School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland.
Children's Health Ireland at Crumlin, Dublin 12, Ireland.
Eur J Pharm Biopharm. 2020 Jun;151:153-161. doi: 10.1016/j.ejpb.2020.04.008. Epub 2020 Apr 11.
Intravenous (IV) sildenafil, a phosphodiesterase type 5 inhibitor, is increasingly being used for the treatment of pulmonary hypertension (PH) in the paediatric population. Sildenafil (Revatio®) is approved for the treatment of pH in adults where it is administered as a bolus injection. However, in paediatrics it is used off-label and administered by continuous IV infusion. In the critically unwell child, limited IV access necessitates the administration of multiple IV infusions through a single IV lumen. The absence of compatibility data between sildenafil and other IV medications commonly used in this context necessitates the use of a dedicated IV line for sildenafil. The overall aim of this study was to establish the physical and chemical compatibility of sildenafil with commonly administered infusions in the paediatric and neonatal intensive care setting.
This study evaluated the chemical and physical compatibility of binary and multiple combinations (n = 42) of sildenafil with adrenaline, noradrenaline, milrinone, vasopressin and heparin. These were tested using three diluents (NaCl 0.9%w/v, Glucose 5%w/v, and Glucose 10%w/v) and two environmental conditions (room temperature and 37 °C) frequently encountered in paediatric or neonatal intensive care units. Prior to drug combination analysis, HPLC methods were developed and optimised to allow for the quantification of drugs in accordance with current pharmaceutical guidance. Binary and multiple drug mixtures of sildenafil were examined for physical and chemical compatibility to establish compatibility.
Of the drug combinations not containing heparin, all were deemed compatible with the exception of the five drug mix of Sildenafil 800 μg/mL, Milrinone 200 μg/mL, Vasopressin 0.4Units/mL, Noradrenaline 60 μg/mL, Adrenaline 60 μg/mL at 37 °C, in 10%w/v glucose. All binary or multi drug combinations containing heparin were deemed incompatible.
This research provides support and information to clinicians looking to co-administer sildenafil with other IV medicines thus removing the requirement to subject their patients to multiple intravenous cannula insertion points where IV access is restricted.
New evidence to support administration of sildenafil infusions in #PedsICU and #nicu- collaboration between @RCSIPharBioMol@FionaSOBrien1 and @OLCHCrumlin @RCSI_Irl @MoninneHowlett #CHI.
静脉内(IV)西地那非,一种磷酸二酯酶 5 抑制剂,越来越多地用于儿科人群的肺动脉高压(PH)的治疗。西地那非(Revatio®)被批准用于治疗成人的 pH 值,在那里它作为推注注射给药。然而,在儿科中,它是在标签外使用的,并通过连续 IV 输注给药。在病情严重的患儿中,有限的 IV 通路需要通过单个 IV 腔道给予多次 IV 输注。由于缺乏关于西地那非与在这种情况下常用的其他 IV 药物之间的相容性数据,因此需要为西地那非使用专用的 IV 线。本研究的总体目标是确定西地那非与儿科和新生儿重症监护环境中常用的输注物的物理和化学相容性。
本研究评估了西地那非与肾上腺素、去甲肾上腺素、米力农、血管加压素和肝素的二元和多元组合(n=42)的化学和物理相容性。这些组合分别使用三种稀释剂(0.9%w/v 的 NaCl、5%w/v 的葡萄糖和 10%w/v 的葡萄糖)和儿科或新生儿重症监护室中经常遇到的两种环境条件(室温(room temperature)和 37°C)进行测试。在进行药物组合分析之前,开发并优化了 HPLC 方法,以根据当前的药物指导原则允许对药物进行定量。检查了含有和不含有肝素的西地那非二元和多元药物混合物的物理和化学相容性,以确定相容性。
在不含肝素的药物组合中,除了在 37°C 下,在 10%w/v 葡萄糖中,含有 800μg/mL 西地那非、200μg/mL 米力农、0.4Units/mL 血管加压素、60μg/mL 去甲肾上腺素和 60μg/mL 肾上腺素的五药混合,所有其他药物组合均被认为是相容的。所有含有肝素的二元或多元药物组合均被认为是不相容的。
这项研究为希望与其他 IV 药物联合使用西地那非的临床医生提供了支持和信息,从而避免了在 IV 通路受限的情况下对患者进行多次静脉内插管的需要。
新证据支持在#儿科 ICU 和#新生儿 ICU 中给予西地那非输注-与@RCSIPharBioMol@FionaSOBrien1 和@OLCHCrumlin @RCSI_Irl @MoninneHowlett 的合作#CHI。