A Qualitative Analysis of the Impact of Preoperative Mindfulness-Based Stress Reduction on Total Knee Arthroplasty Surgical Experiences.

We qualitatively explored the impact of preoperative mindfulness-based stress reduction (MBSR) on total knee arthroplasty (TKA) experiences. Participants (n = 10) who received MBSR prior to TKA participated in semi-structured interviews concerning their experiences with MBSR and its perceived impact on surgery. We analyzed interviews according to reflexive thematic analysis, and coded data into three main themes: 1) Impact of MBSR on surgery experiences; 2) Contributors to change; and 3) Motivations for participation. Participants noted they were able to relax, feel more confident, and cope more effectively during the preoperative period, and that others in their lives noticed positive changes following their participation in MBSR. Participants' openness to mindfulness and health-related beliefs and may have contributed to the positive impacts they experienced from MBSR. Participants described being motivated to participate in MBSR to help them prepare for their surgery and to learn new coping strategies. Participants described a strong level of commitment to the intervention. With further research, integration of MBSR into prehabilitation for TKA may be appropriate.

Outcomes for a Heat Illness Prevention Program in Outdoor Workers: A 9-Year Overview.

OBJECTIVE: To describe the outcomes effect of removing the medical surveillance component from a heat illness prevention program (HIPP) for outdoor workers from a Central Texas municipality. METHODS: Heat-related illness (HRI) frequency and workers' compensation (WC) cost were assessed retrospectively in a cohort of 329 workers from 2011-2019. During 2011-2017, the HIPP included training, acclimatization, and medical surveillance. In 2018-2019, a modified (mHIPP) was implemented that included training and acclimatization, but without medical surveillance. RESULTS: The HRI rate during HIPP averaged 19.5 per 1000 workers during the first 4 years, dropped to 1.01 per 1,000 workers over the next 3 years, (2015-2017), and increased during mHIPP, to 7.6 per 1,000 workers. DISCUSSION: Although the case increase during the mHIPP was small, medical surveillance may be an important component in lowering workforce HRI.

The Need to Say More: A Qualitative Analysis of Added Free Text to Chronic Pain Patient Intake Packages.

BACKGROUND: Many outpatient chronic pain clinics administer extensive patient intake questionnaires to understand patients' pain and how it impacts their lives. At our institution's pain clinic, many patients include free text in these predominantly closed-ended questionnaires, but little is known about the content categories included in this free text. AIM: This study examined free text entries on chronic pain patient intake questionnaires. METHOD: We analyzed 270 occurrences of free text across 43 patient intake questionnaires of people living with chronic pain using a qualitative content analytic approach. RESULTS: We identified two overarching thematic categories of free text: (1) what they say (characterizes the topic of the free text); and (2) why they say it (characterizes perceived limitations of the patient intake questionnaire format). We also documented the frequency highlighting how often themes and their associated sub-themes (detailed below) were indicated. Within the What they say category, three main themes emerged: (1) health (34.9%; e.g., pain); (2) health service use (27.9%; e.g., medication); and (3) psychosocial factors (20.9%; e.g., relationships). Within the Why they say it category, four main themes emerged: (1) adding information (86.0%; e.g., elaborates/contextualizes); (2) narrow response options (65.1%; e.g., varies); (3) problems with the question (18.6%; e.g., not applicable); and (4) response error (4.7%; e.g., answers incorrectly/misinterprets question). CONCLUSIONS: People living with chronic pain appear motivated to add additional, unprompted information to their patient intake questionnaires. The results from this study may inform changes to chronic pain patient intake questionnaires which could facilitate improvements in chronic pain patient-health care provider communication.

Extemporaneous compounding confidence progression from undergraduate to practice: a pharmacy education perspective.

OBJECTIVE: This study examined how undergraduate students, graduate interns and registered pharmacists perceived their competence in extemporaneous compounding. METHODS: A cross-sectional observational study was conducted using a self-administered survey and participants ranked how confident they felt about compounding certain products using a Likert's scale and free-text responses. KEY FINDINGS: Pharmacy students perceived to be as confident as the interns and pharmacists in preparing 'simple' products, such as solutions, suspensions, creams and ointments. A lack of frequent practice was related to poor confidence by all three groups. CONCLUSION: Integration of theoretical, legal and ethical and patient counselling aspects in extemporaneous compounding curriculum could enhance learning and outcomes.

Demographic and clinical characteristics of free-text writers in chronic pain patient intake questionnaires.

BACKGROUND: Chronic pain is a prevalent and burdensome problem within the Canadian health care system, where the gold standard treatment occurs at multidisciplinary pain facilities. Patient intake questionnaires (PIQs) are standard practice for obtaining health information, with many patients including free-text (e.g., writing in margins of questionnaires) on their PIQs. AIMS: This study aims to quantitatively examine whether and how patients who include free-text on PIQs differ from those who do not. METHODS: We retrospectively analyzed 367 PIQs at a Canadian pain facility in Winnipeg, Canada. Patients were categorized into free-text (i.e., any text response not required in responding to questions) or no free-text groups. Groups were compared on sociodemographics, pain, health care utilization, and depressive symptoms with independent samples t-tests and chi-square analyses. RESULTS: Patients with free-text compared to those without had more sources of pain (6.66 vs. 4.63), longer duration of pain (123.2 months vs. 68.1 months), and a greater proportion of past pain conditions (66.3% vs. 55.2%). Additionally, they had tried more treatments for their pain, had seen more specialists, had tried more past medications, were currently on more medications, and had undergone more tests. No differences were identified for depressive symptoms across groups. CONCLUSIONS: This study is the first to examine patient and health-related correlates of free-text on PIQs at a Canadian pain facility. Results indicate that there are significant differences between groups on pain and health care utilization. Thus, patients using free-text may require additional supports and targeted interventions to improve patient-physician communication and patient outcomes.

Contexte: La douleur chronique est un problème répandu et pénible dans le système des soins de santé au Canada, où le traitement de référence se produit dans un centre multidisciplinaire de la douleur. Les formulaires d'admission du patient sont une pratique courante pour obtenir des renseignements sur la santé, et de nombreux patients y incluent du texte libre (en écrivant, par exemple, dans les marges du formulaire).Objectifs: Cette étude vise àexaminer quantitativement si et comment les patients qui incluent du texte libre sur leur formulaire d'admission diffèrent de ceux qui ne le font pas.Méthodes: Nous avons analysé rétrospectivement 367 formulaires d'admission dans un centre canadien de traitement de la douleur à Winnipeg, au Canada. Les patients ont été classés en deux groupes : avec texte libre (c'est-à-dire ayant inscrit une réponse sous forme de texte non requis au moment de répondre aux questions) ou sans texte libre. Les groupes ont été comparés en ce qui concerne les critères sociodémographiques, la douleur, l'utilisation des soins de santé et les symptômes dépressifs, à l'aide de tests t et chi carré pour échantillons indépendants.Résultats: Les patients avec texte libre par rapport à ceux sans texte libre avaient plus de sources de douleur (6,66 comparativement à 4,63), une plus longue durée de la douleur (123,2 mois comparativement à 68,1 mois) et une plus grande proportion de douleur par le passé (66,3 % comparativement à 55,2 %). De plus, ils avaient essayé d'autres traitements pour leur douleur, avaient vu plus de spécialistes, avaient essayé plus de médicaments par le passé, prenaient à ce moment plus de médicaments et avaient subi plus de tests. Aucune différence n'a été recensée pour les symptômes dépressifs entre les groupes.Conclusions: Cette étude est la première à examiner les corrélats liés au patient et à la santé de l'existence de texte libre sur les formulaires d'admission dans un centre de traitement de la douleur au Canada. Les résultats indiquent qu'il existe des différences importantes entre les groupes en ce qui concerne la douleur et l'utilisation des soins de santé. Ainsi, les patients utilisant le texte libre peuvent avoir besoin de soutien additionnel et d'interventions ciblées pour améliorer la communication patient-médecin et les résultats du patient.

Understanding correlates of suicidality among those with usual pain and discomfort: A Canadian nationally representative study.

OBJECTIVE: Suicidality (ideation, plans, attempts) is elevated among those with chronic pain. However, population-based research is limited and studies primarily focus on mechanisms associated with increasing rather than decreasing risk. This study aimed to identify correlates associated with increased and decreased odds of suicidality among Canadians with usual pain/discomfort in a nationally representative sample. METHODS: Cross-sectional data from the 2012 Canadian Community Health Survey-Mental Health supplement (CCHS-MH; N = 25,113) identified individuals with usual pain/discomfort (i.e., chronic pain; n = 5891). Multiple logistic regressions examined correlates that may increase (disability, activity limitations) and decrease (social support, positive mental health, spirituality) odds of suicidality among individuals endorsing usual pain/discomfort. RESULTS: Among those endorsing usual pain/discomfort, between 7.1% (suicide attempt) to 21.0% (suicide ideation) endorsed suicidality, notably higher than those without (2.0% vs 9.6% for suicide attempt and ideation, respectively). Both greater social support and positive mental health were associated with decreased odds of suicide ideation and attempts (adjusted odds ratio (AOR) range = 0.94-0.97). Those whose pain prevented most activities had increased odds of suicide plans and attempts (AOR range = 1.72-1.94). Additionally, greater disability was associated with increased odds of suicide ideation (AOR = 1.01, 95% CI[1.01-1.02], p < .001). A multivariable model including all risk and protective correlates found only positive mental health as significantly associated with decreased odds of suicide ideation and attempts. CONCLUSIONS: These findings may inform targeted screening, prevention, and intervention strategies to promote resilience and mitigate risk, among those with usual pain/discomfort.

Attitudes Toward Testicular Cancer and Self-Examination Among Northern Irish Males.

Testicular cancer incidence rates are increasing worldwide making it the most common malignancy in males aged 15 to 45 years. Without a known way to prevent the disease health professionals must promote awareness and early detection. A literature review identified a scarcity of information regarding awareness and knowledge of, and attitudes toward, testicular cancer and testicular self-examination among men in Northern Ireland. This study aimed to establish baseline data for Northern Ireland using a convenience sample of 150 men, aged 18 to 45 years. The sample was recruited from across the country and so represents a range of education and area deprivation levels. An online survey was used to collect data. Results showed that while 39% of respondents correctly identified the age group at highest risk for testicular cancer, only 17% of respondents had ever heard of a testicular self-examination. Analysis revealed knowledge, awareness, and attitudes differed by age groups and area deprivation quintiles. It is recommended that health promoters in Northern Ireland and elsewhere use these findings to tailor health promotion initiatives to engage men and raise testicular cancer and self-examination awareness.