ライフサイエンスコーパス: caregiver

1 regivers may benefit both the person and the caregiver.

2 tal and physical health (well-being) for the caregiver.

3 th a positive provider recommendation to the caregiver.

4 uality of Life-5 Dimensions [EQ-5D]) for the caregiver.

5 Short Form-12 health survey [SF-12]) for the caregiver.

6 r Ebola virus disease (EVD) and accompanying caregivers.

7 identify elderly stroke survivors and their caregivers.

8 o TCSs experienced by patients and patients' caregivers.

9 for 3 years); 194 patients had participating caregivers.

10 they receive and the implications for stroke caregivers.

11 ts with Alzheimer disease and their informal caregivers.

12 3) identify coping strategies used by family caregivers.

13 ng results seem to have a relevant impact on caregivers.

14 ship issues and include friends, family, and caregivers.

15 ntia to recognize the unique needs of family caregivers.

16 in patients with atopic dermatitis or their caregivers.

17 nd interdependent between patients and their caregivers.

18 12731 patients (mean age, 67 years) and 2479 caregivers.

19 ldren's overall health status as reported by caregivers.

20 ed up to 1 year and did not decrease in some caregivers.

21 en, highlighting the importance of advice to caregivers.

22 ple with life-limiting illness and for their caregivers.

23 as well as education provided to the primary caregivers.

24 between patients with dementia and familial caregivers.

25 s and behavioural problems reported by their caregivers.

26 the percentage of committed and uncommitted caregivers.

27 6.9%]; median hospital stay, 21 days) and 94 caregivers, 157 (98.1%) and 89 (94.7%), respectively, co

28 lescents 40.7%, 95% CI 25.7%-55.6%; children/caregivers 18.5%, 95% CI 10.3%-26.8%), and a change to d

29 , 2014, and Jan 5, 2015, we interviewed 1980 caregivers, 21% of whom were "uncommitted" to accepting

30 (adults 13.6%, 95% CI 11.9%-15.3%; children/caregivers 22.3%, 95% CI 10.2%-34.5%).

31 adolescents 32.4%, 95% CI 0%-75.0%; children/caregivers 26.3%, 95% CI 15.3%-37.4%).

32 lescents 63.1%, 95% CI 46.3%-80.0%; children/caregivers 29.2%, 95% CI 20.1%-38.4%), being away from h

33 th professionals) and Hong Kong (10 patients/caregivers; 45 health professionals).

34 r consensus workshops in Boston (17 patients/caregivers; 52 health professionals) and Hong Kong (10 p

35 likely than white stroke survivors to have a caregiver (62.5% versus 49.7%; P<0.01) and received on a

36 table by both blinded caregivers and nurses (caregivers: 84% for the lorazepam + haloperidol group vs

37 udy should raise awareness in clinicians and caregivers about the unfavorable prognosis in the most d

38 nt communication with our patients and their caregivers about the very real and morbid consequences o

39 ts were English-speaking or Spanish-speaking caregivers accompanying minor children to nonacute medic

40 We then compared percentages of uncommitted caregivers among those with varying knowledge, attitudes

41 analysis was used to examine the relation of caregiver and child barriers and facilitators to their r

42 12.4% had no mention of AERD by any treating caregiver and were classified as "undiagnosed AERD." "Un

43 nd eighteen participants (461 [45%] patients/caregivers and 557 [55%] health professionals) from 79 c

44 Caregivers and adolescents reported contact with mental

45 hat family-based approaches that target both caregivers and children, encourage communication among t

46 of malaria using the CHWs was acceptable to caregivers and communities.

47 arding this diagnosis on the part of medical caregivers and families.

48 In a 3-round Delphi survey, patients/caregivers and health professionals rated the importance

49 n based on the shared priorities of patients/caregivers and health professionals.

50 Caregivers and interviewers were not masked.

51 rk in understanding the associations between caregivers and LVAD patients, as well as interventions t

52 eived to be more comfortable by both blinded caregivers and nurses (caregivers: 84% for the lorazepam

53 use, delirium recall, comfort (perceived by caregivers and nurses), communication capacity, delirium

54 14, 2013, and Oct 17, 2014, we enrolled 2018 caregivers and their infants from 152 villages into the

55 ons are associated with substantial patient, caregiver, and economic costs.

56 evidence now strongly suggests that parents, caregivers, and families need to be supported in providi

57 nt of patients with glioma, for patients and caregivers, and for health-care providers in Europe.

58 s a great burden for elderly patients, their caregivers, and health systems.

59 were high, equally prevalent in patients and caregivers, and interdependent between patients and thei

60 Participants, caregivers, and outcome assessors were blinded.

61 logy clinicians, patients, family and friend caregivers, and palliative care specialists to update th

62 of MNS disorders on affected persons, their caregivers, and society.

63 senting a substantial burden on individuals, caregivers, and society.

64 Patients, caregivers, and study personnel, including those assessi

65 been used by researchers to engage patients, caregivers, and the broader health care community in the

66 Allocation was concealed from participants, caregivers, and the research team.

67 Patients, caregivers, and those assessing blood pressure were blin

68 our and mood, interventions for the needs of caregivers, and timing of advance care planning.

69 inical researchers, clinicians, patients and caregivers, and U.S. federal research funding organizati

70 2688 fathers (83.4%), selecting other infant caregivers; and 11435 mothers (94.8%) and 3201 fathers (

71 Conclusion Informal caregivers are an important part of the care team and th

72 , compared with their relevant counterparts, caregivers are more likely to be uncommitted if they did

73 Additionally, female caregivers are most likely to employ coping strategies,

74 Patients and caregivers are now considered vital members of the study

75 Engaging informal cancer caregivers as part of the care team and conducting ongoi

76 s trial underscores the burden undertaken by caregivers as they provide care for family members with

77 is a clinical emergency, and patients, their caregivers as well as all healthcare professionals shoul

78 dings highlight the importance of caring for caregivers as well as patients when attempting to improv

79 aseline, 2 weeks, and 3 months after HCT and caregiver-assessed QOL and mood at baseline and 2 weeks

80 ures: Change in reported social needs and in caregiver assessment of child's overall health reported

81 Healthcare provider and caregiver attitudes and practices indicated concerns abo

82 In caregivers, BMI was associated positively only with tota

83 conducted to examine the association between caregiver body mass index (BMI) or child BMI z score and

84 7.45; 95% CI, -11.08 to -3.81; P < .001) and caregiver burden (b = -0.50; 95% CI, -1.09 to 0.08; P =

85 e of people with dementia living at home and caregiver burden (when available).

86 y (Clinical Global Impressions Scale [CGI]), caregiver burden (Zarit Burden Scale), and depression (C

87 Effective interventions to reduce family caregiver burden are poorly understood but family caregi

88 pairment, higher service utilization, higher caregiver burden, and increased mortality.

89 Health-care costs and, importantly, caregiver burden, are also reported to be higher in deme

90 Quality of life, caregiver burden, behavioral and psychological symptoms

91 improvement in cognition, functional status, caregiver burden, CGI scores, and depression in the meth

92 also improved cognition, functional status, caregiver burden, CGI scores, and depression.

93 ses and female caregivers experience greater caregiver burden, distress, increased rates of depressio

94 titude, and experiences) of palliative care, caregiver burden, family function, patient quality of li

95 There were significant improvements in caregiver burden, mental health, and depression after po

96 Outcomes were caregiver burden, quality of life, and depression.

97 quality of life, knowledge and satisfaction, caregiver burden, time tradeoffs, and out-of-pocket cost

98 tion of care have resulted in an epidemic of caregiver burden.

99 nmental challenge or maintain proximity to a caregiver but also contribute to behavioral pathology.

100 d at least partially with time in 84% of the caregivers but did not in 16%.

101 Associations between caregiver characteristics and patient mortality and morb

102 No caregiver characteristics were significantly associated

103 The authors enrolled 1,016 caregiver-child dyads.

104 eting the DGA in a national, large sample of caregiver-child dyads.

105 Of the 300 caregiver-child pairs, 153 (51.0%) were randomly assigne

106 16 countries across six continents, patients/caregivers, clinicians, and research funders.

107 We aimed to determine caregivers' commitment to OPV in districts of Afghanista

108 havior Questionnaires were also completed by caregivers.Compared with placebo, prebiotic intake resul

109 blood for plasma FA quantification, and the caregiver completed demographic and activity questionnai

110 Parents or caregivers completed a questionnaire on general and dent

111 Caregivers completed the Brief Problem Monitor-Parent Fo

112 Of 717 parents/caregivers completing FSIs, 185 (25.8%) reported a total

113 Parent or caregiver consent was obtained for 1531 children (95%),

114 Overall, 746 parents/caregivers consented for the study.

115 This finding will be important for women and caregivers considering preventive strategies.

116 How caregivers contribute to positive or negative outcomes f

117 Women and caregivers could not be masked, but those adjudicating o

118 it appears that increasing independence from caregivers cues the termination of the sensitive period

119 However, no previous studies have evaluated caregiver-delivered CST.

120 Caregivers delivering iCST received training and support

121 ze and intermittent lip-smacking) with human caregivers display increased social interest at 2 months

122 In 176 patient-caregiver dyads, we found that worse caregiver mental he

123 gement of symptoms and concerns, patient and caregiver education, and sensitive communication to elic

124 prescribing peer-review meetings, and brief caregiver education.

125 Interventions: After standardized screening, caregivers either received written information on releva

126 6-3.28; p = 0.02), and iCST improved QoL for caregivers (EQ-5D, MD = 0.06, 95% CI 0.02-0.10; p = 0.01

127 ng can also be extremely stressful, and many caregivers experience declines in mental health.

128 Spouses and female caregivers experience greater caregiver burden, distress

129 This examination of caregiver experiences across insurance types revealed im

130 Despite most caregivers expressing hesitation regarding children rece

131 in functioning; thus, many patients require caregivers for assistance with daily living.

132 38 14-year-old adolescents and their primary caregivers from 18 secondary schools in Cambridgeshire,

133 sought to develop and validate a measure of caregivers' functional status during a preschooler's ast

134 Few instruments exist to measure caregivers' functional status during a young child's ast

135 preschoolers' asthma exacerbations on their caregivers' functional status.

136 Compared with health professionals, patients/caregivers gave higher priority to 6 outcomes (mean diff

137 0.82; p = 0.97) for people with dementia, or caregivers' general health status (MD = 0.13, 95% CI -1.

138 at least one category on the seven-category Caregiver Global Impression of Change scale in 62% of th

139 level of treatment aligns with patients' and caregivers' goals and values.

140 Results Patients whose informal caregiver had higher levels of depressive symptoms were

141 t had dose interruption for 2 doses based on caregiver hardship and one patient had treatment interru

142 Interpretation: Community-based support for caregivers has high potential for scalability and could

143 g a child who shared utensils with a primary caregiver (hazards ratio [HR], 2.33; 95% confidence inte

144 plore the impact of providing care on family caregivers' health and well-being, and (3) identify copi

145 help patients with advanced cancer and their caregivers identify and bring up topics of concern, incl

146 ese infants can encounter hurdles may assist caregivers in identifying a potential cause or causes fo

147 ngaging both patients and their families and caregivers in more active partnerships with providers to

148 atric outpatients by targeting providers and caregivers in primary care hospitals in rural China.

149 area among households with pregnant women or caregivers in rural villages with low piped water access

150 ases is emphasized, including involvement of caregivers in the context of managing these patients wit

151 In addition, caregivers in the intervention arm reported significantl

152 Caregivers in the intervention group reported lower leve

153 Studies that involved caregivers in the intervention produced effect sizes (n

154 Nurses are principal caregivers in the neonatal intensive care unit and suppo

155 the psychiatric health of both patients and caregivers in the neuroscience ICU is a priority and tha

156 to represent the roles of both patients and caregivers in the system.

157 s and uncertain outcomes between parents and caregivers in the treatment of infants with T18 and T13.

158 h include engaging and involving parents and caregivers in their treatment.

159 ervices to patients with cancer and/or their caregivers, including family caregivers, were found to i

160 at providing mobile health intervention to a caregiver increased the strength of the intervention eff

161 Patients, parents and caregivers, investigational site personnel, PTC Therapeu

162 0%-14% lower if productivity loss of parents/caregivers is excluded, (ii) 58%-84% higher if the willi

163 evaluate the effectiveness of a home-based, caregiver-led individual cognitive stimulation therapy (

164 of cognitive stimulation delivered by family caregivers may benefit both the person and the caregiver

165 r relatives (hereafter simply referred to as caregivers [mean age, 36.0 years]) who brought the child

166 The caregivers' mean age was 53 years, 70% were women, and 6

167 In this study, we investigated the role that caregiver mental health plays in patient mortality.

168 patient-caregiver dyads, we found that worse caregiver mental health predicted greater patient mortal

169 iving iCST rated the relationship with their caregiver more positively (MD = 1.77, 95% CI 0.26-3.28;

170 For caregivers, most of the barriers to meeting recommendati

171 CU is a priority and that patients and their caregivers must be considered together in a system to fu

172 0.39) larger than those that did not include caregivers (n = 21; Cohen d = 0.13; 95% CI, 0.02-0.25).

173 dergoing autologous/allogeneic HCT and their caregivers (n = 94).

174 Unmet patient and caregiver needs include effective pharmacological and ps

175 Navigating requests from parents or family caregivers not to disclose poor prognosis to seriously i

176 ely to be securely attached to their primary caregiver (odds ratio [OR] = 1.7, p = 0.029, 95% CI [1.0

177 rvention, 150 standard care) and 343 primary caregiver of a child aged 0-59 months with recent diarrh

178 ospective cohort study including the parents/caregivers of 989 hospitalized patients 17 years and you

179 rvention, 167 standard care) and 410 primary caregivers of a child 0-59 months with recent diarrhoea

180 an infant younger than 6 months and primary caregivers of a child younger than 5 years with recent d

181 d negative aspects of caregiving reported by caregivers of black and white stroke survivors.

182 Caregivers of black stroke survivors reported more posit

183 Despite providing more hours of care, caregivers of black stroke were more positive about thei

184 ants included youths aged 10 to 17 years and caregivers of children aged 0 to 9 years.

185 he effect of economic incentives provided to caregivers of children aged 8-17 years on uptake of HIV

186 challenges in access to specialty care, with caregivers of children insured by CHIP reporting the hig

187 ut-of-pocket costs (77% [75%-78%]) than were caregivers of children insured by Medicaid (26% [23%-28%

188 ealth care services (36% [32%-41%]) than did caregivers of children insured by Medicaid, and a lower

189 d a poll using face-to-face interviews among caregivers of children under 5 years of age.

190 f they were aged 15-49 years or were primary caregivers of children younger than 5 years.

191 In this study, most caregivers of critically ill patients reported high leve

192 A multidisciplinary supportive program for caregivers of heart failure patients had positive effect

193 ss the effect of community-based support for caregivers of HIV-infected children and adolescents, who

194 We prospectively enrolled 280 caregivers of patients who had received 7 or more days o

195 Few resources are available to support caregivers of patients who have survived critical illnes

196 Family caregivers of patients with chronic critical illness exp

197 Providers may refer family and friend caregivers of patients with early or advanced cancer to

198 Family caregivers of patients with frontotemporal dementia expe

199 Family caregivers of patients with frontotemporal dementia face

200 Family caregivers of patients with frontotemporal dementia iden

201 : (1) identify the characteristics of family caregivers of patients with frontotemporal dementia, (2)

202 valuating the health and wellbeing of family caregivers of patients with frontotemporal dementia.

203 Caregivers of patients with heart failure experience bur

204 Caregivers of privately insured children were also signi

205 HFs located within the 12 zones and cited by caregivers of the enrolled infants as the most recent HF

206 of these conditions may inform patients and caregivers of the expected disease duration and may help

207 ted more positive aspects of caregiving than caregivers of white stroke survivors (6.8 versus 6.0; P<

208 ore positive about their caregiver role than caregivers of white stroke survivors.

209 All patients achieved administration by a caregiver or self-injection by week 14.

210 Children who are neglected by caregivers or raised in institutional environments are d

211 ns of ASD have been raised by parents, other caregivers, or health care professionals.

212 Caregiver oral health knowledge scores improved in both

213 variables were consistently associated with caregiver outcomes over time.

214 Findings for caregiver outcomes were inconsistent.

215 ther than prognosis, can improve patient and caregiver outcomes.

216 survived critical illness; consequently, the caregivers' own health may suffer.

217 ve the quality of life of patients and their caregivers, particularly in the end-of-life phase.

218 ) shared environment; 3) parenting style; 4) caregiver perceptions; and 5) genomics.

219 ve assessment and integration of patient and caregiver perspectives into trial design.

220 ver, there was no significant improvement in caregivers' physical health at either 3 or 6 months foll

221 ange intervention using emotional drivers on caregiver practice of these behaviours.

222 Complex caregiver practices can improve through interventions bu

223 rstanding of patient severity of illness and caregiver presence.

224 n was used to assess the association between caregiver psychosocial factors and subsequent patient-pe

225 e quality of the caregiving relationship and caregivers' QoL.

226 aire-39 and EuroQol-5D); adverse events; and caregiver quality of life.

227 om the perspectives of the person and of the caregiver (Quality of the Carer Patient Relationship Sca

228 edge of HIV status was ascertained through a caregiver questionnaire, and anonymised HIV testing was

229 mal newborn screening, self-referred after a caregiver raises concern, or identified to be at risk of

230 Patients or their caregivers recorded events in a seizure diary throughout

231 ad advanced nonhematologic cancer (and their caregivers) recruited from practices of 24 participating

232 re model that improves relevant patient- and caregiver-related outcomes in dementia.

233 ects of environmental experiences related to caregiver relationships because it is these experiences,

234 h the Frontal Systems Behavior Scale (FrSBe: caregiver-report based).

235 ildren with special health care needs, whose caregivers reported significantly greater problems acces

236 g 73 infants not vaccinated with IPV, 58% of caregivers reported that vaccine was unavailable.

237 Primary caregivers reported the frequency with which children co

238 e and direction of change in performance and caregiver-reported attention difficulties differed signi

239 setting in western Rwanda, had no effect on caregiver-reported diarrhoea among children younger than

240 dren younger than 5 years, the prevalence of caregiver-reported diarrhoea in the previous 7 days was

241 ortion of children younger than 2 years with caregiver-reported diarrhoea within the past 7 days.

242 The primary outcome was caregiver-reported diarrhoea within the previous 7 days

243 Caregiver-reported history of eczema, asthma, hay fever,

244 Insurance type was ascertained using a caregiver-reported measure of insurance status and each

245 They compared caregiver-reported NPI scores at week 9 in patients rece

246 variable logistic regression models compared caregiver-reported outcomes across insurance types.

247 Caregiver-reported outcomes related to access to primary

248 Outcomes were caregiver-reported use of sun protection by the child (s

249 served at 4 months after enrollment included caregivers' reports of social needs and child health sta

250 nts from 16 countries, including patient and caregiver representatives.

251 black stroke were more positive about their caregiver role than caregivers of white stroke survivors

252 at in part, children utilize their perceived caregiver's choices when making choices for themselves,

253 justment for age, race/ethnicity, and parent/caregiver's education, the mean difference between hyper

254 were high and comparable between patient and caregiver samples.

255 An awake, trained caregiver should be present at all times, and at least t

256 resent at all times, and at least two family caregivers should be trained specifically for the child'

257 Examining flexibility and variation in caregiver socialization and children's learning extends

258 (SIAs) after JAP interventions and compared caregivers' sources of information about SIAs in 2007 be

259 icrobial stewardship targeting providers and caregivers substantially reduced prescribing of antibiot

260 iver burden are poorly understood but family caregivers suggest education and internet-based support

261 few longitudinal studies suggest that early caregiver support also impacts human hippocampal develop

262 rimary study objectives were to (1) identify caregiver support attributes through a retrospective cha

263 nd emotional development, including observed caregiver support.

264 ance records from all provinces, and (iii) a caregiver survey on the household costs and health utili

265 apacity for instant alerts to be sent to the caregiver team.

266 rs, acute respiratory failure survivors, and caregivers that rated the importance of 19 preliminary o

267 preferences and social affiliation with the caregiver to avoidance of predator odors.

268 o difference in the time used by the child's caregiver to care for a sick child (59% before intervent

269 d in CanCORS (N = 689) nominated an informal caregiver to participate in a caregiving survey.

270 prevention and control of diarrhoea requires caregivers to comply with a suite of proven measures, in

271 Traditional home monitoring requires caregivers to record measurements of weight and oxygen s

272 dren in LMICs who would be reported by their caregivers to show low cognitive and/or socioemotional d

273 seases in the specific country by developing caregivers, trainers, researchers, and administrators at

274 ortality after LVAD placement is impacted by caregiver understanding of patient severity of illness a

275 care for patients with dementia and support caregivers using a computer-assisted assessment determin

276 ntion intervention may depend on patient and caregiver values and preferences.

277 Parking costs, transportation, caregiver wages, and lost wages were not considered in o

278 The initial observation by parents/caregiver was reduced vision (n = 1), red eye (n = 1), o

279 lity of multiple injections by providers and caregivers was summarized, and a systematic review of th

280 of life (OHRQoL) in children with cleft and caregiver well-being.

281 prevent secondary complications, and enhance caregiver well-being.

282 treatment, thereby increasing patients' and caregivers' well-being.

283 Caregivers were eligible if they had a child younger tha

284 Health-care providers and caregivers were interviewed at 42 health facilities in A

285 ple with mild to moderate dementia and their caregivers were recruited from memory services and commu

286 ociated with worse mental health outcomes in caregivers were younger age, greater effect of patient c

287 er and/or their caregivers, including family caregivers, were found to inform the update.

288 r children, barriers were mainly reported by caregivers, which may not correspond to the most importa

289 documented by the social worker; P=0.01), a caregiver who has identified a backup plan (P=0.02), and

290 has identified a backup plan (P=0.02), and a caregiver who is able to provide logistical support (P=0

291 Having a caregiver who understands the severity of the illness an

292 During early 2007, the number of caregivers who had heard about SIA rounds from the media

293 Over half of caregivers whose children got 3 or more injectable vacci

294 care significantly associated with increased caregiver willingness to endorse palliative care and wit

295 below the median; OR 1.26, 1.16-1.39), had a caregiver with any education (vs no education; OR 1.31,

296 ment of simple diagnostic tests that provide caregivers with reliable, immediately actionable informa

297 teract with the environment, older adult and caregiver within the case scenario.

298 3 health facilities, 36 vaccinators, and 336 caregivers, within 5 districts and 3 city corporations.

299 ologists, patients with advanced cancer, and caregivers would promote patient-centered communication,

300 and AMED, using the search terms (1) family, caregivers, young adult, adolescent; (2) adolescent deve