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1.
J Perinatol ; 35(11): 965-9, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26355942

RESUMO

OBJECTIVE: The aim of this study was to identify the best sedation/analgesia protocol for laser photocoagulation (PC) of retinopathy of prematurity (ROP). STUDY DESIGN: This multicenter observational study included five hospitals, each using a specific sedation/analgesia protocol: local anesthesia with oxybuprocaine hydrochloride (Group L); intravenous pentazocine (Group P); intravenous fentanyl (Group F); air, oxygen and sevoflurane (AOS) inhalation (Group I). The groups were compared for pain responses, vital signs and adverse events. RESULTS: Heart rates and systemic blood pressures were elevated by PC in Groups L and P and Groups L, P and F, respectively. Moreover, poor analgesic efficacy was recognized in Groups L, P and F. In contrast, Group I experienced hypothermia, enteral feeding intolerance and apnea more frequently. CONCLUSION: From the viewpoint of sedation/pain relief, AOS anesthesia should be the best protocol. However, considering all the various factors together, the most reasonable one can be varied based on the patient's condition and hospital.


Assuntos
Sedação Consciente/métodos , Recém-Nascido Prematuro , Fotocoagulação/métodos , Medição da Dor , Retinopatia da Prematuridade/cirurgia , Administração por Inalação , Estudos de Coortes , Feminino , Fentanila/administração & dosagem , Humanos , Recém-Nascido , Infusões Intravenosas , Japão , Terapia a Laser/métodos , Masculino , Éteres Metílicos/administração & dosagem , Pentazocina/administração & dosagem , Estudos Prospectivos , Retinopatia da Prematuridade/diagnóstico , Medição de Risco , Índice de Gravidade de Doença , Sevoflurano , Resultado do Tratamento
2.
Diabet Med ; 31(11): 1357-62, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24804978

RESUMO

AIMS: To investigate the molecular and clinical characteristics of the largest series of Japanese patients with glucokinase maturity-onset diabetes of the young (GCK-MODY), and to find any features specific to Asian people. METHODS: We enrolled 78 Japanese patients with GCK-MODY from 41 families (55 probands diagnosed at the age of 0-14 years and their 23 adult family members). Mutations were identified by direct sequencing or multiplex ligation-dependent probe amplification of all exons of the GCK gene. Detailed clinical and laboratory data were collected on the probands using questionnaires, which were sent to the treating physicians. Data on current clinical status and HbA1c levels were also collected from adult patients. RESULTS: A total of 35 different mutations were identified, of which seven were novel. Fasting blood glucose and HbA1c levels of the probands were ≤9.3 mmol/l and ≤56 mmol/mol (7.3%), respectively, and there was considerable variation in their BMI percentiles (0.4-96.2). In total, 25% of the probands had elevated homeostatic assessment of insulin resistance values, and 58.3% of these had evidence of concomitant Type 2 diabetes in their family. The HbA1c levels for adults were slightly higher, up to 61 mmol/mol (7.8%). The incidence of microvascular complications was low. Out of these 78 people with GCK-MODY and 40 additional family members with hyperglycaemia whose genetic status was unknown, only one had diabetic nephropathy. CONCLUSIONS: The molecular and clinical features of GCK-MODY in Japanese people are similar to those of other ethnic populations; however, making a diagnosis of GCK-MODY was more challenging in patients with signs of insulin resistance.


Assuntos
Diabetes Mellitus Tipo 2/genética , Angiopatias Diabéticas/epidemiologia , Saúde da Família , Glucoquinase/genética , Resistência à Insulina , Mutação , Doenças Vasculares Periféricas/complicações , Adulto , Idoso , Substituição de Aminoácidos , Diabetes Mellitus Tipo 2/complicações , Diabetes Mellitus Tipo 2/metabolismo , Diabetes Mellitus Tipo 2/terapia , Angiopatias Diabéticas/prevenção & controle , Feminino , Deleção de Genes , Estudos de Associação Genética , Glucoquinase/metabolismo , Hemoglobinas Glicadas/análise , Humanos , Hipoglicemiantes/uso terapêutico , Incidência , Japão/epidemiologia , Masculino , Microvasos/efeitos dos fármacos , Pessoa de Meia-Idade , Doenças Vasculares Periféricas/epidemiologia , Doenças Vasculares Periféricas/prevenção & controle , Polimorfismo de Nucleotídeo Único
3.
J Gastroenterol ; 32(3): 289-94, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9213239

RESUMO

We conducted a case-control study to examine the association of Helicobacter pylori infection as a risk factor in gastric cancer in the Japanese population. Serum IgG antibodies for Helicobacter pylori were determined in 55 consecutive patients with gastric cancer and in 75 age- and sex-matched mass survey subjects and 57 age- and sex-matched cancer-free patients with conditions considered at a high risk for development of gastric cancer (precancerous condition). We examined the histology in all subjects and particular focus was placed on the extent of Helicobacter pylori-associated gastritis. The seroprevalence of Helicobacter pylori in gastric cancer patients (82%) and those with a precancerous condition (89%) was significantly higher (P < 0.005) than that in the mass survey subjects (60%). Positive relative risk associations were found for patients with gastric cancer (odds ratio, 3, with 95% confidence intervals of 1.69-5.33) and those with a precancerous condition (odds ratio, 5.66, with 95% confidence intervals 2.66-12.03). Significant differences were found when comparisons were made among the case-control groups who were H. pylori-positive and had inflammatory cell infiltration (P = 0.0127). The characteristics of Helicobacter pylori in histologically examined gastric mucosa showed differences between Helicobacter pylori-infected and uninfected persons in all groups. However, for none of these groups was there a significant differences between background mucosa for Helicobacter pylori-infected persons with or without gastric cancer. Helicobacter pylori seroprevalence is strongly associated with an increased risk of gastric cancer and with a precancerous condition; histological investigation did not define additional factors that might be associated with increased cancer risk.


Assuntos
Infecções por Helicobacter/complicações , Helicobacter pylori/isolamento & purificação , Neoplasias Gástricas/microbiologia , Adulto , Idoso , Anticorpos Antibacterianos/sangue , Estudos de Casos e Controles , Feminino , Infecções por Helicobacter/patologia , Humanos , Imunoglobulina G/sangue , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Fatores de Risco , Neoplasias Gástricas/patologia
4.
Hum Genet ; 95(5): 577-80, 1995 May.
Artigo em Inglês | MEDLINE | ID: mdl-7759082

RESUMO

Although the locus for X-linked recessive chondrodysplasia punctata (CDPX1) has been mapped to the region between PABX and DXS31 (the critical region is about 3 Mb long), the precise location within the critical region has not been determined. In this paper, we describe a boy with a 46,Y,der(X)t(X;Y)(p22.3;q11)mat karyotype and review the genotype-phenotype correlations in three male patients with the combination of apparent lack of clinical features of CDPX1 and a partial deletion of the critical region. The results suggest that the region defined by the two BssHII sites at 3180 and 3570 kb from the Xp telomere may be the target region for the CDPX1 locus.


Assuntos
Condrodisplasia Punctata/genética , Mapeamento Cromossômico , Genes Recessivos/genética , Ligação Genética/genética , Cromossomo X , Adolescente , Povo Asiático , Southern Blotting , Deleção Cromossômica , Feminino , Mãos/diagnóstico por imagem , Humanos , Japão , Cariotipagem , Masculino , Radiografia
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