Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 29
Filter
1.
Braz. J. Pharm. Sci. (Online) ; 59: e22690, 2023. tab, graf
Article in English | LILACS | ID: biblio-1505850

ABSTRACT

Abstract Improving vaccine immunity and reducing antigen usage are major challenges in the clinical application of vaccines. Microneedles have been proven to be painless, minimally invasive, highly efficient, and have good patient compliance. Compared with traditional transdermal drug delivery, it can effectively deliver a large-molecular-weight drug into the skin, resulting in a corresponding immune response. However, few studies have examined the relationship between microneedle loading dose and immune effects. In this study, the hyaluronic acid (HA) conical and pyramidal dissolving microneedles were prepared by the two-step vacuum drying method, respectively. The model drug ovalbumin (OVA) was added to HA to prepare dissolving microneedles with different loading amounts. The mass ratios of HA to OVA were 5:1, 5:3, and 5:5. The mechanical properties of the dissolving microneedles were characterized using nanoindentation and in vitro puncture studies. The immune effects of the matrix and drug content were studied in Sprague-Dawley (SD) rats. Finally, the diffusion behavior of OVA and the binding mode of HA and OVA in the microneedles were simulated using Materials Studio and Autodocking software. The experimental results showed that the conical microneedles exhibited better mechanical properties. When the mass ratio of HA to OVA was 5:3, the immune effect can be improved by 37.01% compared to subcutaneous injection, and achieved a better immune effect with relatively fewer drugs. This conclusion is consistent with molecular simulations. This study provides theoretical and experimental support for the drug loading and efficacy of microneedles with different drug loadings


Subject(s)
Injections, Subcutaneous/adverse effects , Pharmaceutical Preparations/analysis , Vaccines/analysis , Immunization/classification , Mechanical Tests/instrumentation , Hyaluronic Acid/agonists , Antigens/adverse effects
2.
São Paulo; s.n; s.n; 2022. 136 p. tab, graf.
Thesis in Portuguese | LILACS | ID: biblio-1415619

ABSTRACT

Introdução: A aterosclerose é uma doença inflamatória crônica decorrente de alterações na parede das artérias de médio e grande calibre e associadas a diversos fatores de risco, dentre os quais destaca-se as hiperlipidemias, ou seja, o aumento plasmático das lipoproteínas, mas também outras comorbidades, como a Síndrome Metabólica. Entre as lipoproteínas, a lipoproteína de baixa densidade (LDL) é de grande relevância na aterosclerose. Diferentes espécies de LDL modificada (LDLm) são originadas através de lipólise, glicação e proteólise, além da oxidação, variando em densidade e eletronegatividade, sendo melhor denominada LDL eletronegativa [LDL (-)]. Considerando as diferenças conformacionais entre a estrutura da ApoB-100 da LDL nativa e da LDL (-), em um estudo inicial, nosso grupo desenvolveu um anticorpo monoclonal (2C7) a partir da imunização de camundongos Balb/c com a LDL (-) humana. Em uma etapa seguinte foi mapeado o epítopo reconhecido pelo anticorpo monoclonal anti-LDL (-) através de phage display. O peptídeo ligante do anticorpo monoclonal anti-LDL (-) foi nomeado p2C7. Esse peptídeo não representa regiões da sequência linear da ApoB-100 humana, mas microdomínios conformacionais de epítopos da ApoB-100 da LDL (-), tornando-os candidatos para a imunomodulação da aterogênese. Portanto, investigar a imunomodulação induzida pelos peptídeo p2C7 miméticos da LDL (-), por representar um epítopo imunodominante da LDL (-), poderá abrir novas perspectivas terapêuticas futuras para a imunomodulação da aterosclerose. Objetivo: Avaliar a imunomodulação promovida pelo p2C7 in vivo, utilizando camundongos C57BL/6 LDLr -/- e amostras de plasma humano. Adicionalmente, no estágio (BEPE) realizado no Instituto Karolinska (dezembro de 2019 a março de 2021), investigou-se o imunometabolismo como mediador nas doenças cardiovasculares. Na parte II-A, estão descritos os resultados do estudo inicialmente proposto. Na parte II-B, apresenta-se os resultados que foram desenvolvidos posteriormente, com ampliação do escopo do projeto, abordando-se a inflamação vascular envolvida no aneurisma de aorta abdominal através de ferramentas de bioinformática. Na parte II-C, são apresentados os resultados do estudo do envolvimento da enzima indolamina 2,3 dioxigenase (IDO) na esteatohepatite não-alcoólica (NASH) e aterosclerose em camundongos ApoE-/- and ApoE/IDO/double-knockout. Metodologia: Foi avaliada a presença de anticorpos anti-p2C7 em amostras de plasma humano de indivíduos com ou sem síndrome metabólica. Realizamos a determinação de TNF circulante nas mesmas amostras e prosseguimos com regressões lineares associando os parâmetros inflamatórios com os níveis de anticorpos anti-p2C7. Camundongos C57BL/6 LDLr -/- foram imunizados com p2C7 e os adjuvantes Alum ou Montanide ISA 720, analisando-se os títulos de anticorpos contra p2C7 e LDL (-), a produção de citocinas (IL-10, IL-4, IL-2, IL-6, IFNγ, IL-17, TNFα) e células secretoras de anticorpos. Camundongos C57BL/6 LDLr -/- foram tolerizados contra os peptídeos mimotopos, com injeções intravenosas (veia caudal) e desafiados com a imunização contendo LDL (-) + Alum. Avaliou-se os títulos de anticorpos contra p2C7 e LDL (-) e a produção de citocinas (TNF-α, IFNγ, IL-12, IL-6, IL-10 e MCP-1). Os camundongos foram mantidos em dieta hipercolesterolêmica por 3 meses para formação da placa aterosclerótica. Após este período, os camundongos foram eutanasiados, avaliando-se a formação de placa aterosclerótica na artéria abdominal e arco aórtico, assim como a produção de citocinas (TNF-α, IFNγ, IL-12, IL-6, IL-10 e MCP-1). Camundongos C57BL/6 LDLr -/- foram imunizados com OVA-p2C7 e, após dieta hipercolesterolêmica de 3 meses para formação de placa aterosclerótica, foram avaliados os parâmetros inflamatórios e avaliada a captação de 18F-FDG no arco aórtico através de PET/CT. Resultados: A imunização com o p2C7 (livre) não foi capaz de induzir resposta humoral, não se observando títulos detectáveis de anticorpos reativos à p2C7 ou LDL (-) em nenhum camundongo imunizado, assim como não foram detectadas células secretoras de anticorpos específicos para a LDL (-). O grupo imunizado com Alum ou Montanide + p2C7 teve aumento significativo na produção de TNF- quando comparado com os demais grupos. O protocolo de tolerização foi realizado com sucesso, visto que os camundongos tolerizados apresentaram títulos de anticorpos inferiores aos controles para o epítopo utilizado. Apenas os camundongos tolerizados com o p2C7 apresentaram aumento significativo na produção de IL-6, IL-12, IL-10, TNF-α, IFNγ e MCP 1 após dieta hipercolesterolêmica. A imunização ativa com OVA-p2C7 foi capaz de reduzir a produção de TNF induzida pela dieta hipercolesterolêmica, assim como reduzir a captação de 18F-FDG. Conclusão: o epítopo p2C7 é altamente expresso na LDL (-) de pacientes com maior risco cardiovascular. Além disso, a imunização ativa com p2C7 também se mostra uma ferramenta promissora para prevenir e regular a inflamação causada pela LDL (-) no curso da aterosclerose


Introduction: Atherosclerosis is a chronic inflammatory disease resulting from changes in the wall of medium and large-caliber arteries and associated with several risk factors, among which hyperlipidemias stand out, ie, the increase in plasma lipoproteins, but also other comorbidities, such as Metabolic Syndrome. Among the lipoproteins, low-density lipoprotein (LDL) is of great relevance in atherosclerosis. Different isoforms of modified LDL (LDLm) are originated through lipolysis, glycation and proteolysis, in addition to oxidation, varying in density and electronegativity, being better called electronegative LDL [LDL (-)]. Considering the conformational differences between the ApoB-100 structure of native LDL and LDL (-), in an initial study, our group developed a monoclonal antibody (2C7) from the immunization of Balb/c mice with human LDL (-). In a next step, the epitope recognized by the anti-LDL monoclonal antibody (-) was mapped using phage display. The binding peptide of anti-LDL monoclonal antibodies (-) was named p2C7. This peptide does not represent linear sequence regions of human ApoB-100, but conformational microdomains of LDL (-) ApoB-100 epitopes, making them candidates for the immunomodulation of atherogenesis. Therefore, investigating the immunomodulation induced by p2C7 peptide mimetics of LDL (-) as it represents an immunodominant epitope of LDL (-) could open new future therapeutic perspectives for the immunomodulation of atherosclerosis. Objective: To evaluate the immunomodulation promoted by p2C7 in vivo, using C57BL/6 LDLr -/- mice, and human plasma samples. In addition, in the internship (BEPE), held at the Karolinska Institute (December 2019 to March 2021), immunometabolism as a mediator of Cardiovascular Diseases was studied. In part II-A, the results of the initially proposed study are described. In part II-B, the results that were developed later are presented, expanding the scope of the project, approaching the vascular inflammation involved in the abdominal aortic aneurysm through bioinformatics tools. In part II-C, the results of the study of the involvement of the enzyme indoleamine 2,3 dioxygenase (IDO) in non-alcoholic steatohepatitis (NASH) and atherosclerosis in ApoE-/- and ApoE/IDO/double mice are presented -knockout. Methodology: The presence of anti-p2C7 antibodies in human plasma samples with or without Metabolic Syndrome was evaluated. We measured circulating TNF in the same samples and proceeded with linear regressions associating inflammatory parameters with levels of anti-p2C7 antibodies. C57BL/6 LDLr -/- mice were immunized with p2C7 and the adjuvants Alum or Montanide ISA 720, analyzing the antibody titers against p2C7 and LDL (-), the production of cytokines (IL-10, IL-4, IL -2, IL-6, IFNγ, IL-17, TNFα) and antibody-secreting cells. C57BL/6 LDLr -/- mice were tolerized against mimotope peptides with intravenous injections (caudal vein) and challenged with immunization containing LDL (-) + Alum. Antibody titers against p2C7 and LDL (-) and cytokine production (TNF-α, IFNγ, IL-12, IL-6, IL-10 and MCP-1) were evaluated. The mice were kept on a hypercholesterolemic diet for 3 months for atherosclerotic plaque formation. After this period, the mice were euthanized, evaluating the formation of atherosclerotic plaque in the abdominal artery and aortic arch, as well as the production of cytokines (TNF-α, IFNγ, IL-12, IL-6, IL-10 and MCP -1). C57BL/6 LDLr -/- mice were immunized with OVA-p2C7 and, after a 3-month hypercholesterolemic diet for atherosclerotic plaque formation, inflammatory parameters were evaluated and 18F-FDG uptake was evaluated by PET/CT. Results: Immunization with p2C7 (free) was not able to induce a humoral response, with no detectable titers of antibodies reactive to p2C7 or LDL (-) being observed in any immunized mouse, as well as no detectable antibody-secreting cells for the LDL (-). The group immunized with Alum or Montanide + p2C7 had a significant increase in TNF-α production when compared to the other groups. The tolerance protocol was successfully performed, as the tolerized mice had lower antibody titers than controls for the epitope used. Only mice tolerated with p2C7 showed a significant increase in the production of IL-6, IL-12, IL-10, TNF-α, IFNγ and MCP 1 after a hypercholesterolemic diet. Active immunization with OVA-p2C7 was able to reduce TNF production induced by the hypercholesterolemic diet, as well as to reduce 18F-FDG uptake. Conclusion: the p2C7 epitope is highly expressed in LDL (-) of patients with higher cardiovascular risk. Furthermore, active immunization with p2C7 is also a promising tool to prevent and regulate inflammation caused by LDL (-) in the course of atherosclerosis


Subject(s)
Animals , Male , Female , Mice , Immunization/classification , Atherosclerosis/pathology , Pets , Lipoproteins, LDL/adverse effects , Mice/abnormalities , Arteries/abnormalities , Cardiovascular Diseases/diagnosis , Risk Factors , Aortic Aneurysm, Abdominal/classification , Methodology as a Subject
3.
Australas Emerg Care ; 23(2): 84-89, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31771840

ABSTRACT

BACKGROUND: Pneumonia is one of the most common reasons patients over the age of 65 years present to the Emergency Department (ED). There is a 23-valent pneumococcal vaccine (23vPPV) available under the National Immunisation Program (NIP) with demonstrated 61-71% effectiveness against Invasive Pneumococcal Disease (IPD), but only 51% of adults aged over 65 years are vaccinated in Australia. METHODS: Short semi-structured interviews were conducted with emergency nurses working across a Local Health District in Sydney New South Wales (n=9) in order to determine their knowledge, behaviour and attitudes towards immunisation status screening in the elderly who present to the ED with pneumonia. Questions were structured to the COM-B Model (capability, opportunity and motivation to change behaviour), and a thematic analysis was conducted. RESULTS: There were three major themes identified: (1) The importance of routinisation, (2) Low knowledge levels and, (3) The 'vaccination is for children' heuristic, as well as suggestions for future interventions to improve screening. CONCLUSIONS: These findings clarify how to improve vaccine uptake amongst this vulnerable cohort. They suggest that emergency departments should provide education to nurses. In addition, checklists/tick boxes can prompt nurses whilst conducting routine work, which may lead to increased vaccination uptake.


Subject(s)
Geriatrics/standards , Immunization/classification , Mass Screening/standards , Aged , Aged, 80 and over , Cohort Studies , Emergency Service, Hospital/organization & administration , Emergency Service, Hospital/statistics & numerical data , Female , Geriatrics/methods , Geriatrics/statistics & numerical data , Humans , Immunization/standards , Immunization/statistics & numerical data , Immunization Schedule , Interviews as Topic/methods , Male , Mass Screening/methods , Mass Screening/statistics & numerical data , New South Wales , Qualitative Research
4.
Fish Shellfish Immunol ; 85: 61-65, 2019 Feb.
Article in English | MEDLINE | ID: mdl-29097324

ABSTRACT

Vaccination of rainbow trout against Enteric Redmouth Disease (ERM) caused by Yersinia ruckeri can be successfully performed by administering vaccine (a bacterin consisting of formalin killed bacteria) by immersion, bath or injection. Booster immunization is known to increase the protection of fish already primed by one of these vaccination methods. Oral vaccination of trout (administering vaccine in feed) is an even more convenient way of presenting antigen to the fish but the effect of an oral booster has not previously been described in detail. The present work describes to what extent protection may be enhanced by oral boostering following priming with different administration methods. The study confirms that vaccination by 30 s dip into a bacterin (diluted 1:10) may confer a significant protection compared to non-vaccinated fish. The immunity may be optimized by booster immunization either provided as dip (most effective), bath (less effective) or orally (least effective). Oral immunization may be used as booster after dip but applied as a single oral application it induced merely a slight and statistically non-significant response. It is noteworthy that primary oral immunization followed by an oral booster vaccination showed a trend for an even weaker response. It should be investigated if continued exposure to a low antigen concentration - as performed by two oral immunizations - may induce tolerance to the pathogen and thereby leave the fish more vulnerable.


Subject(s)
Bacterial Vaccines/pharmacology , Fish Diseases/prevention & control , Immunization, Secondary/veterinary , Immunization/classification , Oncorhynchus mykiss/immunology , Yersinia Infections/veterinary , Yersinia ruckeri/immunology , Animals , Bacterial Vaccines/administration & dosage , Fish Diseases/immunology , Fish Diseases/microbiology , Immunization/veterinary , Yersinia Infections/immunology , Yersinia Infections/microbiology , Yersinia Infections/prevention & control
5.
Medsurg Nurs ; 23(4): 256-60, 2014.
Article in English | MEDLINE | ID: mdl-25318340

ABSTRACT

The best way to prevent influenza and its potentially life-threatening complications is by receiving the annual flu immunization at the earliest opportunity. As patient educators, nurses should help individuals, families, and the community receive the benefits of this important illness prevention strategy.


Subject(s)
Immunization/classification , Influenza Vaccines/classification , Influenza Vaccines/therapeutic use , Influenza, Human/prevention & control , Patient Education as Topic/methods , Education, Nursing, Continuing , Humans , United States
6.
Stud Health Technol Inform ; 197: 15-9, 2014.
Article in English | MEDLINE | ID: mdl-24743070

ABSTRACT

Immunisation is an important part of health care and adverse events following immunisation (AEFI) are relatively rare. AEFI can be detected through long term follow up of a cohort or from looking for signals from real world, routine data; from different health systems using a variety of clinical coding systems. Mapping these is a challenging aspect of integrating data across borders. Ontological representations of clinical concepts provide a method to map similar concepts, in this case AEFI across different coding systems. We describe a method using ontologies to be flag definite, probable or possible cases. We use Guillain-Barre syndrome (GBS) as an AEFI to illustrate this method, and the Brighton collaboration's case definition of GBS as the gold standard. Our method can be used to flag definite, probable or possible cases of GBS. Whilst there has been much research into the use of ontologies in immunisation these have focussed on database interrogation; where ours looks to identify varying signal strength.


Subject(s)
Biological Ontologies , Drug-Related Side Effects and Adverse Reactions/classification , Drug-Related Side Effects and Adverse Reactions/etiology , Electronic Health Records/classification , Guillain-Barre Syndrome/classification , Guillain-Barre Syndrome/prevention & control , Immunization/adverse effects , Immunization/classification , Natural Language Processing
7.
BMC Pediatr ; 14: 1, 2014 Jan 04.
Article in English | MEDLINE | ID: mdl-24387002

ABSTRACT

BACKGROUND: Accurate classification of children's immunization status is essential for clinical care, administration and evaluation of immunization programs, and vaccine program research. Computerized immunization registries have been proposed as a valuable alternative to provider paper records or parent report, but there is a need to better understand the challenges associated with their use. This study assessed the accuracy of immunization status classification in an immunization registry as compared to parent report and determined the number and type of errors occurring in both sources. METHODS: This study was a sub-analysis of a larger study which compared the characteristics of children whose immunizations were up to date (UTD) at two years as compared to those not UTD. Children's immunization status was initially determined from a population-based immunization registry, and then compared to parent report of immunization status, as reported in a postal survey. Discrepancies between the two sources were adjudicated by review of immunization providers' hard-copy clinic records. Descriptive analyses included calculating proportions and confidence intervals for errors in classification and reporting of the type and frequency of errors. RESULTS: Among the 461 survey respondents, there were 60 discrepancies in immunization status. The majority of errors were due to parent report (n = 44), but the registry was not without fault (n = 16). Parents tended to erroneously report their child as UTD, whereas the registry was more likely to wrongly classify children as not UTD. Reasons for registry errors included failure to account for varicella disease history, variable number of doses required due to age at series initiation, and doses administered out of the region. CONCLUSIONS: These results confirm that parent report is often flawed, but also identify that registries are prone to misclassification of immunization status. Immunization program administrators and researchers need to institute measures to identify and reduce misclassification, in order for registries to play an effective role in the control of vaccine-preventable disease.


Subject(s)
Immunization/classification , Immunization/statistics & numerical data , Medical Records Systems, Computerized , Parents , Registries/statistics & numerical data , Self Report , Child, Preschool , Humans , Reproducibility of Results , Time Factors
8.
Stud Health Technol Inform ; 192: 258-62, 2013.
Article in English | MEDLINE | ID: mdl-23920556

ABSTRACT

This study developed and implemented a children's immunization management system with English and Traditional Chinese immunization ontology for semantic-based search of immunization knowledge. Parents and guardians are able to search vaccination-related information effectively. Jena Java Application Programming Interface (API) was used to search for synonyms and associated classes in this domain and then use them for searching by Google Search API. The searching results do not only contain suggested web links but also include a basic introduction to vaccine and related preventable diseases. Compared with the Google keyword-based search, over half of the 31 trial users prefer using semantic-based search of this system. Although the search runtime on this system is not as fast as well-known search engines such as Google or Yahoo, it can accurately focus on searching for child vaccination information to provide search results that better conform to the needs of users. Furthermore, the system is also one of the few health knowledge platforms that support Traditional Chinese semantic-based search.


Subject(s)
Computer-Assisted Instruction/methods , Health Education/methods , Health Promotion/methods , Immunization/classification , Immunization/methods , Natural Language Processing , Search Engine/methods , China , Health Literacy , Information Storage and Retrieval , Semantics , Taiwan , Translating
9.
Int J Toxicol ; 29(3 Suppl): 98S-114S, 2010 May.
Article in English | MEDLINE | ID: mdl-20448270

ABSTRACT

Quaternium-15 is an antimicrobial agent used in cosmetics as a cosmetic preservative and antistatic agent. Little systemic toxicity was reported in most single-dose or repeated-dose animal studies. Quaternium-15 was an oral teratogen, but not a dermal teratogen, in rats at doses that exceeded the expected cumulative exposure from cosmetics. The frequency of sensitization increased in North America but not in Europe, where Quaternium-15 is used less often. In almost all animal and human studies, Quaternium-15 at 0.2% was not a sensitizer. The weight of evidence suggested that a 0.2% concentration is not a sensitizer and that cosmetic products containing Quaternium-15 up to that level are safe.


Subject(s)
Allergens/toxicity , Anti-Infective Agents/toxicity , Methenamine/analogs & derivatives , Preservatives, Pharmaceutical/toxicity , Teratogens/toxicity , Administration, Cutaneous , Administration, Oral , Allergens/classification , Animals , Animals, Laboratory , Anti-Infective Agents/administration & dosage , Anti-Infective Agents/classification , Consumer Product Safety , Humans , Immunization/classification , Methenamine/administration & dosage , Methenamine/classification , Methenamine/toxicity , Preservatives, Pharmaceutical/administration & dosage , Rats , Risk Assessment , Skin Tests , Teratogens/classification , Toxicity Tests
10.
Managua; MINSA;OPS;USAID; 2001. 161 p. ilus, tab, graf.
Monography in Spanish | LILACS | ID: lil-446251

ABSTRACT

El documento presenta El manual de normas y procedimientos 2001 actualizado con el objetivo de proporcionar las bases legales del programa que son de orden público y privado, de interés nacional y que son de estricta obligatoriedad para todos los trabajadores del sector. Además presenta la reseña histórica del PAI en la Región, Conceptos básicos de inmunidad, las vacunas del PAI, las prácticas y aplicación de vacunas, los Procedimientos para las prácticas de vacunación, Las normas nacionales de inmunización, Reacciones adversas en las prácticas de vacunación, la cadena de frio, el sistema de gerencia y suministro del PAI (CLM), Sistema de información del PAI, las Normas básicas de la vigilancia epidemiológica de las enfermedades prevenibles por vacuna, Las normas del laboratorio para la toma y manejo de muestras de las enfermedades prevenibles por vacunas.


Subject(s)
Immunization Schedule , Immunization/classification , Immunization/adverse effects , Immunization/standards , Handbook/standards , Nicaragua , Vaccines/administration & dosage , Vaccines/classification , Vaccines/immunology , Vaccines/supply & distribution
11.
Pediatrics ; 106(1 Pt 2): 171-6, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10888688

ABSTRACT

OBJECTIVE: To examine the effect of patient selection criteria on immunization practice assessment outcomes. METHODS: In 3 high- (50%-85%) and 7 low- (<25%) Medicaid pediatric practices in urban eastern Virginia, we assessed immunization rates of children 12 and 24 months old comparing the standard criteria (charts in the active files excluding those that documented the child moved or went elsewhere) with 3 alternative criteria for selecting active patients: 1) follow-up: the chart contained a complete immunization record or the patient was found to be active in the practice through follow-up contact by phone or mail; 2) seen in the past year: the chart indicated that the patient was seen in the practice in the past year; 3) consecutive: patients that were seen consecutively for any reason. RESULTS: Of the 1823 charts assessed in the high- and low-Medicaid practices, follow-up identified 61% and 83% as active patients; 78% and 95% were ever seen in the past year. At 24 months, mean practice immunization rates were lower for standard (70%) than all 3 alternative criteria (78%-86%). Immunization rate differences between standard and alternative criteria were greater in high- (17%-23%) than low-Medicaid practices (5%-13%). CONCLUSION: The standard for practice assessment should be based on a consistent definition of active patients as the immunization rate denominator.


Subject(s)
Immunization/statistics & numerical data , Medicaid/statistics & numerical data , Ambulatory Care/statistics & numerical data , Child, Preschool , Humans , Immunization/classification , Infant , Medical Records , Outcome Assessment, Health Care , Pediatrics/statistics & numerical data , United States , Virginia
12.
Aust N Z J Public Health ; 24(1): 17-21, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10777973

ABSTRACT

OBJECTIVE: The Australian Childhood Immunisation Register (ACIR) currently classifies those children who have the third dose recorded as fully immunised at 12 months of age, even if records of earlier doses are missing. This analysis assesses the impact this "third-dose assumption" has on immunisation coverage estimates for children aged 12 months. METHODS: ACIR records from three equally spaced cohorts of children at 12 months of age, which relied on the third-dose assumption, were examined for variation in doses and vaccine types recorded by jurisdiction and Medicare registration status. RESULTS: Although the percentage reduction in coverage without application of the third-dose assumption decreased through the three cohorts examined, the proportion classified as fully immunised still decreased by 11-12% (to < 75%) if the third-dose assumption was not used in the most recent cohort. "Fully immunised" status among children with delayed Medicare registration or in jurisdictions with a high proportion of paper reporting to the ACIR was disproportionately reduced without use of the assumption. CONCLUSIONS AND IMPLICATIONS: While independent sources of data continue to show that the ACIR incorrectly classifies some children as not fully immunised even with the third-dose assumption, its use seems appropriate for reporting population trends in immunisation coverage. Earlier Medicare registration and increased electronic reporting to the ACIR, together with incentives for parents and providers to ensure complete ACIR records, should eventually eliminate the need for the third-dose assumption.


Subject(s)
Databases, Factual , Immunization/statistics & numerical data , Registries , Australia , Bias , Birth Certificates , Child , Child, Preschool , Cohort Studies , Data Interpretation, Statistical , Humans , Immunization/classification , Infant , Infant, Newborn , National Health Programs/statistics & numerical data , Reproducibility of Results , Time Factors
13.
J AHIMA ; 70(6): 70-2; quiz 75-6, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10537630

ABSTRACT

Although CPT 1999 contains fewer changes than in past years, coders should take some time to learn them by: familiarizing themselves with the new symbols + and [symbol: see text] reviewing Appendix A for a complete list of modifiers as well as modifiers used in the ambulatory surgery center hospital outpatient setting; reviewing Appendix E for a complete list of add-on codes; reviewing Appendix F for a list of modifier-51-exempt codes; consulting the excludes note found above code 69,990 to identify procedures exempt from the use of the new operating microscope code; examining the specific codes used to identify bronchoscopic procedures; reviewing the parenthetical notes found after code 15,001, directing the coder to also assign the appropriate code for lesion excision; reviewing the changes associated with the coding of destruction of lesions understanding the changes in immunization code assignment; consulting payers for specific reimbursement guidelines.


Subject(s)
Abstracting and Indexing/standards , Medical Records/classification , Ambulatory Surgical Procedures/classification , Bronchoscopy/classification , Cicatrix/surgery , Education, Continuing , Humans , Immunization/classification , Medical Record Administrators , Microscopy/classification , Microscopy/instrumentation , Skin Transplantation/classification , Surgical Procedures, Operative/classification , United States
17.
In. México. Secretaría de Salud. Subsecretaría de Coordinación y Desarrollo. Vacunas, ciencia y salud. México,D.F, Secretaría de Salud, dic. 1992. p.521-7, tab.
Monography in Spanish | LILACS | ID: lil-147861

ABSTRACT

La amibiasis es la infección producida por el protozoario parásito Entamoeba histolytica. A pesar de que el término amibiasis incluye a todos los casos humanos de infección producidos por este microorganismo, sólo una parte de los individuos infectados presentan síntomas imputables a la penetración de las amibas en los tejidos. A esta entidad nosológica se le conoce como amibiasis invasora y al grupo de personas infectadas asintomáticamente se les denomina portadores de E. histolytica y presentan amibiasis luminal. Los estudios sobre inmunidad protectora antiamibiana se encuentran todavía en etapa experimental; sin embargo, en animales de laboratorio los resultados obtenidos han sido en general satisfactorios. Los primeros intentos de inducción de protección antiamibiana, llevados a cabo por diferentes grupos, tuvieron éxito en general. Sin embargo, hay una gran falta de homogeneridad en las condiciones utilizadas por cada grupo de investigadores, y principalmente han consistido en el uso de diferentes dosis de antígenos, en los métodos de caracterización de las cepas amibianas utilizadas, las cantidades de inóculo administradas, las vías de inmunización y los modelos animales en que se aplicaron


Subject(s)
Amebiasis/classification , Amebiasis/complications , Amebiasis/diagnosis , Amebiasis/epidemiology , Amebiasis/etiology , Amebiasis/immunology , Amebiasis/pathology , Amebiasis/prevention & control , Amebiasis/therapy , Amebiasis/transmission , Immunization/classification , Immunization/adverse effects , Immunization/history , Immunization/instrumentation , Immunization/methods , Immunization/trends , Mexico
18.
In. México. Secretaría de Salud. Subsecretaría de Coordinación y Desarrollo. Vacunas, ciencia y salud. México,D.F, Secretaría de Salud, dic. 1992. p.85-91, tab.
Monography in Spanish | LILACS | ID: lil-143329

ABSTRACT

La información o recomendaciones en torno a inmunizaciones para viajeros internacionales debe fundamentarse en el reglamento Sanitario Internacional y el conocimiento sobre la situación epidemiológica más reciente del país o países que serán visitados. Esta información deberá ser conocida por los médicos, autoridades sanitarias, agencias de turismo y otras personas encargadas de advertir a los turistas, quienes además de asegurar que el viajero cuente con las inmunizaciones básicas y que su esquema esté actualizado, deberán recomendarle la inmunización contra otras enfermedades según las condiciones locales en los países que va a visitar. Se señalan las enfermedades sujetas al Reglamento Sanitario Internacional (fiebre amarilla, cólera y peste); las enfermedades inmunoprevenibles objeto de vigilancia epidemiológica internacional y las vacunas fuera de Programa Nacional de Inmunizaciones


Subject(s)
Immunization Schedule , Health Surveillance , Immunization/classification , Immunization/nursing , Immunization/instrumentation , Immunization/trends , Mexico/epidemiology , Transients and Migrants/classification , Transients and Migrants/legislation & jurisprudence , Vaccines/administration & dosage , Vaccines/classification , Vaccines/immunology , Vaccines/supply & distribution
19.
In. México. Secretaría de Salud. Subsecretaría de Coordinación y Desarrollo. Vacunas, ciencia y salud. México,D.F, Secretaría de Salud, dic. 1992. p.449-59.
Monography in Spanish | LILACS | ID: lil-143353

ABSTRACT

Hay dos grandes líneas de pensamiento sobre la etiología de la caries dental. Mientras que algunos afirman que se debe a un desequilibrio de la microflora bucal normal, como consecuencia de un alto consumo de carbohidratos, la mayoría de los investigadores dentales coincide en que la caries es una enfermedad infecciosa y transmisible. El Streptococus mutans (caries) coloniza la cavidad bucal del ser humano sólo después de la erupción dentaria, pues para crecer requieren de superficies duras. Su identificación por la tipificación de sus bacteriocinas y plásmidos señala que en el ser humano, la madre es el reservorio primario de la infección y el contagio ocurre si su saliva, o la de otro individuo con caries, llega a la boca del infante. Existen dos estrategias globales para el desarrollo de vacunas contra la caries. Dos grupos de investigadores británicos exploran la inmunización por vía subcutánea, mientras que las vacunas administrables por vía entérica están bajo estudio en cuatro laboratorios de los Estados Unidos, además grupos suecos, franceses y japoneses participan en la búsqueda de una vacuna eficaz; se anotan los avances en cuanto a la inmunización parenteral, inmunización gingival, inmunización pasiva local, vacunas entéricas y presentación de antígenos como partículas y uso de adyuvantes


Subject(s)
Dental Caries/classification , Dental Caries/complications , Dental Caries/congenital , Dental Caries/diagnosis , Dental Caries/epidemiology , Dental Caries/etiology , Dental Caries/genetics , Dental Caries/immunology , Dental Caries/pathology , Dental Caries/prevention & control , Dental Caries/therapy , Immunization/classification , Immunization/history , Immunization/instrumentation , Immunization/methods , Immunization/trends , Mexico
20.
In. México. Secretaría de Salud. Subsecretaría de Coordinación y Desarrollo. Vacunas, ciencia y salud. México,D.F, Secretaría de Salud, dic. 1992. p.479-91, ilus, tab.
Monography in Spanish | LILACS | ID: lil-143355

ABSTRACT

La gonorrea constituye actualmente un problema importante de salud pública, cuyo impacto se refleja en su morbilidad y a través de sus complicaciónes y secuelas crónicas. El agente causal es Neisseria gonorrhoeae, conocido comúnmente como gonococo, y su único hospedero es el humano. Su forma de transmisión es por el contacto sexual o perinatal. cuando en 1985 se realizó el ensayo clínico de una vacuna producida con pili de gonococo en unos 3,000 voluntarios, se pensaba que las investigaciones para producir una vacuna para gonococo estaban cercanas a lograr su propósito. Sin embargo, a partir de entonces se han debido enfrentar problemas inherentes a las complejidades fisiológicas, inmunoquímicas, moleculares y genéticas de la bacteria. La obtención de una vacuna eficaz puede analizarse desde tres puntos de vista: aspectos de la bacteria, del huésped y con los de la vacuna misma. La identificación de los posibles candidatos para una vacuna se han dirigido a seleccionar componentes que sean constantes entre cepas homólogas y cepas heterólogas, que no dañen el sistema inmunológico del huésped y que estén expuestos en la pared celular de las bacterias. Se ha considerado que los pili, la proteína I, la lipoproteína y la proteína receptora de hierro reúnen estas características. En caso de que la protección que otorgue la vacuna únicamente sea para las complicaciones ocacionadas por la diseminación de la bacteria, ésta será insuficiente para interrumpir la cadena de transmisión


Subject(s)
Gonorrhea/classification , Gonorrhea/complications , Gonorrhea/congenital , Gonorrhea/diagnosis , Gonorrhea/epidemiology , Gonorrhea/etiology , Gonorrhea/immunology , Gonorrhea/pathology , Gonorrhea/prevention & control , Gonorrhea/transmission , Immunization/classification , Immunization/nursing , Immunization/history , Immunization/methods , Immunization/trends , Mexico
SELECTION OF CITATIONS
SEARCH DETAIL
...