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292 HOLISTIC MANAGEMENT OF PAIN
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The importance of this model relates to the interconnectedness of the component parts that produce the neurosignature. Practitioners need to interpret this alongside patients, because it is individual and helps to account for why people have dierent pain experiences. It is also of value because it can be used to decipher and explain persistent pain, which can be a major component of living with a leg ulcer. As this model has developed it can be described as not just biopsychosocial but also as having an existential component: the meaning that is given to the pain experience (Dezutter etal.2015).
Today’s scientic research is taking a step further to determine pain. Lyman (2021) writes that ‘pain is not detected by the brain, it is created by it’ and that it is ‘a conscious translation of our unconscious brain’s decision that the body is in danger’ (Lyman 2021). In understanding what this means for our leg ulcer patients it is helpful to look at what some of these inuences are in more detail. As Lyman (2021) also writes, ‘Pain is a decision made by the brain– the vast majority of which is outside our conscious control – to tell our conscious mind that we are in danger.’
CAUSES OFPAIN
The World Union of Wound Healing Societies (2004) provides useful descriptions that help establish the broad term of wound- related pain to be broken down into a number of causes that should assist a clinician in their joint exploration of pain with the patient. These are described as follows:
Background pain from the underlying aetiology of the leg ulcer-
ation and the wound itself, such as local inammation or oedema.
Pain incidents such as daily activity and walking.Procedural or operative pain from the wound treatment itself or
the dressing change.
Patients are unlikely to be experiencing just one kind of pain and so it is important that dierent types are distinguished.
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TYPES OFPAIN
Nociceptive pain is caused by the stimulation of peripheral nerve bres, which sense and respond to aected or damaged areas of the body. The sodium channels within the nerves can act as a volume to the pain intensity (Lyman2021). Nociceptive pain may be dened as ‘an appropriate physiological response to a painful stimulus. It may involve acute or chronic inammation’ (WUWHS2004). Typically this is short- lived (acute) when due to infrequent trauma or procedure, or it can be cyclic in nature if it becomes a regular occurrence (Acton 2007). The sensations experienced are typically localised, with constant aching and throbbing (Table 6.2). Where the innervation becomes persistent there is an overstimulation of nociceptors; the prolonged inammatory response may cause heightened sensitivity in both the wound (primary hyperalgesia) and the surrounding skin (secondary hyperalgesia) (WUWHS2004).
Neuropathic pain develops due to damage to the somatosensory system (NICE2022), thereby occurring when there has been either peripheral or central nervous system dysfunction or damage. The eect is to elicit altered sensations, which are often unpleasant. Descriptors of neuropathic pain include burning, tingling, pins and needles and electrical shocks located in and through the aected area. Related sensitivity to often non- painful stimuli such as light touch, pressure or changes in temperature can provoke intense pain, which can become persistent. This enhanced sensitivity is known as hyperalgesia or allodynia and is dependent on which nerve bres are aected (Wulf and Baron2002; WUWHS2004; Sandkühler2009). Neuropathic pain can be dicult to treat, so requires recognition and management that includes specic pharmacological preparations.
Nociceptive and neuropathic pain may manifest in distinct ways with patients using dierent words or descriptors to describe their experience (Box6.1). Finding words that resonate with the individual will aid in the communication and evaluation of any strategy.
However, on occasions nociceptive and neuropathic pain may also be dicult to distinguish from one another as symptoms overlap and become similar (Jenkins 2020b). This, alongside their joint presentation in the same person, makes for a complex pain prole. When nociceptive pain is inadequately managed, persistent pain may develop with both nociceptive and neuropathic properties
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Box 6.1 Pain Descriptors That May Help
Communicate theLived Experience
Nociceptive Neuropathic
Throbbing Sharp Dull Sore Aching
Source: Adapted from NICE (2022) and EWMA (2002).
(Taverner et al. 2014), although non- healing wounds seem to be associated with neuropathic pain. Hypersensitivity is poorly understood by clinicians and leads to a ‘lack of belief in the extent of the patient’s pain’ (Hopkins and Worboys2005). Understanding the patient’s lived experience of pain, inuenced by variables such as wound care procedures, is critical if we are to determine an eective treatment plan. This inuences the clinician’s approach to compression therapy and the management plan being suggested (see Chapter8).
Pain has been described as acute and short­persistent if of over seven weeks’ duration (EWMA2002). However, there has been more recent debate as to the use of the term ‘chronic’ and how to dene where acute pain ends and long- term pain begins. It has been suggested that another name for chronic pain is persistent pain, with certain characteristics being presented that can be helpful for the practitioner in understanding their patient’s journey. The debate continues (Nicholas etal.2019). Denitions of persistent pain are debated (Upton and Upton 2015; Nicholas etal. 2019), but the characteristics relate to the following:
Shooting Burning Stabbing Tingling Numb Prickling Itchy
lived or chronic and
Pain persisting over seven weeks (Wulf and Baron2002) and over
longer periods. This will be the experience of many leg ulcer patients.
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The specied duration of ‘long period’ is classied as being over
three months (Treede etal.2015). A high percentage of leg ulcer patients do not have their wounds healed in under 12 that the potential for long- term pain complexities is great.
Pain that exists beyond the period of expected healing (Treede
et al. 2015). For venous leg ulcer management this will be 12 weeks, but it is harder to determine for other aetiologies.
Pain that may continue post healing. This is an important
reminder for clinicians as patients may be left with residual sen­sations or even pain after healing; healing the wound is only one of the desirable outcomes for managing patients with lower limb wounds and conditions.
‘Pain that stopped being a symptom and has become the disease’
(Lyman2021; Wulf and Baron2002).
weeks, so
PAIN CYCLES: NEVER- ENDING PAIN
Pain can be disruptive, life altering and self- perpetuating. Cycles of pain relate to the never- ending narrative of living with pain. Energy, sleep, mood and activity are all interrelated and if a patient is struggling in one area it will have an impact on the others. Upton and Andrews (2013) found a signicant correlation between wound pain and sleep disruption. If a patient is anxious, fearful or depressed, this will aect their sleep. Lack of sleep and the necessity of having to cope with pain decrease energy and make it dicult to be active. Pain together with lack of exercise and movement increases pain, particularly where ankle range of motion is aected (Davies etal.2007). This in turn aects mood (Upton2014).
Pain cycles are self- perpetuating and in wound care include those that relate to wound care procedures and specically dressing changes. Upton and Upton (2015) talk about pain at dressing change, which can easily become a perpetual cycle of pain leading to more dressing. The cycle goes like this. There is pain at dressing change, which leads to stress and related anticipatory pain when dressing time approaches. The patient may then adopt avoidance behaviour, which can cause delayed wound healing, exacerbating pain and initiating the need for more dressings, which are now perceived as being painful. As patients become more anxious or stressed in
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anticipation of pain, they will also rate their pain higher (Colloca and Beneddetti2007). Within this cycle it is easy to see how a patient may be labelled non­in. Perhaps less obvious is the role that nurses can play to alleviate or even negate the discomfort experienced.
concordant as they seek to alleviate the cycle they are
IMPACT OFPAIN ONPEOPLE’S LIVES
The experience of pain is individual, but numerous studies have highlighted commonly encountered factors that can potentiate pain. It is important to understand and identify what is likely to increase pain so that there can be mediation and appropriate care can be given and planned for. Table6.2 identies some of these considerations.
Stress, anxiety and fear are closely linked and well documented as being inuencers and predictors of increased pain that delays healing. The impact on sleep is a common feature of quality- of- life studies (Green etal.2017; Hellström etal.2016; Taverner etal.2014; Upton and Andrews2013). Green etal. (2017) found that ‘the lack of sleep seemed to accentuate the debilitating nature of the condition and made day- to- day functioning more challenging’.
CAUSES OFPAIN
The literature is inconclusive about whether the severity of the pain is predicted by the wound aetiology. Experience can tell us it can be, but clinicians need to be mindful not to be aected by the experiences of others. It remains critical that clinicians come to the assessment with an open mind and ready to listen to the patient’s experience. The myth that pervaded for many years was that arterial ulcers are more painful than venous and so clinicians were already making a value judgement on how much pain a patient was likely to be in. It is now recognised that this is erroneous.
Briggs et al. (2007) found that severity of the pain cannot be predicted by the wound type, size or duration of the leg ulcer. Hellström etal. (2016), in their study of elderly patients, found that pain intensity varied with wound type, those with multiple ulceration of dierent diagnoses scoring the highest (Table6.3). Of note is that
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TABLE6.3 
Leg ulcer type Findings Implications
Venous leg
ulceration
Arterial leg
ulceration
Mixed venous/
arterial leg ulceration
Source: Adapted from Hellström etal. (2016).
Leg ulcer types.
50% no pain 31% scored 5–10
27% no pain 54% scored 5–10
39% no pain 47% scored 5–10
A signicant proportion experienced
severe pain. When 50% can experience no or resolved pain, the patient in pain can be ignored or disbelieved.
There remain some patients who
experience nil or resolved pain. However, a signicant number experience severe pain.
It is of note that despite arterial
disease, a signicant number of patients experience nil or resolved pain. However, nearly 50% experience severe pain.
over 70% of patients with bilateral ulceration were identied as having signicant pain. ‘Higher pain intensity was associated with increasing odds of having sleep disturbances’ and increased rapidly, with a score of over 4 on a numerical rating scale. Hellström etal. (2016) also found a number of patients who reported no pain and still had signicant sleep disturbances, thus this remains a critical question in assessment. While a number of patients said they had no pain associated with their ulceration, it remains signicant that a high proportion had scores of 5–10in severity; this may be related to a wound, infection, erosions or unmanaged swelling. This group needs to feel heard and have their experiences explored if pain is to be successfully managed.
Certain conditions may predispose to articulations of particularly painful experiences. This includes inammatory processes manifesting as part of the underlying pathology. Thus, sickle cell disease, vasculitis including pyoderma gangrenosum, and atrophie blanche may all experientially be found as extremely painful. See Chapter 3 on unusual aetiologies and Chapter 8 on compression therapy and its role in reducing inammation.
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PAIN MANAGEMENT SOLUTIONS: ASSESSMENT
Managing pain can be a signicant challenge for those with leg ulceration and the clinicians caring for that person. Management is rooted in intelligent assessments to understand the patient’s story in relation to their current circumstances and presenting symptoms. WUWHS (2004) suggests a layered approach in assessing pain at wound­related procedures consisting of initial, ongoing and review assessments.
This guidance is a helpful way of approaching the whole impact of pain in a more fundamental way. Wound care procedures are just one aspect of living with a leg ulcer and if pain management is to be meaningful, the assessment needs to encompass all stages of the experience for that patient. WUWHS (2004) talks about assessments needing to be carried out by experienced practitioners with good listening skills. Factors such as feelings, perceptions and beliefs, along with the meaning and impact of pain for that person and the surrounding family, require exploration. The need for establishing a conversation with the patient is paramount to acknowledging the patient’s experience (Jenkins2020b; Ballantyne and Sullivan2015). Patients need to be able to tell their story, some of which will be about presenting issues, and to feel that they are being listened to in a non­judgmental but informed way. See Box6.2.
Box 6.2 Asking Questions toUnderstand
Remember: Assess and document regularly! Be prepared to listen. Do not form preconceived ideas.
The pain history Pain trends Where is the pain? What is it like? What makes it worse? What makes it better?
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Patients’ Pain
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Comprehension and the ability to communicate thoughts and beliefs underpin the use of any assessment tool. Where there are language barriers it is important that translation solutions are sought. In situations where cognitive dierences exist or other forms of communication are required, an acknowledgement of this need alongside appropriate and alternative ways of communicating will be required. Equally practitioners need to be aware that patients may be reticent in disclosing information. Green etal. (2017) found that patients did not always disclose their issues with clinicians during consultation, even when these had been identied as important; this underlines the need for clinicians to create a safe space where the disclosure of sensitive or personal information can be heard and holistic care can be provided.
There are numerous assessment tools available to the practitioner (Feldt 2000; Hockenberry et al. 2005; Woo et al. 2008), although Leren etal. (2020) found that they were used inconsistently. Some of these tools are more age specic or helpful where cognitive ability needs to be addressed. Others are very comprehensive, but can be lengthy and time consuming to complete in the clinical eld. Organisations may also have their own guidance about which tools should be used for a cohort of patients. What is important is that the practitioner becomes cognisant with the tool they are using and that there is consistency with other clinicians to monitor and evaluate progress, including any interventions within ongoing care. Where tools are used it is helpful to have them embedded within a narrative that explores the wider context of the lived experience.
Validated quality-
of- life assessment frameworks such as the Quality- of- Life Scale or the Sickness Impact Prole provide much more detailed information. They may be less easy to use in clinical settings where transient sta are not familiar with the tool, or where time has not been allowed for a more detailed exploration of the patient narrative. Green etal. (2017) have developed an assessment template that goes beyond physical considerations to consider quality- of- life factors and concerns.
Validated assessment scales are of value at all stages of leg ulcer management, whether as part of an initial assessment or for ongoing monitoring (Table6.4), and are recommended for review at dressing changes. They are not mutually exclusive and when used with other quality- of- life frameworks can be the source of rich information to inform and evaluate care in an intelligent and comprehensive way.
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TABLE6.4 
Type of assessment tool Description Comments
Visual scales Visual analogue
Numerical Numerical rating
Verbal Visual rating scale (VRS).
Assessment scales.
scale (VAS).
This includes the
Wong-
Baker Faces scale, which presents as a range of faces from happy with ‘no hurt’ through to upset with ‘hurts worse’.
Numerical values are
attached to the faces with the higher scores indicating the worse pain.
scale (NRS).
A numerical value is
placed against the pain rating (0–10 or 0–100), so no pain may be rated as 0 and the worst possible pain as 10.
Uses a scale of descriptor
words, such as ‘none’, ‘mild’, ‘moderate’ or ‘severe’.
Can be useful for children,
but less so for those with cognitive impairment such as those with dementia.
Simple, replicable and
communicable.
Some people nd it
dicult to engage with numbers and nd words or pictures easier.
Some nd the variation in
pain during the day dicult to score, especially if it is episodic neuropathic pain.
Simple, replicable and
communicable.
Can be used on a
standalone basis or with other scales.
Simple, replicable and
communicable.
Source: Adapted from WUWHS (2004).
Pain diaries written by the patient are of value to explore the pattern and nature of ‘why I have pain’ (EWMA2002; Mudge and Orsted2010; Upton2014). These may be helpful where patients are interested in and able to write a narrative, albeit they do not suit everyone.
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Where patients have multiple causes and experiences of pain, these scales oer limited information. Leg ulcer patients may present with any number of variables that are contributing to their pain status, but without a narrative or surrounding detail they can oer only a snapshot of a trend towards either having pain or being without pain. Recognising this and ensuring the patient’s experience is heard and solutions oered are vital. Enabling the patient to describe their pain, ‘giving them descriptive words to choose’ (Acton2007), can help in conversation and understanding.
The clinical team needs to provide a consistent approach to the exploration so that the outcome of the clinical or pharmacological interventions can be observed. Box6.3 gives some guidance on what areas can be explored with the patient. The practitioner also needs to be aware of what will be the preferred or best way of gaining insight and this will depend on the choice of tool for that patient as well as how the conversation is framed.
Those who have learning disabilities or are cognitively impaired, such as those with a form of dementia, will need to have their pain described or interpreted in dierent ways. The Wong­scale may not be helpful for those with cognitive impairment (Upton and Upton2015). Alternative tools may enable a clinician to explore pain through the person’s own descriptors or the use of non- verbal cues (Box 6.4). These scenarios can be better explored with carers who know the patient well and can provide new evidence or comparators. Body language is always an important indicator of
Baker Faces
Box 6.3 Understanding thePain Experience
When and for how long. Type of pain descriptors: nociceptive or neuropathic or a mix. Severity using a visual or numeric tool. Impact and consequences on sleep and daily life. Factors that exacerbate or reduce the pain, coping strategies. Relief rating with analgesia or other interventions. Adverse eects of current or future treatment.
Source: Adapted from Acton (2007).
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