| scholarly article | Q13442814 |
| P2093 | author name string | J Hanson | |
| E Bruera | |||
| K Spachynski | |||
| T MacEachern | |||
| C L Nekolaichuk | |||
| T O Maguire | |||
| P2860 | cites work | Validity of the support team assessment schedule: do staffs' ratings reflect those made by patients or their families? | Q28285426 |
| The development of a method for assessing the quality of life of cancer patients | Q35991872 | ||
| The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease: A review | Q36272221 | ||
| Who should measure quality of life, the doctor or the patient? | Q36466485 | ||
| Pain and its treatment in outpatients with metastatic cancer | Q39485856 | ||
| Pain characteristics and treatment in an outpatient cancer population | Q39544424 | ||
| The impact of pain on the patient with cancer | Q39552090 | ||
| Neuropsychiatric syndromes and psychological symptoms in patients with advanced cancer | Q40513847 | ||
| New developments in the assessment of pain in cancer patients | Q40655379 | ||
| Patient assessment in palliative cancer care | Q40984207 | ||
| The treatment of cancer pain | Q43074092 | ||
| Cancer-related pain--II. Assessment with visual analogue scales. | Q51235829 | ||
| The validation of visual analogue scales as ratio scale measures for chronic and experimental pain. | Q51240433 | ||
| A comparison of the Hopkins Pain Rating Instrument with standard visual analogue and verbal descriptor scales in patients with cancer pain | Q52044041 | ||
| Correlation of patient and caregiver ratings of cancer pain. | Q52052022 | ||
| The assessment of pain intensity in patients with cognitive failure: A preliminary report | Q52073653 | ||
| The prevalence of psychiatric disorders among cancer patients. | Q52096145 | ||
| Prevalence of symptoms among patients with advanced cancer: an international collaborative study. Symptom Prevalence Group. | Q53366829 | ||
| Can professionals improve their assessments? | Q53579257 | ||
| Value of caregiver ratings in evaluating the quality of life of patients with cancer. | Q53603225 | ||
| Responsiveness of a single-item indicator versus a multi-item scale: assessment of emotional well-being in an international adjuvant breast cancer trial. | Q53627233 | ||
| Quality-of-life evaluation: when do terminal cancer patients and health-care providers agree? | Q54492016 | ||
| P433 | issue | 4 | |
| P921 | main subject | patient | Q181600 |
| P304 | page(s) | 311-323 | |
| P577 | publication date | 1999-07-01 | |
| P1433 | published in | Palliative Medicine | Q7127852 |
| P1476 | title | A comparison of patient and proxy symptom assessments in advanced cancer patients | |
| P478 | volume | 13 |
| Q51542786 | A Multicenter Study Comparing Two Numerical Versions of the Edmonton Symptom Assessment System in Palliative Care Patients |
| Q35801735 | A brief symptom index for advanced lung cancer |
| Q60317382 | A comparison of cancer patients and nurse specialist's symptom-assessment scores, in an acute hospital |
| Q45337609 | A comparison of doctors', parents' and children's reports of health states and health-related quality of life in children with chronic conditions |
| Q35990068 | A conceptual model of pain assessment for noncommunicative persons with dementia |
| Q39144954 | A descriptive cross-sectional study of pain in patients with neuroendocrine tumors |
| Q48762319 | A new index of priority symptoms in advanced ovarian cancer. |
| Q24651100 | A review of the reliability and validity of the Edmonton Symptom Assessment System |
| Q53396200 | A supportive care model for dialysis patients. |
| Q41287137 | A survey of patients' experience of pain and other symptoms while receiving care from palliative care services |
| Q36365425 | Added Value from Secondary Use of Person Generated Health Data in Consumer Health Informatics. Contribution of the Consumer Health Informatics IMIA Working Group. |
| Q56452444 | Assessing hospice inpatients with pain using numerical rating scales |
| Q45227417 | Assessing symptoms in gastroesophageal reflux disease: how well do clinicians' assessments agree with those of their patients? |
| Q51919450 | Assessing symptoms of terminally-ill patients by different raters: a prospective study. |
| Q43884738 | Assessment and management of pain in fungating wounds. |
| Q39881885 | Assessment of palliative care cancer patients' most important concerns |
| Q37724775 | Association Between Symptom Burden and Time to Hospitalization, Nursing Home Placement, and Death Among the Chronically Ill Urban Homebound |
| Q35809381 | Association between patient-reported symptoms and nurses' clinical impressions in cancer patients admitted to an acute palliative care unit |
| Q49847846 | Beyond Pain: Nurses' Assessment of Patient Suffering, Dignity, and Dying in the Intensive Care Unit |
| Q37403903 | Botulinum toxin injection and phenol nerve block for reduction of end-of-life pain |
| Q36315390 | Breathlessness and presentation to the emergency department: a survey and clinical record review. |
| Q40336767 | Breathlessness in cancer and chronic obstructive pulmonary disease: using a qualitative approach to describe the experience of patients and carers. |
| Q45968642 | Can individual patients assess differences in quality of life between groups of patients? |
| Q37016830 | Challenge of assessing symptoms in seriously ill intensive care unit patients: can proxy reporters help? |
| Q36892832 | Commentary on Jocham HR et al. (2006) quality of life in palliative care cancer patients: a literature review. Journal of Clinical Nursing 15, 1188-1195. |
| Q92947604 | Comparing Physician and Nurse Eastern Cooperative Oncology Group Performance Status (ECOG-PS) Ratings as Predictors of Clinical Outcomes in Patients with Cancer |
| Q59103454 | Concordance between Experiences of Bereaved Relatives, Physicians, and Nurses with Hospital End-of-Life Care: Everyone Has Their “Own Truth” |
| Q42623938 | Confidant and breast cancer patient reports of quality of life. |
| Q46447397 | Congruence in symptom assessment between hepatocellular carcinoma patients and their primary family caregivers in China |
| Q57806082 | Correlation of affective temperament and psychiatric symptoms in palliative care cancer patients |
| Q37614065 | Depression assessment and classification in palliative cancer patients: a systematic literature review |
| Q34158787 | Describing the subjects in a study |
| Q48187114 | Development and initial validation of the NCCN/FACT symptom index for advanced kidney cancer. |
| Q53046021 | Development and validation of 11 symptom indexes to evaluate response to chemotherapy for advanced cancer. |
| Q57653189 | Development and validation of eleven symptom indexes to evaluate response to chemotherapy for advanced cancer: Measurement compliance with regulatory demands |
| Q81596886 | Development of a prognostic index in cancer patients with low performance status |
| Q53405354 | Differences in assessment of symptoms and quality of life between patients with advanced cancer and their specialist palliative care nurses in a home care setting. |
| Q30408916 | Do nurses provide holistic care to cancer patients? |
| Q51855708 | Do palliative patients and carers agree about patients' psychological functioning? |
| Q47785701 | Edmonton symptom assessment scale: Italian validation in two palliative care settings |
| Q40921209 | Effect of palliative care nurse champions on the quality of dying in the hospital according to bereaved relatives: A controlled before-and-after study |
| Q33564922 | Electro-acupuncture to prevent prolonged postoperative ileus: a randomized clinical trial |
| Q50459272 | Family estimates of risk for neurocognitive late effects following pediatric cancer: From diagnosis through the first three years of survivorship |
| Q34174412 | Health care providers underestimate symptom intensities of cancer patients: a multicenter European study |
| Q85738949 | Health care providers' use and knowledge of the Edmonton Symptom Assessment System (ESAS): is there a need to improve information and training? |
| Q24802387 | Health-related quality of life, utility, and productivity outcomes instruments: ease of completion by subjects with COPD |
| Q34689956 | Heart failure symptom assessment and management: can caregivers serve as proxy? |
| Q38670846 | Hospitalized patients' vs. nurses' assessments of pain intensity and barriers to pain management |
| Q48432152 | How feasible is implementation of distress screening by cancer clinicians in routine clinical care? |
| Q51843645 | Identification of patient-reported distress by clinical nurse specialists in routine oncology practice: a multicentre UK study. |
| Q34067146 | Impact of tracheostomy placement on anxiety in mechanically ventilated adult ICU patients |
| Q48000586 | Information structuring improves recall of emergency discharge information: a randomized clinical trial |
| Q47607000 | Is breathlessness what the professional says it is? Analysis of patient and professionals' assessments from a German nationwide register |
| Q38758990 | Lack of Patient-Clinician Concordance in Cancer Patients: Its Relation With Patient Variables |
| Q40737668 | Late effects in survivors of central nervous system tumors: reports by patients and proxies |
| Q48341221 | Measuring clinical benefit: use of patient-reported outcomes (PRO) in primary brain tumor clinical trials. |
| Q26752745 | Pain Assessment--Can it be Done with a Computerised System? A Systematic Review and Meta-Analysis |
| Q35678133 | Palliative care in primary care: a study to determine whether patients and professionals agree on symptoms |
| Q33672292 | Palliative care in the ICU: relief of pain, dyspnea, and thirst--a report from the IPAL-ICU Advisory Board |
| Q44255133 | Patient reported late effects of gynecological cancer treatment |
| Q34221163 | Patients' versus general practitioners' assessments of pain intensity in primary care patients with non-cancer pain. |
| Q73927602 | Perception of discomfort by relatives and nurses in unresponsive terminally ill patients with cancer: a prospective study |
| Q39295635 | Phantom pain in bilateral upper limb amputation |
| Q79323650 | Poor correlation between physician and patient assessment of quality of life in palliative care |
| Q36758835 | Prevalence of pain in patients with cancer: a systematic review of the past 40 years |
| Q81172989 | Prioritization of patients on waiting lists for hip and knee replacement: validation of a priority criteria tool |
| Q34337722 | Proxies and other external raters: methodological considerations |
| Q47966277 | Proxy reporting in after-death interviews: the use of proxy respondents in retrospective assessment of chronic diseases and symptom burden in the terminal phase of life |
| Q50560728 | Psyche at the end of life: Psychiatric symptoms are prevalent in patients admitted to a palliative care unit. |
| Q90610662 | Quality of life and symptom intensity over time in people with cancer receiving palliative care: Results from the international European Palliative Care Cancer Symptom study |
| Q58128332 | Ratings of symptoms and comfort in dementia patients at the end of life: comparison of nurses and families |
| Q47162011 | Reducing Symptom Distress in Patients With Advanced Cancer Using an e-Alert System for Caregivers: Pooled Analysis of Two Randomized Clinical Trials. |
| Q34988141 | Research design in end-of-life research: state of science |
| Q34590833 | Symptom assessment in cancer patients |
| Q51654989 | Symptom assessment in elderly cancer patients receiving palliative care. |
| Q73990976 | Symptom burden at the end of life: hospice providers' perceptions |
| Q36667788 | Symptom burden in chronically ill homebound individuals |
| Q48550575 | Symptom distress as rated by advanced cancer patients, caregivers and physicians in the last week of life |
| Q35847034 | Symptom experience in the last year of life among individuals with cancer |
| Q48188176 | Symptoms overlooked in hospitalized cancer patients: Impact of concurrent symptoms on oversight [corrected] by nurses |
| Q37889209 | The Edmonton Symptom Assessment System, a proposed tool for distress screening in cancer patients: development and refinement |
| Q28274253 | The Edmonton Symptom Assessment System: a 15-year retrospective review of validation studies (1991--2006) |
| Q79708938 | The Edmonton symptom assessment system--what do patients think? |
| Q44322104 | The benefits of using patient-reported outcomes in cancer treatment: an overview |
| Q50354425 | The effect of different utility measures on the cost-effectiveness of bilateral cochlear implantation |
| Q58128661 | The last two days of life of nursing home patients – a nationwide study on causes of death and burdensome symptoms in the Netherlands |
| Q38430860 | The psychometric properties of cancer multisymptom assessment instruments: a clinical review |
| Q89759358 | Timing is everything: Early do-not-resuscitate orders in the intensive care unit and patient outcomes |
| Q37893348 | What is the methodological rigour of palliative care research in long-term care facilities in Europe? A systematic review |
| Q36760902 | Which measurement scales should we use to measure breathlessness in palliative care? A systematic review |
| Q42234259 | Who should measure quality of life? |
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