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1.
G Ital Med Lav Ergon ; 20(4): 255-9, 1998.
Article in Italian | MEDLINE | ID: mdl-9987619

ABSTRACT

The study reports the results of a group who, in a multicentric trial, using a gait analysis laboratory Italian made, and a standard procedure, examined 127 normal subjects. The gait laboratory is composed of contacts to relieve the support on the ground, goniometric transducers with an articulated parallelogram, active sensors for cutaneous electromyography, patient unit for data collection and transmission, interface modules for signal reconstruction, software for data elaboration. All data was elaborated in order to give normative data for Italian population. There were no differences between right and left side, nor between male and female subjects. Values of the present study was compared with previous foreign literature and a critical comment is proposed.


Subject(s)
Gait , Adult , Electromyography/statistics & numerical data , Female , Humans , Italy , Male , Physical Examination/instrumentation , Physical Examination/methods , Physical Examination/standards , Physical Examination/statistics & numerical data , Reference Values , Sex Characteristics
2.
Eur J Epidemiol ; 11(2): 217-9, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7672079

ABSTRACT

Twenty four subjects were simultaneously administered DT toxoids, OPV and HBV vaccines at the age of 3, 4-5 and 11 months and then followed up for 2 and 4 years in order to evaluate the duration of the immune response and the need and the timing of HBV revaccination. A fall in anti-HBs titre below 10 mIU/ml was observed at the follow up in 4/24 (16.7%) of the subjects. In other 5 children (20.8%) anti-HBs titre was found to be just above 10 mIU/ml. This would suggest that a revaccination is indicated and it could be performed at the age of 5-6 years when children enter school. This schedule is simple, effective and money saving since it reduces the cost/benefit ratio and the number of visits for immunisations, and it is expected to improve the compliance for the vaccination.


Subject(s)
Hepatitis B Antibodies/biosynthesis , Hepatitis B Vaccines/administration & dosage , Immunization , Vaccination , Child , Child, Preschool , Cost-Benefit Analysis , Diphtheria Toxoid/administration & dosage , Diphtheria-Tetanus Vaccine , Follow-Up Studies , Hepatitis B Vaccines/immunology , Humans , Immunization/economics , Immunization Schedule , Immunization, Secondary/economics , Infant , Italy , Office Visits/economics , Patient Compliance , Poliovirus Vaccine, Oral/administration & dosage , Tetanus Toxoid/administration & dosage , Time Factors , Vaccination/economics , Vaccines, Combined/administration & dosage
3.
Eur J Epidemiol ; 9(3): 311-4, 1993 May.
Article in English | MEDLINE | ID: mdl-8405317

ABSTRACT

A combined vaccine against measles, mumps and rubella (MMR) was administered to both a group of children aged 10-12 months simultaneously with booster doses of compulsory diphtheria-tetanus toxoids and oral poliovirus vaccine and a group of children aged 15-24 months who had previously received booster doses of the compulsory vaccines. Apart from one subject belonging to the second group who was non responder and one from the same group who did not seroconvert against the mumps virus alone, 5 to 6 weeks after MMR vaccine administration we found protective levels of antibodies against measles, mumps and rubella viruses in all children. The follow up of both groups at 3 years did not reveal difference between the two groups. Protective levels of serum antibodies against measles and mumps were found in the two groups, although a significant decline of rubella antibodies was shown (p < 0.05). Since the immunogenicity of the vaccines in the two groups did not differ, we recommend that the scientific community reconsider the vaccination schedule until now recommended. In our opinion the MMR vaccine should be administered simultaneously with booster doses of diphtheria-tetanus toxoids and oral poliovirus vaccine at 10-12 months of age because this policy improves parents' compliance, markedly reduces community costs and simplifies routine immunization schedule.


Subject(s)
Antibodies, Viral/blood , Diphtheria Toxoid/administration & dosage , Immunization Schedule , Measles Vaccine/immunology , Mumps Vaccine/immunology , Poliovirus Vaccine, Oral/administration & dosage , Rubella Vaccine/immunology , Tetanus Toxoid/administration & dosage , Age Factors , Drug Combinations , Follow-Up Studies , Health Care Costs , Humans , Immunization, Secondary , Infant , Measles Vaccine/administration & dosage , Measles Vaccine/adverse effects , Measles-Mumps-Rubella Vaccine , Mumps Vaccine/administration & dosage , Mumps Vaccine/adverse effects , Rubella Vaccine/administration & dosage , Rubella Vaccine/adverse effects , Time Factors
4.
Eur J Epidemiol ; 9(2): 199-202, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8519358

ABSTRACT

A combined vaccine against measles (Edmonston-Zagreb 19 strain), mumps (Rubini strain) and rubella (Wistar RA 27/3 strain) was administered to a group of 46 children aged 10-12 months simultaneously with booster doses of compulsory diphtheria-tetanus toxoid and oral poliovirus vaccine. A second group of 53 children aged 15-24 months who had received booster doses of the compulsory vaccines 5 to 12 months before was also vaccinated. The same seroconversion rates (100%) and similar antibody titers for rubella were observed in both groups. The same seroconversion rates for mumps (93%) and similar rates for measles (98 and 94%) were observed in the two groups. Significantly lower antibody titers for measles and mumps were found in the first group, but they were compensated by an earlier protection, a reduction of number of visits for immunization, costs for the community, and improvement in parental compliance. These results confirm that Edmonston-Zagreb 19 and Rubini strains are still immunogenic even when they are combined with Wistar RA 27/3 strain. Moreover, a long term follow-up in order to verify the persistence of protective antibody levels in both groups of children, could suggest that combined measles, mumps and rubella vaccine could be given earlier (at 10-12 months of age), simultaneously with booster doses of diphtheria and tetanus toxoid and of trivalent oral poliovirus vaccine.


Subject(s)
Antibodies, Viral/biosynthesis , Diphtheria Toxoid/immunology , Measles Vaccine/immunology , Mumps Vaccine/immunology , Poliovirus Vaccine, Oral/immunology , Rubella Vaccine/immunology , Tetanus Toxoid/immunology , Child, Preschool , Diphtheria-Tetanus Vaccine , Drug Combinations , Humans , Immunization, Secondary , Infant , Measles-Mumps-Rubella Vaccine
5.
Vaccine ; 9(10): 747-50, 1991 Oct.
Article in English | MEDLINE | ID: mdl-1836919

ABSTRACT

The reactogenicity and immunogenicity of simultaneous administration of recombinant DNA hepatitis B vaccine with diphtheria and tetanus toxoids (DT) and oral poliovirus vaccine (OPV) in 111 infants were compared with those of DT and OPV alone in a control group of 21 infants. All subjects received three doses of the vaccine according to one of three different schedules of vaccination. Reactions following simultaneous administration of vaccines were all but absent, with mild pain reported for four out of 111 subjects, compared with one of 21 in the control group. Seroconversion rates of 98-100% and high anti-HBs geometric mean titres (GMTs) were observed in all study groups after three doses of hepatitis B vaccine. Significantly higher anti-HBs were seen in Group III, where six months is allowed between the second and the third hepatitis B vaccine doses, compared with Group I and II, where only 1-2 months separate the second and third doses. A fourth dose of vaccine was needed in both these groups to obtain anti-HBs levels as high as seen in Group III after three vaccine doses at 3, 4 and 10 months of age. The immune response to DT and OPV was similar in the study groups and the control group. It is concluded that a course of 10 micrograms doses of recombinant hepatitis B vaccine given simultaneously with DT and OPV elicits a strong anti-HBs response and does not interfere with the immune response to the other antigens.


Subject(s)
Diphtheria Toxoid/immunology , Poliovirus Vaccine, Oral/immunology , Tetanus Toxoid/immunology , Vaccines, Synthetic/immunology , Viral Hepatitis Vaccines/immunology , Antibodies, Viral/blood , Diphtheria Toxoid/administration & dosage , Hepatitis B Vaccines , Humans , Infant , Infant, Newborn , Poliovirus Vaccine, Oral/administration & dosage , Tetanus Toxoid/administration & dosage , Vaccines, Synthetic/administration & dosage , Viral Hepatitis Vaccines/administration & dosage
6.
Acta Paediatr Jpn ; 33(4): 455-8, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1838852

ABSTRACT

An extensive vaccination program to be used in highly endemic areas is the main strategy against the spreading of hepatitis B. The purpose of this study was the evaluation of the immune response to the recombinant HB vaccine administered singly or at the same time as other compulsory vaccines anti-diphtheria, anti-tetanus and oral anti-polio. Evidence was found of the serological efficacy both of HB vaccine and compulsory vaccines with a percentage of seroconversion of 100%. However, the infants who received HB vaccine at birth and at the age of 1 month had titers of antiHBs higher than the infants who received HB vaccine at birth and at 3 months. No difference in antibody levels of compulsory vaccines was observed among the study groups and the controls who received only compulsory vaccines. Our results suggest that HB vaccination must be encouraged and pursued in all newborns.


Subject(s)
Diphtheria Toxoid/administration & dosage , Hepatitis B Antibodies/blood , Poliovirus Vaccine, Oral/administration & dosage , Tetanus Toxoid/administration & dosage , Vaccines, Synthetic/administration & dosage , Viral Hepatitis Vaccines/administration & dosage , Diphtheria Toxoid/immunology , Hepatitis B Vaccines , Humans , Infant , Infant, Newborn , Pilot Projects , Poliovirus Vaccine, Oral/immunology , Tetanus Toxoid/immunology , Time Factors , Vaccines, Synthetic/immunology , Viral Hepatitis Vaccines/immunology
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