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1.
J Holist Nurs ; 42(1): 64-78, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37128683

ABSTRACT

Purpose: To evaluate effectiveness of chairside yoga therapy on perceptions of fatigue, pain, nausea, anxiety, and distress among oncology patients concurrently receiving outpatient cancer infusion therapy. Design: This prospective pilot study used pre-/post-survey design in convenience sample of cancer patients in outpatient setting. Methods: Researchers developed and administered the Outpatient Cancer Symptom Assessment Scale (OCSAS) comprised of cancer- or treatment-related symptoms commonly reported in the oncology population (nausea, pain, fatigue, anxiety, and distress). Following IRB approval, symptoms were rated using Likert scale of 0 (not present) to 10 (severe) before and after chairside yoga therapy delivered concurrently with outpatient infusions. Qualitative data was collected related to patients' overall infusion experience. Findings: Participants (n = 82) reported positive patient experiences and statistically less pain (p < 0.001), fatigue (p < 0.001), anxiety (p < 0.001), and distress (p < 0.001) following the yoga intervention compared to baseline. Nausea was not significantly impacted by the yoga intervention. Conclusions: Yoga therapy received concurrently during outpatient cancer infusion is consistent with a holistic and integrative approach to care for the oncology population. Yoga therapy offers promise for reducing symptoms which negatively impact quality of life, including pain, fatigue, anxiety, and distress. Qualitative data suggests patients' overall infusion experience was enhanced with yoga therapy.


Subject(s)
Neoplasms , Yoga , Humans , Outpatients , Quality of Life , Feasibility Studies , Pilot Projects , Prospective Studies , Depression/therapy , Anxiety/therapy , Neoplasms/complications , Neoplasms/therapy , Pain , Fatigue/etiology , Fatigue/therapy , Nausea
3.
Psychiatr Clin North Am ; 38(2): 333-52, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25998120

ABSTRACT

The goal of the Care Pathway Model for Dementia (CARE-D) is to improve quality of life and daily functioning both for individuals diagnosed with dementia and for their families or other caregivers. This is accomplished by developing individualized recommendations focused on a person's strengths and weaknesses as determined by formal neurocognitive and psychosocial evaluations. Careful attention is given to the stage of illness and an individual's stage in life, to connecting families with services that target an individual's cognitive and behavioral symptoms, and to providing education and emotional support specific to symptoms, clinical diagnosis, and prognosis.


Subject(s)
Alzheimer Disease , Behavioral Symptoms , Frontotemporal Dementia , Psychological Techniques , Quality of Life , Age of Onset , Alzheimer Disease/diagnosis , Alzheimer Disease/psychology , Alzheimer Disease/rehabilitation , Alzheimer Disease/therapy , Behavioral Symptoms/diagnosis , Behavioral Symptoms/therapy , Caregivers/psychology , Emotional Intelligence , Frontotemporal Dementia/diagnosis , Frontotemporal Dementia/psychology , Frontotemporal Dementia/rehabilitation , Frontotemporal Dementia/therapy , Humans , Neuropsychological Tests , Social Support
4.
PLoS One ; 10(4): e0122608, 2015.
Article in English | MEDLINE | ID: mdl-25886645

ABSTRACT

BACKGROUND: Japanese encephalitis (JE) virus (JEV) is a mosquito-borne flavivirus found across Asia that is closely related to West Nile virus. There is no known antiviral treatment for any flavivirus. Results from in vitro studies and animal models suggest intravenous immunoglobulin (IVIG) containing virus-specific neutralizing antibody may be effective in improving outcome in viral encephalitis. IVIG's anti-inflammatory properties may also be beneficial. METHODOLOGY/PRINCIPAL FINDINGS: We performed a pilot feasibility randomized double-blind placebo-controlled trial of IVIG containing anti-JEV neutralizing antibody (ImmunoRel, 400mg/kg/day for 5 days) in children with suspected JE at two sites in Nepal; we also examined the effect on serum neutralizing antibody titre and cytokine profiles. 22 children were recruited, 13 of whom had confirmed JE; 11 received IVIG and 11 placebo, with no protocol violations. One child (IVIG group) died during treatment and two (placebo) subsequently following hospital discharge. Overall, there was no difference in outcome between treatment groups at discharge or follow up. Passive transfer of anti-JEV antibody was seen in JEV negative children. JEV positive children treated with IVIG had JEV-specific neutralizing antibody titres approximately 16 times higher than those treated with placebo (p=0.2), which was more than could be explained by passive transfer alone. IL-4 and IL-6 were higher in the IVIG group. CONCLUSIONS/SIGNIFICANCE: A trial of IVIG for JE in Nepal is feasible. IVIG may augment the development of neutralizing antibodies in JEV positive patients. IVIG appears an appealing option for JE treatment that warrants further study. TRIAL REGISTRATION: ClinicalTrials.gov NCT01856205.


Subject(s)
Antibodies, Neutralizing/therapeutic use , Encephalitis, Japanese/drug therapy , Immunoglobulins, Intravenous/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Antibodies, Neutralizing/blood , Child , Child, Preschool , Dexamethasone/therapeutic use , Double-Blind Method , Encephalitis Virus, Japanese/immunology , Encephalitis, Japanese/pathology , Enzyme-Linked Immunosorbent Assay , Female , Follow-Up Studies , Humans , Infant , Interleukin-4/blood , Interleukin-6/blood , Male , Nepal , Placebo Effect , Treatment Outcome
5.
Perspect Gerontol ; 17(2): 37-49, 2012 May.
Article in English | MEDLINE | ID: mdl-26500714

ABSTRACT

In this article, we explore the symptoms, cause, treatment potential, and supportive services for individuals diagnosed with Primary Progressive Aphasia (PPA). Although it is possible to regain certain cognitive abilities with stroke or brain injury, in PPA, language abilities worsen and other symptoms emerge with time, shortening the lifespan. The goal of speech therapy for PPA is not to regain lost language, but rather to maximize communication for as long as possible. In this article, we offer information and tools for speech-language pathologists to help people living with PPA achieve these goals and improve overall quality of life.

6.
Am J Trop Med Hyg ; 83(5): 1146-55, 2010 Nov.
Article in English | MEDLINE | ID: mdl-21036854

ABSTRACT

We evaluated performance of three commercial Japanese encephalitis virus (JEV) IgM antibody capture enzyme-linked immunosorbent assay (MAC ELISA) kits with a panel of serological specimens collected during a surveillance project of acute encephalitis syndrome in India and acute meningitis and encephalitis syndrome in Bangladesh. The serum and cerebral spinal fluid specimens had been referred to the Centers for Disease Control and Prevention (CDC) for confirmatory testing. The CDC results and specimen classifications were considered the reference standard. All three commercial kits had high specificity (95-99.5%), but low sensitivities, ranging from 17-57%, with both serum and cerebrospinal fluid samples. Specific factors contributing to low sensitivity compared with the CDC ELISA could not be determined through further analysis of the limits and dilution end points of IgM detection.


Subject(s)
Encephalitis Virus, Japanese/immunology , Encephalitis, Japanese/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Immunoglobulin M/blood , Immunoglobulin M/cerebrospinal fluid , Antibodies, Viral/blood , Antibodies, Viral/cerebrospinal fluid , Encephalitis, Japanese/immunology , Humans , Reagent Kits, Diagnostic , Sensitivity and Specificity
7.
Am J Trop Med Hyg ; 83(2): 388-94, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20682888

ABSTRACT

Acute febrile illnesses comprise the majority of the human disease burden in sub-Saharan Africa. We hypothesized that arboviruses comprised a considerable proportion of undiagnosed febrile illnesses in Guinea and sought to determine the frequency of arboviral disease in two hospitals there. Using a standard case definition, 47 suspected cases were detected in approximately 4 months. Immunoglobulin M antibody capture enzyme-linked immunosorbent assays and plaque-reduction neutralization assays revealed that 63% (30/47) of patients were infected with arboviruses, including 11 West Nile, 2 yellow fever, 1 dengue, 8 chikungunya, and 5 Tahyna infections. Except for yellow fever, these are the first reported cases of human disease from these viruses in Guinea and the first reported cases of symptomatic Tahyna infection in Africa. These results strongly suggest that arboviruses circulate and are common causes of disease in Guinea. Improving surveillance and laboratory capacity for arbovirus diagnoses will be integral to understanding the burden posed by these agents in the region.


Subject(s)
Arbovirus Infections/epidemiology , Arboviruses/isolation & purification , Acute Disease , Adult , Antibodies, Viral/blood , Arbovirus Infections/diagnosis , Arbovirus Infections/virology , Arboviruses/classification , Arboviruses/immunology , Enzyme-Linked Immunosorbent Assay , Female , Guinea/epidemiology , Humans , Immunoglobulin M/blood , Male , Middle Aged , Neutralization Tests , Young Adult
8.
Am J Trop Med Hyg ; 81(6): 1144-50, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19996450

ABSTRACT

Infection with Japanese encephalitis virus (JEV) is a major public health problem in Asia. Detection of JEV-specific IgM in serum and cerebrospinal fluid (CSF) by the IgM antibody capture enzyme-linked immunosorbent assay (MAC-ELISA) is currently the most widely used diagnostic method to detect JEV infection. Because of the possible presence of IgM cross-reactivity with other flaviviruses in serum and the high ratio of inapparent-to-apparent JEV infections, a positive result in serum only suggests a recent infection and not necessarily an encephalitic illness caused by JEV. Consequently, detection of JEV-specific IgM in CSF assumes great diagnostic relevance. We evaluated two commercial JEV MAC-ELISA kits using 60 CSF samples obtained from patients with acute encephalitis syndrome. The Panbio and XCyton kits had sensitivities of 65-80% and 95% and specificities of 90% and 97.5%, respectively. Performance information on these commercial JEV MAC-ELISA kits for CSF should assist in laboratory-based JE surveillance programs.


Subject(s)
Encephalitis Virus, Japanese/immunology , Encephalitis, Japanese/cerebrospinal fluid , Encephalitis, Japanese/virology , Enzyme-Linked Immunosorbent Assay/methods , Immunoglobulin M/immunology , Reagent Kits, Diagnostic/standards , Adolescent , Adult , Aged , Child , Child, Preschool , Encephalitis, Japanese/immunology , Female , Humans , Male , Middle Aged , Young Adult
9.
Trop Med Int Health ; 14(11): 1365-73, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19747185

ABSTRACT

OBJECTIVES: To describe the results from two years of Japanese encephalitis (JE) sentinel surveillance in Cambodia. METHODS: Sentinel site surveillance for JE in children aged 15 years and under was implemented in Cambodia in mid-2006. It was integrated into the routine meningoencephalitis surveillance system. Six hospitals were selected as sentinel sites. Epidemiological information and diagnostic specimens were collected from each patient presenting with meningoencephalitis. Cerebrospinal fluid and sera were tested for presence of immunoglobulin M antibodies against JE and dengue viruses by an ELISA. Surveillance data from 2006 to 2008 were analysed. RESULTS: Of 586 patients presenting with meningoencephalitis, 110 (19%) were confirmed to have JE. The percentage of confirmed JE cases at individual sentinel sites ranged from 13% to 35% of all meningoencephalitis cases. Mean age was 6.2 years, with 95% of JE cases in children aged 12 years and under. Cases occurred year-round in both 12-month reporting periods. CONCLUSIONS: JE is an important cause of meningoencephalitis in Cambodian children. As JE is a vaccine-preventable disease, an immunization programme could result in a considerable reduction in morbidity and mortality from JE among children in Cambodia.


Subject(s)
Encephalitis, Japanese/epidemiology , Meningoencephalitis/epidemiology , Sentinel Surveillance , Adolescent , Cambodia/epidemiology , Child , Child, Preschool , Encephalitis, Japanese/diagnosis , Encephalitis, Japanese/prevention & control , Humans , Immunoglobulin M/blood , Immunoglobulin M/cerebrospinal fluid , Incidence , Japanese Encephalitis Vaccines/therapeutic use , Meningoencephalitis/prevention & control , Meningoencephalitis/virology , Seasons
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