in patients with bone metastases

Similar documents
Radiology. General radiology department. X-ray

Evaluation of prognostic scoring systems for bone metastases using single center data

Metastatic Spinal Disease

Recognition & Treatment of Malignant Spinal Cord Compression Study Day

Hybrid bone scintigraphy in gastrointestinal malignancies Institutional Experience

1 Introduction. 2 Materials and methods. LI Na 1 LI Yaming 1,* YANG Chunming 2 LI Xuena 1 YIN Yafu 1 ZHOU Jiumao 1

Louisa Fleure. Advanced Prostate Cancer Clinical Nurse Specialist. Guys and St Thomas NHS Trust

Faster Cancer Treatment Indicators: Use cases

Oncologic Emergencies: When to call the Radiation Oncologist

Louisa Fleure. Advanced Prostate Cancer Clinical Nurse Specialist. Guys and St Thomas NHS Trust

Case Report Treatment of Renal Cell Carcinoma with 2-Stage Total en bloc Spondylectomy after Marked Response to Molecular Target Drugs

The management and treatment options for secondary bone disease. Dr Jason Lester Clinical Oncologist Velindre Cancer Centre

Cancer of Unknown Primary (CUP) Protocol

Spinal cord compression as a first presentation of cancer: A case report

Radiotherapy for Patients with Symptomatic Intramedullary Spinal Cord Metastasis

CoRIPS Research Award 089. Beverley Atherton

Radiotherapy symptoms control in bone mets. Francesco Cellini GemelliART. Ernesto Maranzano,MD. Session 5: Symptoms management

Radiology. Undergraduate Radiology Curriculum

Radiological staging of lung cancer. Shukri Loutfi,MD,FRCR Consultant Thoracic Radiologist KAMC-Riyadh

RADIOLOGY (MEDICAL IMAGING)

The management and treatment options for secondary bone disease. Omi Parikh July 2013

Radiotherapy for lymphoma

PATHWAY MANAGEMENT OF METASTATIC SPINAL CORD COMPRESSION (MSCC) THE CHRISTIE, GREATER MANCHESTER & CHESHIRE

Management of a Solitary Bone Metastasis to the Tibia from Colorectal Cancer

Malignant Spinal cord Compression. Dr. Thiru Thirukkumaran Palliative Care Services - Northwest Tasmania

MUSCLE-INVASIVE AND METASTATIC BLADDER CANCER

A Guide to Ewing Sarcoma

PATHWAY FOR INVESTIGATION OF ADULTS PRESENTING WITH ASCITES. U/S Abdo/pelvis shows ascites without obvious evidence of 1 liver disease

Suspecting Tumors, or Could it be cancer?

A PATIENT WITH TWO EPISODES OF THORACIC SPINAL CORD COMPRESSION CAUSED BY PRIMARY LYMPHOMA AND METASTATIC CARCINOMA OF THE PROSTATE, 11 YEARS APART

CP80 Version: V01. Acute Oncology Management Service Date approved: 8 th May 2015 Date ratified: 1 st June 2015 Review date: 1 st June 2017

Lung Cancer Requirements

MUSCLE - INVASIVE AND METASTATIC BLADDER CANCER

Prof. Dr. NAGUI M. ABDELWAHAB,M.D.; MARYSE Y. AWADALLAH, M.D. AYA M. BASSAM, Ms.C.

bone HEALTH IN FOCUS UNDERSTANDING THE IMPORTANCE OF BONE HEALTH WHEN LIVING WITH METASTATIC BREAST CANCER

Update on Management of Malignant Spinal Cord Compression. Heino Hugel Consultant in Palliative Medicine University Hospital Aintree

Impact of pre-treatment symptoms on survival after palliative radiotherapy An improved model to predict prognosis?

APPROPRIATE USE GUIDELINES

Localized Prostate Cancer Have we finally got it right? Shingai Mutambirwa Professor & Chair-Division Urology DGMAH & SMU Pretoria SOUTH AFRICA

DEPARTMENT OF ONCOLOGY ELECTIVE

North of Scotland Cancer Network Clinical Management Guideline for Metastatic Malignancy of Undefined Primary Origin (MUO)

Osteopoikilosis: A Sign Mimicking Skeletal Metastases in a Cancer Patient

Bone metastases of solid tumors Diagnosis and management by

Imaging Of The Pelvis

PET-MRI in malignant bone tumours. Lars Stegger Department of Nuclear Medicine University Hospital Münster, Germany

MSCC CARE PATHWAYS & CASE STUDIES. By Michael Balloch Spine CNS

Bone Metastases. Sukanda Denjanta, M.Sc., BCOP Pharmacy Department, Chiangrai Prachanukroh Hospital

SPECIFIC AIMS PROGRAM IMAGING. V year (1st semester) Scientific Field DIAGNOSTIC IMAGING AND RADIOTHERAPY TUTOR ECTS

Definition Prostate cancer

GUIDELINES FOR RADIOTHERAPY IN SPINAL CORD COMPRESSION THE CHRISTIE, GREATER MANCHESTER & CHESHIRE. Version:

Brain Tumors. What is a brain tumor?

Are extra-colonic findings on CT colonogram clinically significant? A review of 758 consecutive cases

Diagnosis and Classification of Prostate Cancer

Unknown Primary Service for patients at Chesterfield Royal Hospital

Bone PET/MRI : Diagnostic yield in bone metastases and malignant primitive bone tumors

DRAFT FOR CONSULTATION. Clinical Commissioning Policy Proposition: Palliative radiotherapy for bone pain

General Surgery Curriculum Royal Australasian College of Surgeons, General Surgeons Australia & New Zealand Association of General Surgeons

expectancy Cancer spread to bones life expectancy

Metastatic Spinal Cord Compression (MSCC) Clinical guidelines and pathway

Identification of the Risk Factors of Bone Metastatic among Breast Cancer Women in Al-Bashir Hospital

Challenges in the Diagnosis of bone Metastasis in Patients without a History of Malignancy at Their First Clinic Visit

Cancer of Unknown Primary Service

Clinical Case Conference

6 UROLOGICAL CANCERS. 6.1 Key Points

Case Conference: SBRT for spinal metastases D A N I E L S I M P S O N M D 3 / 2 7 / 1 2

Clinical Trial Results Database Page 1

Index. Surg Oncol Clin N Am 16 (2007) Note: Page numbers of article titles are in boldface type.

Metastatic Disease of the Proximal Femur

Current Management of Metastatic Bone Disease

SELF-ASSESSMENT MODULE REFERENCE SPR 2018 Oncologic Imaging Course Adrenal Tumors November 10, :00 12:10 p.m.

Spine MRI and Spine CT Test Request Tip Sheet

Course specification

Managing Bone Pain in Metastatic Disease. Rachel Schacht PA-C Medical Oncology and Hematology Associates Presented on 11/2/2018

Clinical indications for positron emission tomography

Breast Cancer. What is breast cancer?

Denominator Criteria (Eligible Cases): Patient encounter during the performance period (CPT): 78300, 78305, 78306, 78315, 78320

Cancers of unknown primary : Knowing the unknown. Prof. Ahmed Hossain Professor of Medicine SSMC

Questions and Answers About Breast Cancer, Bone Metastases, & Treatment-Related Bone Loss. A Publication of The Bone and Cancer Foundation

1/3/2008. Karen Burke Priscilla LeMone Elaine Mohn-Brown. Medical-Surgical Nursing Care, 2e Karen Burke, Priscilla LeMone, and Elaine Mohn-Brown

Clinical Study Primary Malignant Tumours of Bone Following Previous Malignancy

Doppler ultrasound of the abdomen and pelvis, and color Doppler

Second Single 4 Gy Reirradiation for Painful Bone Metastasis

MANAGEMENT OF PATIENTS WITH METASTATIC SPINAL CORD COMPRESSION

Breast Cancer. What is breast cancer?

National Imaging Associates, Inc. Clinical guidelines

Brain and Central Nervous System Cancers

Recognition & Treatment of Malignant Spinal Cord Compression Study Day

Recommendations for cross-sectional imaging in cancer management, Second edition

Review of Clinical Manifestations of Biochemicallyadvanced Prostate Cancer Cases

PREAMBLE GENERAL DIAGNOSTIC RADIOLOGY

Spine MRI and Spine CT Test Request Tip Sheet

Glossary of Terms Primary Urethral Cancer

Spine MRI and Spine CT Test Request Tip Sheet

Somerset, Wiltshire, Avon and Gloucestershire (SWAG) Cancer Services. Cancer of Unknown Primary Network Site Specific Group. Clinical Guidelines

Medical Diagnostic Imaging

Spine MRI and Spine CT Test Request Tip Sheet

ORIGINAL ARTICLE ABSTRACT

Radiation Therapy for Prostate Cancer

A prediction model of survival for patients with bone metastasis from uterine corpus cancer

Transcription:

Brazilian Treatment Journal delay of and Medical radiological and Biological errors Research (2003) 36: 1419-1424 ISSN 0100-879X 1419 Treatment delay and radiological errors in patients with bone metastases K. Ichinohe 1, M. Takahashi 2 and N. Tooyama 3 Departments of 1 Radiotherapy and 2 Radiology, Fukuroi Municipal Hospital, Fukuroi, Shizuoka, Japan 3 Department of Radiology, Seirei Hospital, Hamamatsu, Shizuoka, Japan Correspondence K. Ichinohe Department of Radiotherapy Fukuroi Municipal Hospital 2515-1 Kunou Fukuroi, Shizuoka Japan Fax: +81-538-43-2511 Received September 20, 2002 Accepted August 19, 2003 Abstract During routine investigations, we are surprised to find that therapy for bone metastases is sometimes delayed for a considerable period of time. To determine the extent of this delay and its causes, we reviewed the medical records of symptomatic patients seen at our hospital who had been recently diagnosed as having bone metastases for the last four years. The treatment delay was defined as the interval between presentation with symptoms and definitive treatment for bone metastases. The diagnostic delay was defined as the interval between presentation with symptoms and diagnosis of bone metastases. The results of diagnostic radiological examinations were also reviewed for errors. The study population included 76 males and 34 females with a median age of 66 years. Most bone metastases were diagnosed radiologically. Over 75% of patients were treated with radiotherapy. The treatment delay ranged from 2 to 307 days, with a mean of 53.3 days. In 490 radiological studies reviewed, we identified 166 (33.9%) errors concerning 62 (56.4%) patients. The diagnostic delay was significantly longer for patients with radiological errors than for patients without radiological errors (P < 0.001), and much of it was due to radiological errors. In conclusion, the treatment delay in patients with symptomatic bone metastases was much longer than expected, and much of it was caused by radiological errors. Considerable efforts should therefore be made to more carefully examine the radiological studies in order to ensure prompt treatment of bone metastases. Key words Bone metastases Delay Radiology Error Radiotherapy Introduction The prognosis of patients with bone metastases is generally poor (1), but several treatment methods have been proposed to improve their quality of life (1-3). Patients complaining of symptoms attributable to bone metastases should therefore be treated as promptly as possible. During routine studies, we were surprised to find that therapy for bone metastases is sometimes delayed for a considerable period of time. Many investigators have studied the causes of delays in treating primary malignancies (4-10), but the reasons for delays in treating bone metastases have yet to be considered. Thus, the aim of this study was to determine the delay in treatment of bone metastases and the reasons for this delay.

1420 K. Ichinohe et al. Material and Methods Between May 1997 and August 2001, 214 symptomatic patients with bone metastases were registered in the radiation department of our hospital. Of these patients, 110 who first presented at our hospital and who had been recently diagnosed as having bone metastases were included in the study. The main presenting symptoms, the date of presentation to a physician, the date of diagnosis, the diagnostic methods used, the date of treatment, medications, and the treatment methods were obtained from the medical records of each patient. The quality of life of the patients was measured with the Karnofsky index of performance status (PS) at first presentation, at the time of diagnosis of bone metastases, during treatment, and at the time of maximum effect after treatment. The diagnostic delay was calculated as the interval between presentation to a physician with symptoms and diagnosis of bone metastases. The treatment delay was calculated as the interval between presentation to a physician with symptoms and initiation of definitive treatment for bone metastases. For the patients treated with radiotherapy, the interval between referral for irradiation and initiation of radiotherapy was calculated. The results of radiological work-ups for diagnosis were also reviewed, focusing on the images where primary cancer, bone metastases or associated findings had been misdiagnosed. The decision of misdiagnosis was based on the consensus of two radiologists (N. Tooyama and M. Takahashi) who were not aware of the patients histories or symptoms. According to the criteria of Kelvin et al. (11), radiological errors were classified as purely perceptive (lesions visible in retrospect), purely technical (lesions not seen in retrospect), interpretative (lesions observed at the time of study but malignancy not included in the differential diagnosis), and technical and perceptive (technical inadequacy contributing to perceptive error). The reasons for these delays were also evaluated. The Mann-Whitney test and the test for proportions were used to evaluate statistical significance. Results The study population included 76 males and 34 females, with a median age of 66 years (range 36-84 years) at presentation. The main presenting symptoms were back pain (N = 52), pain in the extremities (N = 20), thoracic pain (N = 14), pelvic pain (N = 10), muscle weakness (N = 6), numbness in the extremities (N = 4), and others (N = 4). The primary sites were the lung (N = 40), hepatobiliary system (N = 18), gastrointestinal tract (N = 18), prostate (N = 14), breast (N = 6), urinary tract (N = 4), others (N = 6), and unknown (N = 4). Diagnosis of bone metastases was confirmed by a bone biopsy (N = 6) or radiological examination (N = 104), including magnetic resonance imaging (N = 44). Thirtyeight patients had a single bone metastasis, while 72 had multiple bone metastases. Fortyfour patients had a single or multiple spinal metastasis. In 40 (36.4%) patients, symptoms of bone metastases were the first sign of malignancy. The remaining 70 patients were diagnosed as having bone metastases following treatment of their primary tumors. Treatments included radiotherapy (N = 94), orthopedic surgery (N = 6), systemic therapy with hormonal or cytotoxic agents (N = 6), and orchiectomy (N = 4). Eighty-eight patients were supported with analgesic agents (35 patients with nonsteroidal anti-inflammatory drugs, 25 with opioid drugs, 16 with a combination of the two types of drugs, and 12 with others). At presentation, analgesic agents had been prescribed to 74 patients, with 60 (81.1%) of them having presumptive diagnoses of degenerative or other benign diseases. The diagnostic and treatment delays for

Treatment delay and radiological errors 1421 each patient are shown in Table 1. The diagnostic delay was responsible for most of the treatment delay. Six patients were treated with radiotherapy after surgery. Overall, 100 patients were treated with radiotherapy and the interval between referral to the radiation department and initiation of radiotherapy ranged from 0 to 19 days, with a mean of 1.7 days. Six patients were irradiated urgently because of progressive neurological deficits. For the diagnosis of bone metastases, 490 radiological work-ups were performed with a mean of 4.5 radiological studies per patient. These studies consisted of plain radiography (N = 214), computed tomography (CT, N = 94), bone scintigraphy (N = 82), magnetic resonance imaging (N = 78), and other imaging studies (N = 22). Hospital radiologists examined 168 (34.3%) of the reports concerning these patients. These were CT (N = 46), bone scintigraphy (N = 60), magnetic resonance imaging (N = 58), and other imaging studies (N = 4). On reviewing all of these radiological studies, 166 (33.9%) errors were identified (plain radiography = 100; CT = 22; magnetic resonance imaging = 20; bone scintigraphy = 16; other = 8) concerning 62 (56.4%) patients. In 24 of these errors, a variety of primary tumors (lung cancer, colon cancer, rectal cancer, renal cell carcinoma, pancreatic cancer), and associated findings (paraaortic lymphadenopathy, malignant pleural effusion) were overlooked in 18 patients. Of 166 errors, 18 (10.8%) were the responsibility of hospital radiologists. Of all errors, 108 (65.0%) were purely perceptive, 44 (26.5%) were interpretative, eight (4.8%) were perceptive and technical, and six (3.6%) were purely technical. With respect to 70 patients with a history of malignant disease, 70 radiological errors were identified in 34 (48.6%) and 24 (34.3%) were purely perceptive. In one patient, radial bone metastasis was overlooked in a bone scintigraphy but a bone radiography performed on the same day revealed the metastasis. Another patient with severe back pain was first diagnosed as having a benign compression fracture of the thoracic spine on a chest X-ray, but a routine chest X-ray on admission revealed a lung tumor and he was correctly diagnosed as having a thoracic metastasis by CT of the chest on the same day. In a third patient, a lumbar metastasis was misinterpreted as degeneration by bone radiography, but an abdominal CT scan performed on the same day due to concomitant abdominal discomfort revealed the lumbar metastasis and colon cancer. The radiological errors concerning these three patients did not seem to have been responsible for the delayed diagnosis. All patients with radiological errors except these three were subsequently required to undergo observation with or without analgesics until the correct diagnosis had been made. Table 1 shows that the diagnostic delay in patients with radiological errors was much longer than that in those without, and that much of the diagnostic delay was due to the radiological errors. A decrease in PS of 10% or more oc- Table 1. Treatment delay and its causes (N = 110). Range (days) Mean (days) [%] Diagnostic delay (a) 0-307 39.0 [73.2] with radiological error (N = 62) 2-307 54.2* + without radiological error (N = 48) 0-69 19.4* Interval between diagnosis and treatment (b) 0-77 14.3 [26.8] Treatment delay (a + b) 2-307 53.3 [100] *The mean diagnostic delay with radiological error was about 2.8 times longer than the delay without radiological error (P < 0.001, Mann-Whitney test). + Once a patient was misdiagnosed by radiology, he had to wait an average of 46.2 more days until correct radiological examinations were performed (two were doublechecked and correctly diagnosed by a radiologist 1 and 5 days later). These intervals comprised 85.2% of the mean diagnostic delay with radiological errors, and 66.8% of the mean diagnostic delay of all patients. During these intervals, two patients refused further diagnostic work-ups for 7 and 44 days. Further radiological work-ups for two patients were postponed for 49 and 118 days because of previous treatment for complications (malignant pleural effusion and renal failure). The delays in these four patients made up 6.5% of the mean diagnostic delay.

1422 K. Ichinohe et al. curred significantly more frequently in patients with radiological errors than in patients without radiological error (33/62 = 53.2% vs 15/48 = 31.3%, P = 0.02) between presentation and diagnosis. Especially in 18 patients with local pain, radiological errors caused progression of symptoms; 12 of these patients were totally paralytic, and six immobile because of pathologic fracture of the pelvis or the femur at correct diagnosis. After treatment, a 10% or higher increase of PS in patients with and without radiological errors was obtained in 70% and in 77% of the patients, respectively (P = 0.47). Discussion The treatment delay in symptomatic patients with bone metastases was found to range from 2 to 307 days with a mean of 53.3 days. Nearly three quarters (73.2%) of the treatment delay was due to diagnostic delay (Table 1). Although we could not find any previous reports of treatment delay for bone metastases in the literature, the delay in our patients was much longer than we would have expected. Radiological errors occurred frequently in our study. About one third (33.9%) of the radiological studies for diagnostic work-ups were misdiagnosed and these errors were identified in 54.6% of our patients. As also reported in previous studies (5,10,11), these radiological errors caused long delays in diagnosis (Table 1). Furthermore, these errors often reduced the quality of life of our patients. In the present study, the symptoms of 18 patients who had first presented with only local pain had progressed to spinal paralysis or pathological fracture at diagnosis owing to radiological errors. It was disappointing that as many as 42.2% of all radiological errors were identified in 48.6% of patients with a history of malignant disease, and that over one third (34.3%) of these errors were purely perceptive. Since radiology is an important tool for evaluating patients with bone metastases (12,13), it is clear that radiological studies should be conducted more carefully. We regret that in Japan radiologists do not interpret all radiological studies. In the present study, radiologists interpreted only 34.3% of radiological work-ups. To decrease errors, we believe radiologists should be involved more in radiological studies. The effect of delay due to radiological errors on the PS of the patients was evident in this study. Between presentation and diagnosis, PS for the patients with radiological errors had decreased more frequently than for the patients without radiological error (P = 0.02). For the patients without radiological errors, improvement of PS after treatment was slightly more frequent than for the patients with radiological errors, but the difference was not significant. This may be due to the fact that sites of primary cancer, distributions of metastases, and treatment options also influence treatment outcomes. This is outside the scope of the present study. The effect of using biochemical markers of bone metabolism for a prompt diagnosis of bone metastases was not evaluated in this study. In our opinion, these investigations are not as important as radiological studies for the prompt diagnosis of bone metastases because laboratory studies are often nonspecific for bone metastases (14) and radiological studies are mandatory for identifying metastatic bone lesions (12). The interval between diagnosis and treatment showed that there was only a small treatment delay (Table 1). Although no comparable study is available, we are satisfied that the mean interval between referral to the radiation department of our hospital and initiation of radiotherapy was only 1.7 days. The prompt initiation of radiotherapy may be attributed to the fact that relatively small numbers of patients were irradiated each day with a 10-MV linear accelerator, with a staff of two radiation technologists and one radia-

Treatment delay and radiological errors 1423 tion oncologist during the study period. It should be noted that this study has several limitations: i) Pharmacological methods were not considered to be a definitive treatment for bone metastases. This is due to the fact that, although a patient with bone metastases may be treated with drugs only (1-3,15), the initiation of such therapy might be based on an incorrect diagnosis of nonmalignant disease. At presentation, analgesics had been prescribed to over three fourths (81.1%) of our patients without a correct diagnosis of bone metastases. If pharmacological therapies were regarded as definitive treatments of bone metastases, more bias would be introduced in estimating the effect of radiological errors on treatment delay. ii) It should be noted that the error rate in the present study did not necessarily reflect the accuracy of radiological examinations in our hospital. This is because false-positive findings of radiological examinations were not evaluated in the study design, and because not all radiological examinations performed during the study period were evaluated. iii) Other factors which may delay diagnosis include the delay in follow-up consultations, the time spent to present radiological examinations to physicians, and the waiting times for radiological examinations. Although the exact effect of these factors was not known, the policy of our hospital did not change during the 5-year period of this study; CT had to be performed and interpreted within a few days, plain radiography within one day, magnetic resonance imaging and bone scintigraphy within one week. In emergency situations, CT or magnetic resonance imaging had to be performed and interpreted within one day. Therefore, the effect of these factors is likely to have been small. iv) The small number of patients in this study might not represent all symptomatic patients with bone metastases. The patients were limited to those who presented themselves and were diagnosed at our hospital because the full medical records of these patients could easily be obtained. Despite these limitations, the definitive treatment delays could be calculated from the medical records and the causes of these delays could be defined. Although the causes of these delays may differ among hospitals, it is important for physicians to know the exact treatment delay at their own hospital and to clarify its causes. The key to successful management of cancer patients is early diagnosis and prompt treatment (7-10,16). Therefore, considerable efforts should be made to diagnose and treat these patients as quickly as possible. Continual monitoring of the treatment delay will be a useful indicator of the success of our efforts. References 1. Lote K, Walløe A & Bjersand A (1986). Bone metastasis: prognosis, diagnosis and treatment. Acta Oncologica, 25: 227-232. 2. Coleman RE (2000). Management of bone metastases. Oncologist, 5: 463-470. 3. Schachar NS (2001). An update on the nonoperative treatment of patients with metastatic bone disease. Clinical Orthopaedics and Related Research, 382: 75-81. 4. Stebbing JF & Nash AG (1995). Avoidable delay in the management of carcinoma of the right colon. Annals of the Royal College of Surgeons of England, 77: 21-23. 5. Zilling TL, Walther BS & Ahren BO (1990). Delay in diagnosis of gastric cancer: a prospective study evaluating doctors and patients delay and its influence on five year survival. Anticancer Research, 10: 411-416. 6. MacArthur C, Pendleton L & Smith A (1985). Treatment delay in patients with bladder tumours. Journal of Epidemiology and Community Health, 39: 63-66. 7. Silva PPA, Pereira JR, Ikari FK & Minamoto H (1992). Lung cancer and the delay in diagnosis: analysis of 300 cases. Revista da Associação Médica Brasileira, 38: 145-149. 8. Robinson E, Mohilever J, Zidan J & Sapir D (1986). Colorectal cancer: Incidence, delay in diagnosis and stage of disease. European Journal of Cancer and Clinical Oncology, 22: 157-161. 9. Rossi S, Cinini C, Pietro CD, Lombardi CP, Crucitti A, Bellantone R & Crucitti F (1990). Diagnostic delay in breast cancer: correlation with disease stage and prognosis. Tumori, 76: 559-562. 10. Joensuu H, Asola R, Holli K, Kumpulainen E, Nikkanen V & Parvinen LM (1994). Delayed diagnosis and large size of breast cancer after a

1424 K. Ichinohe et al. false negative mammogram. European Journal of Cancer, 30: 1299-1302. 11. Kelvin FM, Gardiner R, Vas W & Stevenson GW (1981). Colorectal carcinoma missed on double contrast barium enema study: a problem in perception. American Journal of Roentgenology, 37: 307-313. 12. Gold RI, Seeger LL, Bassett LW, Bassett LW & Steckel RJ (1990). An integrated approach to the evaluation of metastatic bone disease. Orthopedics, 28: 471-483. 13. Rybak LD & Rosenthal DI (2001). Radiological imaging for diagnosis of bone metastases. Quarterly Journal of Nuclear Medicine, 45: 53-64. 14. Meijer WG, Van Der Veer E & Willemse PHB (1998). Biochemical parameters of bone metabolism in bone metastases of solid tumors (Review). Oncology Reports, 5: 5-21. 15. Ripamonti C & Fulfaro F (2001). Pathogenesis and pharmacological treatment of bone pain in skeletal metastases. Quarterly Journal of Nuclear Medicine, 45: 65-77. 16. Helweg-Larsen S (1996). Clinical outcome in metastatic spinal cord compression: a prospective study of 153 patients. Acta Neurologica Scandinavica, 94: 269-275.