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1.
Aliment Pharmacol Ther ; 20(11-12): 1211-30, 2004 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15606384

RESUMO

Current accepted treatment for chronic hepatitis B uses either the immunomodulator interferon alpha or nucleoside analogues lamivudine or adefovir. Interferon has side effects which mean it is often poorly tolerated. Long-term use of lamivudine is associated with increasing viral resistance for each year it is taken and the rebound viraemia that can occur when the drug is stopped is also of concern to many. Adefovir appears to have less of the resistance issues of lamivudine but is still a relatively new drug and at present its use is principally limited to patients with lamivudine-resistant disease. A number of other nucleoside analogues are currently being developed with some now at the stage of early clinical trials. A proportion share the significant resistance problems of lamivudine but many appear to have more potent anti-viral effect than the drugs currently available. If some of these newer anti-viral agents are approved for use in chronic hepatitis B, the potential for prolonged suppression of hepatitis B virus replication with resultant stabilization or improvement in liver disease may be achieved.


Assuntos
Antivirais/uso terapêutico , Hepatite B Crônica/tratamento farmacológico , Nucleosídeos/uso terapêutico , Combinação de Medicamentos , Farmacorresistência Viral/genética , Infecções por HIV/complicações , Hepatite B/genética , Hepatite B Crônica/complicações , Humanos , Interferon-alfa/uso terapêutico , Cirrose Hepática/complicações , Transplante de Fígado , Mutação , Replicação Viral
2.
Eur J Gastroenterol Hepatol ; 9(10): 989-92, 1997 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9391789

RESUMO

BACKGROUND: Haemorrhagic complications are common in patients with cirrhosis of the liver and contribute to the morbidity and mortality seen in this condition. Several pathological processes are involved in these complications, including a delay and overall reduction in platelet aggregation. OBJECTIVE: To determine whether impaired aggregation in cirrhosis is the result of an intrinsic abnormality in platelet function or is induced by a factor present in the blood of cirrhotic patients. SETTING: Liver unit patients in a teaching hospital. DESIGN: Blood was taken from 11 patients with cirrhosis (Child's B or C) and 11 healthy controls. Crossover experiments were carried out, suspending platelet pellets from patients in platelet-poor plasma from controls, and vice versa. Aggregation of both samples and also of platelet-rich plasma from patients and controls was measured. RESULTS: Aggregation after 1 min was impaired significantly in patient, compared with control, platelets following incubation in either patient (P = 0.0012), or control (P = 0.0242), plasma. Correspondingly, maximum aggregation of patient platelets was also reduced significantly (P = 0.0036) after incubation in patient plasma. Aggregation after 1 min, and maximum aggregation, of control platelets was increased significantly (P = 0.034 and 0.013, respectively) following incubation in patient plasma. Furthermore, there was a trend (non-significant) towards reduced aggregation of patient platelets incubated in control plasma. CONCLUSION: These results confirm both an intrinsic platelet defect causing impaired aggregation and a circulating factor in the plasma of patients with cirrhosis which may compensate for this functional defect.


Assuntos
Cirrose Hepática/sangue , Agregação Plaquetária , Feminino , Humanos , Masculino , Estatísticas não Paramétricas
3.
Scott Med J ; 41(2): 44-6, 1996 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8735501

RESUMO

The aim of the study was to carry out an audit of 283 hysterectomies performed for menstrual disorders over a one year period, and to determine the satisfaction of the women concerned towards their treatment. The medical records of these patients were examined, and they were each sent a questionnaire, 69% of which were completed and returned. The most common presenting symptoms were menorrhagia and dysmenorrhoea. In 53% of cases no clinical abnormality was postulated and in 31% of cases no pathological abnormality was found. The preoperative clinical and pathological diagnoses were in agreement for 59% of patients. Over 90% of women were satisfied with the management of their case by their GP and the gynaecology outpatient clinic. The use of patient-controlled analgesia systems was associated with better post-operative pain relief than intramuscular injections. Thirteen percent of patients required blood transfusion; 21% suffered some form of postoperative complication, most of which were minor. Ninety-four percent of the women were pleased that they had undergone hysterectomy, and 76% wished that they had had the operation sooner. It was concluded that hysterectomy is perceived positively by patients and should not necessarily be considered as a last resort treatment for menstrual disorders.


Assuntos
Histerectomia/estatística & dados numéricos , Auditoria Médica , Distúrbios Menstruais/cirurgia , Satisfação do Paciente , Adulto , Feminino , Humanos , Pessoa de Meia-Idade , Qualidade de Vida , Escócia
4.
Spec Care Dentist ; 18(4): 156-63, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-10218063

RESUMO

A comparison of salivary flow rates was made between two groups of healthy, unmedicated, elderly, Caucasian men and women ranging in age from 60 to 90 years. One group was a control group, while the other group had both active and restored root caries. The control group consisted of 69 individuals with a mean age of 73 years. The root caries group consisted of 39 individuals with a mean age of 71 years. The groups were evaluated for unstimulated (UPAR) and stimulated parotid gland flow rates (SPAR), unstimulated (USUB) and stimulated submandibular/sublingual gland flow rates (SSUB), and stimulated whole saliva flow rates (SWhole). Parotid flow rates were determined with the use of a Carlson-Crittenden cup, while submandibular/sublingual flow rates were determined by means of the NIDR collector. A 2% citrate solution was used for stimulation in glandular collections. Subjects chewed a 1-cm3 cube of paraffin to stimulate whole saliva. The results showed that the control group had higher UPAR, SPAR, USUB, SSUB, and SWhole than the root caries group.


Assuntos
Assistência Odontológica para Idosos , Cárie Radicular/epidemiologia , Cárie Radicular/etiologia , Salivação/fisiologia , Xerostomia/complicações , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Envelhecimento , Baltimore/epidemiologia , Estudos Transversais , Feminino , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Glândula Parótida/metabolismo , Prevalência , Fatores Sexuais , Glândula Submandibular/metabolismo
5.
Spec Care Dentist ; 18(3): 109-12, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9680920

RESUMO

A study was conducted to evaluate the secretion of stimulated whole saliva (SWS) and secretory IgA (sIgA) among three groups of women. One group was a healthy control group, the second group consisted of women diagnosed with metastatic breast cancer before being placed on chemotherapy, while the third group consisted of women on chemotherapy taking CMF (cyclophosphamide, methotrexate, and fluorouracil) for at least one month. There were seven patients in each group. SWS was collected. Salivary sIgA concentrations were determined by enzyme-linked immunoabsorbant assay. The results of the study showed that the mean SWS flow rate for the chemotherapy group (x = 0.96 mL/min) was significantly lower (p > 0.03) than that of the control group (x = 2.33 mL/min) and lower than that of the group with cancer (x = 1.81 mL/min). Additionally, the results showed that the mean sIgA concentrations for the chemotherapy group (x = 10.9 ng/mg of protein) were slightly lower than those of the control group (x = 13.7 ng/mg of protein) and lower than those of the group with cancer (x = 12.6 ng/mg of protein). The results of this study suggest that women placed on CMF for treatment of carcinoma of the breast may have reduced stimulated salivary production.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/efeitos adversos , Imunoglobulina A Secretora/análise , Saliva/imunologia , Salivação/efeitos dos fármacos , Adulto , Idoso , Análise de Variância , Neoplasias da Mama/tratamento farmacológico , Estudos Transversais , Ciclofosfamida/efeitos adversos , Feminino , Fluoruracila/efeitos adversos , Humanos , Metotrexato/efeitos adversos , Pessoa de Meia-Idade , Saliva/metabolismo , Taxa Secretória/efeitos dos fármacos
6.
Dent Clin North Am ; : 389-97, 1967 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-5229545
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