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MEDICINE


ume for cytology (generally 0.5 mL minimum required), bacterial culture if indicated, Sarcocystis neurona and Neospora hughesii antibody detection, and additional diagnostics as indicated by the his- tory and clinical signs.


C1–C2 Spinal Fluid Collection


Fluid from the C1–C2 space occasionally drips spon- taneously from the needle. In two cases, negative pressure was encountered once in the subarachnoid space precluding gentle aspiration. In these cases the CSF dripped freely with the head below withers height and with patience, allowed enough volume to be collected for cytology and minimal additional testing (1.5 mL). Gentle aspiration is typically required to obtain the majority of the samples and routinely yields 5 mL or more with ease. Fluid is aspirated in 1 to 2 mL sequential aliquots as previ- ously described to reduce the amount of blood con- tamination associated with the first sample.5 It is ideal to use 3 to 5 mL Luer Slip syringes (avoid Luer Lock) and it is important to break the seal on the syringe prior to aspirating the sample to prevent exerting excessive pressure on the meninges. The stylet is replaced and the needle is withdrawn smoothly once an adequate sample volume is obtained. C1–C2 collection: typical yield, 5–8 mL.


Troubleshooting C1–C2 Spinal Needle Placement


If multiple attempts at needle placement occur, the needle track creates an artifact that obscures a clear image of the C1–C2 space and spinal cord. If this occurs, attempt the procedure from the other side following identical site preparation. If blood is ob- tained, it is likely that a vertebral vessel was inad- vertently punctured. In this case needle placement is likely too ventral. The procedure can be repeated with a new needle with care to ensure that the needle is placed in the dorsal C1–C2 space. If neg- ative pressure is encountered subsequent to switch- ing syringes (especially after easy aspiration of the previous 1 mL) the stylet is replaced and the needle is advanced an additional millimeter and should result in easy aspiration of the remaining sample. In this case, it is most likely that the original needle placement is just through the dura and becomes displaced from the subarachnoid space during the transition from one syringe to the next.


LS Space Procedure


The LS space is routinely located using anatomic landmarks (midline at the highest point of the hind- quarters, and or palpation of a depression between the cranial borders of the tuber sacrale, and or using an imaginary line drawn between the two caudal borders of the tuber coxae that intersects with mid- line).4 An approximately 15 cm  15 cm square is clipped to provide a sterile field for collection. After the initial aseptic preparation, the subcutaneous tis- sues and muscle is infiltrated with 5 mL of 2% lido-


480 2018  Vol. 64  AAEP PROCEEDINGS


caine with a 1.5-inch 22-gauge needle before final aseptic preparation. Midline can be difficult to dis- tinguish in some cases, the clinician can attempt to palpate the dorsal spinous process of L6 and use the tail to identify midline. The author often relies on a technician or ancillary person to stand well behind the horse (prior to initial needle puncture) to provide verbal direction on the location of midline. The most optimal horse position is for it to stand square with the hindlimbs slightly camped under. In some neurologic cases, this can be nearly impossible and the author appreciates the horse that will at least weight bear on both hind legs. The LS tap can be successful in the horse that is leaning or is not able to stand square with careful palpation and identification of midline. An 8-inch 18-gauge spi- nal needle is advanced perpendicular to the horse’s back in millimeter increments. Two hands are used to control the needle (one at the junction with the horse’s back and the other at the hub of the needle) to prevent the needle from deviating later- ally or in a cranial or caudal direction. When any change in resistance is encountered (sensation of a “pop”), the stylet is withdrawn and a 5-mL Luer Slip syringe that has had the seal broken is attached and used to check for the presence of spinal fluid. When negative pressure is encountered, the stylet is re- placed and the needle is advanced gradually. In most adult light-breed horses, 2 to 3 inches of needle remain out of the horse and the LS space is encoun- tered at a depth of 5 to 6 inches. A longer needle is sometimes required for draft breeds or heavily mus- cled horses. Some horses raise or swish their tail or drop their hindquarters perceivably when the nee- dle is just about to puncture the dura. These horses may or may not react explosively when the dura is punctured. However, many horses give no indication that you are approaching the space and they may or may not react when the needle enters the subarachnoid space.


LS Spinal Fluid Collection


Gentle aspiration is almost always required. A 5-mL Luer Slip syringe with the seal broken is pre- ferred to provide adequate pressure to promote CSF flow. Ensure a solid connection between the needle hub and syringe. Fluid flowed freely from one case. In some cases, the Queckenstedt’s maneuver (tran- siently raising the head and holding off both jugular veins) is instrumental in increasing intracranial pressure thus promoting CSF flow and enhancing collection volume. Fluid is aspirated in 1–2-mL ali- quots as described above. Typical yield, 5 mL.


Troubleshooting LS Spinal Needle Placement


If bone is encountered when the needle is at a depth of 3 to 4 inches, the needle is likely not in the proper location. Redirecting the needle is often unsuccess- ful. Reassessing the location of midline and select- ing a slightly different location is usually required. It is also important to ensure the needle remains


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