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The Mont Reid Surgical Handbook E-Book

The Mont Reid Surgical Handbook E-Book

Amy Makley

(2017)

Additional Information

Book Details

Abstract

Essential reading for residents and medical students, this popular handbook is a must-have resource for convenient, quick access to information on managing common surgical problems. Written by current surgery residents at the University of Cincinnati, the completely updated 7th Edition focuses on the surgical treatments, guidelines, procedures, and topics you need to know.

  • New chapters cover Surgical Risk Assessment, Head and Neck Malignancy, Mediastinal Tumors, Dialysis Access, and Robotics.
  • Rapid References section offers handy formulas and charts in one easy-access location.
  • Thoroughly revised content throughout ensures that you stay up to date.

Table of Contents

Section Title Page Action Price
Front Cover Cover
IFC ES1
THE MONT REIDSURGICAL HANDBOOK i
THE MONT REIDSURGICAL HANDBOOK iii
Copyright iv
FOREWORD v
PREFACE vi
CONTENTS xi
THE MONT REIDSURGICAL HANDBOOK xv
I - Perioperative Care 1
1 - Surgical History and Physical Examination 3
I. INTRODUCTION AND INITIAL CONTACT 3
II. HISTORY 3
A. CHIEF COMPLAINT 3
B. HISTORY OF PRESENT ILLNESS 3
C. REVIEW OF SYSTEMS 4
D. ALLERGIES 4
E. MEDICATION 4
F. PAST MEDICAL HISTORY 5
G. PAST SURGICAL HISTORY 5
H. FAMILY HISTORY 5
I. SOCIAL HISTORY 5
III. PHYSICAL EXAMINATION 5
A. VITAL SIGNS 5
B. GENERAL APPEARANCE 7
C. HEAD AND NECK 8
D. CHEST 10
E. CARDIOVASCULAR 11
F. ABDOMEN 13
G. GENITOURINARY 16
H. SKIN 17
I. MUSCULOSKELETAL 18
J. LYMPHATICS 19
K. NEUROLOGIC 20
2 - Fluids and Electrolytes 23
I. BASIC PHYSIOLOGY 23
A. BODY FLUID COMPOSITION 23
B. SERUM OSMOLALITY AND TONICITY 23
C. FLUID AND ELECTROLYTE HOMEOSTASIS 24
II. ELECTROLYTE DISTURBANCES 25
A. SODIUM 25
B. POTASSIUM 28
C. CALCIUM 29
D. MAGNESIUM 31
E. PHOSPHORUS 32
III. PARENTERAL REPLACEMENT FLUID THERAPY 33
A. CRYSTALLOIDS 33
B. COLLOIDS 34
IV. ACID-BASE DISORDERS 35
A. PHYSIOLOGY 35
B. PRIMARY METABOLIC DISORDERS 35
C. PRIMARY RESPIRATORY DISORDERS 37
D. MIXED ACID-BASE DISORDERS 38
E. EVALUATION OF ACID-BASE DISORDERS (TABLE 2.3) 38
3 - Nutrition 40
I. NUTRITION BASICS 40
II. DETERMINATION OF CALORIC NEEDS 40
III. NUTRITIONAL ASSESSMENT 41
IV. PREOPERATIVE NUTRITIONAL SUPPLEMENTATION 45
V. POSTOPERATIVE NUTRITIONAL SUPPLEMENTATION 45
VI. ENTERAL NUTRITION 45
VII. SHORT-TERM SUPPLEMENTATION 45
VIII. LONG-TERM SUPPLEMENTATION (>6 WEEKS) 46
IX. PRODUCTS 46
X. COMPLICATIONS OF ENTERAL FEEDING 47
XI. PARENTERAL NUTRITION 48
XII. BASIC COMPOSITION OF FORMULATIONS (TABLES 3.1 AND 3.2) 48
XIII. CENTRAL FORMULAS 49
XIV. PERIPHERAL PARENTERAL NUTRITION 50
XV. INFUSION 50
XVI. MONITORING 50
XVII. COMPLICATIONS 50
XVIII. IMMUNONUTRITION 51
XIX. NUTRIENTS/MACROMINERALS/MICRONUTRIENTS/VITAMINS 52
4 - Wound Healing 55
I. PHASES OF WOUND HEALING 55
A. HEMOSTASIS (5–10 MINUTES POST INJURY) 55
C. PROLIFERATIVE (DAY 1–3 WEEKS POST INJURY) 56
II. FACTORS THAT AFFECT WOUND HEALING 57
A. OXYGENATION 57
B. INFECTION 57
C. NUTRITION 57
D. STEROIDS 57
E. SMOKING 57
F. AGE 58
G. FOREIGN BODIES 58
H. EDEMA 58
I. CHEMOTHERAPY 58
J. RADIATION 58
K. DIABETES MELLITUS 58
L. GENERAL HEALTH 58
III. WOUND PREPARATION 58
A. IRRIGATION 58
B. ANTIMICROBIALS 58
C. DÉBRIDEMENT 59
IV. TYPES OF WOUND CLOSURE 59
A. PRIMARY: CLOSURE OF WOUND BY DIRECT APPROXIMATION OF WOUND EDGES 59
B. SPONTANEOUS HEALING (SECONDARY INTENTION): SPONTANEOUS WOUND CONTRACTION AND EPITHELIALIZATION 59
C. TERTIARY HEALING 60
V. MANAGEMENT OF WOUND COMPLICATIONS 60
A. INFECTION 60
B. SEROMA 60
C. DEHISCENCE 60
VI. HYPERTROPHIC SCARS AND KELOIDS 61
A. HYPERTROPHIC SCARS 61
B. KELOIDS 61
5 - Surgical Risk Assessment 64
I. RISKS AND BENEFITS OF SURGERY 64
II. SURGICAL RISK ASSESSMENT 64
III. PREOPERATIVE PREPARATION 73
IV. POSTOPERATIVE CARE 76
6 - Suture Types, Needle Types, and Instruments 81
I. SUTURE MATERIAL 81
A. THE OPTIMAL SUTURE 81
B. SUTURE CHARACTERISTICS 82
C. ABSORBABLE SUTURE 84
D. NONABSORBABLE SUTURE 85
E. SUMMARY 86
II. NEEDLES 87
III. INSTRUMENTS 89
II - Anesthesia 91
7 - Local Anesthesia 93
I. INJECTABLE AGENTS 93
A. MECHANISM OF ACTION 93
B. CLASSES 93
C. TOXICITY 95
D. USE OF EPINEPHRINE 95
II. TECHNIQUES 96
A. BEFORE INJECTING LOCAL ANESTHETIC IN TRAUMATIC INJURIES, BE SURE TO PERFORM AND DOCUMENT A DETAILED SENSORY EXAMINATION, WHICH MAY BE SUBSEQUENTLY MASKED BY YOUR BLOCK 96
B. OPTIMAL TIMING BETWEEN INJECTION AND INCISION 96
C. GENERAL TECHNIQUES TO DECREASE PAIN 96
D. FIELD BLOCKS 96
E. NERVE BLOCKS FOR THE FACE 96
F. NERVE BLOCKS FOR THE UPPER EXTREMITY 99
III. TOPICAL AGENTS 100
A. TOPICAL ANESTHESIA CAN AVOID THE PAIN AND ANXIETY OF NEEDLE INJECTION AND IS ESPECIALLY USEFUL IN THE PEDIATRIC POPULATION. IT CAN ALSO BE USED AS AN ADJUNCT TO DECREASE SUPERFICIAL SKIN PAIN BEFORE PERFORMING MORE TARGETED NERVE BLOCK WITH AN INJECTABLE LOCAL ANESTHETIC AGENT. 100
B. SYSTEMIC BLOOD LEVELS OF THESE COMPOUNDED TOPICAL ANESTHETICS DEPEND ON THE ABSORPTION, PATIENT SIZE, RATE OF ELIMINATION, AN... 100
C. COMMONLY USED PRODUCTS (10) 100
8 - Conscious Sedation 102
I. INTRODUCTION 102
A. DEFINITION 102
B. APPLICATIONS (SELECTED) 102
II. PREPROCEDURAL EVALUATION 102
A. HISTORY 102
B. AIRWAY EXAMINATION 103
III. MONITORING 104
A. Best Achieved by Someone Other than Person Performing Procedure 104
B. PREPROCEDURE 104
C. CLINICAL ASSESSMENT 104
F. BLOOD PRESSURE 105
IV. AVAILABILITY OF EMERGENCY MEDICAL EQUIPMENT AND PERSONNEL 105
A. Immediate Access to Suction, Bag-Mask Ventilation, Intubation Materials, Defibrillator, and Emergency (Advanced Cardiac Life ... 105
B. Anesthesia or Other Trained Airway Staff in Close Proximity1397256787 105
V. TRAINING IN AIRWAY MANAGEMENT 105
III - Surgical Critical Care 123
10 - Surgical Infection 125
I. BACKGROUND AND SCOPE OF PROBLEM 125
II. MOST COMMON INFECTIONS AFFECTING SURGICAL PATIENTS 127
A. CENTRAL LINE–ASSOCIATED BLOODSTREAM INFECTION 127
B. SURGICAL SITE INFECTIONS 128
C. CATHETER-ASSOCIATED URINARY TRACT INFECTIONS 131
D. CLOSTRIDIUM DIFFICILE INFECTION 133
E. VENTILATOR-ASSOCIATED PNEUMONIA 135
F. PURULENT SKIN AND SOFT TISSUE INFECTIONS 136
G. NECROTIZING SOFT TISSUE INFECTION 137
H. INTRAABDOMINAL INFECTIONS 138
III. SEPSIS 139
11 - Hemorrhage and Coagulation 143
I. GENERAL TOPICS 143
A. NORMAL BLOOD VOLUME AND COMPOSITION 143
B. CLASSES OF HEMORRHAGIC SHOCK (TABLE 11.1) 143
C. TYPING, SCREENING, AND CROSSMATCHING 143
D. GENERAL BLOOD PRODUCT ADMINISTRATION GUIDELINES 144
II. LABORATORY TESTS AND REFERENCE VALUES 144
A. COMPLETE BLOOD COUNT 144
B. PROTHROMBIN TIME 144
C. INTERNATIONAL NORMALIZED RATIO 144
D. ACTIVATED PARTIAL THROMBOPLASTIN TIME 144
E. ACTIVATED CLOTTING TIME 144
F. BLEEDING TIME 145
G. PLATELET FUNCTION TESTS 145
H. THROMBIN TIME 145
I. FIBRINOGEN 145
J. VISCOELASTIC TESTS 145
III. SPECIFIC BLOOD PRODUCTS 146
A. WHOLE BLOOD 146
B. PACKED RED BLOOD CELLS 146
C. FRESH FROZEN PLASMA 147
D. PLATELETS 148
E. CRYOPRECIPITATE 148
IV. MASSIVE TRANSFUSION AND DAMAGE CONTROL RESUSCITATION 149
A. DEFINITION OF MASSIVE TRANSFUSION VARIES, BUT MOST COMMONLY USED IS 10 OR MORE UNITS OF BLOOD PRODUCTS IN THE FIRST 24 HOURS 149
B. PREDICTORS OF NEED FOR MASSIVE TRANSFUSION 149
C. PRESENCE AND IMPLEMENTATION OF STANDARDIZED PROTOCOLS IMPROVE SURVIVAL IN PATIENTS REQUIRING MASSIVE TRANSFUSION 149
D. DAMAGE CONTROL RESUSCITATION IS A STRATEGY TO LIMIT ONGOING BLEEDING BY ADDRESSING HYPOTHERMIA, ACIDOSIS, AND COAGULOPATHY. 149
V. TRANSFUSION REACTIONS 149
A. IMMUNE MEDIATED 149
B. NONIMMUNOLOGIC REACTIONS 151
VI. SURGICAL COAGULOPATHY—GENERAL CONSIDERATIONS 151
A. COAGULATION CASCADE (FIG. 11.2) 151
B. MEDICAL HISTORY TO DETERMINE RISK FOR BLEEDING 151
VII. CONGENITAL BLEEDING DISORDERS 153
A. HEMOPHILIA A 153
B. HEMOPHILIA B (CHRISTMAS DISEASE) 153
C. VON WILLEBRAND DISEASE 153
VIII. ACQUIRED BLEEDING DISORDERS 154
A. VITAMIN K DEFICIENCY 154
B. HYPOTHERMIA 154
C. LIVER FAILURE 154
D. END-STAGE RENAL DISEASE 154
E. DISSEMINATED INTRAVASCULAR COAGULATION 154
F. ACQUIRED THROMBOCYTOPENIA 154
H. HYPERFIBRINOLYSIS 155
IX. MEDICATIONS 155
A. ANTIPLATELET AGENTS 155
B. HEPARINS 156
C. WARFARIN 156
D. DIRECT THROMBIN INHIBITORS 156
E. FACTOR XA INHIBITORS (FONDAPARINUX) 157
F. NEW ORAL ANTICOAGULANTS 157
G. ANTIFIBRINOLYTICS 157
12 - Shock 159
I. PATHOPHYSIOLOGY 159
II. HEMODYNAMIC CONSIDERATIONS 159
A. IMPORTANT RELATIONSHIPS 160
B. PRELOAD 160
C. AFTERLOAD 160
III. ORGAN RESPONSE TO SHOCK 161
A. NEUROENDOCRINE RESPONSE 161
B. MICROVASCULAR DYSFUNCTION 161
C. INFLAMMATORY RESPONSE 162
D. PULMONARY 162
E. RENAL 162
IV. MULTIORGAN DYSFUNCTION SYNDROME 162
A. DEFINITION 162
B. CAUSES 162
C. PREVENTIVE MEASURES 163
V. SHOCK STATES 163
A. HYPOVOLEMIC SHOCK 163
B. SEPTIC SHOCK 165
C. NEUROGENIC SHOCK 167
D. CARDIOGENIC SHOCK 168
E. HYPOADRENAL SHOCK/ADRENAL INSUFFICIENCY 169
VI. VASOACTIVE AGENTS 170
13 - Cardiopulmonary Monitoring 171
I. CARDIAC MONITORING 171
A. CARDIAC RHYTHMS 171
B. BLOOD PRESSURE MONITORING 175
C. HEMODYNAMIC MONITORING BASIC PRINCIPLES 175
D. SPECIFIC DEVICES FOR CARDIAC MONITORING 176
II. PULMONARY MONITORING 182
A. PULSE OXIMETRY 182
D. ARTERIAL OR VENOUS BLOOD GAS 183
III. IMPORTANT FORMULAS 183
A. CARDIAC OUTPUT 183
B. ARTERIAL CONTENT OF OXYGEN 183
C. OXYGEN DELIVERY 184
D. OXYGEN CONSUMPTION 184
14 - Mechanical Ventilation 185
I. DETERMINING NEED FOR MECHANICAL VENTILATION 185
A. AIRWAY INSTABILITY 185
B. RESPIRATORY FAILURE 185
C. GUIDELINES 185
II. VENTILATION VERSUS OXYGENATION 185
A. VENTILATION 185
B. OXYGENATION 186
III. NONINVASIVE POSITIVE PRESSURE VENTILATION 186
A. POSITIVE PRESSURE VENTILATION 186
B. INITIAL SETTINGS 186
C. ADVANTAGES 186
D. RESERVED 186
IV. CONVENTIONAL MECHANICAL VENTILATION 186
A. MODES OF VENTILATION 186
B. VENTILATOR STRATEGIES 187
C. LIBERATION FROM MECHANICAL VENTILATION 188
D. FAILURE TO LIBERATE FROM MECHANICAL VENTILATION 188
V. EFFECTS ON CARDIAC PERFORMANCE 189
A. ENDOTRACHEAL INTUBATION AND MECHANICAL VENTILATION PLACE IMPORTANT PHYSIOLOGIC DEMANDS ON PATIENTS 189
B. THE SHIFT FROM NEGATIVE PRESSURE TO POSITIVE PRESSURE VENTILATION CAN COMPROMISE PRELOAD BY 189
C. POSITIVE PRESSURE VENTILATION 189
D. THE EFFECTS OF POSITIVE PRESSURE VENTILATION ON CARDIAC PERFORMANCE 189
VI. NEED FOR TRACHEOSTOMY 189
VII. VENTILATOR CAUTIONS 190
A. DEFINITION OF ACUTE RESPIRATORY DISTRESS SYNDROME 190
B. ACUTE LUNG INJURY/ACUTE RESPIRATORY DISTRESS SYNDROME TREATED WITH PROTECTIVE LUNG STRATEGY 190
C. VENTILATOR-ASSOCIATED PNEUMONIA 190
VIII. PEARLS 190
A. STANDARD INITIAL VENTILATOR SETTINGS 190
IV - Trauma Surgery 193
15 - Primary and Secondary Survey 195
I. EPIDEMIOLOGY 195
A. MORTALITY 195
B. MECHANISMS OF INJURY 195
II. MANAGEMENT OF THE TRAUMA PATIENT 195
A. PRIMARY SURVEY 195
B. FURTHER EVALUATION AND TRANSFER 198
C. SECONDARY SURVEY 198
III. PEDIATRIC TRAUMA 199
A. MECHANISMS OF INJURY 199
B. PRIMARY SURVEY 199
IV. TRAUMA AND PREGNANCY 200
A. EPIDEMIOLOGY 200
B. ANATOMIC AND PHYSIOLOGIC CHANGES DURING PREGNANCY 200
C. MATERNAL EVALUATION 200
D. FETAL ASSESSMENT 200
V. PENETRATING NECK TRAUMA 201
A. ZONE I 201
B. ZONE II 201
C. ZONE III 202
D. NECK EXPLORATION 202
16 - Abdominal Trauma 203
I. PATHOPHYSIOLOGY 203
II. DIAGNOSIS 204
III. TREATMENT 206
V. SPECIAL CIRCUMSTANCES 217
17 - Thoracic Trauma 220
I. EPIDEMIOLOGY OF THORACIC TRAUMA 220
A. THORACIC TRAUMA 220
B. AFRICAN-AMERICAN MALES 220
C. MOTORCYCLE ACCIDENTS 220
II. PHYSICAL EXAMINATION OF THE CHEST 220
A. CHEST AUSCULTATION 220
B. POINT TENDERNESS 220
C. FLAIL CHEST 220
D. SUBCUTANEOUS EMPHYSEMA 220
E. DULLNESS VERSUS RESONANCE ON PERCUSSION 221
F. SEAT BELT SIGNS 221
III. ADJUNCTS TO THE PHYSICAL EXAMINATION 221
A. CHEST RADIOGRAPHS 221
IV. PATHOPHYSIOLOGY OF THORACIC TRAUMA 221
V. BLUNT CHEST TRAUMA 222
VI. PENETRATING CHEST TRAUMA 225
VII. RESUSCITATIVE THORACOTOMY 228
VIII. OTHER THORACIC PROCEDURES IN THE FACE OF TRAUMA 231
A. FOCUSED ASSESSMENT WITH SONOGRAPHY FOR TRAUMA EXAMINATION 231
B. PERICARDIOCENTESIS 231
C. SUBXIPHOID PERICARDIOTOMY 231
D. THORACOSCOPY 231
IX. POSTOPERATIVE CARE OF THE PATIENT WITH A CHEST INJURY 231
A. CHEST TUBE MANAGEMENT 231
X. COMPLICATIONS OF THORACIC TRAUMA 232
18 - Extremity Trauma 234
I. EVALUATION OF THE INJURED LIMB 234
A. GENERAL POINTS 234
B. EVALUATION OF FRACTURES AND DISLOCATIONS 234
II. OPEN FRACTURES 234
A. DEFINITION 234
B. COMPLICATIONS OF OPEN FRACTURES 235
C. GUSTILO-ANDERSON CLASSIFICATION SYSTEM (TABLE 18.1) 235
D. EMERGENCY DEPARTMENT MANAGEMENT OF OPEN FRACTURES 235
III. COMPARTMENT SYNDROME 237
A. DEFINITION 237
B. CAUSES OF COMPARTMENT SYNDROME 237
C. SIGNS AND SYMPTOMS 237
D. DIAGNOSIS OF COMPARTMENT SYNDROME 238
E. SURGICAL TREATMENT OF ACUTE COMPARTMENT SYNDROME 238
IV. PELVIC FRACTURES 239
A. EVALUATION OF PELVIC RING FRACTURES 239
V. VASCULAR INJURY IN EXTREMITY TRAUMA 241
A. HISTORY AND PHYSICAL 241
B. MANAGEMENT OF EXTREMITY TRAUMA 241
C. COMPLICATIONS OF VASCULAR INJURIES 242.e1
VI. AMPUTATION IN TRAUMA 242
19 - Burn Care 243
I. CAUSATIVE FACTORS 243
A. SCALDS 243
B. FLAME 243
C. FLASH 243
D. CONTACT 243
II. INDICATIONS FOR HOSPITAL ADMISSION 243
A. OUTPATIENT SETTING 243
B. BURN UNIT SETTING 244
III. INITIAL MANAGEMENT 244
A. HISTORY 244
B. AIRWAY/BREATHING 244
C. BURN EVALUATION 246
D. FLUID RESUSCITATION 247
E. INITIAL PROCEDURES 248
F. INITIAL TESTS 249
G. MEDICATIONS 249
IV. PATHOPHYSIOLOGIC CHANGES ASSOCIATED WITH BURN INJURIES 250
A. EDEMA 250
B. HEMODYNAMICS 250
V. BURN WOUND CARE 250
A. GOALS OF BURN WOUND CARE 250
B. TOPICAL AGENTS 251
C. LOCAL CARE 251
D. EARLY EXCISION AND GRAFTING 251
E. GRAFTING 252
VI. SUPPORTIVE CARE 253
A. NUTRITION 253
B. PHYSICAL AND OCCUPATIONAL THERAPY 253
C. ANALGESIA 254
VII. MANAGEMENT OF INFECTION IN THE BURN PATIENT 254
A. THE MOST COMMON INFECTION IN BURN PATIENTS IS PNEUMONIA 254
B. PATHOGENESIS OF WOUND SEPSIS IN AN UNTREATED BURN WOUND 254
C. CLINICAL SIGNS 254
D. DIAGNOSIS OF INVASIVE BURN WOUND SEPSIS 254
E. BACTERIOLOGY OF NOSOCOMIAL BURN INFECTION 255
F. PREVENTION OF BURN INFECTION 255
G. TREATMENT OF BURN INFECTION 255
H. NONBACTERIAL INFECTION 255
VIII. ELECTRICAL INJURIES 256
A. TISSUE DESTRUCTION 256
B. TREATMENT 256
C. FLUID RESUSCITATION 256
D. EARLY DEBRIDEMENT 256
E. IMMEDIATE EXTREMITY FASCIOTOMY 256
IX. CHEMICAL INJURIES 256
A. MANAGEMENT 256
X. OUTPATIENT AND CLINIC TREATMENT 257
A. SELECTION 257
B. TREATMENT 257
C. FOLLOW-UP CARE 257
D. WOUNDS 257
XI. COMPLICATIONS OF BURN INJURIES 258
A. GASTROINTESTINAL 258
B. OCULAR 258
C. CUTANEOUS 258
D. MISCELLANEOUS 259
20 - Neurosurgical Emergencies 260
I. EVALUATION AND MANAGEMENT OF THE NEUROTRAUMA PATIENT 260
A. INITIAL ASSESSMENT 260
B. UNCONSCIOUS PATIENT 261
C. PHYSICAL EXAMINATION 262
D. RADIOLOGIC EVALUATION 264
II. CRANIAL TRAUMA 266
A. TRAUMATIC BRAIN INJURY 266
B. ELEVATED INTRACRANIAL PRESSURE 267
C. SPECIFIC TRAUMATIC CRANIAL INJURIES 269
D. PENETRATING TRAUMATIC BRAIN INJURY 273
E. TRAUMATIC BRAIN INJURY PROGNOSIS 274
III. SPINAL TRAUMA 275
A. GENERAL 275
B. ASSESSMENT 275
C. SPECIFIC SPINAL INJURIES 280
IV. PERIPHERAL NERVE TRAUMA 286
A. GENERAL 286
B. EVALUATION 286
C. TREATMENT 288
V. TRAUMATIC CEREBROVASCULAR INJURIES 288
B. BLUNT CEREBROVASCULAR INJURY 288
C. EVALUATION 289
D. TREATMENT 290
V - Gastrointestinal Surgery 293
21 - Acute Abdomen 295
I. PHYSIOLOGY OF ABDOMINAL PAIN 295
A. VISCERAL PAIN 295
B. SOMATIC PAIN 295
C. REFERRED PAIN 296
II. HISTORY 296
A. PAIN 296
B. VOMITING 297
C. BOWEL FUNCTION 298
D. MEDICAL HISTORY 298
E. MEDICATION 298
III. PHYSICAL EXAMINATION 298
A. GENERAL APPEARANCE 298
B. VITAL SIGNS 299
C. ABDOMINAL EXAMINATION 299
D. EXAMINATION OF PELVIC CAVITY 300
IV. LABORATORY EXAMINATION 301
A. WHITE BLOOD CELL COUNT 301
B. HEMATOCRIT 302
C. PLATELET COUNT 302
D. ELECTROLYTES 302
E. ARTERIAL BLOOD GAS 302
F. LIVER FUNCTION TESTS 302
G. AMYLASE LEVEL INCREASE 302
H. URINE STUDIES 302
I. TROPONINS 302
V. RADIOGRAPHIC EVALUATION 302
A. UPRIGHT CHEST RADIOGRAPH 302
B. ABDOMINAL RADIOGRAPH 303
C. ULTRASONOGRAPHY 303
D. COMPUTED TOMOGRAPHY SCAN 303
VI. INITIAL TREATMENT AND PREOPERATIVE PREPARATION 304
A. ASSESSMENT 304
B. DIET 304
C. INTRAVENOUS FLUIDS 304
D. HEMODYNAMIC MONITORING 304
E. NASOGASTRIC TUBE 304
F. FOLEY CATHETER 304
G. TREATMENT 304
22 - Abdominal Wall Hernias 305
I. HISTORICAL PERSPECTIVE 305
A. HENRY MARCY (1837–1924) 305
B. EDOARDO BASSINI (1844–1924) 305
C. SIR ASTLEY COOPER (1768–1841) 305
D. CHESTER MCVAY (1911–1987) 305
E. EDWARD EARLE SHOULDICE (1890–1965) 305
F. IRVING LICHTENSTEIN AND PARVIZ AMID 305
II. TERMINOLOGY 306
A. HERNIA 306
B. REDUCIBILITY 306
C. INCARCERATION 306
D. STRANGULATION 306
III. NATURAL HISTORY 306
A. INCIDENCE 306
IV. ANATOMIC CONSIDERATIONS 306
A. LAYERS OF THE ABDOMINAL WALL 306
B. INGUINAL CANAL 307
C. SPERMATIC CORD 307
D. PROCESSUS VAGINALIS 307
E. DEEP (INTERNAL) INGUINAL RING 307
F. SUPERFICIAL (EXTERNAL) INGUINAL RING 307
G. HESSELBACH TRIANGLE 307
H. INGUINAL (POUPART) LIGAMENT 307
I. ILIOPUBIC TRACT 307
J. LACUNAR (GIMBERNAT) LIGAMENT 308
K. PECTINEAL (COOPER) LIGAMENT 308
L. FEMORAL CANAL 308
M. INFERIOR LUMBAR (PETIT) TRIANGLE 308
N. SUPERIOR LUMBAR (GRYNFELTT) TRIANGLE 308
V. CLASSIFICATION OF HERNIAS 308
A. GROIN HERNIAS (FIG. 22.1) 308
B. VENTRAL HERNIAS 308
C. MISCELLANEOUS HERNIAS 309
VI. CAUSATIVE FACTORS 311
A. INDIRECT INGUINAL HERNIA 311
B. DIRECT INGUINAL HERNIA 311
C. FEMORAL HERNIA 311
D. CONTRIBUTING FACTORS 311
VII. DIAGNOSIS 312
A. HISTORY 312
B. EXAMINATION 312
C. SMALL BOWEL OBSTRUCTION 312
D. DIFFERENTIAL DIAGNOSIS OF GROIN MASS 312
E. REDUCTION OF INCARCERATED HERNIA 312
F. REDUCTION EN MASSE 313
VIII. PREOPERATIVE CONSIDERATIONS 313
A. PATIENT COMORBIDITIES AND RISK FACTORS 313
B. LAPAROSCOPIC VERSUS OPEN REPAIRS 313
IX. INGUINAL/FEMORAL HERNIA REPAIR 314
A. OPEN REPAIR 314
B. FEMORAL HERNIAS 315
C. LAPAROSCOPIC REPAIR 315
X. VENTRAL/UMBILICAL/INCISIONAL HERNIA REPAIR 317
A. OPEN REPAIR 317
B. LAPAROSCOPIC REPAIR 318
XI. POSTOPERATIVE COMPLICATIONS 318
A. RECURRENT HERNIA 318
B. INFECTION 319
C. BLEEDING 319
D. DYSEJACULATION 319
E. TESTICULAR ATROPHY 319
F. DIFFICULTY VOIDING 319
G. NEUROMA/NEURITIS 319
H. PAIN 319
I. URINARY RETENTION 320
23 - Gastrointestinal Bleeding 321
I. HISTORY 321
A. CHARACTERIZATION OF BLEEDING 321
B. CAUSATIVE FACTORS 321
C. ADDITIONAL MEDICAL HISTORY 321
II. PHYSICAL EXAMINATION 322
A. GENERAL APPEARANCE 322
B. VITAL SIGNS 322
C. SKIN 322
D. HEAD AND NECK 322
E. ABDOMEN 322
F. DIGITAL RECTAL EXAMINATION 322
III. INITIAL MANAGEMENT 322
A. ASSESS THE MAGNITUDE OF HEMORRHAGE 322
B. STABILIZE HEMODYNAMIC STATUS 323
C. MONITOR FOR CONTINUED BLOOD LOSS 323
IV. LABORATORY EVALUATION 323
A. TYPE AND CROSSMATCH 323
B. HEMOGLOBIN/HEMATOCRIT/RED BLOOD CELLS CHARACTERISTICS 323
C. PLATELET COUNT 323
D. PROTHROMBIN AND PARTIAL THROMBOPLASTIN TIMES 323
E. THROMBOELASTOGRAPHY 323
F. RENAL PROFILE 326
V. INVESTIGATIVE AND DIAGNOSTIC PROCEDURES 326
A. NASOGASTRIC TUBE 326
B. ENDOSCOPY 326
C. ANGIOGRAPHY 326
E. COMPUTED TOMOGRAPHY 327
VI. NONSURGICAL TREATMENT 327
A. ENDOSCOPIC 327
B. ELECTROCAUTERY 327
C. VASOPRESSIN INFUSION 327
D. EMBOLIZATION 327
VII. DISEASE-SPECIFIC THERAPY 327
A. ACUTE HEMORRHAGIC GASTRITIS 327
B. PEPTIC ULCER DISEASE 327
C. ESOPHAGOGASTRIC VARICES 328
D. MALLORY-WEISS TEAR 328
E. DIEULAFOY LESION (EXULCERATIO SIMPLEX) 329
F. NEOPLASM 329
G. DIVERTICULOSIS 329
H. ARTERIOVENOUS MALFORMATIONS 329
I. MECKEL DIVERTICULUM 330
J. BENIGN ANORECTAL DISEASE 330
K. AORTOENTERIC FISTULA 330
24 - Intestinal Obstruction 331
I. TERMINOLOGY 331
A. ILEUS 331
B. MECHANICAL OBSTRUCTION 331
C. SIMPLE OBSTRUCTION 331
D. CLOSED-LOOP OBSTRUCTION 331
E. STRANGULATION 331
II. CAUSATIVE FACTORS 331
A. SMALL BOWEL OBSTRUCTION 331
B. LARGE BOWEL OBSTRUCTION 332
D. ILEUS 333
III. PRESENTATION 334
A. HISTORY 334
B. PHYSICAL EXAMINATION 335
C. LABORATORY TESTS 335
IV. IMAGING 336
A. PLAIN FILMS 336
B. CONTRAST STUDIES 337
C. COMPUTED TOMOGRAPHY 339
V. MANAGEMENT 339
A. EXPECTANT/PREOPERATIVE MANAGEMENT (FIG. 24.2) 339
B. OPERATIVE MANAGEMENT 341
C. POSTOPERATIVE CARE 343
D. PARALYTIC ILEUS 343
VI. OUTCOMES 343
A. RECURRENCE 343
B. OPERATIVE MORTALITY 343
25 - Peptic Ulcer Disease 345
I. OCCURRENCE 345
II. PRESENTATION AND EVALUATION 345
A. SYMPTOMS 345
B. PHYSICAL EXAMINATION 346
C. LABORATORY STUDIES 346
D. DEFINITIVE DIAGNOSIS 346
E. MODIFIED JOHNSON CLASSIFICATION 346
III. PATHOGENESIS 346
IV. HELICOBACTER PYLORI 348
V. TREATMENT OF UNCOMPLICATED DISEASE 349
A. PREVENTION 349
B. EMPIRIC MEDICAL THERAPY 349
C. CONCERN FOR GASTRIC CANCER 349
D. SURGICAL THERAPY 349
VI. TREATMENT OF COMPLICATED DISEASE 349
A. CONCERN FOR GASTRIC CANCER 349
B. BLEEDING PEPTIC ULCER 350
C. PERFORATED PEPTIC ULCER 350
D. OBSTRUCTION 350
E. INTRACTABILITY—CURRENTLY RARE 351
VII. DETAILS OF SURGICAL OPTIONS 351
A. HIGHLY SELECTIVE VAGOTOMY (OR PROXIMAL GASTRIC OR PARIETAL CELL) 351
B. OMENTAL (GRAHAM) PATCH 351
C. VAGOTOMY AND DRAINAGE 351
D. VAGOTOMY AND ANTRECTOMY 351
E. DISTAL GASTRECTOMY 352
F. POSTOPERATIVE COMPLICATIONS 352
26 - Inflammatory Bowel Disease 355
I. INFLAMMATORY BOWEL DISEASE 355
A. ULCERATIVE COLITIS 355
B. CROHN DISEASE 355
C. INDETERMINATE COLITIS 355
D. ETIOLOGY 355
II. EXTRAINTESTINAL MANIFESTATIONS 355
A. CUTANEOUS 355
B. OCULAR 356
C. MUSCULOSKELETAL 356
D. HEPATOBILIARY 356
III. ULCERATIVE COLITIS 356
A. PATHOPHYSIOLOGY AND DISTRIBUTION 356
B. EPIDEMIOLOGY 357
C. CLINICAL MANIFESTATIONS 357
D. DIAGNOSIS 357
E. COMPLICATIONS 358
F. MEDICAL MANAGEMENT 359
G. SURGICAL MANAGEMENT 361
H. PROGNOSIS 362
IV. CROHN DISEASE 363
A. EPIDEMIOLOGY 363
B. PATHOPHYSIOLOGY AND DISTRIBUTION 363
C. CLINICAL MANIFESTATIONS 363
D. DIAGNOSIS 364
E. COMPLICATIONS 365
F. MEDICAL MANAGEMENT (SEE SECTION III.G) 365
G. SURGICAL MANAGEMENT 366
H. PROGNOSIS 368
V. INDETERMINATE COLITIS 369
A. TYPICALLY PRESENT WITH SYMPTOMS SIMILAR TO ULCERATIVE COLITIS 369
27 - Benign Esophageal Disease 371
I. ANATOMY 371
A. GENERAL DESCRIPTION 371
B. BLOOD SUPPLY AND NERVES 371
C. HISTOLOGY 372
II. PHYSIOLOGY 373
A. SWALLOWING MECHANISM 373
B. SPHINCTERS 373
III. MOTILITY DISORDERS 374
A. ACHALASIA 374
B. DIFFUSE ESOPHAGEAL SPASM 374
C. NUTCRACKER ESOPHAGUS 375
D. HYPERTENSIVE LES 375
E. SCLERODERMA 375
IV. DIVERTICULA 375
A. DEFINITION 375
B. PHARYNGOESOPHAGEAL (ZENKER DIVERTICULUM) 376
C. MIDESOPHAGEAL 376
D. EPIPHRENIC 376
V. GASTROESOPHAGEAL REFLUX 377
A. ANATOMY 377
B. PATHOPHYSIOLOGY 377
C. DIAGNOSIS 377
D. TREATMENT 378
E. HIATAL HERNIA 379
F. BARRETT ESOPHAGUS 380
VI. BENIGN TUMORS OF THE ESOPHAGUS 380
A. LEIOMYOMA 380
B. OTHER BENIGN LESIONS 380
VII. ESOPHAGEAL RUPTURE AND PERFORATION 381
A. CAUSATIVE FACTORS 381
B. CLINICAL PRESENTATION 381
C. DIAGNOSIS 381
D. TREATMENT 381
VIII. CAUSTIC INJURY 383
A. BACKGROUND 383
B. CLINICAL PRESENTATION 383
C. DIAGNOSIS 383
D. TREATMENT 383
28 - Benign Colorectal Disease 386
I. ANATOMY 386
A. RECTUM 386
B. ANAL CANAL 386
C. LEVATOR ANI MUSCLE 386
D. BLOOD SUPPLY AND LYMPHATIC DRAINAGE 386
II. HEMORRHOIDS 387
A. SIGNS AND SYMPTOMS 388
B. DIAGNOSIS 388
C. MEDICAL TREATMENT 388
D. OFFICE TREATMENT 388
E. SURGICAL HEMORRHOIDECTOMY 389
III. ANAL FISSURE 390
A. OVERVIEW 390
B. SIGNS AND SYMPTOMS 390
C. TREATMENT 390
IV. ANORECTAL ABSCESS 391
A. CLASSIFICATION (BASED ON LOCATION) 391
B. SIGNS AND SYMPTOMS 392
C. TREATMENT 392
V. FISTULA IN ANO 393
A. GENERAL 393
B. CLASSIFICATION 393
C. GOODSALL RULE 393
D. SIGNS AND SYMPTOMS 394
E. TREATMENT 394
VI. PILONIDAL DISEASE 394
A. GENERAL 394
B. TREATMENT 395
VII. ANAL AND PERIANAL INFECTIONS 396
A. CONDYLOMATA ACUMINATA 396
B. ANORECTAL HERPES 396
C. GONOCOCCAL PROCTITIS 396
VIII. PRURITUS ANI 397
A. ETIOLOGY 397
B. DIAGNOSIS 397
C. TREATMENT 397
IX. ANAL NEOPLASM 398
A. TUMORS OF THE ANAL CANAL 398
X. RECTAL PROLAPSE 399
A. CLASSIFICATION 399
B. CLINICAL FEATURES 399
C. EVALUATION 400
D. TREATMENT OPTIONS 401
XI. ANOSCOPY 401
A. GENERAL 401
B. TECHNIQUE 401
XII. RIGID SIGMOIDOSCOPY 402
A. GENERAL 402
B. TECHNIQUE 402
29 - Appendix 403
I. OVERVIEW 403
A. ANATOMY 403
B. FUNCTION 403
II. EPIDEMIOLOGY 403
A. GENERAL 403
B. MORBIDITY AND MORTALITY 403
III. PATHOPHYSIOLOGY 404
A. GENERAL 404
B. COMPLICATIONS 404
IV. PRESENTATION 404
A. HISTORY 404
B. PHYSICAL EXAMINATION 404
C. LABORATORY AND RADIOLOGIC FINDINGS 405
V. DIFFERENTIAL DIAGNOSIS 405
VI. COMPLICATIONS 406
A. PERFORATION 406
B. PERITONITIS 406
C. ABSCESS 406
VII. TREATMENT 406
A. GENERAL 406
B. TECHNIQUE 407
C. LAPAROSCOPY 408
D. FUTURE RESEARCH 409
VIII. SPECIAL CIRCUMSTANCES 409
A. OLDER ADULTS 409
B. INFANTS 409
C. PREGNANCY 409
IX. APPENDICEAL TUMORS 410
A. CARCINOID 410
B. ADENOCARCINOMA 410
C. PSEUDOMYXOMA 411
30 - Benign Pancreatic Disease 412
I. ANATOMY 412
A. EMBRYOLOGY 412
B. HISTOLOGY 412
C. GROSS ANATOMY 413
D. VASCULAR/LYMPHATIC ANATOMY 413
E. DUCT SYSTEM 415
II. ACUTE PANCREATITIS 416
A. BASICS 416
B. PATHOGENESIS 416
C. ETIOLOGY/RISK FACTORS 417
D. DIAGNOSIS 419
E. TREATMENT 421
F. PROGNOSIS 422
G. COMPLICATIONS 423
III. CHRONIC PANCREATITIS 427
A. BASICS 427
B. ETIOLOGY 428
C. DIAGNOSIS 429
D. TREATMENT 429
E. COMPLICATIONS 432
31 - Surgical Diseases of the Spleen 434
I. ANATOMY 434
A. AVERAGE ADULT SPLEEN 434
B. ENCAPSULATED 434
C. SPLENOMEGALY DEFINITION 434
D. BLOOD SUPPLY 434
E. STRUCTURAL SUPPORT 434
F. MICROANATOMY 434
G. ACCESSORY SPLEENS 435
II. FUNCTION 435
A. HEMATOLOGIC 435
B. IMMUNOLOGIC 435
III. GENERAL INDICATIONS FOR SPLENECTOMY 435
A. TRAUMA 435
B. RED BLOOD CELL DISORDERS 435
C. MYELOPROLIFERATIVE DISORDERS 436
D. WHITE BLOOD CELLS DISORDERS 436
E. PLATELET DISORDERS 437
F. OTHER SPLENIC DISORDERS 438
IV. SURGICAL TECHNIQUES 439
A. OPEN SPLENECTOMY 439
B. LAPAROSCOPIC SPLENECTOMY 439
C. HAND-ASSISTED TECHNIQUE 439
V. POSTSPLENECTOMY CONSIDERATIONS 439
A. OVERWHELMING POSTSPLENECTOMY INFECTION 439
B. POSTSPLENECTOMY HEMATOLOGIC CHANGES 440
C. HEMORRHAGE 440
D. INFECTION 440
E. PORTAL VEIN THROMBOSIS 440
F. PANCREATITIS, PSEUDOCYST, FISTULA 441
32 - Bariatric Surgery 442
I. EPIDEMIOLOGY OF MORBID OBESITY 442
A. DEFINITIONS 442
B. CAUSES OF OBESITY 442
C. EPIDEMIOLOGY 442
II. COMORBIDITY ASSOCIATED WITH MORBID OBESITY 443
A. NEOPLASIA 443
B. CARDIOVASCULAR DISEASE 443
C. PULMONARY DISEASE 443
D. ENDOCRINE DISEASE 443
E. GASTROINTESTINAL DISEASE 443
F. OTHER COMORBIDITIES ASSOCIATED WITH MORBID OBESITY 443
III. MEDICAL THERAPY FOR MORBID OBESITY 444
IV. TYPES OF PROCEDURES 444
A. MALABSORPTIVE OPERATIONS 444
B. RESTRICTIVE OPERATIONS 444
C. COMBINED OPERATIONS ARE RESTRICTIVE AND MALABSORPTIVE 444
V. PREOPERATIVE WORK-UP 444
A. PATIENT SELECTION CRITERIA 444
B. PREOPERATIVE ASSESSMENT—MULTIDISCIPLINARY APPROACH 445
C. CONTRAINDICATIONS 445
VI. SURGICAL PROCEDURES FOR THE BARIATRIC PATIENT 445
A. LAPAROSCOPIC SLEEVE GASTRECTOMY 445
B. LAPAROSCOPIC ROUX-EN-Y GASTRIC BYPASS 446
C. LAPAROSCOPIC ADJUSTABLE GASTRIC BANDING 447
D. JEJUNOILEAL BYPASS 448
E. VERTICAL BANDED GASTROPLASTY 448
F. BILIOPANCREATIC DIVERSION 448
VII. RESULTS OF BARIATRIC SURGERY 448
A. SURGICAL THERAPY 448
B. RISK REDUCTION 448
E. WEIGHT LOSS 449
VI - Surgical Oncology 451
33 - Tumor Biology, Syndromes, and Genetic Mutations 453
I. SELF-SUFFICIENCY IN GROWTH SIGNALS 453
A. GROWTH FACTORS 453
B. ALTERATION OF GROWTH SIGNALING PATHWAYS 453
C. SOS/RAS/RAF/MITOGEN-ACTIVATED PROTEIN KINASE PATHWAY 453
D. TUMOR GROWTH IS DEPENDENT ON MANY FACTORS 453
II. INSENSITIVITY TO GROWTH-INHIBITORY SIGNALS 453
A. RETINOBLASTOMA PROTEIN 453
III. EVASION OF PROGRAMMED CELL DEATH 454
A. P53 TUMOR-SUPPRESSOR PROTEIN 454
B. EXTRINSIC APOPTOSIS INDUCTION 454
IV. LIMITLESS REPLICATIVE POTENTIAL 454
V. SUSTAINED ANGIOGENESIS 454
VI. TISSUE INVASION AND METASTASIS 455
A. TETHERING MOLECULES ARE ALTERED 455
B. PROTEASES DEGRADE EXTRACELLULAR MATRICES 455
VII. GENETIC INSTABILITY 455
A. THE PREVIOUS SIX (I–VI) CHARACTERISTICS MUST BE OBTAINED THROUGH GENETIC ALTERATION 455
B. MALFUNCTION OF THE “CARETAKER” SYSTEM 455
VIII. FAMILIAL CANCER SYNDROMES 456
A. FAMILIAL ADENOMATOUS POLYPOSIS 456
B. HEREDITARY BREAST-OVARIAN CANCER SYNDROMES 456
D. LI-FRAUMENI SYNDROME 456
E. MULTIPLE ENDOCRINE NEOPLASIA 456
F. VON HIPPEL-LINDAU DISEASE 457
G. COWDEN SYNDROME 457
H. HEREDITARY DIFFUSE GASTRIC CANCER 457
I. PEUTZ-JEGHERS SYNDROME 457
IX. PHARMACOTHERAPY 457
A. TUMOR GROWTH AND KINETICS 457
B. DRUG MECHANISMS AND THERAPEUTICS 457
X. CHEMOTHERAPEUTIC AGENTS: MECHANISMS, USES, AND IMPORTANT TOXICITIES 459
A. ALKYLATING AGENTS 459
B. ANTIMETABOLITES 459
C. ANTITUMOR ANTIBIOTICS 459
D. MITOTIC INHIBITORS 460
E. HORMONAL AGENTS 460
F. IMMUNOTHERAPY 460
G. MISCELLANEOUS 461
RECOMMENDED READINGS 461
34 - Head and Neck Malignancy 462
I. EPIDEMIOLOGY 462
II. WORK-UP OF A NECK MASS 462
III. NECK DISSECTION 463
IV. TREATMENT OF CANCER BY SITE 465
A. CARCINOMA OF THE ORAL CAVITY AND LIP 465
B. OROPHARYNGEAL CARCINOMA 465
C. LARYNGEAL CANCER 465
D. HYPOPHARYNGEAL 466
E. NASOPHARYNGEAL CARCINOMA 467
F. SALIVARY GLAND TUMORS 467
V. NECK DISSECTION INDICATIONS FOR SALIVARY GLAND MALIGNANCY 469
A. RARER SITES OF CARCINOMA 469
35 - Esophageal Malignancy 470
I. ESOPHAGEAL ANATOMY 470
II. EPIDEMIOLOGY 470
III. HISTOLOGY AND RISK FACTORS 470
IV. DIAGNOSIS AND STAGING 471
V. TNM STAGING SYSTEM 472
VI. TREATMENT PLANNING 473
A. IMPLICATIONS FOR THERAPY 474
VII. ESOPHAGECTOMY 474
VIII. ESOPHAGECTOMY APPROACHES 474
IX. ENDOSCOPIC THERAPIES 475
X. CHEMOTHERAPY AND RADIOTHERAPY 476
XI. PALLIATIVE CARE 477
A. DYSPHAGIA AND OBSTRUCTION 477
B. ESOPHAGEAL-AIRWAY FISTULA 477
36 - Gastric Malignancy 478
I. ADENOCARCINOMA OF THE STOMACH 478
A. EPIDEMIOLOGY 478
B. RISK FACTORS 478
C. PATHOLOGIC CLASSIFICATIONS 479
D. CLINICAL MANIFESTATIONS 480
E. SCREENING 480
F. DIAGNOSIS/STAGING 480
I. SURGICAL TREATMENT 481
J. NEOADJUVANT/ADJUVANT THERAPY 483
K. PROGNOSIS (5-YEAR SURVIVAL) 483
II. GASTRIC LYMPHOMA 483
A. GENERAL CONSIDERATIONS 483
B. CLINICAL PRESENTATION 484
C. PATHOLOGY 484
D. DIAGNOSIS 484
E. TREATMENT 484
III. GASTROINTESTINAL STROMAL TUMORS 484
A. GENERAL CONSIDERATIONS 484
B. OTHER CHARACTERISTICS 484
C. DIAGNOSIS 485
D. PATHOLOGIC LESIONS 485
E. TREATMENT 485
37 - Small Bowel Malignancy 486
I. EPIDEMIOLOGY 486
A. INCIDENCE 486
B. TUMOR CHARACTERISTICS 486
C. GENETIC PREDISPOSITION AND PATHOGENESIS 487
II. DIAGNOSIS 488
III. STAGING 490
A. ADENOCARCINOMA 490
B. LYMPHOMA 490
C. SARCOMA AND CARCINOID TUMORS 490
IV. MANAGEMENT 490
A. SURGERY 490
B. CHEMOTHERAPY 490
38 - Malignant Colorectal and Perianal Disease 492
I. COLORECTAL CANCER: EPIDEMIOLOGY 492
A. EACH YEAR IN THE UNITED STATES, 135,000 CASES OF COLORECTAL CANCER WILL BE DIAGNOSED 492
B. ALMOST 50,000 PEOPLE DIE OF COLORECTAL CANCER ANNUALLY IN THE UNITED STATES. 492
II. RISK FACTORS 492
III. SIGNS AND SYMPTOMS 492
IV. SCREENING GUIDELINES FOR COLORECTAL CANCER 493
A. AVERAGE-RISK PATIENT, STARTING AT AGE 50–75 YEARS—ANY OF THE FOLLOWING SCREENING MODALITIES ARE ACCEPTED 493
C. FAMILIAL ADENOMATOUS POLYPOSIS 493
D. HEREDITARY NONPOLYPOSIS COLORECTAL CANCER 493
E. FAMILY HISTORY 493
V. POLYPS 494
VI. PATHOGENESIS 494
A. LOSS OF HETEROZYGOSITY PATHWAY—80% OF CASES 494
B. REPLICATION ERROR REPAIR PATHWAY—20% OF CASES 495
C. ADENOMATOUS POLYPOSIS SYNDROMES 495
D. NONADENOMATOUS POLYPOSIS SYNDROMES 495
E. NONPOLYPOSIS SYNDROMES 495
VII. PREOPERATIVE EVALUATION 496
A. COMPLETE HISTORY 496
B. COLONOSCOPY 496
C. RECTAL CANCER 496
D. CARCINOEMBRYONIC ANTIGEN 496
VIII. TREATMENT OF COLON CANCER 498
A. GENERAL PRINCIPLES 498
B. SURGICAL THERAPY FOR RESECTABLE MASSES 498
C. CHEMOTHERAPEUTIC REGIMENS 498
D. STAGE-SPECIFIC THERAPY 498
IX. RECTAL CANCER 500
A. STAGE-SPECIFIC THERAPY 500
B. OPERATIVE APPROACH 500
C. CHEMOTHERAPEUTIC REGIMENS 501
X. POSTOPERATIVE FOLLOW-UP 501
A. DIAGNOSIS AND TREATMENT 501
B. TREATMENT OF LOCAL RECURRENT DISEASE 502
XI. ANAL CANCER 502
XII. TUMORS OF THE ANAL CANAL 503
XIII. SIGNS AND SYMPTOMS 503
XIV. SCREENING 503
XV. ANATOMY AND CHARACTERIZATION 503
A. ANAL TUMORS ARE CLASSIFIED INTO TWO GROUPS 503
B. ANATOMY 503
XVI. TUMORS OF THE ANAL CANAL 503
A. ANAL INTRAEPITHELIAL NEOPLASIA 503
C. DIAGNOSIS 505
D. STAGING 505
E. TREATMENT 505
F. ADENOCARCINOMA OF THE ANAL CANAL 505
XVII. TUMORS OF THE ANAL MARGIN 505
A. SQUAMOUS CELL CARCINOMA 505
B. DIAGNOSIS AND STAGING 505
C. TREATMENT 505
XVIII. MALIGNANT MELANOMA OF THE ANAL MARGIN/CANAL 506
A. DIAGNOSIS AND STAGING 506
B. TREATMENT 506
39 - Malignant Pancreas Disease 507
I. PANCREATIC ADENOCARCINOMA 507
A. EPIDEMIOLOGY 507
B. CAUSATIVE FACTORS 507
C. PATHOLOGY 508
D. PRESENTATION 508
E. DIAGNOSTIC EVALUATION/STAGING 509
F. SURGICAL THERAPY/RESECTABILITY 511
G. NEOADJUVANT THERAPY 512
H. ADJUVANT THERAPY 512
I. SURVEILLANCE 512
J. SURVIVAL 512
II. PREMALIGNANT CYSTIC NEOPLASMS OF THE PANCREAS 513
A. MUCINOUS CYSTIC NEOPLASMS (MCNS) 513
B. INTRADUCTAL PAPILLARY MUCINOUS NEOPLASMS 513
40 - Diseases of the Breast 515
I. ANATOMY AND PHYSIOLOGY 515
A. ANATOMY BASICS 515
B. LYMPHATIC DRAINAGE 515
C. NERVES 516
D. BLOOD SUPPLY 516
E. PHYSIOLOGY 516
II. HISTORY 516
A. AGE 516
B. MASS 517
C. NIPPLE DISCHARGE (TABLE 40.1) 517
D. BREAST PAIN (MASTODYNIA) 517
E. GYNECOLOGIC HISTORY 517
F. MEDICAL HISTORY 518
G. SURGICAL HISTORY 518
H. FAMILY HISTORY 518
I. CONSTITUTIONAL SYMPTOMS 518
III. PHYSICAL EXAMINATION 518
A. INSPECTION 518
B. PALPATION 518
C. SCREENING 518
IV. RADIOGRAPHIC STUDIES 519
A. MAMMOGRAPHY 519
B. MAMMOGRAPHIC FINDINGS SUGGESTIVE OF MALIGNANCY 519
C. ULTRASONOGRAPHY 519
D. MAGNETIC RESONANCE IMAGING 519
E. DIGITAL BREAST TOMOSYNTHESIS 520
V. EVALUATION OF BREAST MASS 520
A. NIPPLE DISCHARGE 520
B. PALPABLE LESIONS 520
C. FINE-NEEDLE ASPIRATION BIOPSY 520
D. CORE NEEDLE BIOPSY (PERCUTANEOUS) 521
E. EXCISIONAL BIOPSY 521
VI. BENIGN BREAST DISEASE 521
A. GALACTORRHEA 521
B. FIBROCYSTIC CHANGES 521
C. FIBROADENOMA 522
D. PHYLLODES TUMOR AND CYSTOSARCOMA PHYLLODES 522
E. INTRADUCTAL PAPILLOMA 523
F. FAT NECROSIS 523
G. PLASMA CELL MASTITIS AND PERIDUCTAL MASTITIS 523
H. GALACTOCELE 523
I. MASTITIS AND BREAST ABSCESS 524
J. MONDOR DISEASE 524
K. GYNECOMASTIA 524
L. POLAND SYNDROME 525
VII. BREAST CANCER 525
A. EPIDEMIOLOGY 525
B. RISK FACTORS 525
C. CLINICAL PRESENTATION 526
D. TNM CLASSIFICATION 526
E. STAGING 527
F. PATHOLOGIC LESIONS 527
G. SURGICAL TREATMENT OPTIONS 530
H. SURGICAL TREATMENT BY STAGE 531
I. RADIOTHERAPY TO CHEST AND BREAST 532
J. CHEMOTHERAPY AND HORMONAL THERAPY 533
K. BREAST CANCER AND PREGNANCY 534
L. MALE BREAST CANCER 536
41 - Malignant Skin Lesions 538
I. BASAL CELL CARCINOMA 538
A. GENERAL 538
B. DIAGNOSIS 538
C. TREATMENT 538
II. SQUAMOUS CELL CARCINOMA 539
VII - Hepatobiliary Surgery 545
42 - Benign Gallbladder and Biliary Tree 547
I. ANATOMY 547
A. GALLBLADDER 547
B. BILE DUCTS 547
C. ANOMALIES 548
II. CHOLELITHIASIS 548
A. INCIDENCE 548
B. CAUSATIVE FACTORS 548
C. TYPES OF GALLSTONES 549
D. TREATMENT OF ASYMPTOMATIC CHOLELITHIASIS 549
III. SYMPTOMATIC CHOLELITHIASIS 549
A. BILIARY COLIC 549
B. ACUTE CALCULOUS CHOLECYSTITIS 550
IV. CHOLEDOCHOLITHIASIS 552
A. CAUSATIVE FACTORS AND NATURAL HISTORY 552
B. TREATMENT 552
V. CHOLANGITIS 554
A. CAUSATIVE FACTORS AND PATHOPHYSIOLOGY 554
B. CLINICAL FEATURES AND DIAGNOSIS 554
C. TREATMENT 554
VI. ACALCULOUS CHOLECYSTITIS 555
A. EPIDEMIOLOGY AND PATHOGENESIS 555
B. NATURAL HISTORY 555
C. CLINICAL MANIFESTATION AND DIAGNOSIS 555
D. TREATMENT 555
VII. OTHER DISORDERS OF THE GALLBLADDER 556
A. GALLSTONE DISEASE IN PREGNANCY 556
B. BILIARY DYSKINESIA 556
C. BILIARY SLUDGE 556
D. MIRIZZI SYNDROME 556
E. GALLSTONE ILEUS 556
F. EMPHYSEMATOUS CHOLECYSTITIS 557
G. CALCIFIED “PORCELAIN” GALLBLADDER 557
VIII. MEDICAL TREATMENTS 557
A. ORAL DISSOLUTION THERAPY 557
B. EXTRACORPOREAL SHOCK WAVE LITHOTRIPSY 558
IX. LAPAROSCOPIC CHOLECYSTECTOMY 558
A. SETUP 558
B. TECHNIQUE (FIGS. 42.1 AND 42.2) 558
C. POSTOPERATIVE CARE 559
D. COMPLICATIONS 559
43 - Malignant Gallbladder and Biliary Tree 562
I. GALLBLADDER CANCER 562
A. GENERAL CONSIDERATIONS 562
B. PRESENTATION 562
C. TREATMENT 562
II. BILE DUCT CANCER (CHOLANGIOCARCINOMA) 563
A. GENERAL CONSIDERATIONS 563
B. INTRAHEPATIC CHOLANGIOCARCINOMA 563
C. EXTRAHEPATIC CHOLANGIOCARCINOMA 564
44 - Benign Liver Disease, Cirrhosis, and Portal Hypertension 565
I. PATHOPHYSIOLOGY 565
II. MORPHOLOGY 565
III. ETIOLOGY 565
IV. DIAGNOSIS 567
V. CLASSIFICATION 568
VI. CONSEQUENCES OF CIRRHOSIS 569
VII. HEPATIC SYNDROMES 575
45 - Liver Tumors 576
VIII - Transplant Surgery 583
46 - Renal Transplantation 585
I. GENERAL CONSIDERATIONS 585
A. HISTORY AND EPIDEMIOLOGY 585
B. IMMUNOLOGY OF RENAL TRANSPLANTATION 585
C. IMMUNOSUPPRESSION 585
II. EVALUATION OF CANDIDATES FOR TRANSPLANTATION 586
A. INDICATIONS 586
C. RELATIVE CONTRAINDICATIONS 586
D. PATIENT EVALUATION 586
E. INDICATION FOR PRETRANSPLANT NATIVE NEPHRECTOMY 587
III. KIDNEY DONATION 587
A. LIVING DONOR KIDNEY TRANSPLANTATION 587
B. CLASSICALLY DEFINED DONOR CATEGORIES 587
IV. SPECIFIC OPERATIVE CONSIDERATIONS 588
A. LIVING DONOR NEPHRECTOMY 588
B. TRANSPLANT PROCEDURE 588
V. POSTOPERATIVE CONSIDERATIONS 588
A. POSTOPERATIVE CARE 588
B. ASSESSMENT OF GRAFT FUNCTION 589
C. COMPLICATIONS 589
VI. OUTCOMES 590
A. SURVIVAL BENEFIT OF RENAL TRANSPLANTATION 590
B. SURVIVAL 590
47 - Liver Transplantation 593
I. GENERAL CONSIDERATIONS 593
A. HISTORY 593
B. INDICATIONS AND LISTING PROCESS FOR TRANSPLANTATION 593
C. SPECIFIC INDICATIONS 593
D. CONTRAINDICATIONS 594
E. ORGAN SELECTION 594
II. SPECIFIC OPERATIVE CONSIDERATIONS 595
A. TRADITIONAL OPERATIVE TECHNIQUE 595
B. PIGGYBACK TECHNIQUE 596
C. LIVING DONOR HEPATECTOMY 596
III. POSTOPERATIVE CONSIDERATIONS 596
A. POSTOPERATIVE CARE 596
B. IMMUNOSUPPRESSION (PROTOCOLS VARY BY INSTITUTION) 596
C. ASSESSMENT OF GRAFT FUNCTION 597
D. COMPLICATIONS 597
48 - Pancreas Transplantation 600
I. GENERAL CONSIDERATIONS 600
A. HISTORY AND EPIDEMIOLOGY 600
B. INDICATIONS FOR PANCREAS TRANSPLANTATION 600
C. TYPES OF PANCREAS TRANSPLANTS 600
D. ORGAN SELECTION 601
II. SPECIFIC OPERATIVE CONSIDERATIONS 601
A. TRANSPLANT ANATOMY 601
B. MANAGEMENT OF EXOCRINE SECRETIONS 601
III. POSTOPERATIVE CONSIDERATIONS 601
A. POSTOPERATIVE CARE 601
B. COMPLICATIONS 602
C. OUTCOMES 602
IV. ISLET CELL TRANSPLANTATION 603
A. BACKGROUND 603
B. INDICATIONS 603
C. TECHNIQUE 603
D. OUTCOMES 603
V. PANCREAS VERSUS ISLET CELL TRANSPLANTATION 604
IX - Endocrine Surgery 605
49 - Thyroid 607
I. EMBRYOLOGY 607
A. THYROID DEVELOPMENT 607
B. DEVELOPMENTAL ANOMALIES 607
II. ANATOMY 607
A. OVERVIEW 607
B. ARTERIAL SUPPLY 607
C. VENOUS DRAINAGE 608
D. NERVES 608
E. LYMPHATICS 608
F. HISTOLOGY 608
III. PHYSIOLOGY 608
A. IODINE METABOLISM 608
B. THYROID HORMONE SYNTHESIS 608
C. THYROID HORMONE FUNCTION 608
D. THYROID HORMONE REGULATION 609
E. CALCITONIN 609
IV. WORK-UP OF THYROID DISEASE 609
A. CLINICAL PRESENTATION 609
B. LABORATORY DATA 609
C. IMAGING 610
D. BIOPSY 610
V. HYPERTHYROIDISM 610
A. DIFFUSE TOXIC GOITER—GRAVES DISEASE 610
B. TOXIC ADENOMA—PLUMMER DISEASE 611
C. TOXIC MULTINODULAR GOITER 611
D. THYROID STORM 611
VI. HYPOTHYROIDISM 611
A. CHRONIC LYMPHOCYTIC THYROIDITIS—HASHIMOTO THYROIDITIS 611
VII. THYROIDITIS AND NONTOXIC GOITERS 612
A. ACUTE SUPPURATIVE THYROIDITIS 612
B. SUBACUTE THYROIDITIS 612
C. RIEDELS THYROIDITIS (INVASIVE FIBROUS THYROIDITIS) 612
D. NONTOXIC GOITER 613
VIII. THYROID NODULES 613
A. CLINICAL PRESENTATION 613
B. CLINICAL EVALUATION 613
C. MANAGEMENT BASED ON FINE-NEEDLE ASPIRATION RESULTS 613
D. CYSTIC NODULES 613
E. INCIDENTALOMA 614
IX. THYROID NEOPLASMS 614
A. EPIDEMIOLOGY 614
B. PAPILLARY THYROID CARCINOMA 614
C. FOLLICULAR THYROID CARCINOMA 615
D. HĂśRTHLE CELL CARCINOMA 615
E. MEDULLARY THYROID CANCER 615
F. ANAPLASTIC THYROID CANCER 616
G. THYROID LYMPHOMA 616
H. ADJUVANT THERAPY 616
50 - Parathyroid 618
I. PARATHYROID EMBRYOLOGY AND ANATOMY 618
A. EMBRYOLOGY 618
B. ANATOMY 618
C. PHYSIOLOGY 618
II. PRIMARY HYPERPARATHYROIDISM 619
A. GENERAL 619
B. CAUSATIVE FACTORS 619
C. PRESENTATION 619
D. DIAGNOSIS 619
E. MANAGEMENT 620
III. SECONDARY HYPERPARATHYROIDISM 621
A. CAUSATIVE FACTORS 621
B. SYMPTOMS 621
C. TREATMENT 621
IV. TERTIARY HYPERPARATHYROIDISM 621
A. CAUSATIVE FACTOR 621
B. SYMPTOMS 622
C. TREATMENT 622
V. PARATHYROID CARCINOMA 622
51 - Adrenal Gland 623
I. EMBRYOLOGY AND ANATOMY 623
A. GENERAL 623
B. ARTERIAL SUPPLY 623
C. VENOUS DRAINAGE 623
D. CORTEX 623
E. MEDULLA 623
II. ZONA GLOMERULOSA—MINERALOCORTICOIDS 624
X - Vascular Surgery 641
53 - Thromboembolic Disease 643
I. INTRODUCTION 643
A. EPIDEMIOLOGY 643
B. CAUSATIVE FACTORS 643
D. CLINICAL PRESENTATION 644
E. DIFFERENTIAL DIAGNOSES 644
F. DIAGNOSIS 644
G. SEQUELAE 644
II. METHODS OF PROPHYLAXIS AND TREATMENT OF DEEP VENOUS THROMBOSES AND PULMONARY EMBOLI 645
A. DEEP VEIN THROMBOSIS PROPHYLAXIS 645
B. TREATMENT OF DEEP VEIN THROMBOSIS AND PULMONARY EMBOLI 645
C. PROPHYLACTIC INFERIOR VENA CAVA FILTER PLACEMENT 647
III. AN APPROACH TO PROPHYLAXIS 647
A. DETERMINE THE PATIENT’S RISK FACTORS 647
B. PROPHYLAXIS OF CHOICE 647
IV. APPROACH TO THE PATIENT WITH PULMONARY EMBOLUS 648
A. PHYSIOLOGY 648
D. SURGICAL TREATMENT OPTIONS 648
54 - Aneurysms 650
I. EPIDEMIOLOGY 650
A. GENERAL 650
B. CASE REPORT 650
C. RISK FACTORS 650
D. CAUSATIVE FACTORS 651
II. PATHOLOGY 651
A. LOCATION 651
B. CHARACTERISTICS 651
C. ASSOCIATED MANIFESTATIONS OF DIFFUSE ATHEROSCLEROSIS 651
III. NATURAL HISTORY 651
A. GENERAL CONSIDERATIONS 651
B. STATISTICS 652
IV. CLINICAL PRESENTATION 652
A. SYMPTOMS 652
B. PHYSICAL EXAMINATION 652
V. DIAGNOSTIC STUDIES 652
A. PLAIN FILMS 652
B. B-MODE ULTRASOUND 652
C. COMPUTED TOMOGRAPHY SCAN 653
D. MAGNETIC RESONANCE IMAGING 653
E. AORTOGRAPHY 653
VI. ELECTIVE MANAGEMENT OF ABDOMINAL AORTIC ANEURYSM 653
A. OPERATIVE INDICATIONS 653
B. PREOPERATIVE WORK-UP 653
C. PREOPERATIVE PREPARATION 654
VII. OPEN ABDOMINAL AORTIC ANEURYSM REPAIR 654
A. APPROACH 654
B. OPERATIVE STEPS 654
C. INTRAOPERATIVE PROBLEMS 655
D. PROSTHETIC GRAFT 655
E. POSTOPERATIVE COURSE 655
VIII. COMPLICATIONS 656
A. LOWER EXTREMITY ISCHEMIA 656
B. CARDIAC EVENTS 656
C. RENAL INSUFFICIENCY 656
D. STROKE 656
E. COLONIC ISCHEMIA 656
F. SPINAL CORD ISCHEMIA 656
G. SEXUAL DYSFUNCTION 656
H. LATE COMPLICATIONS 657
IX. ENDOVASCULAR ABDOMINAL AORTIC ANEURYSM REPAIR 657
A. INDICATIONS 657
B. PROCEDURE 657
C. LONG-TERM CARE 658
D. COMPLICATIONS 658
E. OUTCOMES 659
X. OPERATIVE MORTALITY 659
A. OPEN REPAIR 659
B. ENDOVASCULAR ABDOMINAL AORTIC ANEURYSM REPAIR 659
XI. RUPTURED ABDOMINAL AORTIC ANEURYSM 659
A. SYMPTOMS 659
B. PRINCIPLES OF MANAGEMENT 659
XII. ABDOMINAL AORTIC ANEURYSM SCREENING (TABLE 54.3) 660
A. ULTRASOUND 660
55 - Peripheral Vascular Disease 661
I. DEFINITIONS 661
II. PERIPHERAL ARTERIAL DISEASE 661
A. EPIDEMIOLOGY 661
B. RISK FACTORS 661
C. NATURAL HISTORY 661
D. PATHOPHYSIOLOGY 662
E. SYMPTOMS 662
F. PHYSICAL EXAMINATION FINDINGS 663
G. LAB WORK 663
H. DIAGNOSTIC STUDIES 663
III. MANAGEMENT OF ATHEROSCLEROTIC PERIPHERAL ARTERIAL DISEASE 666
A. MEDICAL MANAGEMENT 666
B. REVASCULARIZATION THERAPY 666
C. CRITICAL LIMB ISCHEMIA 669
D. ACUTE LIMB ISCHEMIA 669
IV. RENAL ARTERY DISEASE 670
A. EPIDEMIOLOGY 670
B. NATURAL HISTORY 670
C. CLINICAL CONSEQUENCE 670
D. PATHOPHYSIOLOGY 671
E. DIAGNOSIS 672
F. RENAL ARTERY ANEURYSMS 673
V. LOWER EXTREMITY ANEURYSM DISEASE 674
A. EPIDEMIOLOGY 674
B. NATURAL HISTORY 674
C. FEMORAL ARTERY ANEURYSMS 674
D. POPLITEAL ARTERY ANEURYSMS 675
E. FEMORAL ARTERY PSEUDOANEURYSM 676
F. MYCOTIC ANEURYSMS 676
VI. CHRONIC VENOUS INSUFFICIENCY 677
A. OVERVIEW 677
B. DIAGNOSIS 677
C. MANAGEMENT 678
56 - Carotid Disease 680
I. BACKGROUND: STROKE 680
II. DIAGNOSIS 681
A. HISTORY 681
B. PHYSICAL EXAMINATION 682
C. IMAGING 682
III. DIFFERENTIAL DIAGNOSIS OF STROKE/TRANSIENT ISCHEMIC ATTACKS 684
A. ATHEROSCLEROTIC DISEASE 684
B. FIBROMUSCULAR DYSPLASIA 685
C. COILS AND KINKS BECAUSE OF ANATOMIC VARIATION 685
D. CAROTID ANEURYSMS 685
E. CAROTID DISSECTION 685
F. RADIATION ARTERITIS 685
G. TAKAYASU ARTERITIS 685
H. GIANT CELL ARTERITIS 686
IV. MANAGEMENT 686
A. MEDICAL 686
B. SURGICAL—CAROTID ENDARTERECTOMY 686
C. ENDOVASCULAR—CAROTID ARTERY STENTING 687
V. POSTOPERATIVE COMPLICATIONS 687
A. CARDIOVASCULAR 688
B. NEUROLOGIC 688
VI. POSTOPERATIVE CARE 688
57 - Mesenteric Ischemia 689
I. ANATOMY AND PHYSIOLOGY 689
A. VASCULAR SUPPLY 689
B. COLLATERAL VESSELS 689
C. PHYSIOLOGY 689
II. EPIDEMIOLOGY 690
III. ACUTE MESENTERIC ISCHEMIA 690
A. RISK FACTORS 690
B. CLINICAL PRESENTATION 690
C. CAUSATIVE FACTORS 690
D. DIAGNOSIS 691
E. MANAGEMENT 691
IV. CHRONIC MESENTERIC ISCHEMIA 693
A. CAUSATIVE FACTORS 693
B. DIAGNOSIS 693
C. TREATMENT 693
D. PROGNOSIS 693
V. MESENTERIC VENOUS THROMBOSIS 694
A. CAUSATIVE FACTORS—VENOUS THROMBOSIS PREDOMINANTLY A RESULT OF STAGNATION OF BLOOD FLOW, HYPERCOAGULABILITY, AND VASCULAR INJU... 694
B. CLINICAL PRESENTATION 694
C. DIAGNOSIS 694
D. TREATMENT 694
E. PROGNOSIS 695
VI. MEDIAN ARCUATE LIGAMENT SYNDROME (CELIAC ARTERY COMPRESSION SYNDROME) 695
A. CAUSATIVE FACTORS 695
B. PRESENTATION 695
C. DIAGNOSIS 695
D. TREATMENT 695
58 - Dialysis Access 696
I. INTRODUCTION 696
II. GENERAL OVERVIEW OF DIALYSIS ACCESS TYPES 696
A. SHORT-TERM/EMERGENT ACCESS 696
B. LONG-TERM ACCESS 696
III. DIALYSIS CATHETERS 696
A. NONTUNNELED (NONCUFFED CATHETERS) 696
B. TUNNELED CATHETERS (CUFFED) 697
IV. ARTERIOVENOUS FISTULAS AND GRAFTS 697
A. ARTERIOVENOUS FISTULA 697
B. ARTERIOVENOUS GRAFT 697
V. ARTERIOVENOUS FISTULA MATURATION 698
VI. COMPLICATIONS OF ARTERIOVENOUS FISTULAS AND GRAFTS 699
VII. PERITONEAL DIALYSIS 700
59 - The Diabetic Patient 702
I. DEFINITIONS 702
A. DIABETES 702
B. METABOLIC SYNDROME 702
II. MEDICAL THERAPIES 703
A. ORAL ANTIHYPERGLYCEMICS 703
B. INSULIN 703
D. ADJUSTING MEDICATIONS FOR SURGERY 705
E. HYPOGLYCEMIA (BLOOD GLUCOSE LEVEL LESS THAN 70 MG/DL) 705
F. DIABETIC KETOACIDOSIS 706
G. NONKETOTIC HYPEROSMOLAR HYPERGLYCEMIA 707
III. GLYCEMIC CONTROL IN THE CRITICALLY ILL PATIENT 707
A. HYPERGLYCEMIC RESPONSE TO SURGERY AND ANESTHESIA 707
B. IATROGENIC HYPERGLYCEMIA 707
C. GLYCEMIC CONTROL 707
D. SPECIAL POPULATIONS 707
IV. COMPLICATIONS OF DIABETES 708
A. TISSUE HYPOXIA CAUSED BY MICROVASCULAR DISEASE 708
V. DIABETIC FOOT ULCERS 709
XI - Cardiothoracic Surgery 713
60 - Benign Tumors of the Lung 715
I. OVERVIEW 715
II. HISTORY 715
III. PHYSICAL EXAMINATION 715
IV. INITIAL EVALUATION 715
V. IMAGING 716
VI. BIOPSY OPTIONS 716
VII. EPITHELIAL TUMORS 717
A. POLYPS 717
B. PAPILLOMA 717
C. MUCOUS GLAND ADENOMA 717
VIII. MESENCHYMAL TUMORS 718
A. VESSEL ORIGIN 718
IX. MISCELLANEOUS TUMORS 719
A. FIBROMA 719
B. HAMARTOMA 719
C. TERATOMA 720
X. OTHER TUMORS 720
A. LIPOMA 720
B. CHONDROMA 720
XI. INFLAMMATORY PSEUDOTUMORS 721
A. PLASMA CELL GRANULOMA 721
B. PULMONARY HYALINIZING GRANULOMA 721
XII. OTHER BENIGN TUMORS 721
A. MUCINOUS CYSTADENOMA 721
B. NODULAR AMYLOID 722
61 - Malignant Tumors of the Lung 723
I. EPIDEMIOLOGY 723
A. GENERAL 723
B. MORTALITY 723
II. ETIOLOGY 723
A. CIGARETTE SMOKING 723
B. EXPOSURE 723
III. SCREENING 724
A. GENERAL 724
B. SCREENING MODALITIES 724
IV. SOLITARY PULMONARY NODULE 725
A. GENERAL 725
B. DIFFERENTIAL DIAGNOSIS 725
C. RADIOGRAPHIC CHARACTERISTICS OF BENIGN NODULE 725
D. MANAGEMENT OF SOLITARY PULMONARY NODULE 725
V. CLINICAL FEATURES 725
A. RESPIRATORY 725
B. ASSOCIATED SYNDROMES 726
C. EVIDENCE OF METASTATIC OR LOCALLY ADVANCED DISEASE 726
D. METHOD OF SPREAD 726
VI. PATHOLOGY 726
A. HISTOLOGIC CLASSIFICATION 726
B. LOCATION OF PRIMARY TUMORS 727
VII. ADENOCARCINOMA—40% 727
XII - Surgical Subspecialties 769
65 - General Pediatric Surgery 771
I. FLUIDS AND NUTRITION 771
A. MAINTENANCE FLUIDS 771
B. RESUSCITATION FLUIDS 771
C. FLUID BALANCE 771
D. ACID-BASE ANOMALIES 771
E. TOTAL PARENTERAL NUTRITION 772
II. LESIONS OF THE HEAD AND NECK 772
A. THRYOGLOSSAL DUCT CYST 772
B. BRANCHIAL CLEFT ANOMALIES 773
III. THORACIC DISORDERS 773
A. PULMONARY SEQUESTRATION 773
B. CONGENITAL CYSTIC ADENOMATOID MALFORMATION 774
C. CONGENITAL DIAPHRAGMATIC HERNIA 774
IV. ESOPHAGEAL ANOMALIES 776
A. TRACHEOESOPHAGEAL FISTULA 776
B. ISOLATED ESOPHAGEAL ATRESIA—TYPE A (6%) 777
C. SURVIVAL 778
V. GASTROINTESTINAL TRACT 778
A. HYPERTROPHIC PYLORIC STENOSIS 778
B. INTESTINAL OBSTRUCTION IN THE NEONATE 779
D. NECROTIZING ENTEROCOLITIS 782
E. MECKEL DIVERTICULUM 783
F. APPENDICITIS 783
G. GASTROESOPHAGEAL REFLUX 784
VI. ABDOMINAL WALL DEFECTS 785
A. OMPHALOCELE 785
B. GASTROSCHISIS 785
C. UMBILICAL HERNIA 786
D. INGUINAL HERNIA 786
E. SHORT BOWEL SYNDROME 787
VII. ANORECTAL MALFORMATIONS 787
VIII. NEOPLASMS 788
A. NEUROBLASTOMA 788
B. WILMS TUMOR 788
66 - Neurosurgery 790
I. CRANIAL URGENCIES AND EMERGENCIES 790
A. SPONTANEOUS SUBARACHNOID HEMORRHAGE 790
C. MALIGNANT STROKE (FIG. 66.3) 798
D. HYDROCEPHALUS 799
II. SPINAL URGENCIES AND EMERGENCIES 801
A. DEGENERATIVE SPINAL DISEASE 801
III. CNS TUMORS 804
A. BRAIN TUMORS (FIG. 66.5) 804
B. SPINAL TUMORS (FIG. 66.7) 809
IV. CNS INFECTIOUS URGENCIES AND EMERGENCIES (FIG. 66.8) 811
A. EPIDURAL ABSCESS 811
B. SUBDURAL EMPYEMA 813
C. PARENCHYMAL ABSCESS 814
V. OTHER NEUROSURGICAL URGENCIES/EMERGENCIES 814
A. SEIZURES AND STATUS EPILEPTICUS 814
B. BACLOFEN TOXICITY AND WITHDRAWAL 816
VI. HERNIATION SYNDROMES AND BRAIN DEATH 817
A. HERNIATION SYNDROMES CAN RESULT FROM A VARIETY OF BOTH TRAUMATIC AND NONTRAUMATIC CRANIAL PATHOLOGIES; THERE ARE FOUR COMMON ... 817
B. BRAIN DEATH 818
67 - Orthopedic Surgery 821
I. ASSESSMENT OF THE ORTHOPEDIC PATIENT 821
A. BASIC ADVANCED TRAUMA LIFE SUPPORT PRINCIPLES 821
II. ORTHOPEDIC EMERGENCIES 821
A. HEMODYNAMICALLY UNSTABLE PELVIC FRACTURES 821
B. OPEN FRACTURES 823
C. COMPARTMENT SYNDROME 826
D. VASCULAR INJURY ASSOCIATED WITH EXTREMITY TRAUMA 827
E. TRAUMATIC ARTHROTOMIES 828
F. GUNSHOT WOUNDS 830
G. BITE INJURIES 831
68 - Plastic Surgery: Breast Reconstruction 834
I. INTRODUCTION 834
II. RELEVANT ANATOMY FOR RECONSTRUCTION 834
A. VASCULAR SUPPLY (FIG. 68.1) 834
B. INNERVATION 834
III. PREOPERATIVE EVALUATION 834
A. GOALS OF RECONSTRUCTION 834
B. TIMING 835
C. CURRENT TECHNIQUES 836
D. TECHNIQUE SELECTION CRITERIA 836
IV. TECHNIQUES 836
A. PROSTHETIC RECONSTRUCTION USING IMPLANTS AND EXPANDERS 836
B. AUTOLOGOUS TISSUE TRANSFER 837
C. NIPPLE AREOLAR COMPLEX RECONSTRUCTION (FIG. 68.4) 840
V. ONCOPLASTIC SURGERY 841
A. DEFINITION 841
B. CONSIDERATIONS 841
C. TECHNIQUES 841
VI. POSTRECONSTRUCTION FOLLOW-UP 842
XIII - Future of Surgery 845
69 - Robotics and Newer Surgical Technologies 847
I. SINGLE-INCISION LAPAROSCOPIC SURGERY 847
II. ROBOTIC SURGERY 847
III. NATURAL ORIFICE TRANSLUMINAL ENDOSCOPIC SURGERY 849
IV. ENDOLUMINAL AND ENDOVASCULAR SURGERY 850
XIV - Procedures 853
70 - Procedures 855
I. INDICATIONS FOR AN ARTIFICIAL AIRWAY 855
A. ABSOLUTE 855
B. RELATIVE 855
II. NONSURGICAL TECHNIQUES 855
A. INITIAL/TEMPORIZING MANEUVERS 855
B. OROTRACHEAL INTUBATION 856
C. NASOTRACHEAL INTUBATION 858
D. COMPLICATIONS 859
III. SURGICAL AIRWAY OPTIONS AND METHODS 859
A. CRICOTHYROIDOTOMY 859
B. TRACHEOSTOMY 860
C. PERCUTANEOUS TRACHEOSTOMY 861
D. COMPLICATIONS 861
IV. ALTERNATE AIRWAY METHODS 862
A. COMBITUBE 862
B. FIBEROPTIC BRONCHOSCOPY 862
C. LARYNGEAL MASK AIRWAY 862
V. ARTERIAL CATHETERIZATION 862
A. INDICATIONS 862
B. TECHNIQUES 862
C. COMPLICATIONS 864
VI. BLADDER CATHETERIZATION 864
A. INDICATIONS FOR INDWELLING URETHRAL CATHETER 864
B. COMPLICATIONS OF INDWELLING URINARY CATHETER 865
C. CONTRAINDICATIONS OF BLADDER CATHETERIZATION 865
D. TECHNIQUES 865
E. ALTERNATIVES 873
VII. CENTRAL VENOUS LINES 873
A. INDICATIONS 873
C. TECHNIQUES 873
D. COMPLICATIONS 876
VIII. ENTERAL ACCESS 877
A. NASOGASTRIC TUBES 877
B. OROGASTRIC TUBES 878
C. FEEDING TUBES 879
X. PULMONARY ARTERY (SWAN-GANZ) CATHETERIZATION 881
A. INDICATIONS 881
B. DESIGN 882
C. MEASUREMENT 882
D. PITFALLS 884
XI. ABSCESS DRAINAGE 885
A. TECHNIQUE 885
XII. THORACENTESIS 885
A. INDICATIONS 885
B. TECHNIQUE 886
C. POSITIONING 886
D. PROCEDURE 886
E. INTERPRETATION OF RESULTS (TABLE 70.3) 887
F. COMPLICATIONS 888
XV - Rapid References 889
71 - Rapid References 891
Index 895
A 895
B 903
C 908
D 918
E 920
F 923
G 925
H 928
I 933
J 935
K 936
L 936
M 939
N 943
O 947
P 948
Q 956
R 956
S 958
T 964
U 969
V 970
W 971
X 972
Y 972
Z 972