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The PrepStain ® System produces SurePath ® slides that are intended as replacements for conventional gynecologic Pap smears. Refer to the assay package inserts for instructions on using SurePath ® Preservative Fluid to prepare specimens skuamoz papilloma tedavisi use with these assays.

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Air-drying artifact, obscuring, overlapping cellular material and debris are largely eliminated. The numbers of white blood cells are significantly reduced, allowing for easier visualization of epithelial cells, diagnostically relevant cells and infectious organisms.

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Skuamoz papilloma tedavisi SurePath ® process begins with qualified medical personnel using a broom-type sampling device e. Rather than smearing cells collected by the sampling devices on a glass slide, the heads of the sampling devices detach from the handle and are placed into a vial of SurePath ® Preservative Fluid.

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The vial is capped, labeled, and sent with appropriate paperwork to the laboratory for processing. The heads of the sampling devices are never removed from the preservative vial containing the collected sample.

PrepStain® System Product Insert - BD

An enrichment step, consisting of centrifugal sedimentation through Density Reagent, partially removes non-diagnostic debris and excess inflammatory cells from the sample. After centrifugation, the pelleted cells are resuspended, mixed and transferred to a PrepStain ® Settling Chamber mounted on a SurePath ® PreCoat slide.

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The cells are sedimented by gravity, then stained using a modified Papanicolaou staining procedure. The slide is cleared with xylene or a xylene substitute and skuamoz papilloma tedavisi.

The cells, presented within a 13mm diameter circle, are examined under a microscope by trained cytotechnologists and pathologists with access to other relevant patient background information. Wooden spatulas should not be used with the PrepStain ® System.

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Cytotechnologists and pathologists will be trained in morphology assessment on the SurePath ® slides. Training will include a proficiency examination.

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Laboratory customers will be provided with the use of instructional slide and test sets. TriPath Imaging, Inc.

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Used supplies should be skuamoz papilloma tedavisi of properly in accordance with institutional and governmental regulations. Reagents For In Vitro Diagnostic use. For laboratory use only. SurePath® Preservative Fluid contains an aqueous solution of denatured ethanol.

The mixture contains small amounts of methanol and isopropanol. Do not ingest.

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PrepStain® Density Reagent contains sodium azide. On disposal, flush with a large volume of water to prevent buildup of azide. See website: www.

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Toxic if ingested. Do not breathe vapors. Use with adequate ventilation. Avoid contact with skin and eyes.

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Highly flammable. The storage condition for SurePath ® Preservative Fluid without cytologic samples is skuamoz papilloma tedavisi to 36 months from date of manufacture at room temperature 15° to 30° C.

PrepStain® System Product Insert - BD

The storage limit for SurePath ® Preservative Fluid with cytologic samples is 6 months at refrigerated temperature 2° to 10° C or 4 weeks at room temperature 15° to 30° C. Operators should use appropriate hand, eye and clothing protection.

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However, universal precautions for safe handling of biological fluids should be practiced at all times. Healthcare providers may need to acquire a new specimen if the results skuamoz papilloma tedavisi not correlate with the clinical history of the patient. Furthermore, cytology addresses different clinical questions than sexually transmitted disease STD testing; therefore, aliquot removal may not be suitable skuamoz papilloma tedavisi all clinical situations.

Only one aliquot may be removed from the SurePath ® Preservative Fluid Collection Vial prior to performing the PapTest, regardless of the volume of the aliquot.