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1.
Child Abuse Negl ; 154: 106915, 2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38964011

ABSTRACT

BACKGROUND: Single parent families are at higher risk of re-report to Child Protective Services (CPS) than two-parent families. Yet, how single-family homes differ in risk from two-parent families remains under researched. OBJECTIVE: To identify heterogenous patterns of child and caregiver factors among CPS-involved families and the subsequent risk for CPS re-report based on child and family characteristics (i.e., sociodemographic information, family structure, and risk indicators). PARTICIPANTS AND SETTING: Data were from the 2017 National Child Abuse and Neglect Data System Child File (N = 249,026). METHODS: We conducted latent class analysis (LCA) to identify discrete patterns (i.e., classes) based on child and caregiver risk indicators (e.g., substance use, behavioral health). We then used logistic regression to examine family structure and other family characteristics and CPS indicators predicted CPS re-report for each class. RESULTS: Results yielded five distinct classes: 1) Financial Stressors (25 % of the sample); 2) Caregiver Substance Use (16 %); 3) Complex Household Stressors (3 %); 4) Child Disabilities (4 %); and 5) Minimal Household Stressors (53 %). Family structure was significantly associated with CPS re-reports for Classes 1, 2, and 5. For Class 1, single father families had increased odds of CPS re-report compared to other family structures. For Classes 2 and 5, single father families' odds of CPS re-reports were greater than those of married families, but lower than single mother families. CONCLUSIONS: Children growing up in single father families have different likelihoods of repeat CPS involvement compared to those in single mother and married families. Financial stressors and parental substance use within single father families should be addressed.

2.
J Neonatal Perinatal Med ; 11(3): 317-321, 2018.
Article in English | MEDLINE | ID: mdl-30040744

ABSTRACT

BACKGROUND: Normal saline bolus is commonly used in clinical practice for treating hypotension in very preterm infants during resuscitation at an early age despite the paucity of high quality evidence supporting this practice. OBJECTIVES: To determine the effects of early (<7 days after birth) saline boluses given to very preterm infant (VPI) from 23 to 31 weeks GA. METHOD: This is a population-based cohort analysis of the use of normal saline boluses given to VPI. The outcomes were extracted from the Perinatal Follow-Up Program Database which included all VPI from Halifax County admitted to the NICU at the IWK Health Centre, Halifax, Nova Scotia, Canada between January 2006 to December 2010. We excluded infants with major congenital anomalies and those not offered resuscitation in the delivery room. Our primary outcome was the composite of death or disability by 18-36 months while secondary outcomes were neonatal death, BPD, CP, IVH, PVL, ROP, BSITD III (Bayley Scales of Infant and Toddler Development®, Third Edition) Cognitive, Motor and Language score. RESULTS: Death or disability in those who received saline bolus occurred in 15 (53.6%) compared with 9 (32.1%) in non saline group. Significantly higher rates of CP (p = 0.04), lower scores on the BSITDIII for motor (p = 0.04) and language scales (p = 0.03) were noted for infants who received saline boluses. Cognitive scores approached significance (p = 0.05) with lower scores in the saline bolus group. CONCLUSION: Significant differences were found between the two groups in terms of long term neurodevelopmental outcome and one of the short-term outcome (i.e. BPD). Given the limitations of this retrospective study and the small sample size, a larger cohort from Canadian Neonatal Network database is warranted to evaluate the effects of using normal saline boluses during early life on neurodevelopmental.


Subject(s)
Cerebral Palsy/physiopathology , Child Development/physiology , Developmental Disabilities/physiopathology , Infant, Extremely Premature/growth & development , Infant, Premature, Diseases/physiopathology , Saline Solution, Hypertonic/therapeutic use , Cerebral Palsy/epidemiology , Cerebral Palsy/prevention & control , Developmental Disabilities/epidemiology , Developmental Disabilities/prevention & control , Disabled Children/statistics & numerical data , Evidence-Based Medicine , Female , Gestational Age , Humans , Infant , Infant, Newborn , Infant, Premature, Diseases/epidemiology , Infant, Premature, Diseases/prevention & control , Male , Matched-Pair Analysis , Nova Scotia/epidemiology , Retrospective Studies , Severity of Illness Index , Treatment Outcome
4.
Infect Immun ; 79(4): 1566-77, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21245268

ABSTRACT

Genital tract infections caused by Neisseria gonorrhoeae and Chlamydia trachomatis serovars D to K occur at high incidence in many areas of the world. Despite high rates of coinfection with these pathogens, investigations of host-parasite interactions have focused on each pathogen individually. We describe here a coinfection model in which female BALB/c mice were first infected with the mouse Chlamydia species C. muridarum and then inoculated with N. gonorrhoeae following treatment with water-soluble 17ß-estradiol to promote long-term gonococcal infection. Viable gonococci and chlamydiae were recovered for an average of 8 to 10 days, and diplococci and chlamydial inclusions were observed in lower genital tract tissue by immunohistochemical staining. Estradiol treatment reduced proinflammatory cytokine and chemokine levels in chlamydia-infected mice; however, coinfected mice had a higher percentage of vaginal neutrophils compared to mice infected with either pathogen alone. We detected no difference in pathogen-specific antibody levels due to coinfection. Interestingly, significantly more gonococci were recovered from coinfected mice compared to mice infected with N. gonorrhoeae alone. We found no evidence that C. muridarum increases gonococcal adherence to, or invasion of, immortalized murine epithelial cells. However, increased vaginal concentrations of inflammatory mediators macrophage inflammatory protein 2 and tumor necrosis factor alpha were detected in C. muridarum-infected mice prior to inoculation with N. gonorrhoeae concurrently with the downregulation of cathelicidin-related antimicrobial peptide and secretory leukocyte peptidase inhibitor genes. We conclude that female mice can be successfully infected with both C. muridarum and N. gonorrhoeae and that chlamydia-induced alterations in host innate responses may enhance gonococcal infection.


Subject(s)
Chlamydia Infections/complications , Chlamydia Infections/microbiology , Gonorrhea/complications , Gonorrhea/microbiology , Animals , Antibodies, Bacterial/blood , Antibodies, Bacterial/immunology , Chlamydia Infections/immunology , Chlamydia muridarum/immunology , Cytokines/immunology , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Female , Gonorrhea/immunology , Host-Parasite Interactions/immunology , Humans , Immunohistochemistry , Mice , Mice, Inbred BALB C , Neisseria gonorrhoeae/immunology , Reverse Transcriptase Polymerase Chain Reaction
5.
Oncogene ; 29(45): 6051-63, 2010 Nov 11.
Article in English | MEDLINE | ID: mdl-20729921

ABSTRACT

The microtubule-stabilizing drug paclitaxel has activity in relapsed ovarian cancer. dl922-947, an oncolytic adenovirus with a 24-bp deletion in E1A CR2, replicates selectively within and lyses cells with a dysregulated Rb pathway and has efficacy in ovarian cancer. In the aggressive A2780CP xenograft, combination treatment with weekly dl922-947 and paclitaxel has significantly greater efficacy than either treatment alone and can produce complete tumor eradication in some animals. We investigated the mechanisms of paclitaxel's synergy with dl922-947 in ovarian cancer. The host-cell microtubule network is grossly rearranged and stabilized following adenovirus infection, but paclitaxel does not increase this significantly. Paclitaxel does not synergize by increasing infectivity, viral protein expression or virus release. However, destabilizing the microtubule network with nocodazole reduces viral exit, revealing a novel microtubule-dependent pathway for non-lytic adenoviral exit. dl922-947 can override multiple cell cycle checkpoints but induces cell death by a non-apoptotic mechanism. In combination, dl922-947 and low-dose paclitaxel induces aberrant, multipolar mitoses, mitotic slippage and multinucleation, triggering an apoptotic cell death.


Subject(s)
Adenoviridae , Oncolytic Virotherapy , Ovarian Neoplasms/therapy , Paclitaxel/administration & dosage , Tubulin Modulators/pharmacology , Animals , Apoptosis , Cell Line, Tumor , Female , Humans , Mice , Mice, Inbred BALB C , Microtubules/physiology , Mitosis , Paclitaxel/pharmacology , Tubulin Modulators/administration & dosage , Virus Replication , Xenograft Model Antitumor Assays
6.
Arch Dis Child Fetal Neonatal Ed ; 93(3): F176-82, 2008 May.
Article in English | MEDLINE | ID: mdl-17942582

ABSTRACT

OBJECTIVE: To estimate the impact of caesarean delivery on the incidence of selected neonatal outcomes. PATIENTS AND METHODS: A 15-year, population-based, cohort study (1988-2002) using the Nova Scotia Atlee Perinatal Database compared neonatal outcomes in term newborns born by spontaneous and assisted vaginal delivery, with newborns born by caesarean delivery, with and without labour, using multiple logistic regression. RESULTS: From a total of 142 929 deliveries, there were 27 263 caesarean deliveries, 61% of which were performed in labour. Relative risks were adjusted for year of birth, maternal age, parity, smoking, maternal weight at delivery, hypertensive diseases, diabetes, previous caesarean delivery, use of regional anaesthesia, induction of labour, gestational age at delivery and large and small for gestational age, where significant. Caesarean delivery in labour, but not caesarean delivery without labour, had increased risks for depression at birth and neonatal respiratory conditions compared with spontaneous or assisted vaginal delivery. Compared with spontaneous vaginal delivery and assisted vaginal delivery, the risk of major neonatal birth trauma was decreased for infants after caesarean delivery with labour (odds ratio (OR) = 0.34, 95% CI 0.21 to 0.56 and OR = 0.07, 95% CI 0.04 to 0.11, respectively) and caesarean delivery without labour (OR = 0.20, 95% CI 0.08 to 0.52 and OR = 0.04, 95% CI 0.02 to 0.10, respectively). CONCLUSION: Caesarean delivery in labour, compared with vaginal delivery, is more likely to be associated with an increased risk for respiratory conditions and depression at birth than caesarean delivery without labour. Caesarean delivery appears protective against neonatal birth trauma, especially when performed without labour.


Subject(s)
Birth Injuries/epidemiology , Cesarean Section/adverse effects , Depression, Postpartum/epidemiology , Respiratory Tract Diseases/epidemiology , Adult , Breast Feeding , Cesarean Section/statistics & numerical data , Cohort Studies , Delivery, Obstetric/adverse effects , Delivery, Obstetric/statistics & numerical data , Female , Humans , Incidence , Infant, Newborn , Intensive Care, Neonatal , Labor, Obstetric , Nova Scotia/epidemiology , Odds Ratio , Pregnancy , Pregnancy Outcome , Regression Analysis
7.
BJOG ; 113(7): 769-74, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16827759

ABSTRACT

OBJECTIVE: To evaluate predictive factors for respiratory depression at birth in infants >/=37 weeks. DESIGN: A population-based cohort study of respiratory depression at birth at term and post-term. SETTING: Nova Scotia, Canada. POPULATION: All 126 604 nonanomalous, singleton deliveries >/=37 weeks in cephalic presentation from 1988-2002. METHODS: An analysis of maternal, antenatal, intrapartum, and neonatal factors associated with respiratory depression at birth >/=37 weeks. MAIN OUTCOME MEASURES: A composite outcome of delay in initiating and maintaining respiration after birth, 5-minute Apgar score

Subject(s)
Respiratory Insufficiency/prevention & control , Asphyxia Neonatorum/epidemiology , Cohort Studies , Early Diagnosis , Female , Humans , Hypoxia-Ischemia, Brain/epidemiology , Infant, Newborn , Maternal Age , Nova Scotia/epidemiology , Pregnancy , Pregnancy Complications/epidemiology , Prenatal Diagnosis/standards , Prognosis , Respiratory Insufficiency/epidemiology , Risk Assessment , Risk Factors , Seizures/epidemiology
8.
J Obstet Gynaecol ; 25(1): 7-9, 2005 Jan.
Article in English | MEDLINE | ID: mdl-16147683

ABSTRACT

Using a provincial perinatal database for 15 years, 1988-2002. Cases were identified with one or more of the following markers of severe maternal morbidity: blood transfusion > or = 5 units, emergency hysterectomy, uterine rupture, eclampsia, intensive care (ICU) admission. There were 159,896 mothers delivered of whom 313 (2.0/1000) had 385 markers of severe morbidity (257 had one, 42 had two, 12 had three, and two had four). The following rates of morbidity were recorded: blood transfusion > or = 5 units 119 (0.74/1000); emergency hysterectomy 88 (0.55/1000); uterine rupture 49 (0.31/1000); eclampsia 46 (0.28/1000); ICU 83 (0.52/1000). There was a statistically significant association between multiparity > or = 1, and emergency hysterectomy and uterine rupture; between age > or = 35 years, and emergency hysterectomy, uterine rupture and ICU; and between caesarean delivery and blood transfusion > or = 5 units, emergency hysterectomy, uterine rupture, eclampsia and ICU. The main contributing obstetric complications were haemorrhage (64.7%) and complications of hypertensive disorders (16.8%).


Subject(s)
Pregnancy Complications/epidemiology , Adult , Blood Transfusion/statistics & numerical data , Cesarean Section/statistics & numerical data , Critical Care/statistics & numerical data , Eclampsia/epidemiology , Emergency Treatment , Female , Humans , Hypertension/complications , Hysterectomy/statistics & numerical data , Morbidity , Nova Scotia/epidemiology , Postpartum Hemorrhage/epidemiology , Pregnancy , Pregnancy, Multiple/statistics & numerical data , Uterine Hemorrhage/epidemiology , Uterine Rupture/epidemiology
9.
Obstet Gynecol ; 102(3): 477-82, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12962927

ABSTRACT

OBJECTIVE: To estimate the maternal morbidity associated with cesarean deliveries performed at term without labor compared with morbidity associated with spontaneous labor. METHODS: A 14-year, population-based, cohort study (1988-2001) using the Nova Scotia Atlee Perinatal Database compared maternal outcomes in nulliparous women at term undergoing spontaneous labor for planned vaginal delivery with singleton, cephalic presentation and nulliparous women delivering by cesarean without labor. RESULTS: From a total of 18,435 pregnancies, which satisfied inclusion and exclusion criteria, 721 were cesarean deliveries without labor. There were no maternal deaths or transfers for intensive care. There was no difference in wound infection, blood transfusion, or intraoperative trauma. Women undergoing cesarean deliveries without labor were more likely to have puerperal febrile morbidity (relative risk [RR] 2.2; 95% confidence interval [CI] 1.1, 4.5; P=.03), but were less likely to have early postpartum hemorrhage (RR 0.6; 95% CI 0.4, 0.9; P=.01) compared with women entering spontaneous labor. Subgroup analyses of maternal outcomes in women delivering by spontaneous and assisted vaginal delivery and cesarean delivery in labor were also performed. The highest morbidity was found in the assisted vaginal delivery and cesarean delivery in labor groups. CONCLUSION: The increased maternal morbidity in elective cesarean delivery compared with spontaneous onset of labor is limited to puerperal febrile morbidity. Maternal morbidity is increased after assisted vaginal delivery and cesarean delivery in labor compared with cesarean delivery without labor.


Subject(s)
Cesarean Section/adverse effects , Labor, Obstetric , Morbidity/trends , Postpartum Hemorrhage/diagnosis , Uterine Rupture/diagnosis , Adult , Cesarean Section/methods , Cohort Studies , Confidence Intervals , Female , Follow-Up Studies , Gestational Age , Humans , Labor Onset , Labor Presentation , Maternal Age , Maternal Mortality/trends , Nova Scotia , Parity , Postpartum Hemorrhage/epidemiology , Pregnancy , Pregnancy Outcome , Probability , Retrospective Studies , Risk Assessment , Uterine Rupture/epidemiology
10.
Alzheimer Dis Assoc Disord ; 15(3): 137-45, 2001.
Article in English | MEDLINE | ID: mdl-11522931

ABSTRACT

Current levels of participation in Alzheimer disease (AD) research are inadequate, particularly among nonwhites. This study was conducted to examine caregivers' attitudes toward their family members' participation in AD research. Six focus group interviews were conducted with 38 white and 12 African-American caregivers of participants enrolled in clinical research projects. Both white and African-American families participated in research to help their care recipients and future generations, receive support from the clinical and research staff, and obtain feedback about patient status and research results. Among white caregivers, primary barriers to participation in research included the potential for no direct benefit, problems with the procedures and tests involved, lack of time and resources, and difficulty accepting the diagnosis. Among African-American caregivers, primary barriers included general skepticism about the research process and firmly established attitudes about medical treatment and help seeking that serve as disincentives to research participation. To maximize the perceived benefits of research participation, potential participants should have access to regular personal contact with staff, information about health status changes in the care recipient, and the short-term and long-term results of the research studies in which they are participants. In addition, researchers should be sensitive to the concerns that may serve as barriers to participation, particularly among African Americans.


Subject(s)
Alzheimer Disease , Black or African American/psychology , Caregivers/psychology , Patient Selection , Adult , Aged , Attitude to Health , Cultural Characteristics , Family Relations , Humans , Middle Aged , Research/trends , White People/psychology
11.
Gerontologist ; 41(3): 334-47, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11405431

ABSTRACT

PURPOSE: This research reviewed studies that compare two or more racial, ethnic, national, or cultural groups on aspects of the dementia caregiving experience. DESIGN AND METHODS: Electronic databases were searched to find studies published between 1996 and 2000 in peer-reviewed journals that met the above criteria. RESULTS: Twenty-one studies based on 18 samples were identified. These articles included comparisons involving the following groups of caregivers: African Americans, Chinese, Chinese Americans, Koreans, Korean Americans, Latinos, Whites, and residents of 14 European Union countries. Consistent with previous research, White caregivers were more likely to be spouses when compared to other groups. White caregivers tended to report greater depression and appraised caregiving as more stressful than African American caregivers. Findings were mixed regarding differences in coping and social support, but suggested that minority groups may not have more available support than Whites. Common methodological limitations were a lack of noncaregiving control groups and failure to test specific pathways by which the grouping variable (e.g., race) exerts its impact on outcome variables. IMPLICATIONS: Future studies in this area should use both quantitative and qualitative research methods to specify the pathways by which race, ethnicity, and culture affect the caregiving experience, and should expand their focus beyond the primary caregiver to include the effects of caregiving on families and networks.


Subject(s)
Alzheimer Disease/psychology , Attitude , Caregivers/psychology , Cross-Cultural Comparison , Aged , Depression/psychology , Europe , Female , Humans , Male , Social Support
12.
Obstet Gynecol ; 98(6): 1032-7, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11755549

ABSTRACT

OBJECTIVE: To estimate the incidence and factors associated with combined vaginal-cesarean delivery in twin pregnancies. METHODS: We studied all twin births weighing 500 g or more during a 20-year period (1980-1999) at a tertiary care center. Major anomalies, monoamniotic and conjoined twins, and antepartum fetal deaths were excluded. RESULTS: During this 20-year period, 105,987 women delivered, of whom 1565 (1.5%) had twins. Of these, 1151 twin sets fulfilled the study criteria. The mode of delivery was vaginal in 653 (56.8%), cesarean in 448 (38.9%), and vaginal-cesarean in 50 (4.3%). During the 20 years there was a statistically significant increase in combined vaginal-cesarean and elective cesarean deliveries, with a decrease in vaginal deliveries. Parity, gestational age, and birth weight discordance (>25%) were not associated with combined delivery. Compared with vaginal delivery, the nonvertex second twin was associated with a twofold higher risk of cesarean delivery (relative risk [RR] 2.3; 95% confidence interval [CI] 1.3, 3.8; P =.002); and an interdelivery interval of over 60 minutes with an eightfold higher risk (RR 8.2; CI 4.6,14.6; P <.001). Vaginal-cesarean delivery had a 22-fold higher use of general anesthesia compared with vaginal delivery (RR 21.8; CI 5.4, 88.5; P <.001). CONCLUSION: There has been a significant increase in combined vaginal-cesarean and elective cesarean deliveries among twin gestations, with a decrease in vaginal births. Vaginal-cesarean delivery is associated with nonvertex second twin and a prolonged interdelivery interval.


Subject(s)
Delivery, Obstetric/mortality , Pregnancy Outcome , Pregnancy, Multiple , Adult , Cesarean Section/mortality , Female , Humans , Medical Records , Nova Scotia/epidemiology , Pregnancy , Retrospective Studies , Twins
13.
J Geriatr Psychiatry Neurol ; 14(4): 179-87, 2001.
Article in English | MEDLINE | ID: mdl-11794446

ABSTRACT

With the aging of the population, an increasing number of older adults are diagnosed with Alzheimer's disease or a related disorder. Most people with a dementing illness will be cared for at home by a family member, who may experience a variety of physical, emotional, financial, and social burdens associated with the caregiving role. The purpose of this article is to (a) examine the physical and psychological effects of providing care to a family member with a dementing illness, (b) describe the factors that help determine the nature and magnitude of these effects, and (c) discuss several approaches to caregiver intervention designed to reduce the negative impact of this challenging role. Sociodemographic characteristics (e.g., gender, relationship to the patient, culture, race, ethnicity), caregiver resources (e.g., coping, social support, availability of a companion animal), and personal characteristics (e.g., personality, health behaviors) shape the dementia caregiving experience and have implications for interventions designed to prevent or lessen the stress and burden that often accompany the role.


Subject(s)
Caregivers/psychology , Cost of Illness , Dementia/economics , Home Nursing/psychology , Dementia/therapy , Family , Humans , Sex Distribution , Stress, Psychological/psychology , Treatment Outcome
14.
Diabetes Care ; 23(10): 1511-5, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11023145

ABSTRACT

OBJECTIVE: To examine the relationships among cognitive representations of diabetes, diabetes-specific health behaviors, and quality of life using Leventhal and Diefenbach's self-regulation model of illness (Leventhal H, Diefenbach M: The active side of illness cognition. In Mental Representation in Health and Illness. SkeltonJA, Croyle RT, Eds. New York, Springer-Verlag, 1991, p. 247-272). RESEARCH DESIGN AND METHODS: This research involved secondary analysis of a mailed survey completed by 296 adults (ages 20-90 years). Structural equation modeling was conducted to investigate relationships among cognitive representations, diabetes-specific health behaviors, and quality of life. Model differences by diabetes type were also investigated. RESULTS: Findings indicated that certain cognitive representation constructs were related to increased diabetes-specific health behaviors, decreased sense of burden, and positive quality-of-life outcomes. Individuals levels of understanding of diabetes and their perceptions of control over diabetes were the most significant predictors of outcomes. However, diabetes-specific health behaviors were related to an increased sense of burden that was negatively associated with quality of life. Multigroup analyses indicated that this self-regulatory model provided a good fit for individuals with type 1 diabetes, those with type 2 diabetes who take insulin, and those with type 2 diabetes who do not take insulin. CONCLUSIONS: These findings advance what is known about cognitive representations of illness and the self-regulation of diabetes as well as the relationships between cognitive representations of illness, quality of life, and behavioral factors. In particular, results from this study suggest the need for further study to address ways of reducing the burden of diabetes associated with health behaviors and decreased quality of life.


Subject(s)
Cognition , Diabetes Mellitus/psychology , Diabetes Mellitus/rehabilitation , Health Behavior , Quality of Life , Adult , Age Distribution , Aged , Aged, 80 and over , Attitude to Health , Diabetes Mellitus, Type 1/psychology , Diabetes Mellitus, Type 1/rehabilitation , Diabetes Mellitus, Type 2/psychology , Diabetes Mellitus, Type 2/rehabilitation , Female , Health Knowledge, Attitudes, Practice , Humans , Insulin/therapeutic use , Male , Middle Aged , Models, Psychological , Regression Analysis , Reproducibility of Results , Self Care , Surveys and Questionnaires
15.
Alzheimer Dis Assoc Disord ; 14(3): 129-136,Discussion 127-8, 2000.
Article in English | MEDLINE | ID: mdl-10994653

ABSTRACT

The purpose of this study was to examine attitudes, beliefs, and experiences regarding Alzheimer disease (AD) among patients' first-degree relatives, a group that is at increased AD risk and often involved in health care decision-making for affected family members. Children and siblings (N = 203; age range, 30-92 years; 75% female) of people with AD completed a questionnaire (response rate, 90%) that assessed mental representations of AD, including knowledge, cause and treatment beliefs, distress, and perceived threat. In general, relatives were knowledgeable about AD, had an accurate sense of their disease risk, and endorsed etiologically significant factors as causes. Nonetheless, many participants held misconceptions about AD (e.g., most cases are hereditary) and what may be unrealistic expectations for future treatment developments. Levels of perceived distress and threat were generally high and associated with female gender and younger age. AD represented the foremost health concern of approximately one third of first-degree relatives. Health education efforts are needed to address misconceptions about AD genetics and to disseminate information about the availability of effective treatments. Further research on illness representations is needed to better understand coping and decision-making among those at risk for AD.


Subject(s)
Alzheimer Disease/psychology , Family/psychology , Social Perception , Surveys and Questionnaires , Adult , Age Factors , Aged , Aged, 80 and over , Alzheimer Disease/genetics , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Middle Aged , Regression Analysis , Sex Factors , Statistics, Nonparametric
16.
Arch Biochem Biophys ; 379(1): 46-56, 2000 Jul 01.
Article in English | MEDLINE | ID: mdl-10864440

ABSTRACT

Gene expression in the obligate intracellular bacterium Chlamydia trachomatis ranges from nil in the infectious EB form to high in the dividing RB form. Little is known about the mechanisms of gene regulation in chlamydiae and only a few promoter sequences have been characterized. The purpose of our study was to examine the expression of a cluster of genes that are required for translation in C. trachomatis serovar F: infA (encoding Initiation Factor 1), tRNA(Thr), tuf (encoding Elongation Factor Tu), and tRNA(Trp). Primer extension analysis indicated that tuf is expressed in three different mRNAs. Putative promoter sequences for these transcripts were defined as P1 (upstream of tRNA(Thr)), P2 (within infA) and P3 (upstream of infA). Quantitative RT-PCR analysis revealed that P1 transcripts were most abundant at 16 h postinfection (pi), whereas P2 transcripts predominated at 24 h pi. P3 was active at all times pi; however, transcription terminated upstream of tuf at early times pi and continued through tuf at later times. P1 and P3 were active in Escherichia coli, as assessed by CAT expression in promoter-fusion vectors and a chlamydial in vitro transcription system. Site-specific mutagenesis confirmed the importance of the -35 and -10 hexamers in the P1 and P3 promoters. P2 was weakly active in E. coli and inactive in the in vitro transcription system, indicating either that the P2 transcript is processed from a longer transcript or that P2 expression requires a sigma or transcription factor which is not present in E. coli or the in vitro transcription system. Our data suggest that multiple processes play a role in the regulation of tuf gene expression during the developmental cycle.


Subject(s)
Chlamydia Infections/genetics , Chlamydia trachomatis/genetics , Gene Expression Regulation, Bacterial/genetics , Peptide Elongation Factor Tu/genetics , Promoter Regions, Genetic , Amino Acid Sequence , Base Sequence , Cloning, Molecular , Escherichia coli , Genes, Reporter , HeLa Cells , Humans , Molecular Sequence Data , Mutation , Peptide Elongation Factor Tu/chemistry , Protein Biosynthesis , RNA, Messenger/genetics , Restriction Mapping , Reverse Transcriptase Polymerase Chain Reaction
17.
Health Educ Res ; 14(3): 427-31, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10539233

ABSTRACT

A review of articles published in two health education journals is provided to examine the extent to which older adults were included in published research. The review suggests that older adults were included in about 15% of the research articles published in Health Education and Behavior and Health Education Research. Of the articles that include older adults, age differences in study processes and outcomes are rarely examined, and very few studies advance specific hypotheses based on a theoretical or conceptual model of aging or older adulthood. Several recommendations for health education research are suggested.


Subject(s)
Aged , Health Education , Female , Humans , Male , Middle Aged , Research
18.
Arch Phys Med Rehabil ; 80(7): 854-6, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10414774

ABSTRACT

This report describes two cases in which the addition of an extra joint enhanced range of motion and improved function in persons with unilateral lower-limb amputation. Both individuals had significant disability in the workplace and at home before this modification. In the first case, an individual with a hemipelvectomy had inadequate hip-joint flexion for maneuvering during photo shoots. In the second case, the individual's transfemoral prosthesis provided insufficient knee flexion for kneeling and working in tight spaces. In each case, a manual-locking, single-axis knee joint was added adjacent to the joint with the limited range of motion. In both cases, the addition of the second joint provided the increased flexibility needed. The first person's hip-flexion range improved from 125 degrees to 190 degrees, and the second person's knee-flexion range improved from 140 degrees to 170 degrees. In repeated follow-up, both patients remained highly satisfied with the intervention. The addition of an extra joint is an option that should be considered when inadequate range interferes with function.


Subject(s)
Activities of Daily Living , Amputees/rehabilitation , Artificial Limbs , Disabled Persons/rehabilitation , Range of Motion, Articular , Amputees/psychology , Disabled Persons/psychology , Femoral Neoplasms/surgery , Fibrosarcoma/surgery , Hemipelvectomy/rehabilitation , Humans , Liposarcoma/surgery , Male , Middle Aged , Prosthesis Design , Soft Tissue Neoplasms/surgery , Thigh
19.
J Aging Health ; 9(3): 373-95, 1997 Aug.
Article in English | MEDLINE | ID: mdl-10182399

ABSTRACT

This study describes the health behaviors (alcohol consumption, exercise, sleep patterns, smoking, and weight maintenance) of a sample of older adult spouse caregivers (N = 233) and investigates the predictors of decreased self-care since caregiving began. Multiple regression results indicate that caregivers who experience greater developmental burden, report a greater number of depressive symptoms, perform a greater number of activities of daily living (ADL) tasks in caregiving and spend more hours in a day providing care, and who have lower self-efficacy for both self-care and spouse care are at greater risk for negative health behavior change. Results have implications for the identification of caregivers who may be particularly vulnerable to the negative health impact of caregiving.


Subject(s)
Caregivers , Health Behavior , Self Care , Aged , Alcohol Drinking , Body Weight , Caregivers/psychology , Cost of Illness , Exercise , Female , Humans , Male , Mental Disorders , Sleep , Smoking , Spouses/psychology
20.
Gerontologist ; 37(3): 355-64, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9203759

ABSTRACT

This study provides a review and analysis of the empirical research published since 1985 that has examined the impact of race, culture, and/or ethnicity on the dementia caregiving experience. Ten of the 12 studies included in the review focused on comparisons between Black and White caregivers; one examined differences between Black and Hispanic caregivers, and one focused on White and Hispanic caregivers. Compared to White caregivers, non-White caregivers: a) were less likely to be a spouse and more likely to be an adult child, friend, or other family member, b) reported lower levels of caregiver stress, burden, and depression, c) endorsed more strongly held beliefs about filial support, and d) were more likely to use prayer, faith, or religion as coping mechanisms. Strategies for advancing research in this area are discussed.


Subject(s)
Alzheimer Disease/nursing , Caregivers/psychology , Cross-Cultural Comparison , Black or African American/psychology , Aged , Data Collection , Female , Hispanic or Latino/psychology , Humans , Male , Stress, Psychological , White People/psychology
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