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1.
Crit Care Med ; 48(12): 1914-1915, 2020 12.
Article in English | MEDLINE | ID: mdl-33255114
2.
Arch Dis Child ; 92(8): 683-6, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17412743

ABSTRACT

OBJECTIVE: To assess parental stress levels of mothers of children less than 6 years old with eczema and compare these levels with those reported for other chronic childhood illnesses. METHODS: Mothers were recruited from hospital-based out-patient clinics (55%) or while their child was an in-patient (45%) for management of eczema. Maternal stress was measured utilising the Parenting Stress Index-Long Form (PSI) in 33 mothers. The severity of the eczema at the time of interview was documented by the Eczema Area and Severity Index (EASI) score and the Investigators' Global Assessment (IGA) score. RESULTS: The children with eczema had a mean age of 2.8 years. Mothers of children aged 5 years or less with eczema exhibited significantly higher total stress scores (mean PSI 259.6, 95% CI 244.9 to 274.3) as compared to mothers of normal children (PSI 222.8, 95% CI 221.4 to 224.2) and children with other chronic disorders such as insulin-dependent diabetes (PSI 218.1, 95% CI 204.7 to 231.6) and profound deafness (PSI 221.7, 95% CI 206.4 to 237.0). Stress scores in the parental domain (138.2, 95% CI 128.9 to 147.6) did not differ significantly from the scores of parents of children with severe disabilities such as those requiring home enteral feeding (135.2, 95% CI 129.3 to 141.1) and those with Rett syndrome (132.8, 95% CI 125.0 to 140.6). CONCLUSIONS: Moderate to severe childhood eczema should be regarded as a significant illness in which maternal stress is equivalent to that associated with the care of children with severe developmental and physical problems.


Subject(s)
Eczema/psychology , Mothers/psychology , Stress, Psychological/psychology , Adult , Child, Preschool , Female , Humans , Infant , Male , Mother-Child Relations
3.
Gynecol Oncol ; 99(3 Suppl 1): S262-8, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16229879

ABSTRACT

BACKGROUND: While the cervical mucosal immune response to human papillomavirus (HPV) infection is believed to be central to viral clearance, it is not well characterized. We performed this analysis to determine correlates of HPV-16-specific mucosal antibody response in women at high risk for infection with HPV. METHODS: Cervical mucosal and serum samples were obtained from participants in a case control study that measured demographic risk factors of cervical disease and HPV infection. An HPV-16 L1-virus-like particle ELISA was used to detect HPV-16-specific IgA and IgG. Antibody level results were correlated with demographic characteristics, sexual history, cervical disease, and HPV detection. RESULTS: Cervical anti-HPV-16 IgA and IgG inversely correlated with HPV DNA, HPV-16 DNA, and cervical disease. CONCLUSIONS: These findings suggest that mucosal antibodies may protect against HPV infection and cervical disease. However, additional longitudinal studies evaluating serum and mucosal antibody correlates of incident, persistent, and clearing HPV infection are needed. In addition, standardization of mucosal sample collection and testing methods are required.


Subject(s)
Antibodies, Viral/immunology , Human papillomavirus 16/immunology , Papillomavirus Infections/immunology , Uterine Cervical Dysplasia/virology , Uterine Cervical Neoplasms/virology , Adolescent , Adult , Antibodies, Viral/biosynthesis , Case-Control Studies , DNA, Viral/analysis , Enzyme-Linked Immunosorbent Assay , Female , Human papillomavirus 16/genetics , Humans , Immunoglobulin A/biosynthesis , Immunoglobulin A/immunology , Immunoglobulin G/biosynthesis , Immunoglobulin G/immunology , Middle Aged , Mucous Membrane/immunology , Mucous Membrane/virology , Papillomavirus Infections/virology , Uterine Cervical Neoplasms/immunology , Uterine Cervical Dysplasia/immunology
4.
Psychosom Med ; 66(5): 672-8, 2004.
Article in English | MEDLINE | ID: mdl-15385690

ABSTRACT

OBJECTIVE: Stress or emotional traumas are considered risk factors for unexplained fatiguing illnesses. From July to December 2001, the Centers for Disease Control and Prevention conducted a multigeographical pilot study to test the feasibility of a survey to estimate the prevalence of fatiguing illnesses in the United States. We used data obtained during this survey to estimate the effect of the coincidentally occurring terrorist attacks of September 11, 2001, on the regional prevalence of fatiguing illnesses. METHODS: Identified by random-digit dialing, 2,728 households in eight regional strata were interviewed, and 7,317 respondents were screened for severe fatigue of at least 1 month duration. Identified fatigued people of age 18 to 69 years (N = 440) and a sample of nonfatigued people of the same age range (N = 444) were interviewed in detail concerning fatigue, other symptoms, and medical and psychiatric histories. RESULTS: Weighted prevalence estimates based on interviews performed after the attacks were significantly lower compared with estimates based on interviews performed before the attacks (prolonged fatigue: 5,450 vs. 1,530/100,000, p =.010; chronic fatigue: 18,510 vs. 10,070/100,000, p =.002; chronic fatigue syndrome-like illness: 2,510 vs. 960/100,000, p =.014). CONCLUSION: Our findings suggest decreased regional prevalence of fatiguing illnesses in the aftermath of the terrorist attacks. The causes of this effect are unknown but might involve acute psychological and physiological adaptations that modify the perception or manifestation of fatigue. Future studies should be specifically designed to scrutinize the relationship between stress and fatiguing illnesses and the mediating mechanisms of such a relationship.


Subject(s)
Fatigue Syndrome, Chronic/epidemiology , Fatigue/epidemiology , September 11 Terrorist Attacks , Adolescent , Adult , Aged , Centers for Disease Control and Prevention, U.S./statistics & numerical data , Chronic Disease , Female , Health Surveys , Humans , Life Change Events , Male , Middle Aged , Pilot Projects , Prevalence , Residence Characteristics/statistics & numerical data , Risk Factors , September 11 Terrorist Attacks/psychology , Stress Disorders, Post-Traumatic/epidemiology , United States/epidemiology
5.
Popul Health Metr ; 2(1): 1, 2004 Feb 04.
Article in English | MEDLINE | ID: mdl-14761250

ABSTRACT

BACKGROUND: Chronic fatigue syndrome (CFS) is a debilitating illness with no known cause or effective therapy. Population-based epidemiologic data on CFS prevalence are critical to put CFS in a realistic context for public health officials and others responsible for allocating resources. METHODS: We conducted a pilot random-digit-dialing survey to estimate the prevalence of fatiguing illnesses in different geographic regions and in urban and rural populations of the United States. This report focuses on 884 of 7,317 respondents 18 to 69 years old. Fatigued (440) and randomly selected non-fatigued (444) respondents completed telephone questionnaires concerning fatigue, other symptoms, and medical history. RESULTS: We estimated 12,186 per 100,000 persons 18 to 69 years of age suffered from fatigue lasting for at least 6 months (chronic fatigue), and 1,197 per 100,000 described an illness that, though lacking clinical evaluation, met criteria for CFS (CFS-like). Chronic fatigue and CFS-like illness were more common in rural than in urban populations, although the differences were not significant. The prevalence of these fatiguing illnesses did not differ meaningfully among the four regions surveyed, and no significant geographic trends were observed. CONCLUSIONS: This investigation estimated that nearly 2.2 million American adults suffer from CFS-like illness. The study also suggested the need to focus future investigations of fatigue on populations with lower incomes and less education. There was no evidence for regional differences in the occurrence of fatiguing illnesses.

6.
Clin Diagn Lab Immunol ; 9(3): 577-82, 2002 May.
Article in English | MEDLINE | ID: mdl-11986263

ABSTRACT

A strategy was developed for the control, standardization, and critical evaluation of an enzyme-linked immunosorbent assay (ELISA) for the detection of human papillomavirus-specific immunoglobulin G in human sera. Control human sera, polyclonal animal sera, and monoclonal antibodies were used to establish optimal assay parameters, including antigen coating, serum dilutions, and criteria for daily reproducibility, monitoring, and rejection of assays. Three evaluation techniques were used in parallel to define an optimal cutoff absorbance value that yields greater than 93% sensitivity and 98.5% specificity in the assay's ability to discriminate positive and negative control sera. This strategy provides an optimal method by which to determine cutoff absorbance values for ELISA.


Subject(s)
Antibodies, Viral/blood , Capsid Proteins , Enzyme-Linked Immunosorbent Assay/methods , Papillomaviridae/immunology , Papillomavirus Infections/virology , Tumor Virus Infections/virology , Animals , Antibodies, Viral/immunology , Humans , Immunoglobulin G/blood , Immunoglobulin G/immunology , Oncogene Proteins, Viral/genetics , Oncogene Proteins, Viral/immunology , Papillomavirus Infections/blood , Papillomavirus Infections/immunology , Rabbits , Reproducibility of Results , Tumor Virus Infections/blood , Tumor Virus Infections/immunology
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