Safe Administration of Oral and Enteral Liquid Medicines

Total Page:16

File Type:pdf, Size:1020Kb

Safe Administration of Oral and Enteral Liquid Medicines 11/01/2018 A quick poll Hospital, community, industry or other Who liaises with dieticians? Who liaises with Trust procurement team? SAFE ADMINISTRATION OF ORAL AND ENTERAL LIQUID MEDICINES Surinder Ahuja , Medication Safety Officer I Formulary and Governance Pharmacist The Rotherham NHS Foundation Trust 23 November 2017 Group discussion Outline Four topics 1. Patients and enteral routes 1. What are the legal and practical implications of medicines use in these 2. Considerations and risks relating patients, medicines, patients? processes and management 2. What is the national guidance on this subject? 3. Pharmaceutical issues with administration 3. What factors contribute to medication errors? 4. Contribution of product design and devices to patient safety 4. What did the industry do to reduce risk of harm? 5. Identifying and reporting incidents 6. Factors contributing to medication errors 7. Never Events 8. Literature and resources Five Rights of Administration Patient types Right Patient Unable to swallow solid formulations Right Route Children Right Drug Too ill - critical care Right Dose Mental health Right Time Patients with swallowing disorders stroke impairment of oral structures (head and neck cancers) respiratory (COPD) neurological (Parkinson disease, multiple sclerosis) dementia 1 11/01/2018 Swallowing disorders - assessment Enteral routes Assessment by speech and language therapist (SALT) Nasogastric (NG) Nasojejunal (NJ) Recommendation may include: Percutaneous endoscopic Modified diet and fluids gastrostomy (PEG) Water protocol with oral diet Percutaneous endoscopic Nil-by-mouth and water protocol with no oral diet jejunostomy (PEJ) Percutaneous endoscopic gastro- jejunostomy (PEGJ) Enteral tubes Medicines - legal and practical issues Via nose – long, fine-bore tubes Feedback Via percutaneous – short, wide bore tubes Sterile water for use via jejunum Drug absorption Gastric motility Medicines - formulations Medicines - legal issues Standards tablets / capsules Medicines Act (1968): Sugar coated / film coated Prescribers are allowed to prescribe medicine outside their Dispersible /effervescent license: Buccal /sublingual unlicensed patient groups (off label) Chewable or Enteric coated medicines with no license (unlicensed) e.g. medicines with a non-EU license Modified release Prescribing liability rests with the prescriber. Cytotoxics May also rest with the administrator and supplier. Cytostatics eg finasteride, HRT 2 11/01/2018 Medicines use – outside license Pharmaceutical review Consider: Off label use of licensed medicines alternative licensed routes crush and dispersing from oral to rectal, transdermal, injections mixed with food alternative formulations Injections given oral or enteral route from modified release to standard release dose changes Use of unlicensed medicines when switching solid to liquid formulations eg digoxin, phenytoin Specials order liquid medicines timing of feeding and dosage eg phenytoin –stop feed for 2 hours before and after dose Need to consider legal responsibilities of healthcare professionals How to administer? Risks with administering liquid medicines For oral and enteral administration In a hospital setting Liquids dose measured in a syringe Tablets – crush and disperse in water administered parenteral (IV or subcutaneously) Capsules – opened and contents mixed Injections – give orally or enteral Must have safeguards to prevent wrong route administration Require dose changes eg phenytoin Information on handling Use reference sources What are the safeguards? National guidance National guidance Reducing harm from misplaced enteral tubes Promoting safer use of liquid medicines NPSA/NHS England/NHS Improvement: Patient Safety Alerts Feedback Reducing the harm caused by misplaced nasogastric feeding tubes (2005) Promoting safer measurement and administration of liquid medicines via oral and other enteral routes (2007) Problems swallowing? Resources for clients and carers (2007) Reducing the harm caused by misplaced nasogastric feeding tubes in adults, children and infants (2011) Placement devices for nasogastric tube insertion DO NOT replace initial position checks (2013) Nasogastric tube misplacement: continuing risk of death and severe harm (2016) DoH The Medicine Act Never Event List 2015-16 https://www.england.nhs.uk/wp-content/uploads/2015/03/never-evnts-list-15-16.pdf 3 11/01/2018 NPSA Alert 2007: 1 Design, supply and use of oral/enteral syringes 2 Design, supply and use of enteral feeding system only use labelled oral/enteral syringes that cannot be connected to enteral feeding systems should not contain ports that can be connected to intravenous catheters or ports to measure and administer oral liquid intravenous syringes or that have end connectors that can be connected to medicines intravenous or other parenteral lines do not use intravenous syringes to measure and administer oral liquid enteral feeding systems should be labelled to indicate the route of medicines administration make sure stocks of oral/enteral syringes are available in all clinical areas three-way taps and syringe tip adaptors should not be used in enteral that may need to measure and administer oral liquid medicines in a syringe feeding systems because connection design safeguards can be bypassed. when patients or carers need to administer oral liquid medicines with a syringe, supply them with oral or enteral syringes. 3 Organisational procedures, training and audit Poster (NPSA, 2007) medicines and enteral feeding policies and procedures should identify and manage the risk of administering oral liquid medicines by the wrong route these procedures should be part of the organisation’s training and competency assessment programmes annual medicines management audits should include a review of the measurement and administration of oral liquid medicines to ensure compliance with local policies and procedures. The role of industry The role of industry Feedback ISO standard 80369-3 ENFit feeding tubes connectors feeding tube adaptors for interim use enteral syringes bottle adaptors 4 11/01/2018 Learning culture Factor contributing to errors Identifying and reporting incidents Feedback Awareness of risk of harm Awareness of standards/processes/safeguards System for reporting Reporting and learning culture Factors contributing to errors Learning – National Patients Never Event List (2015-16) – Wrong route Individuals - healthcare professional The patient receives one of the following: Team Intravenous chemotherapy administered via the intrathecal route Task Oral/enteral medication or feed/flush administered by any parenteral Communication route Training and education Intravenous administration of a medicine intended to be administered via Equipment the epidural route Environment Organisation Local National A case of two Never Events Trust actions A deep dive into wrong route errors Declared as Never Events Trustwide audit using NPSA Checklist Identified two wrong route incidents Oramorph prescribed Trustwide training - Stop the Shift measured for oral administration (with IV syringe) Training of new staff administered subcutaneously Role out of ENFit syringes at the same time Informed Chief Pharmacist, Revision of SOP (Medicines Policy) Chief Nurse, Medication Safety Group, Patients Safety Group, CCG, CQC Nutrition Policy – section on medicine administration Declared as Never Events Report of the actions taken Investigations Audit of checklist (Pre- registration pharmacist) 5 11/01/2018 Learning from incidents Summary Factors Actions taken Patient Swallowing difficulties, enteral tubes and feeds, ongoing care Patient types Types of enteral tubes Individuals Awareness of risks and harm and take appropriate actions Risk of patient harm National Reporting system, Patient Safety Alerts, Never Events Risks of medicines use in these patients Medicine Act 1968 Pharmaceutical issues Organisational Local SOPs, procurement, audits, reporting and learning culture, medicines information Product design Equipment Availability of oral and ENFit syringes, adaptors Incident reporting and learning and contributing factors ENFit giving sets, ports, connectors National guidance Literatures sources Training & education Competencies, ongoing Task Prescribing, administration, dispensing, medicine information Global Setting standards, industry product design Literature and resources Medicine Act 1968 Never Event List 2015-16 Thank you NPSA/NHS England/NHS Improvement: Reducing the harm caused by misplaced nasogastric feeding tubes (2005) Promoting safer measurement and administration of liquid medicines via oral and other enteral routes (2007) Problems swallowing? Resources for clients and carers (2007) Any questions Reducing the harm caused by misplaced nasogastric feeding tubes in adults, children and infants (2011) Nasogastric tube misplacement: continuing risk of death and severe harm (2016) Medicines: Barnett N and Parmar P. Tailoring medication formulations for patients with dysphagia PJ 2016) Smyth J. The NEWT guideline for administration of medication to patients with enteral feeding tubes or swallowing difficulties (3rd edition) Online access White R and Bradham V Handbook of drug administration via enteral feeding tubes ( Summary of product characteristics Incident reporting and learning: Seven Steps to patient safety (NPSA 2004) Yorkshire contributory factors framework (2012) http://qualitysafety.bmj.com/content/qhc/early/2012/03/14/bmjqs-2011-000443.full.pdf 6.
Recommended publications
  • (12) United States Patent (10) Patent No.: US 6,515,007 B2 Murad (45) Date of Patent: Feb
    USOO6515007B2 (12) United States Patent (10) Patent No.: US 6,515,007 B2 Murad (45) Date of Patent: Feb. 4, 2003 (54) METHODS FOR MANAGING SCALP OTHER PUBLICATIONS CONDITIONS WPIDS AN 1997-389337, JP 09 169638 A, Jun. 30, 1997, (76) Inventor: Howard Murad, 4265 Marina City Dr., bstract.* Penthouse 11, Marina del Rey, CA (US) MEDLINE 79172521, Orfanos et al, Hautarzt, Mar. 1979, 90292 30(3), 124–33, abstract.* * cited by examiner (*) Notice: patentSubject is to extended any disclaimer, or adjusted the term under of this 35 Primary Examiner Rebecca Cook U.S.C. 154(b) by 0 days. (74) Attorney, Agent, or Firm-Pennie & Edmonds LLP (57) ABSTRACT (21) Appl. No.: 09/920,729 ThisS applicationCO relatesCLCSO to a ph CCUCtical compositionCOOOSOO f (22) Filed: Aug. 3, 2001 the prevention, treatment, and management of Scalp O O conditions, Such as dandruff, Seborrheic dermatitis, (65) Prior Publication Data pSoriasis, folliculitis, and hair thinning including a thera US 2002/0009423 A1 Jan. 24, 2002 peutically effective amount of an acidic component of a hydroxyacid or tannic acid, or a pharmaceutically acceptable Related U.S. Application Data Salt thereof. A preferred anti-dandruff composition and - - - method of managing dandruff includes a therapeutically (62) Pisie of Epitol N: SE filed R Aug. 5. effective amount of the acid component, a vitamin A application, now Nolog23,484Pat. No. O.Z f 1,240,filedonii. which 27, is 1998,a division now Pat o OPO and an anti-growthi- agent. A preferred anti-hairi-hai No. 6,207,694. thinning composition and method of managing thinning hair 7 includes a therapeutically effective amount of the acidic (51) Int.
    [Show full text]
  • An Overview On: Sublingual Route for Systemic Drug Delivery
    International Journal of Research in Pharmaceutical and Biomedical Sciences ISSN: 2229-3701 __________________________________________Review Article An Overview on: Sublingual Route for Systemic Drug Delivery K. Patel Nibha1 and SS. Pancholi2* 1Department of Pharmaceutics, BITS Institute of Pharmacy, Gujarat Technological university, Varnama, Vadodara, Gujarat, India 2BITS Institute of Pharmacy, Gujarat Technological University, Varnama, Vadodara, Gujarat, India. __________________________________________________________________________________ ABSTRACT Oral mucosal drug delivery is an alternative and promising method of systemic drug delivery which offers several advantages. Sublingual literally meaning is ''under the tongue'', administrating substance via mouth in such a way that the substance is rapidly absorbed via blood vessels under tongue. Sublingual route offers advantages such as bypasses hepatic first pass metabolic process which gives better bioavailability, rapid onset of action, patient compliance , self-medicated. Dysphagia (difficulty in swallowing) is common among in all ages of people and more in pediatric, geriatric, psychiatric patients. In terms of permeability, sublingual area of oral cavity is more permeable than buccal area which is in turn is more permeable than palatal area. Different techniques are used to formulate the sublingual dosage forms. Sublingual drug administration is applied in field of cardiovascular drugs, steroids, enzymes and some barbiturates. This review highlights advantages, disadvantages, different sublingual formulation such as tablets and films, evaluation. Key Words: Sublingual delivery, techniques, improved bioavailability, evaluation. INTRODUCTION and direct access to systemic circulation, the oral Drugs have been applied to the mucosa for topical mucosal route is suitable for drugs, which are application for many years. However, recently susceptible to acid hydrolysis in the stomach or there has been interest in exploiting the oral cavity which are extensively metabolized in the liver.
    [Show full text]
  • Chapter 1 Controlling Drug Delivery
    chapter 1 Controlling drug delivery Overview In this chapter we will: & differentiate drug delivery systems according to their physical state & differentiate drug delivery systems according to their route of administration & differentiate drug delivery systems according to their type of drug release & discuss drug transport across epithelial barriers. Introduction KeyPoints & Continued developments in Pharmacotherapy can be defined as the treatment chemistry, molecular biology and prevention of illness and disease by means of and genomics support the drugs of chemical or biological origin. It ranks discovery and developments among the most important methods of medical of new drugs and new drug treatment, together with surgery, physical targets. & treatment, radiation and psychotherapy. There The drug delivery system are many success stories concerning the use of employed can control the pharmacological action of a drugs and vaccines in the treatment, prevention drug, influencing its and in some cases even eradication of diseases pharmacokinetic and (e.g. smallpox, which is currently the only subsequent therapeutic human infectious disease completely profile. eradicated). Although it is almost impossible to estimate the exact extent of the impact of pharmacotherapy on human health, there can be no doubt that pharmacotherapy, together with improved sanitation, better diet and better housing, has improved people’s health, life expectancy and quality of life. Tip Unprecedented developments in genomics Combinatorial chemistry is a way to and molecular biology today offer a plethora of build a variety of structurally related new drug targets. The use of modern chemical drug compounds rapidly and synthetic methods (such as combinatorial systematically. These are assembled chemistry) enables the syntheses of a large from a range of molecular entities number of new drug candidates in shorter times which are put together in different ‘ ’ than ever before.
    [Show full text]
  • Delivery of Orally Administered Digestible Antibodies Using Nanoparticles
    International Journal of Molecular Sciences Review Delivery of Orally Administered Digestible Antibodies Using Nanoparticles Toshihiko Tashima Tashima Laboratories of Arts and Sciences, 1239-5 Toriyama-cho, Kohoku-ku, Yokohama, Kanagawa 222-0035, Japan; [email protected] Abstract: Oral administration of medications is highly preferred in healthcare owing to its simplicity and convenience; however, problems of drug membrane permeability can arise with any administra- tion method in drug discovery and development. In particular, commonly used monoclonal antibody (mAb) drugs are directly injected through intravenous or subcutaneous routes across physical barri- ers such as the cell membrane, including the epithelium and endothelium. However, intravenous administration has disadvantages such as pain, discomfort, and stress. Oral administration is an ideal route for mAbs. Nonetheless, proteolysis and denaturation, in addition to membrane impermeability, pose serious challenges in delivering peroral mAbs to the systemic circulation, biologically, through enzymatic and acidic blocks and, physically, through the small intestinal epithelium barrier. A num- ber of clinical trials have been performed using oral mAbs for the local treatment of gastrointestinal diseases, some of which have adopted capsules or tablets as formulations. Surprisingly, no oral mAbs have been approved clinically. An enteric nanodelivery system can protect cargos from proteolysis and denaturation. Moreover, mAb cargos released in the small intestine may be delivered to the systemic circulation across the intestinal epithelium through receptor-mediated transcytosis. Oral Abs in milk are transported by neonatal Fc receptors to the systemic circulation in neonates. Thus, well-designed approaches can establish oral mAb delivery. In this review, I will introduce the imple- mentation and possibility of delivering orally administered mAbs with or without nanoparticles not Citation: Tashima, T.
    [Show full text]
  • Soft Gelatin Capsules)
    ERGOCALCIFEROL- ergocalciferol capsule Blenheim Pharmacal, Inc. ---------- VITAMIN D, ERGOCALCIFEROL Capsules, USP, 1.25 mg SOFTGEL CAPSULES (Soft Gelatin Capsules) (50,000 USP Units) Rx Only DESCRIPTION Ergocalciferol Capsules, USP is a synthetic calcium regulator for oral administration. Ergocalciferol is a white, colorless crystal, insoluble in water, soluble in organic solvents, and slightly soluble in vegetable oils. It is affected by air and by light. Ergosterol or provitamin D 2 is found in plants and yeast and has no antirachitic activity. There are more than 10 substances belonging to a group of steroid compounds, classified as having vitamin D or antirachitic activity. One USP Unit of vitamin D 2 is equivalent to one International Unit (IU), and 1 mcg of vitamin D 2 is equal to 40 IU. Each softgel capsule, for oral administration, contains Ergocalciferol, USP 1.25 mg (equivalent to 50,000 USP units of Vitamin D), in an edible vegetable oil. Ergocalciferol, also called vitamin D 2 ,is 9, 10-secoergosta-5, 7,10(19),22-tetraen-3-ol,(3β,5 Z,7 E,22 E)-; (C 28H 44O) with a molecular weight of 396.65, and has the following structural formula: Inactive Ingredients: D&C Yellow #10, FD&C Blue #1, Gelatin, Glycerin, Purified Water, Refined Soybean Oil. CLINICAL PHARMACOLOGY The in vivo synthesis of the major biologically active metabolites of vitamin D occurs in two steps. The first hydroxylation of ergocalciferol takes place in the liver (to 25-hydroxyvitamin D) and the second in the kidneys (to 1,25-dihydroxy- vitamin D). Vitamin D metabolites promote the active absorption of calcium and phosphorus by the small intestine, thus elevating serum calcium and phosphate levels sufficiently to permit bone mineralization.
    [Show full text]
  • Drug Administration
    Chapter 3: Drug Administration 2 Contact Hours By: Katie Ingersoll, RPh, PharmD Author Disclosure: Katie Ingersoll and Elite do not have any actual or Questions regarding statements of credit and other customer service potential conflicts of interest in relation to this lesson. issues should be directed to 1-888-666-9053. This lesson is $12.00. Universal Activity Number (UAN): 0761-9999-17-079-H01-P Educational Review Systems is accredited by the Activity Type: Knowledge-based Accreditation Council of Pharmacy Education (ACPE) Initial Release Date: April 1, 2017 as a provider of continuing pharmaceutical education. Expiration Date: April 1, 2019 This program is approved for 2 hours (0.2 CEUs) of Target Audience: Pharmacists in a community-based setting. continuing pharmacy education credit. Proof of participation will be posted to your NABP CPE profile within 4 to 6 To Obtain Credit: A minimum test score of 70 percent is needed weeks to participants who have successfully completed the post-test. to obtain a credit. Please submit your answers either by mail, fax, or Participants must participate in the entire presentation and complete online at Pharmacy.EliteCME.com. the course evaluation to receive continuing pharmacy education credit. Learning objectives After completion of this course, healthcare professionals will be able Discuss the administration of medications in patients using enteral to: and parenteral nutrition. Describe the eight rights of medication administration. Discuss special considerations for administering medications in Explain the administration of enteral and parenteral medications. pediatric and geriatric patients. Introduction Medication errors that occur at the point of drug administration poised to reduce the frequency of medication administration errors.
    [Show full text]
  • A Survey of Cannabis Consumption and Implications of an Experimental Policy Manipulation Among Young Adults
    Virginia Commonwealth University VCU Scholars Compass Theses and Dissertations Graduate School 2018 A SURVEY OF CANNABIS CONSUMPTION AND IMPLICATIONS OF AN EXPERIMENTAL POLICY MANIPULATION AMONG YOUNG ADULTS Alyssa K. Rudy Virginia Commonwealth University Follow this and additional works at: https://scholarscompass.vcu.edu/etd © The Author Downloaded from https://scholarscompass.vcu.edu/etd/5297 This Thesis is brought to you for free and open access by the Graduate School at VCU Scholars Compass. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of VCU Scholars Compass. For more information, please contact [email protected]. A SURVEY OF CANNABIS CONSUMPTION AND IMPLICATIONS OF AN EXPERIMENTAL POLICY MANIPULATION AMONG YOUNG ADULTS A thesis proposal submitted in partial fulfillment of the requirements for the degree of Master of Science at Virginia Commonwealth University. by Alyssa Rudy B.S., University of Wisconsin - Whitewater, 2014 Director: Dr. Caroline Cobb Assistant Professor Department of Psychology Virginia Commonwealth University Richmond, Virginia January, 2018 ii Acknowledgement I would like to first acknowledge Dr. Caroline Cobb for your guidance and support on this project. Thank you for allowing me to explore my passions. I am thankful for your willingness to jump into an unfamiliar area of research with me, and thank you for constantly pushing me to be a better writer, researcher, and person. I would also like to acknowledge the other members of my thesis committee, Drs. Eric Benotsch and Andrew Barnes for their support and expertise on this project. I would also like to thank my family for always supporting my desire to pursue my educational and personal goals.
    [Show full text]
  • Oral Films: a Comprehensive Review
    Mahboob et al., International Current Pharmaceutical Journal, November 2016, 5(12): 111-117 International Current http://www.icpjonline.com/documents/Vol5Issue12/03.pdf Pharmaceutical Journal REVIEW ARTICLE OPEN ACCESS Oral Films: A Comprehensive Review *Muhammad Bilal Hassan Mahboob1,2, Tehseen Riaz1,2, Muhammad Jamshaid1, Irfan Bashir1,2 and Saqiba Zulfiqar1,2,3 1Faculty of Pharmacy, University of Central Punjab Lahore, Pakistan 2Foundation for Young Researchers, Pakistan 3Shoukat Khanum Memorial Cancer Hospital & Research Centre, Lahore, Pakistan ABSTRACT In the late 1970s, rapid disintegrating drug delivery system was developed as an alternative to capsules, tablets and syrups for geriatric and pediatric patients having problems in swallowing. To overcome the need, number of orally disintegrating tablets which disinte- grate within one minute in mouth without chewing or drinking water were commercialized. Then later, oral drug delivery technology had been improved from conventional dosage form to modified release dosage form and developed recently rapid disintegrating films rather than oral disintegrating tablets. Oral disintegrating film or strips containing water dissolving polymer retain the dosage form to be quickly hydrated by saliva, adhere to mucosa, and disintegrate within a few seconds, dissolve and releases medication for oro- mucosal absorption when placed in mouth. Oral film technology is the alternative route with first pass metabolism. This review give a comprehensive detail of materials used in ODF, manufacturing process, evaluation tests and marketed products. Key Words: Oral disintegrating film, oral strip, pediatric and geriatric patients. INTRODUCTIONINTRODUCTION An oral film or strips are manufactured as a large Oral administration is the most preferred route due to re- sheet and then cut into individual dosage unit for packag- lieve of ingestion, pain reduction, to accommodate various ing (Desai et al., 2012).
    [Show full text]
  • An Update on Pharmaceutical Strategies for Oral Delivery of Therapeutic Peptides and Proteins in Adults and Pediatrics
    children Review An Update on Pharmaceutical Strategies for Oral Delivery of Therapeutic Peptides and Proteins in Adults and Pediatrics Nirnoy Dan, Kamalika Samanta and Hassan Almoazen * Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA; [email protected] (N.D.); [email protected] (K.S.) * Correspondence: [email protected]; Tel.: +1-(901)-448-2239 Received: 28 October 2020; Accepted: 16 December 2020; Published: 19 December 2020 Abstract: While each route of therapeutic drug delivery has its own advantages and limitations, oral delivery is often favored because it offers convenient painless administration, sustained delivery, prolonged shelf life, and often lower manufacturing cost. Its limitations include mucus and epithelial cell barriers in the gastrointestinal (GI) tract that can block access of larger molecules including Therapeutic protein or peptide-based drugs (TPPs), resulting in reduced bioavailability. This review describes these barriers and discusses different strategies used to modify TPPs to enhance their oral bioavailability and/or to increase their absorption. Some seek to stabilize the TTPs to prevent their degradation by proteolytic enzymes in the GI tract by administering them together with protease inhibitors, while others modify TPPs with mucoadhesive polymers like polyethylene glycol (PEG) to allow them to interact with the mucus layer, thereby delaying their clearance. The further barrier provided by the epithelial cell membrane can be overcome by the addition of a cell-penetrating peptide (CPP) and the use of a carrier molecule such as a liposome, microsphere, or nanosphere to transport the TPP-CPP chimera. Enteric coatings have also been used to help TPPs reach the small intestine.
    [Show full text]
  • A Focus Group Study About Oral Drug Administration Practices at Hospital Wards—Aspects to Consider in Drug Development of Age-Appropriate Formulations for Children
    pharmaceutics Article A Focus Group Study about Oral Drug Administration Practices at Hospital Wards—Aspects to Consider in Drug Development of Age-Appropriate Formulations for Children Maria Rautamo 1,2,3,*, Kirsi Kvarnström 1,2, Mia Sivén 2 , Marja Airaksinen 2, Pekka Lahdenne 4 and Niklas Sandler 3 1 HUS Pharmacy, HUS Helsinki University Hospital, Stenbäckinkatu 9B, 00290 Helsinki, Finland; kirsi.kvarnstrom@hus.fi 2 Faculty of Pharmacy, University of Helsinki, Viikinkaari 5E, University of Helsinki, 00014 Helsinki, Finland; mia.siven@helsinki.fi (M.S.); marja.airaksinen@helsinki.fi (M.A.) 3 Pharmaceutical Sciences Laboratory, Åbo Akademi University, Tykistökatu 6A, 20520 Turku, Finland; [email protected] 4 Department of Children and Adolescents, HUS Helsinki University Hospital, Stenbäckinkatu 9, 00029 Helsinki, Finland; pekka.lahdenne@hus.fi * Correspondence: maria.rautamo@helsinki.fi or maria.rautamo@hus.fi Received: 11 January 2020; Accepted: 27 January 2020; Published: 30 January 2020 Abstract: Oral drug administration to pediatric patients is characterized by a lack of age-appropriate drug products and the off-label use of medicines. However, drug administration practices at hospital wards is a scarcely studied subject. The aim of this study was to explore the oral drug administration practices at pediatric hospital wards, with a focus on experiences and challenges faced, methods used to mitigate existing problems, drug manipulation habits, perceptions about oral dosage forms and future needs of oral dosage forms for children. This was a qualitative study consisting of focus group discussions with physicians, nurses and clinical pharmacists in a tertiary university hospital with the objective of bringing forward a holistic view on this research topic.
    [Show full text]
  • Challenges of Dissolution Methods Development for Soft Gelatin Capsules
    pharmaceutics Review Challenges of Dissolution Methods Development for Soft Gelatin Capsules Festo Damian 1, Mohammad Harati 2, Jeff Schwartzenhauer 3, Owen Van Cauwenberghe 1,4 and Shawn D. Wettig 1,5,* 1 School of Pharmacy, University of Waterloo, 200 University Ave W, Waterloo, ON N2L 3G1, Canada; [email protected] (F.D.); [email protected] (O.V.C.) 2 Department of Natural Sciences, University of Michigan, 2209 Natural Sciences Building, 4901 Evergreen Rd, Dearborn, MI 48128, USA; [email protected] 3 Catalent Pharma Solutions, 2125 Ambassador Dr, Windsor, ON N9C 3R5, Canada; [email protected] 4 Bio Therapeutic Molecules Inc., 70 Southgate Drive, Unit 4, Guelph, ON N1G 4P5, Canada 5 Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Ave W, Waterloo, ON N2L 3G1, Canada * Correspondence: [email protected]; Tel.: +1-519-888-4567 (ext. 42221) Abstract: Recently, the development of soft gelatin capsules (SGCs) dosage forms has attracted a great deal of interest in the oral delivery of poorly water-soluble drugs. This is attributed to the increased number of poorly soluble drugs in the pipeline, and hence the challenges of finding innovative ways of developing bioavailable and stable dosage forms. Encapsulation of these drugs into SGCs is one of the approaches that is utilized to deliver the active ingredients to the systemic circulation to overcome certain formulation hurdles. Once formulated, encapsulated drugs in the form of SGCs require suitable in vitro dissolution test methods to ensure drug product quality and Citation: Damian, F.; Harati, M.; Schwartzenhauer, J.; Van performance. This review focuses on challenges facing dissolution test method development for Cauwenberghe, O.; Wettig, S.D.
    [Show full text]
  • Accuracy of Enteral Syringes with Commonly Prescribed Paediatric
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by UCL Discovery Accuracy of enteral syringes with commonly prescribed paediatric oral liquid medicines Arenas-Lopez S, Gurung K, Tibby SM, Calleja-Hernandez MA, Tuleu C Sara Arenas-López, Consultant Pharmacist Paediatric Critical Care, Evelina London Children’s Hospital, Guy’s & St Thomas NHS Foundation Trust, Westminster Bridge Road, London SE1 7EH Tel: +442071885049 Email: [email protected] Karuna Gurung, MRPharm Student, UCL School of Pharmacy, London, United Kingdom Shane M Tibby, PICU Consultant, Evelina London Children’s Hospital, London SE1 7EH Email: [email protected] Miguel-Angel Calleja-Hernández, Director Pharmacy Service, Hospital Universitario Virgen de las Nieves and Professor at University of Granada, Spain. Email: [email protected] Catherine Tuleu (Corresponding author), Reader in Pharmaceutics, UCL School of Pharmacy, London, United Kingdom [email protected] Keywords: Accuracy-volume-enteral-syringes-liquid-paediatrics-device Word count – Original article: 2482 1 ABSTRACT (273 Words) Aim: To investigate the paediatric volumetric accuracy for two enteral syringe brands, using commercially available liquid drug formulations, across a range of clinically relevant volumes and physicochemical properties. Method: In vitro experiment under laboratory conditions. Ten drug formulations were tested for two syringe brands (Baxa, Medicina) using a range of formulation volumes (0.05 to 5 mL) and syringe sizes (1 to 5 mL). The weight of syringes, empty, filled and after expelling liquids were accurately measured and converted into volume, based on the known formulation densities. Ten replications were performed for each combination of drug, syringe and volume.
    [Show full text]