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Vol. 11, No. 2
February 2005

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Additional Methods
Limitations with the Modeling
Possible Roles of WHO, SPC, and Donor Nations and Agencies
Appendix References
Appendix Table
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Letter

Modeling the Impact of Pandemic Influenza on Pacific Islands

Nick Wilson,*Comments Osman Mansoor,† Douglas Lush,‡ and Tom Kiedrzynski§
*Wellington School of Medicine and Health Sciences, Otago University, Wellington, New Zealand; †Public Health Consulting Ltd, Wellington, New Zealand; ‡New Zealand Ministry of Health, Wellington, New Zealand; and §Secretariat of the Pacific Community, Noumea, New Caledonia


Appendix

Additional Methods

The output of the FluAid model is the number of additional deaths, hospitalizations, and illness attributable to pandemic influenza that will require medical consultations. The model assumes no effective public health interventions to control disease spread (such as quarantine, access to appropriate vaccine, or widespread use of antiviral drugs). Specific details about the FluAid software and the various assumptions in the model are detailed on the Centers for Disease Control and Prevention (CDC) Web site (1) and in other documents (2,3).

Given the lack of accessible data for specific Pacific Island countries and areas, the default values used in FluAid were used to determine the proportion of the population in the high-risk category for each age group, when calculating the death rates, the hospitalization rates, and the illness rates. The model's parameters were based on the available data (mostly from North America and some from Europe) from the 1957 pandemic and subsequent nonpandemic data (2). Persons categorized as high-risk have a preexisting medical condition (e.g., diabetes) that makes them more susceptible to developing medical complications due to influenza. The proportions in this high-risk category used in the model were 6.4% for persons birth–18 years of age, 14.4% for those 19–64 years of age, and 40% for those ≥65 years of age. The output values from the model were for most likely, minimum, and maximum values (each for death, hospitalization, and illness requiring medical consultations).

The FluAid model provides the total disease impact but does not specify its time distribution. The length of influenza epidemics is highly variable (4,5), but for this analysis, the first pandemic wave was assumed to span 8 weeks and have the same distribution over time as a model of a stochastically simulated influenza epidemic (6) i.e., 32.3% of all cases in week 4, the peak week.

The countries and areas included in this analysis were the 20 tropical Pacific Island countries and areas that are members of the Secretariat of the Pacific Community (SPC) (excluding Papua New Guinea, and Pitcairn Island). Mid-2004 total population estimates from SPC (7) were used and adjusted according to World Health Organization (WHO) data on population distribution (8) to fit the age categories required by the model.

The total number of hospital beds in each Pacific Island country and area was based on WHO data (9). However, the data for Tonga were updated from more recent information (S. Kupu, pers. comm.) and updated similarly for Niue as well (10). When countries' data were missing, the information was found through additional Internet searches (i.e., for Nauru and Tokelau). The number of doctors per capita was also obtained from WHO data (9).

Limitations with the Modeling

The uncertainties associated with pandemic influenza mean that any modeling of its future impact is relatively crude. The FluAid model also has a number of specific limitations, which may lend an underestimation of the next pandemic's impact. First, the new strain may be particularly infectious, virulent, or both. The model's upper incidence rate for clinical illness was 35%, when higher rates (e.g., 50%) are plausible. Second, the proportions of the population in various high-risk groups in Pacific Island countries and areas may be larger than used in the model. This is plausible given the relatively high prevalence of chronic conditions such as diabetes in some Pacific Island countries and areas (e.g., a 23% prevalence rate for diabetes amongst adults aged 25–64 years in Samoa [11]). Finally, the level of antimicrobial drug resistance (e.g., Streptococcus pneumoniae) may continue to increase globally, thus the actual death rate may be higher than used in this model (i.e., if alternative treatments for the secondary microbial infections after influenza infection are not readily available).

In contrast, the results could also be overestimated for the following reasons: First, the use of international level public health interventions as recommended by WHO (12) may prevent or delay pandemic influenza reaching some Pacific Island countries and areas or particularly remote island groups (e.g., the provision of health alert notices to incoming travelers and entry screening). Improvements in surveillance systems (with access to rapid detection kits) over time may increase the chances of control measures being successful or subsequent pandemic waves being delayed. Second, some Pacific Island countries and areas could possibly avoid the first pandemic wave and might have access to a vaccine for protection from subsequent pandemic waves (though this may take 6–9 months from the time that a new virus variant is first identified (13). In addition, the use of antiviral agents (14) could prevent infection and reduce illness among key personnel and also those with high-risk conditions, but only if supplies are adequate. A recent study suggests that pandemic influenza could be contained with "the use of antiviral prophylaxis, if 80% of the exposed persons maintained prophylaxis for up to 8 weeks" (6).

Also, improved treatment in the community and hospital settings could lower hospitalization and death rates (relative to those used in this model). Finally, the geographic dispersal of some Pacific Island countries and areas may mean that spread within the country is much slower than the 8 weeks used in this model. This would reduce the peak demand on health services.

Possible Roles of WHO, SPC, and Donor Nations and Agencies

Agencies such as WHO and SPC play valuable roles in improving influenza surveillance, which may facilitate the control of pandemic influenza. Donor nations and agencies can potentially contribute to enhancing regional surveillance efforts by sharing their experience with developing national influenza pandemic plans and by conducting pandemic planning exercises (New Zealand has experience with both of these [15,16]).

Donor support for increasing the size of the health workforce could assist not only at a time of a pandemic but also when dealing with the current threats to health. Such support could include additional funds for health workforce training and placing and retaining staff in areas of greatest need (e.g., remote locations). Reducing the burden of chronic disease (e.g., donor support for enhanced tobacco control) may also reduce the proportion of the population at increased risk of adverse sequelae from infection with influenza.

Investment by donors in expanding current hospital bed capacity in Pacific Island countries and areas may be of value. However, this is likely a lower priority than strengthening primary healthcare services in Pacific Island countries and areas and making plans to mobilize effective community care. Funding for antiviral drugs and influenza vaccine (when available) to healthcare workers and high-risk groups could also be considered.

Appendix References

  1. Centers for Disease Control and Prevention (National Vaccine Program Office). FluAid. [cited 2004 Jul 15]. Available from: http://www2a.cdc.gov/od/fluaid/default.htm
  2. Meltzer MI, Cox NJ, Fukuda K. The economic impact of pandemic influenza in the United States: implications for setting priorities for interventions. Emerg Infect Dis. 1999;5:659–71.
  3. Centers for Disease Control and Prevention. Meltzer MI, Cox NJ, Fukuda K. Modeling the economic impact of pandemic influenza in the United States: implications for setting priorities for intervention. Background paper. Atlanta: CDC;1999. [cited 2004 Jul 15]. Available from http://www.cdc.gov/ncidod/eid/vol5no5/melt_back.htm
  4. Flahault A, Dias-Ferrao V, Chaberty P, Esteves K, Valleron AJ, Lavanchy D. FluNet as a tool for global monitoring of influenza on the Web. JAMA. 1998;280:1330–2.
  5. Spicer CC. The mathematical modelling of influenza epidemics. Br Med Bull. 1979;35:23–8.
  6. Longini IM, Halloran ME, Nizam A, Yang Y. Containing pandemic influenza with antiviral agents. Am J Epidemiol. 2004;159:623–33.
  7. Secretariat of the Pacific Community. Demography/Population Programme. Pacific Island Populations 2004, Part 1. [cited 2004 Jul 20]. Available from http://www.spc.org.nc/demog/English01-02/RecentStats/2004/Pacific%20Island%20Populations%202004.xls
  8. World Health Organization, Western Pacific Region. Country health profiles 2002 revision. Cited 2004 Jul 20]. Available from http://www.wpro.who.int/chips
  9. World Health Organization. The work of WHO in the Western Pacific Region. Report of the regional director—1 July 2002–30 June 2003. Manila: WHO, 2003:217. [cited 2004 Jul 20]. Available from http://www.wpro.who.int/pdf/rcm54/en/rdr/19_stat_annex.pdf
  10. Andrews J. Funding for hospital tops Niue's post-cyclone wishlist. New Zealand Herald, 13 April 2004. [cited 2004 Dec 24]. Available from http://www.nzherald.co.nz/index.cfm?ObjectID=3560161
  11. Government of Samoa. Launching of Steps Survey Results: Brief Summary of Findings. Apia: Government of Samoa, 2004.
  12. World Health Organization. WHO consultation on priority public health interventions before and during an influenza pandemic. Geneva: The Organization; 2004. [cited 2004 Jul 22]. Available from http://www.who.int/csr/disease/avian_influenza/en/final.pdf
  13. Strikas RA, Wallace GS, Myers MG. Influenza pandemic preparedness action plan for the United States: 2002 Update. Clin Infect Dis. 2002;35:590–6.
  14. Jefferson TO, Deeks JJ, Demicheli V, Rivetti D, Rudin M. Amantadine and rimantadine for preventing and treating influenza A in adults. Cochrane Database Syst Rev. 2004;(3):CD001169.
  15. Jennings L. Avian influenza: a public health risk for New Zealand. N Z Med J. 2004;117;U843.
  16. Ministry of Health. Influenza pandemic action plan. Wellington, New Zealand: Ministry of Health, 2002. [cited 2004 Jul 20]. Available from http://www.moh.govt.nz/moh.nsf/ea6005dc347e7bd44c2566a40079ae6f/
    5f5694e4a5736dd2cc256c55000788a3/$FILE/InfluenzaPandemicActionPlan.pdf

 

Appendix Table. Deaths, hospitalizations, and medical consultations predicted for the next influenza pandemic using the FluAid model (at incidence rates [IR] of clinical illness of 15% and 35%)

Country/area

Deaths (15% IR)

Deaths (35% IR)

Hospitalizations
(15% IR)

Hospitalizations
(35% IR)

Consultations
(15% IR)

Consultations
(35% IR)







Most likely

Range

Most likely

Range

Most likely

Range

Most likely

Range

Most likely

Range

Most likely

Range


Melanesia

   Fiji Islands

195

68–402

453

160–937

1,063

293–1,490

2,480

684–3,476

68,604

53,442–93,423

160,077

124,698 – 217,988

   New Caledonia

64

28–124

152

64–292

332

99–449

773

232–1,048

19,311

15,019–26,652

45,060

35,044 – 62,186

   Solomon Islands

82

33–190

192

79–444

459

143–749

1,071

332–1,750

38,667

30,869–50,274

90,223

72,028 – 117,308

   Vanuatu

42

16–94

99

38–219

235

70–363

549

162–846

17,988

14,241–23,765

41,973

33,230 – 55,452

Micronesia

   Federated States of Micronesia

24

9–50

56

21–119

129

39–193

300

89–452

9,358

7,384–12,458

21,834

17,231 – 29,069

   Guam

43

21–85

101

48–197

218

69–308

507

163–719

13,670

10,754–18,527

31,895

25,092 – 43,230

   Kiribati

19

7–42

44

17–97

104

31–158

243

72–369

7,746

6125–10,271

18,074

14,290 – 23,966

   Marshall Islands

10

3–22

23

8–54

58

16–90

137

38–211

4,621

3,650– 6,096

10,782

8,516 – 14,223

   Nauru

1

0–4

4

1–10

11

3–16

25

7–38

842

665–1,111

1,965

1,549 – 2,593

   Northern Mariana Islands

18

4–39

44

11–89

109

25–141

253

59–329

6,304

4,807–8,833

14,711

11,215 – 20,609

   Palau

6

3–11

13

5–26

30

9–40

70

20–92

1,683

1,305–2,335

3,926

3,044 – 5,448

Polynesia

   American Samoa

12

4–28

31

12–67

73

20–107

169

49–251

5,186

4,080–6,933

12,101

9,521 – 16,178

   Cook Islands

5

2–8

10

5–19

20

7–27

47

15–65

1,139

887–1,579

2,657

2,069 – 3,685

   French Polynesia

59

19–121

137

42–281

327

84–447

763

197–1,042

20,461

15,827–28,107

47,742

36,931 – 65,583

   Niue

1

0–1

1

1–2

2

1–3

5

2–7

131

103–179

306

241 – 419

   Samoa

40

19–84

95

42–198

212

67–319

495

157–746

15,186

12,034–20,182

35,435

28,078 – 47,091

   Tokelau

1

0–1

1

1–2

2

1–3

4

2–6

125

100–165

292

233 – 386

   Tonga

25

11–49

57

27–113

124

39–180

290

93–418

8,115

6,402–10931

18,937

14,936 – 25,506

   Tuvalu

3

1–5

6

3–12

13

5–18

30

10–42

788

619–1,074

1,838

1,445 – 2,505

  Wallis and Futuna

3

1–8

8

4–18

18

5–26

44

14–62

1,231

971–1,656

2,873

2,265 – 3,862

Total

653

252–1369

1,527

588–3,195

3,539

1,027–5,130

8,255

2,395–11,971

241,156

189,283–324,553

562,701

441,660 – 757,289

   
     
   
Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Nick Wilson, Department of Public Health, Wellington School of Medicine and Health Sciences, Otago University, PO Box 7343, Wellington South, New Zealand; fax: 64-4-4763646; email: nwilson@actrix.gen.nz

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