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1.
ASAIO J ; 51(5): 504-7, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16322706

RESUMO

The purpose of our research was to study the clinical outcomes of children with congenital heart disease (CHD) requiring extracorporeal membrane oxygenation (ECMO) support after cardiac surgery at a tertiary care children's hospital. Retrospective review of all patients with CHD who required postcardiotomy ECMO between January 2001 and September 2004 (45 months) was undertaken. Various outcome predictors were tested for any association with survival to hospital discharge using univariate analysis. A total of 84 children were placed on ECMO after CHD surgery; 39 (46.4%) were placed on ECMO in the operating room. Median age of the patients was 128 days (1 day to 5 years) and median weight was 4.53 kg (2-18 kg). Active cardiopulmonary resuscitation was ongoing at the time of cannulation in 27 children (32%). Fifty-two children (61.9) survived > 24 hours after decannulation and 31 (36.9%) survived to discharge. High arterial serum lactate levels at the time of ECMO initiation were strongly correlated with nonsurvival (p = 0.004). Nonsurvivors had longer duration on ECMO than survivors (p = 0.003). The odds of survival dropped significantly after 144 hours (day 6) of ECMO. ECMO support results in improved outcomes in patients who suffered hemodynamic collapse post cardiac surgery. Underlying cardiac lesion, age, weight, gender, initial arterial pH, location of ECMO initiation, need for hemofiltration and placement of ECMO after active ongoing cardiopulmonary resuscitation did not increase the mortality risk. Initial arterial serum lactate level and inability to wean off by 6 days were strongly correlated with nonsurvival.


Assuntos
Oxigenação por Membrana Extracorpórea , Cardiopatias Congênitas/terapia , Cirurgia Torácica , Reanimação Cardiopulmonar , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Feminino , Parada Cardíaca/terapia , Mortalidade Hospitalar , Humanos , Masculino , Estudos Retrospectivos , Taxa de Sobrevida , Fatores de Tempo , Resultado do Tratamento , Estados Unidos
2.
J Neurosci ; 19(21): 9201-8, 1999 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-10531423

RESUMO

Pharmacological evidence suggests a functional role for spinal nitric oxide (NO) in the modulation of thermal and/or inflammatory hyperalgesia. To assess the role of NO in nerve injury-induced tactile allodynia, we examined neuronal NO synthase (nNOS) expression in the spinal cord and dorsal root ganglia (DRG) of rats with tactile allodynia because of either tight ligation of the left fifth and sixth lumbar spinal nerves or streptozotocin-induced diabetic neuropathy. RNase protection assays indicated that nNOS mRNA (1) was upregulated in DRG, but not spinal cord, neurons on the injury side beginning 1 d after nerve ligation, (2) peaked (approximately 10-fold increase) at 2 d, and (3) remained elevated for at least 13 weeks. A corresponding increase in DRG nNOS protein was also observed and localized principally to small and occasionally medium-size sensory neurons. In rats with diabetic neuropathy, there was no significant change in DRG nNOS mRNA. However, similar increases in DRG nNOS mRNA were observed in rats that did not develop allodynia after nerve ligation and in rats fully recovered from allodynia 3 months after the nerve ligation. Systemic treatment with a specific pharmacological inhibitor of nNOS failed to prevent or reverse allodynia in nerve-injured rats. Thus, regulation of nNOS may contribute to the development of neuronal plasticity after specific types of peripheral nerve injury. However, upregulation of nNOS is not responsible for the development and/or maintenance of allodynia after nerve injury.


Assuntos
Regulação Enzimológica da Expressão Gênica , Neurônios Aferentes/enzimologia , Óxido Nítrico Sintase/genética , Dor/fisiopatologia , Nervos Espinhais/fisiologia , Transcrição Gênica , Animais , Gânglios Espinais/enzimologia , Gânglios Espinais/fisiologia , Gânglios Espinais/fisiopatologia , Masculino , Óxido Nítrico Sintase Tipo I , Dor/enzimologia , RNA Mensageiro/genética , Ratos , Ratos Sprague-Dawley , Especificidade da Espécie , Nervos Espinhais/lesões , Nervos Espinhais/fisiopatologia , Fatores de Tempo
3.
Mol Cell Neurosci ; 10(3-4): 196-207, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9532581

RESUMO

Increased voltage-gated sodium channel activity may contribute to the hyperexcitability of sensory neurons in inflammatory and neuropathic pain states. We examined the levels of the transcript encoding the tetrodotoxin-resistant sodium channel SNS in dorsal root ganglion neurons in a range of inflammatory and neuropathic pain models in the rat. Local Freund's adjuvant or systemic nerve growth factor-induced inflammation did not substantially alter the total levels of SNS mRNA. When NGF-treated adult rat DRG neurons in vitro were compared with NGF-depleted control neurons, SNS total mRNA levels and the levels of membrane-associated immunoreactive SNS showed a small increase (17 and 25%, respectively), while CGRP levels increased fourfold. SNS expression is thus little dependent on NGF even though SNS transcript levels dropped by more than 60% 7-14 days after axotomy. In the streptozotocin diabetic rat SNS levels fell 25%, while in several manipulations of the L5/6 tight nerve ligation rat neuropathic pain model, SNS levels fell 40-80% in rat strains that are either susceptible or relatively resistant to the development of allodynia. Increased expression of SNS mRNA is thus unlikely to underlie sensory neuron hyperexcitability associated with inflammation, while lowered SNS transcript levels are associated with peripheral nerve damage.


Assuntos
Neurônios Aferentes/metabolismo , Dor/metabolismo , Canais de Sódio/biossíntese , Animais , Axotomia , Células CHO , Células Cultivadas , Cricetinae , Diabetes Mellitus Experimental/genética , Diabetes Mellitus Experimental/metabolismo , Regulação para Baixo/genética , Feminino , Adjuvante de Freund/administração & dosagem , Gânglios Espinais/citologia , Gânglios Espinais/metabolismo , Inflamação/etiologia , Inflamação/genética , Inflamação/metabolismo , Injeções Subcutâneas , Ligadura , Masculino , Canal de Sódio Disparado por Voltagem NAV1.8 , Fatores de Crescimento Neural/administração & dosagem , Fatores de Crescimento Neural/farmacologia , Dor/genética , Dor/fisiopatologia , RNA Mensageiro/análise , RNA Mensageiro/efeitos dos fármacos , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Ratos Wistar , Canais de Sódio/genética , Nervos Espinhais/fisiologia , Transcrição Gênica , Regulação para Cima/genética
4.
Opt Lett ; 18(2): 113-5, 1993 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-19802055

RESUMO

We have demonstrated an upconversion-pumped blue laser on the (1)G(4)-(3)H(6) band of Tm:YAG at cryogenic temperatures. Measurements were also made to assess the possibility of room-temperature upconversion-pumped lasers in Tm:YAG on both the (1)G(4) -(3)H(6) and the (1)D(2)-(3)F(4) bands.

5.
Appl Opt ; 31(6): 698-9, 1992 Feb 20.
Artigo em Inglês | MEDLINE | ID: mdl-20720669
6.
Appl Opt ; 29(15): 2217-8, 1990 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-20563152

RESUMO

Raman conversion from 1.06 to 1.7 ,um with a photon efficiency of 44% has been demonstrated in HD at 77 K.

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