Histological evaluation of the healing potential of the anterior cruciate ligament by means of augmented and non-augmented repair: an in vivo animal study.

The purpose of this animal study was to investigate the healing potential of the anterior cruciate ligament following transaction at the femoral end, by means of both the augmented and the nonaugmented primary repair, focusing on the histological changes during a 12-month postoperative observation period with respect to necrosis and the loss of normal structures during the healing period. Twenty sheep were randomly assigned to nonaugmented primary ACL repair, or to augmented ACL repair using a polyethylene terephthalate (PET) band. At 2, 6, 16, 26 and 52 weeks postoperatively four sheep out of each group were sacrificed. Histological healing was achieved after 16 weeks for the augmented repair group and after 26 weeks for the nonaugmented repair group. The main difference between the two techniques was that the PET augmentation device protected the ligament from necrosis and ligamentization. In this group a consistently normal ligament was seen histologically during the entire postoperative observation period. The nonaugmented repaired ACLs underwent the processes of necrosis and ligamentization.

Intrathecal clonidine for postoperative analgesia in elderly patients: the influence of baricity on hemodynamic and analgesic effects.

Intrathecal (IT) clonidine is an effective analgesic, but it also produces hemodynamic depression and sedation which are likely to be related to IT clonidine's cephalad spread within the cerebrospinal fluid. We hypothesized that IT clonidine's side effects could be reduced without compromising the duration and quality of analgesia by injecting clonidine IT in a hyperbaric solution and elevating the patient's trunk. We prospectively randomized 30 elderly patients to receive IT 150 microg of either isobaric (ISO) or hyperbaric (HYPER) clonidine for postoperative analgesia after surgical repair of traumatic hip fracture. Hemodynamics, IV fluid administration, visual analog pain scores, sedation scores, and clonidine cerebrospinal fluid levels were recorded at fixed intervals. Patients in the ISO group required significantly more crystalloid fluid administration (median, 2500 mL; range, 1500-3000 mL) than those in the HYPER group (median, 1500; range, 500-3000 mL) to maintain adequate arterial blood pressure (P < 0.01). Also, the decrease in heart rate was significantly more pronounced in the ISO than in the HYPER group (P < 0.01). The duration of analgesia was significantly larger in the ISO (median, 400 min; range, 115-400 min) than in the HYPER (median, 265 min; range, 205-400 min) group (P < 0.05). Sedation scores did not differ between groups. We conclude that increasing the baricity of IT clonidine solution in the conditions of our experiment reduces hemodynamic side effects but also analgesia from IT administered clonidine.