Showing posts with label Depression. Show all posts
Showing posts with label Depression. Show all posts

Thursday, November 14, 2013

Surviving men's depression: Women partners' perspectives

Impact Factor:1.137 | Ranking:21/36 in Social Sciences, Biomedical | 81/136 in Public, Environmental & Occupational Health | 5-Year Impact Factor:1.396Source:2012 Journal Citation Reports® (Thomson Reuters, 2013)
Joan L Bottorff joan.bottorff{at}ubc.ca
University of British Columbia, Kelowna, CanadaJohn L Oliffe
University of British Columbia, Vancouver, CanadaMary T Kelly
University of British Columbia, Vancouver, CanadaJoy L Johnson
University of British Columbia, Vancouver, CanadaJoanne Carey
University of British Columbia, Kelowna, CanadaWhile men’s gendered experiences of depression have been described, the perspectives of women partners who are affected by men’s depression have received little attention. Women partners were recruited to explore how men’s depression impacts them and its influence on gender regimes. Individual interviews with 29 women spouses were coded and analysed. Although idealized femininity positions women as endlessly patient and caring, our findings reveal significant challenges in attempting to fulfil these gender ideals in the context of living with a male partner who is experiencing depression. The strain and drain of living with a depressed man was a key element of women’s experiences. Four sub-themes were identified: (1) resisting the emotional caregiver role, (2) shouldering family responsibilities, (3) connecting men to professional care and (4) preserving the feminine self. The findings suggest that men’s depression has great potential to dislocate heterosexual gender regimes, and attention to gender relations should be included to ensure successful care management of men who experience depression.

© 2013 SAGE Publications. Los Angeles, London, New Delhi, Singapore and Washington DC

View the original article here

Monday, November 11, 2013

Treatment resistant depression in primary care: Co-constructing difficult encounters

Impact Factor:1.137 | Ranking:21/36 in Social Sciences, Biomedical | 81/136 in Public, Environmental & Occupational Health | 5-Year Impact Factor:1.396Source:2012 Journal Citation Reports® (Thomson Reuters, 2013)
Many patients with depression do not recover despite medication or therapy. Individuals with treatment resistant depression often have co-morbid anxiety, personality difficulties and drug or alcohol misuse and have been characterised as difficult, heartsink or problem personalities by general practitioners. Yet critical studies of interaction in medical settings suggest that the context may have a role in constructing the patient. A total of 12 audio-recorded routine consultations were analysed following guidelines for qualitative analysis of medical discourse. The interpretation focused on ways in which the context and structure of primary care consultations in a UK setting construct difficult encounters, which may lead to patients with treatment resistant depression being seen as difficult to manage in various ways. Three overarching observations were that presentation of multiple problems in multiple domains clash with the consultation format; that patients’ atypically high level of activity in a time-limited setting prevents patient-centred work; that the question and answer format restricts multifaceted discussions of social and emotional problems, preventing shared understandings emerging. However, although interactions appear uneasy, they are repaired and may be moderately palliative. Suggestions are made for re-orienting general practitioner work with treatment resistant depression towards long-term goal setting outside of the traditional consultation structure in order to develop shared understandings.

© 2013 SAGE Publications. Los Angeles, London, New Delhi, Singapore and Washington DC

View the original article here

Monday, June 24, 2013

SSRI Prevents Depression in Head, Neck Cancer (CME/CE)

By Salynn Boyles, Contributing Writer, MedPage Today Reviewed by F. Perry Wilson, MD, MSCE; Instructor of Medicine, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that this double-blind randomized trial demonstrated that treatment with escitalopram prevented depression in patients undergoing treatment for head and neck cancer.Be aware that the study was not powered to detect differences in treatment or mortality-associated endpoints between the two groups.

Prophylactic escitalopram cut the incidence of depression in head and neck cancer patients by more than 50% and improved quality of life, a clinical trial showed.

Significantly fewer patients taking the antidepressant developed depression, when compared with those on placebo (10% vs 24.6%; stratified log-rank test, P=.04), according to a study in the June 20 issue of JAMA Otolaryngology Head and Neck Surgery.

"Depression is very common among patients with this disease, but it is not easy to predict who will become depressed at the beginning of treatment," University of Nebraska Medical Center professor of head and neck oncology William Lydiatt, MD, told MedPage Today. "That's why the prevention paradigm may offer considerable benefit at an acceptable risk."

As many as half of head and neck cancer patients develop clinical depression within months of their diagnosis and suicide rates are among the highest in patients with a medical illness, Lydiatt noted.

"The burden of treatment is extensive and frequently includes dysphagia, disfigurement, voice alterations, mucositis, need for tracheostomy and feeding tubes, fatigue and depression," the researchers wrote.

They chose the generic version of the popular SSRI Lexapro for the trial to give patients an affordable treatment option that's well tolerated in the elderly.

The randomized, double-blind trial included 148 newly diagnosed head and neck cancer patients entering treatment who did not yet have a diagnosis of depression. The patients were stratified by sex, site of disease, stage, and primary modality of treatment (surgery versus radiation).

Half were treated with escitalopram at a dosage of 10 mg/d for the first week (one tablet) followed by 20 mg/d (two tablets) until week 16, followed by an additional week of 10 mg/d. During the acute phase of the study, dosage was reduced to 10 mg/d when adverse events occurred. Patients not treated with the antidepressant received matching placebo pills.

Among the study's major findings: Patients undergoing radiation as their initial therapy were significantly more likely than those who had surgery to develop depression (hazard ratio, 3.6; 95% CI ,1.38-9.40; P=.009).A Cox progression hazards regression model comparing the two groups, after controlling for age, smoking status, and other variables, demonstrated an advantage for escitalopram (hazard ratio, 0.37; 95% CI, 0.14-0.96: P=.04).Patients who took escitalopram and who completed the study without developing depression rated their overall quality of life as significantly better than those in the placebo group for 3 consecutive months after ending treatment with the antidepressant (overall quality of life, good or outstanding at weeks 20, 24 and 28 - escitalopram group = 96%, 100%, 96%, respectively; placebo group = 77%, 86%, 85%).

Lydiatt said the finding that radiotherapy patients had a higher risk for depression than surgery patients is a big surprise with important potential clinical implications.

"The higher incidence of depression in the cohort receiving radiation suggests that radiation represents a greater and longer duration stress event than surgery," the researchers wrote. "Radiation may also generate greater inflammatory cytokines during treatment, which could contribute to the higher rate (of depression)."

Although overall treatment success and survival were not study endpoints, Lydiatt said he hopes to conduct further research with these outcomes in mind.

"I would not be surprised to see a survival advantage associated with this approach," he said. "Depression is associated with so many negative manifestations in these patients. Depressed patients don't comply with their treatments to the same degree as patients who aren't depressed and they don't take care of themselves as well. They often lose their spark to live.

This study was funded by a grant from the National Institute of Mental Health. Additional support was provided by a research fund grand from the Nebraska Medical Center and the University of Nebraska Medical Center.

Saturday, June 22, 2013

Depression Tied to Mental Loss in Parkinson's (CME/CE)

By Ed Susman, Contributing Writer, MedPage Today Note that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.Note that this study of patients with Parkinson's disease and healthy controls demonstrated a strong association between mild cognitive impairment and worse scores on standardized tests for depression and anxiety.Be aware that the cross-sectional nature of the study precludes a formal assessment of causality.

SYDNEY -- Nonmotor symptoms such as depression and anxiety appear to be more frequent among patients with Parkinson's disease who also are diagnosed with mild cognitive impairment, researchers reported here.

In comparing scores on the Beck Depression Inventory II, patients with Parkinson's disease and mild cognitive impairment registered a mean score of 14.6; those patients with Parkinson's disease but without mild cognitive impairment scored 8.6, while healthy controls scored 5.3 (P<0.05 for all comparisons), said Sabrina Diab, MS, a PhD candidate at the Center for Advanced Research in Sleep Medicine at the Hôpital du Sacre-Coeur in Montreal.

In addition, patients with Parkinson's disease and mild cognitive impairment scored an average of 14.1 on the Beck Anxiety Index, which was statistically significant compared with Parkinson's disease patients without mild cognitive impairment (5.9) and controls (4.1) (all comparisons, P<0.05), Diab said at her poster presentation at the International Congress on Parkinson's Disease and Movement Disorders.

The 5.9 score is below the cut-off for clinical anxiety, Diab said, so while it is statistically significant, it might not be clinically meaningful. She noted the results were significant despite small numbers of patients in each group.

"What we found is that patients who have Parkinson's disease and mild cognitive impairment scored higher on those scales of depression and anxiety versus patients with Parkinson's disease and without mild cognitive impairment, and versus the control group as well," she said. "We think that if you are treating a Parkinson's disease patient with mild cognitive impairment, that person is more likely to have depression and anxiety."

For the study, Diab and colleagues recruited 36 patients with Parkinson's disease who were taking only dopaminergic medications. They diagnosed 16 of those patients with mild cognitive impairment. The patients with Parkinson's disease were compared with 36 healthy controls.

Most of the participants in the trial were men, and their average age was about 65 years. Disease duration was 6.4 years in the Parkinson's patients with mild cognitive impairment compared with 4.3 years for those without cognitive impairment, but that difference was not statistically significant.

When the researchers scrutinized results on measures of sleep, Diab said, "What we have also seen is that patients with Parkinson's disease and mild cognitive impairment, and Parkinson's disease without mild cognitive impairment, scored higher on the Epworth Sleepiness Scale and the Insomnia Severity Index versus the control group.

"For now, we think that mood symptoms are more related to cognitive impairment, and sleeping complaints are more related to Parkinson's disease."

The researchers did not evaluate the type or severity of the depression or of the anxiety disorder.

Alison Yarnall, MD, of the University of Newcastle in England, told MedPage Today, "This is an interesting pilot study, but we need more information. The numbers in this study are small and only 16 of the patients have mild cognitive impairment."

"Anxiety and depression can impact the tests we do for cognitive impairment, so we should take these results with a pinch of salt because it is kind of chicken or egg," commented Yarnall, who did not participate in the study. "Do people with mild cognitive impairment have more depression and anxiety or is their depression and anxiety impairing their testing abilities? We need a larger study to help us tease out what is really happening with these patients."

Diab and Yarnall had no disclosures.

Primary source: Movement Disorders Society
Source reference:
Diab S, et al "Non-motor symptoms in Parkinson's disease with mild cognitive impairment" MDS 2013.