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Background
A high arch that does not flatten underweight bearing is a characteristic of the foot morphology known as pes cavus.
The forefoot, midfoot, hindfoot, or a combination of these may be the site of the malformation. It causes more weight to be placed on the heel and ball of the foot, which frequently causes pain, discomfort, and trouble walking and balancing.
Pes cavus is a frequent occurrence, affecting about 10% of the general population, but it can also indicate a neurologic problem.
Contracture of the plantar fascia, cockup deformity of the great toe, posterior hindfoot deformity, and clawing of the toes are among the range of related abnormalities seen with pes cavus.
Metatarsalgia and calluses may result from the increased weight bearing on the metatarsal heads.
The objective of treatment is to create a plantigrade foot that permits uniform weight distribution. Surgery is indicated if the plantigrade foot should not keep asymptomatic.
A thorough and meticulous evaluation of the foot and ankle is necessary when making surgical decisions to check for abnormalities, strength, and rigidity.
Bony and soft-tissue operations are the two main categories into which surgical procedures fall.
Epidemiology
It is less frequent than pes planus, or flatfoot, and its frequency varies based on the community under study.
Even though not all high-arched foot conditions are symptomatic or clinically significant, certain studies indicate that up to 25% persons may have one. Though it can appear at any age, late childhood or adolescent is usually when it becomes apparent.
Early adulthood is a common time for progressive forms to appear, when underlying neurological disorders are involved.
A systemic or neurological etiology is more likely to be the source of bilateral presentation, whereas spinal cord pathology or trauma may be the origin of unilateral pes cavus.
Anatomy
Pathophysiology
Mann explained how people with Charcot-Marie-Tooth (CMT) disease develop pes cavus. Understanding the deformity by knowledge of the muscles involved and the order in which they are involved.
A muscle agonist-antagonist model is used to identify the deformity. The anterior tibialis and peroneus brevis become weaker in CMT disease.
Forefoot adduction is caused by the posterior tibialis pulling more forcefully than the weak peroneus brevis. The weakening of the gastrocnemius-soleus complex causes the deformity in the hindfoot of polio patients.
Etiology
The causes of Pes Cavus are:
Malunion of calcaneal or talar fractures
Burns
Sequelae resulting from compartment syndrome
Residual clubfoot
Neuromuscular disease
Genetics
Prognostic Factors
There have been some encouraging results recorded. For example, Wetmore and Drennan found that 24% of patients with CMT illness who had triple arthrodesis had good outcomes after an average follow-up of 21 years.
With an average follow-up of 7.5 years, Mann and Hsu reported on 12 feet in patients with CMT illness who had triple arthrodesis.
The outcomes of osteotomies and soft-tissue surgeries were reported by Roper and Tibrewal. A review of ten CMT disease cases was conducted fourteen years following surgery. Recurrent deformity necessitated repeat surgery for two patients.
Excellent results were indicated by the mean modified American Orthopaedic Foot and Ankle Society (AOFAS) Midfoot Score of 76 and the mean Bristol Foot Score of 27.
Clinical History
Increased weight bearing on the lateral foot can cause patients to present with lateral foot pain.
Patients who have weak peroneus brevis and hindfoot varus may show with ankle instability.
A comprehensive history and examination are the first steps in evaluating a patient who arrives with pes cavus to identify the cause.
Based on family history, neuromuscular diseases can be detected. A new unilateral deformity requires a proper workup because it is very suggestive of a spinal cord malignancy.
Physical Examination
Neurological examination
Foot examination
Age group
Associated comorbidity
Associated activity
Acuity of presentation
Mild lateral pain, Metatarsalgia, Ankle instability, Neurological deficits
Differential Diagnoses
Congenital hypomyelinating neuropathy
Charcot–Marie–Tooth disease
Distal hereditary motor neuropathies
Dejerine–Sottas neuropathy
Laboratory Studies
Imaging Studies
Procedures
Histologic Findings
Staging
Treatment Paradigm
The aim of treatment is to create a plantigrade foot that enables the patient to walk about pain-free and with an even weight distribution.
The patient needs to comprehend the purpose of the procedure and be aware that a normal foot cannot be obtained through surgical reconstruction.
Repeat surgery can be required, particularly if the deformity worsens over time. Patient satisfaction requires preoperative patient education.
Poor vascularity is an unequivocal contraindication to surgery. If necessary, revascularization should be carried out prior to rebuilding.
To reduce the risk of infection, the wound should be cured before reconstruction if there is an ulcer.
Performing an extensive arthrodesis as a salvage treatment and, if feasible, preserving the joints are the current trends.
by Stage
by Modality
Chemotherapy
Radiation Therapy
Surgical Interventions
Hormone Therapy
Immunotherapy
Hyperthermia
Photodynamic Therapy
Stem Cell Transplant
Targeted Therapy
Palliative Care
use-of-non-pharmacological-approach-for-pes-cavus
Patient should take physical therapy to stretch tight muscles and strengthen weak muscles to provide relief.
Using extra-depth shoes and orthotics to relieve bony prominences and avoid toe friction may help reduce symptoms.
The function of hindfoot varus deformities can be improved by modifying the lateral wedge sole.
The heel can be neutralized in forefoot-driven hindfoot varus by using an insole that has lateral elevation and a recession beneath the first ray.
It is necessary to have plastozolte linings in the brace and to regularly check the skin for ulcers.
Proper awareness about pes cavus should be provided and its related causes with management strategies.
Appointments with orthopaedist and preventing recurrence of disorder is an ongoing life-long effort.
Use of Nonsteroidal anti-inflammatory drugs (NSAIDs)
Ibuprofen:
It inhibits synthesis of prostaglandins in body tissues at least 2 cyclo-oxygenase isoenzymes with COX-1 and COX-2.
Use of Muscle Relaxants
Baclofen inhibits monosynaptic and polysynaptic reflexes at the spinal level to decrease excitatory neurotransmitter.
Diazepam:
It reduces anxiety and muscle spasm by enhancing GABA.
use-of-intervention-with-a-procedure-in-treating-pes-cavus
Multiple separate procedures must be performed because no single procedure is suitable for every patient.
Without the need for an arthrodesis, the deformity can be corrected by tendon transfers and osteotomies.
Methods for fully resecting the plantar fascia and removing the fascia from the calcaneus have been documented.
The EHL and the extensor digitorum longus (EDL) are moved to the first, third, and fifth metatarsals as part of the extensor shift technique.
use-of-phases-in-managing-pes-cavus
The initial management phase is suitable for mild or early-stage cases.
The progressive intervention phase is for patients with worsening deformity or unrelieved symptoms.
In supportive care and management phase, patients should receive required attention such as lifestyle modification and surgical interventional procedures.
The regular follow-up visits with the orthopedist are scheduled to check the improvement of patients along with treatment response.
Medication
Future Trends
References
A high arch that does not flatten underweight bearing is a characteristic of the foot morphology known as pes cavus.
The forefoot, midfoot, hindfoot, or a combination of these may be the site of the malformation. It causes more weight to be placed on the heel and ball of the foot, which frequently causes pain, discomfort, and trouble walking and balancing.
Pes cavus is a frequent occurrence, affecting about 10% of the general population, but it can also indicate a neurologic problem.
Contracture of the plantar fascia, cockup deformity of the great toe, posterior hindfoot deformity, and clawing of the toes are among the range of related abnormalities seen with pes cavus.
Metatarsalgia and calluses may result from the increased weight bearing on the metatarsal heads.
The objective of treatment is to create a plantigrade foot that permits uniform weight distribution. Surgery is indicated if the plantigrade foot should not keep asymptomatic.
A thorough and meticulous evaluation of the foot and ankle is necessary when making surgical decisions to check for abnormalities, strength, and rigidity.
Bony and soft-tissue operations are the two main categories into which surgical procedures fall.
It is less frequent than pes planus, or flatfoot, and its frequency varies based on the community under study.
Even though not all high-arched foot conditions are symptomatic or clinically significant, certain studies indicate that up to 25% persons may have one. Though it can appear at any age, late childhood or adolescent is usually when it becomes apparent.
Early adulthood is a common time for progressive forms to appear, when underlying neurological disorders are involved.
A systemic or neurological etiology is more likely to be the source of bilateral presentation, whereas spinal cord pathology or trauma may be the origin of unilateral pes cavus.
Mann explained how people with Charcot-Marie-Tooth (CMT) disease develop pes cavus. Understanding the deformity by knowledge of the muscles involved and the order in which they are involved.
A muscle agonist-antagonist model is used to identify the deformity. The anterior tibialis and peroneus brevis become weaker in CMT disease.
Forefoot adduction is caused by the posterior tibialis pulling more forcefully than the weak peroneus brevis. The weakening of the gastrocnemius-soleus complex causes the deformity in the hindfoot of polio patients.
The causes of Pes Cavus are:
Malunion of calcaneal or talar fractures
Burns
Sequelae resulting from compartment syndrome
Residual clubfoot
Neuromuscular disease
There have been some encouraging results recorded. For example, Wetmore and Drennan found that 24% of patients with CMT illness who had triple arthrodesis had good outcomes after an average follow-up of 21 years.
With an average follow-up of 7.5 years, Mann and Hsu reported on 12 feet in patients with CMT illness who had triple arthrodesis.
The outcomes of osteotomies and soft-tissue surgeries were reported by Roper and Tibrewal. A review of ten CMT disease cases was conducted fourteen years following surgery. Recurrent deformity necessitated repeat surgery for two patients.
Excellent results were indicated by the mean modified American Orthopaedic Foot and Ankle Society (AOFAS) Midfoot Score of 76 and the mean Bristol Foot Score of 27.
Increased weight bearing on the lateral foot can cause patients to present with lateral foot pain.
Patients who have weak peroneus brevis and hindfoot varus may show with ankle instability.
A comprehensive history and examination are the first steps in evaluating a patient who arrives with pes cavus to identify the cause.
Based on family history, neuromuscular diseases can be detected. A new unilateral deformity requires a proper workup because it is very suggestive of a spinal cord malignancy.
Neurological examination
Foot examination
Mild lateral pain, Metatarsalgia, Ankle instability, Neurological deficits
Congenital hypomyelinating neuropathy
Charcot–Marie–Tooth disease
Distal hereditary motor neuropathies
Dejerine–Sottas neuropathy
The aim of treatment is to create a plantigrade foot that enables the patient to walk about pain-free and with an even weight distribution.
The patient needs to comprehend the purpose of the procedure and be aware that a normal foot cannot be obtained through surgical reconstruction.
Repeat surgery can be required, particularly if the deformity worsens over time. Patient satisfaction requires preoperative patient education.
Poor vascularity is an unequivocal contraindication to surgery. If necessary, revascularization should be carried out prior to rebuilding.
To reduce the risk of infection, the wound should be cured before reconstruction if there is an ulcer.
Performing an extensive arthrodesis as a salvage treatment and, if feasible, preserving the joints are the current trends.
Orthopaedic Surgery
Patient should take physical therapy to stretch tight muscles and strengthen weak muscles to provide relief.
Using extra-depth shoes and orthotics to relieve bony prominences and avoid toe friction may help reduce symptoms.
The function of hindfoot varus deformities can be improved by modifying the lateral wedge sole.
The heel can be neutralized in forefoot-driven hindfoot varus by using an insole that has lateral elevation and a recession beneath the first ray.
It is necessary to have plastozolte linings in the brace and to regularly check the skin for ulcers.
Proper awareness about pes cavus should be provided and its related causes with management strategies.
Appointments with orthopaedist and preventing recurrence of disorder is an ongoing life-long effort.
Orthopaedic Surgery
Ibuprofen:
It inhibits synthesis of prostaglandins in body tissues at least 2 cyclo-oxygenase isoenzymes with COX-1 and COX-2.
Orthopaedic Surgery
Baclofen inhibits monosynaptic and polysynaptic reflexes at the spinal level to decrease excitatory neurotransmitter.
Diazepam:
It reduces anxiety and muscle spasm by enhancing GABA.
Orthopaedic Surgery
Multiple separate procedures must be performed because no single procedure is suitable for every patient.
Without the need for an arthrodesis, the deformity can be corrected by tendon transfers and osteotomies.
Methods for fully resecting the plantar fascia and removing the fascia from the calcaneus have been documented.
The EHL and the extensor digitorum longus (EDL) are moved to the first, third, and fifth metatarsals as part of the extensor shift technique.
Orthopaedic Surgery
The initial management phase is suitable for mild or early-stage cases.
The progressive intervention phase is for patients with worsening deformity or unrelieved symptoms.
In supportive care and management phase, patients should receive required attention such as lifestyle modification and surgical interventional procedures.
The regular follow-up visits with the orthopedist are scheduled to check the improvement of patients along with treatment response.
A high arch that does not flatten underweight bearing is a characteristic of the foot morphology known as pes cavus.
The forefoot, midfoot, hindfoot, or a combination of these may be the site of the malformation. It causes more weight to be placed on the heel and ball of the foot, which frequently causes pain, discomfort, and trouble walking and balancing.
Pes cavus is a frequent occurrence, affecting about 10% of the general population, but it can also indicate a neurologic problem.
Contracture of the plantar fascia, cockup deformity of the great toe, posterior hindfoot deformity, and clawing of the toes are among the range of related abnormalities seen with pes cavus.
Metatarsalgia and calluses may result from the increased weight bearing on the metatarsal heads.
The objective of treatment is to create a plantigrade foot that permits uniform weight distribution. Surgery is indicated if the plantigrade foot should not keep asymptomatic.
A thorough and meticulous evaluation of the foot and ankle is necessary when making surgical decisions to check for abnormalities, strength, and rigidity.
Bony and soft-tissue operations are the two main categories into which surgical procedures fall.
It is less frequent than pes planus, or flatfoot, and its frequency varies based on the community under study.
Even though not all high-arched foot conditions are symptomatic or clinically significant, certain studies indicate that up to 25% persons may have one. Though it can appear at any age, late childhood or adolescent is usually when it becomes apparent.
Early adulthood is a common time for progressive forms to appear, when underlying neurological disorders are involved.
A systemic or neurological etiology is more likely to be the source of bilateral presentation, whereas spinal cord pathology or trauma may be the origin of unilateral pes cavus.
Mann explained how people with Charcot-Marie-Tooth (CMT) disease develop pes cavus. Understanding the deformity by knowledge of the muscles involved and the order in which they are involved.
A muscle agonist-antagonist model is used to identify the deformity. The anterior tibialis and peroneus brevis become weaker in CMT disease.
Forefoot adduction is caused by the posterior tibialis pulling more forcefully than the weak peroneus brevis. The weakening of the gastrocnemius-soleus complex causes the deformity in the hindfoot of polio patients.
The causes of Pes Cavus are:
Malunion of calcaneal or talar fractures
Burns
Sequelae resulting from compartment syndrome
Residual clubfoot
Neuromuscular disease
There have been some encouraging results recorded. For example, Wetmore and Drennan found that 24% of patients with CMT illness who had triple arthrodesis had good outcomes after an average follow-up of 21 years.
With an average follow-up of 7.5 years, Mann and Hsu reported on 12 feet in patients with CMT illness who had triple arthrodesis.
The outcomes of osteotomies and soft-tissue surgeries were reported by Roper and Tibrewal. A review of ten CMT disease cases was conducted fourteen years following surgery. Recurrent deformity necessitated repeat surgery for two patients.
Excellent results were indicated by the mean modified American Orthopaedic Foot and Ankle Society (AOFAS) Midfoot Score of 76 and the mean Bristol Foot Score of 27.
Increased weight bearing on the lateral foot can cause patients to present with lateral foot pain.
Patients who have weak peroneus brevis and hindfoot varus may show with ankle instability.
A comprehensive history and examination are the first steps in evaluating a patient who arrives with pes cavus to identify the cause.
Based on family history, neuromuscular diseases can be detected. A new unilateral deformity requires a proper workup because it is very suggestive of a spinal cord malignancy.
Neurological examination
Foot examination
Mild lateral pain, Metatarsalgia, Ankle instability, Neurological deficits
Congenital hypomyelinating neuropathy
Charcot–Marie–Tooth disease
Distal hereditary motor neuropathies
Dejerine–Sottas neuropathy
The aim of treatment is to create a plantigrade foot that enables the patient to walk about pain-free and with an even weight distribution.
The patient needs to comprehend the purpose of the procedure and be aware that a normal foot cannot be obtained through surgical reconstruction.
Repeat surgery can be required, particularly if the deformity worsens over time. Patient satisfaction requires preoperative patient education.
Poor vascularity is an unequivocal contraindication to surgery. If necessary, revascularization should be carried out prior to rebuilding.
To reduce the risk of infection, the wound should be cured before reconstruction if there is an ulcer.
Performing an extensive arthrodesis as a salvage treatment and, if feasible, preserving the joints are the current trends.
Orthopaedic Surgery
Patient should take physical therapy to stretch tight muscles and strengthen weak muscles to provide relief.
Using extra-depth shoes and orthotics to relieve bony prominences and avoid toe friction may help reduce symptoms.
The function of hindfoot varus deformities can be improved by modifying the lateral wedge sole.
The heel can be neutralized in forefoot-driven hindfoot varus by using an insole that has lateral elevation and a recession beneath the first ray.
It is necessary to have plastozolte linings in the brace and to regularly check the skin for ulcers.
Proper awareness about pes cavus should be provided and its related causes with management strategies.
Appointments with orthopaedist and preventing recurrence of disorder is an ongoing life-long effort.
Orthopaedic Surgery
Ibuprofen:
It inhibits synthesis of prostaglandins in body tissues at least 2 cyclo-oxygenase isoenzymes with COX-1 and COX-2.
Orthopaedic Surgery
Baclofen inhibits monosynaptic and polysynaptic reflexes at the spinal level to decrease excitatory neurotransmitter.
Diazepam:
It reduces anxiety and muscle spasm by enhancing GABA.
Orthopaedic Surgery
Multiple separate procedures must be performed because no single procedure is suitable for every patient.
Without the need for an arthrodesis, the deformity can be corrected by tendon transfers and osteotomies.
Methods for fully resecting the plantar fascia and removing the fascia from the calcaneus have been documented.
The EHL and the extensor digitorum longus (EDL) are moved to the first, third, and fifth metatarsals as part of the extensor shift technique.
Orthopaedic Surgery
The initial management phase is suitable for mild or early-stage cases.
The progressive intervention phase is for patients with worsening deformity or unrelieved symptoms.
In supportive care and management phase, patients should receive required attention such as lifestyle modification and surgical interventional procedures.
The regular follow-up visits with the orthopedist are scheduled to check the improvement of patients along with treatment response.

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