To enlist: Possible causative agents for meningitis and neonatal/infant meningitis. Concept introduction: Inflammation of meninges is known as meningitis which is an example of anatomical syndrome. Several types of microorganisms are responsible for meningitis and all of them produce similar set of symptoms. Bacteria cause serious form of acute meningitis, however, it is believed that it is caused by previous infection with viruses. Different microorganisms cause meningitis in neonates.

Question

Want to see the full answer?

Answer 1

Question

Chapter 19.3, Problem 4AYP

Summary Introduction

To enlist:

Possible causative agents for meningitis and neonatal/infant meningitis.

Concept introduction:

Inflammation of meninges is known as meningitis which is an example of anatomical syndrome. Several types of microorganisms are responsible for meningitis and all of them produce similar set of symptoms. Bacteria cause serious form of acute meningitis, however, it is believed that it is caused by previous infection with viruses. Different microorganisms cause meningitis in neonates.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Outline a method for using apomixis to maintain feminized CannabisAssume apomixis is controlled by a single dominant gene. You can choose the type of apomixis: obligate or facultative, gametophytic or sporophytic. Discuss advantages and disadvantages of your proposed method.

Kinetics: One-Compartment First-Order Absorption 1. In vivo testing provides valuable insight into a drug’s kinetics. Assessing drug kinetics following multiple routes of administration provides greater insight than a single route of administration alone. The following data was collected in 250-g rats following bolus IV, oral (PO), and intraperitoneal (ip) administration. Using this data and set of graphs, determine:(calculate for each variable) (a) k, C0, V, and AUC* for the bolus iv data (b) k, ka, B1, and AUC* for the po data c) k, ka, B1, and AUC* for the ip data (d) relative bioavailability for po vs ip, Fpo/Fip (e)absolute ip bioavailability, Fip (f) absolute po bioavailability, Fpo

3. A promising new drug is being evaluated in human trials. Based on preliminary human tests, this drug is most effective when plasma levels exceed 30 mg/L. Measurements from preliminary tests indicate the following human pharmacokinetic parameter values: t1/2,elim = 4.6hr, t1/2,abs = 0.34hr, VD = 0.29 L/kg, Foral = 72%. Based on these parameters, estimate the following if a 49 kg woman were to receive a 1000mg oral dose of this drug: (a) Estimate the plasma concentration of the drug at 1hr, 6 hr, and 20hr after taking the drug ( Concentration estimate) (b) Estimate the time for maximum plasma concentration (tmax). (c) Estimate the maximum plasma concentration (Cmax). (d) Estimate the time at which the plasma level first rises above 30 mg/L. (Note this is a trial and error problem where you must guess a time, plug it into the concentration equation, and determine if it is close to 30 mg/L. Hint: based on part (a) it should be apparent that the answer is less than 1hr.) (e)…