2008 Volume 10 Issue 6 Published: 28 December 2008
  

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    论著

  • 论著
    Li Xiaohong;Ding Yan;Ma Junqi;Han Ying
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Objective: To observe and evaluate the safety of levonorgestrelreleasing intrauterine system (LNG-IUS) in the treatment of endometriosis. Methods:A total of 59 patients with endometriosis were studied. The LNG-IUS was inserted into the uterine cavity. The acne, facial pigmentation, premenstrual mammary swelling, the body weight, and quality of life were scored and compared before and 6 months and 12 months after the insertion of the LNG-IUS. The adverse reactions to LNG-IUS were observed. Results: The acne scores before and 6 months after the insertion of the LNG-IUS were 1.00 (0.00, 3.00) and 0.00 (0.00, 2.00), respectively, the difference was not statistically significant (P>0.05); while the acne scores were 0.00 (0.00, 1.00) 12 months after the insertion of the LNG-IUS, the difference was statistically significant (P<0.01). The facial pigmentation scores before and 6 months and 12 months after the insertion of the LNG-IUS were 1.00 (0.00, 1.00); the differences were not stastically significant (all P>0.05). The premenstrual mammary swelling scores before and 6 months and 12 months after the insertion of the LNG-IUS were 220 (0.00, 4.00), 1.50 (0.00, 4.00) and 1.00 (0.00, 3.00), respectively; the differences were statistically significant (P<005, P<0.01). The body weight before and 6 months and 12 months after the insertion of the LNG-IUS were 59.00 (55.00, 64.00)kg, 59.50 (55.00, 64.00)kg, and 59.00 (54.00, 64.00)kg, respectively; the differences were not statistically significant (all P>0.05). The quality of life before the insertion of the LNG-IUS was compared with the quality of life 6 months and 12 months after the insertion of the LNG-IUS; the differences were statistically significant (all P<0.01). The intramenstrual bleeding before and 6 months and 12 months after the insertion of the LNG-IUS were 4 cases (6.78%), 16 cases (27.12%), and 14 cases (23.73%), respectively. Other adverse reactions to LNG-IUS were hair loss (1 patient) and a feeling of swelling over entire body (2 patients). Conclusion: Levonorgestrelreleasing intrauterine system is safe in treatment of endometriosis.
  • 病例报告

  • 病例报告
    Cai Xuzhen;Huang Lina;Zheng Keyan
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    An 68-year-old woman was treated with allopurinol 0.1 g thrice daily for hyperuricemia. She received traditional Chinese medicines (injection) for 3 days during allopurinol treatment period. After 51 days of allopurinol treatment, the patient developed rash. Loratadine and traditional Chinese medicines were given, but her symptoms worsened. Three days before hospitalization, the patient's rash progressed to involve her entire body and dyspnea occurred. After admission, physical examination revealed ulceration of lips and oral mucous membrane, generalized red maculopapule, and superficial desquamation. Laboratory testing showed that BUN level increased from 7.10 mmol/L to 34.19 mmol/L, and SCr level increased from 131 μmol/L to 499 μmol/L. Allopurinol hypersensitivity syndrome was diagnosed. Allopurinol was discontinued. An infusion of dexamethasone 10 mg once daily was given. Finally, the patient died from renal failure and concurrent generalized infection.
  • 病例报告
    Zhang Chaoa;Xie Qianb
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Two male patients developed acute renal failure after receiving an IV infusion of andrographolide injection.The first patient, a 29-year-old patient, received an IV infusion of andrographolide 0.5 g for a fever. He developed lumbago after the infusion. His SCr was 142 μmol/L in the evening at that day. The next day, he was hospitalized and his SCr was 219 μmol/L. On day 2 of hospitalization, the patient’s SCr was 332 μmol/L. Acute renal failure was diagnosed. Fluid replacement and symptomatic therapy were given. Three days later, his SCr decreased to 244 μmol/L. On day 7 of hospitalisation, his SCr decreased to 149 μmol/L. After 9 days of hospilisation, the patient was discharged, and his lumbago disappeared. A followup 10 days after discharge, his renal function normalized.The second patient, a 25-year-old man, received an IV infusion of andrographolide 0.25 g and oral azithromycin 0.25 g for a cold. After about 4 hours of the infusion, the patient developed lumbago.The next day, his SCr was 189.7 μmol/L and his BUN was 889 μmol/L. All drugs were discontinued. On day 3, his lumbago persisted, his SCr was 214 μmol/L and his BUN was 8.8 μmol/L. After receiving supportive therapy, his SCr decreased to 138 μmol/L and his BUN decreased to 6.4 μmol/L. A followup one week after discharge, his renal function normalized.
  • 病例报告
    Hou Juana;Ma Jingtaob;Xu Fangb;Hu Yingb
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    A 60yearold woman with coronary heart disease received intraarterial iodixanol 50 ml prior to undergoing coronary angiography. One hour after surgery, the woman experienced dizziness, nausea, severe headache, and blurred vision. Her BP was 110/70 mmHg and her cranial CT scan was normal. She was given dexamethasone, fluid replacement and symptomatic therapy. Seven hours and a half later, her symptoms resolved completely.
  • 病例报告
    Liang Aiqun
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    A 53-year-old woman with urinary tract infection received an IV infusion of ceftriaxone sodium 2 g dissolved in 100 ml of 0.9% sodium chloride. She had no history of heart disease and drug allergy previously. Twenty-nine minutes after the first infusion initiation, the woman presented with facial and hand flushing followed by frothing from the mouth and cardiopulmonary arrest. Cardiopulmonary resuscitation started immediately and she received IV dexamethasone, IV adrenalin, IV dopamine, closed chest cardiac compressions, endotracheal intubation, and assisted ventilation. But resuscitation was unsuccessful and she died 30 minutes later.
  • 病例报告
    Zhang Wei;Liu Xiujin
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    A 68yearold woman with pulmonary tuberculosis was administered with IV rifamycin 0.5 g once daily, oral isoniazid 0.3 g once daily, and oral ethambutol 0.5 g thrice daily. Her routine blood tests were normal (WBC count 4.91×109/L, neutrophils 0.729) before therapy. After 12 days of therapy, her WBC count and neutrophils decreased to 2.48×109/ L and 0.557, respectively. Leucopenia and neutropenia were considered to be possibly rifamycinrelated. rifamycin was discontinued. Seven days later, the woman’s WBC count and neutrophils returned to within normal limits (4.41×109/L and 0.622, respectively). IV rifamycin 0.5 g once daily was restarted. Seven days later, her WBC count and neutrophils decreased to 2.93×109/L and 0.487, respectively. rifamycin was withdrawn again and switched to IV levofloxacin 0.2 g twice daily. Isoniazid and ethambutol were continued. Ten days later, her routine blood tests were normal.
  • 病例报告
    Yang Bilian;Li Yuanwen;Sun Zhanxue;Li Nan
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 63yearold woman with a 4month history of diabetes took glipizide and acarbose without adverse reactions occurring. Later, the woman received oral famciclovir 0.25 g thrice daily for herpes simplex. Two hours after the first administration, she experienced dizziness, nausea, vomiting, abdominal pain, and diarrhea. Intestinal infection was excluded by stool examination. Famciclovir was withdrawn and switched to an IV infusion of aciclovir 0.5 g once daily. Glipizide and acarbose were continued. Meanwhile, fluid replacement and symptomatic therapy were given. The following day, her dizziness and gastrointestinal symptoms disappeared completely. The patient continuously received IV infusion of aciclovir for four days. Her herpes simplex was entirely crusted and she was fully cured and discharged.

  • 病例报告
    Liu Wen;Chen Hui;Chen huiying
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 41-year-old woman with adhesive ileus underwent terminal ileum resection. The woman was given intravenous injection of hemocoagulase 1 KU dissolved in 20 ml of sodium chloride 0.9% after surgery, once every two hours for three times. No adverse reactions occurred after receiving the first and second dose of the medication. However, during the third infusion, the patient abruptly developed unconsciousness, sighing respiration, cyanosis of lips, pale face, bilateral mydriasis, and cardiac arrest. The infusion was stopped immediately. She underwent closed-chest cardiac message and oxygen with assisted mask ventilation. Lidocaine, adrenaline, and atropine were given intravenously. Thirty minutes later, her heart beat and respiration recovered.

  • 病例报告
    Xing Yan;Lu Shan;Tang Ya'nan;Zhou Wei
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 1year and 9monthold girl with Kawasaki disease took dipyridamole 25 mg for treatment of thrombocytosis (684×109/L). About 15 minutes after taking the first dose, the girl developed vomiting, drenching sweats, pallor, perioral cyanosis, swelling of her lips, and dyspnea. She had a temperature of 36.3℃, a HR of 130 beats/min, a respiration rate of 32 breaths/min, and a BP of 97/54 mmHg. Dipyridamoleinduced anaphylaxis was diagnosed. Intramuscular adrenalin was administered immediately. Her symptoms resolved 5 minutes later. Cetirizine and methylprednisolone were given 30 minutes later. She recovered completely one hour later.

  • 病例报告
    Zheng Shiming
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    An 18 yearold woman received general intravenous anesthesia with propofol for induced abortion. The woman received IM atropine 0.5 mg 30 minutes before being transferred to the operating room. Her blood pressure was 116/68 mmHg, her heart rate was 70 beats/min, and her SPO2 was 97% after she was transferred to the operating room. She developed chest distress followed by dysphoria, pallor, dyspnea and extensive urticaria on her chest after a slow IV injection of propofol about 50 mg. Her blood pressure was 50/30 mmHg, her heart rate was 138 beats/min and her SPO2 was 85%. Propofolinduced anaphylactic shock was suspected. Propofol was discontinued immediately. Adrenalin, dexamethasone, promethazine and dopamine were given. Her symptoms improved ten minutes later.
  • 安全合理用药

  • 安全合理用药
    Luo Ling;Li Qinglin;Liu Jinggen
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Selective serotonin reuptake inhibitors (SSRIs) are a widely used newer class of antidepressants, which can treat different types of depression. The commonly used SSRIs are fluoxatine, paroxetine, sertraline, fluvoxamine, and citalopram. The SSRIs can cause various types of adverse reactions. The main adverse reactions are gastrointestinal disorders, withdrawal reactions, sexual disturbances, and syndrome of inappropriate secretion of antidiuretic hormone (SIADH), etc. SSRIs may increase the risk of suicidal thinking and behaviour in children and adolescents, but the issue remained controversial. The recent studies have suggested that exposure to SSRIs early in pregnancy appeared to be no increase in the risk of congenital malformations; however, exposure to SSRIs late in pregnancy may incresae the risk of pulmonary hypertension and withdrawal reactions of the newborn. In general, breastfeeding with SSRIs is regarded as safe because the amount of drug is very low in breast milk. But the possibility of longterm effects on development in the infant is unknown. As for the elderly, SSRIs may increase the risk of fracture. Adverse reactions resulting from interations of SSRIs with some drugs are given below. MAOIs: serotonin syndrome; diuretics: severe hyponatremia; anticoagulants: increased risk of bleeding; NSAIDs: increased risk of upper gastrointestinal bleeding; tryptophan: serotonin syndrome; astemizole, terfenadine: ventricular arrhythmias and Q-T interval prolongation; haloperidol, maprotiline: severe extrapyramidal symptoms; lithium increase in plasma lithium concentration and lithium toxicity. Overall, SSRIs have fewer adverse effects than tricyclic antidepressants, but the SSRIs do have characteristic adverse reactions of their own. Therefore, doctors should exercise caution when prescribing SSRIs to patients in clinical practice.
  • 调查研究

  • 调查研究
    Zheng Ping;Zhou Fan;Wen Yunheng
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Objective: To investigate the causes of cefradineinduced hematuria in children. Methods: Clinical data from 19 children with hematuria induced by cefradine use in the community from March 2005 to March 2008 were collected. The patients’ sex and age, clinical presentation, dosage and administration of cefradine, the onset time, intensity and outcome of hematuria were investigated and analyzed. Results: Of the 19 children, 16 were males, 3 were females, and their age was ≤ 1 year (3 cases), ~3 years (10 cases), ~7 years (4 cases), and >7 years (2 cases). The routine dosage of cefradine was 50~100 mg/(kg·d) dissolved in 100~250 ml of sodium chloride 0.9% or glucose 5% for an IV infusion. Sixteen patients received 100 mg/(kg·d). One patient received 110 mg/(kg·d), two patients received <100 mg/(kg·d).The daily dosage was used as a single dose in 17 patients. Of the 19 patients, 17 developed gross hematuria and two developed microscopic hematuria. Laboratory tests showed RBC (+++~++++)/HP and urinary protein <0.1 g/24 h. Sixteen patients (84.2%) had normal renal function and 3 patients (15.8%) had mild elevation in SCr and BUN levels. Eighteen patients (94.7%) developed hematuria within 24 hours after receiving drug therapy. One patient’s hematuria onset was over 24 hours. After drug withdrawal, gross hematuria disappeared within 1~2 days and microscopic hematuria disappeared within 3~5 days. At 3month followup after discharge, their routine urine and renal functions normalized. Conclusion: Hematuria following an IV infusion of cefradine in childnen might be linked to the factors of large dose, high concentration, and young age.
  • 病例报告

  • 病例报告
    Wang Hongtao;Yang Wei;Sheng Qiuju;Wang Yunxiu;Liu Zhuogang;Li Yingchun;Liao Aijun
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Two patients receiving highdose methotrexate chemotherapy developed acute renal failure.Patient 1, a 53-year-old woman with nonHodgkin lymphoma, received highdose methotrexate chemotherapy. Initially she was infused with methotrexate 500 mg intravenously within half an hour, followed by 3500 mg via infusion pump within 24 hours. Then calcium folinate was given for rescue. The first dose of calcium folinate was 30 mg/m2, followed by 15 mg/m2 intramuscularly once every 6 hours for 8 doses. The patient had no history of chronic renal disease. Her renal function was normal before chemotherapy (SCr 97.1 μmol/L, BUN 4.78 mmol/L). On day 4 after chemotherapy, she developed mild edema of the face and both hands, and oliguria; her SCr increased to 151 μmol/L. Methylprednisolone, furosemide, and calcium carbonate and vitamin D3 were given; her urinary alkalinisation and monitoring of renal function were performed (a peak SCr level of 275 μmol/L). On day 13 after chemotherapy, her renal function returned to within normal range (SCr 96 μmol/L).Patient 2, a 29-year-old man with acute lymphoblastic leukemia, received highdose methotrexate chemotherapy. Initially he was infused with methotrexate 500 mg intravenously within half an hour, followed by 4500 mg via infusion pump within 24 hours. The regimen of rescue was the same as patient 1. The patient had no history of chronic renal disease. His renal function was normal before chemotherapy (SCr 86.9 μmol/L, BUN 5.35 mmol/L). On day 3 after chemotherapy, he developed generalized edema and oliguria; his SCr increased to 235 μmol/L (peak level 360 μmol/L). The symptomatic treatment was given (the regimen was the same as patient 1). On day 30 after chemotherapy, his renal function returned to within normal range(SCr 89 μmol/L).
  • 病例报告
    Zhang Haiying;Shi Xiaowei;Li Yuzhen
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 46-year-old woman was hospitalized with tuberculous pleurisy. She was treated orally with rifampicin 450 mg once daily, isoniazid 300 mg once daily, pyrazinamide 500 mg thrice daily, and ethambutol 750 mg once daily. Her platelet count was 335×109/L before treatment. After 14 days of therapy, her platelet count decreased to 1.8×109/L, and the dense bleeding points and ecchymoses occurred on her skin of extremities and abdomen. Rifampicin was withdrawn, and platelet transfusion and methylprednisolone treatment was given. The other therapy remained unchanged. One week later, her platelet count increased to 1642×109/L.

  • 病例报告
    Yuan Xiaoying;Zheng Wei
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    42year-old man with pustular psoriasis was treated with acitretin capsules 30 mg once daily. His routine blood test was basically normal before therapy. He had a RBC count of 3.65×1012/L, a WBC count of 9.5×109/L, and a PLT count of 246×109/L. One week after administration, his RBC was 3.67×1012/L, his WBC was 16.5×109/L, and his PLT was 412×109/L, respectively. Pathological examination showed thrombocytosis and bone marrow hyperplasia. An ultrasound examination showed splenomegaly. The dosage of acitretin was reduced to 15 mg/day. Three weeks later, a reexamination revealed a RBC count of 3.72×1012/L, a WBC count of 14.3×109/L, and a PLT count of 446×109/L. The dosage of acitretin was continuously reduced to 10 mg/day. Two weeks later, a reexamination revealed a RBC count of 3.48×1012/L, a WBC count of 10.3×109/L, and a PLT count of 385×109/L. No abnormal abdominal findings were observed on ultrasound examination.
  • 论著

  • 论著
    Zhou Li;Wu Chunqi;Wang Qingxiu;Yang Baohua;Liao Mingyang
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Objective: To study the dose-effect and time-effect relations to spermatogenic cell apoptosis of rats induced by hydroxyurea. Methods:In the dose-effect study, 25 male Wistar rats were divided into 5 groups (5 rats in each groups). Of the 5 groups, 4 were the test groups and 1 was the control group. Each of the four test groups was administered with a different dose of hydroxyurea (100 mg/kg, 200 mg/kg, 400 mg/kg, and 600 mg/kg) by intraperitoneal injection, respectively. The control group was administered with phosphatebuffered solution 2 ml/kg. All rats were killed 12 hours after dosing. In the timeeffect study, 20 male Wistar rats were divided into 4 groups(5 rats in each groups). Of the 4 groups, 3 were the test groups and 1 was the blank control group. The three test groups were administered with hydroxyurea 400 mg/kg by intraperitoneal injection. All rats were killed 6, 12, and 24 hours after dosing. The dead rats and their testes were weighed. The testes were fixed in Bouin's solution and then stained with hematoxylineosin. Morphological changes were observed under light microscope. The TUNEL staining of apoptotic cells and PAS staining for glycogen were performed. The number of apoptotic cells was counted and the stages of seminiferous epithelial cycle were analysed. Results: There were no significant changes in weights of body and testis 6, 12, and 24 hours after dosing compared with before dosing. The results of the doseeffect study showed the rates of apoptoticpositive seminiferous tubule and apoptotic index were markedly elevated with the increase in doses, especially in 400 mg/kg \[(38.7±2.0)% and (496.4±66.8), respectively\] (P<0.01). The results of the timeeffect study showed the mean number of apoptoticpositive spermatogenic cell and apoptotic index reached a peak at 12 hours after dosing \[(12.9±2.10) and (496.4±66.8), respectively\] compared with the control group. TUNELpositive cells were mainly in stage Ⅰ~Ⅳ of seminiferous cycle. Conclusion: The spermatogenic cell apoptosis of rats induced by hydroxyurea is cell-specific and stage-specific.
  • 病例报告

  • 病例报告
    Gao Ling;Yang Xiaoqing
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 48yearold woman was given an IV infusion of cefoperazone/sulbactam 3 g dissolved in 0.9% sodium chloride injection 250 ml for treatment of bronchitis. The patient developed difficulty breathing, agitation, lips cyanosis, and unconsciousness with an unrecordable BP about 10 minutes after starting the infusion. Cefoperazone/sulbactam was discontinued immediately. Despite treatment with oxygen inhalation, adrenaline, dexamethasone, and hydrocortisone, she died.

  • 论著

  • 论著
    Zhang Hong;Deng Xiaohu;Zhang Yamei;Zhang Jianglin;Huang Feng
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Objective: To observe the adverse reactions of etanercept in the treatment of ankylosing spondylitis (AS). Methods:A randomized, doubleblind, placebocontrolled parallel study was conducted. From April 2005 to January 2006, 52 patients with active ankylosing spondylitis were enrolled in the study, and randomly divided into the etanercept and placebo groups (26 patients in each group). The patients' average age in the etanercept group was (27.7±8.5) years, and in the placebo group was (29.7±8.1) years. The trial duration was 12 weeks. The first 6 weeks were a doubleblind phase and the second 6 weeks were an openlabel phase. During the doubleblind phase, the patients in the etanercept group received etanercept subcutaneously in a dose of 25 mg twice a week for 6 weeks and the patients in the placebo group received inactive substance subcutaneously in a dose of 25 mg twice a week for 6 weeks. During the openlabel phase, all the patients in both groups received etanercept subcutaneously in a dose of 25 mg twice a week for 6 weeks. Routine blood test was performed at week 0, 1, 2, 4, 6, 7, 8, 10, and 12, meanwhile the dermal lesion at the site of injections, the skin and its appendages reactions, infections, hematological disorders, liver enzyme levels, autoantibody response, and other adverse reactions were observed and analysed. Results: The incidence of adverse reactions in the etanercept and placebo groups was 23% and 38%, respectively; the difference was not statistically significant (P>0.05); no serious adverse reaction occurred. During the doubleblind phase, 26.9% of the patients in the etanercept group developed local dermal lesions characterized by redness and swelling, induration, and pruritus at the site of injections, and no case of such local dermal lesions was found in the placebo group; the difference between both groups was statistically significant (P<0.05). During the trial period, the incidence of the reactions at the site of injections was 34.6%. During the doubleblind phase, 6 patients (23.1%) in the etanercept group developed neutrocytopenia, but neutrocytopenia was not found in the placebo group; the difference between both groups was statistically significant (P<0.05). The difference in the other adverse reactions including upper respiratory tract infections (5 vs 7), skin reactions (6 vs 3), and increased liver enzyme levels (5 vs 8) between the etanercept and placebo groups was not statistically significant (all P>0.05). Conclusion: Etanercept is a relatively safe agent in treatment of ankylosing spondylitis.
  • 安全合理用药

  • 安全合理用药
    Fang Jianguo;Liu Dan
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Fluoxetine is one of the selective serotonin reuptake inhibitors, which is often used for treating depression and obsessivecompulsive disorder. Fluoxetine cardiotoxicity includes arrhythmia, torsades de pointes ventricular tachycardia, QT internal prolongation syndrome, serious cardiac damage, and death. The mechanism of cardiac adverse reactions caused by fluoxetine remains uncertain presently. Fluoxetine can cause interactions with some drugs that are metabolized by CYP2D6 leading to cardiac adverse reactions. Clinicians should exercise caution when prescribing fluoxetine to patient with cardiovascular disease, female patients, and elderly patients. ECG monitoring might be performed, if necessary.
  • 调查研究

  • 调查研究
    Dong Shenga;Qi Xiaolianb;Hu Yongshenga
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Objective: To analyse the effects of oral sodium valproate on plasma fibrinogen levels. Methods: Clinical data from the patients with decreased plasma fibrinogen levels in our hospital from March 2007 to January 2008 were collected. The patients’sex and age, dosage and administration of sodium valporate, treatment duration, time period after drug withdrawal, changes in fibrinogen levels before and after drug withdrawal, and outcome were investigated retrospectively. Results: Of the 7 patients [6 males and 1 female aged 15~43 years, average age (23.43±9.24) years], four received sustainedrelease sodium valporate tablets and three received sodium valporate tablets. The dosage was 0.1~0.6 g two to three times daily. Treatment duration was (8.9±8.8) months. The time period after drug withdrawal was (6.14±3.80) d. Fibrinogen levels before and after drug withdrawal were (1.56±0.45)g/L and (3.98±2.23)g/L, respectively. The difference was stastistically significant (P<0.05). After stopping sodium valproate and receiving symptomatic therapy, six patients’fibrinogen levels increased to 2.0 g/L, One patient’s fibrinogen level increased from 1.58 g/L to 1.71 g/L 6 days after drug withdrawal. Conclusion: Sodium valproate can decrease plasma fibrinogen levels of patients. Fibrinogen levels should be monitored during sodium valproate therapy for preventing severe bleeding.
  • 药源性疾病

  • 药源性疾病
    Geng Fengying;Yang Yue;Jin Dan;Yang Hua;Ma Hui;Yang Yueming;Wang Yuxin
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Druginduced headaches refer to a headache caused either directly or indirectly by medications, which account for 5%~10% of the headaches. Mechanism of druginduced headaches is unclear. The comnon causes of drug-induced headaches are as follows: vasodilation, benign intracranial hypertension, aseptic meningitis, disulfiram-like reactions, and analgesic overuse. Clinical presentation of druginduced headaches may be accompanied by dizziness, nausea, vomiting, facial flushing, and decreased blood pressure, besides headache symptoms. The most common causative agents include NSAIDs, histamine H2 receptor antagonists, calcium antagonists, and vasodilators. Care must be taken to distinguish a headache during drug therapy from a headache secondary to the primary disease. The symptoms of druginduced headaches may relieve after stopping the offending agents and receiving symptomatic therapy.
  • 病例报告

  • 病例报告
    Liu Ensheng;Lv Xin
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    Two patients receiving succinylated gelatin injection during surgery developed anaphylactic shock.Patient 1, a 16-year-old woman received an IV infusion of succinylated gelatin during undergoing malignant schwannoma resection. After infusion of 20-30 ml, her BP suddenly fell to 26/20 mmHg with a HR of 150 beats/min, and her generalized skin had an ‘orange peel’ appearance. The surgery was stopped immediately. Her condition improved after antianaphylactic and anti-shock treatment. Three days later, she underwent surgery again. The anesthesia remained the same and no adverse reactions occurred.Patient 2, a 46-year-old woman underwent an exploratory laparotomy for recurrence of postoperative ovarian cancer. She received an IV infusion of succinylated gelatin during surgery. After infusion of about 100 ml, her BP abruptly fell to 40/20 mmHg, and her chemosis occurred. The medication was withdrawn at once and her condition improved after antianaphylactic and antishock treatment. Her surgery was continued.

  • 病例报告
    Chen Hui;Zhu Wei;Lian Shi
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    A 78yearold woman was hospitalized with cerebral hemorrhage, right central hemiparalysis and pulmonary infection. On day 21 after admission, her urine and stool examinations showed fungal spore and hyphae. She was considered to have fungal infections. The woman received an IV infusion of fluconazole 0.4 g daily on day 1 of therapy, followed by fluconazole 0.2 g daily. Three days later, she developed an erythematous macular eruption with mild pruritus on her chest and abdomen. Fluconazole was stopped and changed to an IV infusion of itraconazole 0.25 g twice daily. Two days later, her erythematous macular eruption with marked pruritus progressed to cover her trunk and extremities. Itraconazole was discontinued and replaced with an IV infusion of allimin and oral chlorphenamine. Five days later, her skin eruption basically subsided.
  • 病例报告
    Zhu Caiyong;Sun Aijuan;Zhen Ying
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Three patients experienced musculoskeletal pain after treatment with acitretin.The first patient, a 35-year-old woman with palmoplantar pustulosis, ingested acitretin 30 mg/d. After one week of treatment, she experienced myalgia in her right shoulder, back, and right upper limb, so she reduced acitretin dosage to 20 mg/d herself, and her pain symptoms disappeared after a week. Half a month later, she increased acitretin dosage to 30 mg/d again for her poorly controlled palmoplantar pustulosis. Three days later, the myalgia reappeared at the same sites, so her acitretin dosage was decreased to 20 mg/d again, and her pain symptoms disappeared after a week.The second patient, a 42-year-old man with palmoplantar pustulosis, ingested acitretin 30 mg/d. Nine days later, he developed severe generalized musculoskeletal pain, which significantly interfered with his daily activities. The patient discontinued acitretin himself, but his pain did not disappear after a week. Subsequently, he received oral nonsteroidal antiinflammatory drugs, and his symptoms resolved gradually after five days.The third patient,a 57-year-old man with psoriasis, ingested acitretin 30 mg/d. Five days later, he developed bilateral knee joint pain. Acitretin was stopped at once. Three days later, his pain disappeared completely.
  • 中毒救治

  • 中毒救治
    Xu Fengquan;Feng Xinghua
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    Strychni semen is the dried ripe seed of Strychnos nuxvomica L. The crude drug contains alkaloids, of which the main alkaloids are strychnine and brucine. Strychnine is the main toxic component of strychni semen. Generally, the oral intoxicating dose of strychnine in adults is 5~10 mg, and the oral lethal dose is 30 mg. Strychnine can cause excitation of all parts of the central nervous system. Early signs of intoxication are headache, dizziness, nausea, vomiting, anxiety, restlessness, and slight twitching. Generalized convulsion, increasing sensitivity of sense organs, trismus, risus sardonicus, opisthotonus, dysphagia, and dyspnea follow. The patients often die from respiratory arrest. The principle of therapy in strychni semen poisoning is the prevention or control of convulsions and asphyxia. Management includes gastric lavage, the administration of activated charcoal, sedation with diazepam or phenobarbital, respiration support, and symptomatic treatment. The following precautions should be taken for safe use of strychni semen: crude drug should not be used, and the dosage should conform to the dosage limit in Chinese Pharmacopoeia; strychni semen should not combine with some drugs such as spirit, poppy capsule, musk, and so on; strychni semen is contraindicated in pregnant women; strychni semen should be used with caution in patients with liver and renal function insufficiency, neurological disorders, hypertension, and heart disease; overuse and prolonged use of strychni semen should be avoided, otherwise careful monitoring should be performed; the dosage should be adjusted when using strychni semen from different producing area.

  • 中毒救治
    Xie Lijing;Ding Maobai;Sun Chengye
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )
    Coriaria sinica Maxim is a Chinese herbal medicine. The plant contains sesquiterpene lactons, of which the main toxic components are coriamyrtin, tutin, etc. Coriamyrtin and tutin are a antagonist of γ-aminobutyric acid receptor. They cause the stimulation of the central nervous system and the enhancement of the spinal cord reflex, leading to convulsions. All parts of the plants are toxic, especially in unripe fruits. Ingesting the fruits 15~60 g may cause intoxication. The LD50 of coriamyrtin in mice by intramuscular injection is 1.75 mg/kg. Reports of accidental poisoning in children who eating the fruits are frequent. Generally, the onset time of intoxication symptoms after ingestion of Coriaria sinica Maxim is 0.5~3 h. Early symptoms of Coriaria sinica Maxim poisoning are nausea, vomiting, dizziness, headache, chest distress, abdominal disomfort. Anxiety, restlessness, increased blood pressure, accelerated respiration, generalized convulsion follow. The patients often died from cardiopulmonary arrest. Management includes gastric lavage, catharsis, administration with diazepam or phenobarbital, symptomatic and supportive treatment.
  • 中药不良反应

  • 中药不良反应
    Hu Wei;Shi Shaohong;Yang Jiayao
    2008, 10(6): 0-0.
    Abstract ( ) PDF ( )

    A 35-year-old woman was hospitalized with worsening of generalized rash. Before admission, she had taken Baixuanxiatare tablets for one year. After hospitalisation, she received monoammonium glycyrrhizinate, chlorphenamine, diphenhydramine, and acitretin. Four days after admission, because of bloody stools, she underwent enteroscopy, which revealed a dark brown colic mucous membrane. Colon biopsies showed the presence of pigmentladen mononuclear phagocytes within the lamina propria. Melanosis coli was diagnosed. Baixuanxiatare tablets were discontinued and other drugs were continued. One year later, a repeated enteroscopy revealed normal mucosa in the colon. Melanosis coli might be associated with anthraquinonecontaining aloe in Baixuanxiatare tablets.

  • 综述

  • 综述
    Yang Xinghua;Zhan Siyan
    2008, 10(6): 381-6.
    Abstract ( ) PDF ( )
    Objective: The casecrossover study design proposed by Maclure in 1991 is a method to assess the transient effects on the risk of onset of rare acute events. The case-crossover study has the following features: only data from patients are required; this design allows each patient to serve as his/her own control; patient-level confounding variables, such as gender, are readily controlled; this study eliminates the bias in control selection. The case-crossover study is most suitable for evaluating relations within the following characteristics: the individual exposure varies within short time intervals; the disease has abrupt onset and short latency; the induction period is short. The case-crossover study has been applied in assessing several adverse drug events, such as vaccine safety, drug-induced skin reactions, drug exposure and insidious outcome, the suspected risks of illicit drug use. The case-crossover study is worth using in the investigation of acute adverse events.
  • 病例报告

  • 病例报告
    Wang Chunyun
    2008, 10(6): 386-1.
    Abstract ( ) PDF ( )
    A 23-year-old woman with depression successively received fluoxetine, venlafaxine, amfebutamone and amantadine without adverse reactions. Subsequently duloxetine 60 mg was added to the regimen of amfebutamone 225 mg/d and amantadine 0.2 g/d, which was given in the morning. Two to three days later, the woman presented with redness and swelling on the dorsum of her feet without pain; her renal function and rheumatoid factor examinations were normal. Treatment with IV cefalexin was ineffective. Duloxetine was withdrawn after fourteen days of administration. Amfebutamone and amantadine were continued. The redness and swelling on the dorsum of her feet subsided 3-5 days later.
  • 论著

  • 论著
    Zhang Qi;Peng Miaoguan;Jiang Peipei;Huang Yanping;Min Yunbing;Li Meizhong;Huang Jufang;Luo Jinhua;Wang Dan;Wang Ying;Liao Zhihong
    2008, 10(6): 387-5.
    Abstract ( ) PDF ( )
    Objective: To study on relationship between sulphonylureasinduced hypoglycemia and CYP2C9 genotype in patients with type 2 diabetes. Methods: The outpatients with type 2 diabetes receiving sulphonylureas treatment were enrolled in a study from November 2006 to May 2007. The patients’blood glucose levels and CYP2C9 genotype were measured. The relationship between hypoglycemia and CYP2C9 genotype was analyzed. Results: Of 146 patients with type 2 diabetes, 43 were males, 103 were females, and their ages were 23~79 years\[average age (62.5±12.4) years\]. All patients received sulphonylureas. The specific drugs and dosages were as follows: glipizide 5~10 mg/d, gliclazide 80~160 mg/d, sustainedrelease gliclazide 30~60 mg/d, glimepiride 0.5~2 mg/d, and glibenclamide 5~10 mg/d. Seventyfour cases of 146 patients developed hypoglycemia. Of the 74 cases, 19 were sulphonylureasinducedhypoglycemia and 55 were other factorinduced hypoglycemia (as a consequence of delayed meal, less intake of food, excessive exercises, and so on).Of the 146 patients, 13(8.9%) were CYP2C9*1/*3 genotype, and 7 of the 13 cases were in the hypoglycemia group, 6 were in the nonhypoglycemia group. Of 19 cases of sulphonylureasinduced hypoglycemia, 6 were CYP2C9*1/*3 genotype. Of 55 cases of other factorinduced hypoglycemia, 1 was CYP2C9*1/*3 genotype. There was a statistical difference in CYP2C9 genotype between the sulphonylureasinduced hypoglycemia group and the other factorinduced hypoglycemia group or the nonhypoglycemia group (P<0.05). Conclusion: Sulphonylureasinduced hypoglycemia occurring in patients with type 2 diabetes might link to CYP2C9 gene mutation (CYP2C9*1/*3).