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1.
Rev. bras. ciênc. vet ; 29(1): 3-8, jan./mar. 2022. il.
Article in Portuguese | LILACS, VETINDEX | ID: biblio-1393181

ABSTRACT

A ocorrência de processos fisiopatológicos que cursam com desidratação da ingesta no trato gastrointestinal dos equinos é comum na rotina clínica. Fatores como diminuição da motilidade intestinal e sobrecarga intraluminal de conteúdo desidratado podem levar a compactação em segmentos como estômago, ceco e cólons. Este estudo objetivou realizar a comparação entre soluções eletrolíticas enterais hipotônica (SeHIPO) e isotônica (SeISO) e a solução Ringer com lactato de sódio (RL IV) sobre o teor de umidade das fezes de equinos submetidos a um período de desidratação experimental (PD). Foram utilizados seis equinos adultos, todas fêmeas com idades entre 10 e 15 anos, média de 440 kg de peso corpóreo. O PD constou de 36 horas de jejum hídrico e alimentar associadas a duas administrações intravenosas de furosemida, sendo a primeira imediatamente no início (T-36) e a segunda 12 horas após o início do PD. Os tratamentos utilizados foram: SeHIPO e SeISO, ambas administradas por via nasogástrica em fluxo contínuo (HETfc), e RL IV administrada pela via intravenosa. Todos os tratamentos foram administrados a uma taxa de infusão contínua de 15mL kg-1 h-1 durante 8 horas consecutivas. O delineamento experimental utilizado foi o crossover6x3, onde cada animal foi submetido, em sistema de rodízio, aos três tratamentos em momentos distintos. As soluções eletrolíticas enterais demonstraram maior eficácia na recomposição do teor de umidade das fezes quando comparadas à terapia RL IV. A hidratação enteral com soluções isotônicas e hipotônicas administrada em fluxo contínuo são eficazes em restaurar o teor de umidade das fezes, podendo ofertar uma opção econômica, segura e eficiente na reidratação de pacientes e nas afecções que cursam como obstruções intraluminais simples.


The occurrence of pathophysiological processes that curse with digesta dryness in the gastrointestinal tract of horses is common in clinical routine, factors such as decreased intestinal motility and intraluminal overload of dry content can lead to compaction in segments such as cecum and colon. This study aimed to compare a hypotonic enteral solution (SeHIPO), an isotonic enteral solution (SeISO) and a Ringer with sodium lactate solution (RL IV) over the moisture content of equine feces submitted to an experimental dehydration protocol. Six adult horses were used, all females aged between 10 and 15 years, average body weight of 440 kg. The PD consisted of a 36 hours period of water and food fasting associated with two intravenous administrations of furosemide, the first immediately at the beginning (T-36) and the second 12 hours after the beginning of the PD. The treatments used were: SeHIPO (hypotonic enteral solution administered via nasogastric), SeISO (enteral isotonic solution administered via nasogastric) and RL IV (Ringer's solution with sodium lactate administered intravenously), all treatments were administered by continuous infusion at a rate of 15mL kg-1 h-1 for 8 consecutive hours. The experimental design used was the 6x3 crossover, where each animal is submitted, in a rotation system, to the three treatments at different times. Enteral fluid therapy with isotonic and hypotonic solutions administered in continuous flow are effective in restoring the moisture content of feces, and may offer an economical, safe, and efficient option for rehydrating patients and in conditions that progress as simple intraluminal obstructions.


Subject(s)
Animals , Water-Electrolyte Balance , Dehydration/veterinary , Fluid Therapy/veterinary , Ringer's Lactate/therapeutic use , Horses/metabolism , Hypotonic Solutions/therapeutic use , Isotonic Solutions/therapeutic use , Gastrointestinal Tract , Feces , Administration, Intravenous/veterinary
2.
Curr Eye Res ; 47(4): 511-516, 2022 04.
Article in English | MEDLINE | ID: mdl-34898348

ABSTRACT

PURPOSE: Accelerated trans-epithelial cross-linking (ATE-CXL), a therapy to halt keratoconus progression, has the merit of widening the indications for thinner corneas (<380 µm). Since a hypotonic solution affects the swollen cornea, corneas of <380 µm thickness at preoperative measurement can be an indication for ATE-CXL. The aim of this retrospective study was to compare the efficacy and safety of ATE-CXL for keratoconus between corneas with thicknesses <380 µm and ≥380 µm. MATERIALS AND METHODS: Thirty-four eyes of 27 patients who underwent ATE-CXL (30 mW/cm2; 3 minutes) with completion of a 24-month follow-up, were enrolled and divided into two groups: Group 1, thinnest corneal thickness (TCT), <380 µm (n = 10) and Group 2, TCT, ≥380 µm (n = 24). A hypotonic solution was administered to Group 1 until the corneal thickness increased by >380 µm before UV-A irradiation. We measured uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), maximum and average keratometric values (Kmax and AveK), central corneal thickness (CCT), TCT by anterior segment optical coherence tomography, and corneal endothelial cell density (ECD) using specular microscopy. The changes from baseline to 24 months postoperatively between the two groups were compared accordingly. RESULTS: The changes in Kmax and AveK from baseline to 24 months in Group 1 (ΔKmax: -7.8 ± 7.7 D, ΔAveK: -4.3 ± 6.1 D) showed significant decreases compared to those in Group 2 (ΔKmax: 0.2 ± 3.0 D, ΔAveK: 0.6 ± 2.7 D) (p = .004 and p = .001), and there were no significant changes from baseline to 24 months postoperatively in UCVA, BCVA, CCT, TCT, and ECD in both groups. CONCLUSION: ATE-CXL is effective and safe for keratoconic corneas in both groups. The effect of reducing keratometric values was greater in the group with thinner corneas.


Subject(s)
Keratoconus , Photochemotherapy , Collagen/therapeutic use , Cornea/surgery , Corneal Topography , Cross-Linking Reagents/therapeutic use , Follow-Up Studies , Humans , Hypotonic Solutions/therapeutic use , Keratoconus/diagnosis , Keratoconus/drug therapy , Keratoconus/surgery , Photochemotherapy/methods , Photosensitizing Agents/therapeutic use , Retrospective Studies , Riboflavin/therapeutic use , Ultraviolet Rays
4.
Eur J Endocrinol ; 183(1): G9-G15, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32380474

ABSTRACT

COVID-19 has changed the nature of medical consultations, emphasizing virtual patient counseling, with relevance for patients with diabetes insipidus (DI) or hyponatraemia. The main complication of desmopressin treatment in DI is dilutional hyponatraemia. Since plasma sodium monitoring is not always possible in times of COVID-19, we recommend to delay the desmopressin dose once a week until aquaresis occurs allowing excess retained water to be excreted. Patients should measure their body weight daily. Patients with DI admitted to the hospital with COVID-19 have a high risk for mortality due to volume depletion. Specialists must supervise fluid replacement and dosing of desmopressin. Patients after pituitary surgery should drink to thirst and measure their body weight daily to early recognize the development of the postoperative syndrome of inappropriate antidiuresis (SIAD). They should know hyponatraemia symptoms. The prevalence of hyponatraemia in patients with pneumonia due to COVID-19 is not yet known, but seems to be low. In contrast, hypernatraemia may develop in COVID-19 patients in ICU, from different multifactorial reasons, for example, due to insensible water losses from pyrexia, increased respiration rate and use of diuretics. Hypernatraemic dehydration may contribute to the high risk of acute kidney injury in COVID-19. IV fluid replacement should be administered with caution in severe cases of COVID-19 because of the risk of pulmonary oedema.


Subject(s)
Antidiuretic Agents/administration & dosage , Coronavirus Infections/therapy , Deamino Arginine Vasopressin/administration & dosage , Diabetes Insipidus, Neurogenic/therapy , Fluid Therapy/methods , Hypernatremia/therapy , Hyponatremia/therapy , Inappropriate ADH Syndrome/therapy , Pneumonia, Viral/therapy , Brain Injuries/complications , COVID-19 , Coronavirus Infections/complications , Coronavirus Infections/prevention & control , Coronavirus Infections/transmission , Dehydration/therapy , Diabetes Insipidus/complications , Diabetes Insipidus/therapy , Diabetes Insipidus, Neurogenic/complications , Disease Management , Humans , Hyponatremia/etiology , Hyponatremia/prevention & control , Hypotonic Solutions/therapeutic use , Neurosurgical Procedures , Pandemics/prevention & control , Pneumonia, Viral/complications , Pneumonia, Viral/prevention & control , Pneumonia, Viral/transmission , Postoperative Complications/therapy , Practice Guidelines as Topic , Saline Solution/therapeutic use , Shock/etiology , Shock/therapy
5.
Paediatr Int Child Health ; 40(1): 44-49, 2020 02.
Article in English | MEDLINE | ID: mdl-31138063

ABSTRACT

Background: To prevent the risk of iatrogenic hyponatraemia in hospitalised children, isotonic fluid has been recommended as maintenance intravenous fluid (IVF). There are few studies which compare half normal saline with normal saline as maintenance IVF in general paediatric wards.Aim: To compare the safety and efficacy of half normal saline with normal saline as maintenance IVF in general paediatric wards.Methods: Children aged between 3 months and 5 years with an anticipated requirement for IVF for 24 h were randomised to receive either half normal saline (0.45% saline in 5% dextrose) or normal saline (0.9% saline in 5% dextrose). The primary objective was to compare the incidence of hyponatraemia (serum sodium <135 mmol/L with a decrease from baseline of at least 4 mmol/L) at 24 h in children receiving half normal saline with those receiving normal saline. Secondary objectives were to compare the incidence of moderate (sodium <130 mmol/L), severe (sodium <125 mmol/L) and symptomatic hyponatraemia, change in serum sodium level from baseline and the incidence of hypernatraemia.Results: A total of 168 children were randomised to receive either normal saline (n = 84) or half normal saline (n = 84). More than two-thirds of the children were suffering from respiratory diseases (pneumonia and bronchiolitis) and diseases of the nervous system (meningoencephalitis, febrile seizures and epilepsy). The incidence of hyponatraemia at 12 h in children receiving half normal saline was similar to that in those receiving normal saline (6 vs 4.8%; Relative risk (RR) 1.2; 95% CI 0.3.0-4.8; p = 0.73). Although the incidence of hyponatraemia at 24 h in children receiving half normal saline was higher than in those receiving normal saline, the difference was not statistically significant (14.3 vs 6%; RR 2.6; 95% CI 0.9-7.8; p = 0.07). One child in the isotonic group and one in the hypotonic group developed moderate and severe hyponatraemia, respectively. There was no significant difference in the incidence of hypernatraemia between two groups (RR 0.7; 95% CI 0.16-3.3).Conclusion: Half-normal saline as maintenance IVF does not result in a significantly increased risk of hyponatraemia in general paediatric ward patients under 5 years of age.


Subject(s)
Fluid Therapy , Hypotonic Solutions/therapeutic use , Isotonic Solutions/therapeutic use , Saline Solution/therapeutic use , Child, Preschool , Female , Humans , Hyponatremia/chemically induced , Infant , Male
6.
Molecules ; 24(24)2019 Dec 04.
Article in English | MEDLINE | ID: mdl-31817098

ABSTRACT

Hailey-Hailey disease (HHD) is a rare, chronic and recurrent blistering disorder, characterized by erosions occurring primarily in intertriginous regions and histologically by suprabasal acantholysis. Mutation of the Golgi Ca2+-ATPase ATP2C1 has been identified as having a causative role in Hailey-Hailey disease. HHD-derived keratinocytes have increased oxidative-stress that is associated with impaired proliferation and differentiation. Additionally, HHD is characterized by skin lesions that do not heal and by recurrent skin infections, indicating that HHD keratinocytes might not respond well to challenges such as wounding or infection. Hypochlorous acid has been demonstrated in vitro and in vivo to possess properties that rescue both oxidative stress and altered wound repair process. Thus, we investigated the potential effects of a stabilized form of hypochlorous acid (APR-TD012) in an in vitro model of HHD. We found that treatment of ATP2C1-defective keratinocytes with APR-TD012 contributed to upregulation of Nrf2 (nuclear factor (erythroid-derived 2)-like 2). Additionally, APR TD012-treatment restored the defective proliferative capability of siATP2C1-treated keratinocytes. We also found that the APR-TD012 treatment might support wound healing process, due to its ability to modulate the expression of wound healing associated cytokines. These observations suggested that the APR-TD012 might be a potential therapeutic agent for HHD-lesions.


Subject(s)
Acids/chemistry , Hypochlorous Acid/therapeutic use , Hypotonic Solutions/therapeutic use , Pemphigus, Benign Familial/drug therapy , Antioxidants/metabolism , Calcium-Transporting ATPases/metabolism , Cell Line , Cytokines/genetics , Cytokines/metabolism , Gene Expression Regulation/drug effects , Humans , Hypochlorous Acid/pharmacology , Hypotonic Solutions/pharmacology , Keratinocytes/drug effects , Keratinocytes/metabolism , Keratinocytes/pathology , NF-E2-Related Factor 2/metabolism , Oxidation-Reduction , Oxidative Stress/drug effects , Pemphigus, Benign Familial/genetics , Pemphigus, Benign Familial/pathology , Reactive Oxygen Species/metabolism , Solutions , Wound Healing/drug effects
7.
Arq. bras. med. vet. zootec. (Online) ; 71(2): 404-410, mar.-abr. 2019. tab
Article in English | VETINDEX, LILACS | ID: biblio-1011287

ABSTRACT

The present study assessed and compared the effects of hypotonic enteral electrolyte solutions administered by nasoesophageal tube in continuous flow in dogs submitted to water restriction on packed cell volume; total serum protein and serum osmolarity concentrations; blood volume; plasma glucose and lactate levels; blood gas analysis, anion gap, and strong ion difference. Six adult dogs were used (four males and two females). All animals were submitted to both proposed treatments in a crossover design 6×2. The treatments were as follows: ESmalt consisting of 5g sodium chloride, 1g potassium chloride, 1g calcium acetate, 0.2g magnesium pidolate, and 9.6g maltodextrin that were diluted in 1.000mL water (measured osmotic concentration of 215mOsm L−1) and ESdext consisting of 5g sodium chloride, 1g potassium chloride, 1g calcium acetate, 0.2g magnesium pidolate, and 9.6g dextrose that were diluted in 1.000mL water (measured osmotic concentration of 243mOsm L−1). All solutions were administered at 15ml kg−1 h−1 for 4 hours. Both solutions increased the plasma volume in dehydrated dogs without causing adverse effects. However, ESmalt was more effective in promoting the increase in blood volume.(AU)


O presente estudo avaliou e comparou os efeitos de soluções eletrolíticas enterais hipotônicas, administradas por sonda nasoesofágica em fluxo contínuo em cães submetidos a restrição hídrica, sobre o hematócrito, proteínas totais séricas, osmolaridade sérica, volemia, glicose e lactato plasmáticos, hemogasometria, ânion gap e DIF. Foram utilizados seis cães adultos (quatro machos e duas fêmeas). Todos os animais foram submetidos aos dois tratamentos propostos, em um delineamento crossover 6×2. Os tratamentos foram os seguintes: SEmalt - 5g de cloreto de sódio, 1g de cloreto de potássio, 1g de acetato de cálcio, 0,2g de pidolato de magnésio e 9,6g de maltodextrina, diluídos em 1.000mL de água (osmolaridade mensurada: 215mOsm L -1 ); SEdext - 5g de cloreto de sódio, 1g de cloreto de potássio, 1g de acetato de cálcio, 0,2g de pidolato de magnésio e 9,6g de dextrose, diluídos em 1.000mL de água (osmolaridade mensurada: 243mOsm L -1 ). Todas as soluções foram administradas no volume de 15mL kg -1 hora -1 , durante quatro horas, em fluxo contínuo. Ambas as soluções aumentaram o volume plasmático em cães desidratados, sem gerar o aparecimento de efeitos adversos. Porém, a SEmalt foi mais eficaz em promover a expansão da volemia.


Subject(s)
Animals , Dogs , Dehydration/therapy , Dehydration/veterinary , Fluid Therapy/methods , Fluid Therapy/veterinary , Hypotonic Solutions/therapeutic use , Hypovolemia/veterinary , Intubation, Gastrointestinal/veterinary
8.
Ugeskr Laeger ; 181(11)2019 Mar 11.
Article in Danish | MEDLINE | ID: mdl-30864540

ABSTRACT

The standard practice in paediatric departments in Danish hospitals is to prescribe hypotonic maintenance fluids (sodium content 20-40 mmol/l) for children, who are fasting or have a reduced enteral intake. The past decades have provided strong evidence, that this can lead to hypo-natraemia and subsequent neurologic damage or death. We recommend, that prefabricated isotonic solutions containing 140-154 mmol/l of sodium and 5% glucose, with or without an additional 20 mmol/l of potassium, are available as standard maintenance fluid for children in all Danish hospitals.


Subject(s)
Fluid Therapy , Hyponatremia , Hypotonic Solutions , Child , Humans , Hyponatremia/therapy , Hypotonic Solutions/therapeutic use , Isotonic Solutions , Sodium
9.
J Intensive Care Med ; 33(3): 147-158, 2018 Mar.
Article in English | MEDLINE | ID: mdl-28535742

ABSTRACT

Electrolyte disturbances are frequently encountered in critically ill oncology patients. Hyponatremia and hypernatremia as well as hypocalcemia and hypercalcemia are among the most commonly encountered electrolyte abnormalities. In the intensive care unit, management of critical electrolyte disturbances is focused on initial evaluation and immediate treatment plan to prevent severe complications. A PubMed search was performed to identify best available evidence for evaluation and management of dysnatremias, hypocalcemia, and hypercalcemia. Current literature was reviewed regarding the management of electrolyte disturbances. The role of new therapeutic options, for example, vaptans for hyponatremia, teriparatide for hypocalcemia, and denosumab for hypercalcemia, is discussed. Early diagnosis and appropriate management are expected to reduce adverse outcomes.


Subject(s)
Critical Care/methods , Electrolytes/therapeutic use , Neoplasms/complications , Neoplasms/therapy , Water-Electrolyte Imbalance/therapy , Bone Density Conservation Agents/therapeutic use , Critical Illness/therapy , Early Diagnosis , Humans , Hypertonic Solutions/therapeutic use , Hypotonic Solutions/therapeutic use , Water-Electrolyte Imbalance/diagnosis , Water-Electrolyte Imbalance/etiology
10.
J Clin Anesth ; 37: 52-54, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28235528

ABSTRACT

We describe the first case of severe hypernatremia associated to laparoscopic surgery for hydatid cyst in an adult patient after the use of hypertonic saline solution with complete resolution. Severe hypernatremia is an unusual fact at the immediate postoperative period but may have fatal consequences for the patient and need immediate action. The patient reached a serum sodium concentration of 179 mmol/L without adverse effects after 6 days of treatment. Laparoscopy could play a crucial role in Na+ absorption due to high intraabdominal pressure caused by the pneumoperitoneum and its limitations to avoid peritoneal absorption of hypertonic saline solution. The relation between this surgical technique and the severe complication is discussed. More experience is needed in terms of safety for the patient.


Subject(s)
Cholecystectomy, Laparoscopic/adverse effects , Echinococcosis, Hepatic/surgery , Echinococcosis/surgery , Hypernatremia/complications , Pneumoperitoneum, Artificial/adverse effects , Saline Solution, Hypertonic/adverse effects , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/therapeutic use , Antibiotic Prophylaxis/methods , Echinococcosis/diagnostic imaging , Echinococcosis, Hepatic/diagnostic imaging , Ephedrine/administration & dosage , Ephedrine/therapeutic use , Female , Fentanyl/administration & dosage , Fentanyl/therapeutic use , Glucose/administration & dosage , Glucose/therapeutic use , Humans , Hydrocortisone/administration & dosage , Hydrocortisone/therapeutic use , Hyperglycemia/blood , Hyperglycemia/drug therapy , Hypernatremia/blood , Hypernatremia/drug therapy , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/therapeutic use , Hypotonic Solutions/administration & dosage , Hypotonic Solutions/therapeutic use , Infusions, Intravenous , Insulin/administration & dosage , Insulin/therapeutic use , Magnetic Resonance Imaging , Middle Aged , Muscle Hypotonia/drug therapy , Muscle Hypotonia/etiology , Pain, Postoperative/drug therapy , Postoperative Period , Saline Solution, Hypertonic/administration & dosage , Sodium/administration & dosage , Sodium/therapeutic use , Vasoconstrictor Agents/administration & dosage , Vasoconstrictor Agents/therapeutic use
13.
Cornea ; 35(3): 350-4, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26751988

ABSTRACT

PURPOSE: The aim of this study was to evaluate the early term topographic and aberration results of accelerated (9 mW/cm) corneal cross-linking (CXL) treatment in keratoconic thin corneas. METHODS: Forty-nine eyes from 43 patients (mean age of 21.2 ± 7.1) with progressive keratoconic thin corneas (<400 µm without epithelium) who had accelerated corneal CXL with hypoosmolar riboflavin solution throughout the procedure were enrolled. We measured the uncorrected and corrected distance visual acuity, refraction, slit-lamp examination, topographic values, and corneal higher-order aberrations (Pentacam HR, Oculus Optikgeräte GmbH) preoperatively and 1, 3, and 6 months after surgery. RESULTS: Before surgery, the corneal thickness was 404 ± 18 µm, and the thickness was reduced to 360 ± 24 µm after removing the epithelium. After the application of hypoosmolar riboflavin solution, the thickness increased to 432 ± 44 µm. At month 6, there was a significant increase in uncorrected distance visual acuity (P = 0.043) and corrected distance visual acuity (P = 0.024), a decrease in spherical refraction (P = 0.041), maximum keratometry (Kmax, P = 0.003), anterior elevation values (P = 0.008), corneal thickness (P < 0.001), coma (P = 0.022), spherical aberration (P = 0.001), higher-order root mean square (P = 0.004), and total root mean square (P < 0.001), whereas the cylindrical refraction (P = 0.627), anterior (P = 0.665) and posterior astigmatism (P = 0.165) of the cornea, posterior elevation (P = 0.198), and trefoil (P = 0.141) remained unchanged. No patients showed any complications or scar formation during follow-up. CONCLUSIONS: Accelerated corneal CXL with hypoosmolar riboflavin solution throughout the procedure is effective in thin corneas.


Subject(s)
Collagen/metabolism , Cross-Linking Reagents/therapeutic use , Hypotonic Solutions/therapeutic use , Keratoconus/drug therapy , Photochemotherapy/methods , Photosensitizing Agents/therapeutic use , Riboflavin/therapeutic use , Adult , Cornea/metabolism , Cornea/pathology , Corneal Topography , Female , Humans , Keratoconus/pathology , Male , Middle Aged , Visual Acuity , Young Adult
15.
Cornea ; 34(5): 560-6, 2015 May.
Article in English | MEDLINE | ID: mdl-25789693

ABSTRACT

PURPOSE: Little is known about how the osmolarity of ophthalmic formulations affects the ocular surface. Because hyperosmolar eye drops could be therapeutic for treating corneal edema, this article presents an ex vivo model of corneal edema for testing ophthalmic drugs based on their osmolarity. The respective osmolarity of common eye drops found in the German market is also analyzed here. METHODS: For modeling corneal edema, an Ex Vivo Eye Irritation Test was used to simulate an ocular anterior chamber with a physiological corneal barrier. To induce corneal edema, the anterior chamber was supplied with a hypoosmolar medium (148 mOsm/L) for 24 hours. Preserved and preservative-free 5% sodium chloride (hyperosmolar Omnisorb and Ocusalin 5% UD) were used for 1 hour, on 5 corneas each, to test their efficiency to reduce corneal edema in this model. Corneal thickness was determined by optical coherence tomography. Osmolarity of 87 common eye drops was measured by freezing point osmometry. RESULTS: Ex vivo, the tested hypoosmolar condition induced corneal edema from 450 µm (±50 µm) at baseline to 851 µm (±94 µm, P < 0.0001). Omnisorb and Ocusalin 5% UD significantly reduced the corneal thickness by 279 µm (±28 µm, P < 0.001) for Omnisorb and 258 µm (±29 µm, P < 0.001) for Ocusalin 5% UD. Forty-three (49%) of the tested products had an osmolarity below and 44 (51%) above the physiological tear osmolarity of 289 mOsm/L. Osmolarity values of less than 200 mOsm/L were found in lubricant drops. The highest osmolarity was detected in Omnisorb (1955 mOsm/L). CONCLUSIONS: The Ex Vivo Eye Irritation Test has proven to be a reliable novel model of corneal edema for evaluating osmotic eye drops. Osmolarity measurements revealed a wide range from hypotonic to hypertonic formulations for commonly marketed ophthalmic drugs.


Subject(s)
Corneal Edema/drug therapy , Disease Models, Animal , Lubricant Eye Drops , Pharmaceutical Preparations/chemistry , Administration, Topical , Animals , Chemistry, Pharmaceutical , Corneal Edema/chemically induced , Corneal Edema/diagnosis , Hypotonic Solutions/adverse effects , Hypotonic Solutions/chemistry , Hypotonic Solutions/therapeutic use , Lubricant Eye Drops/adverse effects , Lubricant Eye Drops/chemistry , Lubricant Eye Drops/therapeutic use , Organ Culture Techniques , Osmolar Concentration , Osmometry , Preservatives, Pharmaceutical/adverse effects , Preservatives, Pharmaceutical/chemistry , Preservatives, Pharmaceutical/therapeutic use , Rabbits , Saline Solution, Hypertonic/adverse effects , Saline Solution, Hypertonic/chemistry , Saline Solution, Hypertonic/therapeutic use , Tomography, Optical Coherence
16.
Pediatr Emerg Care ; 31(2): 122-6, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25654679

ABSTRACT

AIM: This study aimed to analyze the effect of isotonic versus hypotonic solution as intravenous maintenance fluid on level of plasma sodium in hospitalized children. METHODS: A fully recursive literature search in May 2013 was conducted in PubMed and EMBASE to identify potentially relevant randomized controlled trials. Jadad score and allocation concealment were adopted to evaluate the methodological quality of each trial. RevMan5.2 was used for statistical analysis. RESULTS: Eight randomized controlled trials with 752 patients were included. Combined analysis showed a significant lower risk of hyponatremia with isotonic solution (odds ratio, 0.36; 95% confidence interval, 0.26-0.51). The isotonic intravenous maintenance did not increase the possibility of hypernatremia (odds ratio, 0.86; 95% confidence interval, 0.36-2.06). CONCLUSIONS: The meta-analysis revealed that there was potential risk of hyponatremia for routine infusion of hypotonic maintenance fluid. The use of isotonic solution was warranted in hospitalized pediatric patients.


Subject(s)
Fluid Therapy , Hypotonic Solutions/therapeutic use , Isotonic Solutions/therapeutic use , Child , Humans , Hyponatremia/etiology , Hypotonic Solutions/adverse effects , Infusions, Intravenous , Randomized Controlled Trials as Topic
17.
Pediatr Nephrol ; 30(7): 1163-72, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25576065

ABSTRACT

BACKGROUND: The administration of hypotonic saline solution for maintenance intravenous fluid (IVF) therapy has been the standard of care, but recent evidence has shown this treatment to be associated with hyponatremia-related complications. The aim of this systematic review was to determine which IVF, i.e., a hypotonic or an isotonic saline solution, poses less risk for the development of hyponatremia among hospitalized children who require maintenance IVF therapy. METHODS: Medline, Cochrane Library, LILACS, Current Controlled Trials, reference lists, and abstract proceedings were searched for randomized controlled trials (RCTs) comparing hypotonic and isotonic saline solutions for maintenance IVF therapy in hospitalized children. Two reviewers independently assessed all potentially relevant studies and subsequently extracted data and evaluated the methodological quality of the RCTs. Studies were then combined and analyzed using a random effects model. RESULTS: Eleven RCTs met the inclusion criteria. Our analysis of these 11 RCTs showed that among hospitalized children receiving maintenance IVF therapy, isotonic solutions significantly decreased the risk of developing hyponatremia [relative risk (RR) 0.50, 95% confidence interval (CI) 0.40-0.62] without significantly increasing the risk for hypernatremia (RR 0.83, 95% CI 0.41-1.67). CONCLUSIONS: Current evidence does not support the standard practice of prescribing a hypotonic saline solution as maintenance IVF therapy to hospitalized children. Although there is no single IVF composition ideal for all children, an isotonic saline solution does appear to be the safer choice when maintenance IVF therapy is used in the general pediatric population.


Subject(s)
Fluid Therapy/methods , Hypotonic Solutions/therapeutic use , Isotonic Solutions/therapeutic use , Adolescent , Child , Child, Preschool , Humans , Hyponatremia/therapy , Hypotonic Solutions/adverse effects , Infant , Infusions, Intravenous , Isotonic Solutions/adverse effects , Randomized Controlled Trials as Topic
18.
J Neurol Surg A Cent Eur Neurosurg ; 76(4): 279-90, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25539069

ABSTRACT

BACKGROUND: Dysnatremias are common and prognostically serious in neurocritical care. We studied whether a standardized sodium protocol would improve our neurocritical care of dysnatremias. METHODS: A 5-year prospective study of a standardized sodium protocol for 1,560 patients admitted with various brain diseases in an adult neurologic-neurosurgical intensive care unit (NNICU) was compared with a 5-year retrospective analysis of 1,440 patients without the sodium protocol. Hyponatremia was defined as serum sodium (SNa(+)) < 135 mmol/L and hypernatremia SNa(+ )> 150 mmol/L. The sodium protocol involved measuring SNa(+), serum, and urine osmolality, measured and calculated renal function parameters, fluid intake 40 mL/kg weight/day without hypotonic saline, thiazide, and desmopressin acetate in all normonatremic NNICU patients. RESULTS: In the protocol study, hyponatremia occurred slightly less often (15.7 versus 16.3% of patients; p = 0.684), hypernatremia was significantly higher (respectively 8.5% versus 5.2% of patients; p < 0.001), and no differences were noted in hypo/hypernatremia (p = 0.483). There were no differences in the incidence of hypo-osmolal hyponatremia (respectively 3.5% versus 3.5% of patients; p = 0.987), cerebral salt wasting (CSW; respectively 1.7% versus 1.7% of patients; p = 0.883), syndrome of inappropriate secretion of antidiuretic hormone (SIADH; respectively 0.1% versus 0.3% of patients; p = 0.152), central diabetes insipidus (CDI; respectively 1.0% versus 0.6% of patients; p = 0.149). In hyponatremia there were no differences in the Glasgow Coma Scale (GCS) score upon onset of hyponatremia (p = 0.294), NNICU mortality (respectively 1.0% versus 0.4% patients; p = 0.074), and bad outcome upon discharge from NNICU (respectively 5.1% versus 6.5% of patients; p = 0.101), but in hypernatremia GCS score upon onset (p < 0.001), mortality (respectively 2.8% versus 1.0%; p < 0.001), and bad outcome from NNICU (respectively 6.7% versus 2.7% patients; p < 0.001) were significantly higher. Multivariate logistic regression analysis showed that hypernatremia, compared with hyponatremia, was a significant predictor of mortality during NNICU stay (respectively odds ratio [OR]: 1.14; p = 0.003 versus OR; 5.3; p = 0.002). CONCLUSIONS: The standard sodium protocol lowered the frequency of SIADH, which was encountered in only one patient over 5 years. However, it did not significantly reduce the incidence and improve the outcome of hyponatremia. Hypernatremia occurred more often and had a higher mortality and worse outcome than hyponatremia, but these patients were neurologically worse upon its onset. The prospective study confirmed that CSW, SIADH, and CDI were not common in our neurocritical care.


Subject(s)
Critical Care/methods , Hypernatremia/diagnosis , Hypernatremia/drug therapy , Hyponatremia/diagnosis , Hyponatremia/drug therapy , Nervous System Diseases/therapy , Sodium/therapeutic use , Aged , Deamino Arginine Vasopressin/therapeutic use , Diuretics/therapeutic use , Female , Humans , Hypernatremia/epidemiology , Hyponatremia/epidemiology , Hypotonic Solutions/therapeutic use , Iatrogenic Disease , Incidence , Male , Middle Aged , Nervous System Diseases/complications , Osmolar Concentration , Prospective Studies , Renal Agents/therapeutic use , Retrospective Studies , Sodium/administration & dosage , Sodium/blood , Thiazides/therapeutic use , Treatment Outcome
19.
Biomed Res Int ; 2014: 754182, 2014.
Article in English | MEDLINE | ID: mdl-25197657

ABSTRACT

PURPOSE: To report the 12-month outcomes of corneal collagen cross-linking (CXL) with a hypoosmolar riboflavin and ultraviolet-A (UVA) irradiation in thin corneas. METHODS: Eight eyes underwent CXL using a hypoosmolar riboflavin solution after epithelial removal. The corrected distance visual acuity (CDVA), manifest refraction, the mean thinnest corneal thickness (MTCT), and the endothelial cell density (ECD) were evaluated before and 6 and 12 months after CXL. RESULTS: The MTCT was 413.9 ± 12.4 µm before treatment and reduced to 381.1 ± 7.3 µm after the removal of the epithelium. After CXL, the thickness decreased to 410.3 ± 14.5 µm at the last follow-up. Before treatment, the mean K-value of the apex of the keratoconus corneas was 58.7 ± 3.5 diopters and slightly decreased (57.7 ± 4.9 diopters) at 12 months. The mean CDVA was 0.54 ± 0.23 logarithm of the minimal angle of resolution before treatment and increased to 0.51 ± 0.21 logarithm at the last follow-up. The ECD was 2731.4 ± 191.8 cells/mm(2) before treatment and was 2733.4 ± 222.6 cells/mm(2) at 12 months after treatment. CONCLUSIONS: CXL with a hypoosmolar riboflavin in thin corneas seems to be a promising method for keratoconic eyes with the mean thinnest corneal thickness less than 400 µm without epithelium.


Subject(s)
Collagen/metabolism , Cornea/metabolism , Cross-Linking Reagents/metabolism , Hypotonic Solutions/therapeutic use , Keratoconus/drug therapy , Riboflavin/therapeutic use , Adult , Cell Count , Cornea/drug effects , Cornea/pathology , Corneal Pachymetry , Endothelial Cells/drug effects , Endothelial Cells/pathology , Epithelium, Corneal/drug effects , Epithelium, Corneal/pathology , Female , Humans , Hypotonic Solutions/pharmacology , Keratoconus/pathology , Keratoconus/physiopathology , Male , Riboflavin/pharmacology , Solutions , Visual Acuity
20.
Nefrología (Madr.) ; 34(4): 477-482, jul.-ago. 2014. tab
Article in Spanish | IBECS | ID: ibc-129628

ABSTRACT

Objetivo: Determinar si la utilización de sueros hipotónicos supone un riesgo en la aparición de hiponatremia iatrogénica en los niños hospitalizados por gastroenteritis aguda (GEA). Pacientes y método: Estudio prospectivo realizado con 205 pacientes de edades comprendidas entre 1 y 28 meses e ingresados con diagnóstico de deshidratación leve o moderada por GEA para recibir sueroterapia en la sección de lactantes de un hospital pediátrico de Madrid (España). El grado de deshidratación inicial se estimó con mediciones clínicas estándar. El suero administrado fue glucosalino 0,3 % en 198 casos y en los 7 casos restantes, todos con hipernatremia inicial, se administró suero glucohiposalino 0,2 %. Se analizó la respuesta a los líquidos intravenosos según si el niño se hallaba normo, hipo o hipernatrémico antes de iniciar el tratamiento. Las cifras de sodio en sangre y la excreción fraccional de sodio (EFNa) se consideraron como medidas de resultado. Resultados: Los 205 pacientes incluidos en el estudio se distribuyeron en tres grupos según el resultado inicial de la natremia. En 37 casos se detectó hiponatremia (18,04 %), en 133 niños isonatremia (64,87 %) y en 35 niños hipernatremia (17,07 %). Después de administrar soluciones hipotónicas encontramos en todos los grupos diferencia significativa entre el sodio sérico inicial y el final; en el grupo con hiponatremia el sodio subió y en los grupos con iso e hipernatremia el sodio descendió ligeramente. Se evidenció correlación significativa entre la EFNa y la evolución de la natremia (Na sérico inicial - Na sérico final). No se detectó ningún caso de hiponatremia posinfusión y tampoco se encontró correlación entre el agua libre administrada y la evolución de la natremia. Conclusiones: En lactantes con funcionamiento renal normal no se ha encontrado hiponatremia como resultado de la administración de sueros hiposalinos intravenosos, hallándose diferencias significativas en la EFNa que indican el ajuste renal de la natremia (AU)


Objective: The purpose of this study is to analyse whether the use of hypotonic fluids increases the risk of iatrogenic hyponatraemia in children hospitalised with acute gastroenteritis (AGE). Patients and methods: Prospective study carried out on 205 patients with ages ranging from 1 to 28 months and admitted with a diagnosis of mild or moderate dehydration due to AGE and treated with intravenous hypotonic fluids in a paediatric department in Madrid (Spain). The degree of dehydration at presentation was estimated using standard clinical measures. 198 children received 0.3 % glucosaline solution and in 7 patients, with baseline hypernatraemia, 0.2 % gluco-hyposaline solution was administered. We analysed the results according to whether children were hyponatraemic, normonatraemic or hypernatraemic at presentation. The blood and urine samples were analysed and the concentration of sodium and fractional sodium excretion (EFNa) before and after intervention were considered as outcome measures. Results: The 205 patients included in the study were distributed in 3 groups according to the baseline natraemia results. In 37 cases we detected hyponatraemia (18.04%), in 133 cases isonatraemia (64.87%) and in 35 children hypernatraemia (17.07%). After administering hypotonic fluids we detected a significant difference between initial and final natraemia in all groups; in the group with hyponatraemia, sodium increased and in the groups with iso and hypernatraemia, sodium slightly decreased. A significant correlation between the EFNa and the evolution of natraemia was found. No cases of hyponatraemia post-infusion were seen and there was no correlation between free water administered and natraemia evolution. Conclusions: Results show that the use of hypotonic fluids does not increase the risk of hospital acquired hyponatraemia in hospitalised children with normal renal function. Our children with gastroenteritis did not develop hyponatraemia even though they were all treated with hypotonic intravenous solutions (AU)


Subject(s)
Humans , Male , Female , Infant , Gastroenteritis/complications , Hyponatremia/prevention & control , Saline Solution, Hypertonic/adverse effects , Prospective Studies , Child, Hospitalized/statistics & numerical data , Fluid Therapy/methods , Hypotonic Solutions/therapeutic use
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