Categoria: Congresso 2023

  • La fatica può influenzare l’insorgenza di dolore tardivo nella sindrome post COVID-19. Uno studio osservazionale

    Fatigue can influence the development of late-onset pain in post COVID-19 syndrome. An observational study.

    Introduction

    Coronavirus disease (COVID-19) is an infection caused by the SARS-CoV-2 virus resulting in various pathology phenotypes characterized by different symptom severities. Pain is one of the most described persistent symptoms following SARS-CoV-2 infection (Bakılan et al., 2021; Fernandez-de-Las-Penas et al., 2022; Soares et al., 2021). Causes of pain persistence after COVID-19 infection are poorly established, and different pathogenetic mechanisms have been proposed. Identifying the main features of post-COVID-19 pain is necessary to provide tailored rehabilitative interventions (Fernández-de-las-Peñas et al., 2022). For these reasons, the primary aim of this paper is to identify possible demographic-pathological features and/or clinical signs related to late-onset pain in people one year after COVID-19 infection.

    Methods

    This observational study was approved by the local Ethical Committee and registered on Clinicaltrials.gov. We enrolled patients with a diagnosis of COVID-19 with rehabilitation needs during the acute phase, and with an increase in pain intensity at 52 weeks from the infection’s onset compared to the pre-COVID-19 condition. All the subjects were monitored through periodic screening of post-COVID syndrome using C19-YRS at 12, 26, and 52 weeks. The subjects were evaluated with the Numeric Pain Rating Scale (NPRS), the Leeds Assessment of Neuropathic Symptoms and Signs (LANSS), the Central Sensitization Inventory (CSI), the Pain Catastrophizing Scale (PCS), the Tampa Scale of Kinesiophobia (TSK). The evaluation of the pressure pain threshold (PPT) and temporal summation (TS) was performed in COVID-19 patients and age- and sex-matched controls.

    Results

    Sixty-seven patients completed the evaluation for post-COVID-19 symptoms at 52 weeks. Twenty subjects presented increased in pain intensity >= 2 points at the 52-week C19-YRS pain assessment (Fig. 1). Subjects with and without pain were similar in demographic and clinical characteristics. Comparison of C19-YRS domains at the threetime points (12, 26, 52 weeks) revealed significantly worse outcomes in fatigue, anxiety, mobility, ability to perform usual daily activities and generally health perception. Reduction in all these domains was retained at the 52-week evaluation (Fig. 2). Multiple linear regression revealed that fatigue at 26 weeks significantly predicted pain onset (b = 0.51, p = 0.006). A mean intensity of pain of 6.0 ± 1.9 was recorded; most of the sample did not show possible neuropathic or nociplastic mechanisms (Fig. 4). No differences were found in PPT and TS between subjects with pain and healthy subjects.

    Discussion and Conclusion

    Our study found that almost one out of three patients hospitalized for COVID-19 developed pain 52 weeks after symptom resolution. Pain intensity seems to fluctuate during the first year following COVID-19 infection. Probably the development of pain long after COVID-19 resolution may be due to new mechanisms developed months after infection, not imputable to nociceptive pathway stimulation or central sensitization (Fernandez-de-Las-Penas et al., 2022). Pain perception seems to be influenced by fatigue. This causal relationship may open the doors to new treatment approaches in pain management, targeting fatigue for late-onset pain treatment. Distinguishing between mechanisms of pain is challenging, and an overlapping is frequent. A comprehensive approach following a biopsychosocial model must consider all possible factors related to pain development, acting on the components of a vicious circle where fatigue and mood disorders play a crucial role in pain development and maintenance.

    REFERENCES

    – Bakılan F, Gökmen İG, Ortanca B, et al. Musculoskeletal symptoms and related factors in postacute COVID-19 patients. Int J Clin Pract. 2021;75(11):e14734. doi:10.1111/ijcp.14734

    – Fernández-de-Las-Peñas C, Cancela-Cilleruelo I, Moro-López-Menchero P, et al. Exploring the trajectory curve of long-term musculoskeletal post-COVID pain symptoms in hospitalized COVID-19 survivors: a multicenter study. Pain. 2023;164(2):413-420. doi:10.1097/j.pain.0000000000002718

    – Fernández-de-Las-Peñas C, Nijs J, Neblett R, et al. Phenotyping Post-COVID Pain as a Nociceptive, Neuropathic, or Nociplastic Pain Condition. Biomedicines. 2022;10(10):2562. Published 2022 Oct 13. doi:10.3390/biomedicines10102562

    – Soares FHC, Kubota GT, Fernandes AM, et al. Prevalence and characteristics of new-onset pain in COVID-19 survivours, a controlled study. Eur J Pain. 2021;25(6):1342-1354. doi:10.1002/ejp.1755

  • La gestione fisioterapica del paziente con dolore nociplastico: consenso tra esperti italiani tramite metodo Delphi

    Physiotherapy management of nociplastic pain: A Delphi study of Italian specialists.

    Introduction

    Pain is a significant health problem for people with musculoskeletal disorders, particularly when it lasts over 3 months1. In many cases, the transition from acute to chronic pain seems to be related to neuroplastic changes occurring in the Central Nervous System (CNS), a process called Central Sensitization (CS)2. Although CS is not the only cause, mechanisms of sensitizations of the CNS play an essential role in nociplastic pain3. Early identification of people with suspected CS mechanisms is necessary due to higher severity of pain, reduced quality of life and poor prognosis4. Despite this, no clinical practice guidelines are available to manage people with suspected CS in rehabilitative settings5. For this reason, this Delphi study aims to reach a consensus on the physiotherapy management of people with pain and suspected CS mechanisms in the Italian scenario.

    Methods

    A web-based Delphi process was employed. Experts in the rehabilitation field were recruited following pre-defined eligibility criteria. Consensus criteria were defined for each round to establish the agreement between participants. Panellists evaluated the usefulness of physical therapist competences in managing people with signs of CS through closed-ended questions. For every competence included, panellists have to explain how they act in their clinical practice every time they approach people where a CS mechanism is suspected. Following completion of three Delphi rounds the final list of competencies was generated.

    Results

    23 participants were recruited for the web-based Delphi process. They all completed Round 1 (23/23, 100%), twenty Round 2 and Round 3 (20/23, 87%). Following Round 1, seven areas were identified by the panel as crucial for CS physiotherapy management; 19 competencies out of 40 reached the consensus between experts, and nine additional competencies were added to Round 2 following literary review. Round 2 identified the agreement for all the 29 competencies. During Round 3, all the experts confirmed the final list generated through the consensus process.

    Discussion and Conclusion

    An agreement between experts was found for the final list of competencies that a physiotherapist should implement every time it approaches people with suspected CS mechanisms. A detailed list of steps was defined to better characterize the physiotherapy process applicable in clinical practice. These steps derived from existing procedures described in the literature and were integrated with additional behaviors identified by the participants in this web-based Delphi process. Our results can open the door to a new way to decline the physiotherapy approach to specific health conditions where theory and practice struggle to find a meeting point. Further research is needed to support the clinical utility of the final list of physiotherapy behaviors and its applicability in daily practice.

    REFERENCES

    1. Treede RD, Rief W, Barke A, et al. Chronic pain as a symptom or a disease: the IASP Classification of Chronic Pain for the International Classification of Diseases (ICD-11). Pain. 2019;160(1):19-27.
    2. Camfferman D, Moseley GL, Gertz K, Pettet MW, Jensen MP. Waking EEG Cortical Markers of Chronic Pain and Sleepiness. Pain Med. 2017;18(10):1921-1931.
    3. Shraim MA, Massé-Alarie H, Hall LM, Hodges PW. Systematic Review and Synthesis of Mechanism-based Classification Systems for Pain Experienced in the Musculoskeletal System. The Clinical Journal of Pain. 2020;36(10):793-812.
    4. Breivik H, Collett B, Ventafridda V, Cohen R, Gallacher D. Survey of chronic pain in Europe: prevalence, impact on daily life, and treatment. Eur J Pain. 2006;10(4):287-333.
    5. Nijs J, Goubert D, Ickmans K. Recognition and Treatment of Central Sensitization in Chronic Pain Patients: Not Limited to Specialized Care. J Orthop Sports Phys Ther. 2016;46(12):1024-1028.
  • Mappatura dei PROMs utilizzati per identificare i bisogni insoddisfatti dei sopravvissuti al cancro in base alla classificazione internazionale del funzionamento, della disabilità e della salute (ICF)

    Mapping Patient-Reported Outcome Measures Used to Identify the Unmet Needs of Cancer Survivors onto the International Classification of Functioning, Disability and Health (ICF)

    Introduction

    As the number of cancer survivors (CSs) is increasing worldwide, providing services relevant to their specific, unmet needs is essential. There are currently various patient-reported outcome measures (PROMs) whose aim is to identify the unmet needs of CSs. Still, limited guidance supports healthcare providers in choosing the most appropriate PROMs for this purpose.

    An International Classification of Functioning, Disability, and Health (ICF)–based analysis of existing PROMs may facilitate reliable identification of the areas of impact on health encompassed by them, providing a basis for the selection of a specific PROM based on content comparison.

    The objective of this study was to assess the content and evaluation constructs of the PROMs used to identify the unmet needs of adult CSs suffering from non-cutaneous cancers with a 5-year survival of ≥ 65% and an incidence of ≥ 5%.

    Methods

    A mapping exercise was performed to evaluate the degree to which the PROMs used to identify the unmet needs of adult CSs covered the spectrum of health-related states, outcomes and determinants described by the WHO ICF.

    The materials for the analysis were 14 PROMs whose aim is to identify the unmet needs of our population of interest.

    Each item of all the PROMs was extracted and linked, word by word, to the ICF by two independent reviewers using the Cieza et al. updated procedure of linking rules. Where disagreements occurred, these were resolved through discussion and consultation with a third reviewer. The ICF was used to determine to which chapter of its hierarchical structure each item of the analysed PROMs could be categorized to represent body structures, body functions, activity and participation, or environmental factors.

    The ICF-linked PROMs were then further screened to obtain an overall framework on how comprehensively they covered ICF categories.

    Results

    The study is ongoing. Mapping has been completed, and the data analysis is under way.

    We expect to have the principal results ready to be presented at the AIFI International Scientific Congress “Tailored Physiotherapy. Una strategia per il futuro” in November 2023.

    Preliminary results show that, despite a wide range of variability, each of the 14 PROMs covered the ICF components of body functions, activity and participation, and environmental factors in different proportions, thus revealing their own specificity in capturing different nuances of apparently similar problems.

    Discussion and Conclusion

    The ICF, created by the World Health Organization, provides an internationally recognized framework, definitions and coding language to describe the impact of health conditions on body functioning, activities limitation and restrictions in participation.

    The linking rules enhance the comparability of PROMs by providing a comprehensive overview of the content of the same, the context in which the measurements take place, the perspectives adopted and the types of response options.

    Linking the PROM domains to ICF components enables the adoption of a universal language. This facilitates reliable identification of the areas of impact on health encompassed by these PROMs, revealing their own specificity in capturing different nuances of apparently similar problems and providing a basis for the selection of the most suitable based on content comparison in clinical practice and research.

    REFERENCES

    World Health Organization. Towards a common language for functioning, disability, and health: ICF. The international classification of functioning, disability and health. 2002.

    Cieza A, Geyh S, Chatterji S, Kostanjsek N, Ustün B, Stucki G. ICF linking rules: an update based on lessons learned. J Rehabil Med. 2005;37:212-8.

    Cieza A, Fayed N, Bickenbach J, Prodinger B. Refinements of the ICF Linking Rules to strengthen their potential for establishing comparability of health information. Disabil Rehabil. 2019;41:574-83.

    Cieza A, Brockow T, Ewert T, Amman E, Kollerits B, Chatterji S, et al. Linking health-status measurements to the international classification of functioning, disability and health. J Rehabil Med. 2002;34:205-10.

    World Health O. International classification of functioning, disability and health : ICF. Geneva: World Health Organization; 2001.

  • EQUILIBRIO TRA LE MISURE, MA SUL BILANCINO C’E’ LA SCALA TINETTI

    BALANCE BETWEEN MEASURES, BUT ON THE SLIDEBAR THERE IS TINETTI SCALE

    Introduction

    Balance is a term frequently used by health professionals working in a wide variety of clinical specialties. Nowadays there is not an universally definition of human balance. From a physic point of view, balance is the state of an object, when the resultant load actions (forces or moments) acting upon it are zero. If the line of gravity of an object falls within the base of support, then the object is balanced. This principle can be applicable to the balance of humans, in fact the human body is balanced when muscle forces counteract the force of gravity, and the line of gravity falls inside the base of support. Measuring static and dynamic balance means giving autonomy to the patient and it represents a good way to prevent falls.

    Methods

    To measure balance, we proposed the following scales to 45 patients, admitted to the department of physical medicine and rehabilitation at the Polyclinic of Messina:

    • Berg Balance Scale
    • Time Up And Go Test (TUG)
    • The 30-Second Chair Stand Test
    • Tinetti Scale, it is used to measure balance ability, including fall risk and ambulation. It is composed by 16 items, divided into two different sections (balance and walking), that assess balance and walking performance through the observation of motor skills of great relevance in daily life. Each item is given a score ranging from 0 to 2, (0= inability, 1= ability with aid or adaptation, 2= full ability). The balance functions consists of 9 tests that examine static balance skills in different positions and the execution of position changes. The second section, on the other hand, assesses walking functions through gait characteristics such as symmetry, length, and stride continuity. The maximum score is 28

    Results

    Through the administration of these scales, we saw a significant improvement in patients’ balance and in the perception of their body

    Discussion and Conclusion

    Thanks to these scales, we noticed that balance needs to be assessed, measured, and warned. From the data collected, it emerged that, thanks to physiotherapy, patients are able to improve their balance, preventing falls and injuries. For the physiotherapist Tinetti scale is more appropriate because its items give value to the observational aspects of movement.

    REFERENCES

    Pollock AS, Durward BR, Rowe PJ, Paul JP. What is balance? Clin Rehabil. 2000 Aug;14(4):402-6. doi: 10.1191/0269215500cr342oa. PMID: 10945424.

  • Proposta di due indicatori percentuali per misurare la libertà di movimento articolare e segmentale utili ai fini gestionali

    Proposal of two percentage indices to measure overall joint mobility and segmental mobility useful for managerial purposes

    Introduction

    Outcome measures used in physiotherapy are typically intended and validated for a particular disease, joint or setting [ 1 ]. For clinical purposes, this is the correct approach. However, functional recovery cannot be compared between different anatomical districts or among different diseases. Such a comparison would be extremely useful at the management level to monitor the overall effectiveness of the physiotherapy interventions.

    To address this issue, we developed and tested two indices of joint mobility and segmental mobility that can be used for all joints and with a 0-100 scoring system. Joint mobility depends on the anatomical structural constraints of the joint. Segmental mobility is also affected by other non-anatomical variables, such as pain and muscle strength.

    Methods

    The joint mobility index (JMI) was computed for each joint as follows: 1) the ROM measurement methodology was standardized according to available literature [ 2 ]; 2) joint maximum excursion in each direction was measured and expressed as a percentage of its normative reference value [ 2 ], leading to a 0-100 grading; and 3) the mean value among all possible joint movements (e.g., flexion, extension, abduction, etc.) was computed. JMI was computed for the following joints: shoulder, elbow, wrist, hip, knee, and ankle (non-axial joints).

    With the same approach, the segmental mobility index (SMI) was also computed. This is a multi-dimensional index that takes into account JMI (as computed above), pain at rest, pain during movement, and strength. Pain was assessed using the verbal numeric rating scale [ 3 ]. Muscle strength was measured with the appropriate Manual Muscle Test. Variables were expressed as a percentage of the corresponding normative value and averaged to produce SMI.

    Results

    A form for JMI computation has been created and added to the electronic medical record of our institution. (Figure 1a). It allows for JMI computation for both the affected and contralateral side (when needed), during active and passive movements, and in subsequent assessment (e.g., admission, hospital stay, discharge). An example of its use is presented for the shoulder joint in Figure 1b, where the increase in SMI (last column) can be seen. An example of the use of SMI is presented in Figure 1c. The increase in both numerical values and plot area is clearly visible.

    Discussion and Conclusion

    We developed two indices that can be used to follow the recovery in joint mobility and segmental mobility in patients with different diseases and in different settings. Their feasibility and usefulness are currently under test at our institution.

    ROM measurements and clinical scales remain key in clinical practice and at the single-patient level. The two proposed indices, one unidimensional and one multidimensional, could be useful at the organizational and managerial level thus providing a broad overview of patients’ recovery following physiotherapy interventions in a ward, a unit, or a hospital.

    Further improvements can be added to the current indices, such as the use of age- and gender-matched normative values and the inclusion of other disorders that could hinder segmental mobility (e.g., lymphedema, scar tissue complications, etc.).

    REFERENCES

    1. Haigh R, Tennant A, Biering-Sørensen F, Grimby G, Marincek C, Phillips S, Ring H, Tesio L, Thonnard JL. The use of outcome measures in physical medicine and rehabilitation within Europe. J Rehabil Med. Novembre 2001; 33(6):273-8.
    2. Clarkson HM, Gilewich GB. Valutazione cinesiologica. Esame della mobilità articolare e della forza muscolare. 2° Ed. Milano: Edi.Ermes; 2002. 432 p.
  • MANEGGIO DELLE MISURE

    RIDING SCHOOL AND SEWING: MEASURES AND HORSES

    Introduction

    Autism is a neurodevelopmental disorder that primarily involves language, communication and social interaction. It is characterised  by restricted and stereotyped interests and repetitive behaviors. Due to the range of symptoms present in each patient, autism is now called Autism Spectrum Disorder (or ASD). In fact, the disorder covers a broad spectrum of symptoms, ability levels and disabilities, which may or may not affect the activities of daily living (ADL) and the independence.  Hippotherapy is a therapy that uses the natural gait and movement of a horse to provide motor and sensory input. It aims to improve neurological functions and sensory processes and it is used for patients with physical and mental disorders, including ASD children. The aim is to study, deepen and synthesise research evidence with respect to the role of Hippotherapy as an additional and supportive activity within the rehabilitation project of children with ASD.

    Methods

    To evaluate the reaching of this objective, we proposed the following scales to 7 children with ASD:

    – Time Up and Go Test (TUG), it consists of measuring the time a patient gets up from a chair, he walks 3 meters, he turns around and he walks back to the chair sitting down again. If the patient normally walks with an aid it should be used during the test. A time greater than or equal to 12 seconds indicates that the patient has a compromise balance and he is at risk of future falls.

    – Five Times Sit to Stand Test, it is used to asses functional lower extremity strength, transitional movements and balance. Its score is is based on the amount of time a patient is able to transfer from a seated to a standing position and back to sitting five times. The patient sits on the chair by resting his back and he folds his arms across the chest. The lower is the time to complete the test the better is the outcome.

    The hippotherapy activity has been proposed every week for twice.

    Results

    After 10 sessions of hippotherapy, there was an improvement in both balance and walking.

    Discussion and Conclusion

    : These scales are useful to evaluate balance and motor coordination. We noticed that throught these two scales we added many observations linked to the execution of the task. This dimension corresponds to behavioural difficulties of these children and we think that these observations should be traslated in measurable values

    REFERENCES

    The work is unfunded

  • ESERCIZIO TERAPEUTICO CONOSCITIVO IN PAZIENTE CON LESIONE CRONICA DEL SECONDO RAGGIO DELLA MANO SINSITRA

    COGNITIVE THERAPEUTIC EXERCSES PROPOSAL IN A FINGER INJURY

    Introduction

    Alba is a 50 year-old woman with a chronic bone lesion of the second phalanx of the left hand. After the surgical reconstruction and after a period of 6 weeks with the brace, she begins a rehabilitation program based on the Cognitive Therapeutic Exercise (CTE), in order to recover the mobility of the finger. To the first evaluation the patient presents: semiflexion of the proximal inter-phalangeal (10°-15°) with the impossibility of reaching passively the extension; a minimum flexion of the distal inter-phalangeal (2°-3°) with a possible passive realignment and little movement of active extension.

    Our aim is to describe the importance and the effectiveness of the Cognitive Therapeutic Exercise in a chronic bone lesion management.

    Methods

    The treatment initially involved stretching and soft tissue massage in order to prepare the hand and the finger to CTE exercises.

    These exercises performed by the patient under the supervision of the therapist were:

     

    Slingbar: the patient is seated with her forearm leaning on the table. Her index finger is located on one end of the slingbar, while on the other end the therapist places four different weights (with an increasing weight). The aim of this exercise is to recognize the different weights with closed eyes.

    Crescent: the patient is seated with her forearm leaning on the table. The four fingers (except the thumb) are placed on a crescent-shaped platform, that is balanced on a tip. The therapist places a weight on one of the previously defined positions. The aim of this exercise is to recognize, with closed eyes, in which position the weight is placed, while keeping the platform in balance.

    Results

    With stretching and soft tissue massage, the therapist was able to detach the scar adhesion of the areas injured by the trauma, improving the ROM of the finger and the drainage of the area.

    With the CTE exercises the patient acquired the management, the control and the consciousness of the volar and dorsal  activities of the hand in the space. At the end of the therapeutic program Alba showed an improvement of active and passive ROM of the distal inter-phalangeal (AROM T0: 7°- 10°; T2: 0°-50°. PROM T0:0°-10°;T2: 0°-60°) and an improvement of active and passive ROM of the proximal inter-phalangeal (AROM T0:10°-80°; T2:0°-80°. PROM T0:5°-85°;T2:0°-90°).

    Discussion and Conclusion

    In conclusion, we can say that, even if in literature there are few evidences about CTE method, these exercises were be able to improve the passive and active ROM of the finger and the patient independence in ADL.

    With this work, we want to highlight the cognitive aspect of every exercise performed by the patient. Although the scar treatment and kinesitherapy are suitable to functional recovery, they do not implicate the same cognitive involvement and sensitive stimulation of CTE exercises.

    REFERENCES

    The work is unfunded

  • Quale strumento di misura per la “Fatica Attentiva”?

    What measurement tool for “Attentional Fatigue”?

    Introduction

    Attentional fatigue is experienced as a decreased ability to concentrate, engage in purposeful activity, and maintain social relationships when there are competing demands on attention. According to William James there are two types of attention: involuntary attention, which is effortlessly drawn to nature, things that affect survival, and things that fascinate us; and voluntary attention, which requires effort to direct when there are competing stimuli. Voluntary attention is necessary for concentration, purposeful action, and monitoring one’s behavior in social interactions. Nowadays there is no measuring scale for attentional fatigue that describes its characteristics such as dimensional size, measuring range, principle of operation.

    Methods

    To measure attentional fatigue we created a scale based on the IPDDAI scale (Identificazione Precoce del Disturbo da Deficit di Attenzione e Iperattività). It is an observational questionnaire composed by 10 items (as a reference of the 17 items of the IPDDAI) whose assessment is based on a 4-point Likert scale (0 = not at all/never, 1 = a little/most of the time, 2 = quite a lot/most of the time, 3 = a lot/always). The first 3 items are aimed at the subject’s behavior, item 4 investigates inattention, the next 4 analyze the impulsivity dimension, and the last two are related to self-esteem and relational aspects that could create interference with attention. The physiotherapist proposed this scale to neurologic patients who did not specifically manifest disorders that impaired the ability to pay attention and concentrate.

    Results

    Through the administration of this scale, we saw a significant improvement in patients’ consciousness about their attentional fatigue.

    Discussion and Conclusion

    Although there is no validated scale to measure attentional fatigue, thanks to the scale described before we realized that attentional fatigue is an important dimension that must be monitored. The exercises proposed by the physiotherapist are always calibrated to the person’s attention span. In this exercises, the patient is encouraged to stay focused, in order to develop progressively different components of attentional skill, such as focus, sustained attention, selectivity, divisibility and alternation.

    REFERENCES

    James, W. The Principles of Psychology. Cambridge, MA: Harvard University Press; 1890/1983;

    Marcotto, E., Paltenghi, B., & Cornoldi, C. (2002). La scala IPDDAI: contributo per la costruzione di uno strumento per l’identificazione precoce del disturbo da deficit di attenzione e/o iperattività. Difficoltà di apprendimento, 8 (2), 153-172

  • Artrodesi intersomatica lombare: effetti in acuto degli esercizi di percezione e di attivazione del core sull’equilibrio e sull’allineamento del rachide. Studio pilota.

    Lumbar interbody arthrodesis: acute effects of perception and Core activation exercises on balance and spine alignment. Pilot study.

    Introduction

    Lumbar spondylolisthesis is a pathological condition of the spine characterized by the slipping of one vertebra compared with the underlying one. According to Meyer, severity is classified considering the degree of slip. For low-grades, the first line of treatment is conservative therapy, including: activity modification, bracing, back muscles strengthening exercises, and back brace. If these treatments fail, next treatment option is lumbar interbody fusion surgery (LIF). Following LIF, trunk proprioception, essential for static and dynamic balance, may decrease favoring sensorimotor and movement control alterations. Thus, providing information to the somatosensory system through guided exercises is important. The aim of the study was to evaluate the acute effects of perception and core activation exercises on balance and spine alignment in people undergoing LIF.

    Methods

    From 20th June to 30th September 2022, 20 patients candidates for LIF, were recruited. After signing an informed consent they were randomly assigned to one of the two study groups: Guided Core Activation and Perception Exercises (GE), or Autonomous Self-Correction (GC). Both interventions lasted 10 minutes and were carried out in front of a squared up mirror. Three evaluations were made: before LIF (PRE) and on third day after LIF, before (P1) and after (P2) the intervention assigned to the group. In PRE and P1 participants were asked to assume the most comfortable position. In P2 they were asked to assume the most correct posture possible, using the information learned. Spine alignment (RMS) was evaluated with Spine 3D (Sensormedica, Guidonia, Rome), a non-invasive, three-dimensional optoelectronic detection system that uses Light Detection and Ranging technology, while balance with a stabilometric platform (FreeMed, sensormedica).

    Results

    Data were processed with Jamovi for Mac version 1.6. Quantitative variables are expressed as mean and standard deviation. Normality of data was calculated with Shapiro Wilk’s test. The difference between the variables over time in the two groups was calculated with ANOVA for repeated measures. The significance was set at p<0.05. In P1, compared to PRE, all investigated parameters worsen, non-significantly, in both groups. In P2, compared to P1, all balance parameters worsen significantly in both groups, some more in GE than in GC. Ellipse Area: GE (158.71±120.08; 83.44±102.2), GC (175.11±133.92; 158.54±139.46) p 0.001. Ellipse Eccentricity: GE (0.64±0.33; 0.48±0.29), GC (0.54±0.15; 0.44±0.2) p 0.018. Delta X: GE (11.37±4.23; 9.73±4.88), GC (18.82±10.85; 15.74±9.77) p 0.001. Delta Y: GE (11.18±6.52; 7.46±4.29), GC (16.97±8.52; 13.41±9.36) p 0.001. RMS improves in GE (3.1±1.85; 4.4±2.41) while it worsens in GC (4.9±0.99; 3.8±1.75); both values are not significant.

    Discussion and Conclusion

    Comparing PRE and P1, the worsening of balance parameters is referable to the postoperative sequelae of LIF. It is known that immediately after surgery the perceptual-motor adaptation mechanisms are reduced or absent. In P2 compared to P1, the slight improvement in RMS of GE compared to the worsening of GC is probably due to the exercises performed with the Physiotherapist. Likewise, the greater deterioration of the balance of GE compared to GC is in agreement with the literature. This highlights how, in acute phase, a postural correction greater than the usual one, leads a difficulty of the somato-sensory system to adapt to the new position. Limitations of the study are the small number of the sample and the single session of exercises, justified by the reduced post-LIF hospitalization time. Further studies, with a significant sample size and over time, are needed.

    REFERENCES

    1) Hebert, J. J., Fritz, J. M., Thackeray, A., Koppenhaver, S. L., &amp; Teyhen, D. (2015). Early
    multimodal rehabilitation following lumbar disc surgery: a randomised clinical trial comparing
    the effects of two exercise programmes on clinical outcome and lumbar multifidus muscle
    function. British journal of sports medicine, 49(2), 100–106.
    2) Gilmore, S. J., Hahne, A. J., Davidson, M., &amp; McClelland, J. A. (2020). Physical activity
    patterns of patients immediately after lumbar surgery. Disability and rehabilitation, 42(26),
    3793–3799.
    3) Janssens, L., Brumagne, S., Claeys, K., Pijnenburg, M., Goossens, N., Rummens, S., &amp;
    Depreitere, B. (2016). Proprioceptive use and sit-to-stand-to-sit after lumbar microdiscectomy:
    The effect of surgical approach and early physiotherapy. Clinical biomechanics (Bristol,
    Avon), 32, 40–48.

  • TRATTAMENTO RIABILITATIVO PERSONALIZZATO IN ESITI DI MALATTIA DI HIRSCHSPRUNG: CASE REPORT

    TAILORED REHABILITATION IN A HIRSCHSPRUNG DISEASE: A CASE REPORT

    Introduction

    La malattia di Hirschsprung è caratterizzata dell’assenza del plesso sottomucoso e mioenterico in un tratto del canale alimentare e causa una sintomatologia ostruttiva. Diverse tecniche chirurgiche sono efficaci, tuttavia, a prescindere dalla tecnica, più del 60% dei pazienti lamenta prolungati disturbi, tra cui incontinenza fecale e stipsi, a volte associati a distensione addominale, vomito ed enterocolite. Spesso nell’adolescenza i sintomi non si risolvono fino alla continenza completa con conseguenti effetti negativi sulla vita del paziente e della sua famiglia. L’obiettivo primario di questo case-report è stato valutare l’efficacia di un trattamento riabilitativo personalizzato intensivo sulla sintomatologia e sulla qualità di vita percepita, attraverso scale di valutazione e questionari specifici. L’obiettivo secondario è stato individuare un protocollo di scale e questionari che valutasse in modo completo e ripetibile la disabilità legata alla patologia.

    Methods

    Paziente femmina. Alla nascita ricoverata presso Terapia Intensiva Neonatale per vomito e difficoltà nell’evacuazione e alimentazione.Dopo diagnosi di Hirschsprung è stata sottoposta ad intervento chirurgico. Gennaio 2021 all’età di 7 anni ha eseguito valutazione riabilitativa per persistenza di incontinenza fecale ed urinaria. Alla valutazione del pavimento pelvico tramite palpazione del nucleo fibroso centrale emergeva una scarsa capacità di contrazione selettiva ed utilizzo di compensi addominali e adduttori, sensibilità conservata. Emergevano difficoltà di gestione di encopresi ed enuresi. Impostato un programma personalizzato di 8 settimane con sedute della durata di 1,30 h, una volta a settimana. Il programma prevedeva la compilazione di bowel diary, diario alimentare ed esercizi per miglioramento della presa di coscienza ed endurance del pavimento pelvico,sotto forma di gioco. E’stato impostato un programma di home-training quotidiano

    Results

    E’ stata valutata la QoL attraverso PEDsQL (Pediatric Quality of Life Inventory), la sintomatologia intestinale attraverso le scale Rintala, Wexner incontinenza e Bristol for children, l’incontinenza urinaria con ICIQ-CLUTS (International Consultation on Incontinence Questionnaire-Pediatric Lower Urinary Tract Symptoms). Il CBCL (Child Behaviour CheckList) è stato somministrato ai genitori per l’inquadramento comportamentale; lo stato socio-economico è stato valutato con l’Indice di Hollinshead. La scale e i questionari sono stati somministrati all’inizio (T0), al termine del trattamento (T1) ed al follow-up ad 1 mese (T2). Al termine del trattamento riabilitativo (T1) è stato osservato un miglioramento in tutti i domini indagati che si è mantenuto anche al follow-up (T2), sia per il bambino che per il genitore. Questo ha avuto un effetto positivo sulla QoL, come evidenziato al PEDsQL con correlati miglioramenti del quadro comportamentale evidente al CBCL

    Discussion and Conclusion

    Il trattamento riabilitativo personalizzato, in esiti di chirurgia per M. di Hirschsprung in età pediatrica sembra essere efficace per migliorare la QoL del paziente e della famiglia, in linea con la letteratura. Il protocollo di valutazione proposto prevede questionari e scale già validati in letteratura e di facile reperibilità, è completo poiché indaga tutti i domini interessati dalla patologia, risulta di facile esecuzione e comprensione per il paziente pediatrico e per la sua famiglia, inoltre è facilmente riproducibile.

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