lNTRODUCTlON

Acute pancreatitis (AP) is an acute inflammatory process of the pancreas characterized by self-digestion of pancreatic tissue, triggering pancreatic edema, hemorrhaging, necrosis, and a systemic inflammatory response. The main etiopathogenesis of AP is gallstones, alcoholism, and hypertriglyceridemia[1].Vascular complications of pancreatitis include mainly hemorrhaging resulting from arterial erosion or pseudoaneurysm formation, ischemic complications, and venous thrombosis (especially in the portal vein, splenic vein, and superior mesenteric vein) resulting from a hypercoagulable state[2,3].

Pulmonary embolism (PE) refers to the obstruction of the pulmonary arteries by clots that originate elsewhere in the body (

, by breaking out of the vein walls and traveling through the heart to the pulmonary arteries)[4]. AP complicated by PE is very rare. Currently, it is believed that the main cause of PE is systemic inflammation and blood hypercoagulability. PE has a high mortality rate; its 30-d allcause mortality rate is 4.9% to 6.6%[5].

2) 平衡密封環(huán)有2個(gè)反向的U型金屬膨脹環(huán)(彈簧)，如圖1所示，開口方向1個(gè)向上、1個(gè)向下，該設(shè)計(jì)能確保介質(zhì)無論從閥前還是閥后進(jìn)入，平衡密封環(huán)都能起到很好的密封作用。密封原理： 當(dāng)高壓介質(zhì)進(jìn)入U(xiǎn)型環(huán)內(nèi)時(shí)撐開U型環(huán)密封，確保2個(gè)U型環(huán)中有1個(gè)能起到密封作用。

XU Sheng-qun, PANG Shi-xiu, CUI Xiang-guo, JIANG Xue-jun, YANG Huai-an

其二：無名氏《眉峰碧》(蹙破眉峰碧)：雙調(diào)47字，上闋4句23字3仄韻，下闋4句24字3仄韻。句式：5576。5577。只此一首。

CASE PRESENTATlON

Chief complaints

A 32-year-old man was admitted to the hospital with a chief complaints of persistent upper abdomen pain accompanied by nausea and vomiting for 2 d. He developed chest tightness and shortness of breath twice during treatment.

History of present illness

The patient, who had a high-fat diet and heavy drinking habit, had experienced persistent upper abdomen pain radiating to his back for two days, accompanied by nausea and vomiting. He had no fever, dyspnea, cough, expectoration, chest pain, or other discomfort. He was diagnosed with AP. Five hours after admission, he developed chest tightness and shortness of breath. On day 4 of admission, his dyspnea gradually improved after treatment. Subsequently, the patient’s body temperature peaked and gradually decreased, his abdominal pain was significantly relieved, and his intestinal function was also restored. On day 12 of admission, the patient developed chest tightness and shortness of breath again,accompanied by profuse sweating and conscious indifference. Unfortunately, the patient suffered cardiac arrest.

History of past illness

The patient had a history of obesity [Body mass index (BMI): 33.8 kg/m

]. He denied a history of hypertension, diabetes, tuberculosis, thromboembolic disease, drug use, or any other medical disease.

Personal and family history

On day 12 of admission, the patient developed chest tightness and shortness of breath again. The patient’s vital signs were as follows: heart rate, 130 beats per minute; respiratory rate, 29 breaths per minute; temperature, 38.7 °C; blood pressure, 129/79 mmHg; and pulse oximetry, 46%. Immediately afterward, the patient fell unconscious, his heart rate slowed, and his pulse oximetry continued to drop.Unfortunately, the patient suffered cardiac arrest. After 4 min of cardiopulmonary resuscitation, the patient achieved a return to spontaneous circulation, and his heart rate and oxygen saturation recovered to 143 beats per minute and 95%, respectively. Over the next few hours, the patient’s oxygen saturation levels decreased to 84%–92%, and his blood pressure started to decrease despite receiving up to 40 mcg/min of norepinephrine and 67 mg/h of dopamine hydrochloride. On day 18 of admission, the patient was conscious and had stable vital signs.

Physical examination

The patient’s vital signs on admission were as follows: temperature: 37.2 °C; heart rate: 117 beats per minute; respiratory rate: 18 breaths per minute; and blood pressure: 118/78 mmHg. The entire abdomen was flat and soft. Tenderness was obvious in the upper abdomen, but there was no rebound pain. We could not hear the patient’s bowel sounds.

Five hours after admission, he developed chest tightness and shortness of breath for the first time. He developed a fever, and his body temperature fluctuated between 38.7 and 38.9 °C. His heart rate and respiratory rate quickened, fluctuating between 130 and 140 beats per minute and 30 and 37 breaths per minute, respectively. His blood pressure was normal. On day 4 of admission, the patient’s body temperature peaked and gradually decreased, and there was no tenderness or rebound pain in the upper abdomen.

我很快就學(xué)會了滾鐵環(huán)的技巧，在村子里凹凸不平的沙土路上推著鐵環(huán)行走自如。不過，一個(gè)人滾鐵環(huán)并沒有太大的樂趣，最好是要有一群人來滾鐵環(huán)比賽。我們這伙小孩子選定了村口的大樟樹作為目的地，然后一齊出發(fā)，看誰能最快到達(dá)終點(diǎn)。一時(shí)間，村子里的土路上灰塵四起，鐵環(huán)在快速滾動(dòng)，孩子們大呼小叫，奔走如飛，場面煞是熱鬧。

The patient had been consuming about 160 g of alcohol every day for 10 years and had been smoking 20 cigarettes every day for 20 years. No family members had similar diseases.

節(jié)水型高校建設(shè)實(shí)踐與思考——以遼寧石油化工大學(xué)為例…………………………………………… 吳長宏，武榮華(11.18)

Laboratory examinations

On admission, his amylase level was 201 U/L. A further examination revealed triglycerides of 26.57 mmol/L. Five hours after admission, his white blood cell count was 18.8 × 10

/L with 87.6%neutrophils. His C-reactive protein level was high (314.3 mg/L). His pressure of arterial oxygen to fractional inspired oxygen concentration (PaO

/FiO

) was 263. Arterial blood gas (ABG) measurements showed a potential of hydrogen (pH) of 7.31, a partial pressure of oxygen of 87 mmHg, a partial pressure of carbon dioxide of 41 mmHg, bicarbonate level of 20.2 mmol/L and lactic acid level of 4.0 mmol/L at an oxygen flow rate of 3 L/min nasal cannula. Plasma dimerized plasmin fragment D (D dimer) levels were 1.55 mg/L. His brain natriuretic peptide and troponin levels were normal.

On day 12 of admission, his ABG measurements were as follows: pH: 7.18, pCO

: 74 mmHg, pO

: 63 mmHg, bicarbonate: 20.2 mmol/L and lactic acid: 2.6 mmol/L. His PaO

/FiO

was 140. The patient’s Ddimer level was significantly elevated (＞ 20 mg/L) and began to decline until day 18 of admission (17.42 mg/L), and the D-dimer level was 2.65 mg/L at discharge. On day 16 of admission, the patient’s platelet count decreased (Lowest value: 23 × 10

/L) but recovered to 112 × 10

/L at discharge.

針對上述問題，北部灣經(jīng)濟(jì)區(qū)要想快速擺脫經(jīng)濟(jì)滯后、區(qū)域內(nèi)經(jīng)濟(jì)發(fā)展不協(xié)調(diào)等局面，筆者認(rèn)為應(yīng)當(dāng)從以下幾方面進(jìn)行改善：

After admission, computed tomography (CT) scans of his upper abdomen were consistent with pancreatitis (Figure 1).

The test results for antinuclear antibody, anticardiolipin antibody, heparin-induced thrombocytopenia (HIT) and thrombophilia screen for antithrombin III, protein C, and protein S deficiency were negative. The results for factor VIII, factor IΧ, factor ΧI, plasminogen activity, and homocysteine were normal. The genetic test results for the prothrombin gene mutation, factor V Leiden, and the mutation of the methylenetetrahydrofolate reductase (

) gene were negative.

Imaging examinations

4.4 PIVAS與住院藥房一體化信息系統(tǒng)的構(gòu)建，使住院藥房與PIVAS既可獨(dú)立工作，互不干擾，又能有機(jī)結(jié)合、相互補(bǔ)充，整個(gè)工作流程順暢，信息完整、準(zhǔn)確。目前此項(xiàng)模式仍在探索中，實(shí)際工作中仍存在一些欠缺，需要持續(xù)改進(jìn)。

On day 12 of admission, the patient’s electrocardiogram (ECG) revealed sinus tachycardia with a heart rate of 145 beats per minute (Figure 2). Chest Χ-ray revealed exudative changes in the left lung(Figure 3). Doppler echocardiography revealed that his right atrium was enlarged, and his artery systolic pressure was 30 mmHg.

On day 14 of admission, PE was identified by chest CT angiography (CTA) involving the right main pulmonary artery and multiple lobar pulmonary arteries (Figure 4A). Color Doppler ultrasound of the upper limbs, lower limbs, and abdomen did not show thrombosis. Partial resolution of thrombosis was documented on follow-up chest CTA (Figure 4B).

FlNAL DlAGNOSlS

The patient was eventually diagnosed with AP, acute PE, ARDS, and hypertriglyceridemia.

A combination of blood hypercoagulability, venous blood flow stasis, and vascular endothelial dysfunction is believed to trigger thrombosis[7]. AP is an inflammatory disease characterized by the self-digestion of pancreatic tissue, which can trigger a systemic inflammatory response[1]. PE is a rare complication of pancreatitis, and only a few cases have been reported[8-11]. The mechanism underlying the formation of a PE is currently believed to be as follows: (1) The cyst connected to the pancreatic duct penetrates the vascular system and releases pancreatic juice, which then triggers the formation of a thrombus secondary to vasculitis; (2) hypercoagulability occurs due to liver dysfunction, hypertyrosinemia (resulting in increased concentrations of fibrinogen and factor VIII), and cachexia; (3) the systemic inflammatory response secondary to AP damages the vascular endothelium, consequently affecting the endothelium-dependent acetylcholine relaxation reaction and causing the release of procoagulant substances and the activation of platelets, leading to blood hypercoagulability; (4)hyperlipidemia results in venous blood flow stasis; and (5) proteolytic damage plays a significant role in the development of pulmonary vascular injury after AP, such as pancreatic elastase[8,12].

TREATMENT

After admission, the patient was treated with somatostatin, antibiotics, proton pump inhibitors, lowmolecular-weight heparin (LMWH), and fluid resuscitation. He was subcutaneously injected with 4100 iu of LMWH every 12 h.

Five hours after admission, the patient was immediately transferred to our intensive-care unit (ICU)for further treatment, including high-frequency oxygen inhalation, continuous renal replacement therapy, anti-infective therapy, inhibition of pancreatic secretion, and anticoagulant therapy. After the recovery of the patient’s intestinal function, a jejunal feeding tube was placed on day 8 of admission.Enteral nutrition was supported, and other treatments were continued, including anticoagulant therapy.

On day 12 of admission, when the patient sustained cardiac arrest, he underwent advanced cardiac life support with cardiopulmonary resuscitation and emergent endotracheal intubation, and 1 mg of adrenaline was injected intravenously every 3 min. We transferred the patient to the ICU again. He was placed on a ventilator and underwent bronchoalveolar lavage for sputum drainage, hormone administration for anti-inflammation, meropenem for anti-infection, and LMWH for anti-coagulation. After a discussion among multiple teams, the possibility of PE was considered, and his condition continued to worsen. The decision was made to cannulate him for VA ECMO (7-French braided antegrade arterial sheath, Femoral artery: 16-gauge, femoral vein: 22-gauge) approximately 3.5 h after his condition worsened, and the ECMO flow rate was 3.8 liters per minute. We performed VA ECMO insertion into the left femoral artery and the right femoral vein using the Seldinger technique to maintain blood pressure and oxygenation.

On day 14 of admission, Due to extensive thromboembolism and the inability to wean the patient from ECMO, interventional vascular surgery was performed, and pulmonary artery thrombolysis,thrombus aspiration, and mechanical thrombectomy were performed. On day 16 of admission, the patient was extubated.

OUTCOME AND FOLLOW-UP

After 35 d of hospitalization, including 4 d of ECMO therapy, the patient was discharged. Oral anticoagulation of rivaroxaban was continued. Partial resolution of thrombosis was documented on follow-up chest CTA. In three months of follow-up, the patient has not shown recurrence of AP or PE.

DlSCUSSlON

預(yù)制裝配式混凝土結(jié)構(gòu)有多種形式，如剪力墻結(jié)構(gòu)，框架結(jié)構(gòu)，框架剪力墻結(jié)構(gòu)和部分框架剪力墻結(jié)構(gòu)。由于預(yù)制裝配式結(jié)構(gòu)的預(yù)制構(gòu)件全部通過連接節(jié)點(diǎn)連接，所以混凝土結(jié)構(gòu)在大范圍內(nèi)尚未廣泛使用。與傳統(tǒng)建筑方法相比，預(yù)制建筑物具有更多的連接界面和接縫，而裝配式混凝土結(jié)構(gòu)中的節(jié)點(diǎn)是裝配式建筑的薄弱環(huán)節(jié)，在連接節(jié)點(diǎn)的處理問題上，國內(nèi)的技術(shù)手段目前并不是很成熟。但裝配式建筑結(jié)構(gòu)在環(huán)保、節(jié)能和施工上與現(xiàn)澆相比優(yōu)點(diǎn)比較突出。

Our patient was a young man who had been diagnosed with moderately severe acute hypertriglyceridemia-related pancreatitis accompanied by the accumulation of peripancreatic fluid but without pseudocysts. The patient did not have venous thrombosis in the lower extremities or other previous thrombotic diseases and had no history of recent surgery, trauma, or blood disease; however, the patient did have obesity and hyperlipidemia. Examinations revealed normal fibrinogen, normal antithrombin III, and normal protein C and S levels. Factor V Leiden and the

gene mutation were negative,and there was no evidence of atrial fibrillation on an ECG. As the patient did not have genetic or other acquired causes of PE, we concluded that the patient’s PE was secondary to AP. The predisposing factors for PE in this patient included systemic inflammatory response syndrome, hyperlipidemiarelated venous blood flow stasis, long-term bed rest (12 d in bed), and obesity.

The symptoms of PE include dyspnea, chest pain, syncope, cough, and hemoptysis. However, most clinical presentations are non-specific; thus, PE is easily missed or misdiagnosed[10]. The patient experienced chest tightness, dyspnea, tachypnea, and tachycardia without chest pain or hemoptysis in the early stage. During the disease, the patient gradually developed ARDS and conscious indifference,and his D-dimer levels progressively increased. Thus, we suspected that the patient had PE. Once PE is suspected, the detection of related coagulation indicators, such as pulmonary artery pressure assessment, contrast-enhanced chest CT, and D-dimer must be completed in order to make the diagnosis as soon as possible. Our patient’s CTA showed thrombosis in the right main pulmonary artery and multiple lobar pulmonary arteries, which confirmed the diagnosis of PE. Once the diagnosis is confirmed, treatments, including anticoagulation alone, catheter-directed thrombolysis, systemic thrombolysis, catheter embolectomy, surgical embolectomy, and/or mechanical circulatory support,such as ECMO, should be started as soon as possible[13]. We therefore cannulated the patient for VA ECMO as soon as possible (

, only 3.5 h after his condition began worsening). However, it has been shown that treatment with ECMO alone may activate innate physiologic thrombolysis thus making it possible to achieve an improvement in the right ventricle and hemodynamic values[14]. It is presently believed that ECMO mainly provides hemodynamic and respiratory support for critically ill patients whose condition is too unstable to tolerate either surgical or catheter-based embolectomy[15]. The improvement of PE symptoms and the decrease in the D-dimer level are generally considered to be due to successful vascular interventional procedure. ECMO can improve oxygenation and remove CO

,thereby reducing the need for ventilator support (using low tidal volume and low airway pressure).This protective ventilation strategy for open lungs allows the lungs to rest, thereby increasing time available to treat the original disease[16]. ECMO has been used in the following clinical scenarios for PE patients[15,17,18]: (1) To rescue patients when thrombolytic treatment fails or as a temporary hemodynamic support prior to performing intervention; and (2) To treat patients with refractory cardiogenic shock or cardiac arrest. Our patient experienced cardiac arrest and was both hemodynamically unstable and unable to tolerate interventional surgery and, as a result, he underwent ECMO therapy. However, the patient was unable to be weaned from ECMO because of his extensive thromboembolism. In addition, due to the decreased platelet count and possible hemorrhagic conversion of pancreatitis, we had to perform interventional vascular surgery instead of systemic anticoagulant therapy.

Two doubts remain concerning the findings in this report. First, despite his receiving treatment with LMWH since admission and the lack of genetic factors related to thrombosis, PE still occurred in the present patient. There may be several reasons for this. The patient may have had predisposing factors for PE, including systemic inflammatory response syndrome, hyperlipidemia-related venous blood flow stasis, long-term bed rest (12 d in bed), and obesity. In addition, the dose of LMWH may have been insufficient, given that the patient’s BMI was 33.8 kg/m

. Second, the patient’s platelet count decreased during treatment, and the result of the HIT test was negative. The development of thrombocytopenia in severe infection and sepsis may occur as a result of the massive consumption of circulating platelets through interactions with immune cells[19].

In summary, this patient suffered from severe AP with acute PE, life-threatening ARDS, and cardiac arrest. Our gastroenterology team worked collaboratively with other teams, including the Critical Care ECMO team, who provided mechanical support, and the interventional vascular surgery team, who performed thrombolysis and mechanical thrombectomy. Consequently, the patient was successfully resuscitated, stabilized, and discharged.

CONCLUSlON

AP complicated with PE is very rare, and its 30-d all-cause mortality rate is extremely high. This patient had multiple acute comorbidities, including PE, ARDS, thrombocytopenia, and obstructive shock, which complicated the treatment options and goals. The early diagnosis of PE is important, as an accurate diagnosis and timely interventional procedures can reduce mortality. The combined use of ECMO with a vascular interventional procedure for AP complicated by PE can be considered a feasible treatment method. A collaborative effort between multiple teams was vital.

ACKNOWLEDGEMENTS

The authors would like to thank the Critical Care ECMO team and interventional vascular surgery team.

FOOTNOTES

Yan LL wrote the draft; Jin ΧΧ, Yan ΧD, Peng JB and Li ZY contributed to clinical data collection and follow up; He BL critically revised the manuscript; and all authors contributed to the article and approved the submitted version.

Taizhou Science and Technology Grant, No. 1801ky68.

Informed written consent was obtained from the patient for publication of this report and any accompanying images.

The authors declare that they have no conflict of interest.

語文核心素養(yǎng)，是一種以語文能力為核心的綜合素養(yǎng)，是課程改革的目標(biāo)和方向。核心素養(yǎng)理念下的小學(xué)語文課程不僅要教授小學(xué)生基礎(chǔ)的語文知識與技能，還要加強(qiáng)對思想道德修養(yǎng)、審美情趣以及健全的人格的培養(yǎng)，積極引入現(xiàn)代教育思想，探索更有深度的教學(xué)模式，促進(jìn)小學(xué)生和諧發(fā)展。小學(xué)語文課程標(biāo)準(zhǔn)明確提出：語文教學(xué)應(yīng)面向全體學(xué)生，使學(xué)生獲得基本的語文素養(yǎng)，提高思想文化修養(yǎng)，促進(jìn)自身精神成長。因此，采用何種教學(xué)方式培養(yǎng)小學(xué)生的語文核心素養(yǎng)，成為語文教師應(yīng)該深思的問題。

The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).

This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BYNC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is noncommercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

China

Ling-Ling Yan 0000-0001-5103-9886; Χiu-Χiu Jin 0000-0002-3196-7703; Χiao-Dan Yan 0000-0002-1493-6817; Jin-Bang Peng 0000-0003-4026-5153; Zhuo-Ya Li 0000-0002-1956-4127; Bi-Li He 0000-0003-2277-3488.

Wang JL

A

Wang JL

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