Introduction
People with profound intellectual and multiple disabilities (PIMD) are a heterogeneous group of individuals [
1] characterized by a combination of profound intellectual disability and serious motor deficit, resulting in extreme restriction of autonomy and communication. When the disorder affects an immature brain, the term of polyhandicap is used. Polyhandicap, as a subgroup of PIMD, includes the most severe cases due to the precocity of the brain affection. Recently, the Ithaca European Reference Network for congenital malformations and rare intellectual disabilities has agreed on the term PIMD/Polyhandicap [
2]. While the individuals may present varying disorders and comorbidities, they all depend on human and technical assistance, and they all need permanent health and educational support [
3]. Specific care and services are necessary for people with PIMD/Polyhandicap including physical medicine rehabilitation and other medical specialties, as well as physiotherapy, occupational therapy, psychomotor therapy, and speech therapy. As these individuals are at greater risk of experiencing severe complications (including epilepsy and respiratory infections) [
4], intensive care medical services should be available at all times to prevent deterioration.
The healthcare organization of persons with PIMD/Polyhandicap differs by country, depending both on the specificities of the associated health care system and the related societal views [
5,
6]. In contrast to other European countries with extensive deinstitutionalization processes, the French system relies on institutional settings aiming to offer a graduated response adapted to the individuals health status. The French health system allows these patients to benefit from two main care management modalities: specialized rehabilitation centres and residential facilities [
7,
8]. Specialized rehabilitation centres offer a high level of medical and paramedical physical rehabilitation and a high level of preventive care for inpatients for a theoretically limited duration. Residential facilities offer a high level of psychosocial education and a lower level of medical care. Within these two modalities, there are units dedicated to adult populations (in- or outpatients over 18 years old) and units dedicated to paediatric populations (in- or outpatients units under 18 years old). Some persons (children and adults) are cared for at home care; in this case, the family benefits from help with nursing and medical care.
This offer is supposed to optimize the care management of persons with severe polyhandicap according to their specific needs in terms of age, health severity, and medical and educational care. Few data describing the adequacy of care setting are available. The first related French study [
9], which was performed in 2015, provided important information from a large sample of persons with severe polyhandicap. From the perspective of the population studied therein (child or adult population), this study showed that approximately 10% of the individuals were not care managed in a structure adapted to their age (i.e., persons under than 18 years old who were cared for in a unit dedicated to adults and persons over 18 years old who were cared for in a unit dedicated to children). Almost half of the individuals were not receiving care in an appropriate structure from the perspective of health severity (i.e., some people with the most severe health status were receiving care in residential facilities, and some people with less severe health status were receiving care in specialized rehabilitation centres). If we can assume that being in the adequate structure (age, health severity) better meets the true needs of the persons, health policy decisions to close or open structures could be based on this valuable data.
To improve the global adequacy of care settings, providing better knowledge of the care consumption of these individuals would strongly improve the health policies and resource allocation. To date, there is no robust inventory of the use of medical and paramedical care among individuals, thereby resulting in suboptimal health care.
In this paper, we used a large sample of French persons with severe polyhandicap to examine: 1) the evolution of the adequacy of care setting over a 5-year period (from 2015–16 to 2020–21) and 2) the health (medical and paramedical) care services used by this population. The results were provided for the whole sample and according to the following subgroups: i) residential facilities and specialized rehabilitation centres and ii) children and adults.
Methods
Design and settings
The study used data from the French cohort (EVALuation PoLyHandicap EVAL-PLH) of individuals with severe polyhandicap. Details of the study protocol of the cohort were published elsewhere [
10]. Data were collected at 2 points: the first wave (Time 1, T1) was collected in 2015 and 2016, and the second wave (Time 2, T2) was collected in 2020 and 2021. Persons with severe PIMD who were cared for in 4 specialized rehabilitation centres (SRC) and 9 residential facilities (RFs) were eligible.
Ethics
Regulatory monitoring was performed in accordance with French law that requires the approval of the French ethics committee (Comité de Protection des Personnes Sud Méditerranée V, 20/10/2014, reference number 2014-A00953-44). A written consent form was collected for each participant (from the legal representative). Clinical trial number: NCT02400528 (registered 27/03/2015).
Selection criteria
The inclusion criteria were as follows: age over 3 years at the time of inclusion; polyhandicap defined by: i) a cerebral lesion leading to a combination of motor deficiency (tetraparesia, hemiparesis, paraparesis, extrapyramidal syndrome, cerebellar syndrome, and/or neuromuscular problems), profound intellectual impairment (intelligence quotient IQ < 40) associated with everyday life dependence (Functional Independency Measure FIM < 55), and restricted mobility (Gross Motor Function Classification System GMFCS III, IV, and V); ii) age at onset of the cerebral lesion younger than 3 years old; and iii) usual care setting in specialized rehabilitation centres or residential facilities.
Samples
The evolution of adequacy was studied from the sample of persons who were assessed at the 2 evaluation times, 2015–2016 and 2020–2021 (sample 1) and the sample of persons assessed at T2 (sample 2). The health care consumption was studied from the sample of persons assessed at T2 (sample 2).
Data collection
For each person, the following data were available in the case report form: sex, age, aetiology lesion time (antenatal, perinatal, and postnatal), aetiology nature (nonprogressive and progressive), mobility (GMFCS), independency (FIM score), profound intellectual impairment (IQ), age classes at assessment (two classes: < 18 or > = 18 years), usual care setting (specialized rehabilitation centres or residential facilities), severity of health status. Severe health status was defined by motor handicap (including paraparesis, tetraparesia, extrapyramidal syndrome, or severe general hypotonia), an IQ < 25, a FIM score ≤ 20, and a GMFCS IV and V. Otherwise, persons were considered to have less severe health status. A specific monitoring was performed by the administrative coordinator to identify people who moved or died over time.
Definition of adequacy of care setting
The adequacy of the care setting was based on objective adequacy and subjective adequacy defined as follows:
Adequacy for age: Adequacy was defined as a person under 18 years old who was cared for in a unit dedicated to children or by a person over 18 years old who was cared for in a unit dedicated to adults. Inadequacy was defined as either of 2 situations: a person under 18 years old who was cared for in a unit dedicated to adults or by a person over 18 years old who was cared for in a unit dedicated to children.
Adequacy for health status severity: Adequacy was defined as a person with a severe health status who was cared for in a specialized rehabilitation centre or by a person with less severe health status who was cared for in residential facilities. Inadequacy was defined as either of 2 situations: a person with a severe health status who was cared for in residential facilities or by a person with less severe health status who was cared for in a specialized rehabilitation centre.
Objective adequacy was a combination of age adequacy and severity adequacy. Objective adequacy was defined as age adequacy and severity adequacy. Inadequacy was defined as any other case.
Adequacy for medical care: Adequacy was defined based on the self-perception of the referring physician of the individual about medical care provided in the setting.
Adequacy for educational care: Adequacy was defined based on the self-perception of the referring physician of the individual about educational care provided in the setting.
Subjective adequacy was a combination of medical adequacy and educational adequacy. Subjective adequacy was defined as adequate medical care and adequate educational care. Inadequacy was defined as any other case.
Definition of health care consumption
Health care consumption was assessed using the following indicators:
-
Consumption of medical care: The number of medical consultations during the last year before the assessment were recorded for general practitioner, physical medicine rehabilitation, neurologist (epilepsia, sleep disorders), dentist, orthopaedist (scoliosis, hip luxation), gastrologist, pneumologist, ophthalmologist, paediatrician (for children), and gynaecologist (for girls-women).
-
Consumption of hospitalization stays: During the last year before the assessment, the number of planned conventional hospitalizations, unplanned conventional hospitalizations, and intensive care unit stays were recorded.
-
Occurrence of decompensation: The number of decompensation episodes leading to admission to an acute care unit during the last year before the assessment was recorded.
-
Consumption of paramedical care: For each item, the monthly prescribed sessions and the gap between the number of prescribed and performed sessions were recorded: physiotherapy, occupational therapy, psychomotor therapy, speech therapy, orthoptist, psychologist, special educator, and dietitian. The gap of prescribed/performed sessions was defined by the number of prescribed sessions minus number of performed sessions (D);3 categories were used: no gap (D < 3 sessions), minor gap (3 < = D < = 10), large gap (D > 10).
Statistical analysis
The proportions of each indicator of adequacy were provided for the 2 samples (sample 1, N = 492 paired subjects, and sample 2, N = 619). The description of medical and paramedical consumption was provided for sample 2 (N = 619): i) all the sample; ii) according to the usual care setting (specialized rehabilitation centres or residential facilities), iii) according to the age classes (< or > = 18 years). Quantitative data are expressed as the medians and interquartile ranges (IQR), and qualitative data are expressed as numbers and percentages. The analyses were performed using SPSS software (IBM SPSS PASW Statistics Inc., Chicago, IL, USA).
Discussion
To our knowledge, this study is the first to describe the evolution of important indicators of care management adequacy for people with severe PIMD in France over a 5-year period.
The first important finding was that objective adequacy, defined as a combination of age adequacy (i.e., a child cared for in a child unit or an adult who was cared for in an adult unit) and severity adequacy (i.e., a severe person cared for in a specialized rehabilitation centres or a less severe person cared for in residential facilities), has improved over time (46% and 50% in 2015–2016 and 2020–2021, respectively). However, the rates of inadequacy are still high. Part of this inadequacy concerned persons who were not care managed in an appropriate care setting according to their age. Adults care managed in units dedicated for children represented 95% of these cases. Another part of the objective inadequacy concerned people who were not care managed in an appropriate care setting according to their health severity. This inadequacy may have consequences. The French health decision-making agencies can exhort the institutions to position the patients according to the legal age (18 years) or the severity. And, in case of non-compliance, beds or units can be suppressed.
Based on these 2 observations, several hypotheses could be suggested. First, the inadequacy could be due to a lack of places (in particular, a lack of places in units dedicated to adult persons) and to a heterogeneous offer of care settings on the French territory, thereby resulting in underresourced areas. Due to the scarcity of specialized centres, the person may be moved far from their family’s place of residence. Families and support teams may choose a less appropriate (in terms of age and/or severity) but nearby care setting rather than a more appropriate care setting that is farther away. These findings could also be relevant for health decision-makers in the planning of future health organizations for persons with severe PIMD. Decision-makers should consider increasing the number of beds dedicated to adults and thinking about a wider and more homogeneous geographical offer of places. Second, the objective inadequacy could be due to a reluctance from the families. Indeed, previous studies showed that parents could be worried by the idea that their child is going to change units [
11]. A change of the familiar environment (change of the care team, change of care structure) could be at high risk of decompensation for the person [
12], sometimes leading to the concept of “failure to cope” [
13]. In addition to the families’ reluctance, it is not sensible to think that the care team, knowing and taking care of the persons for a long time, tied to the persons [
14], could be in a passive position regarding the admission of their patients to another centre. Improving the transition between paediatric and adult health care is not only promoted for persons with PIMD but also widely debated in other fields, such as various chronic diseases [
15,
16]. A cultural shift in staff attitudes and effective transition programs are required [
17]. Currently, to change representations and beliefs, it is essential to better connect adult and paediatric care settings [
18], medicosocial and medical structures, and families and health care teams [
19].
The rate of subjective adequacy, defined by a combination of medical adequacy and educational adequacy perceived by the referring physician, was better than the rate of the objective adequacy but decreased over time from 93% (2015–2016) to 87% (2020–2021). Global inadequacy was mainly due to self-perceived inadequacy for educational care, while adequacy for medical care was at the maximal level. This finding is unsurprising. It is now well-recognized that educational care remains essential for PIMD persons [
20,
21]. Behaviourial disorders, teeth grinding, self-injury, and autistic-like traits should be partially controlled [
22]. Many care settings lack resources to enhance educational care. The gap between performed and prescribed sessions of various paramedical care, including special educators, enhances this result. Health care teams consider that educational care, as well as care-like care, such as physiotherapy, occupational therapy, and psychomotor therapy, is essential in the global care management of persons with PIMD. However, care settings cannot provide these services due to insufficient resources. In the future, it would be important to think about care settings that offering mixed care, including more balanced medical and educative care. It would also be relevant to assess the adequacy perceived by familial caregivers: they are also concerned and can provide a complementary point of view.
Finally, this study provided detailed information on the health consumption of PIMD/polyhandicap persons. While various specific medical consultations seem essential to organize preventive and curative treatments, we found that many persons were insufficiently monitored by general practitioners and physical medicine rehabilitation physicians. Specific needs of persons with PIMD require frequent monitoring: optimization of epilepsy treatment [
23], detection of scoliosis or other deformations, diagnosis of gastroesophageal reflux and maintenance of gastrostomy [
24], and pain evaluation [
25,
26]. Experimented paediatricians and gynaecologists may be of high interest in the medical follow-up of the target persons (children and women, respectively). Oral health maintenance must also be considered [
27]. Therefore, suboptimal management improves the risk of health deterioration or decompensation episodes and consequently the risk of unplanned admissions in conventional medical settings or, more troublesomely, intensive care admission. Administrative and medical staff of these settings, both residential facilities and specialized centres, regularly request more financial resources to be able to offer more appropriate care. Future health care decisions could be based on these robust findings.
Some limitations should be discussed. First, the data collection having been carried out during the year 2020–2021, we can hypothesize that the organization of care could have been significantly modified by the SARS-CoV-2 pandemic. Work absenteeism and safety guidelines, such as limiting human contact and postponing non-urgent care, may have reduced access to care, including medical consultations and paramedical care. Previous studies described the impact of the pandemic on the care organizations in France [
28,
29]. The absence of similar data from the 1st wave deprives us of reference. The third wave of the cohort will allow to better explore this hypothesis. Second, we only collect healthcare consumption defined by medical consultations, hospitalizations, and paramedical care. However, future medico-economic studies should be considered on the basis of an exhaustive identification of the costs of care, including direct costs (drugs, medical devices and wheelchairs) and indirect costs.
Acknowledgements
The EVAL-PLH group: Karine Baumstarck 1,2, Ilyes Hamouda 1,2, Marie-Anastasie Aim 3, Any Beltran Anzola 1, Sherezad Khaldi-Cherif 4, Agnès Felce 5, Kim Maincent 6, Katia Lind 4, Pascal Auquier 2, Thierry Billette de Villemeur 7,8, Marie-Christine Rousseau 1,8, and the EVAL-PLH Group including Narjess Boutalbi 6, Lionel Dany 3, Ponha Heng 7, Patrick Julien 6, Isabelle Kemlin 6, Stéphane Lenormand 5, Stéphane Pietra 8, Julie Roger 6, Maria Valkov 8, Daniel Willocq 8.
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