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Haemophilus influenzae type b

Haemophilus influenzae type b is a bacterium that can cause serious infections in children, including meningitis, pneumonia, and septicemia.
It is a leading cause of bacterial meningitis in young children worldwide.
Symptoms may include fever, headache, stiff neck, and altered mental status.
Prompt antibiotic treatment is critical.
Vaccination has significantly reduced the incidence of Hib disease in many countries.
Researchers can use PubCompare.ai's AI-driven tools to identify the most effective protocols and products for Hib research, accelerating discoveries and streamlining thier work.

Most cited protocols related to «Haemophilus influenzae type b»

We retrieved data on DTP, OPV, and Haemophilus influenzae type b (Hib) immunisation coverage using existing surveys [9 (link),15 ,20 ,21 (link)]. DTP, OPV, and the Hib vaccine are all scheduled during the first 6 months of life (at 2, 4, and 6 months), which is the peak age range for SIDS [22 (link)]. To ensure comparability over time, we used the reported coverage of at least three doses of the respective vaccine. From 1995 onwards, any pertussis vaccine was reported including acellular pertussis vaccine (DTaP) [16 ].
The following three surveys provided data on immunisation coverage in the United States: the United States Immunization Survey (USIS; 1968–1985), the National Health Interview Survey (NHIS; 1991–1993), and the National Immunization Survey (NIS; 1994–2009) [9 (link),15 ,20 ,21 (link)]. The USIS started as an area-probability household survey using face-to-face interviews and became a telephone survey in 1971 [9 (link)]. Until 1978, the USIS assessed the immunisation of children between 1 and 4 years of age. Between 1979 and 1985, the survey included only children aged 24–35 months. The collected information was based on either parental recall or an immunisation record that was maintained at home. There was a lack of information on immunisation coverage from 1986–1990. From 1991 onwards, the NHIS assessed the immunisation status of children aged 19–35 months [20 ,23 ,24 ]. The NHIS examined a representative probability sample of households in the United States using face-to-face interviews. If a child’s immunisation records were available, the data were abstracted from the records; otherwise, the collected information was based on parental recall. Then, in 1994, the CDC implemented the NIS for continuous monitoring of immunisation coverage [15 ,21 (link)]. For 1994, we used the Morbidity and Mortality Weekly Report, and for the years 1995–2009, we used the public use files that are published on the CDC website [15 ,16 ]. The NIS is a random-digit-dialling telephone survey of households with children aged 19–35 months. The data were validated with the immunisation history of the child, which was obtained from the family’s health care provider [25 ]. The NIS and NHIS yielded similar results for estimated immunisation coverage levels [15 ]. In the current study, immunisation coverage is presented graphically as the percentage of children who were immunised with DTP, OPV, and the Hib vaccine in each year during the time period from 1968 to 2009.
Publication 2015
Child Face Fingers Haemophilus influenzae type b Haemophilus Vaccines Households Immunization Immunization Coverage Mental Recall National Health Insurance Only Child Parent Pertussis Sudden Infant Death Syndrome Vaccine, Pertussis Vaccines Vaccines, Acellular
For PCR evaluation of respiratory specimens, we used the Fast-track Diagnostics Respiratory Pathogens 33 multiplex PCR kit (FTD Resp-33 kit) (Fast-track Diagnostics, Sliema, Malta). NP/OP specimens were collected in viral transport medium (universal transport medium [UTM], Copan Diagnostics, Bresica, Italy) and refrigerated at 2°C–8°C for a maximum of 8 hours, or frozen at –80°C prior to nucleic acid extraction. Induced sputum, pleural fluid, and lung aspirate specimens were collected in saline in universal containers and either refrigerated at 2°C–8°C for a maximum of 24 hours, or frozen at –80°C prior to nucleic acid extraction.
Total nucleic acid extraction was performed on respiratory specimens using the NucliSENS easyMAG platform (bioMérieux, Marcy l’Etoile, France). Four hundred microliters of each respiratory specimen (NP specimen in UTM, induced sputum aliquot in normal saline, pleural fluid aliquot, or lung aspirate aliquot) was eluted to a final volume of 60–110 μL nucleic acid. Prior to extraction, induced sputum specimens were digested with 1:1 dithiothreitol and incubated at ambient temperature until any mucus was broken down.
The FTD Resp-33 kit is a real-time PCR arranged in 8 multiplex groups for the detection of the following 33 viruses, bacteria, and fungi: influenza A, B, and C; parainfluenza viruses 1, 2, 3, and 4; coronaviruses NL63, 229E, OC43, and HKU1; human metapneumovirus A/B; human rhinovirus; respiratory syncytial virus A/B; adenovirus; enterovirus, parechovirus; bocavirus; cytomegalovirus; Pneumocystis jirovecii; Mycoplasma pneumoniae; Chlamydophila pneumoniae; Streptococcus pneumoniae; Haemophilus influenzae type b; Staphylococcus aureus; Moraxella catarrhalis; Bordetella pertussis; Klebsiella pneumoniae; Legionella species; Salmonella species; and Haemophilus influenzae species. The K. pneumoniae target was not used in any of the final analyses because of difficulties with assay specificity, as has been found elsewhere [9 (link)]. Positive, negative, and internal extraction controls were included in each run.
Quantitative PCR (qPCR) data were generated through the creation of standard curves using 10-fold serial dilutions of plasmid standards provided by FTD on an approximately quarterly basis at each study site, with calculation of pathogen density (copies/milliliter) from the sample cycle threshold (Ct) values. Because the results for the known standards were highly consistent across laboratories, standard curve data from all sites were pooled to create “standardized” standard curves for each pathogen target; data points beyond 2 standard deviations of the mean were excluded. Quantitative PCR was performed at each site using an Applied Biosystems 7500 (ABI-7500) platform (Applied Biosystems, Foster City, California). Cycling conditions were 50°C for 15 minutes, 95°C for 10 minutes, and 40 cycles of 95°C for 8 seconds followed by 60°C for 34 seconds.
Publication 2017
Adenoviruses Bacteria Biological Assay Bocavirus Bordetella pertussis Chlamydophila pneumoniae Cytomegalovirus Diagnosis Dithiothreitol Enterovirus Freezing Fungi Haemophilus influenzae Haemophilus influenzae type b Homo sapiens Human Metapneumovirus Influenza Klebsiella pneumoniae Lanugo Legionella Lung Moraxella catarrhalis Mucus Multiplex Polymerase Chain Reaction Mycoplasma pneumoniae Neoplasm Metastasis NL63, Human Coronavirus Normal Saline Nucleic Acids Para-Influenza Virus Type 1 Parechovirus Pathogenicity Plasmids Pleura Pneumocystis jiroveci Real-Time Polymerase Chain Reaction Respiratory Rate Respiratory Syncytial Virus Rhinovirus Saline Solution Salmonella Sputum, Induced Staphylococcus aureus Streptococcus pneumoniae Technique, Dilution Virus
The birth cohort was formed from 656 consecutive singleton births at the National Hospital in Tórshavn, Faroe Islands, during 1997-2000. Although cesarean deliveries and obstetric complications were usually not included, the cohort can be considered reasonably representative of Faroese births. Health care is free of charge in the Faroes, and childhood immunizations begin with vaccinations at age 3 months against diphtheria and tetanus, along with pertussis, polio, and Haemophilus influenzae type B. Repeat inoculations are given at ages 5 and 12 months, with a booster vaccination against diphtheria and tetanus at age 5 years.
To examine the long-term antibody responses to the immunizations, the birth cohort underwent prospective follow-up until age 7 years. A total of 587 children (89% of the cohort) participated in 1 or more of the examinations, which took place at age 5 years prebooster, approximately 4 weeks after the booster, and at age 7 years.12 (link) Results from 6 children at the most recent examination were excluded, because an additional booster had been given at some point after the routine booster given at age 5 years. The 464 children (71%) participating at age 7 years did not significantly differ from nonparticipants in terms of sex, maternal exposure to PFCs, or antibody concentration at age 5 years.
The study protocol was approved by the ethical review committee serving the Faroe Islands and by the institutional review board at the Harvard School of Public Health, and written informed consent was obtained from all mothers.
Publication 2012
Antibody Formation Birth Cohort Cesarean Section Child Diphtheria Ethical Review Ethics Committees, Research Haemophilus influenzae type b Immunization Immunoglobulins Maternal Exposure Mothers Pertussis Physical Examination Poliomyelitis Secondary Immunization Toxoid, Tetanus Vaccination

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Publication 2009
Anemia, Sickle Cell Bacteremia Child Diagnosis Diphtheria Escherichia coli Haemophilus influenzae Haemophilus influenzae type b Haemophilus influenzae type b polysaccharide vaccine Hepatitis B HIV Infections Immunization Schedule Infection Malaria Pentavalent Vaccines Pertussis Pneumococcal Vaccine Salmonella typhi Staphylococcus aureus Infection Streptococcus pneumoniae Toxoid, Tetanus Youth
The study was carried out in Maela, a long-term camp for displaced persons in rural Northwest Thailand. Maela has a population of ∼40,000 displaced persons from Myanmar, predominantly of Karen ethnicity, who live in a 4 km2 area. Camp residents receive WHO EPI (Expanded Program on Immunization) immunizations. Haemophilus influenzae type B (HiB) and pneumococcal vaccines are not available. Shoklo Malaria Research Unit (SMRU) has provided medical care in this population since 1986.
Between October 2007 and November 2008, all pregnant women attending the SMRU antenatal clinic at 28–30 weeks gestation were invited to consent to their infant's participation in a pneumonia cohort study. Using sealed opaque envelopes containing an allocation code, women were randomly allocated to the pneumococcal carriage sub-cohort at enrolment. For this sub-cohort, women had a nasopharyngeal swab (NPS) taken at delivery and both infant and mother had a NPS taken at monthly surveillance visits from 1–24 months of age. Samples of blood were collected from the mother and umbilical cord at delivery and infant blood samples were taken at each monthly visit.
Publication 2012
BLOOD Displaced Persons Ethnicity Haemophilus influenzae type b Immunization Immunization Programs Infant Malaria Mothers Nasopharynx Obstetric Delivery Pneumococcal Vaccine Pneumonia Pregnancy Pregnant Women Umbilical Cord Vaccine, Pneumococcal Polysaccharide Woman

Most recents protocols related to «Haemophilus influenzae type b»

Pakistan’s routine EPI schedule in 2019 included BCG (bacille Calmette-Guérin) vaccine and oral polio vaccine (OPV) at birth; 3 doses of Penta (containing diphtheria-tetanus-pertussis, hepatitis B, Haemophilus influenzae type b vaccine), pneumococcal vaccine (PCV10), and OPV at 6, 10, and 14 weeks; 2 doses of rotavirus vaccine (Rota) at 6 and 10 weeks; a single dose of inactivated polio vaccine (IPV) at 14 weeks; and 2 doses of measles vaccine at 9 and 15 months.
For Bangladesh, the EPI schedule included BCG vaccine at birth; Penta, PCV, and OPV at 6, 10, and 14 weeks; IPV at 6 and 14 weeks; and measles-rubella (MR) vaccine at 9 and 15 months.
Publication 2023
10-valent pneumococcal conjugate vaccine BCG Vaccine Childbirth Diphtheria-Tetanus Vaccine Haemophilus influenzae type b Hepatitis B Measles Measles Vaccine Oral Poliovirus Vaccine Pertussis Pneumococcal Vaccine Poliovirus Vaccine, Inactivated Rotavirus Vaccines Rubella Tetranitrate, Pentaerythritol Vaccine, Rubella Vaccines
Administratively, South Africa is divided into nine provinces and 52 Districts. The metropolitan municipalities like Cape Town have the largest urban communities and perform the function of both district and local municipalities.25 In the Western Cape Province, the Cape Town Metro Health district has 8 legislated sub-districts serving a population of 4.1 million persons.26 There are 152 PHC facilities, 102 of which are managed by the City of Cape Town (local government) to augment PHC services provided by provincial facilities.26 Like elsewhere in South Africa, routine immunization services in Cape Town are funded through the Expanded Programme on Immunization of South Africa (EPI-SA) and provided free of charge primarily through the PHC facilities.1 (link) While the Western Cape is often regarded as having a better resourced health system and health outcomes compared with other provinces, immunization coverage remains lower than optimal levels. For instance, a recent study has shown that more than a third (36.11%) of children in the province are incompletely immunized.27 (link) The current routine immunization schedule for children in South Africa is outlined in Table 2.

Current routine childhood vaccination schedule in South Africa.

Age eligibilityVaccine offered
BirthBCG, OPV (0)
6 WeeksOPV (1), RV (1), DTaP-IPV-Hib-HepB (1), PCV (1)
10 WeeksDTaP-IPV-HIB-HepB (2)
14 WeeksRV (2), DTaP-IPV-Hib-HepB (3), PCV (2)
6 monthsMeasles (1)
9 MonthsPCV (3)
12 monthsMeasles (2)
18 MonthsDTaP-IPV-Hib-HepB (4)
6 yearsTd (1)
9 yearsHPV (1), HPV (2) (2 doses, 6 months apart)*
12 yearsTd (2)

BCG = Bacille Calmette Guerin, DTaP-IPV-Hib-HepB = hexavalent vaccine (containing diphtheria, tetanus, pertussis, inactivated polio, Haemophilus influenzae type b and hepatitis B vaccines), HPV = human papillomavirus vaccine, OPV = oral polio vaccine, PCV = pneumococcal conjugate vaccine, RV = rotavirus vaccine, Td = tetanus and reduced dose diphtheria vaccine.

*HPV vaccine is given as part of the school health programme rather than the EPI-SA.

Publication 2023
Child Diphtheria diphtheria-tetanus-five component acellular pertussis-inactivated poliomyelitis -Haemophilus influenzae type b conjugate vaccine gamma-hydroxy-gamma-ethyl-gamma-phenylbutyramide Haemophilus influenzae type b Hepatitis B Vaccines Hexavalent Vaccines Human Papilloma Virus Vaccine Immunization Immunization Coverage Immunization Programs Immunization Schedule Oral Poliovirus Vaccine Pertussis Pneumococcal Vaccine Poliomyelitis Rotavirus Vaccines Toxoid, Diphtheria Toxoid, Tetanus Wellness Programs
The GBD estimates the incidence of infectious meningitis for each country (specific objective a). Meningitis was defined as a “disease caused by inflammation of the meninges, the protective membrane surrounding the brain and spinal cord, and that is typically caused by an infection in the cerebrospinal fluid (CSF). Symptoms include headache, fever, stiff neck, and sometimes seizures” (13 (link)). Infectious meningitis is then classified into four groups: meningococcal, H. influenzae type B, pneumococcal, and others.
A systematic review of surveillance systems reports, scientific literature claims data-inpatient visits, and inpatient hospital data, published up to the end of 2013, was done. Cases were recorded with ICD-9 and ICD-10 codes: N. meningitidis (36-36.9 and A39-A39.9), H. influenzae (320 and G00.0), and S. pneumoniae (320.1 and G00.1). General incidence, and per infectious agent, were generated by Bayesian meta-regressions based on 1,348 non-fatal outcomes sources. To differentiate incident from prevalent cases, the lethality, rate of long-term complications, and sequelae fraction (epilepsy, vision impairment, hearing loss, motor and cognitive impairment, intellectual disability, and behavioral problems) were also computed (13 (link)).
The MenAfriNet Consortium and the WHO record suspected meningitis cases per epidemiological week (for the analysis of epidemic curves by subregion and when assessing the yearly trends of BM incidence in relationship with climate variables (specific objective b), this is the level of certainty). Suspected cases are defined as: “any person with sudden onset of fever (>38.5°C rectal or 38°C axillary) and one of the following signs: neck stiffness, altered consciousness or other meningeal signs” and “any toddler with sudden onset of fever (>38.5°C rectal or 38°C axillary) and one of the following signs: neck stiffness, flaccid neck, bulging fontanel, seizure or other meningeal signs” (43 ).
Some of the cases underwent a lumbar puncture for confirmation in CSF. Basic cytochemical and microbiological analysis contribute to a probable level of certainty: “any suspected case with a macroscopic aspect of its CSF turbid, lousy or purulent; or with a microscopic test showing Gram-negative diplococcus, Gram-negative bacillus, Gram-positive diplococcus; or with leukocytes count more than 10 cells/mm3” (12 , 43 ) and “any infant with CSF leukocyte count >100/mm3 or 10–100 cells/mm3 and either and elevated protein (100 mg/dL) or decreased glucose (< 40 mg/dL) level” (12 , 43 ).
Finally, a smaller proportion reached the confirmed definition: “isolation or identification, in CSF or blood, of the causal pathogen (N. meningitidis, H. influenzae type B, S. pneumoniae, etc.) from the CSF of a suspected/probable case by culture, polymerase chain reaction, immunochromatographic dipstick or latex agglutination test” (12 , 43 ).
Suspected cases are reported by providers at a health facility and informed to the district surveillance officer each week, who then compile and notify the data to the provincial and national instances. Notification must be done even in absence of cases and throughout the year. This information is merged by the national instance of each country and then sent to the WHO, and their partners, on a weekly or monthly basis (if no epidemic is registered). Laboratory tests' results must be also included (12 , 43 ).
Publication 2023
Axilla Bacillus Blood Brain Cells Cerebrospinal Fluid Climate Consciousness Disorders, Cognitive Epidemics Epilepsy Fatal Outcome Fever Flaccid Muscle Tone Glucose Haemophilus influenzae Haemophilus influenzae type b Headache Hearing Impairment Immunochromatography Infant Infection Inflammation Inpatient Intellectual Disability isolation Latex Fixation Tests Leukocyte Count Leukocytes Lice Meninges Meningitis Meningococcal Polysaccharide Vaccine Microscopy Neck Neisseria meningitidis pathogenesis Polymerase Chain Reaction Problem Behavior Proteins Punctures, Lumbar Rectum Seizures sequels Spinal Cord Streptococcus pneumoniae Tissue, Membrane
The region where the African country is located (inside or outside the AMB) was the outcome variable of the categorical regression model (main objective). Categorization of African countries into these two groups has been previously proposed by Laxminarayan et al. (41 (link)), Mazamay et al. (1 (link)), and the GBD study (13 (link)).
The number of BM cases per 100,000 population reported by each country in 2016, was extracted from the GBD study and calculated after adding the incident cases of meningitis caused by N. meningitidis, H. influenzae type B, and S. pneumoniae (secondary objective). The punctual location of each country was defined with latitude and longitude coordinates provided by Google Data Explorer. Besides, we calculated geohash (base-32) and transformed it into the decimal system (42 ).
Considering the literature about socioepidemiological features associated with BM, a set of 60 potential regressors was evaluated for each country including geo-environmental aspects, demographic characteristics, socioeconomic conditions, unmet basic needs, smoking and alcohol habits, nutritional variables, coverage of vitamin A supplementation, vaccination rates (immunization against N. meningitidis was not available for most countries), and additional causes of morbidity (for the operational definition of variables, and their source, see the Supplementary Table 1).
Publication 2023
Ethanol Haemophilus influenzae type b Immunization Meningitis Negroid Races Neisseria meningitidis Streptococcus pneumoniae Vaccination Vitamin A
This article presents the findings of secondary analyses of data sourced from the National Family Health Survey (NFHS). NFHS is a large-scale, multi-round survey conducted in a representative sample of households throughout India [9 ]. It is used as a reference to assess the progress the country has achieved across a multitude of programs. These include family planning, maternal and delivery care, child vaccinations, treatment of childhood diseases, feeding practices and nutrition status of children, nutrition status of adults, anemia among children and adults, blood sugar and hypertension level among adults, tobacco and alcohol consumption, screening for cancer among adults, knowledge on HIV/AIDs among adults, women empowerment, and gender-based violence. The data are publicly available in the form of factsheets, state reports, and raw data for national, state, and district levels.
Data for immunization are available for the point of service (public and private) and the coverage estimates for individual antigens (BCG), hepatitis B birth dose, pentavalent (DPT, hepatitis B, and Haemophilus influenzae type b), oral polio vaccine, measles-containing vaccine (MCV), and rotavirus vaccine (RVV). In addition, data are available for key equity parameters including gender, place of residence, religion, birth order, caste, and mother’s schooling. While the NFHS factsheets provide data on key coverage indicators, the equity indicators are included as part of the state reports. The state reports also provide data on other program indicators, the impact of which can be assessed on the immunization program. Coverage of key immunization indicators for districts is available in the state reports.
Using equity differentiated data from NFHS state reports, this article aims to analyze the progress achieved across states of the country in reaching out to ZD children between the last two NFHS rounds (NFHS 5, 2019-2021 and NFHS 4, 2015-2016). ZD proportions were measured using pentavalent 1 coverage as the indicator. The key determinants studied include the change in ZD prevalence at the national, state, and district levels; the proportion of change in equity determinants; the states with maximum improvements; the maximum disparity across these indicators; and the overall reduction in disparities. The data were interpreted in the form of tables and maps. The maps were created using choropleth maps on Datawrapper [10 ] and the map feature on Microsoft Excel.
A correlation analysis was conducted to understand the nature of the association between ZD prevalence and critical maternal and child health (MCH) indicators which include four or more antenatal care (ANC) visits, the timing of pregnancy registration, institutional delivery (birth at a health facility), children under five years old who are stunted (height-for-age), and children under five years old who are wasted (weight-for-height). For each of these indicators, data were collated for both the NFHS rounds (NFHS 5 and NFHS 4), and the Pearson correlation coefficient was obtained using the following formula:
r=∑[(xi-x ¯)(yi-ȳ)] ⁄ √[∑(xi-x ¯)^2 ∑(yi-ȳ)^2]
with the coefficient value r signifying the strength and direction of correlation between the two variables. The strength of association as per the correlation coefficient values was interpreted as follows: no association: 0, weak association: (±) 0.1 to less than 0.3, moderate association: (±) 0.3 to less than 0.5, strong association: (±) 0.5 to less than 1, and perfect association: (±) 1.
Publication 2023
Acquired Immunodeficiency Syndrome Adult Anemia Antigens Blood Glucose Cancer Screening Care, Prenatal Child Childbirth Child Nutritional Physiological Phenomena Debility Gender-Based Violence Haemophilus influenzae type b Hepatitis B High Blood Pressures Households Immunization Immunization Coverage Immunization Programs Measles Vaccine Microtubule-Associated Proteins Mothers Obstetric Delivery Oral Poliovirus Vaccine Pregnancy Rotavirus Vaccines Tobacco Products Vaccination Woman

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ActHIB is a vaccine developed by Sanofi to help prevent Haemophilus influenzae type b (Hib) infections. It contains inactivated Hib bacteria and is administered through intramuscular injection.
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More about "Haemophilus influenzae type b"

Haemophilus influenzae type b (Hib) is a bacterium that can cause serious and potentially life-threatening infections in young children, including meningitis, pneumonia, and septicemia.
It is a leading cause of bacterial meningitis worldwide, particularly affecting infants and toddlers.
Symptoms of Hib infections may include fever, headache, stiff neck, and altered mental status.
Prompt antibiotic treatment is critical for managing these infections.
Vaccination has significantly reduced the incidence of Hib disease in many countries, thanks to vaccines like ActHIB, Prevenar13, Infanrix Hexa, and Synflorix.
Researchers studying Hib can utilize advanced tools like PubCompare.ai's AI-driven protocol comparison to identify the most effective research protocols and products, such as the QIAamp UCP Pathogen Mini Kit, EasyMAG/EasyMag system, and Siemens nephelometric analyzer.
These tools can help streamline research, accelerate discoveries, and optimize the use of the NucliSENS easyMAG system for Hib detection and analysis.
By leveraging the insights gained from MeSH term descriptions and metadescriptions, researchers can better understand the significance of Hib as a pathogen, the importance of early diagnosis and treatment, and the role of vaccination in reducing the burden of this disease.
With the right tools and protocols, researchers can make important advancements in the study and management of Hib infections, ultimately improving outcomes for children worldwide.