key: cord-0017829-ywnl2jok
authors: Kohno, Junko; Kawamura, Tsuyoshi; Kikuchi, Akiko; Akaishi, Tetsuya; Takayama, Shin; Ishii, Tadashi
title: A Japanese traditional medicine Hochuekkito promotes negative conversion of vancomycin-resistant Enterococci
date: 2021-05-28
journal: Sci Rep
DOI: 10.1038/s41598-021-90890-4
sha: e3bd012e5673d036fa874f29c1a06a94764262ff
doc_id: 17829
cord_uid: ywnl2jok

Vancomycin-resistant enterococci (VRE) are prominent causes of nosocomial infections. Japanese traditional (Kampo) medicine promotes intestinal immunity and protects against bacterial infections. We assessed potential differences in the clinical course of VRE-positive patients, based on their characteristics and treatment with Kampo medicines. This retrospective observational study collected data from VRE-positive patients from August 2018 to July 2019 at a tertiary-care hospital in Japan. The data of 122 consecutive VRE-positive inpatients were analyzed. Sixty-nine patients were treated with probiotics, among whom, 18 were further treated with Kampo medicines. Twenty-six of the 122 patients subsequently died. In univariate analyses, subsequent VRE negative conversion significantly reduced the mortality of VRE-detected patients (p = .0003). Administration of probiotics (p = .0065) and Kampo medicines with probiotics (p = .0002), especially of the Kampo medicine hochuekkito (p = .0014), and a higher serum albumin level positively contributed to the subsequent VRE negative conversion. Multivariate analyses demonstrated that Kampo medicines and body mass index contributed to VRE negative conversion. Hochuekkito shortened the time needed for VRE negative conversion (p = 0.0485). Administration of Kampo medicines, especially of hochuekkito, in addition to probiotics in VRE patients may promote VRE negative conversion.

www.nature.com/scientificreports/ immune function, significantly reduced the urine bacterial count 10 weeks after administration 10 . Matsui et al. 12 reported that HET could inhibit MRSA growth and extend the survival time of MRSA-infected mice. Nakae et al. reported that juzentaihoto (JTT) led to negative bacterial cultures in five cases of refractory multidrug-resistant bacterial infection, including a MRSA case with severe burns 13 . These studies indicated that HET and JTT could be effective for reducing MRSA colonization. Particularly, HET was found to support the immune system by inducing anti-inflammatory responses based on intestinal conditions. However, the effect of Kampo medicines on patients with VRE colonization has not been investigated. We herein report an outbreak of VRE at a tertiarycare hospital in Japan. We aimed to assess potential differences in the clinical course of VRE colonization based on patients' characteristics and treatment with either probiotics or Kampo medicines.

Patient background affected mortality. In a total of 122 patients, VRE were detected in culture tests from sputum (n = 1), bile juice (n = 1), wound exudate (n = 1), urine (n = 3), and stool (n = 116). Clinical data on admission before VRE detection showed that 28 of the 122 cases considered (23.0%) were perioperative cases. The use of antibiotics after admission and before VRE detection was recorded in 110 of the 122 cases (90.2%).

As for the nutritional route, 54 of the 122 patients (44.3%) were fed through a nasogastric feeding tube (Table 1) . During the subsequent clinical course of the 122 VRE-positive patients, 26 patients died and 96 survived. Sixtynine patients were treated with probiotics, and 18 patients further received Kampo medicines in addition to probiotics (16, HET; 1, JTT; and 1, ninjin'yoeito (NYT)). Fifty-three patients received neither probiotics nor Kampo medicines. Four patients were diagnosed with infection due to VRE. Three of them died, while one recovered and was moved to another hospital. Only one deceased patient, who had suffered from severe burns, had undergone treatment with linezolid. Enterococcus faecium accounted for all VRE infections in this cohort. The genotype of all examined samples was Van A. No probiotic-related adverse events were observed in this study. One patient treated with Kampo medicines showed hypokalemia but soon improved with the administration of 25 mg of spironolactone. First, we examined the factors that affected the mortality of VRE-positive patients by univariate analyses ( Table 1 ). The demographic, clinical, and therapeutic data were analyzed. None of the evaluated demographic, Table 1 . Comparative analysis of clinical and therapeutic parameters according to subsequent mortality during hospitalization. Kampo medicines (total) means hochuekkito (n = 16), juzentaihoto (n = 1), and ninjin'yoeito (n = 1). VCM vancomycin, VRE vancomycin-resistant enterococcus. *Mean and standard deviation, †median and interquartile range. www.nature.com/scientificreports/ pre-onset clinical or therapeutic factors significantly affected mortality, except for the serum albumin level at hospitalization. On the other hand, the subsequent VRE negative conversion significantly reduced the mortality of patients with VRE colonization (p = 0.0003). Prior vancomycin (VCM) use before confirmation of VRE positivity in the stool negatively affected mortality (p = 0.0032). These data are summarized in Table 1 .

Impact of considered factors on the overall survival rate. Univariate survival analyses were then performed to evaluate the effect of each clinical and therapeutic variable on the overall survival rate. Kaplan-Meier curves, with p-values determined by log-rank tests for each demographic and clinical factor, are shown in Fig. 1 . Sex, presence of diabetes mellitus or hypertension, peri-operational status, and use of probiotics did not significantly affect mortality. However, the administration of Kampo medicines significantly contributed to the survival rate of patients with VRE colonization (p = 0.031).

Since patients' survival rates were improved by the subsequent achievement of VRE negative conversion, we investigated the factors affecting the rate of VRE negative conversion with a univariate analysis. In particular, the following factors were assessed: history of diabetes mellitus, hypertension, and dyslipidemia; perioperative status; preceding use of antibiotics before confirming VRE in the stool; and therapeutic administration of probiotics or Kampo medicines. The results of the univariate analysis are shown in Table 2 . The administration of probiotics (p = 0.0065, n = 69) and Kampo medicines (p = 0.0002, n = 18), including HET (p = 0.0014, n = 16), positively contributed to VRE negative conversion. Moreover, a higher serum albumin level at hospitalization contributed to a higher achievement rate of VRE negative conversion; the other evaluated factors did not contribute to this.

Rate of achievement of VRE negative conversion. Next, we conducted multivariate binary logistic regression analysis to examine the rate of achievement of VRE negative conversion. We included the following factors as explanatory variables: history of diabetes mellitus, body mass index at hospitalization, serum albumin level at hospitalization, use of a nasogastric feeding tube, and treatment with HET. The results of the multivariate analysis are shown in Table 3 www.nature.com/scientificreports/ the achievement of VRE negative conversion in the whole population and in those nourished via nasogastric feeding tubes are shown in Fig. 2 . In the whole population, the period until VRE negative conversion was not significantly different between the two therapeutic groups (HET: n = 16 vs. no use of Kampo: n = 104; p = 0.2394, log-rank test), but it showed differences in those of similar nutrition status with nasogastric feeding tubes (n = 11 vs. n = 40; p = 0.0485).

In the present study, we demonstrated that the mortality of VRE-positive patients was affected by VCM use and subsequent VRE negative conversion. Use of VCM indicated the immune-compromised status of patients suffering from MRSA infection, and the failure of VRE negative conversion indicates the severity of the patient's condition. The administration of Kampo medicines contributed to the achievement of VRE negative conversion in uni-and multivariate analyses. Moreover, Kampo treatment significantly contributed to the speed of VRE negative conversion. Administration of probiotics also contributed to the achievement of VRE negative conversion but did not affect its speed. The risk of VRE infection depends on a patient's nutritional intake, immune status, the condition of the intestinal flora, and the patient's history of antibiotic use. The use of probiotics for eliminating VRE infections is debated 4-6 , but it has been suggested that probiotics promote a healthy intestinal environment 14 . The present study indicates that probiotics may promote VRE negative conversion, but the combined treatment of probiotics and Kampo medicines showed a stronger and faster effect for the achievement of negative conversion. A higher serum albumin level and body mass index, which reflect the nutritional status, positively contributed to the Table 2 . Comparative analysis of clinical and therapeutic parameters according to the subsequent achievement of VRE negative conversion. Kampo medicines (total) means hochuekkito (n = 16), juzentaihoto (n = 1), and ninjin'yoeito (n = 1). VCM vancomycin, VRE vancomycin-resistant enterococcus. *Mean and standard deviation. www.nature.com/scientificreports/ subsequent VRE negative conversion in the present study. Malnutrition is also an independent factor associated with nosocomial infections 15 . HET is a Kampo medicine originally used to promote digestion and absorption and improve the nutritional status by reducing exhaustion caused by inflammation 16 . Combined administration of Kampo medicines and probiotics may promote the health of the intestinal environment, as well as digestion and absorption, resulting in an improved nutritional condition. Further study will be needed to investigate the nutritional status related with the administration of Kampo medicine and the contribution to VRE decolonization. Few studies assessed the effects of Kampo medicines for multidrug-resistant bacteria. Previous studies have indicated that HET has anti-inflammatory effects on the intestinal mucosa, promotes recovery of the immune system, and increases appetite 16 . JTT and NYT also have similar effects 17 . HET, JTT, and NYT contain common crude drugs: The Japanese Pharmacopoeia (JP), Astragalus Root, JP Ginseng, JP Japanese Angelica Root, JP Atractylodes Lancea Rhizome, and JP Glycyrrhiza ( Table 4 ). Combinations of these drugs may be key for cytokine regulation, activation of innate immunity, and healing in compromised patients 16, 17 . Therefore, we can conclude that Kampo medicines can combat VRE colonization in immunocompromised patients through multiple mechanisms.

In infectious diseases, the efficacy of prebiotics and probiotics has been reported. Guadalupe et al. reported an association between the administration of probiotics combined with prebiotics and the prevention or modulation of severe rotavirus gastroenteritis 18 . Rätsep et al. reported that symbiotic use during antimicrobial therapy can prevent C. difficile infection, as well as its potential to reduce recurrences 19 . Kampo medicines have been proven to influence the microbiome; thus, Kampo medicines have prebiotic effects 20, 21 . The bioactive constituents of HET, Table 4 . Composition of the three Kampo formulae used in this study. The formulae contained the following inactive ingredients: JP Magnesium Stearate and JP Lactose Hydrate. The crude drugs in bold are common in all three formulae. HET is indicated for patients with a delicate constitution, reduced digestive function, and severe fatigability of the limbs: summer emaciation, reinforcement of physical strength after illness, tuberculosis, anorexia, gastroptosis, cold, hemorrhoid, anal prolapse, uterine prolapse, impotence, hemiplegia, and hyperhidrosis. JTT and NYT are indicated for the relief of weakness after recovery from disease, fatigue, malaise, anorexia, perspiration during sleep, cold limbs, and anemia. HET hochuekkito, JTT juzentaihoto, NYT ninjin'yoeito, JP The Japanese Pharmacopoeia. www.nature.com/scientificreports/ including astragaloside IV, calycosin, glycyrrhizic acid, enoxolone, saikosaponin D, ferulic acid, and hesperidin, are distributed in the gastrointestinal tract 22 and can influence the gastrointestinal tract condition together with the microbiome. HET includes triterpenoid saponins, which undergo deglycosylation in a metabolic pathway related to the microbiome 23 . In our study, the effect of Kampo medicines was promoted by probiotics, as supported by the metabolism of saponin to aglycon, which is mediated by probiotics 24, 25 . These reports may explain the additional effects of probiotics on Kampo medicines in the gut environment and immune system. In the Kampo theory, HET, JTT, and NYT are considered to belong to the Ginseng Root and Astragalus Root drug group, which improve body energy. They are traditionally used to relieve weakness after recovery from a disease, fatigue and malaise, and anorexia, and listed in some clinical practice guidelines in Japan 26-31 . HET is indicated for patients with a delicate constitution, reduced digestive function, and severe fatigability of the limbs. JTT and NYT are indicated for the relief of weakness after recovery from disease, fatigue, anorexia, perspiration during sleep, cold limbs, and anemia, and NYT is indicated for patients with symptoms such as cough or insomnia. Since these three Kampo medicines contain Glycyrrhiza, they can cause pseudoaldosteronism. Patients should be carefully monitored to prevent the reduction of serum potassium levels, increased blood pressure, and edema. Other side effects, such as hepatic dysfunction and interstitial pneumonia, were also reported. If these side effects are observed, ceasing the administration of Kampo medicines and administering general medications for adverse events could improve symptoms. In the present study, one patient treated with Kampo medicines showed hypokalemia but soon improved with the administration of spironolactone. Considering these side effects, we think it is safe to introduce Kampo medicines.

In Japan, linezolid and Quinopristin-Dalfopristin are currently approved by the Japanese government for the treatment of VRE infections. Daptomycin is also recommended for VRE infections 3 , but decolonization is still important to reduce VRE spread, decrease the risk of infection, and avoid acquiring tolerance to such anti-VRE drugs.

Nosocomial VRE infections may cause death among immunocompromised patients. The present study indicates that Kampo medicines may contribute to reducing VRE carriers and severe infections, thus reducing the risk of VRE infections in vulnerable patients.

There are some limitations to the present study. As it had a retrospective observational design, participant selection was not precisely controlled. Not all VRE genotypes were examined, and other genotypes could have been present. We did not collect data on the specific antibiotics administered. Furthermore, we did not survey the use of proton pump inhibitors. Further data are needed to investigate the contribution of these factors to VRE decolonization in Japanese patients.

In conclusion, the therapeutic use of Kampo medicines in addition to probiotics positively contributed to the higher rate and speed of VRE negative conversion. The Kampo medicines in this study may aid in controlling antibiotic-resistant bacterial nosocomial infections.

Patients. This study assessed consecutive patients with positive VRE in culture examination from a tertiarycare hospital located in the Aomori prefecture of Japan from August 2018 to July 2019. The hospital has an advanced emergency medical center that receives 24,000 emergency patients every year and has 30 beds in the emergency unit. Once the first VRE-positive patient was identified in August 2018, the infection spread from the emergency unit and intensive care unit to other hospital wards. During this period, the hospital examined the stool cultures of all inpatients every week, and the data of all VRE-positive patients were listed by the clinical laboratory department. A total of 122 inpatients whose culture samples were confirmed to be VRE-positive were enrolled in this study. With respect to the list of VRE-positive patients, we retrospectively collected the following data from hospital medical records. VRE detection. Fecal samples were obtained by collecting swabs (E-MS60, EIKEN Co., Ltd, Tochigi, Japan).

Then, samples were cultured on VRE-selective agar (BD BBLTM, Cat. No.251833, Becton, Dickinson, and Company, NJ, USA). If colonies grew, they were further cultured and VCM resistance examined by BD Sensi-Disc, Va30 (Cat. No. 291019, Becton, Dickinson, and Company, NJ, USA). The minimal inhibitory concentration (MIC) was determined using PC1J panel with MicroScan WalkAway96Plus (Beckman Coulter, Inc., CA, USA). VCM resistance was considered at an MIC of > 16 μg/mL. When VRE were detected, their genotype was examined by the Aomori prefecture public health and environmental center using the pulsed-field gel electrophoresis method. We defined VRE negative conversion to be achieved if the colony could not be detected three times consecutively on VRE-selective agar. The date of VRE negative conversion was defined as the date of sample collection for the third culture test among the three consecutive times of negative colony growth in VRE-selective agar.

For the 122 VRE-positive patients enrolled, the following demographic and clinical data were collected: sex, age, body mass index at hospitalization, serum albumin level at hospitalization, history of diabetes mellitus, history of hypertension, surgical operation after hospitalization, and preceding use of antibiotics for treating bacterial infections before confirming VRE positivity in the stool. In addition to these pre-onset factors, the following therapeutic factors were also evaluated: use of oral probiotics (n = 69) and Kampo medicines (n = 18). The outcomes evaluated were the eventual achievement of negative conversion of VRE (binary variable) and the time between confirming VRE positivity in the stool and achievement of VRE negative conversion (continuous variable).

Since February 2019, the hospital recommended that VRE-positive patients be treated with a probiotic formula to improve enteric microbial balance. Prescription of probiotic formulae, selection of formulation, combined use or not, dosage, and duration of administration were based on the attending doctors' decision. The 16 were treated with 7.5 g of HET in three doses per day, 1 with 7.5 g of JTT in three doses per day, and 1 with 9.0 g of NYT in three doses per day. A Kampo specialist and doctors consulting him prescribed these Kampo medicines to VRE-positive patients. The selection of the Kampo formula was as follows: for patients with some diseases and a vulnerable status, the first choice was HET. If the patient was anemic; red blood cells < 3.7 × 10 6 /μL, hemoglobin < 11.5 g/dL, and hematocrit < 35%, JTH was selected. If patients suffered from anemia and respiratory diseases, NYT was prescribed. Table 4 shows the composition of the three Kampo formulae used in this study. Further information regarding these Kampo formulae can be found on the website of the Standards of Reporting Kampo Products 32 . All Kampo formulae used during the study were manufactured by Tsumura and Co. (Tokyo, Japan).

Distributions of normally distributed numeric variables are described as means and standard deviations, and those of non-normally distributed numeric variables as medians and interquartile ranges (25-75 percentiles) . Comparisons between two variables were performed by using either Student's t-test or Mann-Whitney's U-test according to the variables' distribution pattern. Survival analysis was assessed by Kaplan-Meier curves and the log-rank test. Multivariate analysis for the subsequent achievement of VRE negative conversion was assessed by binary logistic regression analysis with explanatory variables of particular clinical interest and additional variables that had a significant impact (p < 0.10) on the achievement of VRE negative conversion in univariate analyses. In multivariate analysis, explanatory variables with a moderate-to-strong correlation were not simultaneously employed to avoid multicollinearity. In each analysis, p-values < 0.05 were considered statistically significant. When multiple comparisons were simultaneously performed, p-values < 0.01 were considered statistically significant by applying the Bonferroni correction method. Statistical analyses were performed using SPSS Statistics Base 22 software (IBM Corp., Armonk, NY, USA) or MATLAB R2015a (Math-Works, Natick, MA, USA).

Ethics declarations. This study was approved by the Institutional Review Board of Hachinohe City Hospital (Institutional Review Board approval number: 1933) and performed in accordance with the ethical standards of the 1964 Declaration of Helsinki. The institutional review board waived the requirement for informed consent due to the retrospective study design.

The datasets analyzed during the current study are available from the corresponding author on reasonable request.

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We thank Mr. Ryoei Taninai, a pharmacist of the Hachinohe City Hospital, for helping with data collection. We would also like to thank Editage (www. edita ge. com) for English language editing.

J.K. and T.K. treated the patients, collected the data, and prepared the draft manuscript. T.A. analyzed the statistical data and wrote the draft manuscript. S.T. and A.K. wrote and revised the draft manuscript. T. I. gave advice and revised the draft manuscript.

A. K., S. T., and T. I. belong to the Department of Kampo and Integrative Medicine at Tohoku University School of Medicine. The department received a grant from Tsumura, a Japanese manufacturer of Kampo medicines; however, the grant was used as per Tohoku University rules. Potential conflicts of interest were addressed by the Tohoku University Benefit Reciprocity Committee and were managed appropriately. The other authors have no additional conflicts of interest to declare.

Correspondence and requests for materials should be addressed to S.T.Reprints and permissions information is available at www.nature.com/reprints.

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