CN109248173A - A kind of cardioplegic solution - Google Patents

A kind of cardioplegic solution Download PDF

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Publication number
CN109248173A
CN109248173A CN201811407410.2A CN201811407410A CN109248173A CN 109248173 A CN109248173 A CN 109248173A CN 201811407410 A CN201811407410 A CN 201811407410A CN 109248173 A CN109248173 A CN 109248173A
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China
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solution
blood
crystal
matrix solution
lidocaine
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CN201811407410.2A
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胡志斌
葛根贤
毛文帅
崔勇
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Zhejiang Provincial Peoples Hospital
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Zhejiang Provincial Peoples Hospital
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/047Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates having two or more hydroxy groups, e.g. sorbitol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/06Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/14Alkali metal chlorides; Alkaline earth metal chlorides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • A61K35/14Blood; Artificial blood
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A61K9/0026Blood substitute; Oxygen transporting formulations; Plasma extender
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/08Solutions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

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  • Heart & Thoracic Surgery (AREA)
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Abstract

A kind of cardioplegic solution, it is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, Bomaili A) solution is as matrix solution, every 1000ml matrix solution contains 20% 16-17ml of mannitol simultaneously, 25% 7.5-8.5ml of magnesium sulfate, 5% sodium bicarbonate 10-12ml, 10% potassium chloride 13.5-16.5ml, 2% 6-7ml of lidocaine, above-mentioned crystal is mixed by the volume fraction of 1:4 with self oxygenated blood and constitutes Blood cardioplegia, final potassium ion (K+) working concentration are as follows: 11.8-13.5 mmol/L;It has the damage that can solve crystal overload in the short time, mitigation high concentration K+ to ischemic myocardium, and reliable effective, single infusion can maintain stop the features such as fighting for a long time for 60-90 minutes.

Description

A kind of cardioplegic solution
Technical field
The present invention relates to a kind of cardioplegic solution, it is mainly used for minimally invasive cardiovascular surgical procedure under general anesthesia extracorporal circulatory system When cardiac arrest during myocardial preservation, belong to raising and guarantee of the medical safety technical field.
Background technique
Human adult heart cardioplegic solution is many kinds of at present, respectively there is advantage and disadvantage, but there is no and generally acknowledge optimal myocardial preservation scheme.Face Generally according to the Buckberg agreement that the nineties in last century establishes on bed, using 4: 1 Blood cardioplegia discontinuous infusions, it is possible to provide fill The substrate and oxygen of foot simultaneously take away metabolite, and Myocardial protective effects are definite.But the frequency that its every 20-30min is filled again, influences to perform the operation Continuity, and repeatedly there are damage cardio-vascular endothelial cells, the aggravation unfavorable factors such as myocardial edema in perfusion.With angiocarpy Surgery especially minimal invasive techniques flourish, and the simplicity of cardioplegic solution management application becomes new demand, that is, seek one kind The cardioplegic solution of reliable and effective single infusion.
Brettschneider liquid (Custodial-HTK liquid) meets single infusion Myocardial protective effects and reliably stablizes, But in the application of adult department of cardiovascular surgery, there are still some problems, such as causes short time a large amount of crystalloid fluids to enter circulation, after perfusion The doubt of hyponatremia, and there are problems that how coronary stenosis patient guarantees that cardioplegic solution is uniformly perfused.The nineties in last century, The del Nido cardioplegic solution that research team of Univ. of Pittsburgh develops also meets single infusion and Myocardial protective effects are full It is intended to infant myocardium protection field to be widely used.At present in North America, there are more and more del Nido liquid to be used for adult Successful experience report, imitate it the physiological property and powerful cardiac muscle cell's membrane stabilizing action of extracellular fluid, contain with existing 4:1 Price similar in blood cardioplegic solution is even more clinical popular.But in adult department of cardiovascular surgery application process, it has been found that one A little problems, such as adhering to single infusion still for the Ischemic Cardiomyopathy there are coronary stenosis there be no evidence to suggest its safety; And since 800ml is crystalloid fluid in adult's perfusion total amount 1L, also bring the problem that the crystal load short time is overweight;There are also del Potassium ion (K+) concentration is 24mmol/L in Nido liquid, constitutes the potential threat of high potassium damage to cardiac muscle.
Therefore, small to meet adult minimal invasive cardiac surgery visual area, exposure is poor;The aorta clamping time extends, and is perfused repeatedly Blood cardioplegia influence the problems such as visual area make cardioplegic solution can reliable and effective single infusion become adult heart surgical department One proposition.
Summary of the invention
It is an object of the invention to overcome the shortcomings of the prior art, and one kind is provided can to solve in the short time crystal negative Lotus is overweight, mitigates damage of the high concentration K+ to ischemic myocardium, and reliable and effective, single infusion can maintain 60-90 minutes long-times The cardioplegic solution of myocardial preservation.
The object of the present invention is achieved by the following technical solutions, a kind of cardioplegic solution, it is with imitative extracellular The Plasma-Lyte A of liquid©For (Multiple electrolytes injection, Bomaili A) solution as matrix solution, every 1000ml matrix is molten Liquid contains 20% mannitol 16-17ml simultaneously, 25% magnesium sulfate 7.5-8.5ml, 5% 10-12ml of sodium bicarbonate, 10% potassium chloride 13.5-16.5ml, 2% 6-7ml of lidocaine, above-mentioned crystal mix composition containing blood by the volume fraction of 1:4 with self oxygenated blood Cardioplegic solution, final potassium ion (K+) working concentration are as follows: 11.8-13.5mmol/L.
As preferred: every 1000ml matrix solution contains 20% mannitol 16.3ml, 25% magnesium sulfate 8ml, 5% carbonic acid simultaneously Hydrogen sodium 11ml, 10% potassium chloride 15ml, 2% lidocaine 6.5ml, above-mentioned crystal and self oxygenated blood are mixed by 1: 4 volume fraction Close the cold crystal Blood cardioplegia for constituting temperature between 8-12 DEG C, final potassium ion (K+) working concentration are as follows: 12.6 mmol/L。
The invention belongs to the improvement to the prior art, crystal overload in the short time can be solved, mitigate high concentration K by having + the damage to ischemic myocardium, reliable effective, single infusion can maintain stop the features such as fighting for a long time for 60-90 minutes.
Specific embodiment
Below in conjunction with specific embodiment, the present invention will be described in detail: a kind of cardioplegic solution of the present invention is Del Nido liquid is improved, is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, Bomaili A) solution As matrix solution, every 1000ml matrix solution contains 20% mannitol 16-17ml simultaneously, 25% magnesium sulfate 7.5-8.5ml, and 5% Sodium bicarbonate 10-12ml, 10% potassium chloride 13.5-16.5ml, 2% 6-7ml of lidocaine, above-mentioned crystal and self oxygenated blood Blood cardioplegia, final potassium ion (K+) working concentration are as follows: 11.8-13.5 mmol/ are constituted by the volume fraction mixing of 1:4 L。
Embodiment 1: the present invention is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, vigorous arteries and veins power A) solution is as matrix solution, and every 1000ml matrix solution contains 20% mannitol 16.3ml, 25% magnesium sulfate 8ml, 5% carbon simultaneously Sour hydrogen sodium 11ml, 10% potassium chloride 15ml, 2% lidocaine 6.5ml, above-mentioned crystal and self oxygenated blood press 1: 4 volume fraction Mixing constitutes cold crystal Blood cardioplegia of the temperature between 8-12 DEG C, final potassium ion (K+) working concentration are as follows: 12.6 mmol/L。
Embodiment 2: the present invention is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, vigorous arteries and veins power A) solution is as matrix solution, and every 1000ml matrix solution contains 20% mannitol 16ml, 25% magnesium sulfate 7.5ml, 5% carbon simultaneously Sour hydrogen sodium 10ml, 10% potassium chloride 13.5ml, 2% lidocaine 6ml, above-mentioned crystal is with self oxygenated blood by the volume fraction of 1:4 Mixing constitutes Blood cardioplegia, final potassium ion (K+) working concentration are as follows: 11.8mmol/L.
Embodiment 3: the present invention is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, vigorous arteries and veins power A) solution is as matrix solution, and every 1000ml matrix solution contains 20% mannitol 17ml, 25% magnesium sulfate 8.5ml, 5% carbon simultaneously Sour hydrogen sodium 12ml, 10% potassium chloride 16.5ml, 2% lidocaine 7ml, above-mentioned crystal is with self oxygenated blood by the volume fraction of 1:4 Mixing constitutes Blood cardioplegia, final potassium ion (K+) working concentration are as follows: 13.5 mmol/L.
The cardioplegic solution of the invention, including the Plasma-Lyte A to imitate extracellular fluid©(compound electrolyte Injection, Bomaili A) solution is matrix solution, containing mannitol, magnesium sulfate, sodium bicarbonate, potassium chloride, lidocaine ingredient, Above-mentioned crystal is mixed the Blood cardioplegia constituted by 1: 4 volume fraction with self oxygenated blood;Terminal potassium ion (K+) concentration is 12.6 mmol/L mitigate superelevation potassium to myocardium potential damage;Do not change original perfusion system pipeline pipeline when use, it can be with Keep brilliant: blood ratio is 1:4;Avoid crystal overload in the short time;Single infusion can maintain 60-90 minutes cardiac muscles for a long time Protection.
Application method are as follows: 1, dosage: inducing cardioplegia dosage is 2000ml for the first time, can maintain 90 minutes myocardial preservations Effect;Perfusion maintenance dose is 400ml again if necessary, and interval time is 60 minutes.2, reperfusion mode: with self oxygenated blood By crystalline substance: the volume fraction of blood 1: 4 is irrigated.3, filling temperature: it is advisable between 8-12 DEG C.

Claims (2)

1. a kind of cardioplegic solution, it is the Plasma-Lyte A to imitate extracellular fluid©(Multiple electrolytes injection, vigorous arteries and veins Power A) solution is as matrix solution, it is characterised in that: every 1000ml matrix solution contains 20% mannitol 16-17ml simultaneously, and 25% Magnesium sulfate 7.5-8.5ml, 5% sodium bicarbonate 10-12ml, 10% potassium chloride 13.5-16.5ml, 2% 6-7ml of lidocaine, on It states crystal and mixes composition Blood cardioplegia, final potassium ion (K+) working concentration by the volume fraction of 1:4 with self oxygenated blood Are as follows: 11.8-13.5 mmol/L.
2. cardioplegic solution according to claim 1, it is characterised in that: it is sweet that every 1000ml matrix solution contains 20% simultaneously Reveal the sodium bicarbonate of alcohol 16.3ml, 25% magnesium sulfate 8ml, 5% 11ml, 10% potassium chloride 15ml, 2% lidocaine 6.5ml, above-mentioned crystal The cold crystal Blood cardioplegia for constituting temperature between 8-12 DEG C is mixed by 1: 4 volume fraction with self oxygenated blood, it is final Potassium ion (K+) working concentration are as follows: 12.6 mmol/L.
CN201811407410.2A 2018-11-23 2018-11-23 A kind of cardioplegic solution Pending CN109248173A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113975377A (en) * 2020-07-27 2022-01-28 成都青山利康药业有限公司 Cardioplegia solution

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103142643A (en) * 2013-03-22 2013-06-12 新疆医科大学第一附属医院 Autoimmune hemolytic anemia (ALHA) cardioplegic solution and preparation method thereof
CN104107431A (en) * 2006-05-29 2014-10-22 低温药理有限公司 Improved tissue maintenance
CN104857021A (en) * 2015-04-30 2015-08-26 王涛 Cold autologous blood cardioplegia solution and preparation method and application thereof
CN104922059A (en) * 2015-05-21 2015-09-23 北京青藤谷禧干细胞科技研究院有限公司 Umbilical cord mesenchymal stem cell injection and preparation method and application thereof
US20160158280A1 (en) * 2013-07-17 2016-06-09 Hibernation Therapeutics, A Kf Llc A method for organ arrest, protection and preservation and reducing tissue injury
WO2020122928A1 (en) * 2018-12-14 2020-06-18 National Taiwan University A stable cardioplegic solution for cardiac surgery

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104107431A (en) * 2006-05-29 2014-10-22 低温药理有限公司 Improved tissue maintenance
CN103142643A (en) * 2013-03-22 2013-06-12 新疆医科大学第一附属医院 Autoimmune hemolytic anemia (ALHA) cardioplegic solution and preparation method thereof
US20160158280A1 (en) * 2013-07-17 2016-06-09 Hibernation Therapeutics, A Kf Llc A method for organ arrest, protection and preservation and reducing tissue injury
CN104857021A (en) * 2015-04-30 2015-08-26 王涛 Cold autologous blood cardioplegia solution and preparation method and application thereof
CN104922059A (en) * 2015-05-21 2015-09-23 北京青藤谷禧干细胞科技研究院有限公司 Umbilical cord mesenchymal stem cell injection and preparation method and application thereof
WO2020122928A1 (en) * 2018-12-14 2020-06-18 National Taiwan University A stable cardioplegic solution for cardiac surgery

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
KANTATHUT NARONGRIT等: "Experience in the use of Del Nido cardioplegia in ramathibodi Hospital", 《JOURNAL OF THE MEDICAL ASSOCIATION OF THALIAND》 *
傅惟定等: "自行设计含血心脏停搏液灌注装置的应用和管理", 《中国体外循环杂志》 *
张开天等: "DelNido心脏停搏液的临床应用", 《中国体外循环杂志》 *
杨丽娜等: "应用Bentall手术治疗马凡氏综合征的体外循环管理策略", 《河北医学》 *
胡志斌等: "间断灌注保存对离体猪心冠状动脉保护效果的观察", 《心血管外科杂志(电子版)》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113975377A (en) * 2020-07-27 2022-01-28 成都青山利康药业有限公司 Cardioplegia solution
CN113975377B (en) * 2020-07-27 2023-11-10 成都青山利康药业股份有限公司 Cardioplegia solution

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