Subject(s)
Glaucoma, Open-Angle/surgery , Sclerostomy , Trabeculectomy , Humans , Intraocular PressureABSTRACT
"That tongue of yours, by which I have been tricked, shall have its power curtailed and enjoy the briefest use of speech." With these words, Hera, of Greek mythology, deprived the nymph Echo of spontaneous speech, constraining her instead to merely repeating the words of others. Echolalia, which derives from the word "echo," is disordered speech in which an individual persistently repeats what is heard. Echolalia has been described in patients with a number of neuropsychiatric illnesses including autism and Tourette's syndrome. Neuropsychiatric systemic lupus erythematosus (NPSLE) is a heterogeneous disease with protean manifestations that may occur in approximately 25% to 50% of patients with systemic lupus erythematosus (SLE). Although the most common manifestations include cognitive dysfunction (50%) and seizures (20%), NPSLE may also present as peripheral neuropathy (15%), psychosis (10%), or other central nervous system abnormalities. We report the case of a 57-year-old woman with SLE and echolalia.
Subject(s)
Echolalia/etiology , Lupus Vasculitis, Central Nervous System/complications , Lupus Vasculitis, Central Nervous System/diagnosis , Anti-Inflammatory Agents/therapeutic use , Cyclophosphamide/therapeutic use , Drug Therapy, Combination , Female , Humans , Immunosuppressive Agents/therapeutic use , Lupus Vasculitis, Central Nervous System/blood , Lupus Vasculitis, Central Nervous System/drug therapy , Lupus Vasculitis, Central Nervous System/immunology , Middle Aged , Steroids , Treatment OutcomeSubject(s)
Antirheumatic Agents/adverse effects , Immunoglobulin G/chemistry , Immunologic Factors/adverse effects , Receptors, Tumor Necrosis Factor/chemistry , Antirheumatic Agents/administration & dosage , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/pathology , Biopsy , Etanercept , Female , Humans , Immunoglobulin G/administration & dosage , Immunologic Factors/administration & dosage , Injections , Middle Aged , Receptors, Tumor Necrosis Factor/administration & dosage , Skin/pathologyABSTRACT
OBJECTIVES: This pilot study was designed to assess the ability of a photoscreening camera to detect amblyogenic factors such as high refractive error, anisometropia, media opacities and strabismus in children, compared to the standard vision screening techniques employed by the local state public health screening personnel. METHODS: Public health personnel in Illinois used the Eyecor prototype to the current commercially available MTI PS-100 photoscreening camera (manufactured by Medical Technology Inc.) to screen 127 non-dilated subjects, ages 7 months to 20 years (mean age, 6 years), for amblyogenic factors. All participants were concurrently subjected to the "standard" vision screening employed routinely by state public health personnel. The study participants included a group of normal inner-city children and one group of special-needs children. The normal children came from both a public school and a private school. The special-needs children included a group of children from a state-run school for the deaf and hard-of-hearing and a separate group of children attending a multi-disciplinary Easter Seals clinic. RESULTS: In the population of normal children, the mean sensitivity and specificity for the observers using the Eyecor Camera system was 81% and 83% with a mean positive predictive value of 83%, and a mean negative predictive value of 55%. Standard vision screening techniques employed by public health service certified vision screeners had a sensitivity of 88%, a specificity of 91%, a positive predictive value of 67% and a negative predictive value of 97% in the same subjects. In the population of special-needs children with hearing impairment and developmental delay, the mean sensitivity and specificity for the observers using the Eyecor Camera system was 74% and 82% with a mean positive predictive value of 69% and a mean negative predictive value of 85%. Standard vision screening techniques employed by public health service certified vision screeners had a sensitivity of 100%, a specificity of 55%, a positive predictive value of 62% and a negative predictive value of 100% in the same subjects. (See Table 1) CONCLUSIONS: This study shows that the Eyecor Photoscreening Camera is useful in screening normal children for amblyogenic factors. Photoscreening was at least as effective as standard screening methodologies performed by certified vision screeners as required by state public health policy. In addition, photoscreening is particularly useful in testing those children "unscreenable" by conventional vision screening procedures.
Subject(s)
Amblyopia/diagnosis , Health Personnel , Photography/methods , Public Health , Vision Screening/methods , Adolescent , Adult , Amblyopia/epidemiology , Child , Child, Preschool , Double-Blind Method , False Positive Reactions , Humans , Illinois/epidemiology , Incidence , Infant , Pilot Projects , Predictive Value of Tests , Prospective Studies , Reproducibility of Results , Risk Factors , Sensitivity and SpecificityABSTRACT
PURPOSE: Some surgeons are wary of using alcohol-preserved sclera for allografts because they fear a toxic effect on surrounding tissue after placement. We set out to determine the amount of ethanol remaining in scleral allograft material after storage in 95% ethanol. METHODS: Sixty half scleras from 30 donors were preserved in 95% ethanol for an average of 31+/-14 days (range, 11 to 50 days). Rehydration was performed by soaking each half sclera in 4 ounces of balanced salt solution. Half scleras were randomly assigned to six groups of 10 each. Assays for ethanol were performed on the following groups: no balanced salt solution soak and balanced salt solution soak for 10 minutes, 20 minutes, 30 minutes, 40 minutes, and 50 minutes. Ethanol assay was performed by Headspace Gas Space Chromatography at ChemaTox Laboratory, Inc, Boulder, Colorado. RESULTS: The 10 half scleras without balanced salt solution soak had a mean ( SD) ethanol level of 175+/-14.1 mg per g of sclera. After 10 minutes of balanced salt solution s oak, the level decreased to 7.57+/-1.56 mg per g, then 3.77+/-3.02 mg per g at 20 minutes, 1.59+/-0.61 mg per g at 30 minutes, 1.07+/-0.30 mg per g at 40 minutes, and 0.96+/-0.26 mg per g at 50 minutes. Approximately 96% of the ethanol is leeched out of the half sclera by 10 minutes and 98% by 20 minutes. CONCLUSIONS: For sclera preserved in 95% ethanol, soaking in balanced salt solution for 20 minutes or longer leeches approximately 98% of the ethanol from the preserved donor sclera.
Subject(s)
Drug Residues/analysis , Ethanol/analysis , Organ Preservation Solutions/analysis , Organ Preservation , Sclera/chemistry , Tissue Donors , Humans , Sodium Chloride , Therapeutic Irrigation , Time FactorsABSTRACT
Pediatric ophthalmologists should respond to quality expectations inherent in all disciplines of medicine. The specialists must be able to collect data to document and prove the quality of their work if it anticipates continued reimbursement for services. Quality of medical practice is assessed by outcomes research, which is different from clinical research. All specialists are systemically measuring individual and group outcomes across the spectrum of American health care systems. Pediatric ophthalmologists, both in private practice and at academic centers, must concentrate their research efforts on the assessment of cost, quality, utilization, and patient-centered health-related quality of life for the most common pathologies in pediatric ophthalmology practice.
Subject(s)
Ophthalmology/standards , Quality Indicators, Health Care/standards , Quality of Health Care , Child , Humans , Infant , Outcome Assessment, Health Care/standardsSubject(s)
Hypergammaglobulinemia/complications , Immunoglobulin G/analysis , Immunoglobulin lambda-Chains/analysis , Lymphoma, Non-Hodgkin/complications , Paraproteinemias/complications , Retinal Vein Occlusion/etiology , Aged , Bone Marrow/pathology , Chlorambucil/therapeutic use , Drug Therapy, Combination , Fluorescein Angiography , Humans , Hypergammaglobulinemia/diagnosis , Hypergammaglobulinemia/drug therapy , Lymphoma, Non-Hodgkin/diagnosis , Lymphoma, Non-Hodgkin/drug therapy , Male , Paraproteinemias/diagnosis , Paraproteinemias/drug therapy , Prednisone/therapeutic use , Retinal Vein Occlusion/diagnosis , Retinal Vein Occlusion/drug therapy , Tomography, X-Ray Computed , Visual Acuity , Vitreous Hemorrhage/diagnosis , Vitreous Hemorrhage/drug therapy , Vitreous Hemorrhage/etiologySubject(s)
Endophthalmitis/microbiology , Eye Infections, Bacterial/etiology , Pneumococcal Infections/etiology , Scleral Buckling/adverse effects , Suture Techniques/adverse effects , Aged , Anti-Bacterial Agents , Drug Therapy, Combination/therapeutic use , Endophthalmitis/therapy , Eye Infections, Bacterial/microbiology , Eye Infections, Bacterial/therapy , Female , Glucocorticoids/therapeutic use , Humans , Lens, Crystalline/surgery , Pneumococcal Infections/microbiology , Pneumococcal Infections/therapy , Reoperation , Retinal Detachment/surgery , Streptococcus pneumoniae/isolation & purification , Time Factors , VitrectomyABSTRACT
OBJECTIVES: To report a series of five patients who developed systemic lupus erythematosus (SLE) after immunization and review the literature on vaccine-associated connective tissue diseases and the theoretical mechanisms that could explain such an association. METHODS: Uncontrolled retrospective analysis of cases identified sporadically over 7 years at three centers. RESULTS: In our series of 5 patients, symptoms of SLE developed within 2 to 3 weeks after secondary immunization. All patients met American College of Rheumatology (ACR) criteria for the diagnosis of SLE. In most patients, symptoms have been persistent. CONCLUSION: Although a coincidental association between vaccination and the onset of SLE cannot be excluded, the temporal relationship with the development of symptoms makes it immunologically plausible that vaccination triggered systemic autoimmunity in these rare cases. We propose that epidemiological studies be performed to examine this potential association in more detail to quantitate the risk and identify possible genetic risk factors.
Subject(s)
Immunization, Secondary/adverse effects , Lupus Erythematosus, Systemic/etiology , Vaccination/adverse effects , Vaccines/adverse effects , Adult , Autoimmunity/drug effects , Female , Humans , Lupus Erythematosus, Systemic/immunology , Male , Retrospective Studies , Risk FactorsABSTRACT
OBJECTIVE: To determine the safety and efficacy of 3 clinically relevant vaccines in patients with systemic lupus erythematosus (SLE). METHODS: We studied 73 consecutive SLE patients immunized with pneumococcal, tetanus toxoid (TT), and Haemophilus influenzae type B (HIB) vaccines. Patients were evaluated preimmunization and 12 weeks postimmunization for disease activity and immunization side effects. RESULTS: Eighty-four percent of the SLE patients developed a 4-fold titer increase in response to at least 1 vaccine, with 51% developing a 2-fold titer increase with all 3 vaccines. The majority of SLE patients developed protective levels of antibody to TT (90%) and HIB (88%). Although protective antibody levels could not be determined for pneumococcus, almost half of the patients (47%) developed a 4-fold antibody response. There was a trend toward a lower antibody response in patients with active disease treated with immunosuppressive therapy. Overall lupus disease activity was unaffected by immunization. CONCLUSION: Immunization is safe in SLE patients, with the overwhelming majority developing protective antibody levels. Therefore, SLE patients should receive immunizations according to the recommendations of the Centers for Disease Control and Prevention and the Immunization Practices Advisory Committee.
Subject(s)
Epitopes/immunology , Immunization , Lupus Erythematosus, Systemic/immunology , Adolescent , Adult , Aged , Antibody Formation/drug effects , Azathioprine/pharmacology , Bacterial Vaccines/administration & dosage , Cyclophosphamide/pharmacology , Haemophilus Vaccines/administration & dosage , Humans , Immunization/adverse effects , Middle Aged , Prednisone/pharmacology , Streptococcus pneumoniae/immunology , Tetanus Toxoid/administration & dosageSubject(s)
Attitude of Health Personnel , Internal Medicine/education , Internship and Residency , Medical Staff/psychology , Military Medicine/organization & administration , Education, Medical, Graduate/organization & administration , Humans , Managed Care Programs/organization & administration , Medical Staff/education , United StatesABSTRACT
Sexual and physical abuse during childhood seem to be common. The purpose of this study was to determine the prevalence of sexual and physical abuse reported by female fibromyalgia (FM) patients in a referral-based rheumatology practice, and whether patients with FM report greater frequencies of abuse than do patients with rheumatoid arthritis (RA).Patients from two tertiary care centers, 205 with FM and 84 with RA, were mailed a self-administered questionnaire requesting information about demographics, mental health care use, and history of sexual and/ or physical abuse. There were responses from 105 FM and 44 RA patients.A history of sexual or physical abuse was reported by 54% of the sample. Any type of abuse was significantly more prevalent among patients with FM (62%) compared with those with RA (34%, p = 0.02). FM patients had a significantly increased prevalence of both sexual abuse (51% vs. 32%, p = 0.028) and physical abuse (39 vs. 16%, p = 0.006) compared with RA patients. FM patients were more likely than RA patients to report a history of multiple sexual abusers, increased duration of sexual abuse, and more violent physical abuse. Irritable bowel syndrome was more common in FM (44%) than RA patients (9%, p < 0.001), and 57% of FM patients had seen a mental health professional compared with 30% of RA patients (p = 0.002).
ABSTRACT
The use of topical ocular antihistamine/decongestant combinations to treat symptoms associated with allergic conjunctivitis is widespread, effective, and generally without adverse effects. Recently, these medications have become available without a prescription, possibly leading patients to the erroneous assumption that they are void of side effects. Likewise, patients may use these drugs for many ocular therapies for which they are unintended, possibly resulting in ocular complications. One significant adverse effect of these antihistamine/decongestant combinations when used inappropriately is pupillary dilation with associated blurry vision. Continued emphasis of the possible deleterious side effects by the clinician is recommended to circumvent these problems.