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1.
Int Urogynecol J ; 25(1): 41-6, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23912506

ABSTRACT

INTRODUCTION AND HYPOTHESIS: Patient preparedness for stress urinary incontinence (SUI) surgery is associated with improvements in post-operative satisfaction, symptoms and quality of life (QoL). This planned secondary analysis examined the association of patient preparedness with surgical outcomes, treatment satisfaction and quality of life. METHODS: The ValUE trial compared the effect of pre-operative urodynamic studies with a standardized office evaluation of outcomes of SUI surgery at 1 year. In addition to primary and secondary outcome measures, patient satisfaction with treatment was measured using a five-point Likert scale (very dissatisfied to very satisfied) that queried subjects to rate the treatment's effect on overall incontinence, urge incontinence, SUI, and frequency. Preparedness for surgery was assessed using an 11-question Patient Preparedness Questionnaire (PPQ). RESULTS: Based on PPQ question 11, 4 out of 5 (81 %) of women reported they "agreed" or "strongly agreed" that they were prepared for surgery. Selected demographic and clinical characteristics were similar in unprepared and prepared women. Among SUI severity baseline measures, total UDI score was significantly but weakly associated with preparedness (question 11 of the PPQ; Spearman's r = 0.13, p = 0.001). Although preparedness for surgery was not associated with successful outcomes, it was associated with satisfaction (r s = 0.11, p = 0.02) and larger PGI-S improvement (increase; p = 0.008). CONCLUSIONS: Approximately half (48 %) of women "strongly agreed" that they felt prepared for SUI. Women with higher pre-operative preparedness scores were more satisfied, although surgical outcomes did not differ.


Subject(s)
Preoperative Care/psychology , Urinary Incontinence, Stress/surgery , Adult , Female , Humans , Middle Aged , Patient Satisfaction , Quality of Life/psychology , Treatment Outcome
2.
Bone Marrow Transplant ; 47(12): 1520-5, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22562079

ABSTRACT

Over the immediate past 4 years, our program has collected hematopoietic progenitor cells by apheresis from 48 individuals aged 61 and over (range 61-71 years of age). We have retrospectively analyzed the collection and transplant results associated with employing these donors, and have compared them with 175 donors aged 60 or less who were collected during the same time period. We have found no significant difference in venous access (P = 0.208), rate of post-transplant engraftment of neutrophils (P = 0.117) and platelets (P = 0.692), or in rate and grade of acute GVHD (P = 0.806). However, we have found that these older donors have a significantly lower mobilization of CD34 + cells as reflected in lower absolute counts of circulating CD34 + cells pre-apheresis (P = 0.016). This, in turn, results in lower CD34 + cell yields in apheresis products (P < 0.001), trending towards requiring more apheresis procedures (22.9 vs 13.7%, P = 0.095) to collect sufficient CD34 + cells for transplantation. We conclude that it is practical when necessary to employ donors aged 60 and above, as well as safe for both donor and intended recipient. However, concern over reduced CD34 + cell mobilization may be sufficient grounds to seek younger donors when possible.


Subject(s)
Blood Component Removal/methods , Hematopoietic Stem Cell Transplantation/methods , Age Factors , Aged , Female , Graft vs Host Disease/immunology , Hematopoietic Stem Cells/immunology , Humans , Male , Middle Aged , Retrospective Studies , Tissue Donors , Transplantation, Homologous
3.
Med Phys ; 39(6Part28): 3972, 2012 Jun.
Article in English | MEDLINE | ID: mdl-28519612

ABSTRACT

PURPOSE: To evaluate the clinical implementation of a deep inspiration breath hold (DIBH) treatment for left breast radiotherapy using surface imaging and visual aid. METHODS: A CT scan of the patient at DIBH is acquired and used for treatment planning. The plan and skin contour, containing isocenter and surface information are exported from the treatment planning system and imported into the surface imaging system (SIS). The skin contour constitutes the treatment reference surface or target DIBH position. A region of interest (ROI) consisting of the sternum and medial breasts is selected in the SIS. A set of video goggles allows the patient to view their breathing signal within the SIS, aiding in producing a reproducible and stable DIBH similar to simulation. Once the patient is set up at free breathing, she performs a DIBH while being monitored with the SIS. Shifts to minimize displacements from their reference DIBH surface are made. The surface image and patient setup are validated with weekly MV images. The beam is enabled when the two surfaces are within a predetermined tolerance. RESULTS: Data for evaluation of the implementation was acquired for 4 patients throughout treatment. Average treatment time was 16.8 minutes and 14.2 minutes for setup. The average displacement from the reference surface was 0.4 mm during DIBHs. The average reduction of heart mean dose and volume receiving 50% of the prescribed dose between DIBH and FB was 38% and 89% respectively. A total of 15 patients have completed this new treatment. 2 were excluded for inability to achieve reproducible and stable DIBH. CONCLUSION: The workflow we have implemented has proven to be effective and efficient for clinical purposes. Surface imaging provides adequate real time information valuable to the treatment process. Visual aid has helped patients achieve DIBH with high reproducibility and stability.

4.
Am J Physiol Regul Integr Comp Physiol ; 295(4): R1351-8, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18635445

ABSTRACT

Matrix metalloprotease (MMP) activity is increased in the postpartum vagina of wild-type (WT) animals. This degradative activity is also accompanied by a burst in elastic fiber synthesis and assembly. The mechanisms that precipitate these changes are unclear. The goals of this study were to determine how vaginal distention (such as in parturition) affects elastic fiber homeostasis in the vaginal wall and the potential significance of these changes in the pathogenesis of pelvic organ prolapse. Vaginal distention with a balloon simulating parturition resulted in increased MMP-2 and MMP-9 activity in the vaginal wall of nonpregnant and pregnant animals. This was accompanied by visible fragmented and disrupted elastic fibers in the vaginal wall. In nonpregnant animals, the abundant amounts of tropoelastin and fibulin-5 in the vagina were not increased further by distention. In contrast, in pregnant animals, the suppressed levels of both proteins were increased 3-fold after vaginal distention. Distention performed in fibulin-5-deficient (Fbln5(-/-)) mice with defective elastic fiber synthesis and assembly induced accelerated pelvic organ prolapse, which never recovered. We conclude that, in pregnant mice, vaginal distention results in increased protease activity in the vaginal wall but also increased synthesis of proteins important for elastic fiber assembly. Distention may thereby contribute to the burst of elastic fiber synthesis in the postpartum vagina. The finding that distention results in accelerated pelvic organ prolapse in Fbln5(-/-) animals, but not in WT, indicates that elastic fiber synthesis is crucial for recovery of the vaginal wall from distention-induced increases in vaginal protease activity.


Subject(s)
Catheterization , Elastic Tissue/metabolism , Extracellular Matrix/metabolism , Vagina/metabolism , Animals , Biomechanical Phenomena , Electrophoresis, Polyacrylamide Gel , Enzyme Precursors/metabolism , Extracellular Matrix Proteins/genetics , Extracellular Matrix Proteins/metabolism , Female , Gelatinases/metabolism , Male , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Mice , Mice, Inbred C57BL , Mice, Inbred Strains , Mice, Knockout , Pelvic Floor/pathology , Pelvic Floor/physiopathology , Perineum/pathology , Perineum/physiopathology , Pregnancy , Pregnancy Complications/etiology , Pregnancy Complications/physiopathology , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Tropoelastin/metabolism , Uterine Prolapse/etiology , Uterine Prolapse/physiopathology , Vagina/injuries , Vagina/physiopathology
5.
Infect Dis Clin North Am ; 15(1): 171-87, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11301814

ABSTRACT

The development of an effective vaccine for Lyme disease represents a major advance in the control of the most prevalent vector-borne disease in the United States. It has a definite place in the total approach to control of this disease. Its use should be restricted to individuals who are at moderate to high risk of exposure to infected vector ticks. Vaccinated individuals should not be complacent about other personal protection measures, because the vaccine is not uniformly effective and protective antibody levels decay rapidly. Booster doses will be necessary, but the intervals have not yet been determined. There is a theoretical concern about the possible induction of inflammatory arthritis through an autoimmune mechanism, but there is no evidence that this condition has clinical relevance. The impact of the current lawsuits on vaccine recommendations and use remains to be determined. Continued surveillance for rare long-term side effects should address the medical risk issue. Alternative primary vaccine administration schedules are currently under study, and could lead to regimens permitting achievement of protective immunity in 6 months or less. Vaccine is not approved for use in children under the age of 15 years.


Subject(s)
Lyme Disease Vaccines , Lyme Disease/prevention & control , Vaccination , Arthritis/etiology , Arthritis/immunology , Autoimmunity , Child , Clinical Trials as Topic , Humans , Immunization Schedule , Immunization, Secondary , Lyme Disease/complications , Lyme Disease/epidemiology , Lyme Disease Vaccines/administration & dosage , Lyme Disease Vaccines/immunology , Safety , United States/epidemiology
7.
Arch Dermatol ; 135(11): 1317-26, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10566829

ABSTRACT

OBJECTIVE: To evaluate the incidence of Borrelia burgdorferi infection in humans with erythema migrans (EM) in 2 southeastern states. DESIGN: Prospective case series. SETTING: Family medicine practice at academic center. PATIENTS: Twenty-three patients with solitary EM lesions meeting Centers for Disease Control and Prevention (CDC) criteria for Lyme disease. INTERVENTIONS: Patients underwent clinical and serologic evaluation for evidence of B burgdorferi infection. All lesions underwent photography, biopsy, culture and histopathologic and polymerase chain reaction analysis for B burgdorferi infection. Patients were treated with doxycycline hyclate and followed up clinically and serologically. MAIN OUTCOME MEASURES: Disappearance of EM lesions and associated clinical symptoms in response to antibiotic therapy; short-term and follow-up serologic assays for diagnostic antibody; growth of spirochetes from tissue biopsy specimens in Barbour-Stoenner-Kelly II media; special histopathologic stains of tissue for spirochetes; and polymerase chain reaction assays of tissue biopsy specimens for established DNA sequences of B burgdorferi. RESULTS: The EM lesions ranged from 5 to 20 cm (average, 9.6 cm). Five patients (22%) had mild systemic symptoms. All lesions and associated symptoms resolved with antibiotic therapy. Overall, 7 patients (30%) had some evidence of B burgdorferi infection. Cultures from 1 patient (4%) yielded spirochetes, characterized as Borrelia garinii, a European strain not known to occur in the United States; 3 patients (13%) demonstrated spirochetallike forms on special histologic stains; 5 patients (22%) had positive polymerase chain reaction findings with primers for flagellin DNA sequences; and 2 patients (9%) were seropositive for B burgdorferi infection using recommended 2-step CDC methods. No late clinical sequelae were observed after treatment. CONCLUSIONS: The EM lesions we observed are consistent with early Lyme disease occurring elsewhere, but laboratory confirmation of B burgdorferi infection is lacking in at least 16 cases (70%) analyzed using available methods. Genetically variable strains of B burgdorferi, alternative Borrelia species, or novel, uncharacterized infectious agents may account for most of the observed EM lesions.


Subject(s)
Erythema Chronicum Migrans/diagnosis , Lyme Disease/diagnosis , Adult , Aged , Anti-Bacterial Agents/therapeutic use , Antibodies, Bacterial/blood , Biopsy , Borrelia/classification , Borrelia burgdorferi Group/genetics , Borrelia burgdorferi Group/growth & development , Borrelia burgdorferi Group/immunology , Coloring Agents , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Doxycycline/therapeutic use , Erythema Chronicum Migrans/drug therapy , Erythema Chronicum Migrans/microbiology , Female , Flagellin/analysis , Flagellin/genetics , Follow-Up Studies , Georgia , Humans , Incidence , Male , Middle Aged , Photography , Polymerase Chain Reaction , Prospective Studies , South Carolina
9.
Telemed J ; 5(4): 349-56, 1999.
Article in English | MEDLINE | ID: mdl-10908450

ABSTRACT

OBJECTIVES: To determine patient satisfaction with telemedicine encounters among adults with sickle cell disease and compare their scores with SCD patients who have standard medical encounters (as controls). METHODS: Adults patients were recruited from a list of participants in sickle cell telemedicine clinics and prospectively at the time of clinic encounter. Patients were assigned to telemedicine or standard encounter groups. Demographic and pertinent clinical data were obtained for all subjects, and the Client Satisfaction Questionnaire (CSQ-8) was administered. Patients were also asked for open-ended comments regarding their satisfaction with the service. Their responses were recorded verbatim. RESULTS: Patients with telemedicine (n = 60) and standard encounters (n = 60) were comparable in gender, genotype, education, employment, and mean number of sickle cell disease-related complications. Patients in the telemedicine group were younger (p< 0.005), more likely to have Medicaid insurance (p = 0.009), and more likely be taking hydroxyurea (p = 0.003) than patients in the control encounter group. Mean CSQ scores for the telemedicine group were high (total: 28.82+/-3.06), and there was no difference for any item between encounter groups (p = 0.389). Patients in the standard encounter group were more likely to provide positive open-ended comments regarding the encounter (95% vs. 70%; p = 0.001). Negative comments were generally in the area of confidentiality. CONCLUSIONS: While some patients expressed concern about confidentiality with telemedicine, the benefits of improved access and continuity of care were recognized, and overall satisfaction with telemedicine was high. These findings support the use of telemedicine as an acceptable health care delivery option for rural, underserved populations with sickle cell disease.


Subject(s)
Patient Satisfaction/statistics & numerical data , Remote Consultation , Sickle Cell Trait , Adult , Confidentiality , Female , Georgia , Humans , Male , Regional Medical Programs , Rural Health Services , Surveys and Questionnaires
11.
Postgrad Med ; 103(5): 51-4, 57-9, 63-4 passim, 1998 May.
Article in English | MEDLINE | ID: mdl-9590986

ABSTRACT

A rational approach to diagnosis and treatment of Lyme disease requires an understanding of the endemic range of the tick vectors for B burgdorferi, the epidemiologic risk factors, and the spectrum of clinical manifestations. A two-step approach to serologic testing (ELISA followed by Western blot analysis of positive or equivocal results) can be useful if the pretest likelihood of Lyme disease is higher than 20%. Consideration should be given to the possibility of (1) a noninfectious disease with clinical features similar to those of Lyme disease or (2) coinfection with a second tick-transmitted organism. Late Lyme disease must be distinguished by clinical characteristics from fibromyalgia (the commonest source of misdiagnosis in several studies). Antibiotic therapy should be tailored to the extent of disease and limited to 4 weeks in most cases. Human vaccines based on an outer-surface protein from B burgdorferi have been tested in large-scale US clinical trials and may soon be approved for use in persons whose occupational or recreational activities place them at risk for B burgdorferi exposure.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Lyme Disease/diagnosis , Lyme Disease/drug therapy , Animals , Arachnid Vectors , Blotting, Western , Enzyme-Linked Immunosorbent Assay , Humans , Lyme Disease/etiology , Lyme Disease/transmission , Prevalence , Risk Factors , Ticks , Time Factors
12.
J Gen Intern Med ; 12(11): 715-7, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9383142

ABSTRACT

The objective of this project was to compare faculty productivity in teaching and nonteaching clinical settings. We hypothesized that teaching activity would have no impact on productivity. A mixed model, repeated measures analysis of variance was used to analyze average relative value units (RVUs) billed and to test for differences between clinics. Data were drawn from 4,956 clinical encounters made within a student, resident, and faculty clinic. Average RVUs per visit were similar in the three settings. Resident supervision increased faculty productivity, while student supervision had no impact on billed RVUs. Thus, RVUs can be used as a measure of faculty clinical productivity in different settings in an academic medical center. Precepting students does not appear to affect clinical productivity.


Subject(s)
Efficiency, Organizational , Faculty, Medical , Relative Value Scales , Humans , Outpatient Clinics, Hospital , Teaching
14.
Ann Intern Med ; 124(9): 785-91, 1996 May 01.
Article in English | MEDLINE | ID: mdl-8610947

ABSTRACT

OBJECTIVE: To determine whether azithromycin or amoxicillin is more efficacious for the treatment of erythema migrans skin lesions, which are characteristic of Lyme disease. DESIGN: Randomized, double-blind, double-dummy, multicenter study. Acute manifestations and sequelae were assessed using a standardized format. Baseline clinical characteristics and response were correlated with serologic results. Patients were followed for 180 days. SETTING: 12 outpatient centers in eight states. PATIENTS: 246 adult patients with erythema migrans lesions at least 5 cm in diameter were enrolled and were stratified by the presence of flu-like symptoms (such as fever, chills, headache, malaise, fatigue, arthralgias, and myalgias) before randomization. INTERVENTION: Oral treatment with either amoxicillin, 500 mg three times daily for 20 days, or azithromycin, 500 mg once daily for 7 days. Patients who received azithromycin also received a dummy placebo so that the dosing schedules were identical. RESULTS: Of 217 evaluable patients, those treated with amoxicillin were significantly more likely than those treated with azithromycin to achieve complete resolution of disease at day 20, the end of therapy (88% compared with 76%; P=0.024). More azithromycin recipients (16%) than amoxicillin recipients (4%) had relapse (P=0.005). A partial response at day 20 was highly predictive of relapse (27% of partial responders had relapse compared with 6% of complete responders; P<0.001). For patients treated with azithromycin, development of an antibody response increased the possibility of achieving a complete response (81% of seropositive patients achieved a complete response compared with 60% of seronegative patients; P=0.043). Patients with multiple erythema migrans lesions were more likely than patients with single erythema migrans lesions (P<0.001) to have a positive antibody titer at baseline (63% compared with 17% for IgM; 39% compared with 16% for IgG). Fifty-seven percent of patients who had relapse were seronegative at the time of relapse. CONCLUSIONS: A 20-day course of amoxicillin was found to be an effective regimen for erythema migrans. Most patients were seronegative for Borrelia burgdorferi at the time of presentation with erythema migrans (65%) and at the time of relapse (57%).


Subject(s)
Amoxicillin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Azithromycin/therapeutic use , Erythema Chronicum Migrans/drug therapy , Penicillins/therapeutic use , Adult , Amoxicillin/adverse effects , Anti-Bacterial Agents/adverse effects , Antibodies, Bacterial/blood , Azithromycin/adverse effects , Double-Blind Method , Enzyme-Linked Immunosorbent Assay , Erythema Chronicum Migrans/immunology , Female , Humans , Male , Penicillins/adverse effects , Prospective Studies , Recurrence , Treatment Failure
17.
Ann Intern Med ; 119(6): 503-9, 1993 Sep 15.
Article in English | MEDLINE | ID: mdl-8357117

ABSTRACT

PURPOSE: To examine the cost-effectiveness of empirical, parenteral antibiotic treatment of patients with chronic fatigue and myalgia and a positive serologic result for Lyme disease who lack classic manifestations. DATA SOURCES: Peer-reviewed journals, opinion of experts in the field, and published epidemiologic reports. STUDY SELECTION: Consensus by authors on articles that indicated methods for patient selection; on criteria used for diagnosis; on immunologic methods used for classifying patients; on the dose and duration of therapy; and on criteria by which responses to therapy were ascertained. DATA EXTRACTION: In a cost-effectiveness model, the costs and benefits of empirical parenteral therapy for patients seropositive for Lyme disease were compared with a strategy in which only patients having classical symptoms of Lyme disease were treated. DATA SYNTHESIS: In areas endemic for Lyme disease, the incidence of false-positive serologic results in patients with nonspecific myalgia or fatigue exceeds by four to one the incidence of true-positive results in patients with nonclassical infections. Treatment of the former group of patients costs $86,221 for each true-positive patient treated. The empirical strategy causes 29 cases of drug toxicity for every case in the more conservative strategy. If patients were willing to pay $3485 to eliminate anxiety about not treating possible true Lyme disease, the empirical strategy would break even. CONCLUSION: For most patients with a positive Lyme antibody titer whose only symptoms are nonspecific myalgia or fatigue the risks and costs of empirical parenteral antibiotic therapy exceed the benefits. Only when the value of patient anxiety about leaving a positive test untreated exceeds the cost of such therapy is the empirical treatment cost-effective.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Fatigue Syndrome, Chronic/drug therapy , Fibromyalgia/drug therapy , Lyme Disease/drug therapy , Lyme Disease/economics , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/economics , Cost-Benefit Analysis , Drug Administration Schedule , Drug Costs , Fatigue Syndrome, Chronic/etiology , Fibromyalgia/etiology , Humans , Infusions, Intravenous , Lyme Disease/complications , Lyme Disease/epidemiology , Prevalence , United States/epidemiology
18.
J Gen Intern Med ; 7(4): 434-6, 1992.
Article in English | MEDLINE | ID: mdl-1506951

ABSTRACT

The authors describe a primary care-based educational and practice model that integrates general medicine resident education in outpatient rheumatology with specialty fellowship training. Compared with the use of traditional specialty clinics, the model provides better access and service to patients and more appropriate training for residents. Revenues from clinical service delivered by faculty-supervised residents and fellows support 80% of the operating costs and educational activities of the model. The conceptual framework for the model reconciles the educational goals and practice philosophies of general medicine and specialty training and is applicable to training in other predominantly outpatient specialty areas.


Subject(s)
Education, Medical , Fellowships and Scholarships/trends , Internal Medicine/education , Internship and Residency/trends , Models, Theoretical , Outpatient Clinics, Hospital , Rheumatology/education , Specialization , Adolescent , Adult , Aged , Ambulatory Care/trends , Connecticut , Curriculum , Health Workforce , Humans , Internal Medicine/trends , Joint Diseases/diagnosis , Joint Diseases/therapy , Medicine/trends , Middle Aged , Outpatient Clinics, Hospital/trends , Rheumatology/trends
19.
J Infect Dis ; 165(6): 1127-32, 1992 Jun.
Article in English | MEDLINE | ID: mdl-1583333

ABSTRACT

Recombinant (r) outer surface proteins (Osp) A and B, flagellin, and an immunogenic region of flagellin (41-G) from Borrelia burgdorferi were evaluated using immunoblot and ELISA for usefulness as substrates in diagnostic testing for Lyme disease. Antibodies to rOspA, rOspB, and r-flagellin were detected by immunoblot and ELISA using the recombinant proteins. Patients with late disease responded to rOspA, rOspB, and r-flagellin, or only to r-flagellin, whereas patients with early disease showed no response or responded only to r-flagellin. Patients who developed antibodies to r-flagellin also responded to 41-G. The data suggest that recombinant B. burgdorferi antigens can serve as substrates for immunoblot and ELISA, which may be helpful in diagnosing Lyme disease.


Subject(s)
Antibodies, Bacterial/blood , Bacterial Outer Membrane Proteins/immunology , Borrelia burgdorferi Group/immunology , Flagellin/immunology , Lyme Disease/diagnosis , Antibodies, Monoclonal/immunology , Antigens, Bacterial/immunology , Enzyme-Linked Immunosorbent Assay , Humans , Immunoblotting , Recombinant Fusion Proteins/immunology , Recombinant Proteins/immunology
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