Mr. Chris Lodge Consultant Orthopaedic Surgeon ยท York
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Surgical Options

Total Hip Replacement

Total hip replacement is one of the most reliably successful operations in all of surgery โ€” transforming the lives of patients whose hip pain and disability can no longer be adequately managed without surgical intervention. This page explains everything you need to know about the procedure, from the components used to the surgical approach and potential risks.

~90,000
THRs performed in the UK each year
1.2M+
Procedures recorded in the NJR since 2003
~68
Average patient age at surgery
20+
Years longevity expected from modern implants

What is Total Hip Replacement?

Total hip replacement (THR) โ€” also known as total hip arthroplasty โ€” is a surgical procedure in which the damaged surfaces of the hip joint are removed and replaced with precisely engineered artificial components, creating a new, smooth, pain-free bearing surface. It is among the most commonly performed and most successful elective surgical procedures worldwide.

Approximately 90,000 total hip replacements are performed in the UK each year. The National Joint Registry (NJR), active since 2003, now holds data on over 1.2 million hip replacements performed in the UK โ€” making it one of the most comprehensively monitored surgical procedures anywhere in the world. Mr. Lodge performs total hip replacement at York Teaching Hospital (NHS) and at Nuffield Health York Hospital and Ramsay Clifton Park Hospital (private), serving patients from across North Yorkshire, West Yorkshire and East Yorkshire. He is a registered NJR surgeon, and data on outcomes from his patients is routinely submitted and monitored to ensure the highest standards are maintained.

The average age of patients undergoing hip replacement in the UK is around 68, though this should not imply that younger patients are not appropriate candidates. Age alone is not a significant limitation to surgery โ€” the decision is based on the severity of symptoms, functional limitation and overall health. Younger patients often benefit enormously from hip replacement and, with modern implants and bearing surfaces, can expect excellent longevity from their reconstruction.

Results from Mr. Lodge's practice, including revision rates from his primary hip surgery, are recorded within the NJR database. Patient-reported outcome measures (PROMs) are collected routinely before and after surgery to monitor how patients progress and ensure care is continuously evidence-based.

How the Operation Works

Total hip replacement involves the surgical removal of the damaged arthritic surfaces of the hip joint and their replacement with carefully selected implant components. The result is a new, artificial ball-and-socket joint โ€” made from combinations of metal, ceramic and plastic โ€” that recreates smooth, pain-free movement.

The operation begins with the surgeon dividing the neck of the femur (thigh bone) to remove the worn femoral head โ€” the ball of the natural hip joint. This allows access to both the socket (the acetabulum, in the pelvis) and the femoral canal (the hollow centre of the thigh bone). The damaged articular cartilage lining the socket is then removed, and a new metal acetabular cup is implanted into the pelvis. A liner โ€” made of ceramic or highly cross-linked polyethylene โ€” is locked or cemented into this cup.

A metal stem is then carefully sized and introduced into the femoral canal and secured in position, either with bone cement or by relying on the bone growing directly onto the implant surface (uncemented fixation). A ceramic or metal femoral head is then attached to the top of the stem. When the hip is reduced โ€” the ball placed back into the socket โ€” the new artificial bearing is created.

All options โ€” from fixation method to bearing surface to head size โ€” are tailored specifically to each patient's anatomy, age, bone quality, activity level and clinical circumstances. These decisions are discussed with you in advance of surgery so that you fully understand the plan for your individual reconstruction.

Pencil illustration of the acetabular cup showing the porous outer surface (left) and the smooth inner socket (right)

Acetabular Cup

A metal shell (usually titanium) pressed or cemented into the pelvic socket, which accepts a liner to form the bearing surface. The porous outer surface allows bone ingrowth for biological fixation. Positioned at a precise angle to optimise stability and movement.

Pencil illustration of the highly cross-linked polyethylene acetabular liner

Acetabular Liner

Sits inside the metal cup and forms the bearing surface against the femoral head. Made from highly cross-linked polyethylene or ceramic. The liner material determines the wear characteristics and longevity of the reconstruction.

Pencil illustration of the uncemented femoral stem showing the tapered body and fluted distal tip

Femoral Stem

A metal stem (titanium or cobalt-chrome) inserted into the femoral canal. May be fixed with cement or rely on bone ingrowth for biological fixation. Carefully sized to restore correct hip biomechanics and leg length.

Pencil illustration of a ceramic femoral head component

Femoral Head

The artificial ball โ€” made from ceramic or cobalt-chrome metal โ€” that attaches to the Morse taper of the femoral stem and articulates against the acetabular liner. Head size is selected to optimise stability and reduce dislocation risk.

How Are Implants Fixed to Bone?

There are two fundamental principles by which hip implants are secured to bone: cemented fixation and uncemented fixation. Both are well-established techniques with excellent long-term results, and the choice between them depends on a number of patient-specific factors.

In some patients, a hybrid fixation is used โ€” where one component is cemented and the other is uncemented. For example, a cemented femoral stem combined with an uncemented acetabular cup is a commonly used and well-evidenced combination. The right approach for each patient is selected on an individual basis and discussed fully before surgery.

Cemented Fixation

Acrylic bone cement used as a grout

  • Acrylic bone cement is pressurised into the bone before the implant is introduced, securing it firmly as the cement hardens
  • Provides immediate, strong fixation โ€” allowing full weight-bearing from the day of surgery in most cases
  • Particularly suitable for older patients or those with softer, more osteoporotic bone
  • The gold standard for femoral fixation in the UK for many decades, with outstanding long-term evidence
  • Cemented stems have among the lowest revision rates in the NJR, particularly in older patients

Uncemented Fixation

Bone grows onto or into the implant surface

  • The implant surface is coated or textured to encourage the patient's own bone to grow onto or into it, achieving biological fixation
  • A "press-fit" technique is used โ€” the implant is slightly larger than the prepared bone cavity, creating immediate mechanical stability while biological fixation develops
  • More commonly used in younger patients with good bone quality and density
  • Allows use of harder bearing surfaces, including ceramic-on-ceramic combinations
  • Produces a more dynamic, physiological bond between implant and skeleton over time

Preserving Bone for the Future

A fundamental principle of Mr. Lodge's approach to hip replacement is preserving bone stock for the future. It is important that any implant placed at a primary hip procedure should be as "revisable" as possible โ€” ideally to a primary-type component โ€” should revision become necessary later in life. This consideration informs the choice of fixation method and implant design for every patient.

Bearing Surface Options

The bearing surface is the articulating interface between the femoral head and the acetabular liner โ€” in effect, the moving part of the hip replacement. The choice of bearing surface is one of the most important decisions in hip replacement surgery, as it directly influences wear, longevity and the risk of complications over time.

Pencil illustration showing the acetabular bearing components of a total hip replacement in exploded view: the porous-coated metal shell at top, the polyethylene liner in the middle, and two femoral head options below โ€” cobalt-chrome metal on the left and ceramic on the right

The bearing components: metal acetabular shell (top), polyethylene liner (middle), and the femoral head options โ€” cobalt-chrome metal (bottom left) and ceramic (bottom right). The combination of liner and head material determines the bearing surface type.

The ideal bearing surface produces minimal wear debris, is biocompatible with the surrounding tissues, allows a large head size to be used, and performs reliably for many decades. The options available today represent significant advances over those used in earlier generations of hip replacement.

Ceramic-on-Highly Cross-linked Polyethylene

Mr. Lodge's default bearing combination. A ceramic femoral head articulates against a third-generation highly cross-linked polyethylene (HXLPE) liner. This pairing combines the superior surface hardness and scratch-resistance of ceramic with the outstanding wear performance of modern polyethylene โ€” delivering a bearing that is both durable and biocompatible.

Recent independent research comparing second- and third-generation cross-linked polyethylene liners in primary total hip arthroplasty has demonstrated linear wear rates in third-generation liners of 0.0172 mm/year at mean ten-year follow-up โ€” rates so low as to be virtually undetectable on routine X-ray. This represents a dramatic improvement over conventional polyethylene and supports the long-term durability of ceramic-on-HXLPE as a reliable, evidence-based bearing choice for the majority of patients.

Mr. Lodge's default bearing
Research Reference

Blackburn CW et al. In Vivo Wear Analysis of Third- versus Second-Generation Moderately Crosslinked Polyethylene Liners in Total Hip Arthroplasty. The Journal of Arthroplasty. 2025. pii: S0883-5403(25)01039-3.

View paper on ScienceDirect โ†’

Dual Mobility โ€” A Specialist Option for High-Risk Patients

For the majority of patients, ceramic-on-highly cross-linked polyethylene provides an excellent and reliable bearing choice. However, in a specific group of patients where the risk of dislocation is significantly elevated, Mr. Lodge may recommend a dual mobility (DM) construct in place of a conventional bearing.

A dual mobility cup works on the principle of two independent articulations: a small ceramic or metal femoral head moves within a large polyethylene mobile liner, which itself moves within the outer metal acetabular shell. This "ball within a ball" design effectively creates a much larger functional femoral head diameter than would otherwise be possible โ€” dramatically increasing the arc of movement required before the head can lever out of the socket and dislocate. Reported dislocation rates with dual mobility articulations in appropriately selected patients range from 0% to 1.1%, even in those at high risk.

Pencil illustration of a dual mobility hip cup showing the large polyethylene mobile liner on the left and the porous-coated outer metal acetabular shell on the right

The dual mobility construct: the large polyethylene mobile liner (left) sits within the porous-coated metal acetabular shell (right). The femoral head articulates within the liner, creating two independent bearing surfaces and a much larger effective head diameter.

Understanding Spinopelvic Mobility โ€” and Why It Matters

The relationship between the spine, pelvis and hip is fundamental to the success of hip replacement surgery. In a normal individual, the pelvis tilts dynamically as a person moves between standing and sitting โ€” rotating posteriorly (tilting backwards) when sitting down. This pelvic movement adjusts the functional orientation of the acetabular cup as the body position changes, helping to maintain stability of the hip throughout its range of movement.

In patients with a stiff lumbar spine โ€” whether due to spinal fusion, severe degenerative disc disease, prior spinal surgery, or significant spinal deformity โ€” this normal compensatory pelvic movement is reduced or lost. The pelvis is unable to tilt as required, and the acetabular cup effectively sits in a functionally different position depending on whether the patient is standing or sitting. A cup position that provides adequate cover in standing may produce relative uncovering โ€” and therefore instability โ€” in sitting, and vice versa. This creates a significantly elevated risk of dislocation that cannot be fully corrected simply by altering the surgical technique or cup positioning.

This combination of impaired spinal and pelvic movement is referred to as adverse spinopelvic mobility (SPM). A large posterior standing pelvic tilt and severe sagittal spinal deformity are also independently recognised risk factors for hip instability after joint replacement. Crucially, adverse spinopelvic mechanics can exist in patients who have no overt back symptoms โ€” making pre-operative assessment of spinal and pelvic parameters an important part of surgical planning for hip replacement in appropriate patients.

Pencil illustration showing two lateral views of the lumbopelvic region: Panel A showing normal spinopelvic mobility with the sacral slope (SS) in standing, and Panel B showing a stiff spine with altered pelvic tilt and retroversion of the acetabulum in the seated position

Spinopelvic mobility: Panel A (standing) shows normal lumbar lordosis and sacral slope (SS). Panel B (seated/flexed) illustrates how a stiff lumbar spine limits the pelvis from tilting backward, causing the acetabulum to face upward and backward โ€” increasing the risk of impingement and dislocation of the hip replacement.

A 2022 study published in The Bone & Joint Journal (Yates et al.) evaluated modular dual mobility articulations specifically in patients with adverse spinopelvic mobility undergoing primary total hip arthroplasty. In a cohort where one or more factors associated with adverse spinopelvic mobility were present, the dual mobility bearing conferred excellent stability โ€” with no revisions for dislocation reported at two-year follow-up, and a Kaplan-Meier survival rate of 99.1%. The authors concluded that dual mobility bearings confer stability in this high-risk group and represent a reliable solution for patients in whom conventional bearing surfaces carry an unacceptably elevated dislocation risk.

Research Reference

Yates PJ et al. Modular dual-mobility articulations in patients with adverse spinopelvic mobility. The Bone & Joint Journal. 2022;104-B(7):820โ€“825.

View on PubMed (PMID 35775170) โ†’

Beyond spinopelvic stiffness, dual mobility constructs are also considered in other patient groups where dislocation risk is elevated for different reasons. These include patients with neurological disorders โ€” such as Parkinson's disease or a history of stroke โ€” where altered muscle tone, coordination and proprioception impair the body's ability to protect the hip joint during movement. In these groups, the inherent mechanical stability provided by the dual mobility design compensates for the reduced muscular and neuromuscular protection that would otherwise guard against dislocation.

Dual mobility is not a default bearing for all patients. It is a targeted solution for those in whom the risk of dislocation with a standard bearing is meaningfully elevated. The decision to use a dual mobility construct is made on an individual basis following careful pre-operative assessment, including review of spinal history, imaging and neurological status, and will be discussed fully with you before surgery.

The Importance of Head Size โ€” Optimising Stability Without Compromising Wear

The diameter of the femoral head component has a direct and well-evidenced influence on the stability of a hip replacement. A larger head increases what is known as the "jump distance" โ€” the distance the femoral head must travel before it can lever out of the socket โ€” and provides a wider impingement-free range of movement. Both of these effects translate into a meaningfully lower risk of dislocation.

Where anatomy and implant sizing permit, Mr. Lodge's approach is to use as large a femoral head as possible. In practice, this most commonly means a 36 mm ceramic head โ€” the size at which the evidence most clearly demonstrates a benefit in terms of dislocation risk reduction, and for which the wear data with modern highly cross-linked polyethylene is particularly reassuring.

Key Evidence: Wear Rates Are Not Compromised by Using a 36 mm Head

A prospective study by Matharu et al. โ€” published in The Bone & Joint Journal (2015, PMID 26530647) โ€” measured femoral head penetration using validated radiographic edge-detection software (PolyWare Auto) in a cohort of 100 total hip arthroplasties using a 36 mm ceramic head against a third-generation highly cross-linked polyethylene (X3) liner, in patients with a mean age of 59 years at a mean follow-up of 5.08 years.

The steady-state linear wear rate was found to be 0.003 mm per year โ€” a figure so small as to be clinically and radiographically undetectable. No case of osteolysis was identified, and all patients demonstrated significant improvement in functional scores. The authors concluded that the combination of a 36 mm ceramic head with a highly cross-linked polyethylene liner produces wear rates that are negligible in clinical terms, and that this bearing combination can be used with confidence in active patients, including those of relatively young age.

Critically, these wear rates are comparable to โ€” and in some datasets indistinguishable from โ€” those seen with smaller 32 mm heads against the same liner material. The concern that using a larger head would accelerate polyethylene wear, which was a legitimate worry with earlier generations of conventional polyethylene, does not apply to modern highly cross-linked polyethylene in the same way. Wear is not compromised; stability is optimised.

Research Reference

Matharu GS, Mansour R, Morton J, Pynsent PB, Dunlop DJ. The rates of wear of X3 highly cross-linked polyethylene at five years when coupled with a 36 mm diameter ceramic femoral head in young patients. The Bone & Joint Journal. 2015;97-B(11):1470โ€“1474.

View on PubMed (PMID 26530647) โ†’

It is important to note that there are practical limits to head size โ€” dictated by the diameter of the acetabular component that can be implanted given each patient's individual anatomy. Not every patient can accommodate a 36 mm head, and in smaller acetabular components a 32 mm head may be required. Where this is the case, wear performance with modern polyethylene remains excellent regardless. The goal is always to use the largest head that can be safely implanted within a correctly sized and positioned socket โ€” maximising stability without compromising fixation or liner integrity.

Heads larger than 36 mm (โ‰ฅ40 mm) are not routinely used in Mr. Lodge's standard primary hip replacement practice. Registry data have shown that very large heads do not confer additional dislocation benefit over 36 mm, and may carry a modestly increased risk of infection and all-cause revision โ€” likely related to the larger surgical exposure required and taper mechanics. Beyond 36 mm, bigger is not consistently better.

The Surgical Approach

The "surgical approach" refers to the route taken to access the hip joint during the operation โ€” that is, which muscles and soft tissues are divided or moved aside to allow the surgeon to see and work on the joint. The choice of approach influences the recovery experience, dislocation risk and the scope of surgery that can be safely performed.

Over the years, several different approaches have been developed and refined, each with their own advantages and proponents. The fundamental requirement of any approach is to provide adequate visualisation of both the acetabulum and the femur, whilst minimising damage to the surrounding muscles, nerves and blood vessels.

The Posterior Approach

Mr. Lodge's practice is based on the posterior approach to the hip โ€” an approach he has used extensively throughout his surgical career and which he considers to be the safest, most reliable and most versatile technique available.

In the posterior approach, the hip is accessed from the back of the buttock. The skin and overlying fascia are divided, and the muscles are carefully split โ€” rather than cut through โ€” to gain access to the posterior hip capsule. The short external rotator muscles are released along with the posterior capsule to expose the hip joint, creating a protective flap that also shields the sciatic nerve during the procedure. This provides excellent circumferential visualisation of the acetabulum and safe access to the femur.

One of the key advantages of the posterior approach is that the hip abductor muscles โ€” the muscles responsible for stabilising the pelvis during walking โ€” are not significantly involved in the exposure. The nerve supply to these muscles is preserved, which means that a limp following this approach is uncommon. The posterior capsule and short external rotators are carefully repaired and reattached at the end of surgery, restoring the soft tissue envelope and reducing the risk of dislocation.

A minimally invasive technique: Where patient anatomy allows, Mr. Lodge uses a reduced "mini" posterior approach โ€” achieving the same surgical access through a smaller incision with less soft tissue disruption, contributing to faster recovery and less post-operative pain. In more complex cases, the incision is extended as needed, but the fundamental approach remains the same.

What About Other Approaches?

The direct anterior approach (DAA) has gained increasing popularity in some centres, particularly in continental Europe and North America, where proponents argue it is a more "muscle-sparing" technique.

The clinical evidence to date has not demonstrated a clear or consistent advantage of the anterior approach over a well-performed posterior approach in terms of functional outcomes, dislocation rates or long-term results. Equally, the anterior approach does have its own learning curve and specific complications. Given Mr Lodgeโ€™s experience and outcome results using the posterior approach โ€” across primary and revision cases โ€” he continues to base his practice on the approach he knows best and has demonstrated the most reliable results with.

Mr. Lodge is always happy to discuss surgical approach in detail at consultation, including what to expect from the recovery and what the scar will look like.

What Are the Risks?

Total hip replacement is one of the most reliably successful procedures in modern surgery. The vast majority of patients experience excellent outcomes with no significant complications. That said, as with any major operation, it is important that you understand the risks involved before giving your consent to proceed.

The potential complications listed below are uncommon, but they are significant enough to warrant careful discussion. All of these will be covered in detail at your pre-operative consent appointment, and you are encouraged to raise any specific concerns at that stage.

Infection

0.25โ€“0.5% rate

Infection is the most serious potential complication following joint replacement surgery. Extensive precautions are taken throughout โ€” including prophylactic antibiotics, laminar flow theatre conditions, an alcoholic skin preparation and sterile occlusive draping โ€” to reduce this risk to a minimum. Superficial wound infections may resolve with antibiotic treatment. Deep infection involving the joint replacement itself is a more serious concern and can occasionally necessitate further surgery. Late infection can also occur โ€” typically triggered by an infection elsewhere in the body, such as a dental, urinary or chest infection โ€” emphasising the importance of treating infections promptly and informing your surgeon if you develop any infection in the future.

Dislocation

<2% in primary THR

Dislocation occurs when the femoral head becomes dislodged from the acetabular socket. It can be a painful and distressing complication. The risk is reduced by careful implant selection and positioning, soft tissue balancing, use of a larger femoral head and meticulous repair of the posterior capsule at the end of the procedure. Patients are given specific guidance on movements to avoid during the early recovery period โ€” particularly deep hip flexion combined with internal rotation โ€” to minimise this risk. The dislocation rate within Mr. Lodge's practice is considerably lower than the published average.

Blood Clots (DVT / Pulmonary Embolus)

Reduced with prophylaxis

Deep venous thrombosis (DVT) โ€” clots in the leg veins โ€” and pulmonary embolus (PE) โ€” clots travelling to the lungs โ€” are recognised risks following hip surgery. To reduce this risk, Mr. Lodge uses regional anaesthetic techniques, mobilises patients as early as possible after surgery, prescribes low molecular weight heparin (LMWH) injections for four weeks after the operation, and asks patients to wear thromboembolic deterrent (TED) stockings. Early symptoms of a DVT include leg swelling, redness and warmth that does not settle with elevation overnight. Any such symptoms should be reported promptly.

Nerve Injury

Rare; usually temporary

The sciatic nerve lies close to the posterior hip and is the nerve most at risk during hip replacement surgery. Injury to the common peroneal branch of the sciatic nerve can cause weakness in lifting the foot (foot drop) and numbness in parts of the lower leg and foot. The majority of cases are temporary and resolve over weeks to months. Permanent nerve injury is rare. The femoral nerve can also occasionally be affected, causing weakness in straightening the knee. Nerve injury is more common in complex or revision surgery, and any specific increased risk will be discussed in advance.

Leg Length Difference, Bleeding & Fracture

Uncommon

A very slight difference in leg length is a recognised consequence of hip replacement. Mr. Lodge uses scaled pre-operative X-ray planning and computer-based templating to minimise this risk. Many patients' legs are slightly shortened by the arthritis prior to surgery, and a sensation of the leg feeling slightly longer after the operation is common โ€” this usually settles as the body adapts. Clinically troublesome leg length inequality is uncommon. Intra-operative fracture of the femur is rare, occurring most often with uncemented fixation; where this does occur, it is addressed at the time of surgery. Significant bleeding requiring transfusion is also uncommon in routine primary hip replacement.

Implant Wear & Loosening

Long-term consideration

Over time, wear occurs in any bearing surface as the components articulate against each other. The biological response to wear debris can cause damage to the surrounding bone โ€” a process called osteolysis โ€” which can lead to implant loosening, requiring revision surgery. Modern bearing surfaces, particularly ceramic-on-ceramic and highly cross-linked polyethylene, have dramatically reduced wear rates compared to earlier generations of hip replacement. Regular long-term follow-up allows early detection of any signs of loosening before significant bone loss occurs.

Overall perspective: In a straightforward primary hip replacement in a patient without significant complexity, the overall chance of experiencing a major complication of the types listed above is in the region of 1โ€“1.5%. Expressed differently, the chance of undergoing surgery without any of these concerns is approximately 98.5โ€“99%. Hip replacement is a highly successful procedure and should not be approached with undue concern โ€” but informed consent requires that these risks are understood and discussed.

What Results Can You Expect?

The results of total hip replacement are extremely reliable. The procedure has one of the highest patient satisfaction rates of any elective surgical procedure, with the overwhelming majority of patients experiencing dramatic improvements in pain, function and quality of life.

Following total hip replacement, patients typically experience a significant and often rapid reduction in pain โ€” frequently within days of surgery. Over the weeks and months that follow, as healing progresses and the surrounding muscles recover, function continues to improve. Most patients are walking freely, with good range of movement and without significant pain, within six to twelve weeks of their operation.

Modern implants, particularly those using ceramic bearing surfaces, are expected to last well beyond twenty years in the majority of patients. Younger, more active patients may eventually require a revision procedure during their lifetime, but with careful implant selection and technique โ€” particularly with regard to bone preservation โ€” revision surgery can usually be performed with a primary-type implant when the time comes.

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