Cerebral Palsy and Ayurveda
<p>Cerebral palsy is a commonest chronic and progressive disease of mental and physical disability among children and affects 3-8% population which fails to respond the present technologies or medication of modern medicine.</p> <p>Objective of the Study: To evaluate a proven herbal neuro regenerative and neuro vigorative composite NEUROVIT in modifying therapeutic outcome and life style improvement of Cerebral palsy cases.</p> <p>Material & Methods: Cases suggestive of Cerebral palsy attending Institute of applied neurology, Aarogyampunarjeevan, Ara Garden Road , Jagdeo path, Baily Road Patna 14 and National Institute of Health & Research, Warisaliganj (Nawada) Bihar were selected for the study. Selected patients were clinically examined as per various grades of activity to adjudge the severity of illness and investigated for baseline biostatus to evaluate therapeutic outcome and safety profile.</p> <p>Result: Herbal composite ensured marked improvement in all parameters i.e. motor power, muscle tone, mental capability and intelligent quotient (IQ) in 96.7% cases without any disease related complication and drug related sequel.</p> <p>Discussion: Cerebral palsy a chronic condition with considerable morbidity more in male and in lower middle class due to health ignorance unhygienic environment and lack of proper antenatal and obstetric care having increased risk multiple birth, neonatal asphyxia and premature delivery.Conclusion: Though Cerebral palsy has no cure in modern medicine in spite of advancement in technologies and therapeutics but cases diagnosed at early age and, treated with herbal composite adjuvant NEUROVIT Syrup in prescribed dose with other supplement achieve marked clinical improvement and improved lifestyle in 96.7% cases.</p>
Introduction
Cerebral Palsy (CP) is a commonest chronic motor disorders in children with considerable morbidity and affect about 3-8% of the population with 15-20% of physically disabled children and incidence of 3/1000.(WHO ) [1, 2, 3, 4]. This affects 2.1 per thousand live births more among poor and male and prevalence average rate is of 2 per thousand most commonly in low birth weight babies. Its incidence increases with premature and low birth weight babies regardless of quality of care. On n the basis of part affected Cerebral palsy being classified as-Monoplegia, Hemiplegia, Diplegia and quadriplegia out of which diplegia is the commonest (30-40%), Hemiplegia (20-30%),quadriplegia (10- 15%),Spastic quadriplegia 61% and diplegia 22% Out of which spastic Cerebral Palsy is the commonest and accounts to 70-75%, dystonic 10-15% and ataxic <5% [5, 6, 7, 8]. Cerebral palsy is not a progressive disorder but manifestations become more prevalent over time and are more likely to have learning disability without affecting IQ including varying degree of intellectual disability with significantly reduced life expectancy depending on severity of condition & quality of care. 5-10 % of children with Cerebral Palsy die in childhood particularly who had seizure and intellectual disability [9, 10, 11, 12]. The ability to ambulate, roll and self feed are the index of increasing life expectancy, in addition independent gross motor functional ability is a very strong determinants of life expectancy [13, 14]. The most accurate index of assessment of general movements occurring spontaneous before 4 months age [15, 16].
- Abdominal muscle tone
- Delayed motor development
- Persistence of primary reflexes
- Typical symptoms suggestive of diagnosis most commonly occurs at the age of 2 years Therapeutic outcome in Cerebral Palsy depends on the age of diagnosis, as early the diagnosis better is prognosis. The present study is based on the hypothesis that neural tissue remains same ,as it never grows or multiply after birth and no available modern molecule can regenerate or repair damaged or diseased nerve cells thus a herbal composite of proven efficacy in helping repair and rejuvenation of nerve cells been evaluated in cases of Cerebral palsy. Ethical Status: Ethical committee of National Institute of Health & Research approved the extended study to approve the established neurogenic effect of herbal composite
Material & Methods
Objective of study
Evaluation of therapeutic efficacy of a proven herbal neurovigorative and neurogenerative composite in modifying therapeutic outcome and improvement of life style in cases of Cerebral palsy .
Duration of Study
January 2004 to December 2017, this include follow up period also
Material
Patients attending at the Institute of Applied Neurology, Aarogyam punarjeevan, Ram Bhawan, Ara Garden Road, Jagdeopath, Baily Road, Patna 14 and National Institute Of Health & Research Warisaliganj (Nawada) Bihar been considered for the evaluation as per following criteria of selection and exclusion and were diagnosed as per- Children with complaints of spasticity or dysfunction in limbs and delayed developmental milestones and already diagnosed cases of Cerebral Palsy were selected for this study (Table 1).
| Criteriia of selection | Criteria of exclusion | ||||
|---|---|---|---|---|---|
| Children with CP up to 10 years of age | Children >10 years of age | ||||
| Children with developmental delay and disability with mild, moderate, or severe degree. | Children with severe infectious diseases such as TB, meningitis degree. | ||||
| Children with any major congenital Malformations such as Congenital Heart Disease (CHD) |
Table 1: Criteriia of Selection/ Exclusion.
Methods
Parents of Selected patients were interrogated for antenatal, natal and postnatal history Birth history Hospital /home delivery Normal/assisted Delayed labour LSCS /HSCS Antenatal drug history Apgar score Clinical stage (Table 2, 3) History of any medication Response of therapy taken
| Motor function | Gradings | ||||||
|---|---|---|---|---|---|---|---|
| Head Holding | 0 = No head holding | ||||||
| I = Head erect and steady momentarily | |||||||
| 2=Supine; lifts head when pulled up by arms | |||||||
| 3= Prone,elevates self by arms and chest | |||||||
| 4= holds head steady when moved around | |||||||
| 5= Head balanced always | |||||||
| Sitting | 0= Not sitting at all | ||||||
| 1= sits momentarily | |||||||
| 2 – Sits for 30 s or more leaning forward | |||||||
| 3 – Sits with the child's back straight | |||||||
| 4 – While sitting, can manipulate a toy | |||||||
| 5 – Raises self to sitting position | |||||||
| Standing | 0 – Does not stand at all | ||||||
| 1 – Stands holding furniture momentarily | |||||||
| 2 – Takes a few steps, both hands hold | |||||||
| 3 – Without | support | , can stand alone | |||||
| 4 – Stands up, all by himself by throwing weight on arms | |||||||
| 5 – Takes a few steps without support. | |||||||
| Gross Motor Function Classification system for Cerebral Palsy (GMFCS) Level | |||||||
| Fine motor | 0 – No grasping at all/absent palmer grasp | ||||||
| 1 – Tries to reach and holds thing with crude methods | |||||||
| 2 – Tries to reach and holds things with good grip | |||||||
| 3 – Transfers object from one hand to another hand | |||||||
| 4 – Uses thumb and index finger and holds small object | |||||||
| 5 – Uses end of thumb and index finger/neat pincer grasp | |||||||
| Language | 0 – Unable to speak or produce sound at all | ||||||
| 1 – Marked cooing | |||||||
| 2 – Monosyllable | |||||||
| 3 – Bisyllables | |||||||
| 4 – Two words with meaning | |||||||
| 5 – Makes simple sentence. | |||||||
| Personal and social | 0 – Absent social smile and recognition | ||||||
| 1 – Social smile and recognition | |||||||
| 2 – Recognizing mother | |||||||
| 3 – Anxiety in front of a stranger | |||||||
| 4 – Attachment toward a toy and displeasure on taking it away | |||||||
| 5 – Resists if toy is pulled | |||||||
| 6 – Mimicry, understands spoken words and responds in an appropriate manner |
Table 2: Patients were assessed for gross motor, gross motor functions and social personal status and were graded as per followin
| Mild | if score of each >3 |
| Moderate | if score is 2 |
| Severe | if score is 1 or less |
Table 3: On the basis of above assessment score patients
Selected patients were given a herbal composite constituting equal part (100mg) of Acorus calamus Herpestismonnieri, Cassia angustifolia, Nardostacachysjatamansi, Convolvulus pluricaulis in each 5ml in dose as per following (Tables 4 & 5):
| <1 yr | 1.25 ml every 12 hrs | <1 year | Male | Female | Total |
| 1-5 years | 2.5 ml every 12 hours | 1-3 | 34 | 17 | 51 |
| 5-10 years | 5ml every 12 hours | 3-5 | 42 | 29 | 71 |
| Along with Calcium, Neuro vitamin and vitamin D3 supplement | >5 | 36 | 20 | 56 | |
| 4 | 2 | 6 | |||
| 116 | 68 | 184 |
Table 5: Dose Schedule of Herbal supplements (NEUROVIT Syrup).
| Maximum | More than 75% improvement of clinical signs and symptoms |
| Moderate | More than 50-75% improvement of clinical signs and symptoms |
| Mild | More than 25-50% improvement of clinical signs and symptoms |
| Non response | Equal or less than 25% improvement of clinical signs and symptoms: |
Table 7: Effect of therapy been assessed and graded.
Observations
Among 184 selected patients 116 were male and 68 were female, out of all 51 cases were of age <1 year while 71 were of <3 years though 6 cases were of >5 years age (Table 6), (Figure 1). Out of all 96(52.2%) were delivered normally while 51(27%) through caesarean section and 100(54.3%) were with poor Apgar score and 84(41.6%) with low birth weight (Table 7). Among the selected patients 62 had taken various therapeutic including physiotherapy in last few years without having any improvement while rest 122 have not taken any medication and attended the centre for the first time, though 69 cases were detected during the treatment for other disease (Figure 2). The commonest clinical presentation was speech problem in 82.6% cases while 52.7% presents with microcephaly, 44.8% with seizure and 12% with behaviour problem (Table 8). Birth history reveals majority (64) with low birth weight, 59 premature delivery and 61 with poor Apgar score (not cried after birth). Considering the severity of the presentation 32 were of severe, 60 moderate and 92 with mild grade of presentation (Figure 3). No patients had any drug adversity or agonizing clinical presentation or any alteration in haematological, hepatic and renal function though 98.9 % patient show marked rise in haemoglobin (Table 9). Out of all 178 (96.7%) children shows grade I (excellent) clinical outcome while 4(2.1%) and 2(1.1%) had grade II and grade III improvement (Table 10), (Figure 4).
| Age group (in year) | Number of patients | ||||||
|---|---|---|---|---|---|---|---|
| < 1 year | Male | Female | Total | ||||
| 1-3 | 34 | 17 | 51 | ||||
| 3-5 | 42 | 29 | 71 | ||||
| >5 | 36 | 20 | 56 | ||||
| 4 | 2 | 6 | |||||
| 116 | 68 | 184 |
Table 4: Distribution of patients as per clinical presentation.

- Particulars
- Number of patients
- %
- Birth history
- Normal parturition
- 96
- 52.2
- Assisted parturition
- 37
- 20.1
- Forcep
- 16
- Episiotomy
- 21
- Higher segment caeserian section
- 31
- 16.8
- Lower segment caeserian section
- 20
- 10.9
- Foetal status
- Normal
- 56
- 30.4
- Low birth weight baby
- 84
- 45.6
- Premature
- 44
- 24
- Poor apgar score
- 100
- 54.3
Table 6: Distribution of patients as per their birth history.

| Number | Percentage | |
|---|---|---|
| Speech problems | 152 | 82.6 |
| Microcephaly | 97 | 52.7 |
| Visual defect | 70 | 38.04 |
| Seizures | 75 | 44.8 |
| Malnutrition | 64 | 34.8 |
| Intellectual disability | 62 | 33.7 |
| Feeding problems | 38 | 20.7 |
| Hearing problems | 19 | 10.3 |
| Behavior problems | 22 | 12 |
| <30 IU | 180 | 184 |
| >30 IU | 4 | 0 |
| SGPT | ||
| <30 IU | 180 | 184 |
| >30 IU | 4 | 0 |
| Renal profile | ||
| Blood urea: | ||
| <26mg% | 182 | 184 |
| >26mg% | 2 | 0 |
| Serum creatinine: | ||
| <1.5mg% | 184 | 184 |
Table 9: Distribution of patients as per clinical presentation.

| Bio parameter | Number of patients | |||||
|---|---|---|---|---|---|---|
| Before therapy | After therapy | |||||
| Hematological | ||||||
| Hemoglobin: | ||||||
| <12gm % | 134 | 2 | ||||
| >1 2gm% | 50 | 182 | ||||
| Hepatic profile | ||||||
| Serum bilirubin: | ||||||
| <1mg% | 180 | 184 | ||||
| >1mg% | 4 | 0 | ||||
| SGOT: | ||||||
| <30 IU | 180 | 184 | ||||
| >30 IU | 4 | 0 | ||||
| SGPT | ||||||
| <30 IU | 180 | 184 | ||||
| >30 IU | 4 | 0 | ||||
| Renal profile | ||||||
| Blood urea: | ||||||
| <26mg% | 182 | 184 | ||||
| >26mg% | 2 | 0 | ||||
| Serum creatinine: | ||||||
| <1.5mg% | 184 | 184 | ||||
| Urine : | ||||||
| Albumin | ||||||
| Present | 2 | 0 | ||||
| Absent | 182 | 184 |
Table 8: Showing post therapy effect on basic bio parameters.
| Index | Number of patients | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Pre therapy | Post therapy | |||||||||||||||
| Grades | 0 | 1 | 2 | 3 | 4 | 5 | 0 | 1 | 2 | 3 | 4 | 5 | ||||
| Head holding | 32 | 35 | 117 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 | ||||
| Sitting | 32 | 40 | 112 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 | ||||
| Standing | 32 | 59 | 93 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 | ||||
| GMFC level | ||||||||||||||||
| Fine motor | 32 | 40 | 112 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 | ||||
| Language | 32 | 55 | 97 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 | ||||
| Personal & Social | 32 | 52 | 100 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 4 | 178 |
Table 10: Shows therapeutic outcome.

Results
| Discussions |
Table 11: Shows therapeutic outcome.
Cerebral palsy a chronic condition with considerable morbidity more in male and in lower middle class due to health ignorance unhygienic environment and lack of proper antenatal and obstetric care having increased risk multiple birth, neonatal asphyxia and premature delivery. Common symptoms and associated conditions observed in spastic quadriplegia and convulsive disorders [19, 20, 21]. As no effective treatment for the underlying brain damage and all sophisticated technology are highly expensive and complicated therapies in the medical research field find a definite cure for the disease. The present study reveals grade I clinical response in majority of early cases and improved quality of life in all the selected cases taking herbal composite NEUROVIT can be explained as - Physical and mental debility due to hypoxia, loss of GABA mediated inhibition of dentate granule and death of GABAergic inhibitory neuron results in attenuation of inhibitory control which in turn results in hyper excitation of the remaining neuron of the hippocampus.
Mossy cells (located in dentate hilus, a part of hippocampus) are extremely sensitive to seizure induced neuronal death and damage following intense synaptic activator i.e., excite-tonic mechanism of activator of NMDA (N methyl D aspartate) a sub type of glutamate receptor which results in excessive intracellular calcium. Release of cellular zinc attenuate GABA response and induce hyper -excitability of neurons. GABA binds to GABA-A(coupled to calcium/chloride channel and a main target of currently prescribed drugs) as excitatory post synaptic potential are the main form of communication between neurons and is mediated by release of excitatory amino acid-Glutamate from presynaptic elements which is mediated by - NMDA (N methyl D aspartic acid/aspartate) - AMPA(Alpha-amino-3 hydroxy 5 methyl isoxazole propionic acid) kinate - Metabotropic GABA-B (Couples to potassium channel, a cause of latency and long duration of action) located in pre-synaptic element of an excitatory pre-neuron and inhibits pre-synaptic neuron by - direct induction of IPSP - inhibition of release of excitatory neuro transmitters Hence clinical supremacy of the adjunct indigenous composite can be attributed to bioregulative action of indigenous composites active ingredients for GABA neurodynamics i.e., Nardostachysjatamansi (Jatamansin, Jatamanose, Nardostachine) Herpestismonnieri(Monnerein) bio regulate GABA biokinetics and prompt neurovigorative while Acorus calamus (Acorin, Beta asarone and calaminidine) and Crotolariaverrucosa (crotallidine and verrucosin) acts as a neurogenic and helps in regeneration and repair of damaged neuron due to epileptic attacks thus improve and check neural debility and alleviate physical disability . In addition Convolvulus pluricaulis (Covolvulin) and Herpestismonnieri (Bacoside A & B) both promote neural growth due to activation of nerve growth factor-Tyrosine kinase A receptor, preserve m RNA level of muscarnic receptors and check accumulation of lipid and protein damage, thus improve both mental ability and capability. Hence bio regulation of altered GABA neuro kinetics prompt neurogenic action improve mental capability and physical capability [22, 23]. Active ingredients of the composite help revitalization of the damaged or diseased nerve cells ,improve neuro transmission by bio regulating neuro transmitter secretion ,not only improves physical status i.e.- relieves paresis, improves muscle power, increases muscle bulk and improve deep tendon reflex ,in addition also improves mental capability and IQ (Figure 5).

Thus NEUROVIT herbal composite seems to be a boon for Cerebral palsy cases in improving quality of life restricting handicap and improving mental capability., earlier the supplement better the outcome.
Conclusion
Cerebral palsy having no proven therapeutics in modern medicine shows promising result with herbal composite of proven neurogenic and neuro vitalising capacity in cases of cerebral palsy detected at early age i.e. <2 years while patients detected late Or tried various medication presenting with severe spasticity, have improvement in presentation i.e. muscle power and tone, spasticity and mental ability.
Thus this Herbal composite NEUROVIT is worth prescribing either alone or as an adjuvant in cases of Cerebral palsy as early as possible.
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