ライフサイエンスコーパス: caregiver

1 taneous injections in their homes by trained caregivers.

2 hildren is still distinct from that of their caregivers.

3 ancer and reduces the risk of depression for caregivers.

4 oblems and 34.9 years (range 8-75 years) for caregivers.

5 range of intervention strategies to support caregivers.

6 nterviewed: 24 children, 39 teenagers and 44 caregivers.

7 rlier detected cognitive impairment or their caregivers.

8 ents with hematologic malignancies and their caregivers.

9 ort, and resulted in a high workload for the caregivers.

10 ls to transform kidney care for patients and caregivers.

11 ter decisional conflict in both patients and caregivers.

12 nd provide medical education to patients and caregivers.

13 5 children, and family planning practices of caregivers.

14 play distinct attachment styles toward human caregivers.

15 new phase in the process of caring by family caregivers.

16 rgenic food, causing a sense of defeat among caregivers.

17 ecause of the lack of perceived benefits for caregivers.

18 the impact of MCS caregiving on patients and caregivers.

19 orks influence QoL of MCS patients and their caregivers.

20 caregiving affects QoL for both patients and caregivers.

21 skills training, and education materials for caregivers.

22 e burden of measurement and documentation on caregivers.

23 morbidity in affected individuals and their caregivers.

24 onsiderable impact on the quality of life of caregivers.

25 e this to the child, and to their parents or caregivers.

26 expressed more positive responses than white caregivers.

27 g and intervention strategies for supporting caregivers.

28 eat and major stressor to patients and their caregivers.

29 th detrimental consequences for patients and caregivers.

30 routine care of patients with ESLD and their caregivers.

31 ehaviors and reducing anxiety among informal caregivers.

32 mmon and can create difficult situations for caregivers.

33 serious illness-related suffering and their caregivers.

34 may account for stress resilience in family caregivers.

35 Only saliva samples were collected from the caregivers.

36 psychosocial impact of PA on PwPA and their caregivers.

37 pectives of persons with PA (PwPA) and their caregivers.

38 om sample collection to return of results to caregivers (0 vs 55 days; p<0.0001), the number of infan

39 We presented morph videos of the caregiver, a familiar person, and a stranger showing eit

40 t from discussions with their clinicians and caregivers about goals, barriers, and strategies regardi

41 Caregiver acceptance was assessed by asking nurses, tech

42 Regardless of emotion, viewing the caregiver activated brain regions associated with emotio

43 dies including more than 240 000 patients or caregivers addressed the treatment of MCI or mild to mod

44 nguage input that infants receive from their caregivers affects their future language abilities; howe

45 partnerships needed to care for patients and caregivers after medical stabilization.

46 participants were mothers or female primary caregivers aged 15 years or older with children aged 6-2

47 n established relationships, fathers or male caregivers aged 18 years or older were also eligible.

48 ren are frequently cared for by non-parental caregivers (alloparents), yet few studies have conducted

49 r or greater than that of pain (P < 0.05 for caregiver and nurse ratings).

50 luate HF caregiving interventions to support caregiver and patient outcomes; (4) summarize existing p

51 elationship change, strain, and burden (both caregiver and patient perceived).

52 Effects of caregiving on the caregiver and patient range from physical and psychologi

53 y was collected through verbal recall by the caregiver and, when available, by HBR.

54 ting to QoL were conducted with patients and caregivers and analyzed using a 2-phase thematic process

55 nts live the day-to-day of recovery, whereas caregivers and clinicians also contemplate more expansiv

56 al domains overlap within patients and their caregivers and contribute to conflict around the decisio

57 Infant dietary data was collected from caregivers and dietary pattern trajectories from 6 to 12

58 ully understand the experiences and needs of caregivers and effective interventions in order to bette

59 nd further places an untenable strain on the caregivers and families of those afflicted.

60 greater understanding of PA impact on PwPA, caregivers and family members and the need for improved

61 ts the importance of the interaction between caregivers and infants and toddlers related to child fee

62 23% caregivers) and rescreening a subset of caregivers and noncaregivers matched on sociodemographic

63 We sought to elicit patients', caregivers', and health care providers' perceptions of h

64 caregiver status (1997-1999; n = 4,036; 23% caregivers) and rescreening a subset of caregivers and n

65 Sensitivity, specificity; patient, caregiver, and clinician decision-making; patient functi

66 ncorporates findings from NHLBI-led patient, caregiver, and clinician focus groups.

67 l were the number of years staff worked as a caregiver, and resident age, gender, and eating function

68 dities, the relationship between patient and caregiver, and the complexity of the treatment regimen.

69 lth (mHealth) applications provide patients, caregivers, and administrators continuous information ab

70 significant burden to affected individuals, caregivers, and an ageing population.

71 r ICU survivor care and their primary family caregivers, and assess mortality, readmission rates, and

72 ts or collecting data, and the participants, caregivers, and assessors were masked to allocation.

73 te services, online connections to other PID caregivers, and bedside mental health services.

74 c data were collected from patients or their caregivers, and clinical and outcome data were retrieved

75 Patients, caregivers, and evaluators were all masked to treatment.

76 ients with medulloblastoma, for patients and caregivers, and for health-care providers in Europe.

77 ients with diffuse gliomas, for patients and caregivers, and for health-care providers.

78 a considerable economic burden on patients, caregivers, and health facilities in Nepal.

79 asurable benefits for patients, their family caregivers, and health services.

80 nel of 14 researchers, clinicians, patients, caregivers, and health system leaders.

81 ric fever from the perspectives of patients, caregivers, and healthcare providers.

82 Patients, caregivers, and investigators were masked to treatment a

83 n Results: Dyspnea was assessed by patients, caregivers, and nurses with a numerical rating scale.

84 f untold numbers of researchers, clinicians, caregivers, and patients.

85 ich places a substantial burden on patients, caregivers, and physicians.

86 citation system of care to include patients, caregivers, and rehabilitative healthcare partnerships,

87 effective coping strategies in patients and caregivers, and review evidence supporting the beneficia

88 , use measures validated for advanced cancer caregivers, and test real-world interventions.

89 sting policies and resources that support HF caregivers; and (5) identify knowledge gaps and future d

90 Interventions to decrease caregiver anxiety and reaction frequency may help reduce

91 ter group also improved on self-reported and caregiver apathy assessments (P = 0.03 and P = 0.02, res

92 ntions, interaction and communication style, caregiver approach, bathing techniques, abilities focuss

93 sistent with the hypothesis that infants and caregivers are foraging vocally for social input.

94 ical and emotional needs of MCS patients and caregivers are identified and addressed.

95 Moreover, given that grandparent caregivers are more likely to report being depressed, it

96 Caregivers are often responsible for helping and support

97 adversity, including reduced efficacy of the caregiver as a safe haven.

98 caregivers in oncology settings: Considering caregivers as part of the unit of care, Assessing the ca

99 atisfaction between physicians, patients and caregivers as well as clinical outcomes in this populati

100 ile still not reaching the complexity of the caregivers at 4 y of age.

101 cal health effects of caregiving, identified caregivers at risk for adverse outcomes, and evaluated a

102 Nurses and patients' personal caregivers at the bedside reported on their perception o

103 Patients and caregivers attended to the personal recovery experience,

104 Lack of caregiver awareness about the 15- to 18-month visit and

105 in both the patient (beta=0.18; P<0.05) and caregiver (beta=0.28; P<0.001) was significantly related

106 esting these neurons facilitate offspring-to-caregiver bonding.

107 r caregivers resulted in a small benefit for caregiver burden (standardized mean difference, -0.24 [9

108 ten go unrecognised despite being related to caregiver burden and a decreased participation in societ

109 lity of life, and neuropsychiatric symptoms; caregiver burden and well-being.

110 e (for example decreased quality of life and caregiver burden).

111 lems associated with the regimen compromised caregivers' capacity to persist.

112 This study aims to understand caregiver challenges and identify areas for health care

113 o [OR], 1.86; 95% CI, 1.15-3.02) and in days caregiver changed plans (OR, 4.24; 95% CI, 2.33-7.70), w

114 ated at follow-up in separate LTR and family caregiver (collateral) assessments.

115 1 showed a significantly greater increase in caregivers compared with controls.

116 ence for the role of vocal interactions with caregivers, compared with overheard adult speech, in the

117 Their primary caregiver completed a validated 123-item quantitative FF

118 Patient and caregiver conflict over the decision to pursue an LVAD w

119 ient Health Questionnaire) and the CarCGQoL (Caregivers Congenital Glaucoma QOL Questionnaire).

120 lf-care of Chronic Illness Inventory and the Caregiver Contribution to Self-care of Chronic Illness I

121 Patient self-care and care partner (or caregiver) contributions to self-care are recommended to

122 improving the ways that patients and family caregivers cope together and manage problems as a dyad.

123 We collected patient and caregiver cost of illness information for 395 patients,

124 sional conflict (beta=0.16; P<0.05), whereas caregiver depression symptoms was not related to their o

125 surgery as life-changing, with providers and caregivers discussing financial and mortality concerns.

126 less care for patients and supporting family caregivers during their caregiving and after the death o

127 was significantly correlated within patient-caregiver dyads (beta=0.47 and 0.44, for depression and

128 l LVAD evaluation was initiated, 162 patient-caregiver dyads completed assessments of decisional conf

129 ns within and between individuals in patient-caregiver dyads considering LVAD were estimated in a spe

130 termine which interventions (such as patient/caregiver education) would be most effective to prevent

131 egy for infection prevention was patient and caregiver education.

132 In spite of caregivers' efforts to focus organ donation discussions

133 c, 16 studies intersected categories of both caregiver experience and needs, and one study intersecte

134 zed around three major categories: i) family caregiver experiences on receiving the diagnosis (n = 23

135 The final 29 studies identified caregiver experiences, needs, and interventions during t

136 AA caregivers expressed more positive responses than white

137 esent SR was to examine the relation between caregiver feeding practices in children from birth to 24

138 rnal diet during pregnancy and lactation and caregiver feeding strategies and practices.

139 ional and physical burden similar to that of caregivers for patients with cancer.

140 onfirmed case incurred by patients and their caregivers from illness onset until after enrollment and

141 ver-SOF includes 1,069 SOF participants (35% caregivers) from 4 US geographical areas (Baltimore, Mar

142 or communicating with children, parents, and caregivers, generated from a workshop of international e

143 Among the 80 caregiver respondents, caregivers had a median age of 34 years (range, 23-62 ye

144 Caregivers had better functioning than noncaregivers at

145 Personal caregivers had good agreement with patient reports of mo

146 ected environmental samples (drinking water, caregiver hands, child hands, surfaces, soil, open drain

147 sed: informational needs are better met, and caregivers have an improved ability to move on with life

148 ctive psychosocial treatments, and involving caregivers have been shown to improve health outcomes fo

149 cognitive impairment may improve patient and caregiver health outcomes.

150 Mental health problems are common among caregivers, however, professional support for them is of

151 Surveyors asked parents/caregivers if the child received any oral poliovirus vac

152 conducted cross-sectional surveys of student caregivers in 22 school pairs (2017 survey, N = 6,070; 2

153 for palliative care in Rohingya refugees and caregivers in Bangladesh.

154 a practical framework for palliative care of caregivers in oncology settings.

155 ropose the CARES framework to guide care for caregivers in oncology settings: Considering caregivers

156 e majority of them are cared for by informal caregivers in the community.

157 ad access to standard CMAM and CNS services; caregivers in the intervention group also received age-a

158 Using the caregiver-infant context, we review the rodent literatur

159 utcomes measured by Manchester Assessment of Caregiver-Infant interaction (MACI), Mullen Scales of Ea

160 We collected patient and caregiver information for 1029 patients with blood cultu

161 emonstrating how infant behaviour and infant-caregiver interaction can be characterised as foraging p

162 Behavioural change was measured through caregiver interview.

163 Caregiver interviews assessed vaccination campaign parti

164 naturalistic early intervention with active caregiver involvement can facilitate early social commun

165 adverse psychosocial impact on patients and caregivers, leading to frustration, stress and isolation

166 giving impacts QoL of MCS patients and their caregivers long term.

167 Certain high-risk subpopulations of caregivers might need more targeted psychosocial support

168 Patients, caregivers, multidisciplinary clinicians, researchers, i

169 Caregivers must modify their strategies as well as optim

170 ious health problems (n = 156, 53% male) and caregivers (n = 155, 69% female) living in Rohingya refu

171 Caregivers need to be aware of this pathological finding

172 Caregiver needs following the diagnosis included knowled

173 differences on secondary outcomes measuring caregiver non-directiveness (0.16, -0.33 to 0.65), careg

174 ue to CHVs handing out preventive SQ-LNSs to caregivers of AM children instead of referring them to t

175 different lifestyle interventions on parents/caregivers of children attending preschools in a socioec

176 orted moderate or severe PA and with parents/caregivers of children or teenagers (aged 4-17 years) wi

177 althcare providers, researchers, and parents/caregivers of children who survived cardiac arrest.

178 A cross-sectional survey of caregivers of children with mild, moderate and severe PA

179 One hundred caregivers of children with PA (aged 4-15 years) complet

180 for (a) individuals with PA and (b) parents/caregivers of children with PA.

181 Caregivers of children with primary immunodeficiency dis

182 Caregivers of children younger than 18 with diagnosed PC

183 from illness onset until the survey dates to caregivers of patients with blood culture positive cases

184 educational interventions on the outcomes of caregivers of patients with heart failure.

185 the ideal intervention format and design for caregivers of patients with heart failure.

186 The specific tasks of caregivers of patients with HF vary widely based on the

187 icipants included adults with PA and parents/caregivers of PwPA who responded by self-report and prov

188 Caregivers of these patients also bear an emotional and

189 of loss to follow-up or unavailability of a caregiver or child at the correct age.

190 Partnered mothers who were mainly unpaid caregivers or who did other unpaid activities had cognit

191 a greater likelihood of time spent at home, caregiver outcomes are better when hospice care is acces

192 econdary outcomes were a range of infant and caregiver outcomes measured by Manchester Assessment of

193 for cognitive impairment improves patient or caregiver outcomes or causes harm.

194 ention found to have a significant impact on caregiver outcomes, as interventions were heterogeneous

195 are needed that are powered specifically for caregiver outcomes, use measures validated for advanced

196 d with 114 months for those noticed by other caregivers (p = 0.0065).

197 ed with 72 months for those noticed by other caregivers (p = 0.0085).

198 ved a monthly supply of SQ-LNSs to stimulate caregivers' participation and supplement children's diet

199 the interactions was sharper for grandparent caregivers, particularly for males.

200 e association of factors at the level of the caregiver, patient, caregiver-patient relationship, and

201 f interventions targeting the caregiver, the caregiver-patient dyad, or the patient and their family.

202 tors at the level of the caregiver, patient, caregiver-patient relationship, and caregiving itself, w

203 king on how persons with PA (PwPA) and their caregivers perceive the psychosocial impact of living wi

204 with mild, moderate and severe PA, based on caregiver perception, was conducted in the United Kingdo

205 r case of enteric fever from the patient and caregiver perspective was US $64.03 (IQR: US $33.90 -$17

206 From the patient and caregiver perspective, we collected direct medical, nonm

207 pairwise interaction P = .03) and change in caregiver plans (OR, 1.37; 95% CI, 0.67-2.82; pairwise i

208 both the intervention and control group; and caregivers' practices were based on self-report, and the

209 and support strategies that could be used by caregivers, practitioners, policymakers, and key stakeho

210 nclear whether interventions for patients or caregivers provide clinically important benefits for old

211 Family caregivers provide substantial care for patients with ad

212 ipants, and assessed inflammation only after caregivers provided care for extended periods of time.

213 based on self-report, and the possibility of caregivers providing socially desirable responses cannot

214 osed with PA (self-report); parent/nonparent caregivers (proxy-report for a child with PA); and paren

215 ults with PA (self-report); 546 were parents/caregivers (proxy-report); and 881 were parents/caregive

216 (r = -0.66, P < .01), indicating that worse caregiver QOL was significantly correlated with more dep

217 analyze data to determine associations with caregiver QOL.

218 rtant for designing interventions to improve caregivers' QOL, thereby maximizing their ability to car

219 Personal caregivers' ratings of dyspnea had substantial agreement

220 nd 12 months among under-5 children based on caregivers' recall.

221 5) a recommendation that patients and their caregivers receive education on oxygen equipment and saf

222 At present, caregivers receive little guidance or information to sup

223 Child development research highlights caregiver regulation of infant physiology and behavior a

224 n computational modeling of decision making, caregiver-related transmission of traumatic stress, and

225 included social attitudes and support, child-caregiver relationship and coping strategies used.

226 ires mutually capable parties, but one-sided caregiver relationships reveal its developmental and evo

227 Caregivers report that children with PA experience high

228 Caregivers reported providing an average of 13.8 hours o

229 It also reduced caregiver-reported ARI despite no evidence of improved a

230 The primary outcome was caregiver-reported child diarrhoea (>=3 loose or watery

231 household drinking water quality and reduced caregiver-reported diarrhea among children <5 years.

232 The PAPRIQUA study aimed to assess the caregiver-reported impact of living with PA on children'

233 .69, -1.27 to -0.10) on the MACI, but higher caregiver-reported receptive (37.17, 95% CI 10.59 to 63.

234 ay be subject to unmeasured confounding, and caregiver-reported vaccination status, which is subject

235 Among the 80 caregiver respondents, caregivers had a median age of 34

236 Psychoeducation interventions for caregivers resulted in a small benefit for caregiver bur

237 utcomes to support their transition into the caregiver role (n = 5).

238 period in the process of transitioning into caregiver role.

239 test data supported the superior role of the caregiver's face and were in line with the findings from

240 tudies that focused more specifically on the caregiver's initial reactions to a diagnosis of Alzheime

241 For the patient and caregiver's perspective, we administered questionnaires

242 had a significant small to medium effect on caregiver's self-efficacy for dealing with problem behav

243 s as part of the unit of care, Assessing the caregiver's situation and needs, Referring to appropriat

244 t for a child with PA); and parent/nonparent caregivers (self-report of PA impact on themselves).

245 egivers (proxy-report); and 881 were parents/caregivers (self-report).

246 , 116 aged 13-17 years) and 881 from parents/caregivers (self-report).

247 ver non-directiveness (0.16, -0.33 to 0.65), caregiver sensitive responding (0.24, -0.15 to 0.63), an

248 everity and child's sex, and associations of caregivers' sex and anxiety with the proxy report of the

249 Microbial diversity and child-caregiver similarity increased most between 1 and 2.5 y

250 mpling decisions, and was similar to that in Caregiver-SOF (39% died; aHR = 0.71, 95% CI: 0.57, 0.89)

251 tality among women invited to participate in Caregiver-SOF (41% died; adjusted hazard ratio (aHR) = 0

252 Caregiver-SOF includes 1,069 SOF participants (35% careg

253 ples representing key points in constructing Caregiver-SOF, and Caregiver-SOF.

254 ey points in constructing Caregiver-SOF, and Caregiver-SOF.

255 tified by screening all SOF participants for caregiver status (1997-1999; n = 4,036; 23% caregivers)

256 essive symptoms was dependent on grandparent caregivers' status and gender.

257 Caregivers suggested several organizational-level soluti

258 Caregivers suggested several organizational-level soluti

259 es enrollee adoption by type of benefit (eg, caregiver support, in-home personal care, palliative nur

260 of four elements; three elements focused on caregiver-surrogate communication (admission meeting, fo

261 rolled trials of interventions targeting the caregiver, the caregiver-patient dyad, or the patient an

262 ctical aspects of caregiving, and Supporting caregivers through bereavement.

263 quality of life (QoL) of patients and their caregivers through the lens of preparedness and mutualit

264 upport (MCS) require the identification of a caregiver to assist with MCS care.

265 y role in supporting and guiding parents and caregivers to communicate with their children about the

266 rs, family members, friends, or neighbors as caregivers to help manage their chronic disease.

267 :1) to invite or not invite fathers and male caregivers to participate.

268 gy is developed, trained alert dogs can help caregivers to protect both the patient and those around

269 tically important to understand the needs of caregivers to support the increasingly complex medical c

270 ve" emotions may prompt protective action by caregivers toward infant primates, and infants show dist

271 Despite the benefits to patients and caregivers, US acute care facilities are largely not usi

272 response to such stress, patients and their caregivers use a variety of strategies to manage the dis

273 Caregivers use clinical examination to timely recognize

274 ndards exist for teaching patients and their caregivers ventricular assist device (VAD) self-care ski

275 derived from the data: (1) 'Hardwired to be caregivers' - vocation versus role, (2) needing a stable

276 work acknowledging the importance of patient-caregiver well-being in serious illness.

277 In the adjusted regression model lower caregiver well-being was significantly associated with l

278 th care system-level improvements to enhance caregiver well-being.

279 ntion, and the availability and knowledge of caregivers were also important, as was the cleanliness o

280 Second, caregivers were concerned that allergenic foods might be

281 A total of 635 parents/caregivers were enrolled: mean age 38 +/- 11 years, 83%

282 core 0) children (n = 119) and their primary caregivers were followed from 1 until 4 y of child age.

283 domized controlled trials with 1036 informal caregivers were included.

284 Incident caregivers were individually matched on multiple demogra

285 Caregivers were invited to a support group.

286 Research staff, clinicians, patients, and caregivers were masked to group assignment.

287 Caregivers were mostly working in university affiliated

288 Schools, and their children's parents/caregivers, were randomized to receive either an "indivi

289 but higher preference by subjects and their caregivers when compared with a conventional MRI coil.

290 t primates, and infants show distress toward caregivers when they appear to violate expectations in t

291 sured the children's anthropometry and asked caregivers whether children had been referred to service

292 n secure attachment formation with a primary caregiver, which is impaired in many children with child

293 and no effects were found for a subset of 45 caregivers who were living with a spouse with dementia.

294 n facility-based testing), or by the child's caregiver with an oral HIV test.

295 vs 4.9%) or other race (14.6% vs 8.7%), had caregivers with a bachelor's degree (29.8% vs 23.5%), an

296 red with the goals of providing patients and caregivers with advice for the management of cachexia.

297 th program to help patients and their family caregivers with long-term self-management of COPD.

298 lly used small convenience samples, compared caregivers with poorly characterized control participant

299 The return of results to caregivers within 30 days (in 18 737 [98.3%] of 19 058 i

300 responsibilities fall to patients and their caregivers, yet stakeholder concerns in these heterogene