Pub Date : 2016-07-01Epub Date: 2016-05-11DOI: 10.1111/vec.12485
Denise T Fantoni, Keila K Ida, Thomas F T Lopes, Denise A Otsuki, José Otávio C Auler, Aline M Ambrósio
Objective: To compare the effects of pressure controlled ventilation (PCV) with volume-controlled ventilation (VCV) on lung compliance, gas exchange, and hemodynamics in isoflurane-anesthetized dogs.
Interventions: Dogs were randomly assigned to be ventilated with 100% oxygen using PCV (n = 20) or VCV (n = 20). The respiratory rate was 20/min and positive end-expiratory pressure (PEEP) was 5 cm H2 O, with a tidal volume of 10 mL/kg. Cardiac output (CO) was measured using thermodilution. Cardiopulmonary and blood gas data were obtained during spontaneous ventilation and after 30 (T30) and 60 minutes (T60) of controlled ventilation.
Measurements and main results: In dogs ventilated with PCV, at T30 and T60, PIP was lower (11.4 ± 1.9 and 11.1 ± 1.5 cm H2 O, respectively) and static compliance (CST ) was higher (51 ± 7 and 56 ± 6 mL/cm H2 O, respectively) than in VCV group (PIP of 14.3 ± 1.3 and 15.5 ± 1.4 cm H2 O; CST of 34 ± 8 and 33 ± 9 mL/cm H2 O, P < 0.0001). Compared with spontaneous ventilation, both groups had decreased alveolar-arterial oxygen difference at T30 and T60 (PCV: 128 ± 32 mm Hg vs 108 ± 20 and 104 ± 16 mm Hg, respectively; VCV: 131 ± 38 mm Hg vs 109 ± 19 and 107 ± 14 mm Hg, respectively; P < 0.01), while CO was maintained at all time points.
Conclusions: Compared to spontaneous ventilation, both ventilatory modes effectively improved gas exchange without hemodynamic impairment. PCV resulted in higher lung CST and lower PIP compared to VCV.
目的:比较压力控制通气(PCV)和容量控制通气(VCV)对异氟醚麻醉犬肺顺应性、气体交换和血流动力学的影响。设计:前瞻性随机研究。单位:兽医教学医院。动物:40只客户拥有的母狗接受选择性卵巢子宫切除术。干预措施:狗被随机分配到使用PCV (n = 20)或VCV (n = 20)进行100%氧气通气。呼吸速率20次/min,呼气末正压(PEEP) 5 cm H2 O,潮气量10 mL/kg。心输出量(CO)采用热稀释法测定。自动通气时、控制通气30分钟(T30)和60分钟(T60)后的心肺和血气数据。测量结果及主要结果:PCV通气犬在T30和T60时,PIP低于VCV组(分别为11.4±1.9和11.1±1.5 cm H2 O),静态顺应性(CST)高于VCV组(PIP分别为14.3±1.3和15.5±1.4 cm H2 O)(分别为51±7和56±6 mL/cm H2 O);CST分别为34±8和33±9 mL/cm H2 O, P < 0.0001)。与自发通气相比,两组在T30和T60时肺泡-动脉氧差均降低(PCV分别为128±32 mm Hg vs 108±20和104±16 mm Hg;VCV分别为131±38 mm Hg vs 109±19和107±14 mm Hg;P < 0.01),而CO在各时间点均保持不变。结论:与自发通气相比,两种通气方式均能有效改善气体交换,且无血流动力学损伤。与VCV相比,PCV导致更高的肺CST和更低的PIP。
{"title":"A comparison of the cardiopulmonary effects of pressure controlled ventilation and volume controlled ventilation in healthy anesthetized dogs.","authors":"Denise T Fantoni, Keila K Ida, Thomas F T Lopes, Denise A Otsuki, José Otávio C Auler, Aline M Ambrósio","doi":"10.1111/vec.12485","DOIUrl":"https://doi.org/10.1111/vec.12485","url":null,"abstract":"<p><strong>Objective: </strong>To compare the effects of pressure controlled ventilation (PCV) with volume-controlled ventilation (VCV) on lung compliance, gas exchange, and hemodynamics in isoflurane-anesthetized dogs.</p><p><strong>Design: </strong>Prospective randomized study.</p><p><strong>Setting: </strong>Veterinary teaching hospital.</p><p><strong>Animals: </strong>Forty client-owned bitches undergoing elective ovariohysterectomy.</p><p><strong>Interventions: </strong>Dogs were randomly assigned to be ventilated with 100% oxygen using PCV (n = 20) or VCV (n = 20). The respiratory rate was 20/min and positive end-expiratory pressure (PEEP) was 5 cm H2 O, with a tidal volume of 10 mL/kg. Cardiac output (CO) was measured using thermodilution. Cardiopulmonary and blood gas data were obtained during spontaneous ventilation and after 30 (T30) and 60 minutes (T60) of controlled ventilation.</p><p><strong>Measurements and main results: </strong>In dogs ventilated with PCV, at T30 and T60, PIP was lower (11.4 ± 1.9 and 11.1 ± 1.5 cm H2 O, respectively) and static compliance (CST ) was higher (51 ± 7 and 56 ± 6 mL/cm H2 O, respectively) than in VCV group (PIP of 14.3 ± 1.3 and 15.5 ± 1.4 cm H2 O; CST of 34 ± 8 and 33 ± 9 mL/cm H2 O, P < 0.0001). Compared with spontaneous ventilation, both groups had decreased alveolar-arterial oxygen difference at T30 and T60 (PCV: 128 ± 32 mm Hg vs 108 ± 20 and 104 ± 16 mm Hg, respectively; VCV: 131 ± 38 mm Hg vs 109 ± 19 and 107 ± 14 mm Hg, respectively; P < 0.01), while CO was maintained at all time points.</p><p><strong>Conclusions: </strong>Compared to spontaneous ventilation, both ventilatory modes effectively improved gas exchange without hemodynamic impairment. PCV resulted in higher lung CST and lower PIP compared to VCV.</p>","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 4","pages":"524-30"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12485","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34538622","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-07-01Epub Date: 2016-05-27DOI: 10.1111/vec.12494
Kaoru Tsuruta, F A Mann, Robert C Backus
Objective: To describe the use of postoperative intrajejunal feeding and to evaluate the association of preoperative plasma albumin concentrations with intrajejunal feeding-related complications and clinical outcome.
Design: Prospective, observational study.
Setting: University veterinary teaching hospital.
Animals: Sixty-four dogs.
Interventions: Jejunostomy tube placement during abdominal surgery.
Measurements and main results: Most dogs (81%) survived. The median intrajejunal feeding period was 2.1 days (range: 1-16 days; n = 64). Only 3 (5%) dogs received their estimated resting energy requirement by intrajejunal feeding. Of dogs that were fed intrajejunally (58 out of 64), most (55 out of 58) received intrajejunal feeding within 24 hours after surgery. Energy provision via the jejunal feeding tube did not differ between dogs with and without complications (P = 0.592), or between nonsurvivors and survivors (P = 0.298). Thirty-five dogs ate voluntarily concurrently with intrajejunal feeding. Of dogs that ate voluntarily concurrently with intrajejunal feeding for ≤50% of the postoperative period, most (74%) survived to discharge. Complications were seen in 22% of dogs, and none were life-threatening; gastrointestinal signs were most common. There was no difference in preoperative plasma albumin concentration between dogs with and without complications (P = 0.432) and between nonsurvivors and survivors (P = 0.727). Fecal score was not significantly different between the 2 liquid diets studied (FormulaV Enteral Care HLP and CliniCare Canine/Feline; P = 0.927).
Conclusions: A jejunostomy tube placed during abdominal surgery was likely to be used at the study institution. Few complications were seen and none were life-threatening. Intrajejunal feeding was initiated early after surgery and did not interfere with the initiation of voluntary oral intake. Fecal scores were high and were useful for an objective assessment of fecal consistency in dogs with intrajejunal feeding.
{"title":"Evaluation of jejunostomy tube feeding after abdominal surgery in dogs.","authors":"Kaoru Tsuruta, F A Mann, Robert C Backus","doi":"10.1111/vec.12494","DOIUrl":"https://doi.org/10.1111/vec.12494","url":null,"abstract":"<p><strong>Objective: </strong>To describe the use of postoperative intrajejunal feeding and to evaluate the association of preoperative plasma albumin concentrations with intrajejunal feeding-related complications and clinical outcome.</p><p><strong>Design: </strong>Prospective, observational study.</p><p><strong>Setting: </strong>University veterinary teaching hospital.</p><p><strong>Animals: </strong>Sixty-four dogs.</p><p><strong>Interventions: </strong>Jejunostomy tube placement during abdominal surgery.</p><p><strong>Measurements and main results: </strong>Most dogs (81%) survived. The median intrajejunal feeding period was 2.1 days (range: 1-16 days; n = 64). Only 3 (5%) dogs received their estimated resting energy requirement by intrajejunal feeding. Of dogs that were fed intrajejunally (58 out of 64), most (55 out of 58) received intrajejunal feeding within 24 hours after surgery. Energy provision via the jejunal feeding tube did not differ between dogs with and without complications (P = 0.592), or between nonsurvivors and survivors (P = 0.298). Thirty-five dogs ate voluntarily concurrently with intrajejunal feeding. Of dogs that ate voluntarily concurrently with intrajejunal feeding for ≤50% of the postoperative period, most (74%) survived to discharge. Complications were seen in 22% of dogs, and none were life-threatening; gastrointestinal signs were most common. There was no difference in preoperative plasma albumin concentration between dogs with and without complications (P = 0.432) and between nonsurvivors and survivors (P = 0.727). Fecal score was not significantly different between the 2 liquid diets studied (FormulaV Enteral Care HLP and CliniCare Canine/Feline; P = 0.927).</p><p><strong>Conclusions: </strong>A jejunostomy tube placed during abdominal surgery was likely to be used at the study institution. Few complications were seen and none were life-threatening. Intrajejunal feeding was initiated early after surgery and did not interfere with the initiation of voluntary oral intake. Fecal scores were high and were useful for an objective assessment of fecal consistency in dogs with intrajejunal feeding.</p>","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 4","pages":"502-8"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12494","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34523758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-07-01Epub Date: 2016-06-15DOI: 10.1111/vec.12496
Lesleigh A Redavid, Claire R Sharp, Mark A Mitchell, Nicole F Beckel
Objectives: To document the incidence of hyperlactatemia in sick cats hospitalized for emergency care and to evaluate the prognostic utility of serial lactate measurements in cats with hyperlactatemia.
Design: Prospective observational study over a 10-month period (July 2010-May 2011).
Setting: Private veterinary referral center with 24-hour hospital care.
Animals: One hundred and twenty-three privately owned cats admitted to a private referral center.
Interventions: Blood was collected by direct venipuncture from the jugular or medial saphenous vein at the time of hospital admission and at 6 and 24 hours following admission.
Measurements and main results: The median plasma lactate concentration for all cats at admission (T0) was 1.89 mmol/L (17.0 mg/dL) (range: 0.3-12.48). Twenty-three percent (28/123) of cats admitted were hyperlactatemic (ie, >2.87 mmol/L; >25.86 mg/dL) upon admission. Lactate concentration at presentation and serial lactate measurements were not found to be related with survival to discharge or correlated with duration of hospitalization. The overall survival rate of all cats in this study was 81%.
Conclusions: This study demonstrated that the incidence of hyperlactatemia in sick cats being admitted for hospitalization in a private referral center was 23%, and that lactate concentration on admission and serial lactate measurements over time were not prognostic in this group of hospitalized cats. Future studies are needed to evaluate the prognostic utility of lactate and serial lactate measurements in specific disease states and in a larger population of critically ill cats.
{"title":"Hyperlactatemia and serial lactate measurements in sick cats.","authors":"Lesleigh A Redavid, Claire R Sharp, Mark A Mitchell, Nicole F Beckel","doi":"10.1111/vec.12496","DOIUrl":"https://doi.org/10.1111/vec.12496","url":null,"abstract":"<p><strong>Objectives: </strong>To document the incidence of hyperlactatemia in sick cats hospitalized for emergency care and to evaluate the prognostic utility of serial lactate measurements in cats with hyperlactatemia.</p><p><strong>Design: </strong>Prospective observational study over a 10-month period (July 2010-May 2011).</p><p><strong>Setting: </strong>Private veterinary referral center with 24-hour hospital care.</p><p><strong>Animals: </strong>One hundred and twenty-three privately owned cats admitted to a private referral center.</p><p><strong>Interventions: </strong>Blood was collected by direct venipuncture from the jugular or medial saphenous vein at the time of hospital admission and at 6 and 24 hours following admission.</p><p><strong>Measurements and main results: </strong>The median plasma lactate concentration for all cats at admission (T0) was 1.89 mmol/L (17.0 mg/dL) (range: 0.3-12.48). Twenty-three percent (28/123) of cats admitted were hyperlactatemic (ie, >2.87 mmol/L; >25.86 mg/dL) upon admission. Lactate concentration at presentation and serial lactate measurements were not found to be related with survival to discharge or correlated with duration of hospitalization. The overall survival rate of all cats in this study was 81%.</p><p><strong>Conclusions: </strong>This study demonstrated that the incidence of hyperlactatemia in sick cats being admitted for hospitalization in a private referral center was 23%, and that lactate concentration on admission and serial lactate measurements over time were not prognostic in this group of hospitalized cats. Future studies are needed to evaluate the prognostic utility of lactate and serial lactate measurements in specific disease states and in a larger population of critically ill cats.</p>","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 4","pages":"495-501"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12496","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34580648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-07-01Epub Date: 2016-06-10DOI: 10.1111/vec.12497
Deborah Silverstein, Lori Waddell, Ken Drobatz
This memorial column pays tribute to Robert T. Chuck, past‐president of AWWA from 1986‐87. He passed away on Dec. 27, 2012. His long career in the water industry in his native Hawaii is outlined, along with his involvement with AWWA and other water industry associations.
{"title":"In Memoriam.","authors":"Deborah Silverstein, Lori Waddell, Ken Drobatz","doi":"10.1111/vec.12497","DOIUrl":"https://doi.org/10.1111/vec.12497","url":null,"abstract":"This memorial column pays tribute to Robert T. Chuck, past‐president of AWWA from 1986‐87. He passed away on Dec. 27, 2012. His long career in the water industry in his native Hawaii is outlined, along with his involvement with AWWA and other water industry associations.","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 4","pages":"469-70"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12497","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34566657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-07-01Epub Date: 2016-04-08DOI: 10.1111/vec.12473
Jonathan A Lidbury, Audrey K Cook, Jörg M Steiner
Objective: To comparatively review the pathogenesis, clinical presentation, diagnosis, and management of hepatic encephalopathy (HE) in dogs and cats.
Data sources: The Medline database was searched for articles related to HE in people, dogs, and cats. Articles published within the last 5 years were given special importance.
Human data synthesis: The pathogenesis of HE is complex and incompletely understood, but ammonia appears to play a central role. Hyperammonemia leads to accumulation of glutamine in astrocytes, with subsequent astrocyte swelling and neurological dysfunction. The development of HE in patients with hepatic cirrhosis is a poor prognostic indicator. The fermentable disaccharide lactulose and the antimicrobial rifaximin are US Food and Drug Administration approved treatments for human HE. Severe protein restriction is no longer recommended for patients with this condition.
Veterinary data synthesis: HE is often associated with portosystemic shunting in dogs and cats. Ammonia plays a central role in the pathogenesis of HE in dogs and cats, but other factors such as manganese and endogenous benzodiazepines may also contribute. Recently, a soy protein-based diet was found to be beneficial in treating canine HE. Severe dietary protein restriction is likely to be detrimental in affected animals. There have been no clinical trials of drugs routinely used in the management HE in veterinary medicine, but lactulose and antimicrobials such as metronidazole are well-established treatments.
Conclusions: HE is a potentially life-threatening condition that is probably underdiagnosed in companion animals. Although various treatment recommendations have been proposed, there is a lack of evidence in the veterinary literature regarding optimal strategies for the management of this condition. As our understanding of the pathogenesis of HE in dogs and cats evolves, novel diagnostic tests and therapeutic agents may become available.
{"title":"Hepatic encephalopathy in dogs and cats.","authors":"Jonathan A Lidbury, Audrey K Cook, Jörg M Steiner","doi":"10.1111/vec.12473","DOIUrl":"https://doi.org/10.1111/vec.12473","url":null,"abstract":"<p><strong>Objective: </strong>To comparatively review the pathogenesis, clinical presentation, diagnosis, and management of hepatic encephalopathy (HE) in dogs and cats.</p><p><strong>Data sources: </strong>The Medline database was searched for articles related to HE in people, dogs, and cats. Articles published within the last 5 years were given special importance.</p><p><strong>Human data synthesis: </strong>The pathogenesis of HE is complex and incompletely understood, but ammonia appears to play a central role. Hyperammonemia leads to accumulation of glutamine in astrocytes, with subsequent astrocyte swelling and neurological dysfunction. The development of HE in patients with hepatic cirrhosis is a poor prognostic indicator. The fermentable disaccharide lactulose and the antimicrobial rifaximin are US Food and Drug Administration approved treatments for human HE. Severe protein restriction is no longer recommended for patients with this condition.</p><p><strong>Veterinary data synthesis: </strong>HE is often associated with portosystemic shunting in dogs and cats. Ammonia plays a central role in the pathogenesis of HE in dogs and cats, but other factors such as manganese and endogenous benzodiazepines may also contribute. Recently, a soy protein-based diet was found to be beneficial in treating canine HE. Severe dietary protein restriction is likely to be detrimental in affected animals. There have been no clinical trials of drugs routinely used in the management HE in veterinary medicine, but lactulose and antimicrobials such as metronidazole are well-established treatments.</p><p><strong>Conclusions: </strong>HE is a potentially life-threatening condition that is probably underdiagnosed in companion animals. Although various treatment recommendations have been proposed, there is a lack of evidence in the veterinary literature regarding optimal strategies for the management of this condition. As our understanding of the pathogenesis of HE in dogs and cats evolves, novel diagnostic tests and therapeutic agents may become available.</p>","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 4","pages":"471-87"},"PeriodicalIF":0.0,"publicationDate":"2016-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12473","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34750749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OBJECTIVE To measure platelet closure time (PCT) in dogs during controlled hemorrhagic shock and after fluid resuscitation with hydroxyethyl starch (HES) 130/0.4 or 0.9% sodium chloride. DESIGN Experimental interventional study. SETTING University veterinary teaching hospital. ANIMALS Eleven healthy Greyhounds. INTERVENTIONS Dogs were anesthetized and had 48 mL/kg of blood removed to induce hemorrhagic shock. Dogs received 20 mL/kg of HES 130/0.4 (n = 6) or 80 mL/kg of 0.9% sodium chloride (NaCl; n = 5) intravenously over 20 minutes. PCT was measured using the Platelet Function Analyzer-100 with collagen and adenosine-diphosphate cartridges at: T0 = 60 minutes after induction of anesthesia prior to hemorrhage, T1 = during hemorrhagic shock, and T2 = 40 minutes after completion of fluid bolus. Packed cell volume and platelet count were concurrently measured. MEASUREMENT AND MAIN RESULTS Hemorrhagic shock did not significantly change PCT, with no difference between T0 and T1. Both the HES 130/0.4 and 0.9% NaCl group had a significantly increased mean PCT at T2 of 91.4 seconds (95% CI 69.3-113.4) and 95.5 seconds (95% CI 78.2-112.8), respectively, compared to T1. The magnitude of change was significantly greater for the 0.9% NaCl group than the HES 130/0.4 group. There was no difference in the magnitude of change in PCV and platelet count between the 2 groups. The PCV and platelet count were >25% and >100,000/μL, respectively, in all dogs, except for dogs in the HES 130/0.4 group at T2 where platelet counts were <100,000/μL. CONCLUSION Controlled hemorrhagic shock in Greyhounds under anesthesia did not cause a significant change in PCT. Both HES 130/0.4 and 0.9% NaCl administration after induction of shock increased PCT. These results do not support that HES 130/0.4 causes relevant platelet dysfunction beyond hemodilution.
{"title":"Platelet closure time in anesthetized Greyhounds with hemorrhagic shock treated with hydroxyethyl starch 130/0.4 or 0.9% sodium chloride infusions.","authors":"D. McBride, G. Hosgood, A. Raisis, L. Smart","doi":"10.1111/vec.12468","DOIUrl":"https://doi.org/10.1111/vec.12468","url":null,"abstract":"OBJECTIVE\u0000To measure platelet closure time (PCT) in dogs during controlled hemorrhagic shock and after fluid resuscitation with hydroxyethyl starch (HES) 130/0.4 or 0.9% sodium chloride.\u0000\u0000\u0000DESIGN\u0000Experimental interventional study.\u0000\u0000\u0000SETTING\u0000University veterinary teaching hospital.\u0000\u0000\u0000ANIMALS\u0000Eleven healthy Greyhounds.\u0000\u0000\u0000INTERVENTIONS\u0000Dogs were anesthetized and had 48 mL/kg of blood removed to induce hemorrhagic shock. Dogs received 20 mL/kg of HES 130/0.4 (n = 6) or 80 mL/kg of 0.9% sodium chloride (NaCl; n = 5) intravenously over 20 minutes. PCT was measured using the Platelet Function Analyzer-100 with collagen and adenosine-diphosphate cartridges at: T0 = 60 minutes after induction of anesthesia prior to hemorrhage, T1 = during hemorrhagic shock, and T2 = 40 minutes after completion of fluid bolus. Packed cell volume and platelet count were concurrently measured.\u0000\u0000\u0000MEASUREMENT AND MAIN RESULTS\u0000Hemorrhagic shock did not significantly change PCT, with no difference between T0 and T1. Both the HES 130/0.4 and 0.9% NaCl group had a significantly increased mean PCT at T2 of 91.4 seconds (95% CI 69.3-113.4) and 95.5 seconds (95% CI 78.2-112.8), respectively, compared to T1. The magnitude of change was significantly greater for the 0.9% NaCl group than the HES 130/0.4 group. There was no difference in the magnitude of change in PCV and platelet count between the 2 groups. The PCV and platelet count were >25% and >100,000/μL, respectively, in all dogs, except for dogs in the HES 130/0.4 group at T2 where platelet counts were <100,000/μL.\u0000\u0000\u0000CONCLUSION\u0000Controlled hemorrhagic shock in Greyhounds under anesthesia did not cause a significant change in PCT. Both HES 130/0.4 and 0.9% NaCl administration after induction of shock increased PCT. These results do not support that HES 130/0.4 causes relevant platelet dysfunction beyond hemodilution.","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"35 1","pages":"509-15"},"PeriodicalIF":0.0,"publicationDate":"2016-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12468","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63497861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-01-01Epub Date: 2015-07-20DOI: 10.1111/vec.12344
Jill S Manion, John M Thomason, Vernon C Langston, Andrew K Claude, Marjory B Brooks, Andrew J Mackin, Kari V Lunsford
Objective: To evaluate the anticoagulant effects of inhaled heparin in dogs.
Design: This study was conducted in 3 phases. In phase 1, bronchoalveolar lavage fluid (BALf) was collected to generate an in vitro calibration curve to relate heparin concentration to the activated partial thromboplastin time (aPTT). In phase 2, heparin was administered via nebulization to determine the threshold dose needed to prolong systemic aPTT. In phase 3, the local anticoagulant activity of inhaled heparin was determined by measurement of BALf anti-Xa activity and aPTT.
Setting: University teaching hospital.
Animals: Six healthy intact female Walker Hounds were used in this study. Two dogs were used for each phase.
Interventions: Inhaled unfractionated sodium heparin was administered in doses ranging from 50,000 to 200,000 IU.
Results: In vitro addition of heparin to BALf caused a prolongation in aPTT. Inhaled heparin at doses as high as 200,000 IU failed to prolong systemic aPTT, and a threshold dose could not be determined. No significant local anticoagulant effects were detected.
Conclusions: Even at doses higher than those known to be effective in people, inhaled heparin appears to have no detectable local or systemic anticoagulant effects in dogs with the current delivery method.
{"title":"Anticoagulant effects of inhaled unfractionated heparin in the dog as determined by partial thromboplastin time and factor Xa activity.","authors":"Jill S Manion, John M Thomason, Vernon C Langston, Andrew K Claude, Marjory B Brooks, Andrew J Mackin, Kari V Lunsford","doi":"10.1111/vec.12344","DOIUrl":"https://doi.org/10.1111/vec.12344","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the anticoagulant effects of inhaled heparin in dogs.</p><p><strong>Design: </strong>This study was conducted in 3 phases. In phase 1, bronchoalveolar lavage fluid (BALf) was collected to generate an in vitro calibration curve to relate heparin concentration to the activated partial thromboplastin time (aPTT). In phase 2, heparin was administered via nebulization to determine the threshold dose needed to prolong systemic aPTT. In phase 3, the local anticoagulant activity of inhaled heparin was determined by measurement of BALf anti-Xa activity and aPTT.</p><p><strong>Setting: </strong>University teaching hospital.</p><p><strong>Animals: </strong>Six healthy intact female Walker Hounds were used in this study. Two dogs were used for each phase.</p><p><strong>Interventions: </strong>Inhaled unfractionated sodium heparin was administered in doses ranging from 50,000 to 200,000 IU.</p><p><strong>Results: </strong>In vitro addition of heparin to BALf caused a prolongation in aPTT. Inhaled heparin at doses as high as 200,000 IU failed to prolong systemic aPTT, and a threshold dose could not be determined. No significant local anticoagulant effects were detected.</p><p><strong>Conclusions: </strong>Even at doses higher than those known to be effective in people, inhaled heparin appears to have no detectable local or systemic anticoagulant effects in dogs with the current delivery method.</p>","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 1","pages":"132-6"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12344","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33921367","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OBJECTIVE To determine whether early insulin administration (≤6 h after admission) results in more rapid resolution of diabetic ketosis (DK) and ketoacidosis (DKA), shorter duration of hospitalization, and higher incidence of complications, and whether more severe ketonuria is associated with longer time to resolution of DK/DKA. DESIGN Retrospective study (January 1, 2003-March 1, 2013). SETTING University teaching hospital. ANIMALS Sixty dogs and cats with DK or DKA receiving short-acting insulin therapy. INTERVENTIONS None. MEASUREMENTS AND MAIN RESULTS Medical records were reviewed and data recorded including signalment; previous history of diabetes; intake temperature, blood pressure, blood glucose, pH, base excess, and degree of ketonuria; time to short-acting insulin therapy and resolution of DK/DKA; length of hospitalization; and complications. Insulin was initiated ≤6 hours in the early group and >6 hours in the late group after hospital admission. Early group patients had more rapid resolution of DK/DKA after starting short-acting insulin therapy (36.4 ± 22.6 vs. 55.4 ± 26.6 h, P = 0.014). There was no difference in duration of hospitalization or complications. More severe ketonuria resulted in longer time to resolution of DK/DKA after initiation of short-acting insulin (severe: 50.9 ± 24.2; moderate: 29.6 ± 19; mild: 23.4 ± 21.9 h, P = 0.005, all individual pairwise comparisons P < 0.05). CONCLUSIONS Early insulin administration is associated with more rapid resolution of DK/DKA without an associated increase in complication rates. DK/DKA took longer to resolve with more severe ketonuria. Prospective studies are warranted to identify specific time targets for insulin administration in DK/DKA patients.
目的探讨早期(入院后≤6 h)给予胰岛素是否能更快地缓解糖尿病酮症(DK)和酮症酸中毒(DKA),缩短住院时间,提高并发症发生率,以及更严重的酮症尿是否与更长的DK/DKA缓解时间相关。设计回顾性研究(2003年1月1日- 2013年3月1日)。大学教学医院。动物:60只患有DK或DKA的狗和猫接受短效胰岛素治疗。干预措施和主要结果:回顾医疗记录并记录数据,包括信号;既往糖尿病史;摄入温度、血压、血糖、pH值、碱过量、尿酮程度;短效胰岛素治疗时间与DK/DKA的缓解;住院时间;和并发症。入院后早期组≤6小时,晚期组≤6小时开始使用胰岛素。早期组患者在开始短效胰岛素治疗后DK/DKA的缓解更快(36.4±22.6∶55.4±26.6 h, P = 0.014)。两组在住院时间和并发症方面无差异。越严重的尿酮症导致短效胰岛素治疗后DK/DKA的消退时间越长(重度:50.9±24.2;中度:29.6±19;轻度:23.4±21.9 h, P = 0.005,各个体两两比较P < 0.05)。结论早期胰岛素治疗与DK/DKA的快速解决相关,且未增加并发症发生率。DK/DKA的缓解时间较长,且酮症患者较多。有必要进行前瞻性研究以确定DK/DKA患者胰岛素给药的具体时间目标。
{"title":"Retrospective comparison of early- versus late-insulin therapy regarding effect on time to resolution of diabetic ketosis and ketoacidosis in dogs and cats: 60 cases (2003-2013).","authors":"Jillian DiFazio, D. Fletcher","doi":"10.1111/vec.12415","DOIUrl":"https://doi.org/10.1111/vec.12415","url":null,"abstract":"OBJECTIVE To determine whether early insulin administration (≤6 h after admission) results in more rapid resolution of diabetic ketosis (DK) and ketoacidosis (DKA), shorter duration of hospitalization, and higher incidence of complications, and whether more severe ketonuria is associated with longer time to resolution of DK/DKA. DESIGN Retrospective study (January 1, 2003-March 1, 2013). SETTING University teaching hospital. ANIMALS Sixty dogs and cats with DK or DKA receiving short-acting insulin therapy. INTERVENTIONS None. MEASUREMENTS AND MAIN RESULTS Medical records were reviewed and data recorded including signalment; previous history of diabetes; intake temperature, blood pressure, blood glucose, pH, base excess, and degree of ketonuria; time to short-acting insulin therapy and resolution of DK/DKA; length of hospitalization; and complications. Insulin was initiated ≤6 hours in the early group and >6 hours in the late group after hospital admission. Early group patients had more rapid resolution of DK/DKA after starting short-acting insulin therapy (36.4 ± 22.6 vs. 55.4 ± 26.6 h, P = 0.014). There was no difference in duration of hospitalization or complications. More severe ketonuria resulted in longer time to resolution of DK/DKA after initiation of short-acting insulin (severe: 50.9 ± 24.2; moderate: 29.6 ± 19; mild: 23.4 ± 21.9 h, P = 0.005, all individual pairwise comparisons P < 0.05). CONCLUSIONS Early insulin administration is associated with more rapid resolution of DK/DKA without an associated increase in complication rates. DK/DKA took longer to resolve with more severe ketonuria. Prospective studies are warranted to identify specific time targets for insulin administration in DK/DKA patients.","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"26 1 1","pages":"108-15"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12415","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63496900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Boller, D. Fletcher, B. Brainard, S. Haskins, K. Hopper, V. Nadkarni, P. Morley, M. McMichael, R. Nishimura, J. Robben, E. Rozanski, E. Rudloff, J. Rush, A. Shih, Sean D. Smarick, Luis H Tello
OBJECTIVE To provide recommendations for reviewing and reporting clinical in-hospital cardiopulmonary resuscitation (CPR) events in dogs and cats and to establish nonambiguous operational definitions for CPR terminology. DESIGN Consensus guidelines. SETTING International, academia, referral practice, general practice, and human medicine. METHODS An international veterinary Utstein task force was convened in April 2013 in San Francisco to determine the scope of the project, the variables to be reported, their definitions, and a reporting template. Factors that were essential for meaningful data reporting and were amenable to accurate collection (ie, core variables) and additional variables useful for research projects and hypothesis generation (ie, supplemental variables) were defined. Consensus on each item was either achieved during that meeting or during the subsequent online modified Delphi process and dialogue between task force members. RESULTS Variables were defined and categorized as hospital, animal, event (arrest), and outcome variables. This report recommends a template for standardized reporting of veterinary in-hospital CPR studies involving dogs or cats. Core elements include the suspected cause(s) and location of arrest, first rhythm identified, the occurrence of return of spontaneous circulation (ROSC) of more than 30 seconds (any ROSC) or more than 20 minutes (sustained ROSC), survival to discharge, and functional capacity at discharge. If CPR is discontinued or the patient is euthanized by owner request, a reason is reported. The task force suggests a case report form to be used for individual resuscitation events. CONCLUSIONS The availability of these veterinary small animal CPR reporting guidelines will encourage and facilitate high-quality veterinary CPR research, improve data comparison between studies and across study sites, and serve as the foundation for veterinary CPR registries.
{"title":"Utstein-style guidelines on uniform reporting of in-hospital cardiopulmonary resuscitation in dogs and cats. A RECOVER statement.","authors":"M. Boller, D. Fletcher, B. Brainard, S. Haskins, K. Hopper, V. Nadkarni, P. Morley, M. McMichael, R. Nishimura, J. Robben, E. Rozanski, E. Rudloff, J. Rush, A. Shih, Sean D. Smarick, Luis H Tello","doi":"10.1111/vec.12436","DOIUrl":"https://doi.org/10.1111/vec.12436","url":null,"abstract":"OBJECTIVE To provide recommendations for reviewing and reporting clinical in-hospital cardiopulmonary resuscitation (CPR) events in dogs and cats and to establish nonambiguous operational definitions for CPR terminology. DESIGN Consensus guidelines. SETTING International, academia, referral practice, general practice, and human medicine. METHODS An international veterinary Utstein task force was convened in April 2013 in San Francisco to determine the scope of the project, the variables to be reported, their definitions, and a reporting template. Factors that were essential for meaningful data reporting and were amenable to accurate collection (ie, core variables) and additional variables useful for research projects and hypothesis generation (ie, supplemental variables) were defined. Consensus on each item was either achieved during that meeting or during the subsequent online modified Delphi process and dialogue between task force members. RESULTS Variables were defined and categorized as hospital, animal, event (arrest), and outcome variables. This report recommends a template for standardized reporting of veterinary in-hospital CPR studies involving dogs or cats. Core elements include the suspected cause(s) and location of arrest, first rhythm identified, the occurrence of return of spontaneous circulation (ROSC) of more than 30 seconds (any ROSC) or more than 20 minutes (sustained ROSC), survival to discharge, and functional capacity at discharge. If CPR is discontinued or the patient is euthanized by owner request, a reason is reported. The task force suggests a case report form to be used for individual resuscitation events. CONCLUSIONS The availability of these veterinary small animal CPR reporting guidelines will encourage and facilitate high-quality veterinary CPR research, improve data comparison between studies and across study sites, and serve as the foundation for veterinary CPR registries.","PeriodicalId":74015,"journal":{"name":"Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)","volume":"67 1","pages":"11-34"},"PeriodicalIF":0.0,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/vec.12436","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63497552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}