Hemodynamic effects of ketamine in children with congenital heart disease and/or pulmonary hypertension

被引:24
作者
Loomba, Rohit S. [1 ]
Gray, Seth B. [2 ]
Flores, Saul [3 ]
机构
[1] Advocate Childrens Hosp, Inst Heart, Dept Pediat, Oak Lawn, IL USA
[2] Hosp Sick Children, Div Cardiol, Dept Pediat, Toronto, ON, Canada
[3] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, Sect Crit Care & Cardiol, Houston, TX 77030 USA
关键词
congenital heart disease; hemodynamics; ketamine; systemic vascular resistance;
D O I
10.1111/chd.12662
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionKetamine is a drug often used for procedural sedation or as adjunct agent for general sedation in children with congenital heart disease. In the clinical realm, there is often confusion regarding the effects of ketamine on hemodynamics, particularly pulmonary vascular resistance and systemic vascular resistance. We performed a meta-analysis of studies investigating the effects of ketamine on hemodynamics. MethodsA systematic review was conducted to identify studies characterizing the hemodynamic effects of ketamine in children with congenital heart disease. Studies were assessed for quality and those of satisfactory quality with pre- and postketamine hemodynamics for each patient were included in the final analyses. Those not limited to pediatric patients and those not limited to patients with congenital heart disease were excluded from the final analyses. ResultsA total of 7 studies with 139 patients were included in the final analyses. Pulmonary vascular resistance, systemic vascular resistance, mean pulmonary artery pressure, mean systemic pressure, heart rate, pH, and arterial oxygen concentration did not significantly change with administration of ketamine. Carbon dioxide concentration did increase significantly by a mean of 1.38mmHg with the administration of ketamine. ConclusionKetamine has minimal impact on hemodynamics in children with congenital heart disease when used at usual clinical doses. Systemic vascular resistance and pulmonary vascular resistance are not significantly altered. Blood gas values are also only minimally affected by ketamine.
引用
收藏
页码:646 / 654
页数:9
相关论文
共 16 条
[1]   Taming the Ketamine Tiger [J].
Domino, Edward F. .
ANESTHESIOLOGY, 2010, 113 (03) :678-684
[2]   Hemodynamic response to ketamine in children with pulmonary hypertension [J].
Friesen, Robert H. ;
Twite, Mark D. ;
Nichols, Christopher S. ;
Cardwell, Kathryn A. ;
Pan, Zhaoxing ;
Darst, Jeffrey R. ;
Wilson, Neil ;
Fagan, Thomas E. ;
Miyamoto, Shelley D. ;
Ivy, D. Dunbar .
PEDIATRIC ANESTHESIA, 2016, 26 (01) :102-108
[3]   EFFECT OF KETAMINE ON PULMONARY-ARTERY PRESSURE - EXPERIMENTAL AND CLINICAL-STUDY [J].
GASSNER, S ;
COHEN, M ;
AYGEN, M ;
LEVY, E ;
VENTURA, E ;
SHASHDI, J .
ANAESTHESIA, 1974, 29 (02) :141-146
[4]  
Han D, 2017, MEDICINE, V96, P4
[5]   PULMONARY AND SYSTEMIC HEMODYNAMIC-RESPONSES TO KETAMINE IN INFANTS WITH NORMAL AND ELEVATED PULMONARY VASCULAR-RESISTANCE [J].
HICKEY, PR ;
HANSEN, DD ;
CRAMOLINI, GM ;
VINCENT, RN ;
LANG, P .
ANESTHESIOLOGY, 1985, 62 (03) :287-293
[6]   NMDA receptor antagonists ketamine and PCP have direct effects on the dopamine D2 and serotonin 5-HT2 receptors -: implications for models of schizophrenia [J].
Kapur, S ;
Seeman, P .
MOLECULAR PSYCHIATRY, 2002, 7 (08) :837-844
[7]   Ketamine: Teaching an old drug new tricks [J].
Kohrs, R ;
Durieux, ME .
ANESTHESIA AND ANALGESIA, 1998, 87 (05) :1186-1193
[8]   Novel drugs and therapeutic targets for severe mood disorders [J].
Mathew, Sanjay J. ;
Manji, Husseini K. ;
Charney, Dennis S. .
NEUROPSYCHOPHARMACOLOGY, 2008, 33 (09) :2080-2092
[9]  
MORRAY JP, 1984, ANESTH ANALG, V63, P895
[10]   Which anesthetic agent alters the hemodynamic status during pediatric catheterization?: Comparison of propofol versus ketamine [J].
Öklü, E ;
Bulutcu, FS ;
Yalçin, Y ;
Ozbek, U ;
Cakali, E ;
Bayindir, O .
JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA, 2003, 17 (06) :686-690