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    6種方法預(yù)防低?;颊咝g(shù)后惡心嘔吐(p ONV)的成本效果分析

    2014-04-18 08:05:52王麗珺倉靜薛張綱
    關(guān)鍵詞:托烷司瓊利多麻醉科

    王麗珺倉 靜薛張綱

    (1復(fù)旦大學(xué)附屬眼耳鼻喉科醫(yī)院麻醉科 上海 200031;2復(fù)旦大學(xué)附屬中山醫(yī)院麻醉科 上海 200032)

    6種方法預(yù)防低危患者術(shù)后惡心嘔吐(p ONV)的成本效果分析

    王麗珺1倉 靜2△薛張綱2

    (1復(fù)旦大學(xué)附屬眼耳鼻喉科醫(yī)院麻醉科 上海 200031;2復(fù)旦大學(xué)附屬中山醫(yī)院麻醉科 上海 200032)

    目的比較6種方法預(yù)防相對低?;颊咴诟骨荤R膽囊切除術(shù)后發(fā)生惡心嘔吐的成本和效果。方法180名擇期行腹腔鏡膽囊切除術(shù)并符合入選標(biāo)準(zhǔn)的男性患者,隨機(jī)分為6組。組1接受異丙酚靶控輸注(targetcontrolled infusion,TCI)+5 mg托烷司瓊;組2接受異丙酚TCI+10 mg地塞米松和1.25 mg氟派利多;組3接受異丙酚TCI+生理鹽水;組4接受七氟醚+5 mg托烷司瓊;組5接受七氟醚+10 mg地塞米松和1.25 mg氟派利多;組6接受七氟醚+生理鹽水。研究終點(diǎn)是術(shù)后24 h內(nèi)惡心嘔吐發(fā)生的次數(shù),采用盲法記錄。結(jié)果各組患者的一般情況、麻醉時間、手術(shù)時間、拔管時間和術(shù)后24 h的痛覺模擬評分差異均無統(tǒng)計學(xué)意義。組2術(shù)后惡心嘔吐的發(fā)生率顯著低于組3(P=0.03),組5顯著低于組6(P=0.01)。接受托烷司瓊和異丙酚或七氟醚發(fā)生術(shù)后惡心嘔吐的相對危險度分別為0.51或0.68;接受地塞米松聯(lián)合氟哌利多和異丙酚或七氟醚發(fā)生術(shù)后惡心嘔吐的相對危險度分別為0.40或0.39;相對于七氟醚,接受異丙酚麻醉發(fā)生術(shù)后惡心嘔吐的相對危險度是0.80。1~6組每分鐘的費(fèi)用-效果比分別為1.07、0.88、1.14、1.05、0.74和1.06。結(jié)論異丙酚、托烷司瓊、地塞米松和氟哌利多發(fā)生術(shù)后惡心嘔吐的相對危險度不同。6種干預(yù)措施中,七氟醚結(jié)合地塞米松和氟哌利多具有最低的每分鐘費(fèi)用-效果比。

    術(shù)后惡心嘔吐(PONV); 七氟醚 異丙酚; 托烷司瓊; 地塞米松; 氟哌利多; 費(fèi)用-效果

    In recent years,new anesthetics,techniques and antiemetics have entered the market. Prophylactic antiemetics are useful in patients at risk of PONV[1].Most previous studies have focused on the prophylaxis management for highrisk patients[2].Researches on patients at relative low risk of PONV were rare.Nowadays,prevention of PONV should be examined not only for their clinical benefits but also their costs.

    The aim of the present investigation was to compare 6 interventions for the prevention of PONV after LC in those at relative low risk of PONV,with the objective of looking at which combination is more economic and effective.

    Materials and Methods

    The local ethics committee approved the study protocol,and all patients gave informed consent to participate in the study.

    SubjectsOne hundred and eithty male patients (ASA I-II)scheduled for elective LC were prospectively studied.Patients were enrolled from Jan.,2008 to Dec., 2008 in Zhongshan hospital.Inclusion criteria were nonsmoker status,no previous history of postoperative nausea and vomiting or motion sickness,and anticipated use of postoperative opioids[1].Exclusion criteria were renal insufficiency(creatinine>1.5 mg/d L),liver dysfunction(aspartate aminotransferase>40 U/L, alanine aminotransferase>40 U/L),abuse of alcohol and drugs,and documented coronary or valvular heart diseases.

    proposalAll patients were instructed to refrain from food for 8 hours and not to drink for 3 houes before anaesthesia.There were no premedication.After a preoperative interview,by using computer-generated random numbers in sequentially numbered sealed envelopes,all patients fulfilling inclusion criteria were randomly separated into six groups:

    In Group 1(n=30),anesthesia was induced by fentanyl 3μg/kg,lidocaine 20 mg, succinylcholine 1-2 mg/kg.target-controlled infusion (TCI)of pump using propofol(Diprivan 1%50 mL, DK550,AstraZeneca,UK)was initiated with the target plasma propofol concentration set at 6μg/ m L,and an endotracheal tube was inserted when the effect site concentration was above 3μg/m L.Vecuronium 0.08 mg/kg was used for the muscle relaxation.Anesthesia was maintained by a target plasma propofol concentration at 4μg/m L which was titrated to the clinical effects.Fentanyl and vecuronium were also added when anesthesia seemed inadequate.5 mg tropisetron(06070006, Southwest Pharmaceutical Co.,Ltd.)was given intravenously at the end of surgery.

    Group 2(n=30)and group 3(n=30) received the same procedure for induction and maintenance of anesthesia,except that in group 2, 10 mg dexamethasone(060805,Shanghai General Pharmaceutical Co.,Ltd)and 1.25 mg droperidol (060501,Shanghai Xudong Pharmaceutical Co., Ltd)were given prior to induction while in group 3,no antiemetics were administration.

    Group 4(n=30)received fentanyl 3μg/kg, lidocaine 20 mg,propofol 2 mg/kg(Diprivan 1%20 mL,DF483,AstraZeneca,UK)and succinylcholine 1-2 mg/kg to induce anesthesia.Sevoflurane(S005B602, Baxter,USA)was administered for the maintenance of anesthesia.Vecuronium 0.08 mg/kg was used for the muscle relaxation.Additional doses of fentanyl and vecuronium were given as necessary.5 mg tropisetron was given intravenously at the end of surgery.

    Group 5(n=30)and group 6(n=30) underwent the same protocol as group 4.But in group 5,10 mg dexamethasone and 1.25 mg droperidol were given prior to induction,while in group 6 no antiemetics were administratied.

    At arrival in the operating theatre,an intravenous cannula was inserted into the patientˊs nondominant hand and all patients received a Lactated Ringerˊs solution at a rate of 10 m L/kg per hour.The designed patientsˊage and weight were entered into the TCI pump(Diprifusor,Graseby, UK)and the infusion line was attached to the intravenous cannula.All patients breathed O2at 5 L/min from a clear plastic mask attached to a circle absorber system during induction,the TCI pump was initiated with the target plasma propofol concentration set at 6μg/m L in group 1,2 and 3. When the effect site concentration was above 3μg/ m L,an endotracheal tube was inserted.After the insertion of the endotracheal tube,the vaporiser was opened to 2.5%and the TCI target reduced to 4μg/m L in the designed groups.A constant fresh gas flow of 1 L/min was used during maintenance (steady state)of anesthesia.Ventilation patterns were adjusted to keep end-expiratory CO2between 35 and 40 mm Hg(1 mm Hg=0.133 k Pa,the same below,continuous capnography).Concentrations of volatile anesthetics was measured by using a solor 8 000 monitor.

    Each patient was inserted a nasogastric tube upon intubation and suction applied to empty the stomach of air and gastric contents.During surgery,the pneumo-peritoneum was insufflated with CO2,with an intra-abdominal pressure of 15 mm Hg.Prior to endotracheal extubation,the nasogastric tube was suctioned again and then removed.When reaching the extubation criteria, the trachea was extubated.In the operating theater,patients were monitored continuously with electrocardiography,pulse oximetry,capnography, and noninvasive blood pressure measurements.

    Depth of anaesthesia was adjusted in all 6 groups in order to maintain heart rate and blood pressure within 15%-20%from baseline,the vaporiser or TCI pump and fentanyl were adjusted as necessary to maintain adequate anaesthesia according to clinical signs.5 mg tropistron were given at the end of surgery in group 1 and 4.10 mg dexamethasone and 1.25 mg droperidol were given prior to induction in group 2 and 5.Saline was given in group 3 and 6.Anesthesia and the administration of antiemetic drugs were provided by anesthesiologists who were not involved in the study and who were experienced in both techniques.

    ObservationindexPatients were monitored for 24 hours postoperatively.Our primary outcome measure was the incidence of any nausea,emetic episodes(retching or vomiting),or both(i.e. postoperative nausea and vomiting).Trained investigators who were fully blinded to the intraoperative management and random treatment assignments recorded the number of emetic episodes.

    Postoperative pain was noted using the visual analog scale(VAS,0:no pain,10:the most pain). Patients were also asked to assess their postoperative state as satisfactory score with regard to the incidence of nausea,vomiting,pain, and adverse events(0:the worst satisfaction, 10Lthe most satisfaction).

    The expense of sevoflurane was calculated by the following formula[3]:

    The volume of vapour produced from 1 m L of liquid for sevoflurane at 20℃and 1 atmosphere pressure is 182.7 m L/min[4].

    Prices for all used substances were taken from our hospital pharmacy list.The costs of stuff and fixed costs such as monitoring equipment or other overhead costs(e.g.hospital overheads)and the social costs were not taken into consideration.

    StatisticalanalysisStatistical analyses were carried out by Stata 7.0.The continuous data were represented as x—±s and compared by the analysis of variance(ANOVA).Non-parametric data were analyzed by the Kruskal-Wallis rank sum test and categorical data were analyzed by the Pearsonˊs Chi-square test.Theαerror was set at 0.05,andβ error at 0.2.P<0.05 was considered to indicate statistical significance.

    Results

    All the 180 patients completed the study and no major events were noticed during anesthesia. The patient characteristics were given in Tab 1. There was no significant difference among all 6 groups according to the age and weight.

    Tab 1 patient characteristics(±s,n=30)

    Data were compared by the analysis of variance(ANOVA).

    Preoperative observations and the amount of anaesthetics used were given in Tab 2.Postoperative observations were described in Tab 3.Time of surgery and time of anesthesia(start of induction of anesthesia until extubation)were similar in all groups.Time of extubation(end of surgery until extubation)and VAS for 24 hours postoperation were not significantly different in six groups.The satisfactory score in group 6 was significantly lower than the other groups(P<0.05).

    Tab 2 Intraoperative observations(±s,n=30)

    Data were compared by the Kruskal-Wallis rank sum test.″-″:Not administrated.

    Tab 3 postoperative observations(±s,n=30)

    VAS:Visual analog scale;PONV.Postoperative nausea and vomiting;Health effect:No.of patients without PONV.VAS and Satisfactory Score were compared by the Kruskal-Wallis rank sum test,(1)P<0.05,vs.the other groups.

    The incidence of PONV in group 2 was significantly lower than that in group 3(P=0.03), and in group 5 was significantly lower than that in group 6(P=0.01).Compared with those received only anesthetics,the relative risk of PONV for patients who received anesthetics combined with antiemetics was reduced to 0.62(95%CI:0.47-0.88).The relative risk of PONV for those received tropisetron and propofol or sevoflurane were 0.51(95%CI:0.21 -1.2)or 0.68(95%CI:0.37-1.24),for those received dexamethasone,droperidol and propfol or sevoflurane were 0.40(95%CI:0.14-1.12)or 0.39 (95%CI:0.16-0.95),for those received propofol was 0.80(95%CI:0.46-1.4)(Tab 4 to Tab 6). Cost associated with each group was shown in Tab 7. Cost-effectiveness ratio was defined as“The total anesthesia cost/The number of patients without PONV”.Patients based on sevoflurane combined with dexamethasone and droperidol had the lowest costeffectiveness ratio per minute in all 6 groups.

    Tab 4 Risk of p ONV according to patientsˊrandomly assigned antiemetics(±s)

    CI:Confidence interval.Data were compared by the Pearsonˊs Chi-square test.

    Tab 7 The primary drug cost and total anesthetic cost associated in each group(RMB,±s)

    Total anesthetic cost referred all anesthesia associated cost during the operation,including drug cost,material cost,operating cost and monitor cost.

    Discussion

    Today,the financial consequences of treating patients seem to be as important as the medical consequences.It is challenging to reduce the cost of anesthesia while maintaining or even improving quality[5].

    PONV is one of the most common complications following surgery.Better anesthetic techniques,along with a new generation of antiemetics,reduced the incidence of PONV in todayˊs practice.Nevertheless,PONV still occurs, with an incidence up to 75%in some high-risk patients[6].It is reported that PONV is one of the most unpleasant postoperative symptoms so that avoiding PONV is as important as avoiding pain postoperatively[7].Patients are willing to spend up to 100 US dollars out of their pocket for an effective antiemetic[8].

    It is well known that the incidence of PONV varies considerably according to the basic risk factors of patients and type of surgery conducted. Those who were of at least two of the following risk factors:female sex,nonsmoker status,previous history of postoperative nausea and vomiting or motion sickness,and anticipated use of postoperative opioids,when underwent laparoscopic cholecystectomy,they are defined as high-risk patients[9].But,in those relative low-risk patients,the most cost-effective way for preventing PONV remains unknown.

    One of the most important way to prevent PONV is to use antiemetics.All the tested antiemetics are proved to be safe.Droperidol is one of the most widely used drugs.A quantitative systematic review showed that for prevention of early nausea(within 6 h postoperatively),relative risk(RR)of droperidol was 0.45 and for prevention of early vomiting,RR was 0.65[10].It may have an effect on dopamine receptor D2. However,low-dose droperidol can cause dysphoria. In Dec.,2001,the FDA issued a new“black box”warning on droperidol because of concerns of serious cardiac arrhythmias secondary to QT prolongation[11].However,there is little evidence that antiemetic doses trigger this condition[12]. None of the patients who received droperidol showed side effects in our study.

    Intravenous dexamethasone generally requires a longer period of time to take effect and a time lag of 12-24 hours to achieve maximal result. Dexamethasone should be given before or immediately after induction of anesthesia rather than waiting until the surgery is nearly completed,probably by reducing surgery-induced inflammation[13].Specific guidelines have been issued on the prevention and management of nausea and vomiting[14].According to theseguidelines,a combination of droperidol 1.25 mg with dexamethasone 10 mg is recommended for operative procedures associated with a high risk of nausea and vomiting,including laparoscopic procedures.We used a combination of droperidol and dexamethasone based on this recommendation and low cost of these agents.In our study,we found that the relative risk of PONV for those received dexamethasone,droperidol and propfol was 0.40 while for those received dexamethasone, droperidol and sevoflurane was 0.39.

    Tropisetron is a new generation of 5-hydroxytryptamine type 3 antagonists.It is metabolized by the liver cytochrome P-450 2D5system,and due to the polymorphism of this system,it metabolizes faster in some individuals. The mean elimination half-life is 8 hours in individuals with fast metabolism and 30 to 40 hours in those with slow metabolism,which could make tropisetron suitable for prevention of PONV in a single dose.Tropisetron is considered relatively safe but more expensive than droperidol and dexamethasone.In our study,the relative risk of PONV for those received tropisetron and propofol or sevoflurane were 0.51 or 0.68.

    We chose target-controlled infusion of propofol and sevoflurane as two of the anesthesia techniques because both of them are reported to provide stable hemodynamics during anesthesia and are used more and more widely for recent years.

    The TCI system was as simple to use as a vaporiser,in that adequate anaesthetic conditions it could always be restored by adjusting the target concentration and no patient required an additional manual bolus of propofol or other intervention. Though it was said that use of sevoflurane as a maintenance anesthesia allowed rapid recovery[15], the extubing time in TCI groups and sevoflurane groups were similar according to our data.This may be explained by using current Diprifusor software in TCI pump which showed the effect site (brain)concentration as a sign of anesthesia recovery.

    It has been reported that PONV occurs less frequently after a propofol-based anesthetic compared with other methods[16].The possible effects of propofol are its interactions with the dopaminergic and the serotoninergic systems. Propofol may depress the synaptic transmissionin cortex region olfactory and decrease the release of excitatory amino acids[17].According to our data, the relative risk of PONV for those who received propofol was 0.80 compared with sevoflurane.

    In our study,the relative risk of PONV for those received anesthetics combined with antiemetics was 0.62 compared with those only received anesthetics. Since propofol is more expensive than sevoflurane and patients usually have to afford the cost of waste drug, the combination of sevoflurane and 10mg dexamethason plus 1.25mg droperidol has the lowest cost-effective ratio per minute for relatively low-risk patients undergoing LC.

    [1] Apfel CC,Zhang K,George E,et al.Transdermal scopolamine for the prevention of postoperative nausea and vomiting:a systematic review and meta-analysis[J]. Clin Ther,2010,32(12):1987-2002.

    [2] Ahmed OHAS,Nasr DAM,Ezzat H.Effect of premedication with mirtazapine versus ondansetron on postoperative nausea and vomiting in breast surgery[J]. Eg JA,2011,27(3):135-139.

    [3] Smith I.Cost considerations in the use of anaesthetic drugs[J].Pharmacoeconomics,2001,19(5):469-481.

    [4] Laster MJ,Fang Z,Eger II EI.Specific gravities of desflurane,enflurane,halothane,isoflurane,and sevoflurane[J].Anesth Analg,1994,78(6):1152-1153.

    [5] Sachin R,Andrew PV.Postoperative analgesia and discharge criteria for day surgery[J].Anaesth Intensive Care Med,2010,11(4):153-156.

    [6] Ryu JH,Jeon YT,Hwang JW,et al.Intravenous,oral,and the combination of intravenous and oral ramosetron for the prevention of nausea and vomiting after laparoscopic cholecystectomy:a randomized,double-blind,controlled trial[J].Clin Ther,2011,33(9):1162-1172.

    [7] Ryu JH,Chang JE,Kim HR,et al.Ramosetron vs. ramosetron plus dexamethasone for the prevention of postoperative nausea and vomiting(PONV)after laparoscopic cholecystectomy:prospective,randomized, and double-blind study[J].Int J Surg,2013,11(2):183 -187.

    [8] Gan T,Sloan F,Dear G,et al.How much are patients willing to pay to avoid postoperative nausea and vomiting?[J].Anesth Analg,2001,92(2):393-400.

    [9] Anna L,Agilan K.Focus on quality:Managing pain and PONV in day surgery[J].Curr Anaesth Crit Care,2007, 18(4):200-207.

    [10] Schaub I,Lysakowski C,Elia N,et al.Low-dose droperidol(≤1 mg or≤15μg·kg-1)for the prevention of postoperative nausea and vomiting in adults:quantitative systematic review of randomised controlled trials[J].Eur J Anaesthesiol,2012,29(6):286-294.

    [11] Habib AS,Gan TJ.The use of droperidol before and after the Food and Drug Administration black box warning:a survey of the members of the Society of Ambulatory Anesthesia[J].J Clin Anesth,2008,20(1):35-39.

    [12] Wax D,Doshi A,Hossain S,et al.Changing patterns of postoperative nausea and vomiting prophylaxis drug use in an academic anesthesia practice[J].J Clin Anesth,2007, 19(5):356-359.

    [13] Ho CM,Wu HL,Ho ST,et al.Dexamethasone prevents postoperative nausea and vomiting:benefit versus risk[J].Acta Anaesthesiol Taiwan,2011,49(3):100-104.

    [14] Myklejord DJ,Yao L,Liang H,et al.Consensus guideline adoption for managing postoperative nausea and vomiting[J].WMJ,2012,111(5):207-213.

    [15] Orhon ZN,Devrim S,Celik M,et al.Comparison of recovery profiles of propofol and sevoflurane anesthesia with bispectral index monitoring in percutaneous nephrolithotomy[J].Korean J Anesthesiol,2013,64(3):223-238.

    [16] Akkurt CO,Temiz M,Inanoglu K,et al.Comparison of recovery characteristics,postoperative nausea and vomiting,and gastrointestinal motility with total intravenous anesthesia with propofol versus inhalation anesthesia with desflurane for laparoscopic cholecystectomy:A randomized controlled study[J].Curr Ther Res,2009,70(2):94-103.

    [17] Golembiewski J,Tokumaru S.Pharmacological prophylaxis and management of adult postoperative/postdischarge nausea and vomiting[J].J Perianesth Nurs,2006,21(6):385-397.

    Cost-effectiveness comparison between 6 interventions for the prevention of postoperative nausea and vomiting(p ONV)on low-risk patients

    WANG Li-jun1,CANG Jing2△,XUE Zhang-gang2
    (1Department of Anesthesiology,Ear Eye Nose and Throat Hospital,Fudan University,Shanghai 200031,China;2Department of Anesthesiology,Zhongshan Hospital,Fudan University,Shanghai 200032,China)

    Objective We conducted this study to compare the cost and effectiveness of prophylactic antiemetic interventions combined with different anesthetic techniques on those relative low-risk patients received laparoscopic oholcystectomy(LC).MethodsOne hundred and eighty male patients fulfilling inclusion criteria scheduled for LC were randomized divided into 6 groups,with 30 patients in each group.Group 1 received target-controlled infusion(TCI)of propofol+5 mg tropisetron.Group 2 received TCI propofol+10 mg dexamethasone+1.25 mg droperidol.Group 3 received TCI propofol without antiemetics.Group 4 received sevoflurane+5 mg tropisetron.Group 5 received sevoflurane +10 mg dexamethasone+1.25 mg droperidol.Group 6 received sevoflurane without antiemetic.Theprimary outcome was nausea and vomiting within 24 hours after surgery,which was evaluated blindly.ResultsNo difference was seen with regard to patient characteristics,time of surgery,anesthesia and extubation and visual analogue score(VAS)for 24 hours after surgery.The incidence of postoperative nausea and vomiting(PONV)in group 2 was significantly lower than in group 3(P=0.03),and in group 5 was significantly lower than that in group 6(P=0.01).The relative risk of PONV for those received tropisetron and propofol or sevoflurane were 0.51 or 0.68,for those received dexamethasone,droperidol and propfol or sevoflurane were 0.40 or 0.39,for those received propofol was 0.80.The relative risk of PONV for those received antiemetics were 0.62 compared with those received only anesthetics.Looking at the total cost including waste,the cost-effectiveness ratio per minute was 1.07,0.88,1.14,1.05,0.74 and 1.06 respectively in group 1 to 6.ConclusionsPropofol,tropisetron,dexamethasone and droperidol had different relative risk of PONV.Dexamethasone plus droperidol and sevoflurane had the lowest cost-effectiveness ratio per minute.

    postoperative nausea and vomiting(PONV); propofol; sevoflurane; tropisetron;dexamethasone; droperidol; cost-effectiveness Postoperative nausea and vomiting(PONV)is one of the most common complications after laparoscopic cholecystectomy(LC).It is associated with the high risk of suture dehiscence,aspirated pneumonia,respiratory tract obstruction and so on, therefore it delays discharge time and increases medical cost.

    R 656

    B

    10.3969/j.issn.1672-8467.2014.01.012

    2013-02-12;編輯:張秀峰)

    △Corresponding author E-mail:cjj286@126.com

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