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1.
Perfusion ; 38(3): 574-579, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-35077261

RESUMO

INTRODUCTION: Despite being a daily clinical application in cardiac operating theaters, an evidence-based approach on how to optimally initiate the heart-lung machine (HLM) to prevent critical phases of cerebral ischemia is still lacking. We therefore designed a study comparing two different initiation times for starting the cardiopulmonary bypass (CPB). METHODS: We conducted a monocentric, randomized, and prospective study comparing the impact of two initiation times, a rapid initiation of 15 s and a slow initiation of 180 s to reach the full target flow rate of 2.5 L/min/m2 times the body surface area, on cerebral tissue oxygenation by near infrared spectroscopy measurements. RESULTS: The absolute values in tissue oxygenation index (TOI) showed no difference between the groups before and after the CPB with a 10% drop in oxygenation index in both groups due to the hemodilution through the HLM priming. Looking at the kinetics a rapid initiation of CPB produced a higher negative rate of change in TOI with a total of 21% in critical oxygenation readings compared to 6% in the slow initiation group. CONCLUSION: In order to avoid critical phases of cerebral ischemia during the initiation of CPB for cardiac procedures, we propose an initiation time of at least 90 s to reach the 100% of target flow rate of the HLM.


Assuntos
Isquemia Encefálica , Ponte Cardiopulmonar , Humanos , Ponte Cardiopulmonar/métodos , Estudos Prospectivos , Oximetria/métodos , Gasometria , Oxigênio , Circulação Cerebrovascular
2.
Spine J ; 14(12): 3011-7, 2014 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-25011093

RESUMO

BACKGROUND CONTEXT: Instrumented fusion of the spine is a surgery commonly performed to stabilize vertebrae causing pain and to correct anatomic deformities. Such surgery can create substantial blood loss. Autotransfusion is a means to limit homologous blood transfusion in this setting. However, a dilemma is created when the high-speed drill used for bone removal comes in contact with implanted titanium spinal hardware. A clinician at this point is forced to decide between two options: to discontinue autotransfusion to avoid the potential transfusion of titanium fragments while risking blood loss and the need for homologous transfusion or to continue autotransfusion while risking transfusion of titanium fragments back into circulation. PURPOSE: To conclusively identify whether titanium fragments created by a high-speed drill are able to pass through standard autotransfusion microaggregate blood filters. STUDY DESIGN: A positive and negatively controlled experiment with blinded sample analysis. OUTCOMES MEASURES: The presence or absence of titanium alloy on a filter with detection by energy-dispersive X-ray spectroscopy (EDX). METHODS: A mock autotransfusion setup was devised for in vitro filtering. Six investigational and two control experiments were conducted. Titanium fragments generated by a high-speed drill were aspirated with saline and filtered with standard autotransfusion reservoirs and microaggregate blood filters. A final filter with a 1-µm pore size was placed distal to the blood filters. After filtration was complete, this final filter was analyzed using EDX. RESULTS: The presence of titanium was confirmed by EDX on five of six investigational filters. The positive and negative control filters were analyzed by EDX and tested positive and negative, respectively, for titanium. CONCLUSIONS: Standard 40 µm reservoir and blood microaggregate filters do not eliminate the smallest fragments of titanium generated by contact between a high-speed drill and a titanium hardware. The mass of titanium able to elude filtration is very small. The impact of transfusing blood contaminated with such a small mass of titanium is not known.


Assuntos
Transfusão de Sangue Autóloga/métodos , Filtração/métodos , Fusão Vertebral/métodos , Titânio/efeitos adversos , Transfusão de Sangue Autóloga/efeitos adversos , Humanos , Fusão Vertebral/efeitos adversos , Titânio/uso terapêutico
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