, and Indigenous children were more likely to sustain severe burns than their non-Indigenous counterparts.6 Similarly, a recent study in New South Wales and the Australian Capital Territory found that children from rural areas more frequently presented with flame burns and burns affecting more than 10% of total body surface area (TBSA) than children from urban areas, and that they have longer hospital stays and higher rates of re-admission after burn injury.7 However, this study did not disaggregate children by Indigenous status, and differences between urban and remote areas may reflect differences in the respective populations, as a higher proportion of Indigenous Australian children (5.1%) than of non-Indigenous children (0.5%) live in remote areas of NSW.8

Although there are differences in burn characteristics at initial presentation, a study in WA found that, once they entered the hospital system, Indigenous people with major burns (50% TBSA) experienced levels of service and had outcomes comparable with those of non-Indigenous patients.9 However, it is not known whether there are differences for patients with less severe burns, or, in particular, for children.

The aim of our study was to explore differences in the characteristics of burn injuries leading to hospitalisation, and in their treatment and outcomes, for Indigenous Australian and non-Indigenous children in NSW.

Methods

Setting

The estimated population of NSW is 6.8 million, 1.3 million of whom are aged 0–14 years.8 At the 2006 census (midpoint of our study), 2.2% of NSW residents identified as Aboriginal and/or Torres Strait Islander (Indigenous Australians), including 7.0% of children aged 0–14 years. Aboriginal people are the original inhabitants of NSW; Torres Strait Islander people comprise 0.1% of the NSW population.8

Study design and data sources

This study was a population-based cohort analysis of linked hospital and mortality data. We used hospital data from the NSW Admitted Patient Data Collection (APDC) linked with mortality data from the NSW Register of Births, Deaths and Marriages (RBDM). The APDC includes records for all separations from NSW public and private sector hospitals and day procedure centres. Patient demographic data, diagnoses and procedures are recorded for each separation and coded according to the Australian modification of the International Statistical Classification of Diseases and Related Problems, tenth revision (ICD-10-AM).10 The RBDM captures details of all deaths registered in NSW. Probabilistic linkage of the datasets was performed by the NSW Centre for Health Record Linkage (http://www.cherel.org.au); de-identified datasets of linked APDC and RBDM data from July 2000 to March 2014 were supplied to the researchers for analysis.

Participants and analysis

The linked data were used to define a cohort of children for the analysis, details of which have been described elsewhere.2 In brief, we selected all children resident in NSW and born in a NSW hospital between 1 July 2000 and 31 December 2012. We then identified children in this cohort who were admitted to a NSW hospital for a first burn injury. Based on the findings of a previous study of the impact of case selection criteria on the identification of patients hospitalised for burn injuries,11 the index burn admission was defined by a primary diagnosis of injury (ICD-10-AM codes, S00–T75, or T79) and an external cause code of exposure to smoke, fire and flames (ICD-10-AM, X00–X09) or contact with heat and hot substances (ICD-10-AM, X10–X19); or by a primary diagnosis of burns (ICD-10-AM, T20–T32). Repeat admissions for the same injury were identified as admissions with either the same primary diagnosis or the same external cause code and primary diagnosis of burn injury as the index admission.

Information about the external cause of the injury (smoke, fire and flames: ICD-10-AM, X00–X09; scalds: ICD-10-AM, X10–X14; contact burns: ICD-10-AM, X15–X19), the body part affected, %TBSA, depth of burn injury, treatment at a hospital with a paediatric tertiary referral burn unit (the Children’s Hospital at Westmead), and inhalation injury (ICD-10-AM, T27, T28.0, T58, T59) were derived from the index admission. Severe burns were defined as partial or full thickness burns affecting more than 10% TBSA.12 Length of stay (LOS) for the index admission was defined as the difference in days between the final discharge day and the date of admission for the index episode of care. Hospitalisations consisting of several continuous episodes of care for the same injury were counted as one hospital stay. The total LOS was defined as the LOS for all admissions related to the index admission. The type of care provided to the child was determined for all burn-related admissions.

Statistical analysis

The proportions of Indigenous and non-Indigenous children with specific burn characteristics were compared in χ2 tests. The influence of these characteristics on differences between Indigenous and non-Indigenous children in LOS was analysed by Cox regression analysis, adjusted for individual (Indigenous status, sex, age), burn (inhalation injury, %TBSA) and area (disadvantage, remoteness) characteristics. Geographic remoteness was defined according to the Accessibility/Remoteness Index of Australia (ARIA+)13 and area-level socio-economic status according to the Australian Bureau of Statistics’ Socio-Economic Index for Areas (SEIFA) Index of Relative Social Advantage and Disadvantage.14 Indigenous status was derived from the child’s birth record in the hospital data. Data were prepared for analysis with SAS 9.3 (SAS Institute) and analysed in Stata 12 (StataCorp).

Ethics approval

Ethics approval for the study was granted by the Population Health Services Research Ethics Committee (reference, HREC/09/CIPHS/18), the Aboriginal Health and Medical Research Council Ethics Committee (reference, 684/09), and the University of Western Sydney Ethics Committee (reference, CI2009/03/141).

Results

Cohort characteristics

A total of 1 124 717 children were included in the cohort, of whom 35 749 (3.1%) were Indigenous Australians. The proportion of Indigenous children living in remote areas (9%; 3312 children) was higher than that for non-Indigenous children (1%; 7574 children). During 2000–2014, 323 Indigenous and 4246 non-Indigenous children were hospitalised for a first burn injury; including repeat admissions, these burns accounted for 5829 hospitalisations of non-Indigenous children and 464 of Indigenous children. The proportions of Indigenous children admitted for a burn injury who lived in remote (15%; 48 children) or disadvantaged areas (76%; 245 children) were higher than for non-Indigenous children (1%; 45 children, and 46%; 1955 children respectively; Box 1).

Burn injury characteristics and outcomes

Scalds were the leading cause of burn injury to both Indigenous (47%) and non-Indigenous children (62%). A larger proportion of Indigenous (18%) than non-Indigenous patients (8%) were admitted for flame burns (Box 2).

The body regions most often injured were different for the two groups of children (P = 0.005). A smaller proportion of Indigenous children presented with burns to the hand or wrist (17%) and a higher proportion with burns to the ankle or foot (12%) than non-Indigenous children (23% and 8% respectively). When stratified by area of residence, the proportion of Indigenous children with burns to the foot and ankle was greater among those living in metropolitan and inner regional areas (14%, 24 children; online Appendix).

A greater proportion of Indigenous than of non-Indigenous patients sustained full thickness burns (16% v 14%) or burns affecting more than 20% TBSA (6% v 2%; Box 2). When stratified by area of residence, the proportion of Indigenous children with burns affecting more than 10% TBSA was greater for those living in outer regional and remote areas (21%, 29 children; online Appendix).

The proportions of Indigenous children with severe burn injuries (17%) or inhalation injuries (4%) were similar to those for non-Indigenous children (12% and 3% respectively; Box 2).

A smaller proportion of Indigenous patients than of non-Indigenous patients were treated at a hospital with a paediatric tertiary burns unit (40% v 50%; P < 0.001); of children with severe burn injuries, 59% of Indigenous and 56% of non-Indigenous children were admitted to a hospital with a paediatric tertiary burns unit (P = 0.69; Box 2).

A larger proportion of Indigenous than of non-Indigenous children with severe burn injuries living in major cities and inner regional areas (63% v 58%) and a higher proportion of those living in outer regional and remote areas (56% v 43%) were treated at a hospital with a specialist burns unit (online Appendix).

Most Indigenous (85%) and non-Indigenous children (84%) were hospitalised once for their burn injury; there was no significant difference in the overall pattern of re-admissions (P = 0.19; Box 2). There were, however, differences in the care received: a lower proportion of Indigenous children underwent surgery (20% v 25% of non-Indigenous children; P = 0.025), and a higher proportion received physical and occupational therapy (13% v 9%; P = 0.015) (Box 3).

A smaller proportion of Indigenous children with burn injuries were treated as day-only patients (31% v 41% of non-Indigenous patients), and a larger proportion stayed in hospital for more than one week (32% v 17%; Box 2).

The mean LOS during the index admission (excluding day patients) for Indigenous children (6.1 days; 95% CI, 4.8–7.4 days) was almost 3 days longer than for non-Indigenous children (3.4 days; 95% CI, 3.2–3.7; P < 0.001). The median LOS for each group of children was one day (Box 4). After adjusting for sex, age, inhalation injury, %TBSA, depth of burn, geographic remoteness, and area disadvantage, LOS was still significantly longer for Indigenous than for non-Indigenous children (P = 0.002). %TBSA, depth of burn, and geographic remoteness were each significantly associated with increased LOS (Box 5).

Discussion

In this data linkage cohort study, we found that a higher of proportion of burn injuries to Indigenous than to non-Indigenous children were caused by flame burns, that their burns more often affected a larger %TBSA, and that they stayed in hospital longer.

The higher proportion of flame burns among Indigenous children admitted to hospital for burn injuries might partially be explained by the higher proportion of Indigenous children living in rural and remote areas, where the incidence of flame burns is higher,7,15 perhaps because there are more outdoor fires in rural areas or because rural children more frequently engage in risky behaviour than those in urban areas.7

A recent study similarly found that a higher proportion of children from rural areas presented to a specialist burn unit with burns affecting more than 10% TBSA;7 however, this analysis did not analyse cases by Indigenous status. Our results suggest that this difference could be partly explained by the higher proportion of Indigenous children living in remote areas.

The mean LOS for a burn injury was almost 3 days longer for Indigenous than for non-Indigenous children. This difference is similar to the reported difference in LOS between children living in remote and urban areas.7 After adjusting for burn injury characteristics, geographic remoteness, and area-level disadvantage, the difference in LOS between Indigenous and non-Indigenous children was still statistically significant, indicating that other factors also influence LOS.

A smaller proportion of Indigenous children than of non-Indigenous children were treated at a hospital with a paediatric tertiary referral burn unit. One explanation could be that a larger proportion of non-Indigenous children live near this hospital, located in western Sydney, so that it is their first point of contact. Inequities in access to medical services experienced by Indigenous Australians and people living in remote areas are recognised.1618 In contrast, we found that a higher proportion of Indigenous than of non-Indigenous children presenting with a severe burn and living in remote areas were treated at a hospital with a tertiary burns unit. About 40% of Indigenous and non-Indigenous children with severe burns were not admitted to a hospital with a tertiary burns unit, but our data did not allow further investigation of the underlying reasons. However, separation from family and community are likely to influence decisions by physicians and families about transferring children from remote areas to specialist burn units, typically located in metropolitan areas.19 Moreover, the introduction of telehealth procedures has facilitated care of patients in remote areas, so that fewer children need to be transferred to a hospital with a specialist burn unit.20

A lower proportion of Indigenous than of non-Indigenous patients underwent surgery, but a higher proportion of Indigenous children received in-hospital physical and occupational therapy, probably because a larger proportion of their injuries were severe burns.

This is the first data linkage cohort study of the characteristics of burn injuries to Indigenous and non-Indigenous children in Australia. However, it was subject to limitations that are inherent to the use of routinely collected hospital data. Our study was restricted to injuries that resulted in a hospitalisation; hospital admission and access may vary between population groups and regions; and higher admission rates in remote areas may reflect differences in access to other health care providers and services.21 Children living in rural and remote areas are more likely to be treated as inpatients because their travelling distances to hospital are longer, making it more difficult to return as day patients.22

There is currently no source of data on injuries incurred in the community and treated in the primary care setting in Australia, and we did not capture presentations at outpatient burn clinics or to Indigenous community-controlled health services.

Inaccuracies in the coding of external cause are possible, as well as in the coding of %TBSA in hospital data.2325 It has been reported that %TBSA is likely to be overestimated by referring hospitals when compared with assessments in specialist burn units.23,24 We may have underestimated the burden of burn injury hospitalisation in our cohort, as some repeat admissions might have been missed because of differences in external or primary diagnosis coding, and because we restricted our analysis to the first burn injury.

In view of the fact that patients admitted to hospital with a tertiary burns unit are reviewed by a physiotherapist, the proportion of children recorded as having received physical and occupational therapy was surprisingly low; the recording of such therapy in the hospital data may have been incomplete.

Anatomic location was not included as a factor in our statistical modelling of LOS because of the small numbers of cases in individual categories.

Further, underreporting of Indigenous status in routinely collected data is a recognised problem that can lead to underestimation of the number of Indigenous children hospitalised for injuries.26 We used Indigenous status as recorded in birth records to minimise the effect of differential misclassification bias, whereby the opportunity to be recorded as Indigenous rises with the number of times a child is admitted to hospital. However, applying different algorithms to identify Indigenous children on the basis of linked hospital data has been shown to increase both their identification and the sizes of differences between Indigenous and non-Indigenous children.2,27 Our estimates of differences between Indigenous and non-Indigenous children may therefore be conservative.

Conclusion

We found that the proportion of burns affecting more than 10% TBSA was higher for Indigenous than for non-Indigenous children, and that, after adjusting for the characteristics of the burn and residential location, Indigenous children spend more time in hospital.

Box 1 –
Characteristics of children admitted to hospital for a first burn injury, New South Wales, 2000–2014

All children

Non-Indigenous children

Indigenous children

P


Total number of children

1 124 717

1 088 968

35 749

Children admitted to hospital for a first burn injury (% of cohort)

4569 (0.41%)

4246 (0.39%)

323 (0.90%)

Age

0.03

< 1 year

798 (17.5%)

745 (17.5%)

53 (16%)

1–4 years

3057 (66.9%)

2854 (67.2%)

203 (63%)

4–13 years

714 (15.6%)

647 (15.2%)

67 (21%)

Sex

0.86

Girls

1902 (41.6%)

1769 (41.7%)

133 (41%)

Boys

2667 (58.4%)

2477 (58.3%)

190 (59%)

Area-level disadvantage

< 0.001

First tertile (most disadvantaged)

2200 (48.2%)

1955 (46.0%)

245 (76%)

Second tertile

1453 (31.8%)

1383 (32.6%)

70 (22%)

Third tertile (least disadvantaged)

916 (20.0%)

908 (21.4%)

8 (2%)

Geographic remoteness

< 0.001

Major cities

2716 (59.4%)

2649 (62.4%)

67 (21%)

Inner regional

1163 (25.5%)

1054 (24.8%)

109 (34%)

Outer regional

597 (13.1%)

498 (11.7%)

99 (31%)

Remote/very remote

93 (2.0%)

45 (1.1%)

48 (15%)

Number of hospitalisations

5829

6293

464


Box 2 –
Characteristics of burn injury, treatment and outcome for children admitted to hospital for a first burn injury, New South Wales, 2000–2014

All children

Non-Indigenous children

Indigenous children

P


Number of children

4569

4246

323

External cause of injury

< 0.001

Smoke, fire and flame

407 (8.9%)

348 (8.2%)

59 (18%)

Scalds

2794 (61.2%)

2641 (62.2%)

153 (47%)

Contact burns

910 (19.9%)

835 (19.7%)

75 (23%)

Other

458 (10.0%)

422 (9.9%)

36 (11%)

Anatomic location

0.005

Head/neck

874 (19.1%)

806 (19.0%)

68 (21%)

Trunk

962 (21.1%)

896 (21.1%)

66 (20%)

Shoulder/upper limb

604 (13.2%)

569 (13.4%)

35 (11%)

Wrist/hand

1027 (22.5%)

973 (22.9%)

54 (17%)

Hip/lower limb

505 (11.1%)

466 (11.0%)

39 (12%)

Ankle/foot

384 (8.4%)

347 (8.2%)

37 (12%)

Other/unspecified

213 (4.7%)

189 (4.5%)

24 (7.4%)

Total body surface area (%TBSA) injured*

0.002

< 10%

3796 (83.1%)

3546 (83.5%)

250 (77%)

10–19%

462 (10.1%)

426 (10.0%)

36 (11%)

≥ 20%

122 (2.7%)

104 (2.4%)

18 (6%)

Depth of injury

< 0.001

Superficial

324 (7.1%)

297 (7.0%)

27 (8.4%)

Partial

3309 (72.4%)

3105 (73.1%)

204 (63%)

Full thickness

645 (14.1%)

593 (14.0%)

52 (16%)

Inhalation injury

133 (2.9%)

120 (2.8%)

13 (4.0%)

0.22

Severe burn‡,§

533 (11.7%)

487 (12.4%)

46 (17%)

0.14

Treated at hospital with tertiary referral burn unit

2260 (49.5%)

2132 (50.2%)

128 (40%)

< 0.001

Severe burn treated at hospital with tertiary referral burn unit

298 (55.9%)

271 (55.6%)

27 (59%)

0.69

Number of re-admissions

0.19

0

3825 (83.7%)

3550 (83.6%)

275 (85%)

1

608 (13.3%)

570 (13.4%)

38 (12%)

2

115 (2.5%)

109 (2.6%)

6 (2%)

> 2

21 (0.5%)

17 (0.4%)

4 (1%)

Length of stay

< 0.001

< 1 day

1841 (40.3%)

1742 (41.0%)

99 (30.7%)

1–7 days

1917 (42.0%)

1795 (42.3%)

122 (37.8%)

8–28 days

510 (11.1%)

454 (10.7%)

56 (17.3%)

> 28 days

301 (6.6%)

255 (6.0%)

46 (14.2%)


* Missing data: 170 non-Indigenous and 19 Indigenous children. † Missing data: 251 non-Indigenous and 40 Indigenous children. ‡ Missing data: 311 non-Indigenous and 45 Indigenous children. § Defined as partial or full thickness burn and > 10% TBSA.

Box 3 –
Treatment of children admitted to hospital for a first burn injury, New South Wales, 2000–2014

All children

Non-Indigenous children

Indigenous children

P


Total number of hospitalisations

6293

5829

464

Mechanical ventilation

75 (1%)

65 (1%)

10 (2%)

0.047

Surgical intervention

1547 (25%)

1453 (25%)

94 (20%)

0.025

Physical/occupational therapy

612 (10%)

552 (9%)

60 (13%)

0.015

Other allied health*

1207 (19%)

1100 (19%)

107 (23%)

0.027


* Includes nutrition and dietetics, social work, speech pathology, pharmacy, pastoral care, play therapy and social work.

Box 4 –
Length of hospital stay for children admitted to hospital for a first burn injury (excluding day patients), New South Wales, 2000–2014

Non-Indigenous children

Indigenous children

P


Number of children

2504

224

Length of stay, first admission (days)

Median (IQR)

1 (1–3)

1 (1–6)

< 0.001

Mean (95% CI)

3.4 (3.2–3.7)

6.1 (4.8–7.4)

< 0.001

Range

1–61

1–77

Length of stay, total (days)

Median (IQR)

2 (1–4)

3 (1–7)

< 0.001

Mean (95% CI)

4.1 (3.8–4.3)

7.1 (5.6–8.5)

< 0.001

Range

1–61

1–79


Box 5 –
Effects of individual and area-level characteristics on differences in hospital length of stay for Indigenous and non-Indigenous children admitted to hospital for a first burn injury, New South Wales, 2000–2014

Characteristic

Hazard ratios*(95% CI)

P


Indigenous status

Non-Indigenous

Reference

Indigenous

0.78 (0.66–0.92)

< 0.002

Sex

Girls

Reference

Boys

1.00 (0.92–1.09)

0.98

Age

0–4 years

Reference

5–13 years

0.98 (0.86–1.12)

0.82

Inhalation injury

No

Reference

Yes

0.80 (0.52–1.23)

0.30

Depth of injury

Superficial

Reference

Partial

0.72 (0.60–0.85)

< 0.001

Full thickness

0.45 (0.36–0.55)

< 0.001

Total body surface area (%TBSA) injured

< 10%

Reference

10–19%

0.53 (0.47–0.60)

< 0.001

≥ 20%

0.23 (0.17–0.29)

< 0.001

Geographic remoteness

Major cities

Reference

Inner regional

0.88 (0.80–0.97)

0.01

Outer regional

0.82 (0.72–0.94)

< 0.001

Remote/very remote

1.00 (0.75–1.33)

1.0

Area-level disadvantage

First tertile (most disadvantaged)

Reference

Second tertile

1.05 (0.95–1.16)

0.34

Third tertile (least disadvantaged)

1.05 (0.93–1.17)

0.45


* Adjusted for all other variables in table.