2020 Volume 22 Issue 8 Published: 28 August 2020
  

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  • Xu Juntang
    Abstract ( ) PDF ( )
    At present, there are two kinds of oral antithrombotic drugs commonly used, including antiplatelet agents and anticoagulants. Before initiation of antithrombotic drugs, the risk of bleeding should be routinely assessed and measures to prevent bleeding should be taken as soon as possible. Methods for improving the efficacy and safety of warfarin include close monitoring during use, anticoagulative management, physician training, and patient education. Novel oral anticoagulants are easy to use, take effect quickly, and their dosage need not be monitored and adjusted in routine clinical practice, but the liver and kidney function should be taken into consideration for dosing regimen. After acute coronary syndrome (ACS) and percutaneous coronary intervention (PCI), dual antiplatelet therapy (DAPT) was routinely given. The risk of bleeding and ischemia/thrombosis should be carefully evaluated and balanced before taking these medications, and the optimal drug combination and the duration of DAPT should be selected.
  • Wang Yu, Xie Yifan, Zhang Zhuoli
    Abstract ( ) PDF ( )
    Febuxostat, a new selective xanthine oxidase inhibitor, is approved by the U.S. Food and Drug Administration in 2009 for the treatment of gout and hyperuricemia. The study on the "cardiovascular safety of febuxostat and allopurinol in patients with gout and cardiovascular comorbidities (CARES)", which was published in 2018, showed that febuxostat could increase the risk of all-cause mortality and cardiovascular related death in gout patients with cardiovascular disease. However, the subsequent clinical studies have not confirmed that febuxostat could increase the risk of cardiovascular events-related death. The inconsistent results of the studies on cardiovascular safety of febuxostat suggest that the gout patients with cardiovascular disease may benefit from continuous uric acid lowering therapy. However, during the process of using febuxostat, the risk of cardiovascular events and cardiovascular events-related death should be alerted, the combination medication and renal function of patients should be paid attention to, and the xanthine oxidase inhibitor withdrawal syndrome should be prevented.
  • Zhang Yatong, Liu Junpeng, Zhao Zinan, Lu Hongliu, Hu Xin
    Abstract ( ) PDF ( )
    Objective To explore the effect of amiodarone combined with rivaroxaban on the plasma concentration of rivaroxaban in patients with non-valvular atrial fibrillation. Methods This study was designed as the prospective cohort study. The subjects were selected from patients with atrial fibrillation who were hospitalized in the Department of Cardiology of Beijing Hospital from January to October 2019 and treated with rivaroxaban (≥3 days). The enrolled patients were divided into the with amio- darone combination group and the without amiodarone combination group. The trough concentration and peak concentration of rivaroxaban were detected by chromogenic substrate method with anti-Xa assay kit. Taking the plasma concentration of patients with a daily dose of 20-mg of rivaroxaban as the standard,plasma concentrations in patients with various daily doses of rivaroxaban were standardized. The measured plasma concentrations,standardized plasma concentrations,and plasma concentrations in patients at daily dose of 20-mg of rivaroxaban were respectively compared between the 2 groups. Results A total of 65 patients were entered in the study, including 12 patients in the with amiodarone combination group (the daily dose of rivaroxaban was 20-mg) and 53 patients in the without amiodarone combination group (the daily doses of rivaroxaban were 20, 15, and 10-mg in 42, 9, and 2 patients, respectively). The differences in gender, age, weight, body mass index, smoking history, CHA2DS2-VASc score, HAS-BLED score, daily dose of rivaroxaban, liver and kidney function, and platelet count of patients between the 2 groups were not statistically significant (P>0.05 for all). The trough and peak plasma concentrations of rivaroxaban in the with amiodarone combination group were higher than those in the without combination amiodarone group, but the differences were not statistically significant [(43±30) ng/ml vs. (38±26) ng/ml, t=0.569, P=0.571; (294±114) ng/ml vs. (251±87) ng/ml, t=1.473, P=0.146]. The differences in standardized trough and peak plasma concentrations of rivaroxaban [(41±28) ng/ml, (273±108) ng/ml] in patients between the 2 groups, and the trough and peak plasma concentration [(40±27) ng/ml,(249±75) ng/ml] of patients at daily dose of 20-mg of rivaroxaban were not statistically significant (P>0.05 for all). Conclusion Amiodarone has no significant effects on the plasma concentration of rivaroxaban in patients with atrial fibrillation, however, it is still necessary to strengthen the patient monitoring in those with combination use of the 2 drugs.
  • Luo Aijing, Liu Juan, Huang Lingjin, Hu Qinghua, Luo Wanjun, Chen Xuliang
    Abstract ( ) PDF ( )
    Objective To explore the effect of network medication guidance on anticoagulation management of warfarin. Methods The study was designed as the retrospective cohort study. Study subjects were selected from patients who underwent cardiac valve replacement during January 2018 and April 2019 in the Department of Cardiovascular Surgery of Xiangya Hospital, Central South University, and took oral warfarin for 3 months or more after operation. According to the mode of revisit, the patients were divided into 4 groups: 1-month post-operation network group (INR review results were uploaded online for more than 2 times within 1 month after operation), 1-month post-operation control group (INR was reviewed in Xiangya Hospital 1 month after the operation and INR data was recorded), 3-month post-operation network group (INR review results were uploaded online for more than 4 times within 3 months after operation), and 3-month post-operation control group (INR was reviewed in Xiangya Hospital 3 months after the operation and INR data was recorded). The gender and age distribution of patients in the network group and the control group, as well as INR and INR compliance rate at 1 or 3 months after operation were compared. Results A total of 420 patients underwent cardiac valve replacement in Xiangya Hospital during the study period, and all of them were prescribed warfarin for anticoagulation. Among the 420 patients, 266 patients (63.3%) had network or Xiangya Hospital revisit records 1 month after operation, 71 of which were included in the 1-month post-operation network group and 178 of which in the 1-month post-operation control group; 132 (31.4%) patients had network or Xiangya Hospital revisit records 3 month after operation, 46 of which were included in the 3-month post-operation network group and 77 of which in the 3-month post-operation control group. Patients in the 1-month post-operation network group had lower age, higher INR compliance rate, and lower incidence of insufficient anticoagulation than those in the 1-month post-operation control group, and the differences were all statistically significant [(49±10) years vs. (53±11) years, P=0.009; 64.8%(46/71) vs. 45.5%(81/178), P=0.006; 21.1%(15/71) vs. 46.6%(83/178), P<0.001]. Patients in the 3-month post-operation network group had higher INR, higher INR compliance rate, and lower incidence of insufficient anticoagulation than those in the 3-month post-operation control group, and the differences were all statistically significant [(2.05±0.45) vs. (1.84±0.62), P=0.044; 67.4% (31/46) vs. 30.9% (30/97), P=0.002; 30.4% (14/46) vs. 54.5% (42/77), P=0.009]. Conclusions Network medication guidance is helpful to improve the effect of warfarin anticoagulation management and improve the INR compliance rate of patients after cardiac valve replacement. The main manifestation of substandard anticoagulation is insufficient anticoagulation, which should be paid attention to.
  • Peng Wenxing, Shi Xiujin, Xu Xiaoyu, Zhou Yang, Zhang Yi, Lin Yang
    Abstract ( ) PDF ( )
    Objective To explore the occurrence and risk factors of bleeding events in acute coronary syndromes (ACS) patients treated with ticagrelor combined with aspirin. Methods The study subjects were selected from ACS patients who were admitted to Beijing Anzhen Hospital, Capital Medical University from January to December 2017 and treated with ticagrelor and aspirin (aspirin 100-mg/d, ticagrelor 180-mg/d). Medical records of the patients who met the inclusion criteria(at age>18 years, with medication duration ≥ 1 year, and with complete follow-up records) were collected and retrospectively analyzed. The patients were divided into bleeding group and non-bleeding group according to whether there were bleeding events within 1 year. Baseline clinical characteristics such as gender, age, type of ACS, comorbidities, combined drugs, history of percutaneous coronary intervention, routine blood parameters, liver and kidney function, and etc. in patients between 2 groups were compared. The risk factors of bleeding events were analyzed using logistic regression method and the odds ratio (OR) and its 95% confidence interval (CI) were calculated. Results A total of 180 patients were entered in the analysis, including 135 males and 58 females, aged (57±10) years, with the range of 31 to 81 years. There were 39 patients in the bleeding group and 141 patients in the non-bleeding group, and the incidence of bleeding events was 21.7%. None of the differences in gender distribution, age, comorbidities, history of percutaneous coronary intervention or combined drugs in patients between the 2 groups were statistically significant (all P>0.05). The platelet count of patients in the bleeding group was significantly lower than that in the non-bleeding group [(197±49) ×109/L vs. (220±60) ×109/L, t=2.254, P=0.025]. The shortest time from medication to the onset of bleeding of the 39 patients in the bleeding group was 14 days and the longest one was 12 months. The cumulative incidences of bleeding events at 3, 6, and 12 months of medication were 12.2% (22/180), 18.3% (33/180), and 21.7% (39/180), respectively. All bleeding events were minor bleeding, and the skin mucous ecchymosis had the highest incidence, which was 15.0% (27/180), followed by gingival bleeding or nosebleed, which was 7.2% (13/180). The incidence of fundus hemorrhage was 1.7% (3/180) and incidences of gastrointestinal bleeding and hematuria were both 0.6% (1/180). Multivariate logistic regression analysis showed that low platelet count was an independent risk factor for bleeding events [OR=0.991, 95%CI: 0.984-0.999, P=0.020]. Conclusions ACS patients have a relative high risk of bleeding events when treated with ticagrelor combined with aspirin, but most of them were minor. For ACS patients with low platelet counts, this anti- platelet regimen should be used with caution and drug monitoring should be done in the whole course.
  • Wang Han, Tian Chunxiang, Ning Ping, Li Gen, Liang Hua
    Abstract ( ) PDF ( )
    Objective To explore the clinical characteristics of granulomatous mastitis (GM)induced by antipsychotics. Methods Antipsychotic-related GM cases were collected in Chengdu Women′s and Children′s Central Hospital. Meanwhile, antipsychotic-related GM literature cases in PubMed, Embase, ScienceDirect, Wanfang, VIP, and CNKI databases up to November 2019 were searched. The age, fertility status, primary mental disease, causative agents, duration of medication, diagnosis and characteristics of breast lumps, serum prolactin level, intervention measures, and prognosis of these patients were collected and analyzed retrospectively. Results A total of 7 clinical patients and 9 literature cases with antipsychotic drug-related GM were collected, and all of them were female, aged 21-55 years, of which 10 patients were never giving birth. They took antipsychotics for 0.5-17.0 years. The causative drugs included risperidone in 8 of the 16 patients. Other antipsychotics included olanzapine, clozapine, sulpiride, aripiprazole, perphenazine, quetiapine, amisulpride, flupentixol and melitracen, and etc. Serum prolactin levels elevated in 12 patients (25.45-84.50-μg/L), were normal in 3 patients, and were not mentioned in 1 patient. Surgical resection was performed in 9 patients. GM were improved significantly in the remaining 7 patients with or without adjusting antipsychotics after receiving oral administration of bromocriptine and/or methylprednisolone. And GM recurred in 1 patient during the followed-up. Conclusion Antipsychotic-related GM may occur in women of any age, regardless of whether they have giving birth. Risperidone is the main antipsychotic drug causing GM.
  • Ni Beibei, Qin Miao, Sun Chen, Li Jing
    Abstract ( ) PDF ( )
    Parenteral nutrition-associated cholestasis (PNAC) is a common and serious complication of newborns receiving parenteral nutrition support for more than 2 weeks. The occurrence of PNAC may be the result of multiple factors. Premature birth, low birth weight, long-term parenteral nutrition, lack of enteral feeding, patent ductus arteriosus, necrotizing enterocolitis, intestinal bacterial overgrowth, bacterial translocation, and imbalance of parenteral nutrition components or containing toxic ingredients are all risk factors of neonatal PNAC. The mechanism of PNAC is not clear, which may be related to the change of bile salt enterohepatic circulation, intestinal flora translocation, improper use of fat emulsions, improper use of amino acids and carbohydrate, and excessive trace elements. The prevention measurements of PNAC mainly include early enteral feeding, optimization of parenteral nutrition components, light protection during the use of nutrient solution, and so on. The therapeutic strategies of PNAC are limited, drugs such as ursodeoxycholic acid, erythromycin, phenobarbital, and rifampicin can be considered.
  • Yuan Wei, Li Yunjing, Xu Ping, Liu Wenhui
    Abstract ( ) PDF ( )
    A 56-year-old male patient with recurrent renal cell carcinoma and splenic metastasis received oral sunitinib 50-mg/d (4 weeks of medication and 2 weeks of withdrawal were defined as 1 cycle; the dosage was reduced to 25-mg/d after 2 cycles). And intravenous infusion of pembrolizumab 100-mg once every 3 weeks was added because of his illness. After 3 cycles of sunitinib and 5 cycles of pembrolizumab treatments, the patient developed muscle and joint pain, joint swelling, movement disorder, abnormal limb sensation and gradually developed symptoms such as difficulty in defecation, choking of drinking water, dysphagia, and dyspnea. The patient was diagnosed as Guillain-Barre syndrome after neurologist consultation, which might be related to the combination use of sunitinib and pembrolizumab. The above 2 drugs were stopped and dexamethasone and human immunoglobulin (pH4) for intravenous injection were given. Three days later, the patient could turn over on his own; 5 days later, his symptoms of dysphagia, dyspnea, and muscle and joint pain were relieved; 10 days later, he could stand beside the bed; one and a half month later, he could walk independently.
  • Li Yun, Li Qing, Jin Yueping, Cai Yuewei
    Abstract ( ) PDF ( )
    A 34-year-old female patient with Helicobacter pylori (Hp) infection received quadruple therapy for eradication of Hp infection, which contained esomeprazole, colloidal bismuth pectin, amoxicillin, and furazolidone. Before the treatment, the patient′s physical examination results were normal except the positive 14C urea breath test. On day 6 of medication, the patient developed fever, nausea, vomiting, and diarrhea, which returned to normal after drug withdrawal. About 20-minutes after taking furazolidone again 3 days later, the patient developed dizziness, amaurosis, vomiting, hand and foot convulsions with chills, unconsciousness, high fever, muscle soreness, fatigue, and generalized skin congestion with rash. Meanwhile her blood pressure was 76/34-mmHg. Laboratory tests showed alanine aminotransferase (ALT) 365-U/L and aspartate aminotransferase (AST) 596-U/L. Anaphylactic shock, and drug-induced liver injury were consi- dered. It was considered that the anaphylactic shock might be related to furazolidone, and liver injury might be related to esomeprazole, amoxicillin, and furazolidone. Symptomatic treatments such as blood pressure-raising, cooling, anti-allergy, and liver-protective drugs were given immediately. Ten days later, the above-mentioned symptoms disappeared completely, her body temperature was 36.3-℃, blood pressure was 126/75-mmHg, ALT was 59-U/L, and AST was 38-U/L.
  • Pei Yuying, Li Nuo, Jia Liqun, Lou Yanni
    Abstract ( ) PDF ( )
    Two patients (patient 1, a 60-year-old female; patient 2, a 62-year-old male) received oral targeted drug crizotinib (250-mg twice daily and 500-mg once daily, respectively) for anaplastic lymphoma kinase-positive non-small cell lung cancer. Both patients developed skin reactions of their hands after half a year of treatment, which were aggravated as the treatment continued. Symptoms of patient 1 presented as large red patches on the hands, forearms, and neck, with mild epidermis hypertrophy and desquamination, accompanied by obvious tenderness. Symptoms of patient 2 presented as chapped, ulcerated, and erosive skin on the fingertips and palms, accompanied by obvious pain. The 2 patients were given soaking treatment with compound granules of traditional Chinese medicine consisting of raw Astragalus, Carthamus, Radix Arnebiae, Geranium, and Radix Angelicae Sinensis, and their symptoms were obviously improved after 4 and 5 weeks, respectively.
  • Liu Qun, Jin Wenwen, Geng Ning, Lin Zhonghua, Xin Yongning
    Abstract ( ) PDF ( )
    A 63-year-old male patient took tamsulosin hydrochloride sustained release capsules 0.2-mg daily and Qianliexin capsules 2 g thrice daily by himself for urinary urgency and urodynia. Twenty- five days later, he developed itchy skin, deep brown urine, nausea, fatigue, and loss of appetite. Laboratory tests showed alanine aminotransferase (ALT) 265-U/L, aspartate aminotransferase (AST) 163-U/L, total bilirubin (TBil) 155.1-μmol/L, direct bilirubin (DBil) 74.7-μmol/L, indirect bilirubin (IBil) 80.4-μmol/L, alkaline phosphatase (ALP) 261-U/L, and gamma-glutamyltransferase (γ-GT) 184-U/L. Liver biopsy showed the cholestatic liver injury. He was diagnosed as acute drug-induced liver injury, which might be related to the above 2 drugs. The above 2 drugs were stopped and oral ursodeoxycholic acid 250-mg thrice daily was given. On day 42 of drug withdrawal, laboratory tests showed ALT 368-U/L, AST 179-U/L,TBil 504.9-μmol/L, DBil 382.8-μmol/L, IBil 122.1-μmol/L, ALP 201-U/L, and γ-GT 58-U/L. On day 91 of drug withdrawal, laboratory tests showed ALT 78-U/L, AST 62-U/L, TBil 138.1-μmol/L, DBil 118.2-μmol/L, IBil 20.2-μmol/L, ALP 140 U/L, and γ-GT 31-U/L. The patient′s liver function returned to normal 135 days after drug withdrawal.
  • Tian Xu, Zhang Hongmei, Sun Lirui, Guo Qiushi, Zhou Wei
    Abstract ( ) PDF ( )
     A 56-year-old female patient received epalrestat 50-mg thrice daily orally because of the diagnosis of diabetic peripheral neuropathy. After 3 times of epalrestat treatment that day (about 10-hours after the first medication), the patient developed red papules on the face and patch-like erythema on the head and neck. On day 2 of epalrestat treatment, the rashes were progressively aggravated and the patient was diagnosed with erythema multiforme-type drug eruption. Considering that it might be caused by epalrestat, the drug was replaced by lipoic acid injection and symptomatic treatments with dexamethasone, vitamin C injection, and calcium gluconate injection were given. Three days later, the patient′s allergic symptoms were alleviated. Anti-allergic drugs were phased out gradually while the other drugs were continued. Six days later, the patient had no discomfort and was discharged from the hospital. At 20 days of follow-up, the rashes did not recur.
  • Shi Dingyi, Sun Yiming
    Abstract ( ) PDF ( )
    A 59-year-old female patient mistakenly took air potato (Dioscorea bulbifera L.) as Polygonum multiflorum (1 steamed piece daily, and 2 on the last day) for healthcare. Ten days later, the patient developed jaundice, fatigue, anorexia, and nausea. Laboratory tests showed alanine aminotransferase (ALT) 1-090-U/L, aspartate aminotransferase (AST) 2-620-U/L, gamma-glutamyltransferase (γ-GT) 98-U/L, total bilirubin (TBil) 566.3-μmol/L, direct bilirubin (DBil) 301.5-μmol/L, and total bile acid (TBA) 351.4-μmol/L. Toxic hepatitis caused by air potato was diagnosed. IV infusions of compound glycyrrhizin injection, reduced glutathione for injection, and Yinzhihuang injection (茵栀黄注射液) and oral ursodeoxycholic acid tablets and traditional Chinese medicine decoction were given. After 25 days of treatments, her liver function were improved obviously, and laboratory tests showed ALT 39-U/L, AST 90-U/L, γ-GT 115-U/L, TBil 60.6-μmol/L, DBil 34.5-μmol/L, and TBA 121.5-μmol/L.
  • Wu Jingfang, Xin Meiyun, Han Lei
    Abstract ( ) PDF ( )
    A 7-year-old boy coughed for 7 days. His parents fed him fresh and ripe cocklebur fruit (Fructus Xanthii) once which was picked and fried by themselves (unknown dose). On the 3rd day after feeding the cocklebur fruit, the boy developed paroxysmal epigastric pain, with vomiting, anorexia, fatigue, drowsiness, and low fever. The laboratory tests showed alanine aminotransferase (ALT) 3-344-U/L, aspartate aminotransferase (AST) 3-501-U/L, serum total bilirubin (TBil) 26.5 μmol/L, direct bilirubin (DBil) 19.0 μmol/L, albumin (ALB) 32.8-g/L, and blood ammonia 120-μmol/L. On the 6th day after feeding the cocklebur fruit, the boy developed aggravated fatigue, irritability, slightly slow response, and light yellowish staining of sclera. The laboratory tests showed ALT 4-565-U/L, AST 4-335-U/L, TBil 32.9-μmol/L, DBil 23.4-μmol/L, ALB 30.2-g/L, and blood ammonia 124-μmol/L. Acute liver failure due to cocklebur fruit poisoning was considered. The boy received blood purification therapy (2 plasmapheresis and 4 days′ hemodiafiltration) and symptomatic treatments. The laboratory tests showed ALT 1-043-U/L, AST 203-U/L, TBil 22.0-μmol/L, DBil 12.3-μmol/L, ALB 39.1-g/L, and blood ammonia 36.3-μmol/L. The blood purification therapy was stopped and the symptomatic treatments was continued. The laboratory tests 2 weeks later showed ALT 24-U/L, AST 35-U/L, TBil 13.8-μmol/L, DBil 4.6-μmol/L, and ALB 47.3-g/L.
  • Ma Shuangshuang, Xu Yunshan, Shen Wei
    Abstract ( ) PDF ( )
     A 26-year-old female patient took oral methimazole 20-mg twice daily due to hyperthyroidism. More than a month later, she developed spastic pain of limb muscles. Laboratory tests showed alanine aminotransferase (ALT) 45-U/L, aspartate aminotransferase (AST) 121-U/L, creatine kinase (CK) 6-090-U/L, and serum potassium 4.1-mmol/L. The dose of methimazole was reduced to 10-mg once daily, but the patient′s myalgia was not improved after 3 days. Adverse reactions due to methimazole were considered and therefore the drug was discontinued. Four days after drug withdrawal, the patient′s myalgia was obviously relieved, and laboratory tests showed ALT 36-U/L, AST 50-U/L, and CK 1-954-U/L. After 18 days of drug withdrawal, her myalgia disappeared, and the ALT, AST, and CK returned to normal.
  • Li Xianmin, Lin Fang, Mu Jingsong
    Abstract ( ) PDF ( )
    A 27-year-old male patient mistakenly took an anti-obesity agent containing sibutramine. Two months later, the patient developed fever and myalgia. Two days later, his above symptoms were aggravated, and unconsciousness, rashes, and oliguria appeared. Laboratory tests showed serum creatinine 748-μmol/L, aspartate aminotransferase 299-U/L, alanine aminotransferase 102-U/L, total bilirubin 101.6-μmol/L, direct bilirubin 85.5-μmol/L, lactate dehydrogenase 3-070-U/L, myoglobin 12-081-μg/L, and creatine kinase 18-517-U/L. Rhabdomyolysis with multisystem injury caused by sibutramine was diagnosed. The anti-obesity agent was discontinued, and continuous renal replacement therapy and symptomatic and supportive treatments such as magnesium isoglycyrrhizinate, acetylcysteine, and terlipressin were given. After 2 weeks, the patient′s symptoms disappeared, the rashes subsided, and the liver and kidney functions and laboratory tests such as creatine kinase and myoglobin returned to normal.