Pasquale De Negri

Dr. Pasquale De Negri


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 November 2001 in Pediatric Anesthesia
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Journal Article
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PNPasquale De Negri
Pasquale De Negri
GIGiorgio Ivani
Giorgio Ivani
CVCiro Visconti
Ciro Visconti
PVPaolo De Vivo
Paolo De Vivo

1 August 1998 in British Journal of Anaesthesia
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Journal Article
Closed access
GIG Ivani
G Ivani
ELE Lampugnani
E Lampugnani
MTMichele Torre
Michele Torre
GMG Calevo Maria
G Calevo Maria
PNPasquale De Negri
Pasquale De Negri
NMN S Morton
N S Morton
In a double-blind, multicentre study 245 children aged 1-10 yr undergoing elective minor surgery as inpatients were randomly allocated to receive a single caudal extradural injection of 1 ml kg-1 of either 0.25% bupivacaine or 0.2% ropivacaine after induction of light general anaesthesia. The groups were comparable for age, weight, vital signs and duration of surgery. The onset time was similar for ropivacaine and bupivacaine (9.7 vs 10.4 min). Further analgesia was not required in 40% of children. The mean time to first analgesia in the remainder was 233 min in the bupivacaine group and 271 min in the ropivacaine group. No motor block was measurable in either group. Ropivacaine 2 mg kg-1 was as effective as bupivacaine 2.5 mg kg-1 for caudal analgesia in children.

1 April 2000 in Acta Anaesthesiologica Scandinavica
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Journal Article
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GIG. Ivani
G. Ivani
PNPasquale De Negri
Pasquale De Negri
ACA. Conio
A. Conio
MAM. Amati
M. Amati
SRS. Roero
S. Roero
PLP. A. Lönnqvist
P. A. Lönnqvist

1 March 1998 in Pediatric Anesthesia
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Journal Article
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GIGiorgio Ivani
Giorgio Ivani
NMNadia Mereto
Nadia Mereto
ELElisabetta Lampugnani
Elisabetta Lampugnani
PNPasquale De Negri
Pasquale De Negri
MTMichele Torre
Michele Torre
PLPer Lönnqvist
Per Lönnqvist

1 December 2012 in Anesthesia & Analgesia
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Journal Article
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SBSergio Bertoglio
Sergio Bertoglio
FFFabio Fabiani
Fabio Fabiani
PNPasquale De Negri
Pasquale De Negri
ACAntonio Corcione
Antonio Corcione
DMDomenico Franco Merlo
Domenico Franco Merlo
LZLucia Zappi
Lucia Zappi
Open colorectal cancer (CRC) surgery induces severe and prolonged postoperative pain. The optimal method of postoperative analgesia in CRC surgery has not been established. We evaluated the efficacy of preperitoneal continuous wound infusion (CWI) of ropivacaine for postoperative analgesia after open CRC surgery in a multicenter randomized controlled trial. Candidates for open CRC surgery randomly received preperitoneal CWI analgesia or continuous epidural infusion (CEI) analgesia with ropivacaine 0.2% 10 mL/h for 48 hours after surgery. Fifty-three patients were allocated to each group. All patients received patient-controlled IV morphine analgesia. Over the 72-hour period after the end of surgery, CWI analgesia was not inferior to CEI analgesia. The difference of the mean visual analog scale score between CEI and CWI patients was 1.89 (97.5% confidence interval = -0.42, 4.19) at rest and 2.76 (97.5% confidence interval = -2.28, 7.80) after coughing. Secondary end points, morphine consumption and rescue analgesia, did not differ between groups. Time to first flatus was 3.06 ± 0.77 days in the CWI group and 3.61 ± 1.41 days in the CEI group (P = 0.002). Time to first stool was shorter in the CWI than the CEI group (4.49 ± 0.99 vs 5.29 ± 1.62 days; P = 0.001). Mean time to hospital discharge was shorter in the CWI group than in the CEI group (7.4 ± 0.41 and 8.0 ± 0.38 days, respectively). More patients in the CWI group reported excellent quality of postoperative pain control (45.3% vs 7.6%). Quality of night sleep was better with CWI analgesia, particularly at the postoperative 72-hour evaluation (P = 0.009). Postoperative nausea and vomiting was significantly less frequent with CWI analgesia at 24 hours (P = 0.02), 48 hours (P = 0.01), and 72 hours (P = 0.007) after surgery evaluations. Preperitoneal CWI analgesia with ropivacaine 0.2% continuous infusion at 10 mL/h during 48 hours after open CRC surgery provided effective postoperative pain relief not inferior to CEI analgesia.

1 June 2007 in The Clinical Journal of Pain
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Journal Article
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PNPasquale De Negri
Pasquale De Negri
TTTiziana Tirri
Tiziana Tirri
GPGianluca Paternoster
Gianluca Paternoster
PMPasqualina Modano
Pasqualina Modano
Vertebroplasty (PV) and balloon kyphoplasty (KP) are minimally invasive vertebral augmentation procedures involving injection of polymethyl methacrylate cement under radiologic control into a fractured vertebral body. They strengthen the bone and improve the intense pain caused by fracture secondary to osteoporosis, metastasis, or trauma and refractory to conservative therapies such as analgesic use, bed rest, and bracing. Aim of the study is to investigate and compare safety and efficacy of KP and PV on pain and mobility in patients with vertebral fractures due to osteoporosis or trauma. Twenty-one patients have been enrolled in a prospective nonrandomized controlled study with painful vertebral compression fractures resistant to common therapies. Patients underwent KP or PV. A Visual Analog Scale has been used to measure pain status at different time up to 6 months; the Oswestry Disability Index (ODI) was chosen to evaluate functional activity before procedure and 6 months later. Mean pain scores decreased significantly from pretreatment to posttreatment with KP and PV as did the ODI scores. No significant differences could be found between both groups for the mean VAS and ODI scores preprocedure and postprocedure. Cement extravasation occurred only during PV. No other adverse events correlated to both techniques have been reported. Our results suggest that both PV and KP offer therapeutic benefit significantly reducing pain and improving mobility in patients with vertebral fracture without significant differences between groups in term of quality. The leakage of cement has been observed only during PV.