中外健康文摘
中外健康文摘
중외건강문적
WORLD HEALTH DIGEST
2013年
18期
37-38
,共2页
芬太尼%二异丙酚%首次安全剂量%试管婴儿%无痛取卵
芬太尼%二異丙酚%首次安全劑量%試管嬰兒%無痛取卵
분태니%이이병분%수차안전제량%시관영인%무통취란
fentanyl%Propfol%the initial dose%IVF%painless OVA
目的探讨芬太尼复合丙泊酚在无痛取卵中丙泊酚的首次安全剂量。方法40例自愿接受无痛取卵的患者,ASA分级Ⅰ-Ⅱ级,年龄29±6岁,体重54±9公斤,随机分成四组,A,B,C,D四组丙泊酚的首次剂量依次为1mg/kg,1.5mg/kg,2mg/kg,2.5mg/kg;观察血压,心率,呼吸,氧饱和度,体动反应,呼吸暂停(呼吸间隔长于20秒);清醒时间(拔出穿刺针至患者问取卵多少的时间);术后疼痛采用VAS评分标准(0分:无痛;1~3分:轻度疼痛:4~6分:中度疼痛:7~10分:重度疼痛)。结果剂量30秒后B,C,D组患者睫毛反射均消失,而A组有8例患者需追加丙泊酚2~3毫升才能满足穿刺要求;在丙泊酚首次剂量下,B,C两组血压,心率变化轻微,B组有1例氧饱和度下降,而C组有四例氧饱和度下降,托下颌面罩吸氧纠正,两组有显著性差异(P▲<0.01);在四组中,D组4例患者需面罩加压给氧,2例心率减慢,对呼吸循环抑制作用最大,较B,C组明显抑制(P▲▲<0.01)。A,B,C组患者清醒时间无显著性差异(P※>0.05)分别为94±35秒,90±32秒,91±34秒;D组182±42秒,与前三组有显著性差异(P※※<0.01);VAS评分:四组患者清醒后疼痛评分无显著性差异(P▲▲▲>0.05)。结论丙泊酚首次剂量1.5mg/kg复合芬太尼1 ug / kg,在取卵操作中具有安全,无痛,苏醒快的特点。
目的探討芬太尼複閤丙泊酚在無痛取卵中丙泊酚的首次安全劑量。方法40例自願接受無痛取卵的患者,ASA分級Ⅰ-Ⅱ級,年齡29±6歲,體重54±9公斤,隨機分成四組,A,B,C,D四組丙泊酚的首次劑量依次為1mg/kg,1.5mg/kg,2mg/kg,2.5mg/kg;觀察血壓,心率,呼吸,氧飽和度,體動反應,呼吸暫停(呼吸間隔長于20秒);清醒時間(拔齣穿刺針至患者問取卵多少的時間);術後疼痛採用VAS評分標準(0分:無痛;1~3分:輕度疼痛:4~6分:中度疼痛:7~10分:重度疼痛)。結果劑量30秒後B,C,D組患者睫毛反射均消失,而A組有8例患者需追加丙泊酚2~3毫升纔能滿足穿刺要求;在丙泊酚首次劑量下,B,C兩組血壓,心率變化輕微,B組有1例氧飽和度下降,而C組有四例氧飽和度下降,託下頜麵罩吸氧糾正,兩組有顯著性差異(P▲<0.01);在四組中,D組4例患者需麵罩加壓給氧,2例心率減慢,對呼吸循環抑製作用最大,較B,C組明顯抑製(P▲▲<0.01)。A,B,C組患者清醒時間無顯著性差異(P※>0.05)分彆為94±35秒,90±32秒,91±34秒;D組182±42秒,與前三組有顯著性差異(P※※<0.01);VAS評分:四組患者清醒後疼痛評分無顯著性差異(P▲▲▲>0.05)。結論丙泊酚首次劑量1.5mg/kg複閤芬太尼1 ug / kg,在取卵操作中具有安全,無痛,囌醒快的特點。
목적탐토분태니복합병박분재무통취란중병박분적수차안전제량。방법40례자원접수무통취란적환자,ASA분급Ⅰ-Ⅱ급,년령29±6세,체중54±9공근,수궤분성사조,A,B,C,D사조병박분적수차제량의차위1mg/kg,1.5mg/kg,2mg/kg,2.5mg/kg;관찰혈압,심솔,호흡,양포화도,체동반응,호흡잠정(호흡간격장우20초);청성시간(발출천자침지환자문취란다소적시간);술후동통채용VAS평분표준(0분:무통;1~3분:경도동통:4~6분:중도동통:7~10분:중도동통)。결과제량30초후B,C,D조환자첩모반사균소실,이A조유8례환자수추가병박분2~3호승재능만족천자요구;재병박분수차제량하,B,C량조혈압,심솔변화경미,B조유1례양포화도하강,이C조유사례양포화도하강,탁하합면조흡양규정,량조유현저성차이(P▲<0.01);재사조중,D조4례환자수면조가압급양,2례심솔감만,대호흡순배억제작용최대,교B,C조명현억제(P▲▲<0.01)。A,B,C조환자청성시간무현저성차이(P※>0.05)분별위94±35초,90±32초,91±34초;D조182±42초,여전삼조유현저성차이(P※※<0.01);VAS평분:사조환자청성후동통평분무현저성차이(P▲▲▲>0.05)。결론병박분수차제량1.5mg/kg복합분태니1 ug / kg,재취란조작중구유안전,무통,소성쾌적특점。
Objective Opproach the fentanyl and propofol in Painless OVA in the first safe dose. Methods Choice 40 cases of the voluntary acceptance of patients with painless OVA,ASA gradeⅠ-Ⅱ, Age of 29±6 years old, body weight of 54±9 kg , were randomly divided into four groupsA,B,C,D with 20 patients each. A, B, C, D four groups give the initial dose of propofol in the following order: 1mg/kg, 1.5mg/kg, 2mg/kg, 2.5mg/kg; The observation of blood pressure, heart rate, respiration, oxygen saturation, dynamic response, apnea ( breathing intervals longer than 20 seconds ); awake time (from pull out the needle to patients asked how long the time ); postoperative pain with VAS standard ( 0:painless; 1~3:mild pain, 4~6 : moderate pain : 7~10: severe pain). The results for the finitial dose of propofol for the B, C, D group of eyelash reflex disappeared after 30 seconds, and 8 cases in group A must add propofol 2~3 ml to satisfy the operation requirements ; In the initial dose of propofol observe,the B and the C ,both the blood pressure and heart rate changes were mild,just 1 cases in group B oxygen saturation falls, but four cases in group C ,the oxygen saturation decend, under the care of lift the chin,give the oxygen face mask to inhaling of oxygen , there was significant difference (P▲<0.01 ); in the four group, 4 cases in group D patients should face mask pressurized oxygen, 2 cases of heart rate slows,was the greatest inhibition effect on respiration and circulation, compared with B, C group was significantly inhibited (P▲▲<0.01). A, B, C group patients awake time had no significant difference (P※>0.05) was 94 ±35 sec, 90 ±32 sec, 91 ±34 seconds; group D, 182±42 seconds , and compared with A,B,C,there was significant difference (P※※<0.01); VAS score: four groups of patients after awake,the pain score significantly difference (P▲▲▲>0.05 ).Conclusion the initial dose of propofol 1.5mg/kg combined with fentanyl 1 ug / kg, on OVA is safe, painless,revive quick.