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Journal articles on the topic 'Intravenous Infusion of Helixor®'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Yong-Il, Ji. "INTRAVENOUS APPLICATION OF HELIXOR® IN GYNECOLOGICAL ONCOLOGY: IS IT SAFE?" International Journal of Research - Granthaalayah 5, no. 10 (2017): 307–12. https://doi.org/10.5281/zenodo.1043407.

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<strong>Background:</strong> Traditional mistletoe (Viscum album L.) therapy has been frequently used in patients with cancer in Europe. The different mistletoe formulations available for oncological use are Iscador®, Iscucin®, AbnovaViscum®, and Lektinol®, as well as Helixor®, which may improve therapeutic outcomes following intravenous (i.v.) administration and therefore, is becoming more commonly used. <strong>Method:</strong> I conducted an observational study in four different University Hospital Centers and the frequency of adverse drug reactions (ADRs) induced by the i.v. infusion of He

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Ji, Yong-Il. "INTRAVENOUS APPLICATION OF HELIXOR® IN GYNECOLOGICAL ONCOLOGY: IS IT SAFE?" International Journal of Research -GRANTHAALAYAH 5, no. 10 (2017): 307–12. http://dx.doi.org/10.29121/granthaalayah.v5.i10.2017.2306.

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Background: Traditional mistletoe (Viscum album L.) therapy has been frequently used in patients with cancer in Europe. The different mistletoe formulations available for oncological use are Iscador®, Iscucin®, AbnovaViscum®, and Lektinol®, as well as Helixor®, which may improve therapeutic outcomes following intravenous (i.v.) administration and therefore, is becoming more commonly used. Method: I conducted an observational study in four different University Hospital Centers and the frequency of adverse drug reactions (ADRs) induced by the i.v. infusion of Helixor® was determined.

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Lederer, Ann-Kathrin, Sabine Rieger, Michael Schink, and Roman Huber. "Pharmakokinetics of Mistletoe Lectins after Intravenous Application of a Mistletoe Product in Healthy Subjects." Pharmaceuticals 17, no. 3 (2024): 278. http://dx.doi.org/10.3390/ph17030278.

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Mistletoe lectins (ML) have cytotoxic and immunomodulating properties, and subcutaneously applied mistletoe products (MP) containing ML have approval for supportive cancer treatment. MP are also given off-label intravenously, but data about pharmacokinetics are widely lacking. Therefore, the aim of our phase I trial was to evaluate the pharmacokinetics and safety of intravenously applied natural ML. Initially, 12 healthy male volunteers were planned to receive a single infusion of 2000 mg Helixor® P. We had to terminate the study prematurely after the inclusion of eight subjects due to elevati

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Steele, Megan L., Jan Axtner, Antje Happe, Matthias Kröz, Harald Matthes, and Friedemann Schad. "Safety of Intravenous Application of Mistletoe (Viscum albumL.) Preparations in Oncology: An Observational Study." Evidence-Based Complementary and Alternative Medicine 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/236310.

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Background. Traditional mistletoe therapy in cancer patients involves subcutaneous applications ofViscum albumL. preparations, with doses slowly increasing based on patient responses. Intravenous infusion of high doses may improve therapeutic outcomes and is becoming more common. Little is known about the safety of this “off-label” application of mistletoe.Methods. An observational study was performed within the Network Oncology. Treatment with intravenous mistletoe applications is described. The frequency of adverse drug reactions (ADRs) to intravenous mistletoe applications was calculated an

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Paller, Channing J., Lin Wang, Wei Fu, et al. "Abstract 1600: Phase I trial of intravenous mistletoe extract in advanced cancer." Cancer Research 83, no. 7_Supplement (2023): 1600. http://dx.doi.org/10.1158/1538-7445.am2023-1600.

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Abstract Purpose: Mistletoe extract is widely used in cancer patients to support therapy and to improve quality of life (QoL). However, its use is controversial due to suboptimal trials and a lack of data supporting its intravenous administration. Patients and Methods: This phase I trial of intravenous Mistletoe (Helixor M) aimed to determine the recommended phase 2 dosing and to evaluate safety. Solid tumor patients progressing on at least one line of chemotherapy received escalating doses of Helixor M three times a week. Assessments were also made of tumor marker kinetics and QoL. Results: T

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Nahata, Milap C. "Intravenous Infusion Conditions." Clinical Pharmacokinetics 24, no. 3 (1993): 221–29. http://dx.doi.org/10.2165/00003088-199324030-00004.

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7

Leggett, Annie. "Intravenous infusion pumps." Nursing Standard 4, no. 28 (1990): 24–26. http://dx.doi.org/10.7748/ns.4.28.24.s37.

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8

Luke, Julia, and Janice Middleton. "Intravenous infusion controllers." Nursing Standard 4, no. 29 (1990): 30–32. http://dx.doi.org/10.7748/ns.4.29.30.s33.

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9

Soto, G., M. Naranjo González, and F. Calero. "Intravenous lidocaine infusion." Revista Española de Anestesiología y Reanimación (English Edition) 65, no. 5 (2018): 269–74. http://dx.doi.org/10.1016/j.redare.2018.01.015.

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10

Holzman, Robert S. "Intravenous Infusion Equipment." International Anesthesiology Clinics 30, no. 3 (1992): 35–50. http://dx.doi.org/10.1097/00004311-199230030-00003.

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Holzman, Robert S. "Intravenous Infusion Equipment." International Anesthesiology Clinics 30, no. 4 (1992): 35–50. http://dx.doi.org/10.1097/00004311-199230040-00004.

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12

Winstanley, Peter, Kim Hammond, and Tracy Elton. "Intravenous cannulation, intravenous infusion and prescription of intravenous fluids." Foundation Years 5 (January 2009): 17–19. http://dx.doi.org/10.1016/j.mpfou.2008.08.005.

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13

Liang, Weihang, and Xuefei Jia. "Research on the Causes and Nursing Interventions of Extravasation During Intravenous Infusion." Journal of Clinical and Nursing Research 8, no. 8 (2024): 46–51. http://dx.doi.org/10.26689/jcnr.v8i8.7165.

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Intravenous infusion, a common clinical drug treatment method, is widely used in the treatment of various diseases. Due to the invasive nature of puncture during intravenous infusion, patients may inevitably experience resistance and tension when facing nursing staff performing infusion procedures. Additionally, the complexity of the nursing staff’s work and the impact of the infusion therapy environment can exacerbate the tension between nurses and patients, leading to risks such as drug leakage and needlestick injuries. This article focuses on the factors influencing extravasation during int

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Kononov, Anatoly, Earl Z. Browne, Frederick Alexander, and Stacy Porvasnik. "Continuous rat intravenous infusion." Microsurgery 15, no. 6 (1994): 443–45. http://dx.doi.org/10.1002/micr.1920150615.

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15

Hrez Ali Al-Sudani, Basim, and Sahar Swadi Raheem. "Postoperative ketamine infusion in comparison with tramadol infusion for postoperative pain relief." AL-QADISIYAH MEDICAL JOURNAL 11, no. 19 (2017): 71–77. http://dx.doi.org/10.28922/qmj.2015.11.19.71-77.

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Background:Systemic narcotics commonly used for postoperative analgesia are associated with many side effects.Many studies regarding the best postoperative analgesic regimen with minimum side effects have been done over the last 20 years.In this study we compare between the postoperative intravenous infusion of tramadol with the postoperative intravenous infusion of ketamine .Method : This stidy was carried out on 120 parturients prepared for an elective caeserian section under general anaesthesia . All patients subjects according to American Society Of Anaesthesiologist ( ASA) classification

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Kurniatie, Menik Dwi. "ANALISIS FAKTOR KEJADIAN PHLEBITIS DENGAN SIMULASI MODEL FISIS ALAT TERAPI INTRAVENA." Jurnal SainHealth 3, no. 1 (2019): 21. http://dx.doi.org/10.51804/jsh.v3i1.336.21-29.

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Intravenous therapy through long-term infusion is at risk for complications such as phlebitis. The influence of medical factors with a history of hypertension and mechanical factors based on the location of the position of infusion is the main study of the causes of phlebitis.One of the causes of phlebitis is the flow of intravenous fluids which is not proportional to the volume of infusion fluid. Intravenous Therapy Devices with the aim of assessing the physical phenomena modeling experiments intravenous therapy with the theory of fluid mechanics and prove the existence of linkage patient's b

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17

Preedy, V. R., and P. J. Garlick. "The response of muscle protein synthesis to nutrient intake in postabsorptive rats: The role of insulin and amino acids." Bioscience Reports 6, no. 2 (1986): 177–83. http://dx.doi.org/10.1007/bf01115004.

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In 12 h fasted rats, rates of muscle protein synthesis were stimulated by refeeding for 1 h and by intragastric or intravenous infusion of an amino acid plus glucose mixture for 1 hr, but not by intravenous infusion of amino acids alone for 1 h. Intravenous injection of anti-insulin serum suppressed the response to feeding and to intragastric infusion, but not to intravenous infusion. It is concluded that the response of muscle protein synthesis to food intake is mediated by both insulin and amino acids acting in concert.

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18

Oros, Dragana, Marko Penčić, Jovan Šulc, et al. "Smart Intravenous Infusion Dosing System." Applied Sciences 11, no. 2 (2021): 513. http://dx.doi.org/10.3390/app11020513.

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Intravenous (IV) infusion therapy allows the infusion fluid to be inserted directly into the patient’s vein. It is used to place medications directly into the bloodstream or for blood transfusions. The probability that a hospitalized patient will receive some kind of infusion therapy, intravenously, is 60–80%. The paper presents a smart IV infusion dosing system for detection, signaling, and monitoring of liquid in an IV bottle at a remote location. It consists of (i) the sensing and computation layer—a system for detection and signaling of fluid levels in the IV bottle and a system for regula

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19

Felker, Evgeny Y., Maxim S. Fataliev, Andrey O. Kolosov, et al. "Intravenous lidocaine infusion in children." Regional Anesthesia and Acute Pain Management 16, no. 2 (2022): 129–38. http://dx.doi.org/10.17816/1993-6508-2022-16-1-129-138.

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BACKGROUND: The problem of adequate analgesia in the early postoperative period is not relevant at present, both in our country and abroad because 50% of children experience pain after surgical interventions despite the ongoing therapy. Inadequate ideal method for assessing the pain syndrome severity, age restrictions with several drugs, and difficult communication with young children, as well as drug selection, lead to inadequate detection in pediatric practice. AIM: This study aimed to evaluate the effectiveness and safety of intravenous infusion of lidocaine in the early postoperative

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20

Ng, S. K. B. "Intravenous immunoglobulin infusion causing pseudohyponatremia." Lupus 8, no. 6 (1999): 488–90. http://dx.doi.org/10.1177/096120339900800617.

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21

Coetzee, Johan F. "Principles of intravenous drug infusion." Anaesthesia & Intensive Care Medicine 6, no. 4 (2005): 141–44. http://dx.doi.org/10.1383/anes.6.4.141.63629.

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22

Nordell, K., L. Mogensen, O. Nyquist, and E. Orinius. "THROMBOPHLEBITIS FOLLOWING INTRAVENOUS LIGNOCAINE INFUSION." Acta Medica Scandinavica 192, no. 1-6 (2009): 263–65. http://dx.doi.org/10.1111/j.0954-6820.1972.tb04813.x.

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23

Mofenson, Howard C., and Thomas R. Caraccio. "Continuous infusion of intravenous naloxone." Annals of Emergency Medicine 16, no. 3 (1987): 374–75. http://dx.doi.org/10.1016/s0196-0644(87)80212-3.

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Mofenson, Howard C., and Thomas R. Caraccio. "Continuous infusion of intravenous naloxone." Annals of Emergency Medicine 16, no. 5 (1987): 600. http://dx.doi.org/10.1016/s0196-0644(87)80713-8.

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25

Coetzee, Johan F. "Principles of intravenous drug infusion." Anaesthesia & Intensive Care Medicine 13, no. 5 (2012): 243–46. http://dx.doi.org/10.1016/j.mpaic.2012.02.011.

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Coetzee, Johan F. "Principles of intravenous drug infusion." Anaesthesia & Intensive Care Medicine 16, no. 12 (2015): 647–50. http://dx.doi.org/10.1016/j.mpaic.2015.09.003.

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27

Chambers, David J. "Principles of intravenous drug infusion." Anaesthesia & Intensive Care Medicine 20, no. 1 (2019): 61–64. http://dx.doi.org/10.1016/j.mpaic.2018.11.005.

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28

Wilkins, Robert G., and Martin Unverdorben. "Accidental Intravenous Infusion of Air." Journal of Infusion Nursing 35, no. 6 (2012): 404–8. http://dx.doi.org/10.1097/nan.0b013e31827079fe.

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29

Cowan, J. C., D. W. Holt, R. S. Bexton, and D. S. Reid. "Flecainide ? an intravenous infusion regimen." European Journal of Clinical Pharmacology 32, no. 2 (1987): 195–98. http://dx.doi.org/10.1007/bf00542195.

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30

Jacobs, James R. "Intravenous Anesthetic Drugs: Infusion Pharmacology." International Anesthesiology Clinics 29, no. 4 (1991): 53–71. http://dx.doi.org/10.1097/00004311-199102940-00006.

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31

Glass, Peter S. A., Oliver J. Dyar, James R. Jacobs, and J. G. Reves. "Intravenous Anesthetic Drugs: Infusion Regimens." International Anesthesiology Clinics 29, no. 4 (1991): 73–82. http://dx.doi.org/10.1097/00004311-199102940-00007.

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32

Bayhakki and Utomo Wasisto. "The Development of a Digital Mobile Infusion Bag: An Instrument for Preventing Occlusion of Intravenous Infusion." Development of a Digital Mobile Infusion Bag: An Instrument for Preventing Occlusion of Intravenous Infusion 8, no. 9 (2023): 4. https://doi.org/10.5281/zenodo.10012219.

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This study aimed to develop a Digital Mobile Infusion Bag, an instrument for preventing the occlusion of intravenous infusion while mobilization. It replaces infusion stand when patients using intravenous infusion want to mobilize. Methods: This quantitative study started from developing the instrument and followed by testing the instrument. At this stage, the authors developed the instrument. Results: A Digital Mobile Infusion Bag has been developed. It was made of materials that are strong enough to withstand a 500 ml plastic infusion bottle. This instrument ensures the safety and comfort of

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33

Luke, David R., and George Foulds. "Toleration of Intravenous Azithromycin." Annals of Pharmacotherapy 31, no. 9 (1997): 965–69. http://dx.doi.org/10.1177/106002809703100901.

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Objective To study the toleration of various infusate concentrations of single intravenous doses of azithromycin. Design Randomized, double-blind, two-treatment, two-period, crossover. Setting Clinical pharmacology unit. Participants Twenty-four healthy men aged 19–41 years. Study Design All subjects were initially randomized to receive single 1-hour intravenous infusions of azithromycin 1 g at infusate concentrations of 1, 2, or 5 mg/mL (n = 6 each) compared with placebo (n = 6). Subjects who were randomized to receive 1 mg/mL concentrations were subsequently administered 5 mg/mL concentratio

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DeDonato, Bethany M., Lisa I. Bickford, and Ryan J. Gates. "Microbial Growth in Neonatal Intravenous Fat Emulsion Administered Over 12 Versus 24 Hours." Journal of Pediatric Pharmacology and Therapeutics 18, no. 4 (2013): 298–302. http://dx.doi.org/10.5863/1551-6776-18.4.298.

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OBJECTIVES To determine whether an extended infusion time (24 hours) of intravenous fat emulsion is associated with an increase in microbial growth, versus a shorter infusion time (12 hours). METHODS Samples were collected from intravenous fat emulsions (n=132), from intravenous fat emulsions prepared in the current 24-hour infusion method (n=55), and from intravenous fat emulsions prepared in the twice-daily (12-hour infusion) method (n=55). In addition, samples were collected from pharmacy (n=22) to test for possible contamination. RESULTS No growth was observed in either arm of the study. C

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Hoff, Rieka, Karolien Vervisch, Kris De Coen, and Koenraad Smets. "Continuous infusion vs. intermittent flushing of peripheral cannulas in neonates using a needleless connector: a prospective cohort study." Journal of Perinatal Medicine 47, no. 4 (2019): 464–69. http://dx.doi.org/10.1515/jpm-2018-0285.

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Abstract Objective To compare the duration of patency of peripheral intravenous cannulas between continuous infusion and intermittent flushing, while using a needleless intravenous connector in newborns admitted to the neonatal intensive care unit (NICU). Methods This is a prospective cohort study, including neonates admitted to the NICU who needed a peripheral intravenous cannula for intermittent administration of intravenous medication. In the first period, neonates received continuous peripheral infusion with NaCl 0.9% at 0.2 mL/h. In the second period, cannulas were flushed with NaCl 0.9%

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Law, Shing T., Harrison W. Farber, and Robert W. Simms. "Use of intravenous epoprostenol as a treatment for the digital vasculopathy associated with the scleroderma spectrum of diseases." Journal of Scleroderma and Related Disorders 2, no. 3 (2017): 208–12. http://dx.doi.org/10.5301/jsrd.5000255.

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Introduction Intravenous prostanoid therapy is recommended for severe systemic sclerosis-related digital vasculopathy. The evidence supporting this recommendation is limited. The aim of this study was to evaluate the safety and efficacy of treating scleroderma spectrum digital vasculopathy with intravenous epoprostenol. Methods Patients with a diagnosis of systemic sclerosis who had received intravenous epoprostenol for scleroderma spectrum digital vasculopathy between 1st October 2003 and 1st September 2015 at Boston University Medical Center were identified using ICD-9 code search, and their

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37

Brundin, T., R. Branstrom, and J. Wahren. "Effects of oral vs. i.v. glucose administration on splanchnic and extrasplanchnic O2 uptake and blood flow." American Journal of Physiology-Endocrinology and Metabolism 271, no. 3 (1996): E496—E504. http://dx.doi.org/10.1152/ajpendo.1996.271.3.e496.

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The metabolic and circulatory responses to intravenous or oral administration of glucose (75 g) were studied in healthy subjects. Pulmonary oxygen uptake increased promptly after oral but not during intravenous glucose infusion. The average 2-h rise above basal in whole body oxygen uptake was 8 +/- 1% (P < 0.001) after oral glucose and 3 +/- 1% (P < 0.05) during intravenous glucose infusion. After oral glucose, splanchnic oxygen uptake rose initially by approximately 15% (P < 0.01) and then declined; its average 2-h postprandial level was not significantly higher than that in the basa

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Dunn, Lauren K., and Marcel E. Durieux. "Perioperative Use of Intravenous Lidocaine." Anesthesiology 126, no. 4 (2017): 729–37. http://dx.doi.org/10.1097/aln.0000000000001527.

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Perioperative lidocaine infusion improves analgesia and recovery after some surgical procedures, possibly through systemic antiinflammatory effects. This commentary provides the clinician with evidence for rational use of perioperative lidocaine infusion in procedures where it is of demonstrated benefit.

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Drouet, Maryline, Feng Chai, Christine Barthélémy, et al. "Influence of Vancomycin Infusion Methods on Endothelial Cell Toxicity." Antimicrobial Agents and Chemotherapy 59, no. 2 (2014): 930–34. http://dx.doi.org/10.1128/aac.03694-14.

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ABSTRACTPeripheral intravenous therapy is frequently used in routine hospital practice and, due to various factors, its most common side effect is phlebitis. The infusion of vancomycin is particularly associated with phlebitis despite its widespread use. French guidelines recommend central intravenous infusion for high concentrations of vancomycin, but peripheral intravenous therapy is often preferred in intensive care units. Methods of vancomycin infusion are either intermittent infusion or continuous infusion. A comparison of these methods underin vitroconditions simulating clinical use coul

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Pruzanski, Waldemar, Matthew L. Sherman, Donald W. Kufe, and Peter Vadas. "Induction of circulating phospholipase A2by intravenous administration of recombinant human tumour necrosis factor." Mediators of Inflammation 1, no. 4 (1992): 235–40. http://dx.doi.org/10.1155/s0962935192000358.

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We have examined the effects of intravenous infusion of recombinant human tumour necrosis factor (rh-TNF) on serum activity of phospholipase A2(PLA2) in patients with malignancies. Nine patients received a 24 h continuous intravenous infusion ranging from 1.0 × 105U/m2to 3.0 × 105U/m2; 14 patients received a 5 day continuous intravenous infusion ranging from 0.5 × 105U/m2/day to 3.0 105U/m2/day. Twenty one of 23 patients responded with marked increases in serum PLA2activity that were detectable 3 h after the beginning of the rh-TNF infusion and reached maximum levels at 18 h with a mean increa

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Appelgren, B. H., S. Arver, and G. B. Sagulin. "Effect of intracerebroventricular calcitonin on renal hydromineral excretion in sheep." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 250, no. 6 (1986): R980—R983. http://dx.doi.org/10.1152/ajpregu.1986.250.6.r980.

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The localization of calcitonin in hypothalamic tissue and cerebrospinal fluid and calcitonin binding sites in circumventricular organs suggests involvement in neural mechanisms, possibly hydromineral balance. Therefore, we compared the effects of intracerebroventricular and intravenous infusions of porcine calcitonin (0.04-0.05 mU X kg-1 X min-1) on renal water, Ca, Mg, Na, and K excretions. The intracerebroventricular administration of calcitonin for 60 min induced a pronounced increase (P less than 0.01) in free water clearance, from a preinfusion value of -0.73 +/- 0.45 to +3.02 +/- 1.15 ml

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Rosyady, Phisca Aditya, Nurina Umy Habibah, Ahmad Raditya Cahya Baswara, Nuni Ihsana, Dedik Sulistiawan, and Widya Rahayu Dinata. "Microcontroller-Based Intravenous Fluid Monitoring System Design." Journal of Applied Engineering and Technological Science (JAETS) 5, no. 2 (2024): 649–60. http://dx.doi.org/10.37385/jaets.v5i2.3230.

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Intravenous fluids are used to replace the body's fluid and electrolyte balance. This is a crucial need for a patient during treatment, so infusion replacement should not be delayed as it can be fatal to the patient. Medical personnel must always pay attention to the patient's infusion. This has always been a problem because the limited number of medical personnel and the large number of patients often make it difficult for medical personnel to carry out their duties. The development of technology increases human creativity and creates various tools to help humans be more effective, including

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Pleasants, Roy A., Leigh M. Vaughan, Dennis M. Williams, and Janet L. Fox. "Compatibility of Ceftazidime and Aminophylline Admixtures for Different Methods of Intravenous Infusion." Annals of Pharmacotherapy 26, no. 10 (1992): 1221–26. http://dx.doi.org/10.1177/106002809202601004.

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OBJECTIVE: Aminophylline and ceftazidime are sometimes used concurrently in patients with respiratory disorders. Parenteral aminophylline usually is administered as a constant infusion, and ceftazidime is given intermittently or less commonly as a constant infusion. We evaluated the stability and compatibility of the two drugs when aminophylline is given as a constant intravenous infusion and ceftazidime is administered simultaneously either through a y-site (piggyback method) or as a continuous infusion (constant infusion method). DESIGN: The chemical stability of intravenous aminophylline an

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Kastrissios, H., G. A. G. Mogg, E. J. Triggs, and J. W. Higbie. "Interpleural Bupivacaine Infusion Compared with Intravenous Pethidine Infusion after Cholecystectomy." Anaesthesia and Intensive Care 19, no. 4 (1991): 539–45. http://dx.doi.org/10.1177/0310057x9101900409.

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Twenty-six cholecystectomy patients received either an interpleural infusion of bupivacaine (Group B, n = 12) or an intravenous infusion of pethidine (Group P, n = 14) for management of postoperative pain over a three-day period. Patients in Group P experienced a significantly (P < 0.05) greater incidence of total side-effects (146) than patients in Group B (66). Pain scores (VAS) and responses to a pain questionnaire were similar for both groups; however, within Group B improvement in mean VAS scores at rest with time were more sustained. Similar reductions in FEV, and FVC from preoperativ

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Harvey, V. J., M. L. Slevin, G. W. Aherne, P. Littleton, A. Johnston, and P. F. Wrigley. "Subcutaneous infusion of bleomycin--a practical alternative to intravenous infusion." Journal of Clinical Oncology 5, no. 4 (1987): 648–50. http://dx.doi.org/10.1200/jco.1987.5.4.648.

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The phase specificity and short half-life of bleomycin make it likely that it would be more effective when administered by continuous infusion. This is supported by studies using cell lines, as well as by animal studies and clinical experience in humans. This study was conducted to compare the pharmacokinetics of intravenous (IV) and subcutaneous infusions of bleomycin. The serum concentrations of bleomycin were measured using a sensitive and specific radioimmunoassay. The results demonstrate similar plasma concentrations and area under the curve for both routes. The subcutaneous infusions wer

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Kuensting, Laura L. "Comparing Subcutaneous Fluid Infusion with Intravenous Fluid Infusion in Children." Journal of Emergency Nursing 39, no. 1 (2013): 86–91. http://dx.doi.org/10.1016/j.jen.2012.04.017.

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Matsukawa, Toshiyoshi, and Takenori Miyamoto. "Angiotensin II-stimulated secretion of arginine vasopressin is inhibited by atrial natriuretic peptide in humans." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 300, no. 3 (2011): R624—R629. http://dx.doi.org/10.1152/ajpregu.00324.2010.

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We investigated the effect of the intravenous infusion of atrial natriuretic peptide (ANP) on the response of plasma arginine vasopressin (AVP) levels to intravenous infusion of angiotensin II (ANG II) in healthy individuals. Intravenous infusion of ANP (10 ng·kg−1·min−1) slightly but significantly decreased plasma AVP levels, while intravenous infusion of ANG II (10 ng·kg−1·min−1) resulted in slightly increased plasma AVP levels. ANG II infused significant elevations in arterial blood pressure and central venous pressure (CVP). Because the elevation in blood pressure could have potentially in

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Nickel, Barb. "Peripheral Intravenous Access: Applying Infusion Therapy Standards of Practice to Improve Patient Safety." Critical Care Nurse 39, no. 1 (2019): 61–71. http://dx.doi.org/10.4037/ccn2019790.

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The most common invasive procedure performed in the hospital setting worldwide is the insertion of a peripheral intravenous catheter. Although use of peripheral intravenous access is common, its presence is far from benign, with a reported 35% to 50% failure rate, even in facilities with a dedicated infusion team. Significant complications related to the presence of a peripheral intravenous site include localized infection, bacteremia, phlebitis, and infiltration or extravasation. Consistent application of evidence-based standards of practice in all aspects of peripheral intravenous catheter c

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Kawamura, Hideki, Toshiro Tanioka, Mariko Kuji, Kazuaki Shibuya, and Masahiro Takahashi. "Effect of Shorter Term of Intravenous Infusion for Reduction of Catheter-Related Bloodstream Infection After Gastrectomy." International Surgery 97, no. 4 (2013): 345–50. http://dx.doi.org/10.9738/cc147.1.

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Abstract After gastrectomy, a longer period of intravenous alimentation is required than for other digestive surgeries, portending a higher risk of catheter-related bloodstream infection (CRBSI). From assessment of CRBSI occurring between 2004 and 2007 (preintervention group), the duration of intravenous infusion between 2008 and 2010 (postintervention group) was changed to shorter-term (6-day) infusion. To verify the effect of changes in injection schedule on the incidence of CRBSI, the occurrence of CRBSI was studied comparatively among preintervention and postintervention cases, excluding c

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Akbar, Shafi M., and Muath M. Ali. "Safety of Administration of Hypertonic Sodium Chloride Solution Through Peripheral IV in Neuroscience Intensive Care Unit, KAMC, Makkah." Journal of Innovations in Medical Research 2, no. 2 (2023): 36–44. http://dx.doi.org/10.56397/jimr/2023.02.06.

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Background: Infusions of 3% sodium chloride are routinely recommended to be given through central venous catheters, not peripheral IV lines. In addition, no data are available on the proper site for administration of a continuous intravenous infusion of 3% sodium chloride solution in adults. Some recent studies have illustrated that this theory may not be relevant, and that 3% sodium chloride may be safe for administration in peripheral IV lines. Aims and Objectives: To evaluate the incidence of infusion-related reactions in neuro intensive care patients treated with continuous intravenous inf

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