Updated: Feb 11, 2008
In 1939, Kanavel, author of the landmark Infections of the Hand, observed, "In almost all cases of serious infection the difficulty is to make a correct diagnosis both as to the nature of the infection and the position of the pus."1 Specific infections covered in this article include paronychia, felon, herpetic whitlow, tenosynovitis, and deep fascial space infections.
Few structures of the body are as complex or as unique as the human hand with the functions of sensation, mobility, and strength in one small area. The hand consists of multiple compartments and planes, the knowledge of which allows one to understand the pathophysiology, diagnosis, and treatment of hand infections.
Paronychia
Infection of the area of the lateral nail fold (paronychium) is typically due to superficial trauma (eg, hangnails, nail biting, manicuring, finger sucking). Artificial nails have also been associated with acute paronychia. Although paronychia typically starts as a cellulitis, its progression to abscess formation is not uncommon. Infection that spreads to the proximal nail edge is termed an eponychia. Occasionally, infection can spread under the nail plate itself, resulting in a subungual abscess.
Chronic paronychia resembles acute paronychia but is usually nonsuppurative. People at risk include those repeatedly exposed to water and/or irritants as well as those who are immunocompromised. Metastatic cancer, subungual melanoma, and squamous cell cancer may rarely present as chronic paronychia.
Felon
The distal palmar phalanx is compartmentalized by tangentially oriented fibrous septa. These septa result in a closed compartment at the distal phalanx, which helps prevent the proximal spread of infection. Infection typically is due to direct inoculation of bacteria by penetrating trauma but may be caused by hematogenous spread and by local spread from an untreated paronychia.
Infection results in edema and increased pressure within the closed compartment. This, in turn, can impair venous outflow and lead to a local compartment syndrome and myonecrosis. Invasion of the bone leads to osteomyelitis.
Herpetic whitlow
Herpes simplex virus (HSV) infection of the distal finger typically results from direct inoculation of the virus into broken skin. Infection by type 1 or type 2 HSV is clinically indistinguishable. As in herpes infections elsewhere in the body, it is believed that the virus can remain dormant in the neural ganglia, leading to recurrent infections.
Tendon sheaths consist of a visceral layer adherent to the tendon and a parietal layer. Notably, the flexor tendon sheath of the thumb is continuous with the radial bursae, whereas the flexor tendon sheath of the fifth digit is continuous with the ulnar bursae. In 80% of individuals, communication exists between the radial and ulnar bursae. The tenosynovial coverings of the second, third, and fourth digits do not communicate with either the radial bursae or the ulnar bursae in most individuals.
Infection within a flexor tendon sheath, as in other infections of the hand, usually is the result of direct inoculation of bacteria from penetrating trauma.
One common cause of penetrating trauma occurs when one person strikes another person in the mouth, resulting in a fight bite. A tooth may penetrate the metacarpophalangeal (MCP) joint capsule or an extensor tendon. Because the injury occurs while the joint is in flexion, deeper injuries to the extensor tendon or the MCP joint capsule or bone can be easily missed when the hand is examined in extension. For more information, see Bites, Human.
Infection can also occur by hematogenous spread, with Neisseria gonorrhoeae as the offending agent in many cases.
Pyogenic flexor tenosynovitis, an infection of the flexor tendon, is most common in the index, middle, and ring fingers and can form as early as 6 hours after the initial penetration.
Infection typically follows the course of the tendon sheath, which results in the spread of infection into the radial or ulnar bursae, depending on the primary tendon sheath involved. Elevated pressure within the tendon sheath due to infection may impair nutrient flow to the tendon. Tendon necrosis, impaired function, or both are disastrous sequelae of untreated elevated tendon sheath pressure.
Deep fascial space infection
The deep fascial spaces of the hand are potential spaces and consist of the dorsal subaponeurotic space, subfascial web space, midpalmar space, and thenar space. The dorsal subaponeurotic space lies dorsal to the extensor tendons of the hand. The subfascial web space is contiguous with the dorsal subcutaneous space of the digits. The midpalmar space is demarcated by the palmar interosseous muscles dorsally and the flexor tendons of the third, fourth, and fifth digits ventrally. Lastly, the thenar space extends from the long metacarpal bone to the thenar eminence and consists of the area between the adductor pollicis muscle dorsally and the flexor tendon of the second digit ventrally.
These compartments are susceptible to infection by direct penetrating trauma, spread from a neighboring compartment, or hematogenous seeding. Because of the dorsal location of the lymphatics, erythema and swelling commonly appear over the dorsum of the hand, even when the injury is of palmar origin.
For more on hand anatomy, see Hand, Anatomy.
Infections of the hand (especially dominant-hand infections) can be devastating and frequently require admission for antibiotic therapy and/or surgical intervention. Possible complications are outlined below (see Complications).
| Bites, Animal | Fractures, Hand |
| Bites, Human | Herpetic Whitlow |
| Cellulitis | Nailbed Injuries |
| Compartment Syndrome, Extremity | Osteomyelitis |
| Felon | Paronychia |
| Fingertip Injuries | Tenosynovitis |
Septic joint
Primary hand tumors
Trauma, lacerations and tendon injury
Vascular disorders
In cases of severe infection causing vascular insufficiency, Doppler ultrasonography may assist in evaluation.
Prompt consultation with an experienced hand surgeon is indicated for patients with evidence of infectious tenosynovitis, deep fascial space infections, or osteomyelitis. Cases of chronic paronychia that do not respond to initial therapy should be referred to a dermatologist.
The goals of pharmacotherapy are to eradicate the infection and to prevent complications. With the rise of methicillin-resistant Staphylococcus aureus as a cause of hand infections, coverage with appropriate antibiotics is important.4 In this era, cephalexin alone is inappropriate coverage for hand infections, and coverage for all infections should include MRSA coverage.
Therapy must cover all likely pathogens in the context of the clinical setting.
First-generation cephalosporin that inhibits bacterial growth by inhibiting bacterial cell wall synthesis. Bactericidal and effective against rapidly growing organisms forming cell walls. Primarily active against skin flora. Typically used for skin structure coverage and as prophylaxis in minor procedures. DOC for immunocompromised patients with paronychia.
250-500 mg PO qid
25-50 mg/kg/d PO divided q6h
Aminoglycosides increase nephrotoxic potential of cephalexin
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in patients with renal impairment
Lincosamide useful as treatment against serious skin and soft tissue infections caused by most staphylococcal strains. Also effective against aerobic and anaerobic streptococci, except enterococci. Inhibits bacterial protein synthesis by inhibiting peptide chain initiation at bacterial ribosome where it preferentially binds to 50S ribosomal subunit, causing bacterial growth inhibition. DOC for paronychia in children and those who wash dishes.
150-450 mg PO qid
20-30 mg/kg/d PO divided qid
Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects of clindamycin; antidiarrheals may delay absorption of clindamycin
Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis
Combination antimicrobial agent that uses a beta-lactamase inhibitor with ampicillin. Covers skin, enteric flora, and anaerobes. DOC for infectious tenosynovitis and deep fascial space infections.
3 g IV q6h
<12 years: Not established
<12 years: 25 mg/kg IV q6h (based on ampicillin component)
Probenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of oral contraceptives
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Patients with renal failure may require dose adjustment; mononucleosis increases incidence of rash with ampicillin-sulbactam therapy; evaluate appearance of rash carefully to differentiate nonallergic ampicillin rash from hypersensitivity reaction
First-generation semisynthetic cephalosporin, which, by binding to 1 or more penicillin-binding proteins, arrests bacterial cell wall synthesis and inhibits bacterial growth. Primarily active against skin flora, including S aureus. Typically used alone for skin and skin-structure coverage. An alternate DOC for infectious tenosynovitis and deep fascial space infections.
1 g IV/IM q6h
20 mg/kg IV/IM q8h
Probenecid prolongs effect of cefazolin; coadministration with aminoglycosides may increase renal toxicity; may yield false-positive urine-dip test for glucose
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in renal impairment; superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy
Potent antibiotic directed against gram-positive organisms and active against Enterococcus species. Useful in treatment of septicemia and skin structure infections. Indicated for patients who cannot receive or whose conditions have not responded to penicillins and cephalosporins or for those who have infections with resistant staphylococci. For abdominal penetrating injuries, combine with agent active against enteric flora and/or anaerobes. DOC (in conjunction with gentamicin) for infectious tenosynovitis and deep fascial space infections in patients who are allergic to penicillin. To avoid toxicity, current recommendation is to assay vancomycin trough levels after third dose drawn 0.5 h prior to next dosing. Use CrCl to adjust dose in patients with renal impairment.
1 g IV q12h
10 mg/kg IV q6h
Erythema, histaminelike flushing, and anaphylactic reactions may occur when administered with anesthetic agents; taken concurrently with aminoglycosides, risk of nephrotoxicity may increase above that with aminoglycoside monotherapy; effects in neuromuscular blockade may be enhanced when coadministered with nondepolarizing muscle relaxants
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in renal failure; neutropenia; red man syndrome is caused by IV infusion that is too rapid (dose administered over a few min) but rarely happens when dose administered as 2-h administration or as PO/IP administration; red man syndrome is not an allergic reaction
Aminoglycoside antibiotic used for gram-negative bacterial coverage. Used commonly in combination with both an agent against gram-positive organisms and an agent that covers anaerobes. DOC (in conjunction with vancomycin) for infectious tenosynovitis and deep fascial space infections in patients who are allergic to penicillin. Dosing regimens are numerous and are adjusted based on CrCl and changes in volume of distribution.
1 mg/kg IV/IM q8h or 5-7 mg/kg IV/IM q24h
2.5 mg/kg IV/IM q8h
Coadministration with other aminoglycosides, cephalosporins, penicillins, and amphotericin B may increase nephrotoxicity; aminoglycosides enhance effects of neuromuscular blocking agents, thus prolonged respiratory depression may occur; coadministration with loop diuretics may increase auditory toxicity of aminoglycosides; possible irreversible hearing loss of varying degrees may occur (monitor regularly)
Documented hypersensitivity; non–dialysis-dependent renal insufficiency
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Narrow therapeutic index (not intended for long-term therapy); caution in renal failure (not on dialysis), myasthenia gravis, hypocalcemia, and conditions that depress neuromuscular transmission; adjust dose in renal impairment
These agents are used to induce and boost active immunity.
Used to induce active immunity against tetanus in selected patients. Immunizing agents of choice for most adults and children >7 y are tetanus and diphtheria toxoids. Necessary to administer booster doses to maintain tetanus immunity throughout life.
Pregnant patients should receive only tetanus toxoid, not a diphtheria antigen-containing product.
In children and adults, may administer into deltoid or midlateral thigh muscles. In infants, preferred site of administration is mid thigh laterally.
Primary immunization: 0.5 mL IM; administer 2 injections 4-8 wk apart; third dose 6-12 mo after second injection
Booster dose: 0.5 mL q10y
Administer as in adults
Patients receiving immunosuppressants, including corticosteroids or radiation therapy, may remain susceptible despite immunization because of poor immune response; cimetidine may enhance or augment delayed-hypersensitivity responses to skin-test antigens; avoid concurrent use of medication with systemic chloramphenicol because it may impair amnestic response to tetanus toxoid; concurrent use of tetanus immune globulin may delay development of active immunity by several days (interaction is nevertheless clinically insignificant and does not preclude concurrent use)
Documented hypersensitivity; a history of any type of neurologic symptoms or signs following administration of this product; Food and Drug Administration (FDA) recommends that elective tetanus immunization be deferred during any outbreak of poliomyelitis because tetanus toxoid injections are an important cause of provocative poliomyelitis
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use to treat actual tetanus infections or for immediate prophylaxis of unimmunized individuals (use tetanus antitoxin instead, preferably human tetanus immune globulin); diminished antibody response to active immunization may be observed in patients receiving immunosuppressive therapy; better to defer primary diphtheria immunization until immunosuppressive therapy discontinued; routine immunization of symptomatic and asymptomatic HIV-infected persons is recommended
These agents are used in the treatment of chronic paronychia. They have anti-inflammatory properties and cause profound and varied metabolic effects. Corticosteroids modify the body's immune response to diverse stimuli.
An adrenocorticosteroid derivative suitable for application to skin or external mucous membranes. Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability.
Apply sparingly to affected areas bid/qid
Apply as in adults
None reported
Documented hypersensitivity; viral, fungal, and bacterial skin infections
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Prolonged use, applying over large surface areas, applying potent steroids, and using occlusive dressings may increase systemic absorption of corticosteroids and may cause Cushing syndrome, reversible HPA-axis suppression, hyperglycemia, and glycosuria
These agents are used in the treatment of chronic paronychia.
Broad-spectrum antifungal agent that inhibits yeast growth by altering cell membrane permeability, causing death of fungal cells. Reevaluate diagnosis if no clinical improvement after 4 wk.
Gently massage into affected area and surrounding skin areas bid for 2-6 wk
Children: Not established
Adolescents: Apply as in adults
None reported
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Not appropriate for treatment of systemic fungal infections; avoid contact with the eyes; if irritation or sensitivity develops, discontinue use and institute appropriate therapy
Kanavel AB. Infections of the Hand. 1939;17-410.
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Wolanyk DE. 17. Infections. In: Hart RG, Uehara DT, Wagner MJ, eds. Emergency and Primary Care of the Hand. Irving,Tx: The American College of Emergency Physicians; 2001:219-246.
hand infection, infections of the hand, paronychia, felon, herpetic whitlow, infectious tenosynovitis, deep fascial space infections, acute paronychia, hangnails, nail biting, manicuring, finger sucking, eponychia, artificial nails, chronic paronychia, metastatic cancer, subungual melanoma, squamous cell cancer, floating nail, subungual abscess, herpes simplex virus infection of the finger, HSV infection of the finger, HSV-1, HSV-2, dorsal subaponeurotic abscess, subfascial web space infection, midpalmar space infection, thenar space infection, Staphylococcus aureus, S aureus, Streptococcus species, Candida albicans, C albicans, atypical mycobacteria, Neisseriagonorrhoeae, N gonorrhoeae, Eikenella corrodens, E corrodens, Pasteurella multocida, P multocida, Capnocytophaga species, frank abscess, osteomyelitis
Rohini Jonnalagadda, MD, Staff Physician, Department of Emergency Medicine, New York University/Bellevue Hospital Center
Rohini Jonnalagadda, MD is a member of the following medical societies: Sigma Xi
Disclosure: Nothing to disclose.
Gregory S Johnston, MD, Assistant Professor, Department of Emergency Medicine, New York University School of Medicine; Chair, Hospital Emergency Preparedness Committee, Bellevue Hospital Center; Consulting Staff, Department of Emergency Medicine, Bellevue Hospital Center, New York University Medical Center, Tisch Hospital, Harbor Veterans Administration Medical Center
Gregory S Johnston, MD is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.
Dan Danzl, MD, Chair, Department of Emergency Medicine, Professor, University of Louisville Hospital
Dan Danzl, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, Kentucky Medical Association, Society for Academic Emergency Medicine, and Wilderness Medical Society
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
Eric L Weiss, MD, DTM&H, Director of Stanford Travel Medicine, Medical Director of Stanford Lifeflight, Assistant Professor, Departments of Emergency Medicine and Infectious Diseases, Stanford University School of Medicine
Eric L Weiss, MD, DTM&H is a member of the following medical societies: American College of Emergency Physicians, American College of Occupational and Environmental Medicine, American Medical Association, American Society of Tropical Medicine and Hygiene, Physicians for Social Responsibility, Southeastern Surgical Congress, Southern Association for Oncology, Southern Clinical Neurological Society, and Wilderness Medical Society
Disclosure: Nothing to disclose.
John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Rick Kulkarni, MD, Assistant Professor of Surgery, Section of Emergency Medicine, Yale-New Haven Hospital
Rick Kulkarni, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: WebMD Salary Employment
The authors and editors of eMedicine gratefully acknowledge the contributions of previous authors, Amy K Rontal, MD, and Heatherlee Bailey, MD, to the development and writing of this article.
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