Siphonguard Device Functional Testing - Codman HAKIM Manual Del Usuario

Tabla de contenido

Publicidad

Idiomas disponibles
  • MX

Idiomas disponibles

  • MEXICANO, página 72
Ojemann RG: Normal pressure hydrocephalus. Clin Neurosurg 18:
337–370, 1971.
Ojemann RG, Black P McL: Evaluation of the patient with dementia and
treatment of normal pressure hydrocephalus. In: Wilkins RH, Regachary SS
(eds). Neurosurgery. McGraw Hill, 1984.
Penn RD, Bacus JW: The brain as a sponge: a computed tomographic look
at Hakim's Hypothesis. Neurosurgery 14: 670–675, 1984.
Raimondi AJ, Yashon D, Matsumoto S, Reyes C: Increased intracranial
pressure without lateralizing signs, the "midline syndrome."
Neurochirurgia 10: 197–209, 1967.
Rayport M, Reiss J: "Hydrodynamic Properties of certain shunt
assemblies for the treatment of hydrocephalus, Part I: Report of a case
of communicating hydrocephalus with increased cerebrospinal fluid
production treated by duplication of shunting device." Part II: Pressure-flow
characteristics of the Spitz-Holter, Pudenz-Meyer, and Cordis-Hakim shunt
systems. J Neurosurg 30: 455–467, 1969.
Reinprecht A, Dietrich W, Bertalanffy A, Czech T: The Medos Hakim
Programmable Valve in the Treatment of Pediatric Hydrocephalus.
Childs Nerv Syst 13: 588–594, 1997.
Zemack G, Romner B: Seven-year clinical experience with the
CODMAN HAKIM programmable valve: a retrospective study of 583 patients.
Neurosurg Focus 7: 4, 1999.
APPENDIX
Preimplantation Performance Testing
Although Integra does not recommend functional testing, some
surgeons may choose to do so. Before testing, it is extremely important
that a CODMAN HAKIM Valve with or without SIPHONGUARD Device be
flushed of all air bubbles. Air bubbles within the CODMAN HAKIM Valve or
SIPHONGUARD Device produce inaccurate manometer test results. The
presence of air bubbles can reduce the cross-sectional area of the flow path,
increase system resistance, and impede the flow of fluid through the system
during testing.

SIPHONGUARD Device Functional Testing

Equipment Required (use all sterile equipment, perform testing under
sterile conditions)
One manometer, wide-bore (e.g. 3.5 mm), graduated in mm (available in
lengths from 38 to 60 cm)
One 4-way stopcock
One syringe, 5 mL
One syringe filter, 5 µm
Tubing adapters
Silicone tubing
One male luer connector with 1/16 in. barb
Saline solution
Flushing Procedure
Note: At a rate of 0.5 mL/minute, unitized versions require 2–3 minutes
to complete flushing. This is the time required for fluid to fill the valve and
exit the distal catheter. Allot additional time to ensure the system is free of
air bubbles.
1.
Assemble manometer, stopcock, syringe, and tubing (Figure A-1).
Figure A-1
2.
Detach syringe from assembly and fill the syringe with sterile saline
solution using the 5 µm filter in-line. Detach the filter after filling
the syringe.
3.
Set the valve opening pressure to 30 mm H
remains in its sterile package.
4.
Remove valve from the sterile package, and connect the valve to the
manometer/syringe assembly.
Note: Do not attach the distal catheter at this time.
O (294 Pa) while the valve
2
9
Manometer
To Valve

Publicidad

Tabla de contenido
loading

Tabla de contenido