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Effect of swimming pools on antibiotic use and clinic attendance for infections in two Aboriginal communities in Western Australia

Desiree T Silva, Deborah Lehmann, Mary T Tennant, Peter Jacoby, Helen Wright and Fiona J Stanley
Med J Aust 2008; 188 (10): 594-598. || doi: 10.5694/j.1326-5377.2008.tb01800.x
Published online: 19 May 2008

Abstract

Objective: To determine whether installation of swimming pools in remote Aboriginal communities reduces infection-related outpatient attendances and prescription of antibiotics.

Design and setting: Swimming pools were opened in Jigalong and Mugarinya, Western Australia, in September 2000. We examined local clinic records to document illnesses occurring in children and adolescents under 17 years of age between 1998 and 2005. In Jigalong, we examined records of those enrolled in an ongoing study evaluating the effect of swimming pools on health. In Mugarinya, we examined clinic records of those residing there permanently.

Main outcome measures: Clinic attendance rates for skin, middle-ear and respiratory tract infections and trauma, and prescription rates for antibiotics were analysed by using a community-based selection method in Jigalong, and a clinic-based selection method in both communities for comparison of the two communities and the two methods.

Results: We examined records of 131 children in Jigalong and 128 children in Mugarinya. After the pools had been installed, clinic attendance rates for skin infections declined by 68% in Jigalong and by up to 77% in Mugarinya. In Jigalong (where the pre-pool prevalence of infections was higher than in Mugarinya), rates of antibiotic prescription declined by 45%, as did clinic attendance for middle-ear infections (61% reduction) and respiratory tract infections (52% reduction).

Conclusion: Swimming pools in remote communities are associated with reduced prevalence of skin infections. Where disease prevalence is high, pools are also associated with reduced rates of antibiotic prescriptions and middle-ear and respiratory tract infections. In communities with resident health staff, examination of clinic records is an efficient method of monitoring the effects of public health interventions on the burden of infectious diseases.

Methods

Swimming pools were opened in Jigalong and Mugarinya in September 2000 and have generally been open from September to April each year. Both communities are in a semi-arid environment, over 1200 km north of Perth (Box 1). During the summer, daily temperatures range from 15ºC to 45ºC, falling to freezing at night in the winter months. In 2001, the census recorded 275 people in Jigalong and 188 in Mugarinya.9

Morbidity data collection

We collected morbidity data by examining medical records for children and adolescents (< 17 years) held at the local clinics. After the swimming pools opened in September 2000, we calculated annual morbidity rates from episodes occurring between 1 October and 30 September. All prescriptions for systemic antibiotics were recorded, and all episodes of ear, skin and respiratory tract infections (listed in Box 2) were documented. For comparison, we also documented changes in the rates of clinic visits for trauma, an illness category that we would not expect to decline after installation of a pool. We have previously reported a low incidence of pool-related trauma.6 Multiple attendances for treatment of an illness were counted as a single episode. However, if antibiotics were changed during the course of a single episode of illness, they were recorded as separate courses of antibiotics.

Inclusion criteria

Two different methods of data selection were used:

The community-based selection method: This was used at Jigalong, where there was an ongoing study that has been described in detail.6 Our research team visited Jigalong every 6 months between September 2000 and February 2005 and examined the children who were present. For the current analysis, we used Jigalong clinic data for an individual child only if that child had been seen by the research team during one of its routine 6-monthly visits during the 12-month period, October to September. If the child had not been seen by the research team during one of the 12-month periods, clinic-based morbidity data for that year were recorded as “missing”. We considered the community-based selection method the most reliable assessment of which children were present during a 12-month period.

The clinic-based selection method: There was no ongoing study in Mugarinya, so a different method of data selection had to be used. We extracted clinic attendance records for children identified by the local nurse (who had worked there for many years and did so throughout the study period) as being resident in the community. A child’s period of residence was defined as being between the start of the 12-month period (1 October) that included the child’s first clinic record and the end of the 12-month period (30 September) that included their last clinic record.

To compare morbidity rates between communities and the results obtained from the two different selection methods, we also analysed Jigalong data by the clinic-based method of selection.

Permission and ethical approval

Written permission to access medical records had been obtained from parents or guardians in Jigalong when they gave consent for their children to participate in the regular surveys.6 Approval for investigators to access the medical files of children in Mugarinya was given by the local community council and the local public health authority. Ethical approval to conduct the study was given by the Western Australian Aboriginal Health Information and Ethics Committee and the Princess Margaret Hospital Ethics Committee (Perth, WA). The Confidentiality of Health Information Committee of the Health Department of WA approved access to clinic data.

Results

Over the 6 years, 131 children were enrolled into the study in Jigalong, and morbidity data from 128 children residing in Mugarinya were analysed. At first enrolment, 40% of the study participants in Jigalong and 55% in Mugarinya were aged < 5 years; 56% in Jigalong and 50% in Mugarinya were boys. In Jigalong, 37–61 children were included in each year’s analysis when we used the community-based selection method, and 79–112 children when we used the clinic-based selection method; in Mugarinya 57–72 children were included each year.

The mean number of middle-ear and respiratory infections per child at the start of the study was lower in Mugarinya than in Jigalong, but skin infections and trauma attendances were similar (Box 3).

In Jigalong, the rates of infectious diseases (adjusted for age and sex) declined significantly from the pre-pool year to 2004–2005 (Box 3, Box 4). With the clinic-based method, middle-ear infections decreased by 61%, skin infections by 68%, and respiratory infections by 52%. The community-based selection method gave similar reductions in morbidity. Antibiotic prescription rates decreased significantly 2 years after the pool was opened and remained low there-after. The prescription rate decreased by 45% from the pre-pool year to 2004–2005.

The rate of antibiotic prescription was lower in Mugarinya than in Jigalong for the entire study period. The number of prescriptions per child per year ranged from 1.4 to 3.0 in Jigalong and 0.8 to 1.4 in Mugarinya. In Mugarinya, the adjusted antibiotic prescription rates changed little after the opening of the pool, and rates of respiratory tract and middle-ear infections increased, but not significantly. There was a significant reduction in rates of skin infections relative to the pre-pool year of between 53% and 77% annually until 2003–2004, but no reduction in 2004–2005. Trauma rates were significantly lower in 2001–2002 and 2002–2003 than in 1999–2000. For all disease categories except trauma, the morbidity rate in 2004–2005 was the highest since the pool was opened.

Log-linear trend analyses (Box 5) confirmed a significant decline in antibiotic prescriptions and infections in Jigalong from 1998 to 2005, irrespective of the selection method. In Mugarinya, trend analysis showed a decline in all skin infections, but no significant changes in rates of other infections, trauma-related events or antibiotic prescriptions.

There were 16 reports in Jigalong and 12 in Mugarinya of otitis externa (“swimmers ear”), a recognised problem among regular users of swimming pools,10,11 with no increase in prevalence over the course of the study.

Discussion

Clinic attendances for skin infections in both Jigalong and Mugarinya declined after the installation of swimming pools. There was also a significant decline in attendance for middle-ear and respiratory infections in Jigalong, where attendance rates for these illnesses were higher in the pre-pool period than in Mugarinya. The reduction in middle-ear and skin infections in Jigalong confirms and extends our earlier findings over a 7-year period.6

The 45% reduction in antibiotic prescriptions in Jigalong is consistent with the reduction in clinic visits for infections, but we found little change in antibiotic prescription rates in Mugarinya.

There were differences in health services available in the two communities. Two doctors and nursing staff lived in Jigalong throughout the study period. By contrast, in Mugarinya there were no resident doctors or nurses, but a nurse with extensive local knowledge had been providing a service for more than 20 years and stayed there 4 days each week. At other times, people had to travel from Mugarinya to Port Hedland for treatment. The fact that medical staff were not always available in Mugarinya to see sick children and to document illness episodes may in part explain the lower clinic attendance rates in Mugarinya. There may also have been differences in prescribing practices between staff in the two communities. However, there may also be a real difference in disease burden between these two communities (a subjective impression of the visiting researchers), which needs to be explored further.

The two methods we used have potential biases. The clinic-based method of selection may have excluded healthy children and hence resulted in an overestimate of morbidity rates. In fact, the morbidity rates in Mugarinya were lower than in Jigalong. In contrast, one might expect the community-based method to underestimate morbidity, because sick children might have remained at home and not been seen by the research team. However, a paediatrician being part of the research team and the team’s request to see sick children during 6-monthly visits may have encouraged people to bring sick children for examination. It is reassuring that the morbidity and antibiotic prescription rates found by the two analytical methods in Jigalong produced remarkably similar results. We aimed to ensure we had the most complete and reliable information on children, but we are unable to determine whether highly mobile teenagers, who might be at greatest risk of illness, might have benefited least from the intervention as they were less likely to use the pool.

In this observational study, attendance at clinics could have declined independently of installation of the pools. In Jigalong, the decline in rates of attendance for infections was not accompanied by reductions in attendance for injuries. The morbidity reductions at Jigalong are therefore unlikely to be the result of changes in overall clinic attendance. We cannot explain the reduction in clinic attendances for trauma at Mugarinya during 2001–2002 and 2002–2003, but this reduction did not coincide with any declines in attendance for infections.

However, in July 2001 pneumococcal conjugate vaccine was introduced in WA for children aged < 5 years, and by 2002 there was > 90% uptake in Jigalong and Mugarinya (Sally Connelly, Regional Immunisation Coordinator, Pilbara Population Health, personal communication, 2007). The vaccine program may have contributed to a reduction in pneumococcus-related respiratory illness, but is unlikely to have influenced attendance rates for middle-ear infections, because studies in the Northern Territory have not detected any effect of pneumococcal conjugate vaccine on the burden of severe middle-ear infections in Aboriginal communities.12 In our study, the reduction in possibly pneumococcus-related infections and other infections (eg, skin infections) actually began before a vaccine could have significantly affected morbidity rates. Furthermore, the reduction in disease burden was not equivalent in the two communities.

In view of high rates of infectious and chronic diseases, swimming pools in remote Aboriginal communities can have short-term and long-term advantages. Fewer prescriptions for antibiotics will reduce costs and antibiotic resistance, both of which are of concern in Aboriginal communities.13 Pyoderma is generally the result of group A streptococcal infections, and has been associated with rheumatic heart disease and glomerulonephritis.5,14-16 Aboriginal Australians have the highest documented rates of these illnesses worldwide.17,18 By reducing pyoderma, swimming pools may lower the incidence of the streptococcus-related chronic illnesses and the associated costs of renal dialysis and heart valve replacements.

Population mobility between Aboriginal communities is high and this can affect the interpretation of study results.19 Nevertheless, in Jigalong, community-based or clinic-based selection methods produced similar results. Therefore, we propose that evaluation of public health interventions for infectious diseases in children is possible using the clinic-based method in communities with resident staff and enough staff to ensure well kept clinic records.

Conclusions

The introduction of swimming pools is associated with a reduction in skin, ear and respiratory infections where documented outpatient attendance rates are high, thereby reducing antibiotic prescription rates and clinic workload. The effect on health of swimming pools being built elsewhere in Australia may be monitored efficiently by examining clinic records.

4 Morbidity rate ratios (95% CIs), adjusted for age and sex, 2000–2005 relative to pre-pool year (1999–2000) in two remote Western Australian Aboriginal communities

Jigalong


Mugarinya


Community-based method


Clinic-based method


Clinic-based method


Reason for attendance

n*

Events

Rate ratio

n

Events

Rate ratio

n

Events

Rate ratio


Systemic antibiotics

1999–2000

60

220

90

334

65

79

2000–2001

39

138

0.9 (0.7–1.2)

99

283

0.8 (0.7–1.0)

69

81

0.9 (0.7–1.3)

2001–2002

46

88

0.6§ (0.5–0.8)

108

205

0.6 (0.5–0.7)

68

71

0.8 (0.6–1.1)

2002–2003

61

93

0.5 (0.4–0.6)

112

159

0.5 (0.4–0.6)

72

72

0.8 (0.5–1.1)

2003–2004

51

77

0.5 (0.4–0.7)

102

153

0.5 (0.4–0.7)

69

71

0.8 (0.6–1.2)

2004–2005

37

67

0.5 (0.4–0.8)

79

122

0.6 (0.4–0.7)

57

89

1.2 (0.9–1.8)

Middle-ear infection

1999–2000

60

58

90

102

65

19

2000–2001

39

54

1.5 (0.9–2.3)

99

99

1.0 (0.7–1.3)

69

27

1.2 (0.6–2.6)

2001–2002

46

23

0.7 (0.5–1.1)

108

73

0.8 (0.6–1.0)

68

38

1.7 (0.9–3.4)

2002–2003

61

42

0.8 (0.4–1.4)

112

57

0.6 (0.4–1.0)

72

27

1.1 (0.5–2.5)

2003–2004

51

15

0.4 (0.2–0.8)

102

30

0.4 (0.3–0.6)

69

33

1.5 (0.7–3.4)

2004–2005

37

15

0.5 (0.3–0.9)

79

20

0.4 (0.2–0.6)

57

36

2.0 (0.9–4.6)

Skin infection

1999–2000

60

138

90

203

65

67

2000–2001

39

56

0.6 (0.5–0.8)

99

131

0.6 (0.5–0.8)

69

36

0.5 (0.3–0.8)

2001–2002

46

44

0.5 (0.3–0.8)

108

101

0.5 (0.4–0.6)

68

18

0.2 (0.1–0.4)

2002–2003

61

36

0.3 (0.2–0.4)

112

76

0.4 (0.3–0.5)

72

30

0.4 (0.2–0.6)

2003–2004

51

37

0.4 (0.3–0.6)

102

73

0.4 (0.3–0.5)

69

32

0.4 (0.3–0.7)

2004–2005

37

26

0.3 (0.2–0.6)

79

43

0.3 (0.2–0.5)

57

45

0.7 (0.5–1.2)

Respiratory infection

1999–2000

60

85

90

104

65

27

2000–2001

39

44

0.8 (0.6–1.2)

99

82

0.8 (0.6–1.2)

69

33

1.1 (0.7–1.8)

2001–2002

46

17

0.4 (0.2–0.6)

108

49

0.5 (0.3–0.8)

68

30

1.0 (0.6–1.7)

2002–2003

61

20

0.3 (0.2–0.4)

112

48

0.5 (0.3–0.9)

72

32

1.0 (0.5–1.7)

2003–2004

51

16

0.3 (0.2–0.7)

102

36

0.4 (0.3–0.7)

69

34

1.2 (0.6–2.1)

2004–2005

37

18

0.4 (0.2–0.8)

79

26

0.5 (0.3–0.8)

57

36

1.4 (0.8–2.4)

Trauma

1999–2000

60

31

90

35

65

14

2000–2001

39

20

0.9 (0.5–1.6)

99

29

0.7 (0.4–1.3)

69

9

0.6 (0.3–1.4)

2001–2002

46

27

1.1 (0.5–2.2)

108

47

1.1 (0.6–1.9)

68

4

0.3 (0.1–0.8)

2002–2003

61

24

0.8 (0.4–1.3)

112

48

1.0 (0.6–1.8)

72

6

0.4 (0.2–1.00)

2003–2004

51

25

0.8 (0.4–1.7)

102

44

1.0 (0.6–1.8)

69

25

1.7 (0.8–3.3)

2004–2005

37

14

0.7 (0.3–1.5)

79

33

1.0 (0.6–1.7)

57

12

1.0 (0.4–2.3)


* Number of children enrolled in the community-based survey who were seen by the research team during the 12 months (October–September) in each year. Number of children resident during the 12 months who were enrolled in the community-based survey. Number of children resident during the 12 months. § Statistically significant ratios (P < 0.05) are shown in bold.

  • Desiree T Silva1
  • Deborah Lehmann1
  • Mary T Tennant1
  • Peter Jacoby1
  • Helen Wright2
  • Fiona J Stanley1

  • 1 Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, Perth, WA.
  • 2 Rural Clinical School of Western Australia, University of Western Australia, Kalgoorlie, WA.


Correspondence: desiree.silva@bigpond.com

Acknowledgements: 

We thank Helen Wright and Jenny Smith for assistance with data extraction from the notes and data entry, and Kirsten Alpers for editorial assistance. We thank the nursing and medical staff at Jigalong and Mugarinya and Kylie Carville for assisting us in obtaining the clinic records. This study was funded by the Western Australian Department of Housing and Works and the Western Australian Health Promotion Foundation (Healthway). Peter Jacoby and Deborah Lehmann are funded through National Health and Medical Council program grant 353514.

Competing interests:

None identified.

  • 1. Anderson I, Crengle S, Kamaka ML, et al. Indigenous health in Australia, New Zealand, and the Pacific. Lancet 2006; 367: 1775-1785.
  • 2. Carville K, Lehmann D, Hall G, et al. Infection is the major component of the disease burden in Aboriginal and non-Aboriginal Australian children. Pediatr Infect Dis J 2007; 26: 210-216.
  • 3. Freemantle CJ, Read AW, de Klerk NH, et al. Patterns, trends, and increasing disparities in mortality for Aboriginal and non-Aboriginal infants born in Western Australia, 1980–2001: population database study. Lancet 2006; 367: 1758-1766.
  • 4. Reid J, Trompf P, editors. The health of Aboriginal Australia. Sydney: Harcourt Brace Jovanovich, 1991.
  • 5. Currie BJ, Carapetis JR. Skin infections and infestations in Aboriginal communities in northern Australia. Australas J Dermatol 2000; 41: 139-145.
  • 6. Lehmann D, Tennant MT, Silva DT, et al. Benefits of swimming pools in two remote Aboriginal communities in Western Australia: intervention study. BMJ 2003; 327: 415-419.
  • 7. Morris PS, Leach AJ, Silberberg P, et al. Otitis media in young Aboriginal children from remote communities in Northern and Central Australia: a cross-sectional survey. BMC Pediatr 2005; 5: 27.
  • 8. Turnidge JD, Bell JM, Collignon PJ. Rapidly emerging antimicrobial resistances in Streptococcus pneumoniae in Australia. Pneumococcal Study Group. Med J Aust 1999; 170: 152-155.
  • 9. Trewin D. Population distribution, Aboriginal and Torres Strait Islander Australians, 2001. Canberra: Australian Bureau of Statistics, 2002. (ABS Cat. No. 4705.0.) http://www.ausstats.abs.gov.au/ausstats/subscriber.nsf/0/85AB4A6668629B77CA256BE400026A25/$File/47050_2001.pdf (accessed Dec 2007).
  • 10. van Asperen IA, de Rover CM, Schijven JF, et al. Risk of otitis externa after swimming in recreational fresh water lakes containing Pseudomonas aeruginosa. BMJ 1995; 311: 1407-1410.
  • 11. van Balen FA, Smit WM, Zuithoff NP, Verheij TJ. Clinical efficacy of three common treatments in acute otitis externa in primary care: randomised controlled trial. BMJ 2003; 327: 1201-1205.
  • 12. McKenzie GA, Carapetis JR, Leach AJ, et al. Pneumococcal vaccination and otitis media in Australian Aboriginal infants [abstract PO 1210]. 5th International Symposium on Pneumococci and Pneumococcal Diseases; 2006 Apr 2–6; Alice Springs.
  • 13. Grimwood K, Collignon PJ, Currie BJ, et al. Antibiotic management of pneumococcal infections in an era of increased resistance. J Paediatr Child Health 1997; 33: 287-295.
  • 14. Carapetis JR, McDonald M, Wilson NJ. Acute rheumatic fever. Lancet 2005; 366: 155-168.
  • 15. Steer AC, Danchin MH, Carapetis JR. Group A streptococcal infections in children. J Paediatr Child Health 2007; 43: 203-213.
  • 16. Streeton CL, Hanna JN, Messer RD, Merianos A. An epidemic of acute post-streptococcal glomerulonephritis among aboriginal children. J Paediatr Child Health 1995; 31: 245-248.
  • 17. Carapetis JR, Currie BJ, Kaplan EL. Epidemiology and prevention of group A streptococcal infections: acute respiratory tract infections, skin infections, and their sequelae at the close of the twentieth century. Clin Infect Dis 1999; 28: 205-210.
  • 18. Carapetis JR, Currie BJ. Clinical epidemiology of rheumatic fever and rheumatic heart disease in tropical Australia. Adv Exp Med Biol 1997; 418: 233-236.
  • 19. Taylor J. Short-term Indigenous population mobility and service delivery. CAEPR discussion paper 118. Canberra: Centre for Aboriginal Economic Policy Research, Australian National University, 1996.

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