2021 Volume 23 Issue 7 Published: 28 July 2021
  

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  • Zhong Zhilei, Chen Qiuyu, Ma Ruilan, Qi Qiucheng, Li Jiaxuan, Yang Jingsi
    Abstract ( ) PDF ( )
    Vaccines have made great contributions to the prevention of infectious diseases, but vaccine hesitancy is widespread in the world. The reasons for vaccine hesitancy are complex, but the main reasons are the lack of public awareness of vaccine-preventable diseases and the lack of confidence in vaccine effectiveness and safety. In the context of the continuous spread of the coronavirus disease 2019 (COVID-19) epidemic, boosting public confidence and ensuring the orderly development of the vaccination work of COVID-19 vaccines and conventional vaccines are necessary to curb the resurgence of the COVID-19 epidemic and prevent the outbreak of various infectious diseases in China. Under the current situation, the main measures to deal with vaccine hesitancy are to play the role of health care institutions, improve public health literacy, normalize the public opinion orientation of the media platform, strengthen the supervision of vaccine clinical research and production, and do a good job in surveillance and compensation for adverse events following immunization.
  • Guan Yue, Mu Fei, Zhang Wei, Qiao Yi, Wang Congcong, Chen Sunin, Guo Guiping, Wang Jingwen
    2021, 23(7): 342-347.
    Abstract ( ) PDF ( )
    Benifits outweigh the risks for patients with autoimmune disease (AID) in remission period to be vaccinated with coronavirus disease 2019 (COVID-19) vaccines. The mRNA vaccines, inactivated vaccines, and recombinant protein subunit vaccines are safe for AID patients, whereas the safety of recombinant adenovirus vector-based vaccines is still uncertain. Some drugs for the treatment of AID may reduce the immune response of the body to the COVID-19 vaccines and affect the immune efficacy of the vaccine, which may be related to the timing of vaccination. Based on several published relevant guidelines and recommendations for the COVID-19 vaccines in AID patients, this article elaborates on vaccination problems to be paid attention to in patients with AID treated with different drugs.
  • Wang Yueyuan, Zhou Yanglin, Yang Liu, Gou Mengqiu, Bian Yuan
    Abstract ( ) PDF ( )
    Solid organ transplant (SOT) recipients are a high-risk population for coronavirus disease 2019 (COVID-19), and the safety and efficacy of COVID-19 vaccines in this population is of great concern. At present, the published studies on COVID-19 vaccines for SOT recipients are mainly about mRNA vaccines and there are a few cases reports on recombinant adenovirus vector-based vaccines. These results show that the COVID-19 vaccines are safe for the SOT recipients, but the immune response rates are lower and the incidence of vaccine breakthrough infections is higher than that in the general population. Based on the results of the current studies, SOT recipients can start to be vaccinated with COVID-19 vaccines 1 to 3 months after organ transplantation. Prevention of COVID-19 after vaccination is still necessary to avoid vaccine breakthrough infections.
  • Tong Zhiqiang, Xing Yue, Jiang Shuai, Li Xiang, Dong Mei
    Abstract ( ) PDF ( )
    Patients with cancer are at high risk for coronavirus disease 2019 (COVID-19). Institutions for disease control and prevention and cancer-related learned societies in many countries recommend prioritizing cancer patients for COVID-19 vaccines. All the COVID-19 vaccines currently approved for emergency use, including inactivated vaccines, mRNA vaccines, recombinant adenovirus vector-based vaccines, and recombinant protein subunit vaccines, can be applied in cancer patients. Cancer patients with stable disease can be vaccinated against COVID-19 at any time, while patients with advanced-stage cancer or undergoing anticancer therapy should decide on the timing of vaccination according to the specific situation such as treatment methods and cancer type, etc.. The benefits of COVID-19 vaccination in cancer patients may outweigh the risks, but the immune response rate may be lower in cancer patients, especially in patients with haematological malignancies, than in healthy individuals.
  • Cai Haodong
    Abstract ( ) PDF ( )
    Patients with chronic kidney disease (CKD) are at high risk for coronavirus disease 2019 (COVID-19). Government agencies or learned societies in many countries recommend prioritizing patients with CKD for COVID-19 vaccines. The immune response rate to the COVID-19 vaccines is lower in hemodialysis patients and kidney transplant recipients compared with that in healthy individuals, and increasing the number of vaccinations each member of these population may improve their immune response rate. There was no significant difference in the incidence of adverse reactions after vaccination between patients with CKD and healthy controls. Patients with stable CKD should be vaccinated against COVID-19 unless there were contraindications to vaccination. The mRNA vaccines, inactivated vaccines, and recombinant protein subunit vaccines are all safe for patients with CKD. Patients with CKD treated with rituximab or high-dose glucocorticoid need to weigh the benefits and risks before vaccination, and COVID-19 vaccines can be given when rituximab treatment ends for more than 6 months or after glucocorticoid reduction.
  • Luo Juan, Yuan Qi, Diao Changdong, Chen Xu, Fan Li, Shi Chen
    Abstract ( ) PDF ( )
    Objective To compare the adverse reactions of oxycodone hydrochloride prolonged- release tablets and fentanyl transdermal system in the treatment of moderate and severe cancer pain. Methods The medical records of patients with moderate to severe cancer pain who used oxycodone hydrochloride prolonged-release tablets (oxycodone group) or fentanyl transdermal systems (fentanyl group) for more than 1 week during hospitalization in Union Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology from January 2018 to December 2019 were collected. The occurrence of adverse reactions after analgesic treatments were retrospectively analyzed. Results A total of 698 patients were enrolled in the analysis, including 535 in the oxycodone group and 163 in the fentanyl group. The incidence of adverse reactions in the oxycodone group was significantly higher than that in the fentanyl group [72.5% (388/535) vs. 51.5% (84/163), χ2=25.139, P<0.001]. The common adverse reactions (with incidence ≥5%) in the oxycodone group were constipation, nausea/vomiting, xerostomia, drowsiness, and dizziness, while those in the fentanyl group were constipation, nausea/vomiting, and dizziness. The incidence of constipation in the oxycodone group was significantly higher than that in the fentanyl group [60.9% (326/535) vs. 40.5% (66/163), χ2=21.209, P<0.001]. The differences in the incidence of other adverse reactions in the 2 groups were not statistically significant (all P>0.05). All adverse reactions were grade 1 or 2, which were improved after symptomatic treatments. No adverse reactions of grade 3 or more severe occurred.Conclusions Both oxycodone hydrochloride prolonged-release tablets and fentanyl transdermal system are safe during the treatment for moderate to severe cancer pain, with mild adverse reactions, which can be relieved by symptomatic treatments. Oxycodone hydrochloride prolonged-release tablets are more likely to cause constipation than fentanyl transdermal system.
  • Liu Hui, Liu Yan, Liu Yuan
    Abstract ( ) PDF ( )
    Objective To explore the clinical characteristics of type 1 diabetes mellitus (T1DM) related to nivolumab (NIVO). Methods Databases including CNKI, Wanfang, VIP, PubMed, Web of Science, and Embase were searched as of December 31, 2020 and case reports on T1DM related to NIVO were collected. The patients′ information including general situation, primary disease, NIVO use, and occurrence, treatment, and outcome of T1DM, etc. were extracted and analyzed by descriptive statistical method. Results A total of 18 patients with NIVO-related T1DM reported in 17 literature were collected, including 9 males and 9 females, aged from 49 to 84 years with an average age of 69 years. The primary diseases were malignant melanoma in 8 patients, non-small cell lung cancer in 6 patients, renal cell carcinoma in 3 patients, and prostate cancer in 1 patient. Sixteen patients were treated with NIVO alone and 2 patients were treated with NIVO combined with ipilimumab. The time from NIVO treatment to diagnosis of T1DM was 34-841 days in 18 patients (<100 days in 7 patients, 100-300 days in 6 patients, and >300 days in 5 patients). Of the 18 patients, 13 (72.2%) developed fulminant T1DM and 11 (61.1%) developed diabetic ketoacidosis (DKA). The main clinical manifestations included fatigue, polyuria, polydipsia, thirst, etc., and delirium or drowsiness could also occur. One case had no clinical symptoms. Laboratory tests showed that the blood glucose levels increased obviously (17.4-52.8-mmol/L) in all 18 patients; 17 patients had HbA1c examination records, among which 16-had elevated level (by 6.5%-13.4%); 14 patients had serum C-peptide test record and the levels were all lower than the lower limit of reference value. After T1DM occurrence, 18 patients were all treated with insulin and other symptomatic treatments; NIVO was stopped in 12 patients (ipilimumab was stopped in 2 patients at the same time) and blood glucose levels returned to normal in 7 patients and were not described in 5 patients; NIVO was not stopped in 4 patients and the blood glucose levels returned to normal in 2 patients and were not recorded in 2 patients. Among the 12 patients who stopped using NIVO, 3 died of tumor progression. Conclusions NIVO-related T1DM mostly occur within 300 days after medication. The clinical manifestations are similar to those of common T1DM. The proportion of fulminant T1DM and DKA are relatively high. The blood glucose levels in most patients can be controlled after stopping NIVO and receiving insulin and other symptomatic treatments.
  • Wang Shuo, Cai Haodong, Mei Dan
    Abstract ( ) PDF ( )
    Vaccine development and vaccination are the most effective means to prevent and control coronavirus disease 2019 (COVID-19). At present, there are 4 types of COVID-19 vaccines approved for emergency use by the World Health Organization and approved conditionally for marketing and emergency use by State Drug Administration of China, including inactivated vaccine, recombinant protein subunit vaccine, messenger RNA vaccine, and adenovirus vector-based vaccine. Pre-marketing clinical studies show that the vaccines above-mentioned can effectively stimulate the body′s immune system to produce antibodies against COVID-19, the overall safety is good. Most of the adverse events after vaccination are mild or moderate. However, COVID-19 vaccination involves a large number and wide range of people, and its safety problems can not be ignored. The medical workers and researchers should be on high alert and conduct long-term monitoring to ensure vaccine safety.
  • Li Yanhua, Tian Xu, Liu Guangchen, Zhang Hongmei
    Abstract ( ) PDF ( )
    A 60-year-old male patient was hospitalized due to acute attack of bronchial asthma and pneumonia and antitussive, antiasthmatic, and anti-inflammatory treatments was given. Then his symptoms were improved. Discharge medication included budesonide and formoterol fumarate powder for inhalation and montelukast sodium. On the 4th day of medication after discharge, the patient developed bilateral metatarsophalangeal joint pain with redness and swelling, abdominal distension, fatigue, and dark urine. Laboratory tests showed serum creatinine (Scr) 112-μmol/L, serum uric acid 228-μmoL/L, urine protein (+), and urine occult blood (++). Gout, rheumatoid arthritis, and other autoimmune diseases were excluded and the possibility of acute kidney injury and metatarsophalangeal joint pain related to montelukast sodium was considered. Montelukast sodium was discontinued, budesonide and formoterol fumarate powder for inhalation was continued, and symptomatic treatment was given at the same time. Seven days later, the pain of metatarsophalangeal joint was improved and the urine color returned to normal. Two weeks later, his Scr level returned to normal (75-μmol/L).
  • Zhao Feiyan, Zhang Xialan, Qin Yuanyuan, Tang Qiuyue, Zhang Dengyu, Shen Xikun, Huang Yuyu
    Abstract ( ) PDF ( )
    A 43-year-old female patient received Fuyanshu capsules 1.6 g orally thrice daily for pelvic inflammation. The traditional Chinese medicine decoction was added 1 week later. After 10 days of combination therapy, the patient developed fatigue, which was gradually aggravated, and yellowish skin and sclera appeared. Seven days later,laboratory tests showed alanine aminotransferase (ALT)>1-000-U/L, aspartate aminotransferase (AST) >750-U/L, gamma-glutamyltransferase (γ-GT) 148-U/L, alkaline phosphatase (ALP) 153-U/L, and total bilirubin (TBil) 56.3-μmol//L. After excluding viral hepatitis, autoimmune liver disease, obstructive jaundice, and other causes, liver injury caused by Fuyanshu capsules combined with traditional Chinese medicine decoction was considered. After Fuyanshu capsules and traditional Chinese medicine decoction were discontinued, reduced glutathione, glycyrrhizic acid preparation, and ursodeoxycholic acid were given. Seven days later, the patient′s symptoms were improved obviously and laboratory tests showed ALT 323-U/L, AST 125-U/L, γ-GT 149-U/L, ALP 109-U/L, and TBil 35.8-μmol/L。Twenty-seven days later, the patient′s symptoms disappeared and laboratory tests showed ALT 62-U/L, AST 42-U/L, γ-GT 67-U/L, ALP 67-U/L, and TBil 18.7-μmol/L. There are 7 same components in Fuyanshu capsule and traditional Chinese medicine decoction. It was considered that the liver injury was related to the increase of hepatotoxicity caused by the combination of the two drugs.
  • Wu Xiaoping, Sun Xiaojing, Li Jinfeng
    Abstract ( ) PDF ( )
    A 52-year-old male patient took one compound paracetamol and amantadine hydrochloride capsule (each capsule contains 250-mg acetaminophen, 100-mg amantadine hydrochloride, 2-mg chlorphenamine maleate, 10-mg artificial bezoar, and 15-mg caffeine) by himself for a cold. Half a day after the medication, the patient developed erythema with itching on the back. The next day the rash worsened and spread throughout the body, involving the mouth, eyes, and scrotal mucosa. Then the skin rash developed into big herpes with epidermal sloughing, and the area of skin damage reached to 90%, accompanied by mild liver injury and blood glucose rise. Epidermolysis bullosa type eruption was diagnosed. High-dose glucocorticoids, immunoglobulins, and symptomatic and supportive treatments were given and her skin lesions largely recovered 3 weeks later. The patient′s epidermolysis bullosa type eruption was consi- dered to be probably related to the acetaminophen in compound paracetamol and amantadine hydrochloride capsules.
  • Liu Haiyan, Miao Qiuli, Song Yanqing, Wang Xiangfeng
    Abstract ( ) PDF ( )
    A 62-year-old female patient with stomach cancer received an IV infusion of oxaliplatin and mannitol injection on day 1 and oral tegafur, gimeracil, and oteracil potassium on days 1-14 in a 21-day cycle after radical mastectomy. Pretreatment with dexamethasone and other drugs was given 3 hours before the infusion to alleviate possible adverse reactions. During the 1st cycle of chemotherapy, the patient had no other adverse reaction except nausea and fatigue, and no intervention was given. About 2 hours after oxaliplatin and mannitol injection in the 2nd cycle, the patient′s limbs were swollen and flushed, and red patches appeared on the skin. Then the erythema increased and merged into patches and her skin on the feet was desquamated. The above symptoms were improved after anti-allergic treatments. About 3 hours after oxaliplatin and mannitol injection in the 3rd cycle, the patient developed dyspnea, and systemic skin flushing and swelling accompanied by scratches. Then visible blisters on part of the skin appeared, which cracked at the flexion of the joints with exudate impregnation. The patient was given anti-allergic therapy such as prednisolone. Four days later, her skin on the whole body showed scaly desquamation, her hands and feet showed gloved desquamation, and she was diagnosed as having exfoliative dermatitis; 9 days later, her skin color became lighter and there was no new rash. Considering that exfoliative dermatitis was caused by oxaliplatin and mannitol injection, the chemotherapy regimen was switched to docetaxel (day 1) and tegafur, gimeracil, and oteracil potassium (days 1-14). The skin allergic reactions did not recur.
  • Gao Yiling, Zhu Minghui, Tang Qiaoyun, Ni Tong, Wang Lin, Ma Jing
    Abstract ( ) PDF ( )
    A 38-year-old female patient with recurrence of breast cancer accompanied by liver metastasis received intravenous infusion of sintilimab 200-mg on the first day and 21 days was a cycle. Before the immunotherapy, her function of liver, kidney, and thyroid was normal. Three days after the medication, the patient developed rash and itching on skin of waist. After that, diffuse erythema and desquamation appeared on skin of her whole body and blisters appeared on both upper limbs and back. At the same time, she developed blurred vision, increased eye secretions, and foreign-body sensation. Laboratory tests showed alanine aminotransferase (ALT) 123-U/L, aspartate aminotransferase (AST) 342 UL, γ-Glutamyltransferase (γ-GT) 907-U/L, alkaline phosphatase (ALP) 424-U/L, serum creatinine (Scr) 95.6-μmol/L, uric acid 691.0-μmol/L, and thyroid-stimulating hormone (TSH) 20.87 mU/L. She was diagnosed with rash, hypothy- roidism, kidney injury, conjunctivitis, and liver injury, which were considered to be associated with sintilimab. After 16 days of symptomatic treatments such as IV infusions of methylprednisolone sodium succinate for injection and magnesium isoglycyrrhizinate injection, oral administration of levothyroxine sodium and Haikun Shenxi capsules (海昆肾喜胶囊), levofloxacin eye drops, and skin care, her rash was subsided, blisters were absorbed, and the discomfort in the eyes disappeared. Laboratory tests showed ALT 111 UL, AST 122-U/L, γ-GT 1-430-U/L, ALP 321-U/L, Scr 56.0-μmol/L, uric acid 243.0-μmol/L, and TSH 13.60 mU/L.