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Robert Dowling

Publications and source records attributed to Robert Dowling.

3 recordsLinked to original sources

Improved pain control after cardiac surgery: results of a randomized, double-blind, clinical trial.

OBJECTIVE: We sought to determine whether a continuous regional infusion of a local anesthetic delivered to the operative site would result in decreased levels of postoperative pain and narcotic requirements for patients who undergo a standard median sternotomy for cardiac surgery. METHODS: A double-blind, randomized, controlled trial was conducted at a single center. Patients who were undergoing elective coronary artery bypass graft surgery alone or combined with laser transmyocardial revascularization received bilateral intercostal nerve blocks with either ropivacaine or saline. At wound closure, 2 catheters with multiple side openings were inserted percutaneously and placed directly over the sternum. The same agent (ropivacaine vs saline) was then administered as a continuous regional infusion for 48 hours through an elastomeric pump. Requirements for postoperative systemic narcotic analgesics and pain assessment scores were recorded for 72 hours after the operation. Secondary outcome measures were hospital length of stay and pulmonary function test results. Pain scores and narcotic use on the second postoperative day were also compared to avoid the confounding influence of anesthesia administered at the time of the operation. RESULTS: The total amount of narcotic analgesia required by the ropivacaine group was significantly less than that of the control group (47.3 vs 78.7 mg, respectively; P =.038). The ropivacaine group required less narcotics on postoperative day 2 as well (15.5 vs 29.4 mg, P =.025). The mean overall pain scores for the ropivacaine group were significantly less than the mean overall scores for the normal saline group (1.6 vs 2.6, respectively; P =.005). Patients receiving ropivacaine had a mean length of stay of 5.2 days compared with 8.2 days for patients in the normal saline group (P =.001). Excluding the data from outliers (length of stay = 39 days), the normal saline group mean length of stay was 6.3 days (P <.01). There was no difference in assessment of pulmonary function. CONCLUSION: Continuous delivery of local anesthetics significantly improved postoperative pain control while decreasing the amount of narcotic analgesia required in patients who underwent standard median sternotomy. There was also a significant decrease in hospital length of stay, which is likely to result in significant cost reductions.

Aged↗

Total artificial heart: destination therapy.

The AbioCor is a revolutionary device. It is the only device of its kind in the clinical world. The role of the AbioCor is to provide permanent replacement of the failing heart for patients who are not transplant candidates. The clinical trial has been successful in the majority (four of seven) of patients implanted thus far. Eight more patients are required to complete the initial feasibility phase of the trial, afterwhich it remains to be seen if the trial will expand to additional patient populations. The powerful features of the pump have been demonstrated in the extremely sick group of candidates that enrolled in the study. The TET system has worked extremely well. Lastly, the milestone of discharging a patient to home on a completely internal artificial heart has been realized. The profile of CardioWest is very different from AbioCor. Although both were initially designed as permanent replacement therapies, the CardioWest has been extremely useful as a bridging device, and it may have a broader application in the future. For the CardioWest, the most favorable groups are patients with cardiomyopathy who decompensate while awaiting transplantation. On the other hand, the AbioCor is indicated in nontransplant candidates with biventricular failure who have a less than 30-day predicted survival. Proper patient selection is critical to achieving success with either device.

Equipment Design↗