| Literature DB >> 29184455 |
Simon N Rogers1,2, Brittany Barber3.
Abstract
The measurement of patient-reported outcome measures (PROMs) following head and neck cancer (HNC) has the capacity to substantially enhance the care of patients and their care-givers following the diagnosis and treatment of HNC. Literature concerning PROMs has increased exponentially in the past 2 decades, producing a vast array of data upon which the multidisciplinary team can reflect. For this review, "Handle On QOL" has been used as a source of references to illustrate the points raised. PROMs are contextualized by considering the clinically-distinct key stages that cancer patients endure: diagnosis, treatment, acute toxicity, early recovery, late effects, recurrence, and palliation. The PROMs are considered in six main categories: 1) those addressing cornucopia of issues not specific to cancer; 2) those addressing issues common to all cancers; 3) questionnaires with items specific to HNC; 4) questionnaires that focus on a particular aspect of head and neck function; 5) those measuring psychological concerns, such as depression, anxiety, or self-esteem; and 6) item prompt lists. Potential benefits of PROMs in clinical practice are discussed, as are barriers to use. The way forward in integrating PROMs into routine HNC care is discussed with an emphasis on information technology.Entities:
Keywords: head and neck cancer; multi-professional; patient reported outcomes; quality of life
Year: 2017 PMID: 29184455 PMCID: PMC5687779 DOI: 10.2147/PROM.S129012
Source DB: PubMed Journal: Patient Relat Outcome Meas ISSN: 1179-271X
Areas most commonly affected by HNC and its treatment
| Carer | Coping |
| Dental status | Disfigurement |
| Emotion | Fatigue |
| Fear of recurrence | Financial/work |
| Information | Lymphedema |
| Nutrition | Oral rehabilitation |
| Pain | Personality |
| Self-esteem | Sociodemographic |
| Speech | Swallowing |
| Shoulder | Trismus |
| Xerostomia | Unknown |
Abbreviation: HNC, head and neck cancer.
Domains housing symptoms experienced during diagnosis and treatment by HNC patients as based on the Patient Concerns Inventory item prompt list
| Physical and functional well-being | Treatment-related |
|---|---|
| Activity | Cancer treatment |
| Appetite | Regret about treatment |
| Bowel habit | PEG tube |
| Breathing | Wound healing |
| Chewing/eating | |
| Coughing | Social care and social well-being |
| Dental health/teeth | Carer |
| Dry mouth | Dependents/children |
| Energy levels | Financial benefits |
| Fatigue/tiredness | Home care/district nurse |
| Hearing | Lifestyle issues (smoking/alcohol) |
| Indigestion | Recreation |
| Mobility | Relationships |
| Mouth opening | Speech/voice/being understood |
| Mucous | Support for my family |
| Nausea | |
| Pain in the head and neck | Psychological, emotional and spiritual well-being |
| Pain elsewhere | Appearance |
| Regurgitation | Angry |
| Salivation | Anxiety |
| Shoulder | Coping |
| Sleeping | Depression |
| Smell | Fear of the cancer coming back |
| Sore mouth | Fear of adverse events |
| Swallowing | Intimacy |
| Swelling | Memory |
| Taste | Mood |
| Vomiting/sickness | Self-esteem |
| Weight | Sexuality |
| Spiritual/religious aspects | |
| Personality and temperament |
Abbreviations: HNC, head and neck cancer; PEG, percutaneous endoscopic gastrostomy tube.
Examples of patient-reported outcomes relating to HRQOL during key stages of HNC
| Diagnosis | • Patient Concerns Inventory-Diagnosis |
| • Satisfaction with Cancer Information profile (SCIP) | |
| Treatment | • Hospital Anxiety Depression Scale (HADS) |
| • Symptom Severity Scale (SSS) | |
| • Visual Analog Scale (VAS) | |
| Acute toxicity | • Late Effects in Normal Tissue (LENT) |
| • Common Terminology Criteria for Adverse Events (CTC-AE) | |
| • Oral Mucositis Weekly Questionnaire-Head and Neck Cancer (OMWQ-HN) | |
| Early recovery | • EuroQOL EQ-5D-5L |
| • European Organization for Research and Treatment of Cancer (EORTC) QLC-C30 | |
| • Functional Assessment of Cancer Therapy-Head and Neck (FACT-H&N) | |
| • University of Washington Quality of Life Scale (UW-QoL v4) | |
| • Patient Concerns Inventory (PCI-HN) | |
| Late effects | • Oral rehabilitation: Liverpool Oral Rehabilitation Questionnaire (LORQ) |
| • Trismus: Gothenburg Trismus Questionnaire (GTQ) | |
| • Swallowing: Swallowing Quality of Life Questionnaire (SWAL-QOL) | |
| • Xerostomia Questionnaire (XQ) | |
| Recurrence | • Vanderbilt Head and Neck Symptom Survey (VHNSS) |
| Palliation | • EORTC QLQ-C15-PAL |
| • Family Assessment of Treatment at the End of life (FATE) | |
| • Schedule for the Evaluation of Individual Quality of Life (SEIQoL) |
Abbreviation: HRQOL, health related quality of life; HNC, head and neck cancer.