高血壓 高尿酸 慢性腎病 胰島素 https://2019medicinenote.blogspot.com/2019/12/blog-post_57.html . 糖尿病相關筆記~目錄 https://2019medicinenote.blogspot.com/2020/01/blog-post_4.html

2026年1月19日 星期一

野外與登山醫學 THE 1992 路易斯湖高海拔疾病定義及量化共識會議 LAKE LouisE CoNSENsus ON THE DEFINITION AND QUANTIFICATION OF ALTITUDE ILLNESS

2026-01-20
路易斯湖在位於加拿大落基山脈的班夫國家公園內. 湖面海拔約 1750 公尺. 
症狀 symptoms 是病患覺得自己有哪些不尋常的症狀. 是病患自己說的. 但嬰幼兒或年長者或其他無法清晰明確表達群體. 也可由照護者代為表達病患症狀. 例如全身虛弱. 例如食慾不振. 
徵象 signs 是指身體檢查發現的特定發現. 例如生命體徵(vital signs)體溫.心跳.血壓.氧氣濃度.
要描述紀錄患者的狀況. 除了 symptoms /signs,  還有一些屬於實驗室檢查. 包括抽血,驗尿. 糞便檢查. 各種疾病快篩. 影像學檢查(x光.超音波.電腦斷層. 核磁共振. 心電圖. 肌電圖. 腦波等等等)

統一名詞翻譯
Dexamethasone 類固醇(地塞米松), 高海拔疾病的研究或文獻. 提到的類固醇幾乎都是指 dexamethasone(類固醇種類很多,不僅地塞米松一種)
HAI= high altitude illness 高海拔疾病(等於高山症)
AMS =acute mountain sickness 急性高山病(不等於高山症)
HAC=E high altitude cerebral edema 高海拔腦水腫
HAPE =high altitude pulmonary edema 高海拔肺水腫
Acetazolamide 丹木斯(乙酰唑胺). 一種利尿劑
Nifedipine 硝苯地平, 是一種降血壓藥物, 分類上屬於鈣離子阻斷劑CCB, 於1969年被合成,1981年在美國核准上市。


The lake louise consensus on the quantification of altitude illness
January 1992-PDF檔案下載處

1991年這次共識會提出HAPE診斷需要有兩個以上的症狀及兩個以上的徵象,

在1991年國際低氧症研討會上,與會者達成共識,對各種高原疾病進行量化。這個過程分為幾個階段,由 Peter Hackett(彼得·哈克特)和Oswald Oelz(奧斯瓦爾德·厄爾茨)主持。
在會議召開前,共識委員會收到了有關高山症定義和量化方法的文件。會議期間,所有代表都有機會參與文件的編寫工作。委員會在會議期間多次召開會議,最後制定了這份共識文件。
本文件反映了截至1991年3月的發展現狀,其內容包括:
a) 高海拔症候群的診斷標準,
b) 對高海拔疾病的各種症狀/徵象進行評分的既定流程。
c) 自我評估問卷,
d) 臨床評估-由觀察者進行

建議在接下來的兩年內,由那些對高原疾病進行實地研究的研究人員使用上述方案,並在 1993 年 2 月 9 日至 13 日於路易斯湖舉行的 1993 年國際缺氧研討會上討論結果

以下診斷標準已被接受。
AMS 急性高山病
在近期海拔升高的情況下,出現頭痛,並伴隨以下至少一種症狀:胃腸道症狀(厭食、噁心或嘔吐)、疲勞或虛弱、頭暈或頭暈、睡眠困難。

HACE
可視為「末期」或重度AMS(急性高山病)。在近期海拔升高的情況下,如果急性高山症患者出現精神狀態改變和/或共濟失調,或非急性高山症患者同時出現精神狀態改變和共濟失調,則應考慮此診斷。


HAPE
在近期海拔升高的情況下,有以下情況:
以下症狀至少出現兩項(症狀是病人自己說的)
靜止時呼吸困難、咳嗽、虛弱或運動能力下降、胸悶或胸悶。
以下徵象至少出現兩項(徵象=身體檢查)
至少有一個肺野出現囉音或喘鳴音、中心性紫紺、呼吸急促、心跳過速。

Campbell 博士評論道:
雖然這並非我的專業領域,但我必須表達一些擔憂,目前提出的所謂分類並非異源性分類。急性高山病(AMS)的定義是基於症狀或綜合徵,而高海拔腦水腫(HACE)的定義則是基於病理生理學。 AMS 的基本病理生理機轉很可能與 HACE 類似。另一方面,HACE 的病理生理機轉也可能導致類似 AMS 的症候群。任何分類(而非簡單的清單)都應盡可能做到同源性分類。
待辦事項:
1)解決 Moran Campbell 對 HACE 定義不明確的擔憂。 
2)Bartsch 建議將呼吸急促和心動過速進行量化。

At the 1991 International Hypoxia Symposium, a consensus process to quantify the various altitude maladies occurred. There were several stages in the process which was chaired by Peter Hackett and Oswald Oelz.
Prior to the conference, a consensus committee was given documents pertaining to definitions and ways to quantify altitude illness. At the conference, all delegates were given the opportunity to have input into the preparation of the document. The committee met on several occasions during the meeting and developed this consensus document.
This document represents the present state of its evolution, as of March, 1991. It consists of:
a) diagnostic criteria of altitude syndromes,
b) an agreed process of scoring the various symptoms/signs of altitude illness.
c) self assessment questionnaires,
d) clinical assessment-performed by an observer


It is proposed that the above schema be used over the next two years by those investigators conducting field research into altitude illness and the outcome discussed at the 1993 International Hypoxia Symposium at Lake Louise, February 9-13, 1993.


The following DIAGNOSTIC CRITERIA were accepted.


AMS
In the setting of a recent gain in altitude, the presence of headache and at least one of the following symptoms: gastrointestinal (anorexia, nausea or vomiting), fatigue or weakness, dizziness or lightheadedness, difficulty sleeping.


HACE
Can be considered "end stage" or severe AMS. In the setting of a recent gain in altitude, the presence of a change in mental status and/or ataxia in a person with AMS, or the presence of both mental status change and ataxia in a person without AMS.


HAPE
In the setting of a recent gain in altitude, the presence of the following:
Symptoms: at least two of:
dyspnea at rest, cough, weakness or decreased exercise performance, chest tightness or congestion.
Signs: at least two of:
rales or wheezing in at least one lung field, central cyanosis, tachypnea, tachycardia.

Comment from Dr. E.J.M. Campbell:
Although this is not my field, I must express some concern that the so-called classification put forward is not heterologous. AMS is defined in symptomatic or syndromal terms whereas HACE is defined in pathophysiological terms. It may well be that AMS has as its basic pathophysiology something not unlike HACE. On the other hand, it may well be that the pathophysiology ofHACE can cause a syndrome like AMS. It is much preferable that any classification (as opposed to simply a list) should be isologous. To be done: 1) Address Moran Campbell's concern about unclear definition of HACE. 2. Bartsch suggests that tachypnea and tachycardia should be quantified.


Emergency treatment of anaphylaxis 英國--全身性嚴重過敏治療指引

2026-01-20 相關筆記連結
1. anaphylaxis 嚴重全身性過敏反應 治療藥物與頻次劑量
2. 野外與登山醫學---對磺胺類藥物過敏的人可否服用丹木斯
3. anaphylaxis 全身性嚴重過敏反應 腎上腺素劑量
4. 名詞翻譯~ Anaphylaxis 全身性嚴重過敏反應
5. anaphylaxis 全身性嚴重過敏反應 診斷標準與治療
6. 野外與登山醫學-epipen 腎上腺素筆-全身性嚴重過敏反應治療用藥
7. 全身性嚴重過敏反應-Fatal anaphylaxis 死亡案例接觸過敏原之後出現症狀的時間 from uptodate

這篇是 (May 2021 英國)全身性嚴重過敏反應治療指引 

重點建議
1. 全身性嚴重過敏反應是會危及生命的過敏反應
2. 辨識是否為全身性嚴重過敏反應可依據
    a. 突然快速的症狀進展
    b. 會出現呼吸道, 呼吸, 或循環問題
    c. 皮膚或黏膜異常, 潮紅, 蕁麻疹, 血管性水腫, 有20%個案不會出現這些
當個案暴露於已知的過敏原之後出現以上症狀, 可能是全身性嚴重過敏反應
可以參照 ABCDE步驟處理危及生命的問題
Airway, Breathing, Circulation, Disability, Exposure (ABCDE) 
當ABC出現問題, 第一線治療藥物是腎上腺素, 以肌肉注射方式施打在大腿前外側
若施打一次的五分鐘內沒反應., 可施打第二次


Key recommendations for clinical practice
• Anaphylaxis is a potentially life-threatening allergic reaction. 

• Recognise anaphylaxis based on: 
1. sudden onset and rapid progression of symptoms 
2. Airway and/or Breathing and/or Circulation problems 
3. skin and/or mucosal changes (flushing, urticaria, angioedema) – but these may be absent in up to 20% of cases. 
The diagnosis is supported if a patient has been exposed to an allergen known to affect them.

• Treat life-threatening features, using the Airway, Breathing, Circulation, Disability, Exposure (ABCDE) approach. 

Adrenaline is the first-line treatment for anaphylaxis. Give intramuscular (IM) adrenaline early (in the anterolateral thigh) for Airway/Breathing/Circulation problems. 
*** A single dose of IM adrenaline is well-tolerated and poses minimal risk to an individual having an allergic reaction. If in doubt, give IM adrenaline. 
*** Repeat IM adrenaline after 5 minutes if Airway/Breathing/Circulation problems persist. 

• Intravenous (IV) adrenaline must be used only in certain specialist settings, and only by those skilled and experienced in its use.
*** IV adrenaline infusions form the basis of treatment for refractory anaphylaxis: seek expert help early in patients whose respiratory and/or cardiovascular problems persist despite 2 doses of IM adrenaline. 

• Follow the National Institute for Health and Care Excellence (NICE) guideline for the assessment and referral of patients suspected to have had anaphylaxis. Specifically:
*** All patients should be referred to a specialist clinic for allergy assessment.
*** Offer patients (or, if appropriate, their parent and/or carer) an appropriate adrenaline injector as an interim measure before the specialist allergy assessment (unless the reaction was druginduced).
*** Patients prescribed adrenaline auto-injectors (and/or their parents/carers) must receive training in their use, and have an emergency management or action plan 

• Further research is needed to better identify and treat patients at greatest risk of severe anaphylaxis.
*** Anaphylaxis reactions should be reported to the UK Anaphylaxis Registry at www.anaphylaxie.net (to register, email anaphylaxis.registry@ic.ac.uk).
*** Follow guidance for reporting and debriefing of adverse events.

Summary of changes from previous guideline
This guideline replaces the previous guideline from Resuscitation Council UK (RCUK): Emergency treatment of anaphylactic reactions – Guidelines for healthcare providers (originally published January 2008, annotated July 2012 with links to NICE guidance).
• Greater emphasis on intramuscular adrenaline to treat anaphylaxis, and repeated after 5 minutes if Airway/Breathing/Circulation problems persist. 
• A specific dose of adrenaline is now included for children below 6 months of age. 
• Increased emphasis on the importance of avoiding sudden changes in posture and maintaining a supine position (or semi-recumbent position if that makes breathing easier for the patient) during treatment. 
• There are 2 algorithms:
*** Initial treatment of anaphylaxis, with emphasis on repeating the dose of adrenaline after 5 minutes and giving an IV fluid bolus if Airway/Breathing/Circulation problems persist.
*** Treatment of refractory anaphylaxis, defined as anaphylaxis where there is no improvement in respiratory or cardiovascular symptoms despite two appropriate doses of IM adrenaline.

• IV fluids are recommended for refractory anaphylaxis, and must be given early if hypotension or shock is present. 
• Antihistamines are considered a third-line intervention and should not be used to treat Airway/Breathing/Circulation problems during initial emergency treatment.  
*** Non-sedating oral antihistamines, in preference to chlorphenamine, may be given following initial stabilisation especially in patients with persisting skin symptoms (urticaria and/or angioedema).

• Corticosteroids (e.g. hydrocortisone) are no longer advised for the routine emergency treatment of anaphylaxis. 
• New guidance is offered relating to the duration of observation following anaphylaxis, and timing of discharge.

1. Introduction
1.1 Purpose of this guideline 
Increasing numbers of people are presenting to UK hospitals with anaphylaxis. 4,5 Despite previous guidelines, at least 50% of reactions are not treated with IM adrenaline (the firstline treatment of anaphylaxis)6 and treatment, investigation and follow-up of patients with anaphylaxis is suboptimal.
This guideline replaces the previous guideline from Resuscitation Council UK: Emergency treatment of anaphylactic reactions – Guidelines for healthcare providers (originally published January 2008, annotated July 2012 with links to NICE guidance).1 There are no randomised controlled clinical trials in humans providing unequivocal evidence for the optimal treatment of anaphylaxis; such evidence is unlikely to be forthcoming.11,12 Nonetheless, the evidence-base for specific management strategies has increased, and international guidelines have been updated.
This guideline provides:
• an updated consensus about the recognition and treatment of anaphylaxis in all healthcare settings 
• a focus on the treatments that patients with anaphylaxis should receive, that are relevant to all healthcare providers 
• recommendations for treatment that are easy to implement, and that will be appropriate for most anaphylaxis reactions 
• new guidance on the treatment of refractory anaphylaxis. 

This guideline does not cover every possible anaphylaxis scenario, and has been written to be as simple as possible to facilitate teaching, learning and implementation. Improved implementation should reduce harm and deaths from anaphylaxis.

1.2 略

1.3 Key points 
Treatment of anaphylaxis should be based on general life-support principles:
• Call for help early. 
• Use the Airway, Breathing, Circulation, Disability, Exposure (ABCDE) approach to recognise and treat problems. Treat the greatest threat to life first. 
• Give IM adrenaline to treat Airway/Breathing/Circulation problems. 
• Initial treatment should not be delayed by a lack of a complete history or definite diagnosis. 
• Repeat IM adrenaline after 5 minutes if features of anaphylaxis do not resolve.

Patients having anaphylaxis in any setting should expect the following as a minimum: 
• recognition that they are seriously unwell 
• an early call for help (resuscitation team or ambulance) 
• initial assessment and treatment based on an ABCDE approach 
• prompt treatment with IM adrenaline 
• investigation and specialist follow-up in an allergy clinic. 

Both IM and IV routes are recommended for the treatment of anaphylaxis in the perioperative setting. IV adrenaline should be used for anaphylaxis only by experienced specialists in an appropriate setting (e.g. critical care and peri-operative settings). See Section 5.1.2 for more information.

1.4略

2. Anaphylaxis
2.1 Definition of anaphylaxis 
The World Allergy Organisation Anaphylaxis Committee defines anaphylaxis as: 11
 "A serious systemic hypersensitivity reaction that is usually rapid in onset and may cause death. Severe anaphylaxis is characterized by potentially life-threatening compromise in airway, breathing and/or the circulation, and may occur without typical skin features or circulatory shock being present.” 

Anaphylaxis is a clinical diagnosis; a precise definition is not important for treatment.

Anaphylaxis is characterised by: 
• Sudden onset and rapid progression of symptoms. 
• Airway and/or Breathing and/or Circulation problems. 
• Usually, skin and/or mucosal changes (flushing, urticaria, angioedema).

 The diagnosis is supported if a patient has been exposed to an allergen known to affect them. However, in up to 30% of cases there may be no obvious trigger. Remember: 
• Skin or mucosal changes alone are not a sign of anaphylaxis. 
• Skin and mucosal changes can be subtle or absent in 10–20% of reactions (e.g. some patients present initially with only bronchospasm or hypotension).

Gastrointestinal symptoms (e.g. nausea, abdominal pain, vomiting) in the absence of Airway and/or Breathing and/or Circulation problems do not usually indicate anaphylaxis. Abdominal pain and vomiting can be symptoms of anaphylaxis due to an insect sting or bite. 
Anaphylaxis lies along a spectrum of severity in terms of allergic symptoms.11 (Figure 1)

2.2略

2.3 Pathophysiology of anaphylaxis 
In anaphylaxis, the activation of multiple inflammatory pathways causes Airway/Breathing/ Circulation problems: 
• Tissue oedema and smooth muscle contraction in the airways (causing bronchospasm and wheeze). This is the most common presentation for food-induced anaphylaxis. 
• Fluid extravasation (tissue oedema, hypovolaemia), and a profound reduction in venous tone.28,29 
*** If severe, this mix of hypovolaemic and distributive shock cannot be overcome by compensatory mechanisms and combine to cause reduced blood flow back to the heart and an underfilled ventricles. 29 
• Depressed myocardial function has also been reported, which can cause cardiogenic shock. Electrocardiographic changes have been noted. Release of mediators may cause arrhythmia such as supraventricular tachycardia; a reduction in coronary perfusion may cause or contribute to ST-segment or T-wave changes.29 
• Fluid leakage into the bowel and smooth muscle contraction (resulting in abdominal and pelvic cramps).

In a landmark paper, Fisher described 205 adult patients with peri-operative anaphylaxis, many of whom had central venous monitoring in place. 31 He reported: 
• low right-heart filling pressures in all patients without cardiac disease; despite having elevated pressures, 9 of 11 patients with cardiac disease appeared to need volume expansion to achieve a stable blood pressure 
• increases in haematocrit in 22 patients were indicative of extravasation of up to 35% of circulating blood volume within 10 minutes of reaction onset. 

These data emphasise the need for aggressive fluid resuscitation in anaphylactic shock. 

Changes in posture from supine to standing or sitting upright have been associated with cardiovascular collapse and death during anaphylaxis.32,33 The change in posture further reduces venous return to the heart; this can lead to a further reduction in cardiac output and can compromise myocardial perfusion. 
Keeping a patient with cardiovascular instability flat, with or without the legs raised, will maximise venous return to the heart and is therefore a key component of the initial response to anaphylaxis (see section 4.3). Patients with predominantly respiratory symptoms (and no evidence of cardiovascular instability) may prefer to be in a semi-recumbent position. Pregnant patients should lie on their left side to prevent aortocaval compression, if necessary, with the bed in a head-down position (see Section 4.7).

3. Recognition of anaphylaxis
Look for: 
• Sudden onset of Airway and/or Breathing and/or Circulation problems. 
• Usually, skin and/or mucosal changes (flushing, urticaria, angioedema).

Skin or mucosal changes alone are not a sign of anaphylaxis and may be absent in up to 20% of reactions.
Confusion may arise because some patients have systemic reactions that are not anaphylaxis. Generalised urticaria, angioedema, and rhinitis are not considered to be anaphylaxis because life-threatening features – an Airway and/or Breathing and/or Circulation problem – are not present. However, if in doubt, give IM adrenaline and seek expert help. 
Most reactions develop quickly over minutes: the timing is dependent on the trigger (see Table 2 and Figure 4). Allergens given by a parenteral route (e.g. IV drug, intramuscular injection, insect sting) cause a more rapid onset of symptoms than reactions to an ingested food or drug.
Different symptoms are often associated with different triggers, as shown in Table 2. Most anaphylaxis in children is due to food, which may explain why respiratory presentations of anaphylaxis are more common in this age group. In around 5 -10% cases, no obvious trigger can be identified. 

3.2 Airway / Breathing / Circulation problems 
Patients can have either an A or B or C problem, or any combination. Use the ABCDE approach to recognise these and treat early.

Airway problems
Airway swelling (throat and tongue swelling causing difficulty in breathing/swallowing; patients may feel their throat is closing) 
• Hoarse voice 
• Stridor (a high-pitched inspiratory noise caused by upper airway obstruction)

Breathing problems
• Increased work of breathing 
• Bronchospasm (wheeze) and/or persistent cough 
• Patient becoming tired with the effort of breathing (fatigue) 
• Hypoxaemia (SpO 2 <94%) which may cause confusion and/or central cyanosis 
• Respiratory arrest

Circulation problems
• Signs of shock: o pale, clammy o significant tachycardia (increased heart rate) o hypotension (low blood pressure) 
• Dizziness, decreased conscious level or loss of consciousness 
• Arrhythmia 
• Cardiac arrest

Breathing problems can vary from mild bronchospasm to life-threatening asthma with no other features to suggest anaphylaxis.42 Anaphylaxis can present primarily as respiratory arrest.19,22,27 Consider anaphylaxis in a person with sudden onset breathing difficulties, especially if known to be allergic to a food or insect sting. 

Circulation problems (often referred to as anaphylactic shock) can be caused by vasodilation, by capillary leak with loss of fluid from the circulation, and by direct myocardial depression (see Figure 5). Characteristically, these cause a compensatory tachycardia.20,29 Bradycardia (a slow heart rate) is usually a late feature, often preceding cardiac arrest, 29 but has also been reported in insect/venom anaphylaxis, occurring with the onset of hypotension.44 

Anaphylaxis can also cause myocardial ischaemia and electrocardiogram (ECG) changes,31 even in individuals with normal coronary arteries.43 Anaphylaxis can also affect a patient’s neurological status (Disability problems) because of decreased brain perfusion or the effect of local allergic mediators in the central nervous system. There may be confusion, agitation and loss of consciousness. Patients are usually anxious and may experience a “sense of impending doom”.45 Patients may also have gastrointestinal symptoms (abdominal pain, incontinence, vomiting). These symptoms are more likely to indicate anaphylaxis in the context of reactions due to insect bite or sting, snake bite or parenteral administration of drugs.

3.3 Skin and/or mucosal changes
These are assessed as part of the Exposure when using the ABCDE approach. 
• These are often the first feature of allergic reactions and are present in over 80% of anaphylaxis.37 
• They can be subtle (e.g. patchy erythema) or dramatic (generalised rash). 
• They may involve the skin, the mucosal membranes (e.g. lips), or both. 
• There may be urticaria (also called hives, nettle rash, weals or welts), which can appear anywhere on the body. Weals may be pale, pink or red, can be different shapes and sizes, and are often surrounded by a red flare. They are usually itchy. 
• Angioedema involves swelling of deeper tissues, most commonly in the eyelids and lips, and sometimes the tongue and in the throat. 

Although skin changes can be worrying or distressing for patients and those treating them, skin changes without life-threatening Airway/Breathing/Circulation problems are not anaphylaxis. Reassuringly, most patients who present with skin changes caused by an allergic reaction do not go on to develop anaphylaxis.

3.4 Differential diagnosis 
• Following an ABCDE approach will help with treating the differential diagnoses. 
• In all of the circumstances below, IM adrenaline is unlikely to cause harm and might be clinically useful. 

Life-threatening conditions: 
• Sometimes anaphylaxis can present with symptoms and signs that are very similar to life-threatening asthma – this is most common in children. • Hypotension is a late sign in children. • Seek expert help early if there are any doubts about the diagnosis and treatment. 
Other conditions which can mimic anaphylaxis (but do not respond to adrenaline): 
• inducible laryngeal obstruction (ILO, formerly known as vocal cord dysfunction) 
• ACE inhibitor-induced angioedema, which can be life-threatening and typically does not respond to adrenaline.

Non-life-threatening conditions (these usually respond to simple measures): 
• faint (vasovagal episode) – this can occur in the context of non-anaphylaxis allergic reactions (see below) 
• panic attack 
• breath-holding episode in a child 
• spontaneous (non-allergic) urticaria or angioedema. 

There may be difficulty distinguishing between anaphylaxis and a panic attack. Patients with prior anaphylaxis may be prone to panic attacks if they think they have been re-exposed to the allergen that caused a previous reaction. The sense of impending doom and breathlessness leading to hyperventilation are symptoms that can resemble anaphylaxis. Sometimes, there may be flushing, or blotchy skin associated with anxiety adding to the diagnostic difficulty. 

Diagnostic difficulty may also occur with vasovagal attacks after immunisation or other procedures, but the absence of rash, breathing difficulties, and swelling are useful distinguishing features, as is the slow heart rate in a vasovagal attack (whereas anaphylaxis is usually associated with a tachycardia). Symptoms should resolve rapidly on lying flat. If rapid recovery does not happen, consider anaphylaxis as a cause.

下圖. 如何鑑別迷走神經反射造成暈厥或全身性嚴重過敏反應

























頑固性全身性嚴重過敏反應
多數全身性嚴重過敏反應打一次腎上腺素就會改善. 10% 需打第二劑才有反應. 2.2% 需要施打超過兩次才有反應
4.8 Refractory anaphylaxis 
Most of the anaphylaxis reactions occurring in a community setting will respond to initial treatment with IM adrenaline, although currently around 10% receive a second dose and 2.2% (95% confidence interval, 1.1- 4.1%) receive more than two doses. 6
All healthcare professionals should be able to identify patients with Breathing and/or Circulation problems of anaphylaxis which do not respond to initial treatment with IM adrenaline, and to escalate care quickly by calling for support from the resuscitation team or from the ambulance service for urgent transfer to hospital.







CXR heart failure with bilateral pleural effusion

the same patient  2016-2026