Group B streptococcal infection medical therapy: Difference between revisions
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==Overview== | ==Overview== | ||
Group B streptococcal (GBS) infection should be suspected as a causative agent for bacterial meningitis in infants less than two years of age, among whom empirical antibiotic therapy should be initiated immediately.<ref name="pmid15494903">{{cite journal| author=Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM et al.| title=Practice guidelines for the management of bacterial meningitis. | journal=Clin Infect Dis | year= 2004 | volume= 39 | issue= 9 | pages= 1267-84 | pmid=15494903 | doi=10.1086/425368 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15494903 }} </ref> [[Ampicillin]] or [[penicillin]] are recommended for the treatment of confirmed neonatal GBS [[meningitis]].<ref name="pmid15494903">{{cite journal| author=Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM et al.| title=Practice guidelines for the management of bacterial meningitis. | journal=Clin Infect Dis | year= 2004 | volume= 39 | issue= 9 | pages= 1267-84 | pmid=15494903 | doi=10.1086/425368 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15494903 }} </ref> Intrapartum antibiotic treatment should be administered to asymptomatic pregnant women who are carriers of GBS because it provides prophylaxis against the transmission of the infection to the neonate. [[Penicillin]] remains the agent of choice for intrapartum antibiotic prophylaxis, with [[ampicillin]] as an acceptable alternative.<ref name=CDCMMWR>Verani J.R., McGee L, and Schrag S.J. Prevention of Perinatal Group B Streptococcal Disease. Revised Guidelines from CDC, 2010.[http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5910a1.htm?s_cid=rr5910a1_w CDC.gov]</ref> [[Penicillin]] and [[ampicillin]] are generally effective for the treatment of GBS infection in non-pregnant adults.<ref name="pmid11462195">{{cite journal| author=Farley MM| title=Group B streptococcal disease in nonpregnant adults. | journal=Clin Infect Dis | year= 2001 | volume= 33 | issue= 4 | pages= 556-61 | pmid=11462195 | doi=10.1086/322696 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11462195 }} </ref> | |||
==Medical Therapy in Neonatal Meningitis== | ==Medical Therapy in Neonatal Meningitis== | ||
===Empirical Antibiotic Therapy in Neonatal Meningitis=== | ===Empirical Antibiotic Therapy in Neonatal Meningitis=== | ||
GBS should be suspected as a causative agent for bacterial meningitis in infants less than two years of age | Group B streptococcal (GBS) infection should be suspected as a causative agent for bacterial meningitis in infants less than two years of age, among whom empirical antibiotic therapy should be initiated immediately according to the Infectious Diseases Society of America (IDSA) guidelines.<ref name="pmid15494903">{{cite journal| author=Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM et al.| title=Practice guidelines for the management of bacterial meningitis. | journal=Clin Infect Dis | year= 2004 | volume= 39 | issue= 9 | pages= 1267-84 | pmid=15494903 | doi=10.1086/425368 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15494903 }} </ref> | ||
Shown below is a table | Shown below is a table summarizing the choice of empirical medical therapy in neonatal meningitis.<ref name="pmid15494903">{{cite journal| author=Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM et al.| title=Practice guidelines for the management of bacterial meningitis. | journal=Clin Infect Dis | year= 2004 | volume= 39 | issue= 9 | pages= 1267-84 | pmid=15494903 | doi=10.1086/425368 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15494903 }} </ref> | ||
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===Targeted Antibiotic Therapy in Neonatal Meningitis=== | ===Targeted Antibiotic Therapy in GBS Neonatal Meningitis=== | ||
Shown below is a table | Shown below is a table summarizing the choice of targeted medical therapy in neonatal meningitis according to the IDSA guidelines.<ref name="pmid15494903">{{cite journal| author=Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM et al.| title=Practice guidelines for the management of bacterial meningitis. | journal=Clin Infect Dis | year= 2004 | volume= 39 | issue= 9 | pages= 1267-84 | pmid=15494903 | doi=10.1086/425368 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15494903 }} </ref> | ||
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* Positive GBS vaginal-rectal screening culture in late gestation during current pregnancy | * Positive GBS vaginal-rectal screening culture in late gestation during current pregnancy | ||
Intrapartum antibiotic treatment of asymptomatic pregnant women who are carriers of GBS because it provides prophylaxis against the transmission of the infection to the newborn. | Intrapartum antibiotic treatment of asymptomatic pregnant women who are carriers of GBS is recommended because it provides prophylaxis against the transmission of the infection to the newborn. | ||
Intrapartum antibiotic prophylaxis is not indicated in this circumstance if a cesarean delivery is performed before onset of labor on a woman with intact amniotic membranes. | Intrapartum antibiotic prophylaxis is not indicated in this circumstance if a cesarean delivery is performed before onset of labor on a woman with intact amniotic membranes. | ||
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The following are key components of intrapartum antibiotic prophylaxis agents and dosing:<ref name=CDCMMWR>Verani J.R., McGee L, and Schrag S.J. Prevention of Perinatal Group B Streptococcal Disease. Revised Guidelines from CDC, 2010.[http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5910a1.htm?s_cid=rr5910a1_w CDC.gov]</ref> | The following are key components of intrapartum antibiotic prophylaxis agents and dosing:<ref name=CDCMMWR>Verani J.R., McGee L, and Schrag S.J. Prevention of Perinatal Group B Streptococcal Disease. Revised Guidelines from CDC, 2010.[http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5910a1.htm?s_cid=rr5910a1_w CDC.gov]</ref> | ||
* [[Penicillin]] remains the agent of choice for intrapartum antibiotic prophylaxis, with ampicillin as an acceptable alternative ( | * [[Penicillin]] remains the agent of choice for intrapartum antibiotic prophylaxis, with [[ampicillin]] as an acceptable alternative (class A, level of evidence I). | ||
* Penicillin-allergic women who do not have a history of [[anaphylaxis]], [[angioedema]], [[respiratory distress]], or [[urticaria]] following administration of a [[penicillin]] or a [[cephalosporin]] should receive [[cefazolin]] ( | * Penicillin-allergic women who do not have a history of [[anaphylaxis]], [[angioedema]], [[respiratory distress]], or [[urticaria]] following administration of a [[penicillin]] or a [[cephalosporin]] should receive [[cefazolin]] (class B, level of evidence II). | ||
* Antimicrobial susceptibility testing should be ordered for antenatal GBS cultures performed on [[penicillin]]-allergic women at high risk for [[anaphylaxis]] because of a history of [[anaphylaxis]], [[angioedema]], [[respiratory distress]], or [[urticaria]] following administration of a [[penicillin]] or a [[cephalosporin]] (AII). To ensure proper testing, clinicians must inform laboratories of the need for antimicrobial susceptibility testing in such cases ( | * Antimicrobial susceptibility testing should be ordered for antenatal GBS cultures performed on [[penicillin]]-allergic women at high risk for [[anaphylaxis]] because of a history of [[anaphylaxis]], [[angioedema]], [[respiratory distress]], or [[urticaria]] following administration of a [[penicillin]] or a [[cephalosporin]] (AII). To ensure proper testing, clinicians must inform laboratories of the need for antimicrobial susceptibility testing in such cases (class A, level of evidence III). | ||
* Penicillin-allergic women at high risk for [[anaphylaxis]] should receive [[clindamycin]] if their GBS isolate is susceptible to [[clindamycin]] and [[erythromycin]], as determined by antimicrobial susceptibility testing; if the isolate is sensitive to [[clindamycin]] but resistant to [[erythromycin]], [[clindamycin]] may be used if testing for inducible [[clindamycin]] resistance is negative (CIII). Penicillin-allergic women at high risk for [[anaphylaxis]] should receive [[vancomycin]] if their isolate is intrinsically resistant to [[clindamycin]] as determined by antimicrobial susceptibility testing, if the isolate demonstrates inducible resistance to [[clindamycin]], or if susceptibility to both agents is unknown ( | * Penicillin-allergic women at high risk for [[anaphylaxis]] should receive [[clindamycin]] if their GBS isolate is susceptible to [[clindamycin]] and [[erythromycin]], as determined by antimicrobial susceptibility testing; if the isolate is sensitive to [[clindamycin]] but resistant to [[erythromycin]], [[clindamycin]] may be used if testing for inducible [[clindamycin]] resistance is negative (CIII). Penicillin-allergic women at high risk for [[anaphylaxis]] should receive [[vancomycin]] if their isolate is intrinsically resistant to [[clindamycin]] as determined by antimicrobial susceptibility testing, if the isolate demonstrates inducible resistance to [[clindamycin]], or if susceptibility to both agents is unknown (class C, level of evidence III). | ||
* The recommended dosing regimen of [[penicillin G]] is 5 million units intravenously, followed by 2.5--3.0 million units intravenously every 4 hours ( | * The recommended dosing regimen of [[penicillin G]] is 5 million units intravenously, followed by 2.5--3.0 million units intravenously every 4 hours (class A, level of evidence II). The range of 2.5--3.0 million units is recommended to achieve adequate drug levels in the fetal circulation and amniotic fluid while avoiding [[neurotoxicity]]. The choice of dose within that range should be guided by which formulations of [[penicillin G]] are readily available in order to reduce the need for pharmacies to specially prepare doses. | ||
Shown below is an algorithm depicting the choice of antibiotics for the primary prevention of early-onset GBS neonatal infection based on the 2010 revised CDC guidelines.<ref name=CDCMMWR>Verani J.R., McGee L, and Schrag S.J. Prevention of Perinatal Group B Streptococcal Disease. Revised Guidelines from CDC, 2010.[http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5910a1.htm?s_cid=rr5910a1_w CDC.gov]</ref> | |||
{{Family tree/start}} | |||
{{Family tree | | | A01 | | | A01= <div style="float: left; text-align: left; width: 20em; padding:1em;">'''Is the patient allergic to penicillin?''' </div>}} | |||
{{Family tree | |,|-|^|-|.| | }} | |||
{{Family tree | B01 | | B02 | B01= No| B02= Yes}} | |||
{{Family tree | |!| | | |!| | }} | |||
{{Family tree | C01 | | C02 | C01= <div style="float: left; text-align: left; width: 20em; padding:1em;">[[Penicillin G]], 5 million units IV initial dose, <br> then 2.5-3.0 million units every 4 hours until delivery<br><br> OR<br> <br> [[Ampicillin]], 2 g IV initial dose, <br> then 1 g IV every 8 hours until delivery </div>| C02= <div style="float: left; text-align: left; width: 20em; padding:1em;">'''Does the patient a history of any of the following after receiving penicillin or cephalosporin?''' <br> [[Anaphylaxis]] <br> [[Angioedema]] <br> [[Respiratory distress]] <br> [[Urticaria]] </div>}} | |||
{{Family tree | | | |,|-|^|-|.| | }} | |||
{{Family tree | | | D01 | | D02 | D01= No| D02= Yes}} | |||
{{Family tree | | | |!| | | |!| | }} | |||
{{Family tree | | | E01 | | E02 | E01= <div style="float: left; text-align: left; width: 20em; padding:1em;">[[Cefazolin]], 2 g IV initial dose, <br> then 1 g IV every 8 hours until delivery </div>| E02= <div style="float: left; text-align: left; width: 20em; padding:1em;">'''Is the isolate susceptible to [[clindamycin]] and [[erythromycin]]?''' </div>}} | |||
{{Family tree | | | | |,|-|-|^|.| | }} | |||
{{Family tree | | | | F01 | | F02 | F01= No| F02= Yes}} | |||
{{Family tree | | | | |!| | | |!| | }} | |||
{{Family tree | | | | G01 | | G02 | G01= <div style="float: left; text-align: left; width: 20em; padding:1em;">[[Vancomycin]], 1 g IV every 12 hours until delivery </div>| G02= <div style="float: left; text-align: left; width: 20em; padding:1em;">[[Clindamycin]], 900 mg IV every 8 hours until delivery </div>}} | |||
{{Family tree/end}} | |||
===Chorioamnionitis=== | ===Chorioamnionitis=== | ||
The treatment of [[chorioamnionitis]] requires the immediate administration of antibiotics until delivery. In addition, antipyretics must be administered. | The treatment of [[chorioamnionitis]] requires the immediate administration of broad spectrum antibiotics until delivery. In addition, antipyretics must be administered.<ref name="pmid20569811">{{cite journal| author=Tita AT, Andrews WW| title=Diagnosis and management of clinical chorioamnionitis. | journal=Clin Perinatol | year= 2010 | volume= 37 | issue= 2 | pages= 339-54 | pmid=20569811 | doi=10.1016/j.clp.2010.02.003 | pmc=PMC3008318 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20569811 }} </ref> | ||
The broad spectrum antibiotics regimen, particularly among pregnant women who were administered prophylactic intrapartum penicillin G for GBS, includes:<ref name="pmid20569811">{{cite journal| author=Tita AT, Andrews WW| title=Diagnosis and management of clinical chorioamnionitis. | journal=Clin Perinatol | year= 2010 | volume= 37 | issue= 2 | pages= 339-54 | pmid=20569811 | doi=10.1016/j.clp.2010.02.003 | pmc=PMC3008318 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20569811 }} </ref> | |||
* [[Ampicillin]] 2 g every 6 hours, PLUS | |||
* [[Gentamicin]] 1.5 mg/kg every 8-24 hours | |||
If the patient is undergoing C-section, the following antibiotics must be added to the initial broad spectrum antibiotics to cover for [[anaerobe]]s: | |||
* [[Clindamycin]] 900 mg IV, OR | |||
* [[Metronidazole]] 500 mg IV<ref name="pmid15495005">{{cite journal| author=French LM, Smaill FM| title=Antibiotic regimens for endometritis after delivery. | journal=Cochrane Database Syst Rev | year= 2004 | volume= | issue= 4 | pages= CD001067 | pmid=15495005 | doi=10.1002/14651858.CD001067.pub2 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15495005 }} </ref> | |||
==Medical Therapy in Adults== | |||
[[Penicillin]] and [[ampicillin]] are generally effective for the treatment of GBS infection in non pregnant adults; however, it is best that the antibiotic treatment is guided by the susceptibility testing results. The duration of antibiotic therapy should be a minimum of 2 weeks but longer duration of treatment should be attempted in fulminant infections.<ref name="pmid11462195">{{cite journal| author=Farley MM| title=Group B streptococcal disease in nonpregnant adults. | journal=Clin Infect Dis | year= 2001 | volume= 33 | issue= 4 | pages= 556-61 | pmid=11462195 | doi=10.1086/322696 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11462195 }} </ref> | |||
[[Gentamicin]] might be considered as an addition to the initial antibiotic regimens.<ref name="pmid11462195">{{cite journal| author=Farley MM| title=Group B streptococcal disease in nonpregnant adults. | journal=Clin Infect Dis | year= 2001 | volume= 33 | issue= 4 | pages= 556-61 | pmid=11462195 | doi=10.1086/322696 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11462195 }} </ref> | |||
The dose of antibiotics might be higher than that in other types of infection, particularly in [[meningitis]].<ref name="pmid11462195">{{cite journal| author=Farley MM| title=Group B streptococcal disease in nonpregnant adults. | journal=Clin Infect Dis | year= 2001 | volume= 33 | issue= 4 | pages= 556-61 | pmid=11462195 | doi=10.1086/322696 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11462195 }} </ref> | |||
==References== | ==References== | ||
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[[Category:Streptococcaceae]] | [[Category:Streptococcaceae]] | ||
[[Category:Obstetrics]] | [[Category:Obstetrics]] | ||
[[Category:Mature chapter]] | [[Category:Mature chapter]] | ||
[[Category:Pediatrics]] | |||
[[Category:Neonatology]] | |||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} |
Latest revision as of 17:51, 18 September 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rim Halaby, M.D. [2]
Overview
Group B streptococcal (GBS) infection should be suspected as a causative agent for bacterial meningitis in infants less than two years of age, among whom empirical antibiotic therapy should be initiated immediately.[1] Ampicillin or penicillin are recommended for the treatment of confirmed neonatal GBS meningitis.[1] Intrapartum antibiotic treatment should be administered to asymptomatic pregnant women who are carriers of GBS because it provides prophylaxis against the transmission of the infection to the neonate. Penicillin remains the agent of choice for intrapartum antibiotic prophylaxis, with ampicillin as an acceptable alternative.[2] Penicillin and ampicillin are generally effective for the treatment of GBS infection in non-pregnant adults.[3]
Medical Therapy in Neonatal Meningitis
Empirical Antibiotic Therapy in Neonatal Meningitis
Group B streptococcal (GBS) infection should be suspected as a causative agent for bacterial meningitis in infants less than two years of age, among whom empirical antibiotic therapy should be initiated immediately according to the Infectious Diseases Society of America (IDSA) guidelines.[1]
Shown below is a table summarizing the choice of empirical medical therapy in neonatal meningitis.[1]
Age | Possible pathogens causing the bacterial meningitis | Empirical treatment |
< 1 month | Ampicillin + cefotaxime OR Ampicillin + aminoglycoside | |
1-23 months | Vancomycin + third generation cephalosporin |
Targeted Antibiotic Therapy in GBS Neonatal Meningitis
Shown below is a table summarizing the choice of targeted medical therapy in neonatal meningitis according to the IDSA guidelines.[1]
Recommended therapy for GBS meningitis | Alternative therapy for GBS meningitis |
Ampicillin OR Penicillin Consider adding an aminoglycoside |
Third generation cephalosporin (Ceftriaxone or cefotaxime) |
Recommended Dosage of Antibiotics
Shown below is a table summarizing the recommended dosage of antibiotics according to the IDSA guidelines.[1]
Antibiotic agent | Dosage |
Amikacin | 0-7 days: 15-20 mg/kg
8-28 days: 30 mg/kg Infants > 28 days: 20-30 mg/kg |
Ampicillin | 0-7 days: 150 mg/kg
8-28 days: 200 mg/kg Infants > 28 days: 300 mg/kg |
Cefotaxime | 0-7 days: 100-150 mg/kg
8-28 days: 150-200 mg/kg Infants > 28 days: 225-300 mg/kg |
Ceftazidime | 0-7 days: 100-150 mg/kg
8-28 days: 150 mg/kg Infants > 28 days: 150 mg/kg |
Ceftriaxone | Infants > 28 days: 80-100 mg/kg |
Gentamicin | 0-7 days: 5 mg/kg
8-28 days: 7.5 mg/kg Infants > 28 days: 7.5 mg/kg |
Penicillin G | 0-7 days: 0.15 mg/kg
8-28 days: 0.2 mg/kg Infants > 28 days: 0.3 mg/kg |
Tobramycin | 0-7 days: 5 mg/kg
8-28 days: 7.5 mg/kg Infants > 28 days: 7.5 mg/kg |
Vancomycin | 0-7 days: 20-30 mg/kg
8-28 days: 30-45 mg/kg Infants > 28 days: 60 mg/kg |
Consider lower dosages and longer intervals of antibiotics in case of very low-birth weight neonates.
Medical Therapy for Pregnant Women
Asymptomatic Carriers
Treatment for GBS is indicated in cases of:
- GBS bacteriuria during any trimester of the current pregnancy
- Positive GBS vaginal-rectal screening culture in late gestation during current pregnancy
Intrapartum antibiotic treatment of asymptomatic pregnant women who are carriers of GBS is recommended because it provides prophylaxis against the transmission of the infection to the newborn.
Intrapartum antibiotic prophylaxis is not indicated in this circumstance if a cesarean delivery is performed before onset of labor on a woman with intact amniotic membranes.
The following are key components of intrapartum antibiotic prophylaxis agents and dosing:[2]
- Penicillin remains the agent of choice for intrapartum antibiotic prophylaxis, with ampicillin as an acceptable alternative (class A, level of evidence I).
- Penicillin-allergic women who do not have a history of anaphylaxis, angioedema, respiratory distress, or urticaria following administration of a penicillin or a cephalosporin should receive cefazolin (class B, level of evidence II).
- Antimicrobial susceptibility testing should be ordered for antenatal GBS cultures performed on penicillin-allergic women at high risk for anaphylaxis because of a history of anaphylaxis, angioedema, respiratory distress, or urticaria following administration of a penicillin or a cephalosporin (AII). To ensure proper testing, clinicians must inform laboratories of the need for antimicrobial susceptibility testing in such cases (class A, level of evidence III).
- Penicillin-allergic women at high risk for anaphylaxis should receive clindamycin if their GBS isolate is susceptible to clindamycin and erythromycin, as determined by antimicrobial susceptibility testing; if the isolate is sensitive to clindamycin but resistant to erythromycin, clindamycin may be used if testing for inducible clindamycin resistance is negative (CIII). Penicillin-allergic women at high risk for anaphylaxis should receive vancomycin if their isolate is intrinsically resistant to clindamycin as determined by antimicrobial susceptibility testing, if the isolate demonstrates inducible resistance to clindamycin, or if susceptibility to both agents is unknown (class C, level of evidence III).
- The recommended dosing regimen of penicillin G is 5 million units intravenously, followed by 2.5--3.0 million units intravenously every 4 hours (class A, level of evidence II). The range of 2.5--3.0 million units is recommended to achieve adequate drug levels in the fetal circulation and amniotic fluid while avoiding neurotoxicity. The choice of dose within that range should be guided by which formulations of penicillin G are readily available in order to reduce the need for pharmacies to specially prepare doses.
Shown below is an algorithm depicting the choice of antibiotics for the primary prevention of early-onset GBS neonatal infection based on the 2010 revised CDC guidelines.[2]
Is the patient allergic to penicillin? | |||||||||||||||||||||
No | Yes | ||||||||||||||||||||
Penicillin G, 5 million units IV initial dose, then 2.5-3.0 million units every 4 hours until delivery OR Ampicillin, 2 g IV initial dose, then 1 g IV every 8 hours until delivery | Does the patient a history of any of the following after receiving penicillin or cephalosporin? Anaphylaxis Angioedema Respiratory distress Urticaria | ||||||||||||||||||||
No | Yes | ||||||||||||||||||||
Cefazolin, 2 g IV initial dose, then 1 g IV every 8 hours until delivery | Is the isolate susceptible to clindamycin and erythromycin? | ||||||||||||||||||||
No | Yes | ||||||||||||||||||||
Vancomycin, 1 g IV every 12 hours until delivery | Clindamycin, 900 mg IV every 8 hours until delivery | ||||||||||||||||||||
Chorioamnionitis
The treatment of chorioamnionitis requires the immediate administration of broad spectrum antibiotics until delivery. In addition, antipyretics must be administered.[4]
The broad spectrum antibiotics regimen, particularly among pregnant women who were administered prophylactic intrapartum penicillin G for GBS, includes:[4]
- Ampicillin 2 g every 6 hours, PLUS
- Gentamicin 1.5 mg/kg every 8-24 hours
If the patient is undergoing C-section, the following antibiotics must be added to the initial broad spectrum antibiotics to cover for anaerobes:
- Clindamycin 900 mg IV, OR
- Metronidazole 500 mg IV[5]
Medical Therapy in Adults
Penicillin and ampicillin are generally effective for the treatment of GBS infection in non pregnant adults; however, it is best that the antibiotic treatment is guided by the susceptibility testing results. The duration of antibiotic therapy should be a minimum of 2 weeks but longer duration of treatment should be attempted in fulminant infections.[3]
Gentamicin might be considered as an addition to the initial antibiotic regimens.[3]
The dose of antibiotics might be higher than that in other types of infection, particularly in meningitis.[3]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Tunkel AR, Hartman BJ, Kaplan SL, Kaufman BA, Roos KL, Scheld WM; et al. (2004). "Practice guidelines for the management of bacterial meningitis". Clin Infect Dis. 39 (9): 1267–84. doi:10.1086/425368. PMID 15494903.
- ↑ 2.0 2.1 2.2 Verani J.R., McGee L, and Schrag S.J. Prevention of Perinatal Group B Streptococcal Disease. Revised Guidelines from CDC, 2010.CDC.gov
- ↑ 3.0 3.1 3.2 3.3 Farley MM (2001). "Group B streptococcal disease in nonpregnant adults". Clin Infect Dis. 33 (4): 556–61. doi:10.1086/322696. PMID 11462195.
- ↑ 4.0 4.1 Tita AT, Andrews WW (2010). "Diagnosis and management of clinical chorioamnionitis". Clin Perinatol. 37 (2): 339–54. doi:10.1016/j.clp.2010.02.003. PMC 3008318. PMID 20569811.
- ↑ French LM, Smaill FM (2004). "Antibiotic regimens for endometritis after delivery". Cochrane Database Syst Rev (4): CD001067. doi:10.1002/14651858.CD001067.pub2. PMID 15495005.