Patricia Fogarty-Mack
Columbia University
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Anesthesiology | 1997
John Guy; Bradley J. Hindman; Kristy Z. Baker; Cecil O. Borel; Mazen A. Maktabi; Noeleen Ostapkovich; Jerry Kirchner; Michael M. Todd; Patricia Fogarty-Mack; Verna Yancy; Martin D. Sokoll; A. McAllister; Carl Roland; William L. Young; David S. Warner
BackgroundRemifentanil hydrochloride is an ultra-short-acting, esterase-metabolized micro-opioid receptor agonist. This study compared the use of remifentanil or fentanyl during elective supratentorial craniotomy for space-occupying lesions.MethodsSixty-three adults gave written informed consent for
Neurosurgery | 1996
William L. Young; Abraham Kader; Eugene Ornstein; Kristy Z. Baker; Noeleen Ostapkovich; John Pile-Spellman; Patricia Fogarty-Mack; Bennett M. Stein
To study the pathophysiology of idiopathic postoperative brain swelling or hemorrhage after arteriovenous malformation resection, termed normal perfusion pressure breakthrough (NPPB), we performed cerebral blood flow (CBF) studies during 152 operations in 143 patients, using the xenon-133 intravenous injection method. In the first part of the study, CBF was intraoperatively measured (isoflurane/N2O anesthesia) during relative hypocapnia in 95 patients before and after resection. The NPPB group had a greater increase (P < 0.0001) in mean +/- standard deviation global CBF (28 +/- 6 to 47 +/- 16 ml/100 g/min, n = 5) than did the non-NPPB group (25 +/- 7 to 29 +/- 10 ml/100 g/min, n = 90); both arteriovenous malformation groups showed greater increase (P < 0.05) than did controls undergoing craniotomy for tumor (23 +/- 6 to 23 +/- 6 ml/100 g/min, n = 22). Ipsilateral and contralateral CBF changes were similar. In a second cohort of patients with arteriovenous malformations, CBF was measured at relative normocapnia and it increased (P < 0.002) from pre- to postresection (40 +/- 13 to 49 +/- 15 ml/100 g/min, n = 57). There were no NPPB patients in this latter cohort. The feeding mean arterial pressure was measured intraoperatively before resection or at the last embolization before surgery (n = 64). The feeding mean arterial pressure (44 +/- 16 mm Hg) was 56% of the systemic arterial pressure (78 +/- 12 mm Hg, P < 0.0001) and was not related to changes in CBF from pre- to postresection. There was an association between increases in global CBF from pre- to postresection and NPPB-type complications, but there was no relationship of these CBF changes to preoperative regional arterial hypotension. These data do not support a uniquely hemodynamic mechanism that explains cerebral hyperemia as a consequence of repressurization in hypotensive vascular beds.
Anesthesiology | 1998
Noeleen Ostapkovich; Kristy Z. Baker; Patricia Fogarty-Mack; Michael B. Sisti; William L. Young
BACKGROUND Remifentanil, a rapidly metabolized mu-opioid agonist, may offer advantages for neurosurgical procedures in which prolonged anesthetic effects can delay assessment of the patient. This study compared the effects of remifentanilnitrous oxide on cerebral blood flow (CBF) and carbon dioxide reactivity with those of fentanyl-nitrous oxide anesthesia during craniotomy. METHODS After institutional approval and informed patient consent were obtained, 23 patients scheduled to undergo supratentorial tumor surgery were randomly assigned to remifentanil or fentanyl infusion groups in a double-blinded manner. Midazolam, thiopental, and pancuronium induction was followed by equipotent narcotic loading infusions of remifentanil (1 microg x kg(-1) x min(-1)) or fentanyl (2 microg x kg(-1) x min(-1)) for 5-10 min. Patients were ventilated with 2:1 nitrous oxideoxygen, and opioid rates were reduced and then titrated to a stable hemodynamic effect. After dural exposure, CBF was measured by the intravenous 133xenon technique at normocapnia and hypocapnia. Reactivity of CBF to carbon dioxide was calculated as the absolute increase in CBF per millimeters of mercury increase in the partial pressure of carbon dioxide (PaCO2). Data were analyzed by repeated-measures analysis of variance, unpaired Students t-tests, or contingency analysis. RESULTS In the remifentanil group (n = 10), CBF decreased from 36+/-11 to 27+/-8 ml x 100 g(-1) x min(-1) as PaCO2 decreased from 33+/-5 to 25+/-2 mmHg. In the fentanyl group (n = 8), CBF decreased from 37+/-11 to 25+/-6 ml x 100 g(-1) x min(-1) as PaCO2 decreased from 34+/-3 to 25+/-3 mmHg. Absolute carbon dioxide reactivity was preserved with both agents: 1+/-1.2 ml x 100 g(-1) x min(-1) x mmHg(-1) for remifentanil and 1.5+/-0.5 ml x 100 g(-1) x min(-1) x mmHg(-1) for fentanyl (P = 0.318). CONCLUSION Remifentanil and fentanyl have similar effects on absolute CBF, and cerebrovascular carbon dioxide reactivity is maintained.
Stroke | 1997
Shailendra Joshi; William L. Young; John Pile-Spellman; Patricia Fogarty-Mack; Robert R. Sciacca; Lotfi Hacein-Bey; Hoang Duong; Yvonne Vulliemoz; Noeleen Ostapkovich; Tara Jackson
BACKGROUND AND PURPOSE The mechanism of adaptation to chronic cerebral hypotension in normal brain adjacent to cerebral arteriovenous malformations (AVMs) is unknown. To clarify these mechanisms, we performed cerebral blood flow (CBF) studies in structurally and functionally normal vascular territories during 53 distal cerebral angiographic procedures in 37 patients with AVMs. METHODS CBF was measured using the superselective intra-arterial 133Xe method before and after a 3-minute infusion of either verapamil (1 mg.min-1, n = 23), acetylcholine (1.33 micrograms.kg-1.min-1, n = 7), nitroprusside (0.5 microgram.kg-1.min-1, n = 16) or nitroglycerin (0.5 microgram.kg-1.min-1, n = 7). RESULTS Mean +/- SD systemic (76 +/- 13 mm Hg) and distal cerebral arterial (55 +/- 16 mm Hg; range, 20 to 97 mm Hg) pressures were not different among groups. Verapamil increased CBF (45 +/- 12 to 65 +/- 21 mL.100 g-1.min-1, P < .001). There was no effect of acetylcholine (no change [46 +/- 9 to 46 +/- 9 mL.100 g-1.min-1], NS) or nitroglycerin (36 +/- 14 to 36 +/- 13 mL.100 g-1.min-1, NS). Nitroprusside decreased CBF (40 +/- 12 to 31 +/- 11 mL.100 g-1.min-1, P < .001). The percent change in CBF after drug administration was proportional to cerebral arterial pressure for verapamil only (r = .57, P = .0051). CONCLUSIONS When infused intra-arterially in clinically relevant doses in both hypotensive and normotensive normal vascular territories remote from an AVM nidus, calcium channel blockade caused vasodilation, but there was an absence of response to nitric oxide-mediated vasodilators. These data suggest that (1) the nitric oxide pathway probably is not involved in the adaptation to chronic cerebral hypotension in AVM patients and (2) if our findings in vessels remote from or contralateral to the AVM are applicable to vessels of patients with other forms of cerebrovascular disease, clinically relevant doses of intra-arterial nitrovasodilators may not be useful in the manipulation of cerebrovascular resistance.
Survey of Anesthesiology | 1998
John Guy; Bradley J. Hindman; Kristy Z. Baker; Cecil O. Borel; Mazen A. Maktabi; Noeleen Ostapkovich; Jerry Kirchner; Michael M. Todd; Patricia Fogarty-Mack; Vema Vancy; Martin D. Sokoll; A. McAllister; Carl Roland; William L. Young; David S. Warner
Background Remifentanil hydrochloride is an ultra‐short‐acting, esterase‐metabolized micro‐opioid receptor agonist. This study compared the use of remifentanil or fentanyl during elective supratentorial craniotomy for space‐occupying lesions. Methods Sixty‐three adults gave written informed consent for this prospective, randomized, double‐blind, multiple‐center trial. Anesthesia was induced with thiopental, pancuronium, nitrous oxide/oxygen, and fentanyl (n = 32; 2 micro gram [center dot] kg [center dot] sup ‐1 min sup ‐1) or remifentanil (n = 31; 1 micro [center dot] kg sup ‐1 [center dot] min sup ‐1). After tracheal intubation, infusion rates were reduced to 0.03 micro gram [center dot] kg sup ‐1 [center dot] min sup ‐1 (fentanyl) or 0.2 micro gram [center dot] kg sup ‐1 [center dot] min sup ‐1 (remifentanil) and then adjusted to maintain anesthesia and stable hemodynamics. Isoflurane was given only after specified infusion rate increases had occurred. At the time of the first burr hole, intracranial pressure was measured in a subset of patients. At bone flap replacement either saline (fentanyl group) or remifentanil ([nearly equal] 0.2 micro gram [center dot] kg sup ‐1 [center dot] min sup ‐1) were infused until dressing completion. Hemodynamics and time to recovery were monitored for 60 min. Analgesic requirements and nausea and vomiting were observed for 24 h. Neurological examinations were performed before operation and on postoperative days 1 and 7. Results Induction hemodynamics were similar. Systolic blood pressure was greater in the patients receiving fentanyl after tracheal intubation (fentanyl = 127 +/‐ 18 mmHg; remifentanil = 113 +/‐ 18 mmHg; P = 0.004). Intracranial pressure (fentanyl = 14 +/‐ 13 mmHg; remifentanil = 13 +/‐ 10 mmHg) and cerebral perfusion pressure (fentanyl = 76 +/‐ 19 mmHg; remifentanil = 78 +/‐ 14 mmHg) were similar. Isoflurane use was greater in the patients who received fentanyl. Median time to tracheal extubation was similar (fentanyl = 4 min: range = ‐1 to 40 min; remifentanil = 5 min: range = 1 to 15 min). Seven patients receiving fentanyl and none receiving remifentanil required naloxone. Postoperative systolic blood pressure was greater (fentanyl = 134 +/‐ 16 mmHg; remifentanil = 147 +/‐ 15 mmHg; P = 0.001) and analgesics were required earlier in patients receiving remifentanil. Incidences of nausea and vomiting were similar. Conclusion Remifentanil appears to be a reasonable alternative to fentanyl during elective supratentorial craniotomy.
Journal of Neurosurgical Anesthesiology | 1997
Patricia Fogarty-Mack; John Pile-Spellman; L Hacien-Bey; Noeleen Ostapkovich; Shailendra Joshi; Y Vulliemoz; William L. Young
In this study the authors determined the effect of papaverine on regional cerebral blood flow (rCBF) in the angiographically normal arteriolar beds of patients with arteriovenous malformations (AVMs) who underwent transfemoral superselective angiography. Middle cerebral artery (MCA) branch vessels were catheterized during 10 procedures performed in nine patients. The mean (+/- standard deviation) largest AVM diameter was 4.4 +/- 1 cm. Regional CBF was measured by recording the washout of a bolus of xenon-133 injected through the microcatheter. In a dose-ranging study. rCBF and MCA pressure in two patients were repeatedly measured after 3-minute infusions of papaverine at 0.07, 0.7, and 7 mg/minute. In a single-dose study, an additional eight patients received only the highest dose of papaverine administered over a 3-minute period. In the dose-ranging study, CBF increased from baseline in a dose-dependent fashion. In the single-dose study, papaverine increased in rCBF 103%, from 48 +/- 11 to 95 +/- 23 ml/100 g/minute at an MCA pressure of 55 +/- 23 mm Hg. Increase in rCBF was linearly related (y = 2.2x - 17, r2 = 0.84; p = 0.001) to baseline MCA pressure (range 22-84 mm Hg). Papaverine increases rCBF in a direct proportion to baseline MCA pressure, even at low baseline pressures. Selective infusion of vasodilators should be investigated in acute cerebral hypotension to facilitate either primary or collateral recruitment of CBF by aiding spontaneous autoregulatory vasodilation. In addition, rCBF monitoring may be useful in determining the most effective intraarterial dose of papaverine while minimizing complications due to hyperemia.
American Journal of Neuroradiology | 1996
Patricia Fogarty-Mack; John Pile-Spellman; Lotfi Hacein-Bey; Andre Osipov; John DeMeritt; Ethan Jackson; William L. Young
Foundations of Anesthesia (Second Edition)#R##N#Basic Sciences for Clinical Practice | 2006
Patricia Fogarty-Mack; William L. Young
Journal of Neurosurgical Anesthesiology | 1996
Shailendra Joshi; H Duong; Lotfi Hacein-Bey; Patricia Fogarty-Mack; John Pile-Spellman; William L. Young
Journal of Neurosurgical Anesthesiology | 1996
Patricia Fogarty-Mack; John Guy; Bradley J. Hindman; Kristy Z. Baker; Cecil O. Borel; Mazen A. Maktabi; Noeleen Ostapkovich; V Yancy; Michael M. Todd; Jerry Kirchner; Martin D. Sokoll; William L. Young; A. McAllister; Carl Roland; David S. Warner