PubMed · 13444983
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
W MIKULOWSKI. 1957. About agonal Diphtheria.. https://pubmed.ncbi.nlm.nih.gov/13444983/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
Respiratory diphtheria can be severe or fatal in unvaccinated persons; even with appropriate treatment, 5%-10% of patients with diphtheria die. For >50 years, vaccination against diphtheria has been recommended for children and adults in the United States. Persons who are unvaccinated or vaccinated inadequately can contract diphtheria during travel to areas where the disease is endemic, putting them and their close contacts at risk for severe illness. This report describes fatal respiratory diphtheria in an unvaccinated Pennsylvania resident who had visited Haiti, a country where the disease is endemic. The case highlights the need for all international travelers to be up-to-date with all recommended vaccinations, including a primary series of diphtheria toxoid-containing vaccine.
(1) Two six-component vaccines available in France (Hexavac and InfanrixHexa) are designed for primary and booster vaccination of infants. A single intramuscular injection delivers a five-component vaccine (diphtheria, tetanus, poliomyelitis, Haemophilus influenzae type b and acellular pertussis) and a hepatitis B vaccine. (2) The clinical evaluation dossier on InfanrixHexa includes four trials versus separate injections of a five-component vaccine and a hepatitis B vaccine at two distinct sites. (3) For primary vaccination, no difference in immunogenicity was found between InfanrixHexa and separate vaccination for 5 of the 6 components. The serological response to Haemophilus was weaker with InfanrixHexa, but whether or not this translates into worse long-term clinical protection is unknown. (4) After primary vaccination, major adverse events were a little rarer with InfanrixHexa than with separate vaccination. There was no difference in adverse events between InfanrixHexa and separate vaccination after the recommended booster between the ages of 16 and 18 months. (5) Evaluation data on Hexavac published by Aventis Pasteur MSD are very limited. We found only one trial in the primary vaccination setting, versus vaccination at two distinct sites with a five-component vaccine and a hepatitis B vaccine. (6) The serological response to hepatitis B virus and Haemophilus was significantly weaker with Hexavac than with separate vaccination, but no difference was found regarding the other four components. It is not known if this difference has any clinical implications. There was no difference in adverse events between Hexavac and separate vaccination. (7) The vaccination schedule depends on whether or not separate hepatitis B vaccine is required at birth. A six-component vaccine and a five-component vaccine can be used alternately.
BACKGROUND: In the United States, the national childhood immunization schedule calls for children to receive four doses of DTaP (diphtheria and tetanus toxoids and acellular pertussis) vaccine administered at 2, 4, 6, and 15 to 18 months. Dose 4 of DTaP is among the most frequently missed vaccines for children who are not adequately immunized. METHODS: Using the 2001 National Immunization Survey, the effect of the timeliness of the first three DTaP doses was assessed on completion of the four-dose series by age 24 months and on time by age 12 to 18 months. RESULTS: Missing Dose 4 was more prevalent among children who received Dose 3 late (but <16 months) than among children who received Dose 3 on time (24% vs 10%). Similarly, receiving Dose 4 late (or not at all) was more prevalent among children who received Dose 3 late (but <9 months) (39% vs 22%). An invalid Dose 4 was administered to 4.6% of those with Dose 3 late but before 9 months and to 10.6% of those with no Dose 3 before 9 months, compared to 1.2% of those with Dose 3 on time. CONCLUSIONS: Physicians and staff can identify children at risk for missing the fourth DTaP dose or receiving it late by assessing timeliness of receipt of DTaP Dose 3 and implementing steps to ensure that at-risk children receive Dose 4 as recommended.