Key result
Preoperative abnormal laboratory results significantly predicted postoperative abnormalities for sodium (OR 2.15; 95% CI 1.82-2.54), potassium (OR 4.22), and creatinine (OR 3.00) following TJA.
Why the study?
Routine chemistry-7 testing after total joint arthroplasty has been questioned with the rise of short-stay procedures, warranting evaluation of the incidence, risk factors, and clinical interventions for abnormal postoperative panels.
What are the incidence and risk factors for abnormal routine postoperative chem-7 panels in patients undergoing total joint arthroplasty?
Cohort (n=3,162)
What are the incidence and risk factors for abnormal routine postoperative chem-7 panels in patients undergoing total joint arthroplasty?
Routine postoperative chem-7 testing in total joint arthroplasty may only be necessary for patients with abnormal preoperative labs, preexisting renal disease, bilateral TJA, or those on specific medications like ACE inhibitors, ARBs, or diuretics.
BACKGROUND: The routine use of traditional chemistry-7 (chem-7) laboratory tests following total joint arthroplasty (TJA) has been called into question with the advent of short-stay procedures. Our objective was to determine the incidence, risk factors, and clinical interventions associated with inpatient abnormal routine postoperative chem-7 panels. METHODS: From 2015 to 2017, 3,162 patients underwent a total of 3,721 TJA procedures, including primary total hip arthroplasty (THA) (n = 1,939; 52.1%) or primary total knee arthroplasty (TKA) (n = 1,782; 47.9%). Patients underwent routine preoperative and postoperative chem-7 testing. Clinical interventions were identified. With use of mixed-effects multivariate logistic regression, potential risk factors for abnormal chemistry panel values (including preoperative chem-7 results, type of surgery, age, sex, race, comorbidities, American Society of Anesthesiologists [ASA] score, and medications) were analyzed. RESULTS: The rates of abnormal preoperative laboratory results were 3.4% for sodium (Na+), 7.4% for potassium (K+), 15.8% for blood urea nitrogen (BUN), and 26.4% for creatinine (Cr). The incidence of abnormal postoperative results was low for K+ (9.7%) and higher for Na+ (25.6%), BUN (55.6%), and Cr (27.9%). Preoperative abnormal laboratory results were a significant predictor of a postoperative abnormality for Na+ (odds ratio [OR] = 2.15; 95% confidence interval [CI] = 1.82 to 2.54), K+ (OR = 4.22; 95% CI = 3.03 to 5.88), and Cr (OR = 3.00; 95% CI = 2.45 to 3.68). Bilateral TJA was associated with increased odds of abnormal postoperative Na+ (OR = 1.56; 95% CI = 1.44 to 1.68). Renal disease was associated with increased odds of abnormal postoperative Cr (OR = 15.21; 95% CI = 5.67 to 40.77). Patients taking loop diuretics had increased odds of abnormal postoperative K+ (OR = 2.10; 95% CI = 1.42 to 3.11) and Cr (OR = 2.28; 95% CI = 1.56 to 3.33). Regarding intervention, 6.7% of hypokalemic patients received potassium chloride (KCl) fluid/tablets. Forty percent of hyponatremic patients received sodium chloride (NaCl) fluid/tablets. The electrolyte-related medicine consultation rate was 0.3% (13 of 3,721). CONCLUSIONS: On the basis of our findings, we recommend postoperative chem-7 testing for patients with an abnormal preoperative laboratory result (Na+, K+, BUN, Cr), preexisting renal disease, bilateral TJA, and prescribed angiotensin-converting enzyme inhibitors (ACE), angiotensin II receptor blockers (ARB), and diuretics. LEVEL OF EVIDENCE: Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.
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Tischler et al. (2021) conducted a cohort in Total joint arthroplasty (n=3,162). Abnormal preoperative laboratory results vs. Normal preoperative laboratory results was evaluated on Abnormal postoperative sodium (Na+) level (OR 2.15, 95% CI 1.82 to 2.54). Preoperative abnormal laboratory results significantly predicted postoperative abnormalities for sodium (OR 2.15; 95% CI 1.82-2.54), potassium (OR 4.22), and creatinine (OR 3.00) following TJA.
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