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1.
BMC Pulm Med ; 20(1): 66, 2020 Mar 18.
Article in English | MEDLINE | ID: mdl-32188435

ABSTRACT

BACKGROUND: Uncontrolled severe asthma in children is burdensome and challenging to manage. This study aims to describe outcomes in children with uncontrolled severe asthma managed in a nurse-led severe asthma clinic (SAC). METHODS: This retrospective analysis uses data collected from children referred by a paediatric respiratory specialist to a nurse-led SAC for uncontrolled severe asthma between 2014 and 2019. The pre-clinical assessments included a home visit to assess modifiable factors that could be addressed to improve control. A comprehensive lung function analysis was conducted at each visit. Interventions were personalised and included biologic agents. Statistical analysis was performed using nonparametric, two-tailed Mann-Whitney U-test, the parametric Student's t-test, or analysis of variance (ANOVA) as appropriate. RESULTS: Twenty-three children with a median age of 12 years were seen once, and 16 were followed up. Compared to a non-asthmatic (NA) and asthmatic (A) age-matched cohort, children with severe asthma (SA) had a lower FEV1, and FVC% predicted before and after bronchodilator inhalation, and a higher mean Lung Clearance Index [LCI] (10.5 [SA] versus 7.3 [NA] versus 7.6 [A], p = 0.003). Almost 80% of children with SA had an abnormal LCI, and 48% had a reduced FEV1% at the first SAC visit. Asthma control and FEV1% predicted significantly improved at a follow-up visit, while LCI remained abnormal in the majority of children (83%). CONCLUSION: Over time, many children with severe asthma showed improved clinical outcomes and lung function while lung ventilation inhomogeneities persisted. Future appropriately controlled studies are required to determine if a nurse-led multidisciplinary SAC is associated with better outcomes.


Subject(s)
Asthma/physiopathology , Lung/physiopathology , Outpatient Clinics, Hospital , Practice Patterns, Nurses' , Administration, Inhalation , Adolescent , Asthma/drug therapy , Asthma/nursing , Australia , Bronchodilator Agents/therapeutic use , Child , Child, Preschool , Female , Humans , Male , Respiratory Function Tests , Retrospective Studies , Spirometry , Treatment Outcome
2.
Clin Infect Dis ; 65(12): 2099-2104, 2017 Nov 29.
Article in English | MEDLINE | ID: mdl-29099909

ABSTRACT

BACKGROUND: Natural infection with Bordetella pertussis is thought to result in 4-20 years of immunity against subsequent symptomatic pertussis infection. However, these estimates are based on studies in unvaccinated or whole-cell pertussis-vaccinated children. We conducted a population-based study of pertussis infection and reinfection during a 5-year period in California in an cohort vaccinated exclusively with acellular pertussis (aP) vaccine. METHODS: California surveillance data were reviewed to identify all children with 2 reported incidents of pertussis with symptom onset between 1 January 2010 and 31 December 2015. Case investigation reports were reviewed, and children with ≥2 episodes of symptomatic pertussis infection that met the case definition were included. RESULTS: Of 26259 pertussis cases reported in children (aged <18 years), 27 children met the inclusion criteria. Recurrent cases occurred among children of all ages; 5 (19%) were <6 months of age at the time of their first illness. The time from initial infection to reinfection was <1 year in 11 (41%) cases. Twenty-one children (78%) had received ≥3 doses of diphtheria and tetanus toxoids and aP vaccine at the time of their first pertussis infection, 1 (4%) had received 1 dose, and 5 (19%) were unvaccinated. CONCLUSIONS: Recurrent cases of pertussis infection are extremely rare. Based on this surveillance data, approximately 0.1% of children who were infected with pertussis experienced a clinically significant second episode of pertussis within 4 years. More research is needed to understand the immune response to B. pertussis infection in children vaccinated with aP vaccines.


Subject(s)
Diphtheria-Tetanus-acellular Pertussis Vaccines/administration & dosage , Diphtheria-Tetanus-acellular Pertussis Vaccines/adverse effects , Population Surveillance , Whooping Cough/epidemiology , Adolescent , Bordetella pertussis/immunology , Bordetella pertussis/isolation & purification , California/epidemiology , Child , Child, Preschool , Cohort Studies , Diphtheria-Tetanus-acellular Pertussis Vaccines/immunology , Female , Humans , Infant , Male , Recurrence , Whooping Cough/etiology , Whooping Cough/microbiology , Whooping Cough/prevention & control
4.
J Infect Dis ; 210 Suppl 1: S380-9, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316859

ABSTRACT

BACKGROUND: Vaccine-associated paralytic poliomyelitis (VAPP) is a rare adverse event associated with oral poliovirus vaccine (OPV). This review summarizes the epidemiology and provides a global burden estimate. METHODS: A literature review was conducted to abstract the epidemiology and calculate the risk of VAPP. A bootstrap method was applied to calculate global VAPP burden estimates. RESULTS: Trends in VAPP epidemiology varied by country income level. In the low-income country, the majority of cases occurred in individuals who had received >3 doses of OPV (63%), whereas in middle and high-income countries, most cases occurred in recipients after their first OPV dose or unvaccinated contacts (81%). Using all risk estimates, VAPP risk was 4.7 cases per million births (range, 2.4-9.7), leading to a global annual burden estimate of 498 cases (range, 255-1018). If the analysis is limited to estimates from countries that currently use OPV, the VAPP risk is 3.8 cases per million births (range, 2.9-4.7) and a burden of 399 cases (range, 306-490). CONCLUSIONS: Because many high-income countries have replaced OPV with inactivated poliovirus vaccine, the VAPP burden is concentrated in lower-income countries. The planned universal introduction of inactivated poliovirus vaccine is likely to substantially decrease the global VAPP burden by 80%-90%.


Subject(s)
Poliomyelitis/epidemiology , Poliovirus Vaccines/administration & dosage , Poliovirus Vaccines/adverse effects , Adolescent , Adult , Child , Child, Preschool , Developed Countries , Developing Countries , Female , Global Health , Humans , Infant , Infant, Newborn , Male , Prevalence , Risk Assessment , Young Adult
5.
J Infect Dis ; 210 Suppl 1: S434-8, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25316865

ABSTRACT

Polio eradication requires the removal of all polioviruses from human populations, whether wild poliovirus or those emanating from the oral poliovirus vaccine (OPV). The Polio Eradication & Endgame Strategic Plan 2013-2018 provides a framework for interruption of wild poliovirus transmission in remaining endemic foci and lays out a plan for the new polio end game, which includes the withdrawal of Sabin strains, starting with type 2, and the introduction of inactivated poliovirus vaccine, for risk mitigation purposes. This report summarizes the rationale and evidence that supports the policy decision to switch from trivalent OPV to bivalent OPV and to introduce 1 dose of inactivated poliovirus vaccine into routine immunization schedules, and it describes the proposed implementation of this policy in countries using trivalent OPV.


Subject(s)
Disease Eradication/methods , Disease Eradication/organization & administration , Poliomyelitis/epidemiology , Poliomyelitis/prevention & control , Poliovirus Vaccines/administration & dosage , Poliovirus Vaccines/immunology , Vaccination/methods , Global Health , Humans , Poliomyelitis/transmission
6.
Am J Public Health ; 103(10): 1736-40, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23948003

ABSTRACT

Health risks from poor malaria control, unsafe water, and indoor air pollution are responsible for an important share of the global disease burden-and they can be addressed by efficacious household health technologies that have existed for decades. However, coverage rates of these products among populations at risk remain disappointingly low. We conducted a review of the medical and public health literatures and found that health considerations alone are rarely sufficient motivation for households to adopt and use these technologies. In light of these findings, we argue that health education and persuasion campaigns by themselves are unlikely to be adequate. Instead, health policymakers and professionals must understand what users value beyond health and possibly reengineer health technologies with these concerns in mind.


Subject(s)
Environmental Health , Health Promotion , Housing , Technology , Attitude , Global Health , Humans , Poverty Areas , Risk
7.
Pediatr Pulmonol ; 52(10): 1340-1348, 2017 10.
Article in English | MEDLINE | ID: mdl-28737279

ABSTRACT

PURPOSE: The purpose of this study was to compare (i) the exercise capacity and (ii) lung function prior to and immediately post cardiopulmonary exercise tests (CPET) of children who underwent early life lung resection for Congenital Pulmonary Airway Malformations (CPAM) to healthy control children. METHOD: Eight children with CPAM (four males, age 9.6 ± 1.8 years) and eight control children without respiratory disease (three males, age 9.4 ± 1.4 years) performed a CPET on a cycle ergometer, during which maximal oxygen consumption (V̇O2max ) and heart rate were measured. Prior to and immediately post CPET, lung function measures including Nitrogen Multiple Breath Washout (MBW) and spirometry were performed. RESULTS: There were no significant between group differences in pre CPET lung function (P > 0.05) or maximal exercise capacity (V̇O2max CPAM: 39.4 mL. kg-1. min-1 , Control: 40.5 mL. kg-1. min-1 ). Post CPET, FEV1 was significantly lower in the CPAM group, with two participants diagnosed subsequently with exercise induced bronchospasm based on post-CPET spirometry and follow-up clinical investigations. CONCLUSION: Early life lung resection for CPAM does not appear to have negative implications for exercise capacity later in childhood. Clinicians should be aware that dyspnoea following exercise may be due to asthma rather than residual effects of CPAM in these children.


Subject(s)
Exercise Tolerance , Lung , Respiratory System Abnormalities , Child , Exercise Test , Female , Forced Expiratory Volume , Heart Rate , Humans , Lung/abnormalities , Lung/physiopathology , Lung/surgery , Male , Oxygen Consumption , Respiratory System Abnormalities/physiopathology , Respiratory System Abnormalities/surgery , Spirometry
9.
Diagn Microbiol Infect Dis ; 83(1): 41-5, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26081239

ABSTRACT

Interferon-gamma release assays have limited sensitivity for detecting latent tuberculosis infection. In this study, we determine if the addition of immunomodulators to the QuantiFERON-TB Gold In-Tube (QFT-GIT) increased test sensitivity without compromising specificity. We prospectively compared QFT-GIT results with and without incubation with 2 immunomodulators (lipopolysaccharide [LPS] and polyinosine-polycytidylic acid [PolyIC]) in 2 cohorts-113 culture-confirmed tuberculosis (TB) subjects in Hanoi, Vietnam, and 226 documented QFT-GIT-negative, low TB risk health care workers undergoing annual TB screening at a US academic institution. Sensitivity of the tests in TB subjects was 84.1% with the standard QFT-GIT and 85.8% and 74.3% after incubation with LPS and PolyIC, respectively. Specificity in low TB risk health care workers was 100% with the standard QFT-GIT by design and 86.7% with LPS and 63.3% with PolyIC. In conclusion, use of the 2 immunomodulators did not improve sensitivity of the QFT-GIT in TB patients and reduced specificity in low-risk health care workers.


Subject(s)
Immunologic Factors/metabolism , Interferon-gamma Release Tests/methods , Mycobacterium tuberculosis/immunology , T-Lymphocytes/immunology , Tuberculosis/diagnosis , Adult , Aged , Female , Health Personnel , Humans , Lipopolysaccharides/metabolism , Male , Middle Aged , Poly I-C/metabolism , Prospective Studies , Sensitivity and Specificity , T-Lymphocytes/drug effects , United States , Vietnam
10.
Acad Med ; 85(3): 470-5, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20182120

ABSTRACT

Because translational research is not clearly defined, developers of translational research programs are struggling to articulate specific program objectives, delineate the knowledge and skills (competencies) that trainees are expected to develop, create an appropriate curriculum, and track outcomes to assess whether program objectives and competency requirements are being met. Members of the Evaluation Committee of the Association for Clinical Research Training (ACRT) reviewed current definitions of translational research and proposed an operational definition to use in the educational framework. In this article, the authors posit that translational research fosters the multidirectional and multidisciplinary integration of basic research, patient-oriented research, and population-based research, with the long-term aim of improving the health of the public. The authors argue that the approach to designing and evaluating the success of translational training programs must therefore be flexible enough to accommodate the needs of individual institutions and individual trainees within the institutions but that it must also be rigorous enough to document that the program is meeting its short-, intermediate-, and long-term objectives and that its trainees are meeting preestablished competency requirements. A logic model is proposed for the evaluation of translational research programs.


Subject(s)
Education, Medical , Translational Research, Biomedical/standards
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