Communicable Diseases Surveillance - Additional reports

This report published in Communicable Diseases Intelligence Volume 25, No 2, April 2001 contains an analysis and tables of monthly notifiable diseases and laboratory data, and quarterly surveillance reports.

Page last updated: 28 May 2001

A print friendly PDF version is available from this Communicable Diseases Intelligence issue's table of contents.




Gonococcal Surveillance

John Tapsall, The Prince of Wales Hospital, Randwick, NSW, 2031 for the Australian Gonococcal Surveillance Programme.

The Australian Gonococcal Surveillance Programme (AGSP) reference laboratories in the various States and Territories report data on sensitivity to an agreed 'core' group of antimicrobial agents quarterly. The antibiotics currently routinely surveyed are penicillin, ceftriaxone, ciprofloxacin and spectinomycin, all of which are administered as single dose regimens and currently used in Australia to treat gonorrhoea. When in vitro resistance to a recommended agent is demonstrated in 5 per cent or more of isolates from a general population, it is usual to remove that agent from the list of recommended treatment.1 Additional data are also provided on other antibiotics from time to time. At present all laboratories also test isolates for the presence of high level (plasmid-mediated) resistance to the tetracyclines, known as TRNG. Tetracyclines are however not a recommended therapy for gonorrhoea in Australia. Comparability of data is achieved by means of a standardised system of testing and a program-specific quality assurance process. Because of the substantial geographic differences in susceptibility patterns in Australia, regional as well as aggregated data are presented.

Reporting period 1 July to 30 September 2000

The Australian Gonococcal Surveillance Programme (AGSP) laboratories examined a total of 794 isolates in this quarter, slightly less than the 859 available in this period in 1999. About 33 per cent of this total was from New South Wales, 25 per cent from Victoria, 17 per cent from Queensland, 13 per cent from the Northern Territory, 9 per cent from Western Australia and 2.5 per cent from South Australia. There were few isolates from other centres.

Penicillins

Figure 10 shows the proportions of gonococci fully sensitive (MIC £ 0.03 mg/L), less sensitive (MIC 0.06 - 1 mg/L), relatively resistant (MIC ³ 1 mg/L) or else penicillinase producing (PPNG) aggregated for Australia and by State and Territory. A high proportion of PPNG and relatively resistant strains fail to respond to treatment with penicillins (penicillin, amoxycillin, ampicillin) and early generation cephalosporins.

Figure 10. Gonococci isolated, Australia, 1 July to 30 September 2000, by penicillin susceptibility and region

Figure 10. Gonococci isolated, Australia, 1 July to 30 September 2000, by penicillin susceptibility and region

FS fully sensitive to penicillin, MIC ≤ 0.03 mg/L
LS less sensitive to penicillin, MIC 0.06 - 0.5 mg/L
RR relatively resistant to penicillin, MIC ≥ 1 mg/L
PPNG penicillinase producing Neisseria gonorrhoeae


About 20 per cent of all isolates were penicillin resistant by one or more mechanisms - 8.8 per cent PPNG and 11.6 per cent by chromosomal mechanisms (CMRNG). The penicillin-resistant isolates comprised about 31 per cent of all isolates in South Australia, about 27 per cent in New South Wales, 21 per cent in Victoria, 19 per cent in Queensland and 15 per cent in Western Australia. In the Northern Territory 3 isolates out of 100 examined were penicillin resistant - 1 PPNG and 2 CMRNG.

The number of PPNG isolated in Australia (70) was higher in this quarter than in the corresponding period in 1999 (56). Numerically most PPNG were found in New South Wales   (23), Victoria (18) and Queensland (16) whereas the highest proportion of PPNG was found in isolates from Western Australia (14%). In Queensland, Victoria, New South Wales and South Australia the proportion of PPNG ranged between 9 and 11 per cent of isolates examined. A single PPNG was present in the Northern Territory. Acquisition data on PPNG indicated local infection with these strains was occurring throughout Australia. South East Asian countries remained the main source of external acquisition.

Once again more isolates (92) were resistant to the penicillins by separate and distinct chromosomal mechanisms. These CMRNG were especially prominent in New South Wales where 49 such isolates were detected. Victoria (25) and Queensland (11) were also prominent sources of CMRNG. Two strains of this type were present in the Northern Territory.

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Ceftriaxone and spectinomycin

Most isolates in Australia were again susceptible to these injectable agents. A small number of strains exhibited decreased ceftriaxone susceptibility.

Quinolone antibiotics

Quinolone resistant N. gonorrhoeae (QRNG) are defined as those isolates with an MIC to ciprofloxacin equal to or greater than 0.06 mg/L. QRNG are further subdivided into less sensitive (ciprofloxacin MICs 0.06 - 0.5 mg/L) or resistant (MIC ³ 1 mg/L) groups. The distribution of QRNG in Australia in this quarter is shown in Figure 11.

Figure 11. Quinolone-resistant N. gonorrhoeae, Australia, 1 July to 30 September 2000, by region

Figure 11. Quinolone-resistant N. gonorrhoeae, Australia, 1 July to 30 September 2000, by region

LS QRNG = Ciprofloxacin MICs 0.06 - 0.5 mg/L
R QRNG = Ciprofloxacin MICs ≤ 1 mg/L



The total number (142) and proportion (19.8%) of all QRNG was again high and very similar to numbers and proportions seen in the corresponding quarter of 1999 (152 isolates, 18%). In the current quarter, the QRNG were widely dispersed and were present in all centres except the Northern Territory. High rates were maintained in New South Wales (26%), Victoria (21%) South Australia (21%) and Queensland (17%). A lower proportion of Western Australian isolates (7%) was QRNG.

Forty-nine of the New South Wales, 13 of the Victorian and 20 Queensland QRNG exhibited high level resistance (MIC ciprofloxacin ³ 1 mg/L) and 3 higher level QRNG were also seen in South Australia and Western Australia. MICs ranged up to 16mg/L.

A significant shift occurred in New South Wales in this quarter insofar as the proportion of less sensitive strains decreased and fully resistant isolates acquired through local contact predominated. In Victoria about 60 per cent of the QRNG were still in the 'less sensitive' MIC range 0.06 - 0.5 mg/L and were found almost exclusively in males. QRNG were increasingly acquired through local contact but also from overseas from such diverse sources as Bahrain, Cambodia, China, Madagascar, Malaysia, the Philippines, Thailand, the United Kingdom and Vietnam.

High level tetracycline resistance

The number (69) and proportion (8.7%) of TRNG detected was less than in the corresponding period of 1999 (85, 10%). TRNG represented 21 per cent of isolates from Queensland, 10 per cent from Western Australia, 8 per cent from Victoria and 5 per cent from New South Wales and South Australia. A single TRNG was found in the Northern Territory. Most TRNG were imported into Australia from Cambodia, Indonesia, Thailand and Vietnam.

References

1. Anonymous. Management of sexually transmitted diseases. World Health Organization 1997; Document WHO/GPA/ TEM94.1 Rev.1 p 37.

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Rotavirus Surveillance

The National Rotavirus Reference Centre (NRRC) undertakes surveillance and characterisation of rotavirus strains causing annual epidemics of severe diarrhoea in young children throughout Australia.

There are currently fourteen laboratories contributing data and rotavirus specimens for the characterisation of representative rotavirus serotypes.

The NRRC is happy to give and receive notifications of rotavirus outbreaks Australia-wide. The NRRC can be contacted at the Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Flemington Road, Parkville, Victoria 3052. Telephone: (03) 9345 5069, Facsimile: (03) 9345 6240, E-mail: masendyp@cryptic.rch.unimelb.edu.au. For more information see Commun Dis Intell 2000;24:10.

June 2000 to April 2001

The 2000 rotavirus season of most Australian collaborating centres appears to have come and gone and the task of completing the rotavirus serotyping is well under away. Molecular and serological serotyping techniques have been employed to serotype rotavirus positive specimens received Australia-wide. Serotype G3 rotaviruses appeared sporadically in Australia during a 4-year Australia-wide epidemiological survey between 1993-1996,1 however none have been identified in any of the centres for the sampling period, June 2000 to December 2000. The Serotype G1 rotaviruses have been detected in all centres studied.

Serotype G4 viruses were found in the following 9 centres: Brisbane, Melbourne, Adelaide, Perth, Gove, Narrabri, Horsham, Darwin and Sydney. The G4 viruses were the most prevalent serotype (57%) in specimens received from The Prince of Wales Hospital in south-east Sydney. G4 viruses were also identified from The Children's Hospital at Westmead in Sydney's west (21%), but serotype G2 specimens were found to be the most prevalent serotype (45.6%) in this location. Serotype G2 viruses from Sydney's south-east were low in comparison (7.7%).

This unusual serotype distribution of the G2 and G4 viruses in Sydney suggests different serotypes can exhibit different distribution within a relatively small geographical area. G2 rotaviruses have also been detected in Melbourne, Hobart, Adelaide, Perth, Gove, Narrabri, Horsham and Darwin. Serotype G9 viruses which were identified for the first time in Australia in 1997, appeared in Sydney, Perth, Melbourne and Horsham, with G9 the most prevalent serotype in Horsham (72.7%) for the sampling period June 2000 to January 2001.

Rotavirus collection continues, and the National Rotavirus Reference Centre welcomes any notifications of rotavirus outbreaks.

References

1. Bishop RF, Masendycz PJ, Bugg HC, Carlin JB, Barnes GL. Epidemiological patterns of rotaviruses causing severe gastroenteritis in young children throughout Australia from 1993 to 1996. J Clin Microbiol 2001;39:1085-1091.

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HIV and AIDS Surveillance

National surveillance for HIV disease is coordinated by the National Centre in HIV Epidemiology and Clinical Research (NCHECR), in collaboration with State and Territory health authorities and the Commonwealth of Australia. Cases of HIV infection are notified to the National HIV Database on the first occasion of diagnosis in Australia, by either the diagnosing laboratory (Australian Capital Territory, New South Wales, Tasmania, Victoria) or by a combination of laboratory and doctor sources (Northern Territory, Queensland, South Australia, Western Australia). Cases of AIDS are notified through the State and Territory health authorities to the National AIDS Registry. Diagnoses of both HIV infection and AIDS are notified with the person's date of birth and name code, to minimise duplicate notifications while maintaining confidentiality.

Tabulations of diagnoses of HIV infection and AIDS are based on data available 3 months after the end of the reporting interval indicated, to allow for reporting delay and to incorporate newly available information. More detailed information on diagnoses of HIV infection and AIDS is published in the quarterly Australian HIV Surveillance Report, and annually in HIV/AIDS and related diseases in Australia Annual Surveillance Report. The reports are available from the National Centre in HIV Epidemiology and Clinical Research, 376 Victoria Street, Darlinghurst NSW 2010. Internet: http://www.med.unsw.edu.au/nchecr. Telephone: (02) 9332 4648. Facsimile: (02) 9332 1837.

HIV and AIDS diagnoses and deaths following AIDS reported between 1 October and 31 December 2000, as reported to 31 March 2001, are included in this issue of Communicable Diseases Intelligence (Tables 8 and 9).

Table 8. New diagnoses of HIV infection, new diagnoses of AIDS and deaths following AIDS occurring in the period 1 October to 31 December 2000, by sex and State or Territory of diagnosis

  ACT NSW NT Qld SA Tas Vic WA Totals for Australia
This period 2000 This period 1999 Year to date 2000 Year to date 1999
HIV diagnoses Female
0
2
1
2
0
0
5
0
10
20
73
75
Male
0
52
0
25
3
0
31
0
111
161
620
656
Sex not reported
0
0
0
0
0
0
0
0
0
0
0
0
Total1
0
54
1
27
3
0
36
0
121
183
695
733
AIDS diagnoses Female
0
2
0
0
0
0
0
0
2
4
20
19
Male
0
22
1
7
2
0
12
0
44
38
187
156
Total1
0
24
1
7
2
0
12
0
46
42
207
176
AIDS deaths Female
0
0
0
0
1
0
0
0
1
0
7
4
Male
0
15
0
1
2
0
7
0
25
29
115
115
Total1
0
15
0
1
3
0
7
0
26
29
122
120

1. Persons whose sex was reported as transgender are included in the totals.



Table 9. Cumulative diagnoses of HIV infection, AIDS and deaths following AIDS since the introduction of HIV antibody testing to 31 March 2001, by sex and State or Territory

  State or Territory Australia
ACT NSW NT Qld SA Tas Vic WA
HIV diagnoses Female
28
634
10
163
63
5
228
119
1,250
Male
228
11,236
108
2,070
694
78
4,022
925
19,361
Sex not reported
0
243
0
0
0
0
24
0
267
Total1
256
12,134
118
2,240
757
83
4,288
1,049
20,925
AIDS diagnoses Female
9
201
0
50
25
3
72
26
386
Male
87
4,742
36
853
350
45
1,679
356
8,148
Total1
96
4,955
36
905
375
48
1,759
384
8,558
AIDS deaths Female
4
114
0
33
16
2
49
17
235
Male
68
3,249
24
577
234
29
1,294
252
5,727
Total1
72
3,371
24
612
250
31
1,350
270
5,980

1. Persons whose sex was reported as transgender are included in the totals.



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Childhood immunisation coverage

Tables 10 and 11 provide the latest quarterly report on childhood vaccination coverage from the Australian Childhood Immunisation Register (ACIR).

The data show the percentage of children fully vaccinated at age 12 months for the cohort born between 1 October and 31 December 1999 and at 24 months of age for the cohort born between 1 October and 31 December 1998 according to the Australian Standard Vaccination Schedule.

A full description of the methodology used can be found in Commun Dis Intell 1998;22:36-37.

Table 10. Percentage of children immunised at 1 year of age, preliminary results by disease and State for the birth cohort 1 October to 31 December 1999; assessment date 31 March 2001

Vaccine
State or Territory Australia
ACT NSW NT Qld SA Tas Vic WA
Total number of children
990
20,721
778
11,641
4,375
1,453
15,119
6,074
61,151
Diphtheria, Tetanus, Pertussis (%)
92.9
91.0
89.0
91.8
91.5
93.1
92.2
90.1
91.5
Poliomyelitis (%)
92.8
90.9
89.6
91.8
91.5
93.2
92.3
90.0
91.4
Haemophilus influenzae type b (%)
95.4
94.3
94.0
94.4
95.0
95.6
95.3
93.6
94.6
Fully immunised (%)
92.7
90.7
88.6
91.4
91.4
92.6
92.1
89.6
91.2
Change in fully immunised since last quarter (%)
+0.0
+0.2
-0.6
-0.6
-0.8
+1.0
0.0
-0.7
-0.1


Table 11. Proportion of children immunised at 2 years of age, preliminary results by disease and State for the birth cohort 1 October to 31 December 1998; assessment date 31 March 2001

Vaccine
State or Territory Australia
ACT NSW NT Qld SA Tas Vic WA
Total number of children
1,085
21,388
781
11,504
4,501
1,609
15,618
6,279
62,765
Diphtheria, Tetanus, Pertussis (%)
89.6
87.3
82.0
90.4
89.7
91.4
88.5
86.5
88.3
Poliomyelitis (%)
93.9
92.2
93.0
93.5
94.5
95.3
94.0
91.9
93.1
Haemophilus influenzae type b (%)
94.9
94.4
93.6
94.7
95.5
95.5
95.5
93.5
94.7
Measles, Mumps, Rubella (%)
93.0
91.4
91.1
93.3
94.1
94.3
93.0
91.2
92.4
Fully immunised (%)2
87.6
82.7
78.9
87.8
87.5
89.7
85.1
82.6
84.8
Change in fully immunised since last quarter (%)
-0.2
+0.8
-1.1
-0.5
-1.1
+1.1
-1.3
-0.5
-0.3

1. The 12 months age data for this cohort was published in Commun Dis Intell 2000;24:109.
2. These data relating to 2 year old children should be considered as preliminary. The proportions shown as 'fully immunised' appear low when compared with the proportions for individual vaccines. This is at least partly due to poor identification of children on immunisation encounter forms.
Acknowledgment: These figures were provided by the Health Insurance Commission (HIC), to specifications provided by the Commonwealth Department of Health and Aged Care. For further information on these figures or data on the Australian Childhood Immunisation Register please contact the Immunisation Section of the HIC: Telephone 02 6124 6607.


This article was published in Communicable Diseases Intelligence Volume 25, No 2, April 2001.

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