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1.
Artif Organs ; 23(9): 817-21, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10491028

RESUMO

The aim of this study is to assess the clinical performance of 6 different low-flux dialysis membranes under steady-state conditions in terms of urea and phosphate clearances. Ten stable hemodialysis patients were examined. The following dialyzers were studied, all in 1.5- to 1.6-m2 format: cuprammonium, cellulose acetate, cellulose diacetate, hemophane, polysulfone (low-flux), and polysynthane. The following parameters were examined: urea reduction ratio, phosphate reduction ratio, "instantaneous dialyzer clearance" for urea and phosphate, and total amount of urea and phosphate removed in the dialysate over a 1-week (three dialyses) period. Although there were differences between the membranes, all produced results within a narrow range. There was no one membrane that produced superior clearances in all categories. The cellulose acetate membrane was the least satisfactory membrane. Phosphate clearances were at best one third that of urea clearances. When choosing a low-flux dialysis membrane, urea and phosphate clearances are so similar amongst different membranes that other criteria are likely to have a greater influence on the choice of membrane.


Assuntos
Materiais Biocompatíveis/química , Membranas Artificiais , Diálise Renal/instrumentação , Adulto , Idoso , Celulose/análogos & derivados , Celulose/química , Soluções para Diálise/análise , Desenho de Equipamento , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Fosfatos/análise , Fosfatos/sangue , Polímeros/química , Sulfonas/química , Fatores de Tempo , Ureia/análise , Ureia/sangue
2.
J Reprod Med ; 41(5): 352-4, 1996 May.
Artigo em Inglês | MEDLINE | ID: mdl-8725762

RESUMO

OBJECTIVE: To describe the occurrence of subinvolution of the placental bed following molar pregnancy. STUDY DESIGN: A review of archival histology and clinical charts. RESULTS: Four cases of subinvolution of the placental bed after a molar pregnancy were found in an institutional review; three were preceded by a complete mole and one by a partial mole. In all four cases the arteries were widely distended and mainly devoid of thrombus formation. Plentiful persistent interstitial trophoblast was seen within the decidua and myometrium, and endovascular trophoblast was seen embedded within the arterial walls in all four and intraluminally in two of the cases. CONCLUSION: The condition may be underdiagnosed after molar pregnancy and is a likely cause of continued bleeding following evacuation of the hydatidiform mole.


Assuntos
Mola Hidatiforme/complicações , Placenta/irrigação sanguínea , Placenta/patologia , Complicações Neoplásicas na Gravidez/patologia , Neoplasias Uterinas/complicações , Adulto , Decídua/patologia , Feminino , Humanos , Mola Hidatiforme/diagnóstico , Miométrio/patologia , Gravidez , Complicações Neoplásicas na Gravidez/diagnóstico , Estudos Retrospectivos , Trofoblastos/patologia , Neoplasias Uterinas/diagnóstico
3.
Aust N Z J Obstet Gynaecol ; 36(2): 210-2, 1996 May.
Artigo em Inglês | MEDLINE | ID: mdl-8798318

RESUMO

Uterine rupture is extremely rare in the absence of any of the commonly recognized risk factors. We describe here a case of incomplete uterine rupture in a woman in her first pregnancy who had no previous instrumentation to the genital tract. Her only significant history was that of 2 episodes of minor antepartum haemorrhage occurring prior to induction of labour with artificial rupture of membranes and intravenous oxytocin. The rupture was manifested by 450 mL blood in the peritoneal cavity when an emergency Caesarean section was performed for persistent fetal bradycardia.


Assuntos
Paridade , Ruptura Uterina/etiologia , Adulto , Bradicardia/etiologia , Cesárea , Feminino , Doenças Fetais/etiologia , Humanos , Gravidez , Fatores de Risco , Ruptura Uterina/complicações
4.
Ann Intern Med ; 124(5): 469-76, 1996 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-8602704

RESUMO

OBJECTIVE: To determine the prevalence of vitamin B12 deficiency in patients who have had gastric surgery. DESIGN: Cross-sectional study. SETTING: Philadelphia Veterans Affairs Medical Center. PARTICIPANTS: 61 patients who had had gastric surgery and 107 controls. MEASUREMENTS: Serum levels of vitamin B12, folate, methylmalonic acid, and total homocysteine measured before and after treatment in participants with vitamin B12 deficiency. Vitamin B12 deficiency was defined as one of the following: 1) a serum vitamin B12 level less than 221 pmol/L and an elevated methylmalonic acid level; 2) a serum vitamin B12 level less than 221 pmol/L and an elevated total homocysteine level that decreased with vitamin B12 treatment; or 3) in patients unavailable for treatment, a serum vitamin B12 level less than 221 pmol/L, a folate level greater than 9 nmol/L, and an elevated total homocysteine level. RESULTS: Study patients and controls were similar in age, sex, and racial distribution. Nineteen patients (31%) and 2 controls (2%) had vitamin B12 deficiency (P < 0.001). Twelve (63%) of the 19 vitamin B12-deficient patients had elevated total homocysteine levels. In all participants with vitamin B12 deficiency who received treatment (15 of 21), methylmalonic acid and total homocysteine levels decreased substantially, confirming the deficiency before treatment. CONCLUSION: Patients who have had gastric surgery have a high prevalence of vitamin B12 deficiency. Prompt recognition and treatment of the deficiency with resultant normalization of elevated total homocysteine and methylmalonic acid levels may prevent the development of cardiovascular, hematologic, and neurologic abnormalities. Our data support both frequent screening and vitamin B12 replacement therapy in patients who have had gastric surgery and have serum vitamin B12 levels less than 221 pmol/L.


Assuntos
Homocisteína/sangue , Ácido Metilmalônico/sangue , Complicações Pós-Operatórias/sangue , Estômago/cirurgia , Deficiência de Vitamina B 12/diagnóstico , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos Transversais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Vitamina B 12/sangue , Deficiência de Vitamina B 12/sangue , Deficiência de Vitamina B 12/tratamento farmacológico
5.
Arch Intern Med ; 155(17): 1900-6, 1995 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-7677557

RESUMO

BACKGROUND: Coronary artery disease strikes early and may prove particularly severe in persons of African-American descent. Therefore, we studied the lipid-lowering efficacy and safety of pravastatin sodium (20 mg/d), a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, in 245 African-American patients with primary hypercholesterolemia. METHODS: After 4 weeks on an American Heart Association phase I low-fat diet, patients were randomized in a double-blind manner to either pravastatin or placebo in a 3:1 ratio. RESULTS: After 12 weeks of pravastatin treatment, low-density lipoprotein cholesterol levels declined 25.8%, total cholesterol levels 20.3%, and triglyceride levels 6.2%, while high-density lipoprotein cholesterol levels remained essentially unchanged. Overall, 72% of pravastatin-treated patients achieved reductions in low-density lipoprotein cholesterol level in excess of 20%, and 44% attained declines in excess of 30% (both P < .01 vs placebo). Pravastatin was generally well tolerated in this population, with one patient (0.5%) exhibiting a reversible myopathy with creatine kinase elevations to 10 times the upper limit of normal. No substantial elevations of aminotransferase levels of two to three times the upper limit of normal occurred in either the pravastatin or the placebo group. Drug compliance was high, exceeding 90%. CONCLUSION: Pravastatin appears to be an effective and safe lipid-lowering agent and is the first 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor to be studied extensively in this underrepresented population.


Assuntos
Anticolesterolemiantes/uso terapêutico , População Negra , Hipercolesterolemia/tratamento farmacológico , Pravastatina/uso terapêutico , Anticolesterolemiantes/efeitos adversos , Método Duplo-Cego , Inibidores Enzimáticos/uso terapêutico , Feminino , Humanos , Hipercolesterolemia/sangue , Lipídeos/sangue , Masculino , Pessoa de Meia-Idade , Pravastatina/efeitos adversos
6.
Spec Care Dentist ; 15(4): 159-65, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-9002920

RESUMO

A sample of 44 adults with severe disabilities completed a randomized single-blind cross-over study testing chlorhexidine swabbing under various conditions: with/without prior dental prophylaxis, reduced frequency of application (2 vs. 5 times per week), and prolonged use (42 weeks). All subjects received therapeutic doses of 10 mL 0.12% chlorhexidine gluconate (Peridex, Procter & Gamble) and 10 mL 0.05% NaF applied with a Toothette (Sage Products). Clinical effectiveness of chlorhexidine swabbing compared with placebo was previously reported. In the present study, while initial benefits were observed to be independent of dental prophylaxis, significant reductions in periodontal scores were sustained by a combination of dental prophylaxis and swabbing protocol, at reduced frequency of application and over prolonged time. High levels of acceptance and compliance by subjects/caregivers were maintained. Subjects/caregivers reported improvements in dental health as well as in attitude, quality of life, and smile. Chlorhexidine swabbing at maintenance frequency, combined with periodic dental prophylaxis, may offer an effective and pragmatic long-term preventive regimen for persons with disabilities.


Assuntos
Anti-Infecciosos Locais/administração & dosagem , Clorexidina/análogos & derivados , Assistência Odontológica para a Pessoa com Deficiência/métodos , Dispositivos para o Cuidado Bucal Domiciliar , Antissépticos Bucais/uso terapêutico , Higiene Bucal/métodos , Adulto , Clorexidina/administração & dosagem , Estudos Cross-Over , Índice CPO , Cálculos Dentários/prevenção & controle , Placa Dentária/prevenção & controle , Índice de Placa Dentária , Feminino , Gengivite/prevenção & controle , Humanos , Masculino , Higiene Bucal/instrumentação , Índice Periodontal , Método Simples-Cego , Fluoreto de Sódio/uso terapêutico , Estatísticas não Paramétricas
8.
Am J Cardiol ; 74(2): 149-54, 1994 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-8023779

RESUMO

Seventy-four patients with plasma low-density lipoprotein cholesterol levels > or = 160 mg/dl after an American Heart Association phase 1 diet were randomized to double-blind treatment with fluvastatin, 20 mg/day, or placebo for 6 weeks. Immediate-release niacin was then added to both treatment regimens and titrated to a maximum of 3 g/day for a further 9 weeks. After 6 weeks of fluvastatin monotherapy, low-density lipoprotein cholesterol levels decreased by 21% (p < 0.001 vs placebo), and after the addition of niacin, response was potentiated to 40% compared with 25% for the niacin control group at study end point (p < 0.001). Fluvastatin, alone and in combination with niacin, also significantly improved high-density lipoprotein cholesterol (increases of about 30%) and triglyceride profiles (decreases of approximately 28%) from baseline. Lipoprotein(a) decreased by 37% in those receiving fluvastatin-niacin but was unaltered in those receiving fluvastatin alone. No serious adverse events were ascribed to fluvastatin, and no cases of myositis were observed. Small, transient, asymptomatic increases in aspartate aminotransferase were noted with fluvastatin-niacin treatment but were not considered clinically relevant. Although the fluvastatin-niacin combination in this study was without evidence of significant transaminitis, myopathy, or rhabdomyolysis, it would seem prudent to continue to monitor its safety with longer term use. In conclusion, fluvastatin, both as monotherapy and in combination with niacin, proved to be an effective, safe, and well-tolerated therapeutic alternative for hypercholesterolemia.


Assuntos
Anticolesterolemiantes/uso terapêutico , Ácidos Graxos Monoinsaturados/uso terapêutico , Hipercolesterolemia/tratamento farmacológico , Indóis/uso terapêutico , Niacina/uso terapêutico , Adulto , Idoso , Alanina Transaminase/sangue , Anticolesterolemiantes/administração & dosagem , Anticolesterolemiantes/efeitos adversos , Aspartato Aminotransferases/sangue , Colesterol/sangue , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Método Duplo-Cego , Combinação de Medicamentos , Tolerância a Medicamentos , Ácidos Graxos Monoinsaturados/administração & dosagem , Ácidos Graxos Monoinsaturados/efeitos adversos , Feminino , Fluvastatina , Seguimentos , Humanos , Hipercolesterolemia/sangue , Hipercolesterolemia/dietoterapia , Indóis/administração & dosagem , Indóis/efeitos adversos , Lipoproteína(a)/sangue , Masculino , Pessoa de Meia-Idade , Niacina/administração & dosagem , Niacina/efeitos adversos , Cooperação do Paciente , Placebos , Triglicerídeos/sangue
9.
Spec Care Dentist ; 13(6): 229-35, 1993.
Artigo em Inglês | MEDLINE | ID: mdl-8042130

RESUMO

A controlled pilot study determined oral health in persons with quadriplegia due to spinal cord injury, and compared dental disease rates in spinal cord injury and other disability groups. Seventeen adults with spinal cord injury and 17 controls were assessed for dental/medical/social history; manual function; head, neck, and oral lesions; salivary flow; DMFS; and gingivitis, periodontal pockets, plaque, and calculus. Findings were compared with those from prior studies according to the same protocol, for groups of similar age with mental retardation, cerebral palsy, traumatic brain injury, and chronic mental illness. No significant differences between spinal cord injury and control subjects were noted, except that fewer spinal cord injury subjects brushed daily or flossed (p < 0.05); dependent subjects tended to have more plaque and gingivitis than those brushing independently. Subjects with spinal cord injury and mental illness had less gingivitis than those with mental retardation and cerebral palsy (p < 0.001); on calculus, subjects with spinal cord injury ranked lower than subjects with mental illness (p < 0.05). On DFS, mentally ill subjects and those with traumatic brain injury ranked higher than mentally retarded and cerebral palsy groups, with spinal cord injury subjects intermediate. Mentally retarded and traumatic-brain-injured subjects had fewer teeth than other groups (p < 0.05). The findings suggest differences in oral health status and oral care for various disabled populations.


Assuntos
Assistência Odontológica para a Pessoa com Deficiência/estatística & dados numéricos , Cárie Dentária/complicações , Doenças Periodontais/complicações , Quadriplegia/complicações , Traumatismos da Medula Espinal/complicações , Adulto , Análise de Variância , Lesões Encefálicas/complicações , Paralisia Cerebral/complicações , Distribuição de Qui-Quadrado , Índice CPO , Índice de Placa Dentária , Feminino , Necessidades e Demandas de Serviços de Saúde/estatística & dados numéricos , Humanos , Deficiência Intelectual/complicações , Masculino , Transtornos Mentais/complicações , Doenças Periodontais/epidemiologia , Projetos Piloto , Prevalência
10.
Spec Care Dentist ; 12(2): 57-62, 1992.
Artigo em Inglês | MEDLINE | ID: mdl-1440118

RESUMO

Chlorhexidine is effective when used as an oral rinse, but many disabled people cannot use such a protocol. A double-blind cross-over study tested the efficacy of applying chlorhexidine with a sponge-swab, in a sample of 76 severely disabled adults, drawn from diverse rehabilitation settings. Two randomly assigned groups applied 10 mL 0.12% chlorhexidine gluconate (Peridex, Procter & Gamble) or 10 mL placebo, using a "Toothette" (Halbrand) once daily, 5 times per week for 10 weeks. All subjects received 10 mL 0.05% NaF, applied similarly but separately from the test/placebo agent. Pre- and post-trial measures included perceived level of function and oral status, that is, DMFS, plaque, calculus, pocket depth, and tooth stain. The protocol received high levels of compliance and acceptance. Compared with placebo, swabbing with chlorhexidine resulted in consistent, and, in part, significant improvements in plaque, gingivitis, and periodontal pocket depth. Side effects of chlorhexidine, that is, tooth stain and calculus, were relatively minor. Perceived improvements in dental health were associated with improved physical health, appearance, and mouth odor. The results indicate that chlorhexidine swabbing is a useful oral disease preventive protocol for persons with disability.


Assuntos
Clorexidina/análogos & derivados , Assistência Odontológica para a Pessoa com Deficiência , Dispositivos para o Cuidado Bucal Domiciliar , Adulto , Análise de Variância , Clorexidina/administração & dosagem , Clorexidina/uso terapêutico , Cálculos Dentários/prevenção & controle , Placa Dentária/prevenção & controle , Índice de Placa Dentária , Método Duplo-Cego , Feminino , Gengivite/terapia , Humanos , Masculino , Cooperação do Paciente , Satisfação do Paciente , Índice Periodontal , Bolsa Periodontal/terapia
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