Libin Madeline B, Weltman Joel G, Prittie Jennifer
Department of Emergency and Critical Care, Animal Medical Center, New York, NY, USA.
Vet Med (Auckl). 2020 Jul 15;11:57-69. doi: 10.2147/VMRR.S253759. eCollection 2020.
To evaluate whole blood chloride concentration and hospital-acquired AKI in hospitalized canine patients. Secondary outcome measures included the volume-adjusted chloride load, in-hospital mortality and length of ICU stay.
This is a prospective, observational study. Sixty dogs admitted to the ICU and receiving IV fluid therapy for >24 hours from February 2018 to July 2019. Corrected chloride and creatinine concentrations were obtained twice daily. Total volume of IV fluid and total chloride load were recorded. Volume-adjusted chloride load (VACL) was calculated by dividing the chloride administered by the volume of fluid administered. Hospital-acquired AKI was defined as an increase in creatinine of ≥26.5 μmol/L (0.3 mg/dL) or 150% from baseline to maximum. Survival to hospital discharge or non-survival and ICU length of stay were also recorded.
Fifteen out of 60 patients developed hospital-acquired AKI. Maximum corrected chloride was significantly different in AKI group (median 122.3 mmol/L) vs non-AKI group (median 118.1 mmol/L; p=0.0002). Six out of 60 patients developed hyperchloremia. Hyperchloremic patients were significantly more likely to develop in-hospital AKI (p=0.03). Patients hospitalized ≥2 days had a significantly higher [Cl] compared to those with shorter ICU stay (121.8 ± 5.9 mmol/L vs 117.5 ± 4.3 mmol/L; p=0.002). Eight out of 60 patients were non-survivors. Maximum corrected chloride and creatinine concentrations were not significantly different between survivors and non-survivors. VACL was not significantly different between AKI or mortality groups.
Maximum corrected chloride concentration was significantly higher in dogs with hospital-acquired AKI, even amongst dogs without hyperchloremia. Additionally, maximum corrected chloride concentrations were significantly higher in dogs hospitalized in the ICU longer compared to those hospitalized for fewer than two days. There was no significant difference in VACL in any of the outcome groups. Results from this study suggest alterations in chloride may be observed alongside the development of acute kidney injuries. Future studies in critically ill dogs are warranted.
评估住院犬科患者的全血氯化物浓度及医院获得性急性肾损伤(AKI)。次要观察指标包括容量校正氯化物负荷、院内死亡率及重症监护病房(ICU)住院时长。
这是一项前瞻性观察性研究。2018年2月至2019年7月期间,60只入住ICU且接受静脉输液治疗超过24小时的犬。每天两次获取校正后的氯化物和肌酐浓度。记录静脉输液总量及总氯化物负荷。容量校正氯化物负荷(VACL)通过氯化物给药量除以液体给药量计算得出。医院获得性AKI定义为肌酐从基线至最高值增加≥26.5μmol/L(0.3mg/dL)或增加150%。记录出院存活或未存活情况及ICU住院时长。
60例患者中有15例发生医院获得性AKI。AKI组的最高校正氯化物与非AKI组(中位数118.1mmol/L)有显著差异(中位数122.3mmol/L;p = 0.0002)。60例患者中有6例发生高氯血症。高氯血症患者发生院内AKI的可能性显著更高(p = 0.03)。入住ICU≥2天的患者的[Cl]显著高于住院时间较短的患者(121.8±5.9mmol/L对117.5±4.3mmol/L;p = 0.002)。60例患者中有8例未存活。存活者与未存活者的最高校正氯化物和肌酐浓度无显著差异。AKI组或死亡组之间的VACL无显著差异。
即使在无高氯血症的犬中,医院获得性AKI犬的最高校正氯化物浓度也显著更高。此外,入住ICU时间较长的犬的最高校正氯化物浓度显著高于住院少于两天的犬。各观察指标组的VACL无显著差异。本研究结果表明,急性肾损伤发生时可能会观察到氯化物的变化。有必要对危重病犬进行进一步研究。