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Only high-risk close contacts of known cases should receive prophylactic antibiotics, according to the Centers for Disease Control and Prevention (CDC). The CDC defines high-risk as (1) infants who are <12 months, (2) those especially vulnerable to the complications of pertussis, or (3) those, such as health care workers, in close contact with high-risk individuals (strength of recommendation [SOR]: C, based on consensus/expert opinion). Evidence is insufficient to support a benefit of prophylactic antibiotic treatment for all household pertussis contacts to prevent the development or spread of illness (SOR: B, based on a systematic review of studies).
Give special attention to high-risk close contacts, especially infants
Jose Rodriguez, MD
Florida State University College of Medicine, Tallahassee
Recently, in the medical college where I teach, a student came down with pertussis. Several weeks after the onset of symptoms, she was diagnosed and determined to be no longer contagious. When she coughed in class, however, I worried that she could have infected us all. No one received prophylactic antibiotics. To date, I do not know of anyone who was in close contact with this student who has come down with the illness. However, direct special attention to high-risk close contacts, especially infants, as they can have devastating results from infection.
Evidence summary
A Cochrane review1 of antibiotic use for pertussis prophylaxis, including studies published through 2002, found only 2 randomized, well-controlled trials (RCTs) that compared attack rates between contacts receiving placebo or antibiotic therapy. Neither trial included infants under age 6 months. The reviewers concluded that evidence was insufficient to determine a treatment benefit. The larger study2 included 310 household or family contacts, randomized by household to 10 days of erythromycin estolate or placebo. Positive cultures or clinical pertussis developed in 4.8% of treated contacts and 6.1% of controls (relative risk [RR]=0.8; 95% confidence interval [CI], 0.3–2.2). Adverse side effects occurred in 34% of the erythromycin group and 16% of controls (RR=2.2; 95% CI, 1.4–3.3; number needed to harm=5.6).
Focus on those at high risk
Despite the paucity of RCTs, the CDC and other public health agency guidelines recommend postexposure prophylaxis for certain close contacts to protect high-risk individuals, defined as those who could develop severe disease or experience adverse outcomes if pertussis developed.3-6
High-risk individuals include:
- Infants <1 year old
- Pregnant women in their third trimester
- the immunocompromised
- those with underlying medical condition such as chronic lung disease, respiratory insufficiency, or cystic fibrosis
- those who have close contact with any of the above high-risk individuals (eg, household members or health-care workers providing face-to-face care).
Close contact is defined as:
- confinement in a closed space for >1 hour with a known case, or
- direct contact with respiratory, oral, or nasal secretions from a symptomatic person, or
- face-to-face exposure within 3 feet of a symptomatic patient.
TABLE
Recommendations for pertussis prophylaxis
ORGANIZATION | RECOMMENDATION |
---|---|
Canadian guidelines4 | Reserve prophylaxis for:
|
Public Health Seattle and King County5 | Prophylax only high-risk individuals with
|
CDC6 | During institutional outbreaks
|
Clinical trials involving such patients have not been conducted.6,7 Maintenance of active vaccination status is an effective means to prevent the spread of pertussis among the general population and has been suggested as a means to control local outbreaks,6 though it has no role in immediate postexposure prophylaxis for an individual. In one RCT, no (0/60) fully immunized child in a household with pertussis developed whooping cough, with or without antibiotic prophylaxis. Among unimmunized children, pertussis developed in 4/20 receiving erythromycin prophylaxis and 2/11 receiving placebo.
Macrolides (erythromycin, clarithromycin, or azithromycin) are recommended for postexposure prophylaxis. Trimethoprim-sulfamethoxazole is a second-line agent.5 A short course of erythromycin (7 days), azithromycin (3–5 days), or clarithromycin (7 days) is as effective as a 2-week course of erythromycin in eradicating Bordetella pertussis from the nasopharynx.
Recommendations from others
Recommendations from others are in the TABLE.
1. Altunaiji S, Kukuruzovic R, Curtis N, Massie J. Antibiotics for whooping cough (pertussis). Cochrane Database Syst Rev 2005;(1):CDC004404.-
2. Halperin SA, Bortolussi R, Langley JM, Eastwood BJ, De Serres G. A randomized, placebo-controlled trial of erythromycin estolate chemoprophylaxis for household contacts of children with culture-positive bordetella pertussis infection. Pediatrics 1999;104(4):e42.-
3. Dodhia H, Crowcroft NS, Bramley JC, Miller E. UK guidelines for use of erythromycin chemoprophylaxis in persons exposed to pertussis. J Pub Health Med 2002;24:200-206.
4. Recommended antimicrobial agents for the treatment and postexposure prophylaxis of pertussis 2005. Atlanta, Ga: Centers for Disease Control and Prevention. Available at: www.cdc.gov/mmwr/preview/mmwrhtml/rr5414a1.htm?s_cud=rr5414a1_e. Accessed on March 30, 2007.
5. Dodhia H, Miller E. Review of the evidence for the use of erythromycin in the management of persons exposed to pertussis. Epidemiol Infect 1998;120:143-149.
6. Grob PR. Prophylactic erythromycin for whooping-cough contacts. Lancet 1981;1(8223):772.-
7. Tubbs C, Niemi H, Mayo HG, Warren M. What is the best treatment for pertussis? J Fam Pract 2005;54:1096-1098.
Only high-risk close contacts of known cases should receive prophylactic antibiotics, according to the Centers for Disease Control and Prevention (CDC). The CDC defines high-risk as (1) infants who are <12 months, (2) those especially vulnerable to the complications of pertussis, or (3) those, such as health care workers, in close contact with high-risk individuals (strength of recommendation [SOR]: C, based on consensus/expert opinion). Evidence is insufficient to support a benefit of prophylactic antibiotic treatment for all household pertussis contacts to prevent the development or spread of illness (SOR: B, based on a systematic review of studies).
Give special attention to high-risk close contacts, especially infants
Jose Rodriguez, MD
Florida State University College of Medicine, Tallahassee
Recently, in the medical college where I teach, a student came down with pertussis. Several weeks after the onset of symptoms, she was diagnosed and determined to be no longer contagious. When she coughed in class, however, I worried that she could have infected us all. No one received prophylactic antibiotics. To date, I do not know of anyone who was in close contact with this student who has come down with the illness. However, direct special attention to high-risk close contacts, especially infants, as they can have devastating results from infection.
Evidence summary
A Cochrane review1 of antibiotic use for pertussis prophylaxis, including studies published through 2002, found only 2 randomized, well-controlled trials (RCTs) that compared attack rates between contacts receiving placebo or antibiotic therapy. Neither trial included infants under age 6 months. The reviewers concluded that evidence was insufficient to determine a treatment benefit. The larger study2 included 310 household or family contacts, randomized by household to 10 days of erythromycin estolate or placebo. Positive cultures or clinical pertussis developed in 4.8% of treated contacts and 6.1% of controls (relative risk [RR]=0.8; 95% confidence interval [CI], 0.3–2.2). Adverse side effects occurred in 34% of the erythromycin group and 16% of controls (RR=2.2; 95% CI, 1.4–3.3; number needed to harm=5.6).
Focus on those at high risk
Despite the paucity of RCTs, the CDC and other public health agency guidelines recommend postexposure prophylaxis for certain close contacts to protect high-risk individuals, defined as those who could develop severe disease or experience adverse outcomes if pertussis developed.3-6
High-risk individuals include:
- Infants <1 year old
- Pregnant women in their third trimester
- the immunocompromised
- those with underlying medical condition such as chronic lung disease, respiratory insufficiency, or cystic fibrosis
- those who have close contact with any of the above high-risk individuals (eg, household members or health-care workers providing face-to-face care).
Close contact is defined as:
- confinement in a closed space for >1 hour with a known case, or
- direct contact with respiratory, oral, or nasal secretions from a symptomatic person, or
- face-to-face exposure within 3 feet of a symptomatic patient.
TABLE
Recommendations for pertussis prophylaxis
ORGANIZATION | RECOMMENDATION |
---|---|
Canadian guidelines4 | Reserve prophylaxis for:
|
Public Health Seattle and King County5 | Prophylax only high-risk individuals with
|
CDC6 | During institutional outbreaks
|
Clinical trials involving such patients have not been conducted.6,7 Maintenance of active vaccination status is an effective means to prevent the spread of pertussis among the general population and has been suggested as a means to control local outbreaks,6 though it has no role in immediate postexposure prophylaxis for an individual. In one RCT, no (0/60) fully immunized child in a household with pertussis developed whooping cough, with or without antibiotic prophylaxis. Among unimmunized children, pertussis developed in 4/20 receiving erythromycin prophylaxis and 2/11 receiving placebo.
Macrolides (erythromycin, clarithromycin, or azithromycin) are recommended for postexposure prophylaxis. Trimethoprim-sulfamethoxazole is a second-line agent.5 A short course of erythromycin (7 days), azithromycin (3–5 days), or clarithromycin (7 days) is as effective as a 2-week course of erythromycin in eradicating Bordetella pertussis from the nasopharynx.
Recommendations from others
Recommendations from others are in the TABLE.
Only high-risk close contacts of known cases should receive prophylactic antibiotics, according to the Centers for Disease Control and Prevention (CDC). The CDC defines high-risk as (1) infants who are <12 months, (2) those especially vulnerable to the complications of pertussis, or (3) those, such as health care workers, in close contact with high-risk individuals (strength of recommendation [SOR]: C, based on consensus/expert opinion). Evidence is insufficient to support a benefit of prophylactic antibiotic treatment for all household pertussis contacts to prevent the development or spread of illness (SOR: B, based on a systematic review of studies).
Give special attention to high-risk close contacts, especially infants
Jose Rodriguez, MD
Florida State University College of Medicine, Tallahassee
Recently, in the medical college where I teach, a student came down with pertussis. Several weeks after the onset of symptoms, she was diagnosed and determined to be no longer contagious. When she coughed in class, however, I worried that she could have infected us all. No one received prophylactic antibiotics. To date, I do not know of anyone who was in close contact with this student who has come down with the illness. However, direct special attention to high-risk close contacts, especially infants, as they can have devastating results from infection.
Evidence summary
A Cochrane review1 of antibiotic use for pertussis prophylaxis, including studies published through 2002, found only 2 randomized, well-controlled trials (RCTs) that compared attack rates between contacts receiving placebo or antibiotic therapy. Neither trial included infants under age 6 months. The reviewers concluded that evidence was insufficient to determine a treatment benefit. The larger study2 included 310 household or family contacts, randomized by household to 10 days of erythromycin estolate or placebo. Positive cultures or clinical pertussis developed in 4.8% of treated contacts and 6.1% of controls (relative risk [RR]=0.8; 95% confidence interval [CI], 0.3–2.2). Adverse side effects occurred in 34% of the erythromycin group and 16% of controls (RR=2.2; 95% CI, 1.4–3.3; number needed to harm=5.6).
Focus on those at high risk
Despite the paucity of RCTs, the CDC and other public health agency guidelines recommend postexposure prophylaxis for certain close contacts to protect high-risk individuals, defined as those who could develop severe disease or experience adverse outcomes if pertussis developed.3-6
High-risk individuals include:
- Infants <1 year old
- Pregnant women in their third trimester
- the immunocompromised
- those with underlying medical condition such as chronic lung disease, respiratory insufficiency, or cystic fibrosis
- those who have close contact with any of the above high-risk individuals (eg, household members or health-care workers providing face-to-face care).
Close contact is defined as:
- confinement in a closed space for >1 hour with a known case, or
- direct contact with respiratory, oral, or nasal secretions from a symptomatic person, or
- face-to-face exposure within 3 feet of a symptomatic patient.
TABLE
Recommendations for pertussis prophylaxis
ORGANIZATION | RECOMMENDATION |
---|---|
Canadian guidelines4 | Reserve prophylaxis for:
|
Public Health Seattle and King County5 | Prophylax only high-risk individuals with
|
CDC6 | During institutional outbreaks
|
Clinical trials involving such patients have not been conducted.6,7 Maintenance of active vaccination status is an effective means to prevent the spread of pertussis among the general population and has been suggested as a means to control local outbreaks,6 though it has no role in immediate postexposure prophylaxis for an individual. In one RCT, no (0/60) fully immunized child in a household with pertussis developed whooping cough, with or without antibiotic prophylaxis. Among unimmunized children, pertussis developed in 4/20 receiving erythromycin prophylaxis and 2/11 receiving placebo.
Macrolides (erythromycin, clarithromycin, or azithromycin) are recommended for postexposure prophylaxis. Trimethoprim-sulfamethoxazole is a second-line agent.5 A short course of erythromycin (7 days), azithromycin (3–5 days), or clarithromycin (7 days) is as effective as a 2-week course of erythromycin in eradicating Bordetella pertussis from the nasopharynx.
Recommendations from others
Recommendations from others are in the TABLE.
1. Altunaiji S, Kukuruzovic R, Curtis N, Massie J. Antibiotics for whooping cough (pertussis). Cochrane Database Syst Rev 2005;(1):CDC004404.-
2. Halperin SA, Bortolussi R, Langley JM, Eastwood BJ, De Serres G. A randomized, placebo-controlled trial of erythromycin estolate chemoprophylaxis for household contacts of children with culture-positive bordetella pertussis infection. Pediatrics 1999;104(4):e42.-
3. Dodhia H, Crowcroft NS, Bramley JC, Miller E. UK guidelines for use of erythromycin chemoprophylaxis in persons exposed to pertussis. J Pub Health Med 2002;24:200-206.
4. Recommended antimicrobial agents for the treatment and postexposure prophylaxis of pertussis 2005. Atlanta, Ga: Centers for Disease Control and Prevention. Available at: www.cdc.gov/mmwr/preview/mmwrhtml/rr5414a1.htm?s_cud=rr5414a1_e. Accessed on March 30, 2007.
5. Dodhia H, Miller E. Review of the evidence for the use of erythromycin in the management of persons exposed to pertussis. Epidemiol Infect 1998;120:143-149.
6. Grob PR. Prophylactic erythromycin for whooping-cough contacts. Lancet 1981;1(8223):772.-
7. Tubbs C, Niemi H, Mayo HG, Warren M. What is the best treatment for pertussis? J Fam Pract 2005;54:1096-1098.
1. Altunaiji S, Kukuruzovic R, Curtis N, Massie J. Antibiotics for whooping cough (pertussis). Cochrane Database Syst Rev 2005;(1):CDC004404.-
2. Halperin SA, Bortolussi R, Langley JM, Eastwood BJ, De Serres G. A randomized, placebo-controlled trial of erythromycin estolate chemoprophylaxis for household contacts of children with culture-positive bordetella pertussis infection. Pediatrics 1999;104(4):e42.-
3. Dodhia H, Crowcroft NS, Bramley JC, Miller E. UK guidelines for use of erythromycin chemoprophylaxis in persons exposed to pertussis. J Pub Health Med 2002;24:200-206.
4. Recommended antimicrobial agents for the treatment and postexposure prophylaxis of pertussis 2005. Atlanta, Ga: Centers for Disease Control and Prevention. Available at: www.cdc.gov/mmwr/preview/mmwrhtml/rr5414a1.htm?s_cud=rr5414a1_e. Accessed on March 30, 2007.
5. Dodhia H, Miller E. Review of the evidence for the use of erythromycin in the management of persons exposed to pertussis. Epidemiol Infect 1998;120:143-149.
6. Grob PR. Prophylactic erythromycin for whooping-cough contacts. Lancet 1981;1(8223):772.-
7. Tubbs C, Niemi H, Mayo HG, Warren M. What is the best treatment for pertussis? J Fam Pract 2005;54:1096-1098.
Evidence-based answers from the Family Physicians Inquiries Network