附錄 D — 附錄 D. 肺移植病人照護時間表 / Appendix D. Lung Transplant Patient Care Timeline
本附錄整合 UTH Manual 2022 之標準流程與臨床實務經驗,提供肺移植病人從轉介至長期追蹤的完整時間表。
⚠️ 標記 = 需臨床團隊依三總本院流程確認 📋 標記 = 需補充三總本院數據
This appendix integrates the UTH Manual 2022 standard protocols with clinical practice experience, providing a comprehensive timeline from referral through long-term follow-up for lung transplant patients.
⚠️ Marker = Requires clinical team confirmation based on TSGH institutional protocols 📋 Marker = TSGH institutional data to be supplemented
D.1 D.1 移植前評估期 / D.1 Pre-Transplant Evaluation Period
D.1.1 D.1.1 轉介與門診初評 / D.1.1 Referral and Initial Outpatient Assessment
| 階段 | 內容 | 時程 |
|---|---|---|
| 轉介收案 | 由胸腔內科/外科或外院轉介 | Day 0 |
| 門診初評 | mMRC 呼吸困難評估、基本肺功能、6MWT、CXR | 第 1 次門診 |
| 病史整理 | 製作 PowerPoint 摘要(含 CXR、CT、心導管等影像)[UTH-Manual-2022] | 初評後 1 週內 |
| Phase | Content | Timeline | |——|——|——| | Referral intake | Referred from pulmonology/thoracic surgery or external hospital | Day 0 | | Initial clinic evaluation | mMRC dyspnea assessment, basic PFT, 6MWT, CXR | First clinic visit | | Medical record summary | Prepare PowerPoint summary (including CXR, CT, cardiac catheterization images) [UTH-Manual-2022] | Within 1 week of initial evaluation |
D.1.2 D.1.2 完整評估(住院 3-5 天) / D.1.2 Comprehensive Evaluation (3-5 Day Admission)
依 UTH Manual 登錄系統,完整評估項目如下 [UTH-Manual-2022]:
Per UTH Manual registry system, comprehensive evaluation items [UTH-Manual-2022]:
第 1 天 - 胸部 X 光、胸部 CT - 肺功能完整檢查(FEV1、FVC、DLCO、TLC) - 動脈血氣體分析(A-aDO2 計算) - 基本血液檢查
Day 1 - Chest X-ray, chest CT - Complete pulmonary function testing (FEV1, FVC, DLCO, TLC) - Arterial blood gas analysis (A-aDO2 calculation) - Basic blood tests
第 2 天 - mMRC 評分 - 6 分鐘步行測試(6MWT) - 心臟超音波 - ⚠️ 右心導管(mPAP > 35 mmHg 時)
Day 2 - mMRC scoring - 6-minute walk test (6MWT) - Echocardiography - ⚠️ Right heart catheterization (if mPAP > 35 mmHg)
第 3 天 - HLA 分型 - PRA(Panel Reactive Antibody)檢測 - CMV/EBV 血清學 - 感染症篩檢(HIV、HTLV-1、HBs、HCV)
Day 3 - HLA typing - PRA (Panel Reactive Antibody) testing - CMV/EBV serology - Infectious disease screening (HIV, HTLV-1, HBs, HCV)
第 4-5 天 - 多專科會診(牙科、精神科、復健科、營養、社工) - 疫苗接種評估與補打(麻疹、德國麻疹、水痘、腮腺炎等)[UTH-Manual-2022] - 必要時:冠狀動脈造影(CAG)
Day 4-5 - Multidisciplinary consultations (dental, psychiatry, rehabilitation, nutrition, social work) - Vaccination assessment and catch-up (measles, rubella, varicella, mumps, etc.) [UTH-Manual-2022] - If needed: coronary angiography (CAG)
D.1.3 D.1.3 適應症審查會議 / D.1.3 Indication Review Meeting
| 步驟 | 內容 | 時程 |
|---|---|---|
| 院內 MDT 討論 | 胸腔外科、胸腔內科、麻醉科、ICU、感染科 | 評估完成後 1-2 週 |
| ⚠️ 中央適應檢討委員會 | 提交申請,等待審查結果(適應/不適應/條件適應) | 院內通過後 |
| 結果通知 | 書面通知病人與家屬 | 委員會審查後 |
| Step | Content | Timeline | |——|——|——| | Institutional MDT discussion | Thoracic surgery, pulmonology, anesthesia, ICU, infectious disease | 1-2 weeks after evaluation completion | | ⚠️ Central Indication Review Committee | Submit application, await review result (approved/not approved/conditional) | After institutional approval | | Result notification | Written notification to patient and family | After committee review |
D.1.4 D.1.4 登錄等候 / D.1.4 Waitlist Registration
| 項目 | 說明 |
|---|---|
| JOT 登錄 ⚠️ | 日本為 JOT 系統;三總依衛福部器官捐贈移植登錄中心流程 |
| 登錄時提交 | 完整評估資料、HLA 分型、PRA、CMV 狀態、體重/身高(size matching 用) |
| Status 分級 | 依病情嚴重度分級(⚠️ 台灣分級制度待確認) |
| Item | Description | |——|——| | JOT registration ⚠️ | Japan uses JOT system; TSGH follows MOHW Organ Donation and Transplant Registry Center procedures | | Documents at registration | Complete evaluation data, HLA typing, PRA, CMV status, weight/height (for size matching) | | Status classification | Based on disease severity (⚠️ Taiwan classification system to be confirmed) |
D.2 D.2 等候期管理 / D.2 Waitlist Period Management
D.2.1 D.2.1 定期追蹤時間表 / D.2.1 Periodic Follow-Up Schedule
| 頻率 | 項目 |
|---|---|
| 每 1-2 個月 | 門診回診:mMRC、體重、SpO2、氧氣需求變化 |
| 每 3 個月 | 肺功能追蹤(FVC、FEV1 趨勢) |
| 每 6 個月 | 胸部 CT、完整血液檢查、HLA 抗體追蹤 |
| 每年 | 右心導管(如 PAH 疑慮)、6MWT、疫苗更新 |
| Frequency | Items | |——|——| | Every 1-2 months | Clinic visit: mMRC, weight, SpO2, oxygen requirement changes | | Every 3 months | PFT follow-up (FVC, FEV1 trends) | | Every 6 months | Chest CT, complete blood work, HLA antibody tracking | | Annually | Right heart catheterization (if PAH concern), 6MWT, vaccine update |
D.2.2 D.2.2 等候期臨床重點 / D.2.2 Waitlist Clinical Key Points
根據臨床實務觀察 [UTH-Manual-2022]:
Based on clinical practice observations [UTH-Manual-2022]:
- 體重監測:等候期體重下降為常見問題,需密切追蹤營養狀態
- 氧氣需求變化追蹤:記錄安靜時/活動時氧氣流量變化趨勢
- ADL 評估:步行距離、自理能力、是否需輪椅
- Status 升級評估:病情惡化時需重新評估,向登錄中心申請 Status 變更
- Weight monitoring: Weight loss during waitlist period is common; close nutritional status tracking required - Oxygen requirement trending: Record resting and exertional oxygen flow rate changes - ADL assessment: Walking distance, self-care ability, wheelchair dependency - Status upgrade evaluation: When condition worsens, reassess and apply for status change with registry center
D.2.3 D.2.3 移植協調師訪視 / D.2.3 Transplant Coordinator Visits
根據臨床實務,協調師定期訪視內容包含 [UTH-Manual-2022]:
Per clinical practice, coordinator periodic visit content includes [UTH-Manual-2022]:
| 項目 | 內容 |
|---|---|
| 病情追蹤 | 呼吸症狀、氧氣使用、體重變化、ADL |
| JOT 採血更新 | 定期更新登錄中心所需血液檢體 |
| 心理評估 | 等候焦慮、end-of-life 意願確認 |
| 家屬狀況 | 照顧者支持、住宿安排、經濟狀況 |
| 衛教 | 手術準備、術後預期、復健期展望 |
| Prehabilitation | 確認復健運動執行狀況(步行、呼吸訓練) |
| Item | Content | |——|——| | Disease tracking | Respiratory symptoms, oxygen use, weight changes, ADL | | Registry blood sample update | Periodically update blood specimens required by registry center | | Psychological assessment | Waitlist anxiety, end-of-life wishes confirmation | | Family situation | Caregiver support, housing arrangements, financial status | | Education | Surgical preparation, postoperative expectations, rehabilitation outlook | | Prehabilitation | Confirm rehabilitation exercise compliance (walking, breathing exercises) |
D.2.4 D.2.4 Prehabilitation 方案 / D.2.4 Prehabilitation Protocol
| 項目 | 建議內容 |
|---|---|
| 有氧運動 | 每日步行(依耐受度調整)或使用步行機 30 分鐘/天 |
| 肌力訓練 | 下肢肌力(深蹲等)、呼吸肌訓練 |
| 營養支持 | 高蛋白高熱量飲食、⚠️ 營養補充品(如 PulmoCare) |
| 訪問復健 | 週 1-2 次訪問復健師(呼吸復健 + 床上肌力訓練) |
| Item | Recommended Content | |——|———-| | Aerobic exercise | Daily walking (adjusted per tolerance) or walking machine 30 min/day | | Strength training | Lower extremity strength (squats, etc.), respiratory muscle training | | Nutritional support | High-protein, high-calorie diet; ⚠️ nutritional supplements (e.g., PulmoCare) | | Visiting rehabilitation | 1-2x/week visiting rehabilitation therapist (pulmonary rehab + bed-level strength training) |
D.3 D.3 收到器官通知 → 入院 / D.3 Organ Offer Notification to Admission
D.3.1 D.3.1 通知流程(逐時) / D.3.1 Notification Process (Hourly)
Hour 0 器官捐贈中心通知 → 移植協調師接獲通知
├─ 確認供體資訊(ABO、size match、CMV 狀態、HLA)
├─ 評估 size matching(VCD/VCR ±30% 成人;±12% 兒童)[UTH-Manual-2022]
└─ 通知主刀醫師,決定是否接受
> *```*
> *Hour 0 Organ donation center notification → Transplant coordinator receives notification*
> * ├─ Confirm donor information (ABO, size match, CMV status, HLA)*
> * ├─ Evaluate size matching (VCD/VCR ±30% adult; ±12% pediatric) [UTH-Manual-2022]*
> * └─ Notify lead surgeon, decide whether to accept*
Hour 0-1 通知受者入院
├─ 協調師聯繫病人/家屬
├─ 確認交通方式與預計到院時間
└─ 啟動手術團隊 call-in
> *Hour 0-1 Notify recipient for admission*
> * ├─ Coordinator contacts patient/family*
> * ├─ Confirm transportation method and estimated arrival time*
> * └─ Activate surgical team call-in*
Hour 1-3 受者到院
├─ 急診或直接入住病房
├─ 術前採血(CBC、生化、凝血、Type & Screen、ABG)
├─ 胸部 X 光
├─ COVID-19 PCR ⚠️
├─ Crossmatch 檢體送出
└─ 麻醉科術前評估
> *Hour 1-3 Recipient arrives at hospital*
> * ├─ Emergency department or direct ward admission*
> * ├─ Pre-op blood work (CBC, chemistry, coagulation, Type & Screen, ABG)*
> * ├─ Chest X-ray*
> * ├─ COVID-19 PCR ⚠️*
> * ├─ Crossmatch specimen sent*
> * └─ Anesthesia pre-op evaluation*
Hour 2-4 術前準備
├─ 手術同意書簽署
├─ 麻醉同意書簽署
├─ ⚠️ 術前免疫抑制劑給予:
│ ├─ MMF (CellCept) 500 mg PO [UTH-Manual-2022]
│ └─ Methylprednisolone (Solu-Medrol) 500 mg IV
├─ 術前抗生素(PIP/TAZ 4.5g)
└─ 轉送手術室
Hour 2-4 Pre-op preparation * ├─ Surgical consent signing ├─ Anesthesia consent signing ├─ ⚠️ Pre-op immunosuppressant administration: │ ├─ MMF (CellCept) 500 mg PO [UTH-Manual-2022] │ └─ Methylprednisolone (Solu-Medrol) 500 mg IV ├─ Pre-op antibiotics (PIP/TAZ 4.5g) └─ Transfer to operating room ```*
D.3.2 D.3.2 家屬安排 / D.3.2 Family Arrangements
| 項目 | 說明 |
|---|---|
| 家屬等候室 | 安排家屬至手術等候區 |
| 聯絡窗口 | 協調師或護理師定期更新手術進度 |
| 住宿安排 | 如遠道家屬,協助安排院內或附近住宿 ⚠️ |
| Item | Description | |——|——| | Family waiting area | Arrange family in surgical waiting area | | Contact person | Coordinator or nurse provides periodic surgical progress updates | | Accommodation | Assist with in-hospital or nearby accommodation for families traveling from afar ⚠️ |
D.4 D.4 手術日(Day 0) / D.4 Surgery Day (Day 0)
D.4.1 D.4.1 麻醉準備序列 / D.4.1 Anesthesia Preparation Sequence
根據 UTH Manual 及臨床實務 [UTH-Manual-2022]:
Per UTH Manual and clinical practice [UTH-Manual-2022]:
| 時序 | 步驟 |
|---|---|
| T-60 min | 病人入手術室,確認身分、手術部位 |
| T-45 min | 動脈導管(A-line)建立 |
| T-30 min | 全身麻醉誘導(Propofol、Fentanyl、肌肉鬆弛劑) |
| T-20 min | 雙腔氣管內管或支氣管阻斷器插管 |
| T-15 min | 中央靜脈導管(CV line)— 右內頸靜脈 |
| T-10 min | Swan-Ganz 肺動脈導管置入 |
| T-5 min | 經食道超音波(TEE)置入 |
| T-0 | 消毒鋪單完成,準備開刀 |
| Sequence | Step | |——|——| | T-60 min | Patient enters OR, identity and surgical site verification | | T-45 min | Arterial line (A-line) placement | | T-30 min | General anesthesia induction (Propofol, Fentanyl, muscle relaxant) | | T-20 min | Double-lumen endotracheal tube or bronchial blocker insertion | | T-15 min | Central venous catheter (CV line) — right internal jugular vein | | T-10 min | Swan-Ganz pulmonary artery catheter insertion | | T-5 min | Transesophageal echocardiography (TEE) placement | | T-0 | Prep and drape complete, ready to operate |
D.4.2 D.4.2 手術步驟與時間估算 / D.4.2 Surgical Steps and Time Estimates
典型 BLTx(雙肺移植)手術流程,依臨床實務資料:
Typical BLTx (bilateral lung transplant) surgical workflow, per clinical practice data:
≈ Hour 0 Clamshell incision(第 4 肋間雙側開胸)
心包逆 T 字切開
> *```*
> *≈ Hour 0 Clamshell incision (4th intercostal bilateral thoracotomy)*
> * Pericardial inverted-T incision*
≈ Hour 0.5 Central ECMO cannulation
├─ SVC:脫血管(如 20Fr)
├─ IVC:脫血管(如 20Fr)
└─ 升主動脈:送血管(如 15Fr)
確認 full flow
> *≈ Hour 0.5 Central ECMO cannulation*
> * ├─ SVC: drainage cannula (e.g., 20Fr)*
> * ├─ IVC: drainage cannula (e.g., 20Fr)*
> * └─ Ascending aorta: return cannula (e.g., 15Fr)*
> * Confirm full flow*
≈ Hour 1-2 第一側肺(通常右肺)全摘
├─ 肺門剝離
├─ 肺動脈 stapling
├─ 肺靜脈 stapling
└─ 支氣管 stapling
> *≈ Hour 1-2 First side pneumonectomy (usually right lung)*
> * ├─ Hilum dissection*
> * ├─ Pulmonary artery stapling*
> * ├─ Pulmonary vein stapling*
> * └─ Bronchus stapling*
≈ Hour 2-3 第一側移植肺吻合
├─ 支氣管吻合(4-0 PDS)
├─ 肺動脈吻合(5-0 Pronova)
└─ 左房吻合(4-0 Pronova)
→ 再灌流(reperfusion)
> *≈ Hour 2-3 First side donor lung implantation*
> * ├─ Bronchial anastomosis (4-0 PDS)*
> * ├─ Pulmonary artery anastomosis (5-0 Pronova)*
> * └─ Left atrial anastomosis (4-0 Pronova)*
> * → Reperfusion*
≈ Hour 3-5 第二側肺全摘 + 移植肺吻合(同上步驟)
→ 再灌流
> *≈ Hour 3-5 Second side pneumonectomy + donor lung implantation (same steps)*
> * → Reperfusion*
≈ Hour 5-6 ECMO weaning
├─ 逐步降低 ECMO flow
├─ 監測 mPAP、血壓、SpO2
├─ 必要時啟動 iNO(10-20 ppm)[UTH-Manual-2022]
├─ 氣管支鏡抽痰
└─ 確認血行動力學穩定後 ECMO 離脱
> *≈ Hour 5-6 ECMO weaning*
> * ├─ Gradual ECMO flow reduction*
> * ├─ Monitor mPAP, BP, SpO2*
> * ├─ Initiate iNO (10-20 ppm) if needed [UTH-Manual-2022]*
> * ├─ Bronchoscopic suctioning*
> * └─ Confirm hemodynamic stability before ECMO decannulation*
≈ Hour 6-7 關胸
├─ 置入胸腔引流管(4 條)
├─ 心膜重建(Gore-Tex sheet)
├─ 胸骨鋼絲固定
└─ 逐層閉合
> *≈ Hour 6-7 Chest closure*
> * ├─ Place chest drains (4 tubes)*
> * ├─ Pericardial reconstruction (Gore-Tex sheet)*
> * ├─ Sternal wire fixation*
> * └─ Layered closure*
≈ Hour 7-8 術後氣管支鏡檢查
確認吻合口通暢、無再灌流障礙
> *≈ Hour 7-8 Post-operative bronchoscopy*
> * Confirm anastomotic patency, no reperfusion injury*
≈ Hour 8+ 轉送 ICU
≈ Hour 8+ Transfer to ICU ```
典型時間參數 [根據臨床實務]:
Typical Time Parameters [per clinical practice]:
| 參數 | 典型值 |
|---|---|
| 總手術時間 | 8-10 小時 |
| Cold ischemic time (CIT) | 第一肺 4-6 hr;第二肺 6-8 hr |
| Warm ischemic time (WIT) | 45-70 min/側 |
| Total ischemic time | 6-8 hr(第一肺);7-9 hr(第二肺) |
| Parameter | Typical Value | |——|——–| | Total surgical time | 8-10 hours | | Cold ischemic time (CIT) | First lung 4-6 hr; second lung 6-8 hr | | Warm ischemic time (WIT) | 45-70 min/side | | Total ischemic time | 6-8 hr (first lung); 7-9 hr (second lung) |
D.4.3 D.4.3 術中免疫抑制劑 / D.4.3 Intraoperative Immunosuppression
| 時間點 | 藥物 | 劑量 |
|---|---|---|
| 術前(麻醉誘導前) | MMF (CellCept) | 500 mg PO |
| 術中(再灌流前) | Solu-Medrol | 500 mg IV(部分中心用 500-1000 mg) |
| Timing | Drug | Dose | |——–|——|——| | Pre-op (before anesthesia induction) | MMF (CellCept) | 500 mg PO | | Intraoperative (before reperfusion) | Solu-Medrol | 500 mg IV (some centers use 500-1000 mg) |
D.4.4 D.4.4 術中 ECMO 管理要點 [UTH-Manual-2022] / D.4.4 Intraoperative ECMO Management Points [UTH-Manual-2022]
- Central V-A ECMO 為標準配置
- iPAH 病人:術後需 ICU 維持 ECMO 2-3 天後再嘗試脫離
- ECMO weaning 失敗時:回復 flow,排除原因(PH、出血、氣道分泌物)後再試
- iNO 20 ppm 可輔助 ECMO 脫離
- Central V-A ECMO is the standard configuration - iPAH patients: Post-op ICU ECMO maintenance for 2-3 days before weaning attempt - ECMO weaning failure: Restore flow, troubleshoot cause (PH, bleeding, airway secretions) before re-attempting - iNO 20 ppm can assist ECMO weaning
D.5 D.5 ICU 照護時間表(POD 0-14) / D.5 ICU Care Timeline (POD 0-14)
D.5.1 D.5.1 POD 0(手術當日,ICU 入室) / D.5.1 POD 0 (Surgery Day, ICU Admission)
| 項目 | 內容 |
|---|---|
| 呼吸器設定 | Lung protective:Vt 6-8 mL/kg, PEEP 5 cmH2O, plateau < 30 cmH2O [UTH-Manual-2022] |
| iNO | 如術中使用,維持 10-20 ppm,12-24 小時後逐漸 weaning [UTH-Manual-2022] |
| 血行動力學 | Swan-Ganz 監測 mPAP、CVP、CO/CI、SvO2 |
| 輸液 | 限制性輸液策略,30-40 mL/kg/day [UTH-Manual-2022] |
| 目標 | SvO2 ≥ 60%、CI ≥ 2.5 |
| 藥物啟動 | Tacrolimus IV 持續輸注(見 D.6) |
| 抗生素 | PIP/TAZ 4.5g q8h [UTH-Manual-2022] |
| 抗黴菌 | Micafungin 100 mg/day IV(ECMO 中 200 mg)[UTH-Manual-2022] |
| 抗病毒 | Ganciclovir 5 mg/kg/day IV [UTH-Manual-2022] |
| ABG | 入室後立即,此後 q4-6h |
| CXR | 入室後立即(baseline) |
| Labs | CBC、生化、凝血(入室時) |
| Item | Content | |——|——| | Ventilator settings | Lung protective: Vt 6-8 mL/kg, PEEP 5 cmH2O, plateau < 30 cmH2O [UTH-Manual-2022] | | iNO | If used intraoperatively, maintain 10-20 ppm, gradually wean after 12-24 hours [UTH-Manual-2022] | | Hemodynamics | Swan-Ganz monitoring mPAP, CVP, CO/CI, SvO2 | | Fluids | Restrictive fluid strategy, 30-40 mL/kg/day [UTH-Manual-2022] | | Targets | SvO2 ≥ 60%, CI ≥ 2.5 | | Drug initiation | Tacrolimus IV continuous infusion (see D.6) | | Antibiotics | PIP/TAZ 4.5g q8h [UTH-Manual-2022] | | Antifungal | Micafungin 100 mg/day IV (200 mg on ECMO) [UTH-Manual-2022] | | Antiviral | Ganciclovir 5 mg/kg/day IV [UTH-Manual-2022] | | ABG | Immediately upon admission, then q4-6h | | CXR | Immediately upon admission (baseline) | | Labs | CBC, chemistry, coagulation (on admission) |
D.5.2 D.5.2 POD 1 / D.5.2 POD 1
| 項目 | 內容 |
|---|---|
| 免疫抑制 | mPSL 250 mg IV × 1 [UTH-Manual-2022] |
| Tacrolimus 監測 | 第 1 次 trough level(啟動後 6 小時)[UTH-Manual-2022] |
| 第 2 次 Tac level | 啟動後 16 小時 |
| Basiliximab | POD 1 給予 Simulect 20 mg + NS 50 mL(30 分鐘滴注)(如使用)[UTH-Manual-2022] |
| IVIg | POD 1-2 Venoglobulin 7.5 g(如使用)[UTH-Manual-2022] |
| CellCept | 開始 PO/NG:BW < 50 kg → 500 mg/day;BW ≥ 50 kg → 1000 mg/day(分 2 次)[UTH-Manual-2022] |
| CXR | 每日 |
| 氣管支鏡 | 視情況進行(確認吻合口、抽痰) |
| Item | Content | |——|——| | Immunosuppression | mPSL 250 mg IV x 1 [UTH-Manual-2022] | | Tacrolimus monitoring | 1st trough level (6 hours after initiation) [UTH-Manual-2022] | | 2nd Tac level | 16 hours after initiation | | Basiliximab | POD 1: Simulect 20 mg + NS 50 mL (30-minute infusion) (if used) [UTH-Manual-2022] | | IVIg | POD 1-2: Venoglobulin 7.5 g (if used) [UTH-Manual-2022] | | CellCept | Start PO/NG: BW < 50 kg → 500 mg/day; BW ≥ 50 kg → 1000 mg/day (divided BID) [UTH-Manual-2022] | | CXR | Daily | | Bronchoscopy | As needed (check anastomosis, suction) |
D.5.3 D.5.3 POD 1-3:mPSL 高劑量期 / D.5.3 POD 1-3: High-Dose mPSL Phase
| 日 | Methylprednisolone | 其他重點 |
|---|---|---|
| POD 1 | 250 mg IV × 1 | 第一次 Tac level,CellCept 開始 |
| POD 2 | 250 mg IV × 1 | 持續呼吸器管理,開始評估拔管可能 |
| POD 3 | 250 mg IV × 1 | 胸腔引流量評估,開始腸道營養評估 |
| Day | Methylprednisolone | Other Key Points | |—-|——————-|———-| | POD 1 | 250 mg IV x 1 | First Tac level, CellCept started | | POD 2 | 250 mg IV x 1 | Continue ventilator management, begin extubation readiness assessment | | POD 3 | 250 mg IV x 1 | Chest drain output evaluation, begin enteral nutrition assessment |
D.5.4 D.5.4 POD 4-6:mPSL 減量期 / D.5.4 POD 4-6: mPSL Taper Phase
| 日 | Methylprednisolone | 其他重點 |
|---|---|---|
| POD 4 | 125 mg IV × 1 | Basiliximab 第 2 劑(POD 4)[UTH-Manual-2022] |
| POD 5 | 125 mg IV × 1 | 評估拔管(目標 72 小時內拔管) |
| POD 6 | 125 mg IV × 1 | 拔管後開始口服藥物轉換準備 |
| Day | Methylprednisolone | Other Key Points | |—-|——————-|———-| | POD 4 | 125 mg IV x 1 | Basiliximab 2nd dose (POD 4) [UTH-Manual-2022] | | POD 5 | 125 mg IV x 1 | Extubation assessment (target within 72 hours) | | POD 6 | 125 mg IV x 1 | Post-extubation oral medication transition preparation |
D.5.5 D.5.5 POD 7-9:mPSL 最終減量 / D.5.5 POD 7-9: Final mPSL Taper
| 日 | Methylprednisolone | 其他重點 |
|---|---|---|
| POD 7 | 62.5 mg IV × 1 | 開始 Tacrolimus IV → oral 轉換 [UTH-Manual-2022] |
| POD 8 | 62.5 mg IV × 1 | 追蹤 Tac oral trough level |
| POD 9 | 62.5 mg IV × 1 | 抗黴菌轉 ITCZ oral(20 mL suspension) |
| Day | Methylprednisolone | Other Key Points | |—-|——————-|———-| | POD 7 | 62.5 mg IV x 1 | Begin Tacrolimus IV → oral conversion [UTH-Manual-2022] | | POD 8 | 62.5 mg IV x 1 | Track Tac oral trough level | | POD 9 | 62.5 mg IV x 1 | Switch antifungal to ITCZ oral (20 mL suspension) |
D.5.6 D.5.6 POD 10-14:穩定期 / D.5.6 POD 10-14: Stabilization Phase
| 日 | 重點 |
|---|---|
| POD 10 | Prednisolone 30 mg PO 開始(取代 IV mPSL)[UTH-Manual-2022] |
| POD 10 | Tacrolimus 完成 IV → oral 轉換 |
| POD 10-14 | PSL 每週減量 2.5 mg → 目標 5 mg/day 維持 [UTH-Manual-2022] |
| POD 10-14 | Valganciclovir 900 mg/day PO 取代 GCV IV [UTH-Manual-2022] |
| POD 14 | Baktar (TMP-SMX) 開始(1 錠 × 1/day,週一三五)[UTH-Manual-2022] |
| Day | Key Points | |—-|——| | POD 10 | Prednisolone 30 mg PO begins (replaces IV mPSL) [UTH-Manual-2022] | | POD 10 | Tacrolimus IV → oral conversion complete | | POD 10-14 | PSL taper 2.5 mg/week → target 5 mg/day maintenance [UTH-Manual-2022] | | POD 10-14 | Valganciclovir 900 mg/day PO replaces GCV IV [UTH-Manual-2022] | | POD 14 | Baktar (TMP-SMX) starts (1 tab x 1/day, Mon-Wed-Fri) [UTH-Manual-2022] |
D.5.7 D.5.7 呼吸器脫離與拔管時程 / D.5.7 Ventilator Weaning and Extubation Timeline
| 目標時程 | 內容 |
|---|---|
| POD 1-2 | 開始 weaning trial(降 PEEP、降 PS) |
| POD 2-3(目標 72 小時) | 拔管 [UTH-Manual-2022] |
| 拔管後 | HFNC 或 NIV 過渡 |
| 拔管延遲 > 7-14 天 | 評估氣管切開 [UTH-Manual-2022] |
| Target Timeline | Content | |———-|——| | POD 1-2 | Begin weaning trial (reduce PEEP, reduce PS) | | POD 2-3 (target 72 hours) | Extubation [UTH-Manual-2022] | | Post-extubation | HFNC or NIV transition | | Extubation delay > 7-14 days | Evaluate tracheostomy [UTH-Manual-2022] |
D.5.8 D.5.8 營養支持時程 [UTH-Manual-2022] / D.5.8 Nutritional Support Timeline [UTH-Manual-2022]
| 時間 | 內容 |
|---|---|
| POD 0 | TPN 開始(Elneopa 等) |
| POD 1-2 | 管灌營養開始:50 mL/hr Glutamine F,逐步增量 |
| POD 2-3 | 轉 PulmoCare 管灌 |
| 拔管後 | 口服飲食開始(流質 → 軟食 → 普通飲食) |
| 目標 | Harris-Benedict BEE × 1.2-1.8;蛋白質 1.2-2.0 g/kg/day |
| Timeline | Content | |——|——| | POD 0 | TPN initiated (Elneopa, etc.) | | POD 1-2 | Tube feeding starts: 50 mL/hr Glutamine F, gradually increase | | POD 2-3 | Switch to PulmoCare tube feeding | | Post-extubation | Oral diet begins (liquids → soft → regular diet) | | Target | Harris-Benedict BEE x 1.2-1.8; protein 1.2-2.0 g/kg/day |
D.5.9 D.5.9 復健啟動時程 / D.5.9 Rehabilitation Initiation Timeline
| 時間 | 內容 |
|---|---|
| POD 1-2 | 床上被動運動、關節活動度 |
| POD 2-3 | 床邊坐起 |
| POD 3-5 | 輪椅移位(即使有多條管路) |
| 拔管後 | 站立、步行訓練 |
| POD 7-14 | 每日步行距離逐增 |
| Timeline | Content | |——|——| | POD 1-2 | Bed-level passive exercises, ROM | | POD 2-3 | Bedside sitting | | POD 3-5 | Wheelchair transfer (even with multiple lines) | | Post-extubation | Standing, walking training | | POD 7-14 | Progressive daily walking distance increase |
D.5.10 D.5.10 氣管支鏡檢查時程 / D.5.10 Bronchoscopy Schedule
| 時間 | 目的 |
|---|---|
| 術後即刻(OR 內) | 確認吻合口通暢、有無再灌流障礙 |
| POD 1-3 | 抽痰、評估吻合口癒合 |
| POD 7(第 1 週) | protocol biopsy + BAL |
| POD 14(第 2 週) | 追蹤吻合口、排斥評估 |
| ⚠️ 之後依各中心 protocol | 每 1-2 週至出院 |
| Timeline | Purpose | |——|——| | Immediately post-op (in OR) | Confirm anastomotic patency, assess reperfusion injury | | POD 1-3 | Suctioning, anastomotic healing assessment | | POD 7 (Week 1) | Protocol biopsy + BAL | | POD 14 (Week 2) | Anastomosis follow-up, rejection assessment | | ⚠️ Thereafter per center protocol | Every 1-2 weeks until discharge |
D.6 D.6 免疫抑制劑時間表 / D.6 Immunosuppression Timeline
D.6.1 D.6.1 總覽流程圖 / D.6.1 Overview Flowchart
術前 ─────────── 術中 ──── POD 0 ── POD 1 ── POD 4 ── POD 7-10 ── POD 10 ── 出院後
> *```*
> *Pre-op ─────────── Intra-op ──── POD 0 ── POD 1 ── POD 4 ── POD 7-10 ── POD 10 ── Post-discharge*
MMF 500mg PO ──────────── → CellCept 500-1500mg/day PO 持續 ──────────→
> *MMF 500mg PO ──────────── → CellCept 500-1500mg/day PO continuous ──────────→*
Solu-Medrol ──── 500mg IV
mPSL 250mg×3d → 125mg×3d → 62.5mg×3d
PSL 30mg PO → 減量至 5mg
> *Solu-Medrol ──── 500mg IV*
> * mPSL 250mg×3d → 125mg×3d → 62.5mg×3d*
> * PSL 30mg PO → taper to 5mg*
Tac IV 0.03mL/kg/hr ──────────→ Tac oral
(×1.5-2 IV rate)
> * Tac IV 0.03mL/kg/hr ──────────→ Tac oral*
> * (×1.5-2 IV rate)*
Basiliximab ── D1 ──── D4
```Basiliximab ── D1 ──── D4*
D.6.2 D.6.2 Tacrolimus 詳細時程 [UTH-Manual-2022] / D.6.2 Tacrolimus Detailed Timeline [UTH-Manual-2022]
| 階段 | 給法 | 劑量/目標 |
|---|---|---|
| POD 0(ICU 入室) | Prograf 1A (2mg/0.4mL) + NS 50mL IV drip | 0.03 mL/kg/hr |
| BW 30kg → 0.9 mL/hr | ||
| BW 50kg → 1.5 mL/hr | ||
| BW 70kg → 2.1 mL/hr | ||
| POD 1(6hr) | 第 1 次 trough level 抽血 | 目標 15-20 ng/mL |
| POD 1(16hr) | 第 2 次 trough level 抽血 | |
| 此後 | 每日 trough level(ICU: A-line 抽取) | |
| POD 7-10 | IV → Oral 轉換 | 口服劑量 = IV rate × 1.5-2 倍 |
| 例:IV 0.8 mL/hr → oral 1.2-1.6 mg q12h | ||
| ⚠️ 併用 ITCZ 或 VRCZ 時 | 口服劑量 = IV rate × 1.0 倍 |
| Phase | Route | Dose/Target | |——|——|———–| | POD 0 (ICU admission) | Prograf 1A (2mg/0.4mL) + NS 50mL IV drip | 0.03 mL/kg/hr | | | | BW 30kg → 0.9 mL/hr | | | | BW 50kg → 1.5 mL/hr | | | | BW 70kg → 2.1 mL/hr | | POD 1 (6hr) | 1st trough level blood draw | Target 15-20 ng/mL | | POD 1 (16hr) | 2nd trough level blood draw | | | Thereafter | Daily trough level (ICU: draw from A-line) | | | POD 7-10 | IV → Oral conversion | Oral dose = IV rate x 1.5-2 | | | | Example: IV 0.8 mL/hr → oral 1.2-1.6 mg q12h | | | ⚠️ With concurrent ITCZ or VRCZ | Oral dose = IV rate x 1.0 |
Tacrolimus 目標濃度 [UTH-Manual-2022]:
Tacrolimus Target Levels [UTH-Manual-2022]:
| 時期 | 目標 trough (ng/mL) |
|---|---|
| 0-3 個月 | 14-17 |
| 3-6 個月 | 10-15 |
| > 6 個月 | 8-12 |
| Period | Target Trough (ng/mL) | |——|———————| | 0-3 months | 14-17 | | 3-6 months | 10-15 | | > 6 months | 8-12 |
D.6.3 D.6.3 Corticosteroid 詳細時程 [UTH-Manual-2022] / D.6.3 Corticosteroid Detailed Timeline [UTH-Manual-2022]
| 時間 | 藥物 | 劑量 | 給法 |
|---|---|---|---|
| 術中(再灌流前) | Solu-Medrol | 500 mg | IV bolus |
| POD 1-3 | mPSL | 250 mg/day | IV × 1/day |
| POD 4-6 | mPSL | 125 mg/day | IV × 1/day |
| POD 7-9 | mPSL | 62.5 mg/day | IV × 1/day |
| ⚠️ 替代方案 | mPSL | 62.5 → 40 → 30 mg(逐步) | 部分中心 3 天一減 |
| POD 10 | Prednisolone (PSL) | 30 mg | PO |
| POD 10 起 | PSL 減量 | 每週減 2.5 mg | PO |
| 維持劑量 | PSL | 5 mg/day | PO,長期 |
| Timing | Drug | Dose | Route | |——|——|——|——| | Intraoperative (before reperfusion) | Solu-Medrol | 500 mg | IV bolus | | POD 1-3 | mPSL | 250 mg/day | IV x 1/day | | POD 4-6 | mPSL | 125 mg/day | IV x 1/day | | POD 7-9 | mPSL | 62.5 mg/day | IV x 1/day | | ⚠️ Alternative | mPSL | 62.5 → 40 → 30 mg (stepwise) | Some centers use 3-day steps | | POD 10 | Prednisolone (PSL) | 30 mg | PO | | From POD 10 | PSL taper | 2.5 mg/week reduction | PO | | Maintenance dose | PSL | 5 mg/day | PO, long-term |
體重別 Prednisone 參考劑量 [UTH-Manual-2022]:
Weight-Based Prednisone Reference Dosing [UTH-Manual-2022]:
| 時期 | 劑量公式 | 60 kg | 40 kg |
|---|---|---|---|
| 3 個月 | 0.25 mg/kg/day | 15 mg | 10 mg |
| 6 個月 | 0.15 mg/kg/day | 9 mg | 6 mg |
| 9 個月 | 0.08-0.1 mg/kg/day | 5-6 mg | 3-4 mg |
| Period | Dose Formula | 60 kg | 40 kg | |——|———-|——-|——-| | 3 months | 0.25 mg/kg/day | 15 mg | 10 mg | | 6 months | 0.15 mg/kg/day | 9 mg | 6 mg | | 9 months | 0.08-0.1 mg/kg/day | 5-6 mg | 3-4 mg |
D.6.4 D.6.4 Basiliximab (Simulect) [UTH-Manual-2022] / D.6.4 Basiliximab (Simulect) [UTH-Manual-2022]
- 適應:Tacrolimus 啟動延遲或腎功能不佳時使用
- POD 1:Simulect 20 mg + NS 50 mL,30 分鐘以上滴注
- POD 4:Simulect 20 mg + NS 50 mL,30 分鐘以上滴注
- Indication: When Tacrolimus initiation is delayed or renal function is poor - POD 1: Simulect 20 mg + NS 50 mL, infuse over 30 minutes or more - POD 4: Simulect 20 mg + NS 50 mL, infuse over 30 minutes or more
D.6.5 D.6.5 MMF (CellCept) [UTH-Manual-2022] / D.6.5 MMF (CellCept) [UTH-Manual-2022]
| 時間 | 劑量 | 備註 |
|---|---|---|
| 術前 | 500 mg PO | 術前 9 小時前(第一劑) |
| 術前 | — | 術前 7 小時前(已由前晚給予) |
| POD 0(21:00) | CellCept 500 mg | NG/PO |
| POD 1 起 | BW < 50 kg:500 mg/day;BW ≥ 50 kg:1000 mg/day | 分 2 次(7:00、19:00) |
| 排斥時 | 可增至 3000 mg/day(ACR)或 1500 mg/day 以上 | |
| 副作用監測 | WBC < 1500/μL 時減量或暫停 |
| Timing | Dose | Notes | |——|——|——| | Pre-op | 500 mg PO | 9 hours before surgery (first dose) | | POD 0 (21:00) | CellCept 500 mg | NG/PO | | POD 1 onward | BW < 50 kg: 500 mg/day; BW ≥ 50 kg: 1000 mg/day | Divided BID (7:00, 19:00) | | During rejection | May increase to 3000 mg/day (ACR) or ≥ 1500 mg/day | | | Side effect monitoring | Reduce or hold when WBC < 1500/uL | |
D.6.6 D.6.6 替代方案:Cyclosporine (Neoral) [UTH-Manual-2022] / D.6.6 Alternative: Cyclosporine (Neoral) [UTH-Manual-2022]
| 項目 | 內容 |
|---|---|
| 適應 | Tacrolimus 無法耐受時 |
| 起始劑量 | 5 mg/kg PO 分 2 次 |
| Trough 目標 | 0-3 月:250-350;3-6 月:200-300;>6 月:150-250 ng/mL |
| Item | Content | |——|——| | Indication | When Tacrolimus is not tolerated | | Starting dose | 5 mg/kg PO divided BID | | Trough target | 0-3m: 250-350; 3-6m: 200-300; >6m: 150-250 ng/mL |
D.7 D.7 感染預防時間表 / D.7 Infection Prevention Timeline
D.7.1 D.7.1 周術期抗生素 [UTH-Manual-2022] / D.7.1 Perioperative Antibiotics [UTH-Manual-2022]
| 時間 | 藥物 | 劑量 | 備註 |
|---|---|---|---|
| 術前 | PIP/TAZ | 4.5g IV | 切皮前 30 分鐘 |
| POD 0 起 | PIP/TAZ | 4.5g q8h IV | 持續至少 7-14 天 |
| 依供體培養結果調整 | |||
| 供體有 MRSA | 加 Vancomycin | 1g q12h | |
| 供體有 Pseudomonas | 改 Ceftazidime 或 Meropenem | ||
| ESBL 陽性 | Meropenem | 1g q8h |
| Timing | Drug | Dose | Notes | |——|——|——|——| | Pre-op | PIP/TAZ | 4.5g IV | 30 minutes before incision | | POD 0 onward | PIP/TAZ | 4.5g q8h IV | Continue at least 7-14 days; adjust per donor culture results | | Donor MRSA | Add Vancomycin | 1g q12h | | | Donor Pseudomonas | Switch to Ceftazidime or Meropenem | | | | ESBL positive | Meropenem | 1g q8h | |
D.7.2 D.7.2 抗黴菌預防 [UTH-Manual-2022] / D.7.2 Antifungal Prophylaxis [UTH-Manual-2022]
| 階段 | 藥物 | 劑量 | 期間 |
|---|---|---|---|
| ICU(POD 1 起) | Micafungin (MCFG) | 100 mg/day IV(ECMO 中 200 mg) | 至脫離 ECMO + ICU |
| 口服轉換後 | Itraconazole (ITCZ) suspension | 20 mL/day | 至少 7 天後可轉膠囊 |
| 維持期 | ITCZ capsule | 50-200 mg/day | 至少 3-6 個月 |
| 吸入 | Amphotericin B (Fungizone) 霧化 | ICU 期間開始,⚠️ 視中心 protocol |
| Phase | Drug | Dose | Duration | |——|——|——|——| | ICU (from POD 1) | Micafungin (MCFG) | 100 mg/day IV (200 mg on ECMO) | Until ECMO decannulation + ICU discharge | | Oral transition | Itraconazole (ITCZ) suspension | 20 mL/day | May switch to capsules after 7 days or more | | Maintenance | ITCZ capsule | 50-200 mg/day | At least 3-6 months | | Inhaled | Amphotericin B (Fungizone) nebulized | | Starting in ICU, ⚠️ per center protocol |
D.7.3 D.7.3 CMV 預防 [UTH-Manual-2022] / D.7.3 CMV Prevention [UTH-Manual-2022]
| D/R 狀態 | 預防策略 | 藥物 | 劑量 | 期間 |
|---|---|---|---|---|
| D+/R-(最高風險) | Prophylaxis | GCV IV 5 mg/kg/day → VGC PO 900 mg/day | 術後立即開始 | ≥ 12 個月(0-6 月 900 mg → 6-12 月 450-900 mg) |
| D+/R+ 或 D-/R+ | Prophylaxis | VGC PO 900 mg/day | 口服可能後開始 | 6 個月 |
| D-/R- | 低風險 | Acyclovir PO 400 mg × 2/day | 6 個月 |
| D/R Status | Strategy | Drug | Dose | Duration | |———–|———-|——|——|——| | D+/R- (highest risk) | Prophylaxis | GCV IV 5 mg/kg/day → VGC PO 900 mg/day | Start immediately post-op | 12 months or more (0-6m: 900 mg → 6-12m: 450-900 mg) | | D+/R+ or D-/R+ | Prophylaxis | VGC PO 900 mg/day | Start when oral intake possible | 6 months | | D-/R- | Low risk | Acyclovir PO 400 mg x 2/day | | 6 months |
CMV 監測時程: - ICU 期間:C7-HRP 或 CMV-PCR 每週 1-2 次 - 出院後 3 個月內:每 1-2 週 - 3-12 個月:每月 - Preemptive therapy 閾值:C7-HRP ≥ 10/50,000;CMV-PCR ≥ 1500 IU/mL(R+)或 ≥ 500 IU/mL(R-)[UTH-Manual-2022]
CMV Monitoring Schedule: - ICU period: C7-HRP or CMV-PCR 1-2x/week - First 3 months post-discharge: Every 1-2 weeks - 3-12 months: Monthly - Preemptive therapy threshold: C7-HRP ≥ 10/50,000; CMV-PCR ≥ 1500 IU/mL (R+) or ≥ 500 IU/mL (R-) [UTH-Manual-2022]
D.7.4 D.7.4 PCP 預防 [UTH-Manual-2022] / D.7.4 PCP Prevention [UTH-Manual-2022]
| 藥物 | 劑量 | 起始 | 期間 |
|---|---|---|---|
| TMP-SMX (Baktar/Bactrim) | 1 錠/day,週一三五 | POD 14(或口服可能後) | 終生 |
| 替代(TMP-SMX 過敏) | Atovaquone (Samitrel) 1500 mg/day | 終生 |
| Drug | Dose | Start | Duration | |——|——|——|——| | TMP-SMX (Baktar/Bactrim) | 1 tab/day, Mon-Wed-Fri | POD 14 (or when oral intake possible) | Lifelong | | Alternative (TMP-SMX allergy) | Atovaquone (Samitrel) 1500 mg/day | | Lifelong |
D.7.5 D.7.5 吸入藥物時程 [UTH-Manual-2022] / D.7.5 Inhaled Medication Schedule [UTH-Manual-2022]
| 藥物 | 頻率 | 起始 | 備註 |
|---|---|---|---|
| Meptin(Procaterol)霧化 | q4h → PRN | ICU 入室即開始 | 支氣管擴張 |
| Atrovent(Ipratropium)霧化 | q4h | ICU 入室 | |
| QVAR(Beclomethasone)吸入 | 2 puffs BID-QID | 口服可能後 | 局部抗炎 |
| Tobramycin 霧化 | PRN | Pseudomonas 培養陽性時 | 180-270 mg |
| Amphotericin B 霧化 | PRN | Aspergillus 風險時 | 25 mg |
| Drug | Frequency | Start | Notes | |——|——|——|——| | Meptin (Procaterol) nebulized | q4h → PRN | Start immediately upon ICU admission | Bronchodilator | | Atrovent (Ipratropium) nebulized | q4h | ICU admission | | | QVAR (Beclomethasone) inhaled | 2 puffs BID-QID | When oral intake possible | Local anti-inflammatory | | Tobramycin nebulized | PRN | When Pseudomonas culture positive | 180-270 mg | | Amphotericin B nebulized | PRN | When Aspergillus risk present | 25 mg |
D.8 D.8 出院準備與出院標準 / D.8 Discharge Preparation and Criteria
D.8.1 D.8.1 出院標準檢核表 / D.8.1 Discharge Criteria Checklist
| 項目 | 標準 |
|---|---|
| ☐ 呼吸 | 脫離呼吸器、室內空氣或低流量 O2 穩定 |
| ☐ 肺功能 | FEV1 穩定或改善中 |
| ☐ CXR | 穩定,無新浸潤 |
| ☐ 免疫抑制 | 口服三聯療法穩定(Tac + MMF + PSL),Tac level 達標 |
| ☐ 感染 | 無活動性感染 |
| ☐ 營養 | 口服攝入足夠 |
| ☐ 活動 | 可獨立步行或輕度協助 |
| ☐ 傷口 | 癒合良好 |
| ☐ 排斥 | 氣管支鏡 biopsy 無顯著排斥(≤ A1) |
| ☐ 教育 | 完成衛教(見下表) |
| Item | Criteria | |——|——| | Respiratory | Weaned from ventilator, stable on room air or low-flow O2 | | Pulmonary function | FEV1 stable or improving | | CXR | Stable, no new infiltrates | | Immunosuppression | Stable oral triple therapy (Tac + MMF + PSL), Tac level on target | | Infection | No active infection | | Nutrition | Adequate oral intake | | Mobility | Independent walking or minimal assistance | | Wound | Healing well | | Rejection | Bronchoscopy biopsy with no significant rejection (≤ A1) | | Education | Completed education (see below) |
D.8.2 D.8.2 出院衛教項目 / D.8.2 Discharge Education Items
| 項目 | 內容 |
|---|---|
| 藥物指導 | 三聯免疫抑制劑服藥時間(早 8:30 服 Prograf/CellCept/Prednisone)[UTH-Manual-2022] |
| 抗感染藥物(ITCZ、Baktar、VGC) | |
| GI 保護藥物(PPI、Metoclopramide 等) | |
| 自我監測 | 每日體溫、體重、SpO2 |
| 居家肺量計(HiChek 等)使用 [UTH-Manual-2022] | |
| 感染預防 | 手部衛生、口腔衛生(每餐後刷牙) |
| 避免人群密集處、戴口罩 | |
| 食物安全(避免生食) | |
| 回診預約 | 告知追蹤頻率(見 D.9) |
| 緊急聯絡 | 提供 24 小時聯絡電話、何時需緊急就醫 |
| Item | Content | |——|——| | Medication guidance | Triple IS timing (morning 8:30 take Prograf/CellCept/Prednisone) [UTH-Manual-2022] | | | Anti-infective drugs (ITCZ, Baktar, VGC) | | | GI protective drugs (PPI, Metoclopramide, etc.) | | Self-monitoring | Daily temperature, weight, SpO2 | | | Home spirometer (HiChek, etc.) use [UTH-Manual-2022] | | Infection prevention | Hand hygiene, oral hygiene (brush after every meal) | | | Avoid crowded places, wear mask | | | Food safety (avoid raw foods) | | Follow-up | Inform follow-up frequency (see D.9) | | Emergency contacts | Provide 24-hour contact number, when to seek emergency care |
D.8.3 D.8.3 出院藥物清單範例 [UTH-Manual-2022] / D.8.3 Sample Discharge Medication List [UTH-Manual-2022]
| 類別 | 藥物 | 劑量 |
|---|---|---|
| 免疫抑制 | Tacrolimus (Prograf) | 依 trough 調整 |
| MMF (CellCept) | 500-1500 mg/day 分 2 次 | |
| Prednisolone | 減量中(目標 5 mg/day) | |
| 抗黴菌 | ITCZ suspension/capsule | 20 mL/day 或 50-200 mg |
| 抗病毒 | Valganciclovir (Valixa) | 依 CMV 風險 450-900 mg |
| PCP 預防 | TMP-SMX (Baktar) | 1 錠 週一三五 |
| 吸入劑 | QVAR + Procaterol | BID-QID |
| 腸胃 | Metoclopramide 15 mg、Pantoprazole | |
| Lubiprostone (Amitiza) 48 μg 或 Senokot | 便秘預防 | |
| 益生菌 | Miyairi-BM 或 Biofermin-R | 1 g |
| 助眠 | Ramelteon (Rozerem) 8 mg | PRN |
| 骨質 | Alendronate 35 mg 週一、Vit D3 | 見 D.10 |
| Category | Drug | Dose | |——|——|——| | Immunosuppression | Tacrolimus (Prograf) | Per trough adjustment | | | MMF (CellCept) | 500-1500 mg/day divided BID | | | Prednisolone | Tapering (target 5 mg/day) | | Antifungal | ITCZ suspension/capsule | 20 mL/day or 50-200 mg | | Antiviral | Valganciclovir (Valixa) | Per CMV risk 450-900 mg | | PCP prevention | TMP-SMX (Baktar) | 1 tab Mon-Wed-Fri | | Inhaled | QVAR + Procaterol | BID-QID | | GI | Metoclopramide 15 mg, Pantoprazole | | | | Lubiprostone (Amitiza) 48 ug or Senokot | Constipation prevention | | Probiotic | Miyairi-BM or Biofermin-R | 1 g | | Sleep aid | Ramelteon (Rozerem) 8 mg | PRN | | Bone health | Alendronate 35 mg Monday, Vit D3 | See D.10 |
D.9 D.9 出院後追蹤時間表 / D.9 Post-Discharge Follow-Up Schedule
D.9.1 D.9.1 門診回診頻率 [UTH-Manual-2022] / D.9.1 Clinic Visit Frequency [UTH-Manual-2022]
| 時期 | 頻率 | 內容 |
|---|---|---|
| 出院後第 1-4 週 | 每週 1-2 次 | 基本 Labs + Tac level + CXR |
| 第 1-3 個月 | 每 1-2 週 | Labs + Tac level + 肺功能 + CXR |
| 第 3-6 個月 | 每 2 週至每月 | Labs + Tac level + 肺功能 |
| 第 6-12 個月 | 每月 | Labs + Tac level + CT(每 3-6 月) |
| > 12 個月 | 每 2-3 個月 | 年度全套檢查 |
| Period | Frequency | Content | |——|——|——| | Post-discharge weeks 1-4 | 1-2 times/week | Basic labs + Tac level + CXR | | Months 1-3 | Every 1-2 weeks | Labs + Tac level + PFT + CXR | | Months 3-6 | Every 2 weeks to monthly | Labs + Tac level + PFT | | Months 6-12 | Monthly | Labs + Tac level + CT (every 3-6 months) | | > 12 months | Every 2-3 months | Annual comprehensive workup |
D.9.2 D.9.2 每次回診檢查項目 [UTH-Manual-2022] / D.9.2 Tests at Each Visit [UTH-Manual-2022]
基本項目(每次): - CBC、生化(肝腎功能) - Tacrolimus (或 CsA) trough level - CXR - 居家肺量計數據回顧
Basic items (every visit): - CBC, chemistry (liver/renal function) - Tacrolimus (or CsA) trough level - CXR - Home spirometer data review
定期追加項目:
Periodic additional items:
| 頻率 | 項目 |
|---|---|
| 每 1-2 週(前 3 月) | CMV (C7-HRP)、EBV-DNA、Aspergillus antigen |
| 每月(3-12 月) | CMV 監測、IgG/IgA/IgM |
| 每 3-6 個月 | 胸部 CT、HLA 抗體(DSA)追蹤 |
| 每次 | Aspergillus antigen、Candida antigen、β-D-glucan |
| Frequency | Items | |——|——| | Every 1-2 weeks (first 3 months) | CMV (C7-HRP), EBV-DNA, Aspergillus antigen | | Monthly (3-12 months) | CMV monitoring, IgG/IgA/IgM | | Every 3-6 months | Chest CT, HLA antibody (DSA) tracking | | Every visit | Aspergillus antigen, Candida antigen, beta-D-glucan |
D.9.3 D.9.3 protocol 氣管支鏡時程 / D.9.3 Protocol Bronchoscopy Schedule
| 時間點 | 內容 |
|---|---|
| POD 7 | 第 1 次 protocol biopsy + BAL |
| POD 14 | 第 2 次 biopsy |
| 1 個月 | Surveillance biopsy |
| 3 個月 | Surveillance biopsy |
| 6 個月 | Surveillance biopsy |
| 12 個月 | Surveillance biopsy |
| ⚠️ 之後 | 依臨床需求(FEV1 下降 > 10% 時需加做) |
| Time Point | Content | |——–|——| | POD 7 | 1st protocol biopsy + BAL | | POD 14 | 2nd biopsy | | 1 month | Surveillance biopsy | | 3 months | Surveillance biopsy | | 6 months | Surveillance biopsy | | 12 months | Surveillance biopsy | | ⚠️ Thereafter | Per clinical need (add when FEV1 decline > 10%) |
每次 BAL 送檢: - 細菌培養(含 Aspergillus、Cryptococcus、Mucor、Nocardia) - 抗酸菌染色/培養(TB/NTM) - CMV PCR - 細胞學
Each BAL submission: - Bacterial culture (including Aspergillus, Cryptococcus, Mucor, Nocardia) - Acid-fast stain/culture (TB/NTM) - CMV PCR - Cytology
D.10 D.10 長期里程碑 / D.10 Long-Term Milestones
D.10.1 D.10.1 時間軸總覽 / D.10.1 Timeline Overview
| 時間點 | 里程碑事件 |
|---|---|
| 3 個月 | Tac level 目標調降至 10-15 ng/mL |
| mPSL 減量目標:0.25 mg/kg/day | |
| 首次骨密度檢查(DEXA)[UTH-Manual-2022] | |
| 評估是否需 mTOR inhibitor | |
| 考慮疫苗(滅活疫苗) | |
| 6 個月 | Tac level 目標調降至 8-12 ng/mL |
| mPSL 減量目標:0.15 mg/kg/day | |
| 首次年度實驗室全套 | |
| CMV 預防藥物評估(D+/R+ 或 D-/R+ 可考慮停藥) | |
| 抗黴菌藥物評估(可考慮停 ITCZ) | |
| 9 個月 | mPSL 目標:0.08-0.1 mg/kg/day (5-6 mg) |
| 12 個月 | 年度全面體檢 |
| 胸部 CT | |
| 完整肺功能 | |
| 6MWT | |
| HLA 抗體(DSA) | |
| 骨密度追蹤 | |
| 血脂、血糖、HbA1c | |
| 癌症篩檢(皮膚科、子宮頸抹片等) | |
| CMV/EBV 監測 | |
| 每年(> 1 年後) | 年度全套檢查(同上) |
| DEXA | |
| 疫苗評估更新 | |
| CLAD 篩檢(FEV1 趨勢分析) | |
| PTLD 監測(EBV-DNA) | |
| 皮膚癌篩檢 |
| Time Point | Milestone Event | |——–|———–| | 3 months | Tac level target lowered to 10-15 ng/mL | | | mPSL taper target: 0.25 mg/kg/day | | | First bone density scan (DEXA) [UTH-Manual-2022] | | | Evaluate need for mTOR inhibitor | | | Consider vaccination (inactivated vaccines) | | 6 months | Tac level target lowered to 8-12 ng/mL | | | mPSL taper target: 0.15 mg/kg/day | | | First annual comprehensive laboratory panel | | | CMV prophylaxis evaluation (D+/R+ or D-/R+ may consider discontinuation) | | | Antifungal evaluation (may consider stopping ITCZ) | | 9 months | mPSL target: 0.08-0.1 mg/kg/day (5-6 mg) | | 12 months | Annual comprehensive examination | | | Chest CT, complete PFT, 6MWT | | | HLA antibody (DSA), bone density follow-up | | | Lipids, glucose, HbA1c | | | Cancer screening (dermatology, cervical smear, etc.) | | | CMV/EBV monitoring | | Annually (> 1 year) | Annual comprehensive workup (same as above) | | | DEXA, vaccine assessment update | | | CLAD screening (FEV1 trend analysis) | | | PTLD monitoring (EBV-DNA), skin cancer screening |
D.10.2 D.10.2 骨質疏鬆預防與治療 [UTH-Manual-2022] / D.10.2 Osteoporosis Prevention and Treatment [UTH-Manual-2022]
| 項目 | 內容 |
|---|---|
| 篩檢 | YAM < 80% 或 T-score ≤ -2.5 SD 即需治療 |
| 一線治療 | Alendronate 35 mg PO 每週一次 |
| Vitamin D | Eldecalcitol 0.75 μg/day 或 Alfacalcidol 1.0 μg/day |
| 二線 | Denosumab (Pralia) 60 mg SC 每 6 個月 |
| 追蹤 | DEXA 每年;骨折風險評估 |
| Item | Content | |——|——| | Screening | Treat when YAM < 80% or T-score ≤ -2.5 SD | | First-line | Alendronate 35 mg PO weekly | | Vitamin D | Eldecalcitol 0.75 ug/day or Alfacalcidol 1.0 ug/day | | Second-line | Denosumab (Pralia) 60 mg SC every 6 months | | Follow-up | DEXA annually; fracture risk assessment |
D.10.3 D.10.3 代謝症候群管理 [UTH-Manual-2022] / D.10.3 Metabolic Syndrome Management [UTH-Manual-2022]
高血壓(目標 < 130/80 mmHg): 1. ARB 為首選(Candesartan 4-8 mg、Telmisartan 20-40 mg) 2. CCB:避免 Diltiazem、Verapamil(↑CNI 濃度);可用 Amlodipine(↑CNI 約 25%) 3. ⚠️ 禁用 Aliskiren(與 Cyclosporine 交互作用)
Hypertension (target < 130/80 mmHg): 1. ARB first-line (Candesartan 4-8 mg, Telmisartan 20-40 mg) 2. CCB: Avoid Diltiazem, Verapamil (increase CNI levels); may use Amlodipine (increases CNI ~25%) 3. ⚠️ Aliskiren contraindicated (interaction with Cyclosporine)
高血脂(目標 LDL < 120-140 mg/dL): 1. Statin:選用 Pitavastatin 或 Rosuvastatin(低 CYP3A4 交互作用) 2. 避免 Atorvastatin、Simvastatin(高 CYP3A4 交互作用)
Hyperlipidemia (target LDL < 120-140 mg/dL): 1. Statin: Choose Pitavastatin or Rosuvastatin (low CYP3A4 interaction) 2. Avoid Atorvastatin, Simvastatin (high CYP3A4 interaction)
糖尿病(目標 HbA1c < 7.0%): 1. 首選 DPP-4 inhibitor(Sitagliptin、Linagliptin — 不需腎劑量調整) 2. 避免 Metformin(移植後腎功能波動) 3. ⚠️ α-glucosidase inhibitor 與 MMF/AZA 有交互作用
Diabetes (target HbA1c < 7.0%): 1. First-line: DPP-4 inhibitor (Sitagliptin, Linagliptin — no renal dose adjustment needed) 2. Avoid Metformin (post-transplant renal function fluctuations) 3. ⚠️ Alpha-glucosidase inhibitors interact with MMF/AZA
D.10.4 D.10.4 CLAD 監測 [UTH-Manual-2022] / D.10.4 CLAD Monitoring [UTH-Manual-2022]
| 指標 | 警示值 | 處置 |
|---|---|---|
| FEV1 下降 > 10% | Possible CLAD | 追蹤確認 |
| FEV1 下降 > 20% 持續 3 週以上 | Probable → Definite CLAD | 氣管支鏡 + CT + HLA 抗體 |
| TLC 下降 > 10% | 疑 RAS | 加做 CT 鑑別 BOS vs RAS |
| Indicator | Alert Value | Action | |——|——–|——| | FEV1 decline > 10% | Possible CLAD | Follow-up confirmation | | FEV1 decline > 20% sustained > 3 weeks | Probable → Definite CLAD | Bronchoscopy + CT + HLA antibodies | | TLC decline > 10% | Suspect RAS | Add CT to differentiate BOS vs RAS |
CLAD 治療選項 [UTH-Manual-2022]: 1. Azithromycin 250 mg QOD 2. Montelukast 10 mg/day 3. Pulse steroid(mPSL 500 → 250 → 125 mg × 3 天) 4. Thymoglobulin 1.5 mg/kg(嚴重時)
CLAD Treatment Options [UTH-Manual-2022]: 1. Azithromycin 250 mg QOD 2. Montelukast 10 mg/day 3. Pulse steroid (mPSL 500 → 250 → 125 mg x 3 days) 4. Thymoglobulin 1.5 mg/kg (severe cases)
D.11 D.11 特殊族群注意事項 / D.11 Special Population Considerations
D.11.1 D.11.1 iPAH(特發性肺動脈高壓)患者 [UTH-Manual-2022] / D.11.1 iPAH (Idiopathic Pulmonary Arterial Hypertension) Patients [UTH-Manual-2022]
- 術後 ECMO 維持 2-3 天,不急於脫離
- PEEP 管理需更保守
- 升壓藥優先序:Catecholamine → Milrinone → Prostacyclin (PGE1 0.01-0.02 μg/kg/min)
- 可能需 OnO/Octanoate 1-2 μg/kg/min
- Post-op ECMO maintenance for 2-3 days, do not rush to wean - PEEP management requires more conservative approach - Vasopressor priority: Catecholamine → Milrinone → Prostacyclin (PGE1 0.01-0.02 ug/kg/min) - May require OnO/Octanoate 1-2 ug/kg/min
D.11.2 D.11.2 小兒患者 / D.11.2 Pediatric Patients
- Size matching 標準:predicted VC 差異 ±12%(兒童專用公式)[UTH-Manual-2022]
- Central ECMO cannulation 技術細節需調整(較小管徑)
- 營養支持:考慮兒童專用配方
- 心理支持:多職種團隊(兒童生活輔導員、心理師、社工)
- 家屬住宿與照顧安排
- Size matching criteria: predicted VC difference ±12% (pediatric-specific formula) [UTH-Manual-2022] - Central ECMO cannulation technical details require adjustment (smaller caliber) - Nutritional support: Consider pediatric-specific formulas - Psychological support: Multidisciplinary team (child life specialist, psychologist, social worker) - Family accommodation and care arrangements
D.11.3 D.11.3 再移植患者 [UTH-Manual-2022] / D.11.3 Retransplantation Patients [UTH-Manual-2022]
- 手術難度高(嚴重沾黏)
- CLAD 為最常見適應症
- 術後出血風險高
- 免疫抑制可能需調整(已致敏化)
- Higher surgical difficulty (severe adhesions) - CLAD is the most common indication - Higher postoperative bleeding risk - Immunosuppression may require adjustment (already sensitized)
D.12 D.12 緊急情況時間表 / D.12 Emergency Situation Timeline
D.12.1 D.12.1 何時緊急就醫 / D.12.1 When to Seek Emergency Care
| 症狀 | 可能原因 | 建議 |
|---|---|---|
| 發燒 > 38°C | 感染、排斥 | 立即就醫 |
| SpO2 下降 > 3-5% baseline | PGD、排斥、感染 | 立即就醫 |
| FEV1 下降 > 10% | 排斥、CLAD、感染 | 24 小時內就醫 |
| 呼吸困難急性加重 | 多種原因 | 立即就醫 |
| 咳血 | 吻合口問題、感染 | 立即就醫 |
| Symptom | Possible Cause | Recommendation | |——|———-|——| | Fever > 38 degrees C | Infection, rejection | Seek immediate care | | SpO2 decline > 3-5% from baseline | PGD, rejection, infection | Seek immediate care | | FEV1 decline > 10% | Rejection, CLAD, infection | Seek care within 24 hours | | Acute worsening dyspnea | Multiple causes | Seek immediate care | | Hemoptysis | Anastomotic problems, infection | Seek immediate care |
參考文獻 [UTH-Manual-2022] 東京大學醫學部附屬病院 呼吸器外科,肺移植手冊 2022 年版(繁體中文翻譯版 2024)。 📋 三總本院 protocol 待補充對照。
References [UTH-Manual-2022] University of Tokyo Hospital Department of Thoracic Surgery, Lung Transplant Handbook 2022 Edition (Traditional Chinese Translation 2024). 📋 TSGH institutional protocol to be supplemented for comparison.