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1.
J Med Imaging Radiat Sci ; 49(4): 365-370, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30514552

ABSTRACT

INTRODUCTION: Radiation therapy (RT) after prostatectomy is an important curative treatment option for patients with prostate cancer. It can be delivered immediately after surgery as adjuvant treatment, or after biochemical PSA failure as salvage treatment. There is currently a lack of consensus regarding whether salvage RT in the event of biochemical failure or immediate adjuvant RT is the optimal postprostatectomy RT treatment. Although both types of postprostatectomy RT are generally well tolerated, patients may develop some toxicity that can impact their quality of life and the duration and frequency of treatments can be challenging for patients. It is imperative that patients be provided with evidence-based information so that they are able to make a treatment decision most aligned with their values. METHODS: To help address patients' informational needs, an online education resource was created for patients with prostate cancer considering postoperative RT. Patients and their families were asked to evaluate the effectiveness of this resource using a validated purpose-based information assessment. RESULTS: Nineteen patients were approached and 14 participated, but only five patients returned their evaluations (35%). Sixty percent found the information to be important with regards to each of the six commonly identified purposes in the purpose-based information assessment: organizing, understanding, decision-making, planning, emotional support, and discussing. Only one participant found the information hard to understand and had difficulty finding specific information. DISCUSSION: Patients should be encouraged to actively participate in their treatment decision-making process involving postprostatectomy RT. For patients to make well-informed decisions, patients must be provided with clear and accessible information so that they may understand their disease and the treatment options. CONCLUSION: An online education resource has been developed that most study respondents found clear and helpful for a variety of identified purposes. Overall, this online education resource has the potential to reach a large number of patients and their caregivers who desire specific information and involvement in future treatment decisions.


Subject(s)
Education, Distance/methods , Patient Education as Topic/methods , Prostatic Neoplasms/radiotherapy , Aged , Caregivers/education , Clinical Decision-Making/methods , Evidence-Based Medicine/methods , Humans , Male , Middle Aged , Patient Participation/methods , Pilot Projects , Prostatectomy , Prostatic Neoplasms/surgery , Radiotherapy, Adjuvant
2.
J Cancer Educ ; 29(2): 382-8, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24532366

ABSTRACT

Providing cancer patients with more information regarding their treatments allows them to feel more in control, increases self efficacy, and can decrease anxiety. The aims of the present study were to develop an interprofessional group education session and to evaluate the usefulness and acceptability of this session. In addition, informational distress levels pre- and post-education were evaluated. A prostate radiation therapy (RT) education session was developed and facilitated by an interprofessional team. Topics discussed included how RT works, side effects and management, and support services available. Prior to the education session, participants reported their informational RT distress levels using the validated Distress Thermometer (DT). Post-education session, the DT was readministered. In addition, participants completed an acceptability survey to assess format, structure, and usefulness of the education session. Participants agreed that the session contained valuable and useful information helping them understand expectations during treatment, including resource availability, side effects and management, as well as procedural expectation during treatment. All stated they would recommend the session to other patients. The interprofessional nature of the sessions was deemed useful. Suggested areas for improvement included addition of a dietitian, information on long-term side effects, statistics of radiotherapy side effects, impact of radiotherapy on sexual function, and overall quality of life. The group education session significantly improved informational distress levels (p = 0.04). Educating prostate cancer patients utilizing an interprofessional group format can decrease anxiety and stress related to their RT treatment. Future development of group education sessions for other disease site groups may be valuable.


Subject(s)
Cooperative Behavior , Interdisciplinary Communication , Patient Education as Topic , Prostatic Neoplasms/psychology , Stress, Psychological/prevention & control , Aged , Anxiety/prevention & control , Depression/prevention & control , Humans , Male , Middle Aged , Pilot Projects , Quality of Life , Self Efficacy , Surveys and Questionnaires
3.
Mol Ther ; 17(1): 26-33, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19018253

ABSTRACT

Patients with recessive dystrophic epidermolysis bullosa (RDEB) have incurable skin fragility, blistering, and scarring due to mutations in the gene that encodes for type VII collagen (C7) that mediates dermal-epidermal adherence in human skin. We showed previously that intradermal injection of recombinant C7 into transplanted human DEB skin equivalents stably restored C7 expression at the basement membrane zone (BMZ) and reversed the RDEB disease features. In this study, we evaluated the feasibility of protein therapy in a C7 null mouse (Col7a1(-/-)) which recapitulates the features of human RDEB. We intradermally injected purified human C7 into DEB mice and found that the injected human C7 stably incorporated into the mouse BMZ, formed anchoring fibrils, and corrected the DEB murine phenotype, as demonstrated by decreased skin fragility, reduced new blister formation, and markedly prolonged survival. After 4 weeks, treated DEB mice developed circulating anti-human C7 antibodies. Most surprisingly, these anti-C7 antibodies neither bound directly to the mouse's BMZ nor prevented the incorporation of newly injected human C7 into the BMZ. Anti-C7 antibody production was prevented by treating the mice with an anti-CD40L monoclonal antibody, MR1. We conclude that protein therapy may be feasible for the treatment of human patients with RDEB.


Subject(s)
Collagen Type VII/administration & dosage , Collagen Type VII/therapeutic use , Epidermolysis Bullosa Dystrophica/therapy , Animals , Antibodies/immunology , Basement Membrane/metabolism , Collagen Type VII/immunology , Collagen Type VII/metabolism , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Epidermolysis Bullosa Dystrophica/pathology , Humans , Injections, Intradermal , Mice , Mice, Knockout , Microscopy, Electron, Transmission , Recombinant Proteins/administration & dosage , Recombinant Proteins/therapeutic use , Skin/metabolism , Skin/pathology , Skin/ultrastructure
4.
Cutis ; 82(2): 123-30, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18792544

ABSTRACT

Delusions of parasitosis (DOP), a psychiatric disorder in which patients erroneously insist that they are infested with parasites, remains a fascinating entity with elusive origins. Typically, these patients are resistant to psychiatric referral and treatment with psychotropic medications. We discuss the classification, epidemiology, clinical presentation, etiology, associated features, and differential diagnosis of this disorder. The authors reviewed case reports and clinical trials and tabulated the epidemiologic data, which show DOP is more common than previously thought.


Subject(s)
Delusions/psychology , Parasitic Diseases/psychology , Antipsychotic Agents/therapeutic use , Delusions/classification , Delusions/diagnosis , Delusions/drug therapy , Diagnosis, Differential , Humans
5.
Curr Dir Autoimmun ; 10: 195-205, 2008.
Article in English | MEDLINE | ID: mdl-18460887

ABSTRACT

Epidermolysis bullosa acquisita (EBA) is an acquired, mechanobullous disease characterized by autoimmunity to type VII collagen. Type VII collagen makes anchoring fibrils, structures that connect the epidermis and its underlying basement membrane zone to the papillary dermis. EBA patients exhibit skin fragility, blisters, scars and milia formation reminiscent of genetic dystrophic epidermolysis bullosa (DEB). DEB patients have diminutive or absent anchoring fibrils due to a genetic defect in the gene encoding type VII collagen. EBA patients have a decrease in normally functioning anchoring fibrils secondary to an abnormality in their immune system in which they produce 'pathogenic' IgG anti-type VII collagen antibodies. The pathogenicity of these autoantibodies has been demonstrated by passive transfer animal models, in which anti-type VII collagen antibodies injected into a mouse produced an EBA-like blistering disease in the animal. EBA has several distinct clinical presentations. It can present with features similar to DEB, bullous pemphigoid, cicatricial pemphigoid, Brunsting-Perry pemphigoid or IgA bullous dermatosis. Treatment for EBA is unsatisfactory, however, some therapeutic success has been reported with colchicine, dapsone, photophoresis, infliximab and intravenous immunoglobulin.


Subject(s)
Autoimmune Diseases/immunology , Basement Membrane/immunology , Collagen Type IV/immunology , Dermis/immunology , Epidermis/immunology , Epidermolysis Bullosa Acquisita/immunology , Animals , Autoimmune Diseases/drug therapy , Autoimmune Diseases/genetics , Autoimmune Diseases/pathology , Autoimmunity/genetics , Basement Membrane/pathology , Collagen Type IV/genetics , Dermis/pathology , Epidermis/pathology , Epidermolysis Bullosa Acquisita/drug therapy , Epidermolysis Bullosa Acquisita/genetics , Epidermolysis Bullosa Acquisita/pathology , Epidermolysis Bullosa Dystrophica/drug therapy , Epidermolysis Bullosa Dystrophica/genetics , Epidermolysis Bullosa Dystrophica/immunology , Epidermolysis Bullosa Dystrophica/pathology , Humans , Immunization, Passive , Immunosuppressive Agents/therapeutic use , Mice
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