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Article

Incidence and Determinants of Piperacillin/Tazobactam-Associated Hypokalemia: A Retrospective Study

by
Heenam Seo
1,2 and
Eunyoung Kim
2,*
1
Department of Pharmacy, Kangbuk Samsung Hospital, Seoul 03181, Korea
2
Clinical Data Science, Evidence-Based Clinical Research, Regulatory Science Laboratory, Departments of Health Science, Clinical Pharmacy and Pharmacology, College of Pharmacy, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Korea
*
Author to whom correspondence should be addressed.
Antibiotics 2022, 11(8), 1138; https://doi.org/10.3390/antibiotics11081138
Submission received: 30 July 2022 / Revised: 16 August 2022 / Accepted: 20 August 2022 / Published: 22 August 2022
(This article belongs to the Section Antibiotic Therapy in Infectious Diseases)
Browse Figure
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Abstract

:
Piperacillin/tazobactam (TZP) is a commonly used antibiotic for treating moderate-to-severe infections because of its broad-spectrum activity and recommendation as an alternative to carbapenem. TZP-associated severe hypokalemia has been consistently reported; however, related studies are very rare. This study aimed to evaluate the incidence and risk factors of TZP-associated hypokalemia (TAH). A retrospective cohort study was conducted on hospitalized adult patients who received TZP from 1 January 2015 to 31 December 2017 at a tertiary teaching hospital. Of the 713 patients, 13.9% had TAH. As a result of multivariate logistic regression analysis, older age (OR 1.03, 95% CI: 1.02–1.05, p < 0.001), female sex (OR 1.88, 95% CI: 1.18–3.00, p = 0.008), longer duration of TZP therapy (OR 1.08, 95% CI: 1.04–1.13, p < 0.001), and higher TZP daily dose (OR 1.10, 95% CI: 1.01–1.20, p = 0.049) were independently associated with TAH. In contrast, higher baseline serum potassium level (OR 0.13, 95% CI: 0.07–0.26, p < 0.001) was related to lower TAH. Furthermore, hypokalemia mostly occurred in the early days of TZP therapy (median onset time: 4 days). Thus, close monitoring of serum potassium levels, especially upon therapy initiation, is essential to prevent TAH.

1. Introduction

Hypokalemia is an electrolyte disorder commonly encountered in clinical practice. Mild hypokalemia is generally asymptomatic; however, severe hypokalemia might cause respiratory depression, paralytic ileus, and life-threatening cardiac arrhythmias [1,2,3,4]. Additionally, it has been reported that a low serum potassium level is associated with mortality and morbidity [5,6,7,8,9,10,11] in patients with cardiovascular disease, renal conditions, and others. Thus, it is important to identify or review the causes of hypokalemia to prevent or promptly and appropriately manage the disorder.
Piperacillin/tazobactam (TZP), a combination of semisynthetic ureidopenicillin and a β-lactamase inhibitor [12], is one of the most commonly used antibiotics for a variety of moderate-to-severe infections owing to its broad-spectrum activity. It is an alternative to carbapenems to prevent carbapenem resistance [13,14,15].
Pooled data from clinical trials indicated that TZP is generally safe and well tolerated [13]. However, TZP use has a variety of side effects [14]. Hypokalemia has been known as one of the rare electrolyte abnormalities of TZP. The reported incidence of TZP-associated hypokalemia (TAH) was 1.5% in patients with urinary tract infection [16] and less than 1% in patients with nosocomial pneumonia [14]. However, recent studies reported a notably high incidence of TAH. A randomized controlled trial comparing the efficacy and safety between fosfomycin injection and TZP in complicated urinary tract infections reported a 12.6% incidence of TAH [17]. Another retrospective study by Kuramoto et al. [18] assessing the incidence and risk factors of TAH reported a much higher incidence of 24.8%. In addition, serious TAH cases, mostly accompanied by arrhythmia and treatment discontinuation, have been continuously reported [19,20,21,22,23,24,25]. Nevertheless, the risk factors of TAH have not been well known because of the lack of related studies. However, Kuramoto et al. [18] study indicated older age was the only independent risk factor for TAH.
Considering the widespread use of TZP, it is essential to perform an in-depth analysis of TAH for the safe use of TZP. Therefore, we evaluated hypokalemia’s incidence and risk factors and assessed the time of TAH onset after starting TZP therapy.

2. Results

2.1. Demographic and Clinical Characteristics of Patients

In total, 2699 adult patients were treated with TZP for more than three days between 1 January 2015 and 31 December 2017. Of these, 1986 patients were omitted based on the exclusion criteria. Finally, 713 subjects were included for analysis (Figure 1). The demographic and clinical characteristics of 713 patients at baseline are shown in Table 1. The median age of all patients was 67 years (interquartile range [IQR] 56–77 years), and 34.4% were female. Approximately 5.9% of patients stayed in the intensive care unit (ICU) while receiving TZP therapy. The baseline median serum potassium level was 4.2 mEq/L (IQR 3.9–4.5 mEq/L), and the baseline median serum creatinine level was 0.7 mEq/L (IQR 0.5–0.9 mEq/L). The median daily dose and duration of TZP therapy were 14.3 g (IQR 12.8–16.9 g) and 7 days (IQR 5–11 d), respectively. The most common indication for TZP therapy was pneumonia (37.3%). In addition, 314 (44.0%) of 713 patients were using at least one potential potassium-increasing medication, and the most common drug was non-steroidal anti-inflammatory drugs (NSAIDs) (26.5%).

2.2. Incidence and Severity of Hypokalemia

Of the 713 patients, hypokalemia occurred in 99 patients (13.9%); 9.3% of patients suffered from mild hypokalemia, while 4.6% had moderate-to-severe hypokalemia.
The comparison between the hypokalemic and the normokalemia groups is also presented in Table 1. The hypokalemia group included patients of significantly older age, females, with lower median baseline serum potassium level, longer median duration of TZP therapy, and a higher median TZP daily dose, compared to the normokalemia group.

2.3. Risk Factors of Hypokalemia

The results of univariate logistic regression revealed that older age, female sex, duration of TZP therapy, and TZP daily dose were associated with a higher risk of hypokalemia. In contrast, higher serum potassium levels at baseline were associated with a reduced risk of TAH (Table 2). There were no variables with VIF (>3); four statistically significant covariates from univariate analysis were included in the final multivariate logistic regression. Multivariate analysis also showed that, older age (odds ratio [OR] 1.03, 95% confidence interval [CI]: 1.02–1.05, p < 0.001), female sex (OR 1.88, 95% CI: 1.18–3.00, p = 0.008), longer duration of TZP therapy (OR 1.08, 95% CI: 1.04–1.13, p < 0.001), and higher TZP daily dose (OR 1.10, 95% CI: 1.01–1.20, p = 0.049) were positively associated with TAH, whereas higher baseline serum potassium levels (OR 0.13, 95% CI: 0.07–0.26, p < 0.001) was negatively associated with TAH (Table 2).

2.4. Other Outcomes

Our study indicated that hypokalemia occurred during the early days after the start of TZP therapy, with four days as the onset time and five days as the nadir time (Table 3). In addition, we identified that the decrease in serum potassium from baseline to nadir was 3.5 times greater in the hypokalemia group (0.7 mEq/L vs. 0.2 mEq/L, p < 0.001) with approximately three times higher in the proportion of patients with ≥0.5 mEq/L decrease in serum potassium after TZP therapy (82.8% vs. 28.8%, p < 0.001) (Table 4).

3. Discussion

This is the first study to evaluate the incidence and associated risk factors of TAH in adult patients using data that excluded the medications and medical conditions influencing serum potassium levels with a large sample size. We found that hypokalemia was common in more than 10% of the patients and was more frequent in older and female patients, as well as in those with a longer duration of TZP therapy and higher TZP daily dose administration. In addition, we indicated that TAH occurred in the early days after TZP administration. These findings have important implications for the safe use of TZP.
The high frequency of hypokalemia in TZP treatment in our study is in line with the findings of previous studies [17,18]. The incidence of TAH in the present study was similar to the result of the study by Kaye et al. [17] (13.9% vs. 12.6%), whereas this was considerably lower than that by Kuramoto et al. [18] (13.9% vs. 24.8%). In terms of severity, the proportion of moderate-to-severe hypokalemia was much higher in our study compared to the findings by Kaye et al. [17] (4.5% vs. 1.3%). However, as expected, our result was lower than that of Kuramoto et al. [18] (4.5% vs. 6.4%). The differences in these results may be due to the differences in the inclusion cohorts between the studies.
In this study, females and older age were independent risk factors for developing hypokalemia in patients treated with TZP. In several studies, the female sex has been reported as a risk factor for hypokalemia [26,27,28,29]. Kleinfeld et al. [27] evaluated the relationship between the prevalence of hypokalemia and the age and sex of patients. They found that the incidence of hypokalemia was higher in females than in males, regardless of age. This might be due to differences in the body-mass composition [27]. Potassium content in the body is associated with muscle mass. Females, particularly elderly individuals, tend to have a lower body muscle mass than males or younger individuals, resulting in low total exchangeable potassium levels and a higher risk of developing hypokalemia [18,27,30]. A previous study suggested that a high body mass index (BMI) prevents hypokalemia occurrence [18]. However, in our study, body weight and BMI did not affect the TAH. It is a plausible result because weight and BMI do not reflect the body’s muscle mass. Older age was another risk factor for hypokalemia in the present study. This is consistent with the results obtained by Kuramoto et al. [18]. As mentioned above, the elderly may have lower body mass, and hypokalemia may occur more frequently [27]. In addition, they commonly present with malnutrition and chronic comorbidities with concomitant polypharmacy, such as insulin for diabetes mellitus, β agonists for pulmonary disease, and diuretics for several medical conditions [31], which affect the decrease in serum potassium level [27].
The occurrence of hypokalemia among patients treated with the drugs belonging to the penicillin class is typically known to be associated with high-dose therapy. This is because penicillin, including piperacillin in TZP, can act as non-reabsorbable anions that generate a transmembrane potential gradient in the cortical collecting tubules and augment potassium secretion, leading to hypokalemia [3,32]. This study also demonstrated that a higher dose therapy is a significant predictor of TAH.
In addition, prolonged TZP therapy was significantly associated with TAH in our study. A study comparing the safety of nafcillin and oxacillin also found that a longer duration of treatment was a risk factor for hypokalemia occurrence after adjusting for other confounding factors [33]. The underlying reasons for these results are not clear. However, the possibility of augmentation of potassium excretion due to drug accumulation by repeated administration may be considered.
Higher baseline serum potassium is essential in lowering hypokalemia development in TZP and other penicillin therapy [18,26,33]. The result of the present study corresponded well with the results of the previous studies.
Furthermore, we found that hypokalemia occurred early after the initiation of TZP therapy, and the median time to onset was four days. This result was generally consistent with those of previous studies. However, slight differences in the median onset time were observed: five days in the previous study with TZP [18], four days with oxacillin [33], and three days with nafcillin [33].
This study has some limitations. First, this is a retrospective study; therefore, individual researchers might have been subject to bias. Second, this is a single-center study; selection bias could affect its results, and therefore, for this reason, they might not be generalizable at the national or global level. Third, although we attempted to exclude as many factors affecting potassium levels as possible, excluding all possible contributors of hypokalemia except TZP was almost impossible. Patients treated with drugs that may increase serum potassium were not excluded. Therefore, caution is advised when generalizing the findings. Finally, we did not evaluate the complications of hypokalemia. Thus, further prospective studies are needed to determine more specific TAH-associated outcomes, including the clinical impact of hypokalemia.

4. Materials and Methods

4.1. Study Design and Population

A retrospective observational study was performed over three years (between 1 January 2015 and 31 December 2017) at Kangbuk Samsung Medical Center (Seoul, Korea), a tertiary-care teaching hospital with 800 beds.
Patients aged ≥18 years who received TZP for at least three days were included. Patients were excluded if they had no serum potassium level recorded at baseline or during TZP therapy; had abnormal serum potassium levels at baseline; maintained normal potassium levels with potassium preparations or potassium binders at baseline or during TZP therapy; and received dialysis and continuous renal replacement therapy. Kuramoto et al. [18] excluded patients on well-known hypokalemia-inducing drugs during TZP therapy to identify the incidence and risk factors of TAH. However, several medical conditions are also major causes of hypokalemia [1,3,34]. Thus, cases who received medications or had medical conditions that can contribute to hypokalemia development during TZP therapy were also excluded to specifically assess the impact of TZP on hypokalemia occurrence. The medications with the potential to decrease the serum potassium levels included diuretics (except for potassium-sparing diuretics alone), aminoglycosides, mineralocorticoids and glucocorticoids, amphotericin B, anticancer drugs, laxatives and enemas, β2 agonists, xanthines, and insulins [1,3,34]. Among anticancer drugs, the following medications reported in the literature for hypokalemia were excluded: cisplatin and other platinum drugs, cyclophosphamide, ifosfamide, cetuximab, panitumumab, temsirolimus, methotrexate, abiraterone, and eribulin [35]. Coexisting medical conditions that influence serum potassium levels were also considered. These included alkalosis, vomiting, diarrhea, tube drainage, hypomagnesemia, hypokalemic thyrotoxic periodic paralysis, primary hyperaldosteronism, Cushing’s syndrome, and renal tubular acidosis [1,3,34]. Finally, patients with hyperkalemia during TZP therapy were omitted.
This study was approved by the Institutional Review Boards of Kangbuk Samsung Medical Center (approval no. 2018-11-004). As this was a retrospective study, informed consent was not required. All clinical investigations were conducted per the guidelines of the 2008 Declaration of Helsinki.

4.2. Variables and Definitions

Data were extracted from electronic medical records. The collected data included patient demographic information (age, sex, weight, and height) and the status of ICU care during TZP treatment. It also included serum potassium, creatinine, magnesium, albumin, aspartate aminotransferase, and alanine aminotransferase levels; information related to TZP (daily dose, duration of therapy, and indication); and medications with the potential to increase the serum potassium levels, such as angiotensin-converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers (ARBs), β-blockers, NSAIDs, digoxin, and sulfamethoxazole/trimethoprim [34,36]. BMI was calculated.
Hypokalemia and hyperkalemia were defined as serum potassium levels of <3.5 mEq/L and 5.5 > mEq/L, respectively. Alkalosis was defined as an arterial pH of >7.45. A serum magnesium level of <1.8 mg/dL was considered hypomagnesemia according to our institutional laboratory reference values. Patients included were classified into the normokalemia and hypokalemia groups based on potassium levels during TZP therapy. The hypokalemia group was further classified into mild (>3–3.4 mEq/L) and moderate-to-severe (≤3.0 mEq/L) groups. The baseline serum level was defined as the value recorded up to seven days before the start of TZP therapy. If multiple potassium levels were recorded before TZP therapy, the value obtained closest to the start of TZP therapy was considered the baseline.

4.3. Clinical Outcomes

The incidence, severity, and risk factors of TAH were evaluated. Additionally, clinical characteristics were assessed, including elapsed time to onset of hypokalemia and median difference of serum potassium before and after TZP therapy.

4.4. Statistical Analyses

Categorical variables were expressed as the frequency and proportion of variables and compared using the Pearson’s χ2 test or Fisher’s exact test. Continuous variables were described as the median and IQR and compared using the Mann–Whitney U test. To explore the risk factors, multivariate logistic regression was used. Variables with p < 0.05 from univariate analysis were included. However, variables with a variance inflation factor (VIF) exceeding 3 were excluded to avoid multicollinearity issues. Enter method was used. Statistical analyses were conducted using PASW Statistics 18.0 (IBM, Armonk, NY, USA). Statistical significance was set at p < 0.05 for two-tailed tests.

5. Conclusions

We found that the incidence of hypokalemia was considerably high in adult patients receiving TZP. Furthermore, we identified several factors affecting the onset of hypokalemia. In addition, we demonstrated that hypokalemia developed early under TZP treatment. Thus, close monitoring of serum potassium levels should be considered during TZP therapy, particularly at its beginning.

Author Contributions

Conceptualization, H.S. and E.K.; methodology, H.S. and E.K.; formal analysis, H.S.; investigation, H.S.; data curation, H.S.; writing—original draft, H.S.; writing—review and editing, H.S. and E.K.; visualization, H.S.; supervision, E.K.; project administration, H.S. and E.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by a grant from the National Research Foundation of Korea (NRF) grant funded by the Korean government (Ministry of Science and ICT, MICT)(NRF2021R1F1A1062044) and by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (Grant Number 2021R1A6A1A03044296), which had no further role in the study design, data collection, analysis, and interpretation, the writing of the report, or in the decision to submit the paper for publication.

Institutional Review Board Statement

The study was conducted according to the Declaration of Helsinki and approved by the Institutional Review Boards of Kangbuk Samsung Medical Center (approval no. 2018-11-004).

Informed Consent Statement

An informed consent was waived due to the study’s retrospective nature on anonymous clinical data.

Data Availability Statement

The data presented in this study are available upon reasonable request from the corresponding author.

Acknowledgments

The authors express their deepest gratitude to Kyu-Beck Lee and Sung Ho Lee from the Sungkyunkwan University School of Medicine for their advice on the study and comments on this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Antibiotics 11 01138 g001 550
Figure 1. Patient flow diagram. TZP: piperacillin/tazobactam. a Diuretics (except for potassium-sparing diuretics alone), aminoglycosides, mineralocorticoids and glucocorticoids, amphotericin B, anticancer drugs, laxatives and enemas, β2 agonists, xanthines, and insulins were included; anticancer medications were cisplatin and other platinum drugs, cyclophosphamide, ifosfamide, cetuximab, panitumumab, temsirolimus, methotrexate, abiraterone, and eribulin. b Alkalosis, vomiting, diarrhea, tube drainage, hypomagnesemia, hypokalemic thyrotoxic periodic paralysis, primary hyperaldosteronism, Cushing’s syndrome, and renal tubular acidosis were included.
Figure 1. Patient flow diagram. TZP: piperacillin/tazobactam. a Diuretics (except for potassium-sparing diuretics alone), aminoglycosides, mineralocorticoids and glucocorticoids, amphotericin B, anticancer drugs, laxatives and enemas, β2 agonists, xanthines, and insulins were included; anticancer medications were cisplatin and other platinum drugs, cyclophosphamide, ifosfamide, cetuximab, panitumumab, temsirolimus, methotrexate, abiraterone, and eribulin. b Alkalosis, vomiting, diarrhea, tube drainage, hypomagnesemia, hypokalemic thyrotoxic periodic paralysis, primary hyperaldosteronism, Cushing’s syndrome, and renal tubular acidosis were included.
Antibiotics 11 01138 g001
Table
Table 1. Demographic and clinical characteristics at baseline.
Table 1. Demographic and clinical characteristics at baseline.
VariableTotalHypokalemiaNormokalemiap Value
n = 713n = 99n = 614
Age (years)67 (56–77)74 (61.5–79.0)66 (56–76)<0.001
Female sex245 (34.4)46 (46.5)199 (32.4)0.006
ICU residence42 (5.9)5 (5.1)37 (6.0)0.702
Serum potassium (mEq/L) 4.2 (3.9–4.5)3.9 (3.7–4.1)4.2 (4.0–4.5)<0.001
Serum creatinine (mEq/L) 0.7 (0.5–0.9)0.7 (0.5–0.9)0.7 (0.5–0.9)0.707
Serum magnesium (mEq/L) 2.0 (1.9–2.2)1.9 (1.8–2.1)2.0 (1.9–2.2)0.493
ALB (g/L)3.2 (2.9–3.6)3.1 (2.8–3.6)3.2 (2.9–3.7)0.675
AST (IU/L)27 (18–44)34 (18.8–53.5)26 (17–43)0.511
ALT (IU/L)22 (18–38)21 (11–38)22 (15–38)0.885
Duration of TZP therapy (days)7 (5–11)8 (5.5–13.0)7 (5–11)0.008
TZP daily dose (g) 14.3 (12.8–16.9)15.8 (13.5–17.2)13.5 (12.7–16.8)0.019
BW (kg)58 (50–66)56 (50–64)58.3 (50.2–66.1)0.115
BMI (kg/m2)21.9 (19.6–24.5)22.2 (19.7–24.2)21.9 (19.6–24.6)0.824
Indication for TZP treatment
Pneumonia 266 (37.3)29 (29.3)237 (38.6)0.076
Intra–abdominal infection 197 (27.6)35 (35.4)162 (26.4)0.064
Urinary tract infection76 (10.7)12 (12.1)64 (10.4)0.611
Neutropenic fever42 (5.9)5 (5.1)37 (6.0)0.702
Bacteremia/Sepsis 38 (5.3)8 (8.1)30 (4.9)0.189
Skin and soft tissue infection 38 (5.3)7 (7.1)31 (5.1)0.406
Others81 (11.4)8 (8.1)73 (11.9)0.268
Drugs that may increase serum potassium
NSAIDs 189 (26.5)32 (32.3)157 (25.6)0.158
ARBs104 (14.6)18 (18.2)86 (14.0)0.275
β blockers28 (3.9)2 (2.0)26 (4.2)0.293
Potassium-sparing diuretics 24 (3.4)1 (1.0)23 (3.8)0.161
ACEIs16 (2.2)2 (2.0)14 (2.3)0.909
Sulfamethoxazole/trimethoprim 14 (2.0)1 (1.0)13 (2.1)0.461
Digoxin12 (1.7)2 (2.0)10 (1.6)0.779
Data are presented n (%) or median (interquartile range); ICU: intensive care unit; ALB: albumin; AST: aspartate aminotransferase; ALT: alanine aminotransferase; TZP: piperacillin/tazobactam; BW: body weight; BMI: body mass index; NSAIDs: non-steroidal anti-inflammatory drugs; ARBs: angiotensin II receptor blockers; ACEIs: angiotensin-converting enzyme inhibitors.
Table
Table 2. Logistic regression analysis of independent risk factors for TZP-associated hypokalemia.
Table 2. Logistic regression analysis of independent risk factors for TZP-associated hypokalemia.
VariableUnivariate AnalysisMultivariate Analysis a
OR (95% CI)p ValueOR (95% CI)p Value
Age (year)1.03 (1.01–1.05) 0.0011.03 (1.02–1.05)<0.001
Female sex1.81 (1.18–2.78)0.0071.88 (1.18–3.00)0.008
ICU residence0.83 (0.32–2.16)0.702
Serum potassium (mEq/L) 0.15 (0.08–0.27) <0.0010.13 (0.07–0.26)<0.001
Serum creatinine (mEq/L) 1.05 (0.64–1.71)0.850
Serum magnesium (mEq/L)0.32 (0.02–7.05)0.471
ALB (g/L)1.00 (0.61–1.65)0.998
AST (IU/L)1.00 (0.99–1.00)0.930
ALT (IU/L)1.00 (0.99–1.01)0.943
Duration of TZP therapy (days)1.07 (1.03–1.11)<0.0011.08 (1.04–1.13)<0.001
TZP daily dose (g)1.10 (1.01–1.20)0.0241.10 (1.01–1.20)0.049
Body weight (kg)0.99 (0.97–1.0)0.128
BMI (kg/m2)1.01 (0.95–1.07)0.730
Indication for TZP treatment
Pneumonia 0.66 (0.42–1.05)0.077
Intra–abdominal infection 1.53 (0.97–2.39)0.065
Urinary tract infection1.19 (0.62–2.29)0.612
Neutropenic fever0.83 (0.32–2.16)0.702
Bacteremia/Sepsis 1.71 (0.76–3.85)0.194
Skin and soft tissue infection 1.43 (0.61–3.35)0.408
Others0.65 (0.30–1.40)0.271
Drugs that may increase serum potassium
NSAIDs 1.39 (0.88–2.20)0.159
ARBs1.36 (0.78–2.39)0.276
β blockers0.47 (0.11–2.0)0.304
Potassium-sparing diuretics 0.26 (0.04–1.96)0.193
ACEIs0.89 (0.11–7.27)0.909
Sulfamethoxazole/trimethoprim 0.47 (0.06–3.65)0.472
Digoxin 1.25 (0.27–5.77)0.779
OR: odds ratio; CI: confidence interval: ICU: intensive care unit; ALB: albumin; AST: aspartate aminotransferase; ALT: alanine aminotransferase; TZP: piperacillin/tazobactam; BMI: body mass index; NSAIDs: non-steroidal anti-inflammatory drugs; ARBs: angiotensin II receptor blockers; ACEIs: angiotensin-converting enzyme inhibitors. a Values are adjusted for age, sex, baseline serum potassium level, duration of TZP therapy, and TZP daily dose.
Table
Table 3. Clinical characteristics of patients with hypokalemia.
Table 3. Clinical characteristics of patients with hypokalemia.
CharacteristicsValue
Elapsed time to onset of hypokalemia (days)4.0 (2.5–6.0)
Serum potassium at the onset time of hypokalemia (mEq/L)3.3 (3.1–3.4)
Elapsed time to nadir of hypokalemia (days)5.0 (3.0–7.0)
Serum potassium at the nadir time of hypokalemia (mEq/L)3.2 (3.0–3.3)
Data are presented median (interquartile range).
Table
Table 4. Comparison of clinical characteristics between hypokalemia group and normokalemia group.
Table 4. Comparison of clinical characteristics between hypokalemia group and normokalemia group.
CharacteristicsHypokalemiaNormokalemiap Value
n = 99n = 614
Difference between baseline and nadir serum potassium level0.7 (0.5–1.0)0.2 (0.0–0.5)<0.001 a
Patients with ≥0.5 mEq/L decrease in serum potassium level from baseline82 (82.8)177 (28.8)<0.001 b
Monitoring of serum potassium levels4 (3–6)3 (2–4)<0.001 a
Data are presented n (%) or median (interquartile range); a p-values from the Mann–Whitney U test; b p values from the χ2 test.
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Seo, H.; Kim, E. Incidence and Determinants of Piperacillin/Tazobactam-Associated Hypokalemia: A Retrospective Study. Antibiotics 2022, 11, 1138. https://doi.org/10.3390/antibiotics11081138

AMA Style

Seo H, Kim E. Incidence and Determinants of Piperacillin/Tazobactam-Associated Hypokalemia: A Retrospective Study. Antibiotics. 2022; 11(8):1138. https://doi.org/10.3390/antibiotics11081138

Chicago/Turabian Style

Seo, Heenam, and Eunyoung Kim. 2022. "Incidence and Determinants of Piperacillin/Tazobactam-Associated Hypokalemia: A Retrospective Study" Antibiotics 11, no. 8: 1138. https://doi.org/10.3390/antibiotics11081138

APA Style

Seo, H., & Kim, E. (2022). Incidence and Determinants of Piperacillin/Tazobactam-Associated Hypokalemia: A Retrospective Study. Antibiotics, 11(8), 1138. https://doi.org/10.3390/antibiotics11081138

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