Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 10, Number 7—July 2004
Research

Rapid Assessment Tool for Haemophilus influenzae type b Disease in Developing Countries1

On This Page
Methods
Results
Discussion
Cite This Article
Figures
Figure 1
Figure 2
Figure 3
Figure 4
Tables
Table 1
Table 2
Downloads
Article
RIS [TXT - 2 KB]
Article Metrics
Metric Details
43
citations of this article
EID Journal Metrics on Scopus
Related Articles
MDR Escherichia coli and Klebsiella pneumoniae
Computerized Systems for Pneumonia Surveillance
COVID-19 and Non-HIV P. jirovecii Pneumonia
More articles on Pneumonia
Author affiliations: *Centers for Disease Control and Prevention, Atlanta, Georgia, USA; †World Health Organization, Geneva, Switzerland; ‡Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA; §World Health Organization, Cairo, Egypt

Cite This Article

Abstract

Haemophilus influenzae type b (Hib) still causes a substantial number of deaths among children in developing countries, despite the availability of effective conjugate vaccines. A major obstacle in developing a Hib vaccine has been limited awareness about the impact of Hib disease. A tool was developed to estimate the national rates of Hib meningitis and pneumonia by assessing retrospective local data over 7 to 10 days. Data from 11 countries in Africa, the Middle East, and Asia were studied and showed rates of Hib meningitis from >50 cases per 100,000 children >5 years in Ghana and Uganda to <15 per 100,000 in Iran, Jordan, and Uzbekistan. Results were affected by the quality of available data. The Hib rapid assessment tool can be useful to countries that desire a timely assessment of Hib disease rates.

Figure 1

Thumbnail of Global status of countries using Hib conjugate vaccine in their national immunization program in 2001 (J. Wenger, WHO, unpub. data).

Figure 1. Global status of countries using Hib conjugate vaccine in their national immunization program in 2001 (J. Wenger, WHO, unpub. data).

Among infants and young children, Haemophilus influenzae type b (Hib) is the leading cause of bacterial meningitis deaths and the second leading cause of bacterial pneumonia deaths worldwide and accounts for approximately 400,000 deaths of children each year (1,2). These deaths are preventable through Hib conjugate vaccines (1). In the United States, Hib conjugate vaccines were first introduced into the routine immunization program for infants in 1990. Subsequently, most industrialized, western countries have introduced these vaccines. Hib conjugate vaccines, however, are still not widely used in developing countries, where the greatest rates of Hib-related disease and deaths occur. Before 2002, only 2 of 51 countries with an infant death rate >70 per 1,000 live births were routinely vaccinated against Hib (Figure 1).

The major obstacles to introducing Hib conjugate vaccines into developing countries have been their cost and the population’s limited awareness about the impact of Hib disease. The Hib conjugate vaccine, even after a decade of use, is still expensive, costing approximately $U.S. 2.50 per dose, and thus, external financial resources are needed to procure the vaccine in most developing countries. Since 1999, the Global Alliance for Vaccines and Immunization (GAVI) through the Vaccine Fund has provided a mechanism of financing Hib conjugate vaccines for 5 years to the 75 poorest countries (http://www.vaccinealliance.org/home/index.php). Despite this opportunity, few countries initially requested the Hib vaccine through GAVI, partly because of limited awareness about the rate of Hib disease.

Diagnosing Hib disease is difficult; Hib primarily causes meningitis and pneumonia, two common syndromes often treated empirically. To diagnose Hib meningitis, lumbar punctures must be performed and cerebrospinal fluid rapidly processed in a microbiologic laboratory with the technical capability and supplies to culture Hib. Hib pneumonia is even more difficult to diagnose. Although blood cultures are highly specific for Hib, they have a sensitivity of 20%, thus allowing the role of Hib as a cause of pneumonia to be underestimated (3,4).

Several methods have been used to define the rate of Hib disease in developing countries. Randomized, controlled trials of the Hib conjugate vaccine in The Gambia, which looked at radiographic evidence of pneumonia as a study endpoint, showed that approximately 20% of consolidated pneumonia (diagnosed by chest x-ray) is prevented by vaccination and therefore presumably caused by Hib (5). In Chile, a retrospective analysis of pneumonia after a randomized, controlled trial of Hib vaccine showed a 22% reduction in consolidation or pleural effusion in the group that received vaccine (6). Despite the quality of the data produced, such trials are too expensive, time-consuming, and complex to be widely used to measure Hib disease. A more widely used method to measure Hib disease has been population-based laboratory surveillance for Hib meningitis (7). Such surveillance, although dependent on the rate of lumbar punctures and laboratory quality, can produce reliable data on the incidence rate of Hib meningitis, which can be compared across countries. Population-based surveillance for meningitis, however, requires at least a year to produce results and does not give an estimate of Hib pneumonia.

Alternatives to these longitudinal, time-consuming, resource-intense methods of measuring Hib disease are being sought, particularly for use in regions of the world, such as Africa, where studies have consistently shown high rates of Hib disease (8–12). In countries in these regions, more limited data on the local rate of Hib disease may be adequate to allow evidence-based decisions about introducing Hib vaccine and to provide a basis for national advocacy for, and commitment to, such decisions.

On the basis of these considerations, we created a rapid assessment tool to measure the national rate of severe Hib disease. We discuss the methods used in the rapid assessment tool and its results in the first 11 countries where it was used.

Methods

Logistics

Requests for Hib rapid assessments were made by national ministries of health. The Hib rapid assessment tool was usually completed in 7 to 10 days. The assessment teams consisted of local representatives from the ministry of health and one or two consultants familiar with the tool. National data relevant to the tool was collected by reviewing national health statistics and medical literature, focusing on national or regional journals. The assessment often included several days in the capital city reviewing available data and working with the ministry of health. Most of the assessment involved collecting, evaluating, and synthesizing existing data from hospitals. Data were entered into standardized spreadsheets that assist in the calculation of the national disease impact. The assessment often ended with a meeting to discuss the findings with key persons in the ministry of health and leading pediatricians.

The tool uses two different, complementary methods to estimate Hib rates. The first one works from the “bottom up,” beginning with a local estimate of Hib meningitis incidence rates; the second works from the “top down,” starting with the country’s under-5 mortality rate, which is the number of children per 1,000 live births who die before their fifth birthday.

Meningitis Incidence Rate Method

This method uses retrospective data to calculate an incidence rate of Hib meningitis, from which the annual numbers of cases of and deaths attributable to Hib meningitis and pneumonia are estimated. The first step for this method is selecting an appropriate site where the incidence of Hib meningitis can be accurately calculated. The ideal site is a region of the country where the catchment population of a hospital or a few hospitals can be well defined, where most children with meningitis go to these hospitals, and where the private sector rarely uses the Hib vaccine. In addition, physicians in these hospitals should routinely perform lumbar punctures on children with suspected meningitis, and the hospitals should have laboratories that culture H. influenzae and conduct cytologic tests on cerebrospinal fluid. Although few laboratories in our assessments performed serotyping, we assumed that, in the absence of vaccination, all H. influenzae in cerebrospinal fluid was caused by type b (Hib), which is consistent with available studies (13,14).

Figure 2

Thumbnail of The meningitis incidence rate method for calculating Haemophilus influenzae type b (Hib) disease rate by using the Hib rapid assessment tool. White boxes are data input points and gray boxes are disease rate estimates.

Figure 2. The meningitis incidence rate method for calculating Haemophilus influenzae type b (Hib) disease rate by using the Hib rapid assessment tool. White boxes are data input points and gray boxes are...

Calculating Hib meningitis incidence rate begins by counting the number of cases of culture-confirmed meningitis in children <5 years of age during a defined period in a defined catchment population (Figure 2). The percentage of culture-confirmed meningitis caused by Hib is then calculated. Cerebrospinal fluid samples from neonates are excluded because Hib is very rare in the first month of life (15). Next, the number of purulent cerebrospinal fluid samples during the same period is counted. For the purposes of this tool, purulence is defined in a way that increases the specificity for bacterial meningitis: visible turbidity, >100 leukocytes/mm3, or 10–99 leukocytes/mm3 with glucose <40 mg/dL and protein >100 mg/dL. The culture-confirmed cases are excluded, which leaves a count of culture-negative, purulent cerebrospinal fluid samples. The tool assumes that these are bacterial in origin, and the number ascribed to Hib is calculated by applying the same percentage of culture-confirmed meningitis caused by Hib to the culture-negative, purulent specimens. The rationale for this step is that a certain percentage of Hib meningitis cases may not be culture-confirmed because of prior antimicrobial drug use or laboratory-related factors. The number of culture-confirmed Hib cases and estimated culture-negative Hib cases is added. Then this number is inflated by a factor on the basis of information from local pediatricians to account for children with suspected meningitis who did not get a lumbar puncture. The number of children <5 years of age in the catchment region of the hospitals is used as the denominator to calculate the Hib meningitis incidence rate.

In the last step, the total number of children <5 years of age in the country is used to estimate the annual number of cases of Hib meningitis in the country. By using a ratio of five Hib pneumonia cases for each case of Hib meningitis, which was found in two randomized studies of Hib conjugate vaccine, the annual number of cases of Hib pneumonia is estimated (5,6). By using the case-fatality proportions of Hib meningitis and Hib pneumonia, obtained locally if possible, the annual number of deaths attributable Hib in the country is also estimated.

Under-5 Mortality Rate Method

Figure 3

Thumbnail of The under-5 mortality rate method for calculating Haemophilus influenzae type b (Hib) disease rate by using the Hib rapid assessment tool. White boxes are data input points and gray boxes are disease rate estimates.

Figure 3. The under-5 mortality rate method for calculating Haemophilus influenzae type b (Hib) disease rate by using the Hib rapid assessment tool. White boxes are data input points and gray boxes are...

This method starts with the birth cohort in the country (Figure 3). To calculate the number of childhood deaths in the country, the under-5 mortality rate is applied to the birth cohort. The neonatal death rate, if available, is subtracted from this number. Then the percentage of childhood deaths caused by acute respiratory illness is estimated. This percentage is extrapolated from a study that showed that the higher the under-5 mortality rate, the greater percentage of deaths that are caused by respiratory illness (16). In the next step, the percentage of all acute respiratory illness deaths due to Hib is estimated to be 13%. This figure was obtained by subtracting the number of respiratory deaths unlikely to be caused by Hib, during the neonatal period and caused by measles and pertussis, and multiplying the remaining number of respiratory deaths by 20%, the percentage of severe pneumonia thought to be caused by Hib (5,6,17). This calculation yields the annual number of pneumonia deaths caused by Hib. Then, meningitis cases and meningitis deaths are calculated by using the case-fatality proportion of Hib pneumonia, the 5:1 Hib pneumonia:meningitis ratio, the Hib meningitis case-fatality proportion, and the annual number of Hib pneumonia cases.

Review of the Rapid Assessment Tool

The tool was pilot-tested in several countries, and a draft version was reviewed at a meeting of technical experts convened by the World Health Organization in October 2000. Suggested revisions to the tool made at the meeting were subsequently incorporated. The minutes of this meeting (http://www.who.int/vaccines-documents/DocsPDF01/www604.pdf), along with the completed tool including worksheets, are available on the Internet (http://www.who.int/vaccines-documents/DocsPDF01/www625.pdf).

Results

The Hib rapid assessment tool has been used in 11 developing countries in sub-Saharan Africa, the Middle East, and Asia (Table 1 and Table 2). The assessment of the meningitis incidence rate was performed most often in smaller cities, where the denominator population could be more easily delineated, although several assessments were performed in larger cities, such as Alexandria, Egypt, and Shiraz, Iran. In most countries, at least one hospital had cultured H. influenzae from cerebrospinal fluid. The exceptions were Uzbekistan, Yemen, and Ghana. Alternative strategies were used to estimate the incidence rate of Hib meningitis in these countries. In Uzbekistan, where laboratories had been unable to culture Hib from cerebrospinal fluid and the leukocyte counts were not being performed properly, data from a prospective, population-based study in Moscow, which has a very similar health care system, were applied to the rate of lumbar punctures performed in Uzbek children to yield an estimate of the Hib meningitis incidence (A. Platonov, pers. comm.). In Ghana, Gram stain results of cerebrospinal fluid, rather than culture, were used to estimate the rate of Hib meningitis. In Yemen, data about purulent meningitis from another hospital in the capital and review of data from the local literature were used to estimate the rate of Hib meningitis.

The percentage of culture-confirmed meningitis caused by Hib was 33%–67%. Most hospitals were able to perform leukocyte counts on cerebrospinal fluid, but a few hospitals routinely measured protein and glucose. The incidence rate of culture-confirmed Hib meningitis varied greatly, depending on the ability to find hospitals consistently able to culture Hib from cerebrospinal fluid. Except for a few countries (i.e., Uganda, Oman, and Kyrgyzstan), the rates of culture-confirmed meningitis were very low, <10 per 100,000 children <5 years of age. When we used the rapid assessment tool, the estimated rates of Hib meningitis tended to be several-fold higher than those based on culture-confirmed Hib. When we used the tool, the estimated incidence rate of Hib meningitis among children <5 years of age was >50 cases per 100,000 children <5 years of age in Ghana and Uganda to <15 cases in Iran, Jordan, and Uzbekistan. The under-5 mortality rate method yielded estimates of national Hib disease rates that were higher than those obtained from the meningitis incidence rate method (mean 2.8, 95% confidence interval 1.7–3.9.)

Discussion

Figure 4

Thumbnail of Comparison of incidence rates of Haemophilus influenzae type b (Hib) meningitis per 100,000 children &lt;5 years of age between the rapid assessment tool (gray bars) and prospective, population-based laboratory surveillance (white bars), by region (8–10,12,19–26). (UAE, United Arab Emirates).

Figure 4. Comparison of incidence rates of Haemophilus influenzae type b (Hib) meningitis per 100,000 children <5 years of age between the rapid assessment tool (gray bars) and prospective, population-based laboratory surveillance (white...

The Hib rapid assessment tool estimated rates of Hib meningitis in Africa and the Middle East that were similar to those obtained from population-based studies in the same regions (Figure 4, 8–12, 18–22). In countries in Eastern Europe and Asia where the impact of Hib meningitis is less well-defined, the tool yielded variable results, although not too discrepant from rates found from prospective, population-based surveillance performed in other countries in the same areas (23–26). These results demonstrate that the Hib rapid assessment tool can yield estimates of Hib disease rates similar to expected rates in many countries. Without some of the adjustments made by the tool, the incidence rate of culture-confirmed Hib meningitis would have been low in most of these countries. One strength of the tool is that its adjustments compensate for artificial reasons for low incidence rates of culture-confirmed Hib meningitis, such as low rates of lumbar puncture and the lack of appropriate microbiologic capacity.

While not meant to replace more rigorous and accurate methods used to measure Hib disease, such as prospective, population-based surveillance, the tool addresses a unique need for countries desiring local Hib disease rate estimates to assist them in making a decision to introduce Hib vaccine. The strengths of the tool in addressing this need are that it is rapid, inexpensive, uses locally obtained data, accounts for biases in these data that might underestimate the true rate of Hib disease, and provides disease impact output as the number of cases and deaths from Hib disease, which is often more tangible to decision makers than incidence rates. Moreover, the process of performing the rapid assessment engages pediatricians and decision makers in a dialogue about the clinical, epidemiologic, and laboratory aspects of Hib disease and vaccine. Consequently, the Hib rapid assessment process helps countries develop the capacity to critically evaluate existing local data and perceptions about Hib disease rates.

The Hib rapid assessment tool has several limitations. Whereas in most countries we found hospitals that effectively cultured Hib, in several countries we were unable to find any site with demonstrated capacity to culture Hib. In these countries, we were unable to use the meningitis incidence rate method as outlined in the tool. As mentioned, alternative strategies based on local and regional data were used here, which might have introduced inaccuracies. Nonetheless, the estimates of Hib impact in these countries were similar to those observed in population-based studies from the same regions (Figure 4).

A second limitation of the tool is that even when a hospital that has cultured Hib is found, the output from the tool using the meningitis incidence rate method will always be constrained by the quality of the data. Although the tool corrects for missed cases of Hib meningitis, it does not correct completely for substantial underdiagnosis of Hib meningitis. If clinical or microbiologic factors have led to such underdiagnosis, this will necessarily be reflected in the rate estimates made by the tool. This limitation was exemplified during the rapid assessment in Kyrgyzstan, where the tool found a rate of Hib meningitis of 20.4 per 100,000 in 1999 to 2000, a period when the infectious disease hospital in Bishkek was involved in a study with Aventis-Pasteur, which supplied the laboratory with appropriate reagents and materials to isolate Hib. From 2001 through 2002, after the study ended, the rate obtained from tool in the same hospital decreased to 4.7 per 100,000.

A third limitation of the rapid assessment tool is that several assumptions are incorporated into the calculations. These assumptions, although based on the available literature, may not apply to all populations. For example, the 5:1 ratio of Hib pneumonia to meningitis, which was based on the results of two randomized controlled vaccine trials in The Gambia and Chile, may not apply to all parts of the world (5,6). In countries with lower under-5 mortality rates, the 5:1 ratio may be too high, while in countries with high under-5 mortality rates, the 5:1 ratio may be too low. Moreover, this ratio may vary in different parts of the world, as suggested from the results of a recently completed Hib conjugate vaccine efficacy trial in Lombok, Indonesia, which suggested the incidence of Hib meningitis to be high and the incidence of radiographically defined Hib pneumonia to be relatively low (27).

A fourth concern is that the under-5 mortality rate method yielded higher estimates of Hib disease rates than the meningitis incidence rate method. One reason for this difference is that the neonatal death rate was not subtracted from the under-5 mortality rate in most countries (except Kyrgyzstan, Uzbekistan, and Bhutan). This omission may have led to overestimating Hib disease since neonatal deaths account for a large proportion of childhood deaths, but Hib deaths are rare in neonates (13). Also, because the under-5 mortality rate method starts with pneumonia deaths and works backwards to meningitis cases, more assumptions are made in the last estimate. Therefore, in reconciling the estimates obtained from the two methods, the meningitis prevalence may be more accurate than the meningitis incidence rate method, while estimation of the pneumonia incidence may have an accuracy in between those obtained from the two methods.

The results of the Hib rapid assessment tool need to be interpreted in light of its limitations and the validity of its assumptions critically evaluated in each country where it is used, particularly in regions, such as Asia, where the impact of Hib disease is still uncertain. Nonetheless, the tool has been useful to some countries in deciding whether to adopt Hib vaccine into their national immunization programs. Of the countries we studied, three (Ghana, Uganda, and Oman) introduced Hib vaccine, and three others (Bhutan, Kyrgyzstan, and Yemen) requested Hib vaccine on their initial application to GAVI. Subsequent to the assessments in these countries, the tool has been used in several other developing countries that were considering the introduction of Hib vaccine (Western Pacific Islands [28], Albania, Thailand, Nepal, and Sudan). Several countries (Uganda, Albania, and Egypt) have used results of the rapid assessment tool in cost-effectiveness analyses of Hib vaccine introduction. As more developing countries consider Hib vaccination programs, estimating the local impact of Hib disease will continue to be an important part of the effort to introduce and sustain Hib vaccination programs. The experience with measuring Hib disease rates, including the rapid assessment tool, might also provide a valuable base for considering the introduction of other new vaccines, including pneumococcal and meningococcal conjugates.

Dr. Feikin is a medical epidemiologist in the Respiratory Diseases Branch at CDC. He specializes in vaccines for the prevention of bacterial pneumonia in developing countries.

Top

Acknowledgments

We thank those who participated in these assessments from the ministries of health and hospitals in these countries; the other consultants who assisted in these assessments, Shatrughan Bastola, Selma Khamassi, Salah Al-Awaidy, Robin Biellik, Mamadon Malifa Balde, Jean Bosco Ndihokubwayo, Richard Adegbola, Alexander Platonov, Amany Gayed, Fouad Youssef, and Frank Mahoney; and the technical reviewers for evaluating the tool at the meeting in Geneva in October 2000.

The Bureau for Global Health, United States Agency for International Development provided funding for many of these assessments.

Top

References

  1. Levine  OS, Schwartz  B, Pierce  N, Kane  M. Development, evaluation and implementation of Haemophilus influenzae type b vaccines for young children in developing countries: current status and priority actions. Pediatr Infect Dis J. 1998;17:S95–13. DOIPubMedGoogle Scholar
  2. Peltola  H. Worldwide Haemophilus influenzae type b disease at the beginning of the 21st century: global analysis of the disease burden 25 years after the use of the polysaccharide vaccine and a decade after the advent of conjugates. Clin Microbiol Rev. 2000;13:302–17. DOIPubMedGoogle Scholar
  3. Shann  F. Etiology of severe pneumonia in children in developing countries. Pediatr Infect Dis. 1986;5:247–52. DOIPubMedGoogle Scholar
  4. Isaacs  D. Problems in determining the etiology of community-acquired childhood pneumonia. Pediatr Infect Dis J. 1989;8:143–8.PubMedGoogle Scholar
  5. Mulholland  K, Levine  O, Nohynek  H, Greenwood  BM. Evaluation of vaccines for the prevention of pneumonia in children in developing countries. Epidemiol Rev. 1999;21:43–55.PubMedGoogle Scholar
  6. Levine  OS, Lagos  R, Munoz  A, Villaroel  J, Alvarez  AM, Abrego  P, Defining the burden of pneumonia in children preventable by vaccination against Haemophilus influenzae type b. Pediatr Infect Dis J. 1999;18:1060–4. DOIPubMedGoogle Scholar
  7. Levine  OS, Schuchat  A, Schwartz  B, Wenger  JD, Elliott  JA. Generic protocol for population-based surveillance for Haemophilus influenzae type b. Document number WHO/VRD/GEN/95.05 1995. Geneva: World Health Organization; 1995.
  8. Cadoz  M, Denis  F, Mar  ID. An epidemiological study of purulent meningitis cases admitted to hospital in Dakar, 1970–1979. Bull World Health Organ. 1981;59:575–84.PubMedGoogle Scholar
  9. Campagne  G, Schuchat  A, Djibo  S, Ousseini  A, Cisse  L, Chippaux  JP. Epidemiology of bacterial meningitis in Niamey, Niger, 1981–96. Bull World Health Organ. 1999;77:499–508.PubMedGoogle Scholar
  10. Adegbola  RA, Mulholland  EK, Falade  AG, Secka  O, Sarge-Njai  R, Corrah  T, Haemophilus influenzae type b disease in the western region of The Gambia: background surveillance for a vaccine efficacy trial. Ann Trop Paediatr. 1996;16:103–11.PubMedGoogle Scholar
  11. Bijlmer  HA, van Alphen  L, Greenwood  BM, Brown  J, Schneider  G, Hughes  A, The epidemiology of Haemophilus influenzae meningitis in children under five years of age in The Gambia, West Africa. J Infect Dis. 1990;161:1210–5.PubMedGoogle Scholar
  12. Tall  T, Elola  A, Prazuck  T, Traore  A, Nacro  B, Vincent-Ballereau  F. Meningites a Haemophilus influenzae a Bobo-Kioulasso (Burkina Faso). Med Mal Infect. 1992;22:1173–7. DOIGoogle Scholar
  13. Adams  WG, Deaver  KA, Cochi  SL, Plikaytis  BD, Zell  ER, Broome  CV, Decline of childhood Haemophilus influenzae type b (Hib) disease in the Hib vaccine era. JAMA. 1993;269:221–6. DOIPubMedGoogle Scholar
  14. Broome  CV. Epidemiology of Haemophilus influenzae type b infections in the United States. Pediatr Infect Dis J. 1987;6:779–82. DOIPubMedGoogle Scholar
  15. Bacterial etiology of serious infections in young infants in developing countries: results of a multicenter study. The WHO Young Infants Study Group. Pediatr Infect Dis J. 1999;18:S17–22. DOIPubMedGoogle Scholar
  16. Garenne  M, Ronsmans  C, Campbell  H. The magnitude of death from acute respiratory infections in children under 5 years in developing countries. World Health Stat Q. 1992;45:180–91.PubMedGoogle Scholar
  17. World Health Organization. Implementation of the global strategy for health for all by the Yyear 2000, second evaluation; and eighth report on the world health situation. Document A45/3 1992. Geneva: The Organization; 1992.
  18. Shaltout  AA, Auger  LT, Awadallah  NB, Hijazi  Z, Johny  M, Hajj  KE, Morbidity and death of bacterial meningitis in Arab children. J Trop Med Hyg. 1989;92:402–6.PubMedGoogle Scholar
  19. Zaki  M, Daoud  AS, ElSaleh  Q, West  PW. Childhood bacterial meningitis in Kuwait. J Trop Med Hyg. 1990;93:7–11.PubMedGoogle Scholar
  20. Uduman  SA, Adeyemi  E, El-Khadir  A, Jose  K, Benedict  S, Bener  A. Haemophilus influenzae type b still remains a leading cause of meningitis among unvaccinated children—a prospective CSF analysis study. J Trop Pediatr. 2000;46:331–4. DOIPubMedGoogle Scholar
  21. Novelli  VM, el-Baba  F, Lewis  RG, Bissell  PS. Haemophilus influenzae type b disease in an Arab Gulf state. Pediatr Infect Dis J. 1989;8:886–7. DOIPubMedGoogle Scholar
  22. Almuneef  M, Alshaalan  M, Memish  Z, Alalola  S. Bacterial meningitis in Saudi Arabia: the impact of Haemophilus influenzae type b vaccination. J Chemother. 2001;13(Suppl 1):34–9.PubMedGoogle Scholar
  23. Kojouharova  M, Gatcheva  N, Setchanova  L, Robertson  SE, Wenger  JD. Epidemiology of meningitis due to Haemophilus influenzae type b in children in Bulgaria: a prospective, population-based surveillance study. Bull World Health Organ. 2002;80:690–5.PubMedGoogle Scholar
  24. Zielinski  A, Tomaszunas-Blaszczyk  J, Kuklinska  D. Epidemiology of childhood bacterial meningitis in Poland. Incidence of bacterial meningitis with special reference to Haemophilus influenzae type b among children 0-59 months old in the former Kielce and Bydgoszcz districts in Poland in 1998–1999. Eur J Epidemiol. 2001;17:779–82. DOIPubMedGoogle Scholar
  25. Bennett  JV, Platonov  AE, Slack  MPE, Mala  P, Burton  AH, Robertson  SE. Haemophilus influenzae type b (Hib) meningitis in the pre-vaccine era: a global review of incidence, age distributions, and case-fatality. World Health Organization. Document number WHO/V&B/02.18. Available from: www.who.int/vaccines-documents/
  26. Steinhoff  MC. Invasive Haemophilus influenzae disease in India: a preliminary report of prospective multihospital surveillance. IBIS (Invasive Bacterial Infections Surveillance) Group. Pediatr Infect Dis J. 1998;17:S172–5. DOIPubMedGoogle Scholar
  27. Gessner  BD; Hib study group. A randomized, controlled clinical trial of the effect of Haemophilus influenzae type b (Hib) vaccine on pneumonia and meningitis in children living on Lombok Island, Indonesia. In: Program and Abstracts of the 43rd Annual Interscience Conference on Antimicrobial Agents and Chemotherapy: September 14-17, 2003; Chicago, IL. Abstract G-2054a. Washington: American Society for Microbiology; 2003.
  28. Russell  FM, Carapetis Jr, Mansoor O, Darcy A, Fakakovi T, Metai A, et al. High incidence of Haemophilus influenzae type b infection in children in Pacific Island countries. Clin Infect Dis. 2003;37:1593–9. DOIPubMedGoogle Scholar

Top

Figures
Tables

Top

Cite This Article

DOI: 10.3201/eid1007.030737

1Some of the content of this manuscript has previously been presented in a document on the Web site of the World Health Organization (http://www.who.int/vaccines-documents/DocsPDF01/www625.pdf).

Table of Contents – Volume 10, Number 7—July 2004

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

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

Daniel Feikin, Centers for Disease Control and Prevention, 1600 Clifton Rd., Mailstop C23, Atlanta, GA 30333, USA; fax: 404-639-3970

Send To

10000 character(s) remaining.

Top

Page created: January 27, 2011
Page updated: January 27, 2011
Page reviewed: January 27, 2011
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external